What a bloody week… You came a bit earlier than we expected and gave me the worst post op constipation that i nearly had to phone the samaratins but my god you are perfect. I cannot thank @deliverysuitegrh enough. The way you looked after us through such a scary time was above and beyond. you are all bloody superstars. I am so blessed Welcome to the world little Benji, ya nutter Born 06/06/24
I was setting up the video to do a Christmas dance and I stepped on an upturned plug.
Christmas is coming
Yeah suck on that penguin
Tag someone to let them know you’re missing them over the Xmas period
SHAG MARRY AVOID
HARRY POTTER EDITION
SHAG the Weasley twins… naughty ginger bastards
MARRY weird caretaker bloke so he can put a few shelves and hang my new telly up on the wall
AVOID wormtail because he has clammy hands and would probably love bomb me at the beginning of our relationship with shit teddies that you get from the fair
Your answers please
Am I going to go to hell for this? For all those asking, little Benji is doing brilliantly. Hes putting on so much weight and is our little miracle ❤️❤️❤️
Am I going to go to hell for this? For all those asking, little Benji is doing brilliantly. Hes putting on so much weight and is our little miracle ❤️❤️❤️
Am I going to go to hell for this? For all those asking, little Benji is doing brilliantly. Hes putting on so much weight and is our little miracle ❤️❤️❤️
SHAG MARRY AVOID
Shag les Battersby, coz I reckon he’d really try in bed
Marry Ian beale for financial security
Avoid cain dingle cos he’s a fucking nasty bastard whod be trying to play footsie with my mum under the table at our wedding
Your answers please
Finally found the lyrics to emmerdale….
had no idea my daughter was standing behind me 🤣🤣🤣🤣🤐
Literally me at the euros. @ukgods
For today and today only , I am trying to raise as much money as I can for the charity BXM inspired,
A charity that provides funding for children and young people whose parents are unable to afford to send them on outdoor educational trips. I was often unable to go on school trips as a child as my parents couldn’t afford it. It is awful that any child should miss out.
BXM also run lots of carefully developed programs for young people, Raising aspirations and combatting mental health issues.
Today, I will be doing personalised video messages! Perfect Christmas present for anyone that doesn’t mind getting insulted by kerry mucklowe.
All monies raised go to BXM charity
THERE ARE ONLY 50 AVAILABLE!
LINK IN BIO
YOUVE RAISED NEARY 10K FOR LITTLE EDWARD!
Dancing in absolute jubilation!!! You absolute bloody beauts. I am so lucky to have you all
If you can’t donate , please share
LINK IN BIO
Cannot quite believe ive been so preoccupied in baby bollocks that i haven’t congratulated my second cousin (yes im gonna bloody claim it)the powerhouse human rights lawyer @suigenerisjen on winning freedom for julian assange. If you havent read her book ‘silenced women’ you fucking should, because this woman is changing the world. I love that in a family full of strong women that i ended up being the jester and not the lawyer. SO SO PROUD !!!👏 🥲
Cannot quite believe ive been so preoccupied in baby bollocks that i haven’t congratulated my second cousin (yes im gonna bloody claim it)the powerhouse human rights lawyer @suigenerisjen on winning freedom for julian assange. If you havent read her book ‘silenced women’ you fucking should, because this woman is changing the world. I love that in a family full of strong women that i ended up being the jester and not the lawyer. SO SO PROUD !!!👏 🥲
Cannot quite believe ive been so preoccupied in baby bollocks that i haven’t congratulated my second cousin (yes im gonna bloody claim it)the powerhouse human rights lawyer @suigenerisjen on winning freedom for julian assange. If you havent read her book ‘silenced women’ you fucking should, because this woman is changing the world. I love that in a family full of strong women that i ended up being the jester and not the lawyer. SO SO PROUD !!!👏 🥲
Took me an entire afternoon to film this! Pre order your signed copy of Hexy B*tch from the link in my bio! (Can’t guarantee you’ll get a ghost with a long thin knob but you’ll definitely get a signature!)
Thankyou so much to everyone who has donated to little edward. Was sent this video from his family. You are all so bloody incredible. If you can’t donate please share so we can get this bubba the help he needs. LINK IN BIO
All 50 videos have sold out!
Thankyou so much to everyone who bought a video and also to those whove donated!
To all those who have bought a video , you should receive it at some point today or tomorrow
The most amazing thing is we’ve managed to raise 10k for disadvantaged children. What a bloody incredible gift that is.
THANKYOU ALL SO MUCH
X X X X X X
What happens if you cross Scooby-Doo, Mystic Meg and some ghost hunting equipment from the dark web… you get a new book from me, that’s bloody what!
Come through a portal to the afterlife in the back room of an Oxfordshire pub, turn left at the pagan swingers, and meet me by the pet psychics. It’s going to get hexy, bitches.
Hexy B*tch, will be released this October (just in time for Halloween) and is available to pre-order NOW: https://linktr.ee/daisymaycooperbook
This little bubba needs our help. Please find it in your hearts to donate and share, (link in bio) . If each one of my followers donated 2 quid we could change little edwards life ❤ ♥
Edward who was born on 7th September 2020 and diagnosed with Spinal Muscular Atrophy (SMA) type 1, at 7 weeks old on 29th October. Our world has been turned upside down, in the most extreme way. Edward has brought purpose to our life and makes each day shine in the brightest way possible. He is the most beautiful, happy baby and it breaks our heart that he has this condition.
Spinal Muscular Atrophy (SMA) is a rare, genetic neuromuscular condition causing progressive muscle wasting (atrophy) and weakness leading to loss of movement. This may affect crawling and walking ability, arm, hand, head and neck movement, breathing and swallowing. There are different forms of SMA and a wide spectrum of how severely children and adults are affected.
We live in the UK and there is a treatment available called Spinraza, which increases survival motor neuron (SMN) protein production. We are extremely grateful to have this treatment available to us, as only a few years ago, babies with SMA did not have this hope and would likely not live to reach the age of 2.
Although we have this treatment option available, there is a new pioneering much more advanced treatment called Zolgensma. Zolgensma is a gene therapy medicine for treating SMA. It targets the genetic root cause of SMA with a one-time-only dose and replaces the function of the missing or nonworking survival motor neuron 1 (SMN1) gene with a new, working copy of a human SMN gene. It is currently only available in the USA and with a large price tag, £1.2m!
We are reaching out to our family, friends and the general public to help us raise funds to get our son this life saving treatment. This can be done by donating, sharing our story to everyone and anyone you know, setting up fundraising ideas or events – whatever you can do will be truly appreciated. We can’t do this without you and will be eternally grateful for any donations or support, large or small.
Zolgensma will give Edward the best chance to live a fulfilling life. From a Mum a
Bloody love this charity and everything it stands for
Follow @bxminspired to find out more
