Spinal Muscular Atrophy is a rare, genetic,
deteriorating, life limiting condition, that has no cure!! Isabel was diagnosed
at 16 months with type 2!! She is a very funny, bright, amazing little girl
that is being robbed of her physical abilities! Isabel can sit and occasionally
roll!! Having this condition means she has never been able to stand, walk or
crawl! SMA can rob her of the ability to swallow, eat, breath and even move her
fingers! She and others deserve a cure!! Everyday Isabel SMAshes SMA she keeps
fighting and i will help fight for her and all the other SMA warriors that
deserve a cure- every donation no matter how small will make such a difference,
and change the lives of SMA!!! Let's SMAsh the BATH HALF!!