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!!!