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Margarida Vale is raising money for The SMA Trust
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2017 The Great Manchester Run · 28 May 2017 ·

The SMA TrustVerified by JustGiving
RCN 1097765
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

In May, I'll be running the Manchester 10K for the SMA Trust. But I need your help to fundraise money for this amazing charity, that finds treatments and is looking for a cure for this genetic neuromuscular condition. 

Sponsor me to run the 10K so that I can reach my fundraising goal of £150! 

For those who are unaware of what Spinal Muscular Atrophy is, here's a brief summary:

SMA is a genetic neuromuscular disease, affecting nerves responsible for muscle function. Although classified as rare, SMA is the leading genetic cause of death of infants and toddlers. Children with a less severe form of SMA face the prospect of progressive muscle wasting, loss of mobility and motor function. 1 in every 6,000 to 10,000 births is affected by SMA. The SMA trust is the only UK charity solely dedicated to funding medical research into Spinal Muscular Atrophy.

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Donation summary

Total
£156.38
+ £20.00 Gift Aid
Online
£156.38
Offline
£0.00

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