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Isabel has spinal muscular atrophy type 2 she was diagnosed at 16 months old- this is a rare genetic degenerative life limiting muscle wasting condition that currently has no cure!!! Isabel has never been able to stand, walk or crawl! This means any task that isabel requires the use of her muscles is very difficult- from streching, sitting, breathing and eating. She is an inquizative little 3 year old that doesnt let SMA define her- even when her body is failing her! To give Isabel the indepenace that any 3 year old deserves, We are looking to fundraise for specialist equipment and services to enable her body to be as indepandant for long as possible- thank you for all your support!!!
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Karen Freeman started crowdfunding
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Oct 7, 2017
Best wishes for the futureHope all your birthday wishes come true x
Sep 29, 2017
A lovely smile. Hope this small donation helps. x
Sep 28, 2017
My beautiful granddaughter is 4 years old and you remind me so much of her. She is a real treasure and I am so thankful she is in great health. I'll be thinking of you and hope you get to your total.
Sep 27, 2017
Sep 27, 2017
Let's get this page going!!!
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