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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

On 24th July 2015 I'll be setting off from Whitehaven in Cumbria on a 3 day mission unaided across England on my mountain bike ending up in Scarborough 205 miles later.

I'm raising money for the SMA trust in memory of my little girl Rowan who passed away aged just 18 months old. Rowan was diagnosed with SMA (Spinal Muscular Atrophy) which is a genetic muscle wasting condition that currently has no cure. Please help me raise some much needed funds to help find a cure.

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Donation summary

Total
£2,562.40
+ £497.50 Gift Aid
Online
£2,562.40
Offline
£0.00

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