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Scarlett's 50km ride for The Society For Mucopolysaccharide Diseases (The MPS Society)

Rebecca Prayoga is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)
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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

A message from Scarlett:

Hi, I'm Scarlett and I'm 10. At 4 years old my friend Luna was diagnosed with MPS VI or Maroteaux–Lamy syndrome. MPS is a degenerative genetic disorder which affects the whole body, and it's really rare! The MPS Society has helped Luna and her family, and I wanted to do something to help too.

I realised the MPS Society does Active April, where they challenge people to walk, run or wheel 50km in the month of April to fundraise. As a keen mountain biker, I wanted to challenge myself by cycling 50km in one day!!

I would appreciate anything you can donate. Thank you!! ❤️

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Donation summary

Total
£1,510.00
+ £343.75 Gift Aid
Online
£1,510.00
Offline
£0.00

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