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Nick Brooks

Nick's 12 Hour Tennis Marathon

Fundraising for The SMA Trust
£2,107
raised of £1,350 target
by 63 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

SMA is a genetic neuromuscular disease, which means it is inherited and affects nerves responsible for muscle function. Although classified as rare, SMA is the leading genetic cause of death of infants and toddlers, with approximately 95% of the most severely diagnosed cases resulting in death by the age of 18 months. Children with a less severe form of SMA face the prospect of progressive muscle wasting, loss of mobility and motor function.

1 in 40 to 60 people is an SMA carrier, i.e. approximately 1.6 million people in the UK

1 in every 6,000 to 10,000 births is affected by SMA. At any one time, it is thought that there are between 650 and 1,300 children and adults in the UK living with SMA.

On September 30th I will be completing a 12 consecutive hours of tennis in aid of The SMA Trust.  This will be taking place at the Berkhamsted Tennis Club, and we are encouraging you all to come along and cheer him on, donate a few pennies - and even play some tennis if you like!

https://smatrust.org

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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
£2,107.00
+ £371.00 Gift Aid
Online donations
£2,107.00
Offline donations
£0.00

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