SMA is a genetic disease that affects motor neurones. 1:40 of us is a carrier and in its most severe form children rarely live beyond 2 – making SMA the leading genetic cause of death in babies and toddlers.
The SMA Trust is solely dedicated to funding research into a cure and treatments for SMA
Story
I am sure most of you know the 'story'...
This one is in memory of our beloved Lily Beatrice, who died in September 2012, aged 9 months 2 days.
There is currently no cure for SMA. Your donation will allow research into this devastating condition to continue, giving hope to those living with the disease.
Thank you xxxx
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