Katie Piper Top 100 Instagram Photos and Posts

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Most liked photo of Katie Piper with over 756.5K likes is the following photo

Most liked Instagram photo of Katie Piper
We have around 101 most liked photos of Katie Piper with the thumbnails listed below. Click on any of them to view the full image along with its caption, like count, and a button to download the photo.

Katie Piper Instagram - Age is a gift, not everyone is given. So with that, Happy 40th Birthday to me 🎂

📷: @zakwalton
Katie Piper Instagram - Sometimes the only thing you have control over is perspective and we’re all guilty of seeing the bad in things before the good. 

We’re all on incredibly different paths, so the good in someone else’s life, might not be what you’d see as good in your own. 

It’s a really interesting exercise to write down things that you see as negatives and turn them in to something good. Take time to view your own life, in a way that benefits you, because you’re the only one that’s living it.

I’ll be talking more about this in my broadcast channel, you can join in my bio 🤍
Katie Piper Instagram - A little life update 🌸 

🇺🇸 Spent 3 weeks in the US recently, travelling and meeting inspiring people and hearing stories that have been on my mind ever since, cant wait to share those with you.
👧 That also meant 3 weeks away from the kids, which I forget every time how hard that is, especially with a time difference, so tried to leave little notes for them to open whilst I was away so they felt connected to me.
👨‍👩‍👧‍👧 Feeling privileged to spend special times in the sun with family, the girls are growing up so much and their bond together is amazing to watch.
📝 I’ve been trying to come back to quotes I’ve saved in times I question what’s happening in life and what’s on the brain today is “Flow - don’t force”, I’m reading that as “embrace what’s happening around you and make it work in your favour, rather than pushing things where they maybe shouldn’t go.”
Katie Piper Instagram - After many years battling with my eye health, I’ve reached the end of road somewhat, and the decision has been made to try a prosthetic eye shell. 

This marks the start of a journey to have an artificial eye, with an incredible medical team behind me. As always I’m incredibly grateful to all those in the NHS and private health care system for their talent and kindness.

I will share my journey, I’m hopeful and nervous about being able tolerate it and would love to hear from any of you in the comments if you’ve been on this journey or have any advice…
Katie Piper Instagram - After many years battling with my eye health, I’ve reached the end of road somewhat, and the decision has been made to try a prosthetic eye shell. 

This marks the start of a journey to have an artificial eye, with an incredible medical team behind me. As always I’m incredibly grateful to all those in the NHS and private health care system for their talent and kindness.

I will share my journey, I’m hopeful and nervous about being able tolerate it and would love to hear from any of you in the comments if you’ve been on this journey or have any advice…
Katie Piper Instagram - I met my younger self for coffee today… I realised she spent all of her time worrying about problems that weren’t really there, when life was carefree and fun, until it wasn’t anymore. I reassured her that she’ll get through the dark times that are ahead, darker than she’d ever imagine, but toward a light brighter than she’d have thought too. To arrive at a place where worry is a wasted emotion, because from life, to almost death and back again, she is strong, independent and powerful.
Katie Piper Instagram - No hair, no makeup, just enjoying the moment 💖
Katie Piper Instagram - No hair, no makeup, just enjoying the moment 💖
Katie Piper Instagram - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!
Katie Piper Instagram - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!
Katie Piper Instagram - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!
Katie Piper Instagram - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!
Katie Piper Instagram - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!
Katie Piper Instagram - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - Back to reality 🎬 paradise will have to wait for now!
Katie Piper Instagram - We can never know what’s going on in peoples lives, but we should continue to show them care and respect regardless. Wishing the Princess of Wales well and a strong recovery in private 💛
Katie Piper Instagram - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷
Katie Piper Instagram - Merry Christmas and happy holidays everyone! 😍 We were woke up at what felt like 1am by the girls (it was still pitch black outside, lets put it that way) but they were SO excited for Santa to have been and that’s my favourite part of Christmas, seeing them so excited and capturing those memories of them together (my other favourite part, is FINALLY the end of elf on the shelf, that elf might be little but he’s a lot of work inventing new scenarios for him every night) 🥲

Sending love from our family to yours, and I hope you all have a lovely day 🥰
Katie Piper Instagram - Merry Christmas and happy holidays everyone! 😍 We were woke up at what felt like 1am by the girls (it was still pitch black outside, lets put it that way) but they were SO excited for Santa to have been and that’s my favourite part of Christmas, seeing them so excited and capturing those memories of them together (my other favourite part, is FINALLY the end of elf on the shelf, that elf might be little but he’s a lot of work inventing new scenarios for him every night) 🥲

Sending love from our family to yours, and I hope you all have a lovely day 🥰
Katie Piper Instagram - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Katie Piper Instagram - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Katie Piper Instagram - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Katie Piper Instagram - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Katie Piper Instagram - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Katie Piper Instagram - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Katie Piper Instagram - Growing up so fast! When one of them is only 10 and basically taller than me 🥺 special moments on our family holiday 💕
Katie Piper Instagram - Growing up so fast! When one of them is only 10 and basically taller than me 🥺 special moments on our family holiday 💕
Katie Piper Instagram - Growing up so fast! When one of them is only 10 and basically taller than me 🥺 special moments on our family holiday 💕
Katie Piper Instagram - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏
Katie Piper Instagram - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏
Katie Piper Instagram - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏
Katie Piper Instagram - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏
Katie Piper Instagram - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏
Katie Piper Instagram - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏
Katie Piper Instagram - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏
Katie Piper Instagram - 48 years of marriage 🌹 

It’s my parents wedding anniversary today and I asked them how do you get that number in a marriage. It was a short sweet reply: 

“Patience and understanding, play deaf sometimes”

Happy Anni mum and dad 🩷
Katie Piper Instagram - 48 years of marriage 🌹 

It’s my parents wedding anniversary today and I asked them how do you get that number in a marriage. It was a short sweet reply: 

“Patience and understanding, play deaf sometimes”

Happy Anni mum and dad 🩷
Katie Piper Instagram - 48 years of marriage 🌹 

It’s my parents wedding anniversary today and I asked them how do you get that number in a marriage. It was a short sweet reply: 

“Patience and understanding, play deaf sometimes”

Happy Anni mum and dad 🩷
Katie Piper Instagram - The epidemic of abuse, violence against women continues in plain sight. 
Women being killed and raped in the most extreme ways and children being abused. Reading headlines reporting on Rebecca Cheptegei murder.
 ‘Olympian dies after being set on fire with petrol’… erasing the terrible act of pre-meditated murder that she endured.

Watching the strength, courage and bravery of Gisele Pelicot has moved me, as she attended court this week, waived her right to anonymity to stand against her abuser, her husband, who over the course of 10 years drugged her and invited 51 men to violently rape her. But was not allowed to use the word “rape” in court.

I know from my work with @womens_aid that sadly these stories are no less prevalent behind closed doors. Women attacked, killed, their children murdered by people known to them, beaten and raped, women are not safe.
Katie Piper Instagram - Saved recently ✨#affirmations
Katie Piper Instagram - Saved recently ✨#affirmations
Katie Piper Instagram - Saved recently ✨#affirmations
Katie Piper Instagram - Saved recently ✨#affirmations
Katie Piper Instagram - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Katie Piper Instagram - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Katie Piper Instagram - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Katie Piper Instagram - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Katie Piper Instagram - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Katie Piper Instagram - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Katie Piper Instagram - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Katie Piper Instagram - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Katie Piper Instagram - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Katie Piper Instagram - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Katie Piper Instagram - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Katie Piper Instagram - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Katie Piper Instagram - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Katie Piper Instagram - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Katie Piper Instagram - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper Instagram - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Katie Piper - 756.5K Likes - Age is a gift, not everyone is given. So with that, Happy 40th Birthday to me 🎂

📷: @zakwalton

756.5K Likes – Katie Piper Instagram

Caption : Age is a gift, not everyone is given. So with that, Happy 40th Birthday to me 🎂 📷: @zakwalton
Likes : 756500
Katie Piper - 172.5K Likes - Sometimes the only thing you have control over is perspective and we’re all guilty of seeing the bad in things before the good. 

We’re all on incredibly different paths, so the good in someone else’s life, might not be what you’d see as good in your own. 

It’s a really interesting exercise to write down things that you see as negatives and turn them in to something good. Take time to view your own life, in a way that benefits you, because you’re the only one that’s living it.

I’ll be talking more about this in my broadcast channel, you can join in my bio 🤍

172.5K Likes – Katie Piper Instagram

Caption : Sometimes the only thing you have control over is perspective and we’re all guilty of seeing the bad in things before the good. We’re all on incredibly different paths, so the good in someone else’s life, might not be what you’d see as good in your own. It’s a really interesting exercise to write down things that you see as negatives and turn them in to something good. Take time to view your own life, in a way that benefits you, because you’re the only one that’s living it. I’ll be talking more about this in my broadcast channel, you can join in my bio 🤍
Likes : 172468
Katie Piper - 85.4K Likes - A little life update 🌸 

🇺🇸 Spent 3 weeks in the US recently, travelling and meeting inspiring people and hearing stories that have been on my mind ever since, cant wait to share those with you.
👧 That also meant 3 weeks away from the kids, which I forget every time how hard that is, especially with a time difference, so tried to leave little notes for them to open whilst I was away so they felt connected to me.
👨‍👩‍👧‍👧 Feeling privileged to spend special times in the sun with family, the girls are growing up so much and their bond together is amazing to watch.
📝 I’ve been trying to come back to quotes I’ve saved in times I question what’s happening in life and what’s on the brain today is “Flow - don’t force”, I’m reading that as “embrace what’s happening around you and make it work in your favour, rather than pushing things where they maybe shouldn’t go.”

85.4K Likes – Katie Piper Instagram

Caption : A little life update 🌸 🇺🇸 Spent 3 weeks in the US recently, travelling and meeting inspiring people and hearing stories that have been on my mind ever since, cant wait to share those with you. 👧 That also meant 3 weeks away from the kids, which I forget every time how hard that is, especially with a time difference, so tried to leave little notes for them to open whilst I was away so they felt connected to me. 👨‍👩‍👧‍👧 Feeling privileged to spend special times in the sun with family, the girls are growing up so much and their bond together is amazing to watch. 📝 I’ve been trying to come back to quotes I’ve saved in times I question what’s happening in life and what’s on the brain today is “Flow – don’t force”, I’m reading that as “embrace what’s happening around you and make it work in your favour, rather than pushing things where they maybe shouldn’t go.”
Likes : 85426
Katie Piper - 64.3K Likes - After many years battling with my eye health, I’ve reached the end of road somewhat, and the decision has been made to try a prosthetic eye shell. 

This marks the start of a journey to have an artificial eye, with an incredible medical team behind me. As always I’m incredibly grateful to all those in the NHS and private health care system for their talent and kindness.

I will share my journey, I’m hopeful and nervous about being able tolerate it and would love to hear from any of you in the comments if you’ve been on this journey or have any advice…

64.3K Likes – Katie Piper Instagram

Caption : After many years battling with my eye health, I’ve reached the end of road somewhat, and the decision has been made to try a prosthetic eye shell. This marks the start of a journey to have an artificial eye, with an incredible medical team behind me. As always I’m incredibly grateful to all those in the NHS and private health care system for their talent and kindness. I will share my journey, I’m hopeful and nervous about being able tolerate it and would love to hear from any of you in the comments if you’ve been on this journey or have any advice…
Likes : 64298
Katie Piper - 64.3K Likes - After many years battling with my eye health, I’ve reached the end of road somewhat, and the decision has been made to try a prosthetic eye shell. 

This marks the start of a journey to have an artificial eye, with an incredible medical team behind me. As always I’m incredibly grateful to all those in the NHS and private health care system for their talent and kindness.

I will share my journey, I’m hopeful and nervous about being able tolerate it and would love to hear from any of you in the comments if you’ve been on this journey or have any advice…

64.3K Likes – Katie Piper Instagram

Caption : After many years battling with my eye health, I’ve reached the end of road somewhat, and the decision has been made to try a prosthetic eye shell. This marks the start of a journey to have an artificial eye, with an incredible medical team behind me. As always I’m incredibly grateful to all those in the NHS and private health care system for their talent and kindness. I will share my journey, I’m hopeful and nervous about being able tolerate it and would love to hear from any of you in the comments if you’ve been on this journey or have any advice…
Likes : 64298
Katie Piper - 64.1K Likes - I met my younger self for coffee today… I realised she spent all of her time worrying about problems that weren’t really there, when life was carefree and fun, until it wasn’t anymore. I reassured her that she’ll get through the dark times that are ahead, darker than she’d ever imagine, but toward a light brighter than she’d have thought too. To arrive at a place where worry is a wasted emotion, because from life, to almost death and back again, she is strong, independent and powerful.

64.1K Likes – Katie Piper Instagram

Caption : I met my younger self for coffee today… I realised she spent all of her time worrying about problems that weren’t really there, when life was carefree and fun, until it wasn’t anymore. I reassured her that she’ll get through the dark times that are ahead, darker than she’d ever imagine, but toward a light brighter than she’d have thought too. To arrive at a place where worry is a wasted emotion, because from life, to almost death and back again, she is strong, independent and powerful.
Likes : 64127
Katie Piper - 54.3K Likes - No hair, no makeup, just enjoying the moment 💖

54.3K Likes – Katie Piper Instagram

Caption : No hair, no makeup, just enjoying the moment 💖
Likes : 54301
Katie Piper - 54.3K Likes - No hair, no makeup, just enjoying the moment 💖

54.3K Likes – Katie Piper Instagram

Caption : No hair, no makeup, just enjoying the moment 💖
Likes : 54301
Katie Piper - 42.4K Likes - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!

42.4K Likes – Katie Piper Instagram

Caption : Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 Celebrating another year of life for the man that have given so many people their lives back!
Likes : 42372
Katie Piper - 42.4K Likes - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!

42.4K Likes – Katie Piper Instagram

Caption : Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 Celebrating another year of life for the man that have given so many people their lives back!
Likes : 42372
Katie Piper - 42.4K Likes - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!

42.4K Likes – Katie Piper Instagram

Caption : Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 Celebrating another year of life for the man that have given so many people their lives back!
Likes : 42372
Katie Piper - 42.4K Likes - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!

42.4K Likes – Katie Piper Instagram

Caption : Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 Celebrating another year of life for the man that have given so many people their lives back!
Likes : 42372
Katie Piper - 42.4K Likes - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!

42.4K Likes – Katie Piper Instagram

Caption : Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 Celebrating another year of life for the man that have given so many people their lives back!
Likes : 42372
Katie Piper - 42.4K Likes - Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 
Celebrating another year of life for the man that have given so many people their lives back!

42.4K Likes – Katie Piper Instagram

Caption : Happy Birthday to the G.O.A.T, a man who has helped me more times than I can remember over the years, my doctor @drmohammadajawad 🎂 Celebrating another year of life for the man that have given so many people their lives back!
Likes : 42372
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 28.3K Likes - Back to reality 🎬 paradise will have to wait for now!

28.3K Likes – Katie Piper Instagram

Caption : Back to reality 🎬 paradise will have to wait for now!
Likes : 28264
Katie Piper - 22.7K Likes - We can never know what’s going on in peoples lives, but we should continue to show them care and respect regardless. Wishing the Princess of Wales well and a strong recovery in private 💛

22.7K Likes – Katie Piper Instagram

Caption : We can never know what’s going on in peoples lives, but we should continue to show them care and respect regardless. Wishing the Princess of Wales well and a strong recovery in private 💛
Likes : 22718
Katie Piper - 19.3K Likes - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

19.3K Likes – Katie Piper Instagram

Caption : Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 19315
Katie Piper - 19.3K Likes - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

19.3K Likes – Katie Piper Instagram

Caption : Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 19315
Katie Piper - 19.3K Likes - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

19.3K Likes – Katie Piper Instagram

Caption : Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 19315
Katie Piper - 19.3K Likes - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

19.3K Likes – Katie Piper Instagram

Caption : Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 19315
Katie Piper - 19.3K Likes - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

19.3K Likes – Katie Piper Instagram

Caption : Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 19315
Katie Piper - 19.3K Likes - Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

19.3K Likes – Katie Piper Instagram

Caption : Last few shots, because I haven’t stopped thinking about this dress since I wore it last week 🥹🤍 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 19315
Katie Piper - 17.5K Likes - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

17.5K Likes – Katie Piper Instagram

Caption : Not your average Monday….Red carpet ready 💋 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 17513
Katie Piper - 17.5K Likes - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

17.5K Likes – Katie Piper Instagram

Caption : Not your average Monday….Red carpet ready 💋 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 17513
Katie Piper - 17.5K Likes - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

17.5K Likes – Katie Piper Instagram

Caption : Not your average Monday….Red carpet ready 💋 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 17513
Katie Piper - 17.5K Likes - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

17.5K Likes – Katie Piper Instagram

Caption : Not your average Monday….Red carpet ready 💋 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 17513
Katie Piper - 17.5K Likes - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

17.5K Likes – Katie Piper Instagram

Caption : Not your average Monday….Red carpet ready 💋 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 17513
Katie Piper - 17.5K Likes - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

17.5K Likes – Katie Piper Instagram

Caption : Not your average Monday….Red carpet ready 💋 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 17513
Katie Piper - 17.5K Likes - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

17.5K Likes – Katie Piper Instagram

Caption : Not your average Monday….Red carpet ready 💋 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 17513
Katie Piper - 17.5K Likes - Not your average Monday….Red carpet ready 💋

Photography by @zakwalton
Styled by @harrietnicolsonstylist 
Makeup by @toby_salvietto 
Hair by @hairbychrislong 
Nails by @nailsbychloej using @biosculpturegelgb 

Dress @elizabethemanuelofficial
Shoes @sophiawebster
Bag @mae_cassidy
Jewellery @aariya_diamonds

17.5K Likes – Katie Piper Instagram

Caption : Not your average Monday….Red carpet ready 💋 Photography by @zakwalton Styled by @harrietnicolsonstylist Makeup by @toby_salvietto Hair by @hairbychrislong Nails by @nailsbychloej using @biosculpturegelgb Dress @elizabethemanuelofficial Shoes @sophiawebster Bag @mae_cassidy Jewellery @aariya_diamonds
Likes : 17513
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17.3K Likes - Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon - what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. 

Ive never experienced such a special place like this 🩷

17.3K Likes – Katie Piper Instagram

Caption : Happy 40th birthday Richie ❤️🥳Celebrating the new decade at the @shangrilalondon – what a place to turn 40! ✨Thank you to every single person who made the day so wonderful. Ive never experienced such a special place like this 🩷
Likes : 17256
Katie Piper - 17K Likes - Merry Christmas and happy holidays everyone! 😍 We were woke up at what felt like 1am by the girls (it was still pitch black outside, lets put it that way) but they were SO excited for Santa to have been and that’s my favourite part of Christmas, seeing them so excited and capturing those memories of them together (my other favourite part, is FINALLY the end of elf on the shelf, that elf might be little but he’s a lot of work inventing new scenarios for him every night) 🥲

Sending love from our family to yours, and I hope you all have a lovely day 🥰

17K Likes – Katie Piper Instagram

Caption : Merry Christmas and happy holidays everyone! 😍 We were woke up at what felt like 1am by the girls (it was still pitch black outside, lets put it that way) but they were SO excited for Santa to have been and that’s my favourite part of Christmas, seeing them so excited and capturing those memories of them together (my other favourite part, is FINALLY the end of elf on the shelf, that elf might be little but he’s a lot of work inventing new scenarios for him every night) 🥲 Sending love from our family to yours, and I hope you all have a lovely day 🥰
Likes : 17007
Katie Piper - 17K Likes - Merry Christmas and happy holidays everyone! 😍 We were woke up at what felt like 1am by the girls (it was still pitch black outside, lets put it that way) but they were SO excited for Santa to have been and that’s my favourite part of Christmas, seeing them so excited and capturing those memories of them together (my other favourite part, is FINALLY the end of elf on the shelf, that elf might be little but he’s a lot of work inventing new scenarios for him every night) 🥲

Sending love from our family to yours, and I hope you all have a lovely day 🥰

17K Likes – Katie Piper Instagram

Caption : Merry Christmas and happy holidays everyone! 😍 We were woke up at what felt like 1am by the girls (it was still pitch black outside, lets put it that way) but they were SO excited for Santa to have been and that’s my favourite part of Christmas, seeing them so excited and capturing those memories of them together (my other favourite part, is FINALLY the end of elf on the shelf, that elf might be little but he’s a lot of work inventing new scenarios for him every night) 🥲 Sending love from our family to yours, and I hope you all have a lovely day 🥰
Likes : 17007
Katie Piper - 16.8K Likes - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”

16.8K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it. Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare. People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them. I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime. At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am. Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice. There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet – and nobody should be made to feel like they don’t belong here. Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Likes : 16793
Katie Piper - 16.8K Likes - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”

16.8K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it. Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare. People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them. I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime. At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am. Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice. There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet – and nobody should be made to feel like they don’t belong here. Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Likes : 16793
Katie Piper - 16.8K Likes - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”

16.8K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it. Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare. People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them. I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime. At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am. Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice. There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet – and nobody should be made to feel like they don’t belong here. Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Likes : 16793
Katie Piper - 16.8K Likes - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”

16.8K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it. Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare. People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them. I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime. At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am. Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice. There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet – and nobody should be made to feel like they don’t belong here. Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Likes : 16793
Katie Piper - 16.8K Likes - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”

16.8K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it. Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare. People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them. I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime. At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am. Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice. There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet – and nobody should be made to feel like they don’t belong here. Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Likes : 16793
Katie Piper - 16.8K Likes - Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it.

Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare.

People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them.

I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime.

At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am.

Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice.

There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet - and nobody should be made to feel like they don’t belong here.

Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”

16.8K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @vmrory1993, he says “I’m Rory, I’m 30, and I was born with a birthmark called a venous malformation on my upper lip and right cheek, which I had around 20 operations on when I was younger to reduce the size of it. Growing up I had to endure a great deal of prejudice and mental abuse which by the time I had reached my teenage years had completely shattered my confidence. I was very shy and felt like I was living a never ending nightmare. People told me that I was ugly. People told me that they would kill themselves if they looked like me. People told me I would never achieve certain things in life, and because my confidence was so low I started to believe them. I have now achieved everything that people told me that I wouldn’t, and more. With strength and positivity I have completely overcome the adversity I’ve faced in the past, and I want to show everyone that you can get through any low points that you might experience in your lifetime. At one point I thought I was always going to be unhappy and shy, but here I am now happier and more confident than I ever thought I would be.I have even turned down the opportunity for further surgery to make my face ‘symmetrical’ because I am happy the way that I am. Prejudice is a horrible thing, and nobody should ever be judged or subjected to abuse purely because of what they look like, their race, their sexuality or any other reason. There are people who have been killed due to prejudice, there are people who end their own lives due to prejudice. There are people who aren’t comfortable in their own skin, all because of the prejudice that they have to face which is absolutely heart breaking. We live in a very multi cultural and diverse planet – and nobody should be made to feel like they don’t belong here. Diversity is a beautiful thing, which should be celebrated and I am determined to continue do my best to help and inspire others. Never judge a book by its cover.”
Likes : 16793
Katie Piper - 16.5K Likes - Growing up so fast! When one of them is only 10 and basically taller than me 🥺 special moments on our family holiday 💕

16.5K Likes – Katie Piper Instagram

Caption : Growing up so fast! When one of them is only 10 and basically taller than me 🥺 special moments on our family holiday 💕
Likes : 16508
Katie Piper - 16.5K Likes - Growing up so fast! When one of them is only 10 and basically taller than me 🥺 special moments on our family holiday 💕

16.5K Likes – Katie Piper Instagram

Caption : Growing up so fast! When one of them is only 10 and basically taller than me 🥺 special moments on our family holiday 💕
Likes : 16508
Katie Piper - 16.5K Likes - Growing up so fast! When one of them is only 10 and basically taller than me 🥺 special moments on our family holiday 💕

16.5K Likes – Katie Piper Instagram

Caption : Growing up so fast! When one of them is only 10 and basically taller than me 🥺 special moments on our family holiday 💕
Likes : 16508
Katie Piper - 16K Likes - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏

16K Likes – Katie Piper Instagram

Caption : Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time. I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids is such a gift 🙏
Likes : 15984
Katie Piper - 16K Likes - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏

16K Likes – Katie Piper Instagram

Caption : Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time. I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids is such a gift 🙏
Likes : 15984
Katie Piper - 16K Likes - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏

16K Likes – Katie Piper Instagram

Caption : Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time. I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids is such a gift 🙏
Likes : 15984
Katie Piper - 16K Likes - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏

16K Likes – Katie Piper Instagram

Caption : Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time. I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids is such a gift 🙏
Likes : 15984
Katie Piper - 16K Likes - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏

16K Likes – Katie Piper Instagram

Caption : Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time. I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids is such a gift 🙏
Likes : 15984
Katie Piper - 16K Likes - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏

16K Likes – Katie Piper Instagram

Caption : Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time. I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids is such a gift 🙏
Likes : 15984
Katie Piper - 16K Likes - Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time.  I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids  is such a gift 🙏

16K Likes – Katie Piper Instagram

Caption : Rest, Relaxation and Family Time with my entire family has been much needed and just how I love to spend my down time. I never take these moments for granted. Getting together with my siblings, parents and getting all of the cousins together and watch them play and grow up together just like we once did as kids is such a gift 🙏
Likes : 15984
Katie Piper - 14.4K Likes - 48 years of marriage 🌹 

It’s my parents wedding anniversary today and I asked them how do you get that number in a marriage. It was a short sweet reply: 

“Patience and understanding, play deaf sometimes”

Happy Anni mum and dad 🩷

14.4K Likes – Katie Piper Instagram

Caption : 48 years of marriage 🌹 It’s my parents wedding anniversary today and I asked them how do you get that number in a marriage. It was a short sweet reply: “Patience and understanding, play deaf sometimes” Happy Anni mum and dad 🩷
Likes : 14429
Katie Piper - 14.4K Likes - 48 years of marriage 🌹 

It’s my parents wedding anniversary today and I asked them how do you get that number in a marriage. It was a short sweet reply: 

“Patience and understanding, play deaf sometimes”

Happy Anni mum and dad 🩷

14.4K Likes – Katie Piper Instagram

Caption : 48 years of marriage 🌹 It’s my parents wedding anniversary today and I asked them how do you get that number in a marriage. It was a short sweet reply: “Patience and understanding, play deaf sometimes” Happy Anni mum and dad 🩷
Likes : 14429
Katie Piper - 14.4K Likes - 48 years of marriage 🌹 

It’s my parents wedding anniversary today and I asked them how do you get that number in a marriage. It was a short sweet reply: 

“Patience and understanding, play deaf sometimes”

Happy Anni mum and dad 🩷

14.4K Likes – Katie Piper Instagram

Caption : 48 years of marriage 🌹 It’s my parents wedding anniversary today and I asked them how do you get that number in a marriage. It was a short sweet reply: “Patience and understanding, play deaf sometimes” Happy Anni mum and dad 🩷
Likes : 14429
Katie Piper - 14.2K Likes - The epidemic of abuse, violence against women continues in plain sight. 
Women being killed and raped in the most extreme ways and children being abused. Reading headlines reporting on Rebecca Cheptegei murder.
 ‘Olympian dies after being set on fire with petrol’… erasing the terrible act of pre-meditated murder that she endured.

Watching the strength, courage and bravery of Gisele Pelicot has moved me, as she attended court this week, waived her right to anonymity to stand against her abuser, her husband, who over the course of 10 years drugged her and invited 51 men to violently rape her. But was not allowed to use the word “rape” in court.

I know from my work with @womens_aid that sadly these stories are no less prevalent behind closed doors. Women attacked, killed, their children murdered by people known to them, beaten and raped, women are not safe.

14.2K Likes – Katie Piper Instagram

Caption : The epidemic of abuse, violence against women continues in plain sight. Women being killed and raped in the most extreme ways and children being abused. Reading headlines reporting on Rebecca Cheptegei murder. ‘Olympian dies after being set on fire with petrol’… erasing the terrible act of pre-meditated murder that she endured. Watching the strength, courage and bravery of Gisele Pelicot has moved me, as she attended court this week, waived her right to anonymity to stand against her abuser, her husband, who over the course of 10 years drugged her and invited 51 men to violently rape her. But was not allowed to use the word “rape” in court. I know from my work with @womens_aid that sadly these stories are no less prevalent behind closed doors. Women attacked, killed, their children murdered by people known to them, beaten and raped, women are not safe.
Likes : 14179
Katie Piper - 11.4K Likes - Saved recently ✨#affirmations

11.4K Likes – Katie Piper Instagram

Caption : Saved recently ✨#affirmations
Likes : 11409
Katie Piper - 11.4K Likes - Saved recently ✨#affirmations

11.4K Likes – Katie Piper Instagram

Caption : Saved recently ✨#affirmations
Likes : 11409
Katie Piper - 11.4K Likes - Saved recently ✨#affirmations

11.4K Likes – Katie Piper Instagram

Caption : Saved recently ✨#affirmations
Likes : 11409
Katie Piper - 11.4K Likes - Saved recently ✨#affirmations

11.4K Likes – Katie Piper Instagram

Caption : Saved recently ✨#affirmations
Likes : 11409
Katie Piper - 11.2K Likes - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”

11.2K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for. Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Likes : 11238
Katie Piper - 11.2K Likes - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”

11.2K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for. Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Likes : 11238
Katie Piper - 11.2K Likes - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”

11.2K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for. Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Likes : 11238
Katie Piper - 11.2K Likes - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”

11.2K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for. Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Likes : 11238
Katie Piper - 11.2K Likes - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”

11.2K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for. Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Likes : 11238
Katie Piper - 11.2K Likes - Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. 

I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. 

My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for.

Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. 

I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. 
My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”

11.2K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @stomachick.x_x, she says “In 2014 at just 21, an age I nearly didn’t make it past. I endured one of the hardest times and I’ve gone through for major life saving & life changing surgery for an ileostomy stoma bag due to a rare life-threatening bowel disease known as Hirschsprung’s. I also have multiple other complex conditions/ disabilities. I was told my bowel was packing up & was no longer working as it should to keep me alive. I spent most of my teens in & out of hospital, on tons of different medications, painkillers & endless laxatives. Even trialing medication that weren’t out yet and dealing with a tonne of different debilitating symptoms, from not opening my bowels for five months, extreme bloating weight/blood loss, nausea/vomiting & excruciating pain & more. My surgery was complex & 5 days later I was rushed back in & nearly died due to a perforated & twisted bowel, sepsis, & multiple other complications which I required multiple IV meds, tubes NG/ feeding & blood transfusions for. Being chronically disabled has resulted in me having a lot of surgery & tons of procedures in the last 10 years. Loss of organs & my ability to have children naturally & potentially at all. I recently had my 13th surgery which was during my IVF treatment. Which has sadly failed. I still deal with a lot with my health & I’m on morphine daily. But going through extensive trauma at such a young age has shown me how precious life is & having your health can be. My Stoma saved my life, I will always continue to try to erase the stigma around ostomy bags & invisible illnesses, as well as showing my true beautiful self.”
Likes : 11238
Katie Piper - 10.6K Likes - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”

10.6K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features. Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting. People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love. I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Likes : 10637
Katie Piper - 10.6K Likes - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”

10.6K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features. Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting. People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love. I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Likes : 10637
Katie Piper - 10.6K Likes - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”

10.6K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features. Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting. People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love. I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Likes : 10637
Katie Piper - 10.6K Likes - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”

10.6K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features. Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting. People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love. I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Likes : 10637
Katie Piper - 10.6K Likes - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”

10.6K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features. Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting. People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love. I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Likes : 10637
Katie Piper - 10.6K Likes - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”

10.6K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features. Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting. People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love. I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Likes : 10637
Katie Piper - 10.6K Likes - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”

10.6K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features. Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting. People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love. I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Likes : 10637
Katie Piper - 10.6K Likes - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”

10.6K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features. Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting. People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love. I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Likes : 10637
Katie Piper - 10.6K Likes - Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features.

Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting.

People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love.

I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”

10.6K Likes – Katie Piper Instagram

Caption : Todays #MindsetMonday comes from @littlelady2you, “I was born 2 weeks late in Hope Hospital, in 1975. I spent a lot of time in hospital due to several chest infections, one of which lead to pneumonia. Also, I was in the children’s hospital a lot because they didn’t know what was wrong with me, so they said the reason was ‘failure to thrive’. When I was 18 months old, we went to Great Ormond Street Hospital in London to see Professor Tanner, he knew I had Russell Silver Syndrome (RSS) because of my features. Russell-Silver Syndrome is a rare disorder. The main characteristics are poor growth before and after birth and low birth weight. I only weighed 3lbs 8oz when I was born. My head was large compared to the rest of my body: my mum said I looked like ET (you have always got to have humour). Feeding was difficult because I had bad reflux, hypoglycaemia, curving of the pinky finger, a triangular face, a small jaw, and one side of my body was longer than the other. The average female with RSS grows to 4 feet 7 inches; I am only 4 foot 2 inches. From birth until I was about 2 years old, I spent a lot of time in the hospital. At one point, I was in there for 26 weeks when I was 18 months old because I kept vomiting. People can be very patronising and would quite often pat me on the head and say isn’t she cute. By sharing my story, I’m hoping that people will have a better understanding of RSS because everyday in my life I have to put up with people pointing, staring and making comments. I have had people trying to take photos or film me, which I find very rude and upsetting. After school I went to college then met my husband we married then 12 months later we had our son who is now 16 years old. Sadly in 2010 I lost him and became a widow at 35 years old. My son has been a young carer from an early age in his life, I am very proud of him. I hope sharing this helps people have a better understanding of RSS and see it doesn’t hold me back, I wouldn’t let it. I am in a job I love. I have great family & friends that support me. RSS is who I am so I wouldn’t want to change that, let’s be kind to each other.”
Likes : 10637
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996
Katie Piper - 10K Likes - BRB at @bafta ✨

Styling: @beckyfashionstylist 
Dress: @arcinaori 
Necklace: @officialfaberge 
Photography: @zakwalton 
Makeup: @toby_salvietto 
Hair: @hairbychrislong 

Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️

10K Likes – Katie Piper Instagram

Caption : BRB at @bafta ✨ Styling: @beckyfashionstylist Dress: @arcinaori Necklace: @officialfaberge Photography: @zakwalton Makeup: @toby_salvietto Hair: @hairbychrislong Thank you @parkplaza for the views ✨and @bafta @pandocruises for a perfect evening ❣️
Likes : 9996