Gareth Mayor

Gareth's Movember

Fundraising for The SMA Trust
£377
raised of £250 target
by 19 supporters
Donations cannot currently be made to this page
The SMA Trust

Verified by JustGiving

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

Story

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Spinal Muscular Atrophy is the biggest genetic killer of under 2s. Around 1 in 60 people in the UK have the defective gene, approximately 1.5 million people, but even when two gene carriers produce a child, there is still only a 1 in 4 chance the child will be affected and a 1 in 2 chance they will themselves be a carrier, therefore the family may be completely unaware.

Elsa was a normal 6 month old until she contracted bronchialitis in December 2014 and was then subsequently diagnosed with SMA Type 1.  SMA affects the motor neurons and is the child version of MND (think ice bucket challange) and Type 1 is so severe that around 90% of all children pass away before their second birthday.  Elsa passed just 6 weeks after diagnosis.

I'm growing a tache for November but instead of Men's Health, I'm donating my fundraising to The SMA Trust in the hope that they will one day find a cure for this terrible disease.

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
£377.00
+ £93.00 Gift Aid
Online donations
£377.00
Offline donations
£0.00

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