💞 POWER OF MYTH. Self portraits in my bedroom
💞
.
Link to interview on all things @lovecrafthbo in bio
💞 POWER OF MYTH. Self portraits in my bedroom
💞
.
Link to interview on all things @lovecrafthbo in bio
💞 POWER OF MYTH. Self portraits in my bedroom
💞
.
Link to interview on all things @lovecrafthbo in bio
💗 “And it’s inside myself that I must create someone who will understand….It is because I dove into the abyss that I am beginning to love the abyss I am made of.” – Clarice Lispector 💗
💗❤️ Do some self love tomorrow and buy #periodpower. it’s the stuff they keep from us that makes us feel crazy. 💗❤️
💗 “And it’s inside myself that I must create someone who will understand….It is because I dove into the abyss that I am beginning to love the abyss I am made of.” – Clarice Lispector 💗
💗❤️ Do some self love tomorrow and buy #periodpower. it’s the stuff they keep from us that makes us feel crazy. 💗❤️
💗 “And it’s inside myself that I must create someone who will understand….It is because I dove into the abyss that I am beginning to love the abyss I am made of.” – Clarice Lispector 💗
💗❤️ Do some self love tomorrow and buy #periodpower. it’s the stuff they keep from us that makes us feel crazy. 💗❤️
💗 “And it’s inside myself that I must create someone who will understand….It is because I dove into the abyss that I am beginning to love the abyss I am made of.” – Clarice Lispector 💗
💗❤️ Do some self love tomorrow and buy #periodpower. it’s the stuff they keep from us that makes us feel crazy. 💗❤️
💗 “And it’s inside myself that I must create someone who will understand….It is because I dove into the abyss that I am beginning to love the abyss I am made of.” – Clarice Lispector 💗
💗❤️ Do some self love tomorrow and buy #periodpower. it’s the stuff they keep from us that makes us feel crazy. 💗❤️
🌸 💕💘 What an honor to the attend the endometriosis foundation of America’s 15th annual #blossomball 🌸
💕
I felt emotional and inspired being in a room full of people who are fighting for #endometriosis patients all over the world.
🌸
Not only is this event an incredible fundraiser, but a way to continue sharing endometriosis stories.
🌸
Thank you to @collinastrada for fitting me like a fairy 🧚🏼♂️🌸 @paristexas_it for my 6 inch heels 👠 and to @misha212 and @davidvoncannon for my glam 💘
🌸
If you’d like to help support @EndoFound’s mission of increasing disease recognition, providing education & advocacy and funding landmark #endometriosis research, please consider donating at the link in my bio!
🌸💕💘🌸💕💘🌸💕💘
🌸 💕💘 What an honor to the attend the endometriosis foundation of America’s 15th annual #blossomball 🌸
💕
I felt emotional and inspired being in a room full of people who are fighting for #endometriosis patients all over the world.
🌸
Not only is this event an incredible fundraiser, but a way to continue sharing endometriosis stories.
🌸
Thank you to @collinastrada for fitting me like a fairy 🧚🏼♂️🌸 @paristexas_it for my 6 inch heels 👠 and to @misha212 and @davidvoncannon for my glam 💘
🌸
If you’d like to help support @EndoFound’s mission of increasing disease recognition, providing education & advocacy and funding landmark #endometriosis research, please consider donating at the link in my bio!
🌸💕💘🌸💕💘🌸💕💘
🌸 💕💘 What an honor to the attend the endometriosis foundation of America’s 15th annual #blossomball 🌸
💕
I felt emotional and inspired being in a room full of people who are fighting for #endometriosis patients all over the world.
🌸
Not only is this event an incredible fundraiser, but a way to continue sharing endometriosis stories.
🌸
Thank you to @collinastrada for fitting me like a fairy 🧚🏼♂️🌸 @paristexas_it for my 6 inch heels 👠 and to @misha212 and @davidvoncannon for my glam 💘
🌸
If you’d like to help support @EndoFound’s mission of increasing disease recognition, providing education & advocacy and funding landmark #endometriosis research, please consider donating at the link in my bio!
🌸💕💘🌸💕💘🌸💕💘
🌸 💕💘 What an honor to the attend the endometriosis foundation of America’s 15th annual #blossomball 🌸
💕
I felt emotional and inspired being in a room full of people who are fighting for #endometriosis patients all over the world.
🌸
Not only is this event an incredible fundraiser, but a way to continue sharing endometriosis stories.
🌸
Thank you to @collinastrada for fitting me like a fairy 🧚🏼♂️🌸 @paristexas_it for my 6 inch heels 👠 and to @misha212 and @davidvoncannon for my glam 💘
🌸
If you’d like to help support @EndoFound’s mission of increasing disease recognition, providing education & advocacy and funding landmark #endometriosis research, please consider donating at the link in my bio!
🌸💕💘🌸💕💘🌸💕💘
🌸 💕💘 What an honor to the attend the endometriosis foundation of America’s 15th annual #blossomball 🌸
💕
I felt emotional and inspired being in a room full of people who are fighting for #endometriosis patients all over the world.
🌸
Not only is this event an incredible fundraiser, but a way to continue sharing endometriosis stories.
🌸
Thank you to @collinastrada for fitting me like a fairy 🧚🏼♂️🌸 @paristexas_it for my 6 inch heels 👠 and to @misha212 and @davidvoncannon for my glam 💘
🌸
If you’d like to help support @EndoFound’s mission of increasing disease recognition, providing education & advocacy and funding landmark #endometriosis research, please consider donating at the link in my bio!
🌸💕💘🌸💕💘🌸💕💘
💕 For the March issue of @vogueaustralia I was given the opportunity to sit down with @hannahroserose and talk about my experience with endometriosis for the first time.
Endometriosis isn’t just a heavy bleed or bad blood. It’s an insidious disease that creeps around a woman’s insides and grows roots in places that should be voids. It turns soft parts hard and calloused and confuses simple lines of communication inside the body. As most chronic illness goes, endometriosis can impact your entire life and hurt not only yourself but the people you love.
For 15 years I was told my symptoms did not fit the “criteria” for an endometriosis diagnosis simply because my periods were not heavy. Unfortunately due to the lack of knowledge in the medical field, this is the norm as It takes women, on average, 7 to 10 years to be diagnosed.
Thank you to Aussie vogue for giving me the platform to talk about something that is too often left in the dark and for Hannah who listened with intrigue and kindness.
I was lucky to have a good man and a good dog who refused to leave my side post op and continue to do so.
For some references on where to get more information, these handles are great
@thatendogoddess
@endometriosisaustralia
@endometriosis.uk
@endofound
@alexachung wrote a fantastic article published in @britishvogue about her own experience, and endoblack.org is a great website advocating for women of colour with endometriosis.
The link to my article is up there in my bio and free to read on the @vogueaustralia site.
💕
#endometriosis
💕
💕 For the March issue of @vogueaustralia I was given the opportunity to sit down with @hannahroserose and talk about my experience with endometriosis for the first time.
Endometriosis isn’t just a heavy bleed or bad blood. It’s an insidious disease that creeps around a woman’s insides and grows roots in places that should be voids. It turns soft parts hard and calloused and confuses simple lines of communication inside the body. As most chronic illness goes, endometriosis can impact your entire life and hurt not only yourself but the people you love.
For 15 years I was told my symptoms did not fit the “criteria” for an endometriosis diagnosis simply because my periods were not heavy. Unfortunately due to the lack of knowledge in the medical field, this is the norm as It takes women, on average, 7 to 10 years to be diagnosed.
Thank you to Aussie vogue for giving me the platform to talk about something that is too often left in the dark and for Hannah who listened with intrigue and kindness.
I was lucky to have a good man and a good dog who refused to leave my side post op and continue to do so.
For some references on where to get more information, these handles are great
@thatendogoddess
@endometriosisaustralia
@endometriosis.uk
@endofound
@alexachung wrote a fantastic article published in @britishvogue about her own experience, and endoblack.org is a great website advocating for women of colour with endometriosis.
The link to my article is up there in my bio and free to read on the @vogueaustralia site.
💕
#endometriosis
💕
💕 For the March issue of @vogueaustralia I was given the opportunity to sit down with @hannahroserose and talk about my experience with endometriosis for the first time.
Endometriosis isn’t just a heavy bleed or bad blood. It’s an insidious disease that creeps around a woman’s insides and grows roots in places that should be voids. It turns soft parts hard and calloused and confuses simple lines of communication inside the body. As most chronic illness goes, endometriosis can impact your entire life and hurt not only yourself but the people you love.
For 15 years I was told my symptoms did not fit the “criteria” for an endometriosis diagnosis simply because my periods were not heavy. Unfortunately due to the lack of knowledge in the medical field, this is the norm as It takes women, on average, 7 to 10 years to be diagnosed.
Thank you to Aussie vogue for giving me the platform to talk about something that is too often left in the dark and for Hannah who listened with intrigue and kindness.
I was lucky to have a good man and a good dog who refused to leave my side post op and continue to do so.
For some references on where to get more information, these handles are great
@thatendogoddess
@endometriosisaustralia
@endometriosis.uk
@endofound
@alexachung wrote a fantastic article published in @britishvogue about her own experience, and endoblack.org is a great website advocating for women of colour with endometriosis.
The link to my article is up there in my bio and free to read on the @vogueaustralia site.
💕
#endometriosis
💕
💕 For the March issue of @vogueaustralia I was given the opportunity to sit down with @hannahroserose and talk about my experience with endometriosis for the first time.
Endometriosis isn’t just a heavy bleed or bad blood. It’s an insidious disease that creeps around a woman’s insides and grows roots in places that should be voids. It turns soft parts hard and calloused and confuses simple lines of communication inside the body. As most chronic illness goes, endometriosis can impact your entire life and hurt not only yourself but the people you love.
For 15 years I was told my symptoms did not fit the “criteria” for an endometriosis diagnosis simply because my periods were not heavy. Unfortunately due to the lack of knowledge in the medical field, this is the norm as It takes women, on average, 7 to 10 years to be diagnosed.
Thank you to Aussie vogue for giving me the platform to talk about something that is too often left in the dark and for Hannah who listened with intrigue and kindness.
I was lucky to have a good man and a good dog who refused to leave my side post op and continue to do so.
For some references on where to get more information, these handles are great
@thatendogoddess
@endometriosisaustralia
@endometriosis.uk
@endofound
@alexachung wrote a fantastic article published in @britishvogue about her own experience, and endoblack.org is a great website advocating for women of colour with endometriosis.
The link to my article is up there in my bio and free to read on the @vogueaustralia site.
💕
#endometriosis
💕
💕 For the March issue of @vogueaustralia I was given the opportunity to sit down with @hannahroserose and talk about my experience with endometriosis for the first time.
Endometriosis isn’t just a heavy bleed or bad blood. It’s an insidious disease that creeps around a woman’s insides and grows roots in places that should be voids. It turns soft parts hard and calloused and confuses simple lines of communication inside the body. As most chronic illness goes, endometriosis can impact your entire life and hurt not only yourself but the people you love.
For 15 years I was told my symptoms did not fit the “criteria” for an endometriosis diagnosis simply because my periods were not heavy. Unfortunately due to the lack of knowledge in the medical field, this is the norm as It takes women, on average, 7 to 10 years to be diagnosed.
Thank you to Aussie vogue for giving me the platform to talk about something that is too often left in the dark and for Hannah who listened with intrigue and kindness.
I was lucky to have a good man and a good dog who refused to leave my side post op and continue to do so.
For some references on where to get more information, these handles are great
@thatendogoddess
@endometriosisaustralia
@endometriosis.uk
@endofound
@alexachung wrote a fantastic article published in @britishvogue about her own experience, and endoblack.org is a great website advocating for women of colour with endometriosis.
The link to my article is up there in my bio and free to read on the @vogueaustralia site.
💕
#endometriosis
💕
💕 For the March issue of @vogueaustralia I was given the opportunity to sit down with @hannahroserose and talk about my experience with endometriosis for the first time.
Endometriosis isn’t just a heavy bleed or bad blood. It’s an insidious disease that creeps around a woman’s insides and grows roots in places that should be voids. It turns soft parts hard and calloused and confuses simple lines of communication inside the body. As most chronic illness goes, endometriosis can impact your entire life and hurt not only yourself but the people you love.
For 15 years I was told my symptoms did not fit the “criteria” for an endometriosis diagnosis simply because my periods were not heavy. Unfortunately due to the lack of knowledge in the medical field, this is the norm as It takes women, on average, 7 to 10 years to be diagnosed.
Thank you to Aussie vogue for giving me the platform to talk about something that is too often left in the dark and for Hannah who listened with intrigue and kindness.
I was lucky to have a good man and a good dog who refused to leave my side post op and continue to do so.
For some references on where to get more information, these handles are great
@thatendogoddess
@endometriosisaustralia
@endometriosis.uk
@endofound
@alexachung wrote a fantastic article published in @britishvogue about her own experience, and endoblack.org is a great website advocating for women of colour with endometriosis.
The link to my article is up there in my bio and free to read on the @vogueaustralia site.
💕
#endometriosis
💕
💕 For the March issue of @vogueaustralia I was given the opportunity to sit down with @hannahroserose and talk about my experience with endometriosis for the first time.
Endometriosis isn’t just a heavy bleed or bad blood. It’s an insidious disease that creeps around a woman’s insides and grows roots in places that should be voids. It turns soft parts hard and calloused and confuses simple lines of communication inside the body. As most chronic illness goes, endometriosis can impact your entire life and hurt not only yourself but the people you love.
For 15 years I was told my symptoms did not fit the “criteria” for an endometriosis diagnosis simply because my periods were not heavy. Unfortunately due to the lack of knowledge in the medical field, this is the norm as It takes women, on average, 7 to 10 years to be diagnosed.
Thank you to Aussie vogue for giving me the platform to talk about something that is too often left in the dark and for Hannah who listened with intrigue and kindness.
I was lucky to have a good man and a good dog who refused to leave my side post op and continue to do so.
For some references on where to get more information, these handles are great
@thatendogoddess
@endometriosisaustralia
@endometriosis.uk
@endofound
@alexachung wrote a fantastic article published in @britishvogue about her own experience, and endoblack.org is a great website advocating for women of colour with endometriosis.
The link to my article is up there in my bio and free to read on the @vogueaustralia site.
💕
#endometriosis
💕
💕 For the March issue of @vogueaustralia I was given the opportunity to sit down with @hannahroserose and talk about my experience with endometriosis for the first time.
Endometriosis isn’t just a heavy bleed or bad blood. It’s an insidious disease that creeps around a woman’s insides and grows roots in places that should be voids. It turns soft parts hard and calloused and confuses simple lines of communication inside the body. As most chronic illness goes, endometriosis can impact your entire life and hurt not only yourself but the people you love.
For 15 years I was told my symptoms did not fit the “criteria” for an endometriosis diagnosis simply because my periods were not heavy. Unfortunately due to the lack of knowledge in the medical field, this is the norm as It takes women, on average, 7 to 10 years to be diagnosed.
Thank you to Aussie vogue for giving me the platform to talk about something that is too often left in the dark and for Hannah who listened with intrigue and kindness.
I was lucky to have a good man and a good dog who refused to leave my side post op and continue to do so.
For some references on where to get more information, these handles are great
@thatendogoddess
@endometriosisaustralia
@endometriosis.uk
@endofound
@alexachung wrote a fantastic article published in @britishvogue about her own experience, and endoblack.org is a great website advocating for women of colour with endometriosis.
The link to my article is up there in my bio and free to read on the @vogueaustralia site.
💕
#endometriosis
💕
📷 @miloflips 🖤
📷 @miloflips 🖤
For her latest starring role in Kevin Costner’s multimillion dollar American Civil War epic #Horizon, @abbeylee learnt to ride a horse and more than holds her own against the Oscar-winning actor and director. And she did it all while living with debilitating private pain. In her digital cover story, the actor and model speaks for the first time about coming out the other side of a 15 year battle with endometriosis. “I’ve got a lot of reasons to stop and a lot of reasons why it would be too hard. A lot of reasons to give up,” she tells @hannahroserose in the digital cover interview. “But there’s something in me that keeps wanting to drive forward… You’ve got one life, don’t you?” Read the full digital cover story at the link in bio.
@AbbeyLee wears @Prada and @TiffanyandCo. Photography @maxpapendieck, stylist @kaila.matthews, story @hannahroserose, hair @sophierobertshair, make-up @gillielove, set design: @natturnbull, EP & talent direction @rikki_keene, production @charlottemelissarose