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MPS Society

Iain Gibson is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)
“Lands End to John O'Groats bike ride”

on 29 February 2012

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The MPS Society provides specialist support to children, adults and families in the UK who are affected by MPS, Fabry and related lysosomal storage diseases and we fund research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions with no cure.

Story

<p>I am currently trying to raise money for the MPS society which helps people who suffer from Mucopolysaccharide Deisease that affects the break down waste products in the body. This leads to further health problems as the cells waste products keep building up.</p> <p>The idea came from talking to a colleauge at work about a challenge me and my dad had set to ride from Lands End to John O'Groats (over 1000 miles!) and she gave me the idea to raise the money for this charity and raise awareness on the way.</p> <p>For more information please have a look at this page:</p> <p>http://mpssociety.co.uk/</p> <p>And for information on how I am doing, please see my blog:</p> <p>http://le2jogmps.tumblr.com/</p> <p><br>Thank you for your donations and support</p>

Donation summary

Total
£164.00
+ £32.50 Gift Aid
Online
£164.00
Offline
£0.00

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