To honour the release of You and me on @itvxofficial here are some pictures of me manically pumping in various states of public indecency 😂❤️ me and @classiccam__ who I love, sick views, @lilyingenewmark sleeping on the job, me flooding the dressing room on day 1, @hugehairclaire_1968 putting me in a crop top and shorts 7 months after birth lol and a special visitor!!!
To honour the release of You and me on @itvxofficial here are some pictures of me manically pumping in various states of public indecency 😂❤️ me and @classiccam__ who I love, sick views, @lilyingenewmark sleeping on the job, me flooding the dressing room on day 1, @hugehairclaire_1968 putting me in a crop top and shorts 7 months after birth lol and a special visitor!!!
To honour the release of You and me on @itvxofficial here are some pictures of me manically pumping in various states of public indecency 😂❤️ me and @classiccam__ who I love, sick views, @lilyingenewmark sleeping on the job, me flooding the dressing room on day 1, @hugehairclaire_1968 putting me in a crop top and shorts 7 months after birth lol and a special visitor!!!
To honour the release of You and me on @itvxofficial here are some pictures of me manically pumping in various states of public indecency 😂❤️ me and @classiccam__ who I love, sick views, @lilyingenewmark sleeping on the job, me flooding the dressing room on day 1, @hugehairclaire_1968 putting me in a crop top and shorts 7 months after birth lol and a special visitor!!!
To honour the release of You and me on @itvxofficial here are some pictures of me manically pumping in various states of public indecency 😂❤️ me and @classiccam__ who I love, sick views, @lilyingenewmark sleeping on the job, me flooding the dressing room on day 1, @hugehairclaire_1968 putting me in a crop top and shorts 7 months after birth lol and a special visitor!!!
To honour the release of You and me on @itvxofficial here are some pictures of me manically pumping in various states of public indecency 😂❤️ me and @classiccam__ who I love, sick views, @lilyingenewmark sleeping on the job, me flooding the dressing room on day 1, @hugehairclaire_1968 putting me in a crop top and shorts 7 months after birth lol and a special visitor!!!
To honour the release of You and me on @itvxofficial here are some pictures of me manically pumping in various states of public indecency 😂❤️ me and @classiccam__ who I love, sick views, @lilyingenewmark sleeping on the job, me flooding the dressing room on day 1, @hugehairclaire_1968 putting me in a crop top and shorts 7 months after birth lol and a special visitor!!!
To honour the release of You and me on @itvxofficial here are some pictures of me manically pumping in various states of public indecency 😂❤️ me and @classiccam__ who I love, sick views, @lilyingenewmark sleeping on the job, me flooding the dressing room on day 1, @hugehairclaire_1968 putting me in a crop top and shorts 7 months after birth lol and a special visitor!!!
To honour the release of You and me on @itvxofficial here are some pictures of me manically pumping in various states of public indecency 😂❤️ me and @classiccam__ who I love, sick views, @lilyingenewmark sleeping on the job, me flooding the dressing room on day 1, @hugehairclaire_1968 putting me in a crop top and shorts 7 months after birth lol and a special visitor!!!
2022. The year we packed up the circus and went. So many friends and so much family. I breastfed everywhere and anywhere. No sleep. A year full of so much love found in moments of absolute chaos.
2022. The year we packed up the circus and went. So many friends and so much family. I breastfed everywhere and anywhere. No sleep. A year full of so much love found in moments of absolute chaos.
2022. The year we packed up the circus and went. So many friends and so much family. I breastfed everywhere and anywhere. No sleep. A year full of so much love found in moments of absolute chaos.
2022. The year we packed up the circus and went. So many friends and so much family. I breastfed everywhere and anywhere. No sleep. A year full of so much love found in moments of absolute chaos.
2022. The year we packed up the circus and went. So many friends and so much family. I breastfed everywhere and anywhere. No sleep. A year full of so much love found in moments of absolute chaos.
A cool mum
The new season of Barry is so fucking good @hbo
Mrs Winkler
Me: I love Pilates I just wanna be mindful with my body. Me as soon as I box: I wanna go pro and dedicate my life to beast mode 😂😂😂
Today is rare disease day. Over the last 4 years I have been helping to raise awareness about CCHS. An extremely rare disease that means that those affected can not breathe unaided once they are asleep. @cchsnetwork is the charity ran by our best friend Adam who literally grew this foundation alone with other parents for his son @teddyjoefox to raise money to fight this, fund research and pay for medical bills which they receive NO government help with. As with all rare diseases the funding is overlooked and they lead this fight alone. This year I was introduced to @keepmebreathinginsta an English family who are doing the same work for their son Casper in the uk! They have made tremendous developments! Next month doctors from France and the US will be flying to London to discuss their plans for a pacemaker meaning that EVERY child who has CCHS will hopefully one day be able to live and breathe freely from a machine. This is huge because it will be available to every mutation of the gene unlike medications which are usually specific to a certain type of CCHS. I feel it’s important to point out that this alone won’t free every symptom of CCHS but it will allow independence which is all any parent wants for their child. I feel so grateful to be able to share this news with you and hopefully we can all be a part of changing peoples lives!!! A miracle if this happens and we keep raising money and awareness!!
Today is rare disease day. Over the last 4 years I have been helping to raise awareness about CCHS. An extremely rare disease that means that those affected can not breathe unaided once they are asleep. @cchsnetwork is the charity ran by our best friend Adam who literally grew this foundation alone with other parents for his son @teddyjoefox to raise money to fight this, fund research and pay for medical bills which they receive NO government help with. As with all rare diseases the funding is overlooked and they lead this fight alone. This year I was introduced to @keepmebreathinginsta an English family who are doing the same work for their son Casper in the uk! They have made tremendous developments! Next month doctors from France and the US will be flying to London to discuss their plans for a pacemaker meaning that EVERY child who has CCHS will hopefully one day be able to live and breathe freely from a machine. This is huge because it will be available to every mutation of the gene unlike medications which are usually specific to a certain type of CCHS. I feel it’s important to point out that this alone won’t free every symptom of CCHS but it will allow independence which is all any parent wants for their child. I feel so grateful to be able to share this news with you and hopefully we can all be a part of changing peoples lives!!! A miracle if this happens and we keep raising money and awareness!!
Today is rare disease day. Over the last 4 years I have been helping to raise awareness about CCHS. An extremely rare disease that means that those affected can not breathe unaided once they are asleep. @cchsnetwork is the charity ran by our best friend Adam who literally grew this foundation alone with other parents for his son @teddyjoefox to raise money to fight this, fund research and pay for medical bills which they receive NO government help with. As with all rare diseases the funding is overlooked and they lead this fight alone. This year I was introduced to @keepmebreathinginsta an English family who are doing the same work for their son Casper in the uk! They have made tremendous developments! Next month doctors from France and the US will be flying to London to discuss their plans for a pacemaker meaning that EVERY child who has CCHS will hopefully one day be able to live and breathe freely from a machine. This is huge because it will be available to every mutation of the gene unlike medications which are usually specific to a certain type of CCHS. I feel it’s important to point out that this alone won’t free every symptom of CCHS but it will allow independence which is all any parent wants for their child. I feel so grateful to be able to share this news with you and hopefully we can all be a part of changing peoples lives!!! A miracle if this happens and we keep raising money and awareness!!
My first born child ALEX LAWTHER has made this beautiful film starring @archmadekwe and Emma D’arcy ❤️ it will premier at @tribeca as one of their official selections. I could not be prouder of you Alex!!! The best cast and crew!! Follow @peopleintrouble tickets go on sale MAY 2ND!!
Jessica Barden takes us inside the pool scene in You & Me 🫶
Ben & Emma > Jack & Rose
#YouAndMe #ITVX
Thank you so much for wanting to share your journey with me Jake ❤️ you are such a special person
This #WorldCancerDay I’m helping @BloodCancer_UK to shine a light on blood cancer. Why? Because despite being the fifth most common cancer, over 50% of UK adults can’t name a single symptom.
This lack of awareness is causing unnecessary harm. People are being diagnosed too slowly, and many aren’t even told that their myeloma, leukaemia, lymphoma, MDS or MPN is a type of cancer – leaving many people affected by blood cancer in the dark about what support and services they are entitled to. That’s why I’m joining Blood Cancer UK on their mission to bring blood cancer out of the shadows.
So, this World Cancer Day, help us spread the word, and shine a light on blood cancer by sharing this video, and your own story with the hashtag #ThisIsBloodCancer. Because together we can raise awareness and beat blood cancer once and for all.
