Katy, Simon and Lindsay run the London marathon for MPS

Katy Brown is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)
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London Marathon 2018 · 22 April 2018 ·

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

Our eldest son Sam suffers from Morquio Syndrome, a type of MPS. It causes shortness in stature, progressive physical disability and is life limiting. 

We could not survive without the MPS Society. They provide invaluable support to us and other families living with these rare, devastating conditions. In the fight for the NHS to fund treatment for Morquio, the MPS Society were pivotal and unrelenting in their commitment to ensure children like Sam could access the treatment they so need and deserve.

Please support us and donate to this amazing cause. None of us have ever run a marathon before so we are slightly daunted but training hard!

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Donation summary

Total
£3,110.00
+ £604.55 Gift Aid
Online
£3,110.00
Offline
£0.00

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