![Main fundraiser photo](https://images.gofundme.com/Mh_eDJ6M9ghyzf1JP6dCpTCA1v8=/720x405/https://d2g8igdw686xgo.cloudfront.net/6450890_1555849156940584_r.jpeg)
Isabelle's hope
Donation protected
Our beautiful Isabelle is our youngest child to two gorgeous big sisters Maisy and Matilda
She was a perfectly healthy very happy baby, everything seemed ok until just after her first birthday when Isabelle started to regress and loose all the skills she had just learnt. Now Isabelle has lost all purposeful movement of her body.
Isabelle is communicating via an eye gaze computer and she IS so funny and so bright. It's our mission to show the world just how amazing she is. Isabelle is just like any other girl her age is and we don't want her disability getting in her way.
There's lots and lots of different resources, software and therapies that would make a huge difference to her life. Things like physio , hippotherapy, hydrotherapy and private speech specialists are so vital to ensure Isabelle reaches her full potential.
Rett syndrome is a very rare severe disability. It's a random fault in the genes, nothing causes it and it's not hereditary
Girls develop normally for the first 12-18 months of their life's, many learn to walk and talk and do as any other baby would.
If you'd rather the funds go to the fantastic charity that supports families just like ours with invaluable advice, support and education you can make a donation directly at www.rettuk.org
![](https://2dbdd5116ffa30a49aa8-c03f075f8191fb4e60e74b907071aee8.ssl.cf1.rackcdn.com/6450890_1445775769.4852_funddescription.jpg)
![](https://2dbdd5116ffa30a49aa8-c03f075f8191fb4e60e74b907071aee8.ssl.cf1.rackcdn.com/6450890_1445775901.5433_funddescription.jpg)
![](https://2dbdd5116ffa30a49aa8-c03f075f8191fb4e60e74b907071aee8.ssl.cf1.rackcdn.com/6450890_1445775967.731_funddescription.jpg)
She was a perfectly healthy very happy baby, everything seemed ok until just after her first birthday when Isabelle started to regress and loose all the skills she had just learnt. Now Isabelle has lost all purposeful movement of her body.
Isabelle is communicating via an eye gaze computer and she IS so funny and so bright. It's our mission to show the world just how amazing she is. Isabelle is just like any other girl her age is and we don't want her disability getting in her way.
There's lots and lots of different resources, software and therapies that would make a huge difference to her life. Things like physio , hippotherapy, hydrotherapy and private speech specialists are so vital to ensure Isabelle reaches her full potential.
Rett syndrome is a very rare severe disability. It's a random fault in the genes, nothing causes it and it's not hereditary
Girls develop normally for the first 12-18 months of their life's, many learn to walk and talk and do as any other baby would.
If you'd rather the funds go to the fantastic charity that supports families just like ours with invaluable advice, support and education you can make a donation directly at www.rettuk.org
![](https://2dbdd5116ffa30a49aa8-c03f075f8191fb4e60e74b907071aee8.ssl.cf1.rackcdn.com/6450890_1445775769.4852_funddescription.jpg)
![](https://2dbdd5116ffa30a49aa8-c03f075f8191fb4e60e74b907071aee8.ssl.cf1.rackcdn.com/6450890_1445775901.5433_funddescription.jpg)
![](https://2dbdd5116ffa30a49aa8-c03f075f8191fb4e60e74b907071aee8.ssl.cf1.rackcdn.com/6450890_1445775967.731_funddescription.jpg)
Organizer
Jenny Barnett
Organizer