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Steve Fox's Fundraising Page

claire stevens is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)
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Flora London Marathon 2009 · 26 April 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

Thanks for visiting my fundraising page.

Many of you will know about Oliver and Samuel Stevens who suffer from Hunter Syndrome, a debilitating life-limiting illness. They have been receiving desperately needed Enzyme Replacement Therapy since April 2007 and are currently in good health but there are many more children suffering from similar conditions for whom vital treatment still remains a dream.                                                                 The MPS Society provides support for sufferers and their families and funds research into new treatments to give affected children the  help, hope and possibly the future they deserve.                                                                                                     

I will be running the marathon with their Dad, Bob, and I know Claire, Oliver and Samuel will be there, cheering us on!!!
Donating through Justgiving is quick, easy and totally secure. It’s also the most efficient way to sponsor me: The Society For Mucopolysaccharide Diseases gets your money faster and, if you’re a UK taxpayer, Justgiving makes sure 25% in Gift Aid, plus a 3% supplement, are added to your donation.

So please sponsor me now!

Thank you for visiting my page and wish me luck!

Steve

PS please check out Oliver and Samuel's website- www.oliverandsamuel.com

Donation summary

Total
£1,028.50
+ £91.95 Gift Aid
Online
£341.00
Offline
£687.50

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