Margarida Vale

Margarida's page

Fundraising for The SMA Trust
£157
raised of £150 target
by 16 supporters
Donations cannot currently be made to this page
Event: 2017 The Great Manchester Run, on 28 May 2017
The SMA Trust

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RCN 1097765
We fund research into SMA to help find a cure and treatments

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.

Donations are one click away!

About the charity

The SMA Trust

Verified 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

Donation summary

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

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