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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

Arthur William Granville was born on 30th December 2013.

At 9 weeks old he was officially diagnosed with SMA Type 1.

We are raising money for The SMA Trust who use donations to fund important research into SMA.


 

Donation summary

Total
£6,363.10
+ £525.35 Gift Aid
Online
£2,901.20
Offline
£3,461.90

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