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Joanna's page

Joanna Moore is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)
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Windsor Half Marathon 2009 · 27 September 2009 ·

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

On Sunday 27th September I am running the Windsor 1/2 marathon.  Having NEVER run over a mile in my life this was a silly but optimistic plan. 

The only good thing about it is that I may be able to raise some money for the small but amazing charity, the MPS society.  MPS stands for Mucopolysaccharide and the charity represent the children that have one of the incredibly disabling genetic disease that fall under the umbrella of MPS.  They also help the families of these children who every day provide full time care for their loved one.

Thankyou so much for your help - I will try my absolute hardest to cross the finish line despite it feeling like an impossible dream!

Donation summary

Total
£85.00
+ £22.56 Gift Aid
Online
£85.00
Offline
£0.00

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