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Marie's Bupa Great South Run 2013 page for Anabelle

Marie Shepherd is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)

Team: Remembering Anabelle Shepherd

In memory of Anabelle Shepherd
Donations cannot currently be made to this page

Bupa Great South Run 2013 · 27 October 2013 ·

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 taking the time to visit my JustGiving page.

In March 2012 my niece Anabelle at 13 months was diagnosed with a rare genetic disorder called MPS 1, Hurler Syndrome which without a bone marrow transplant meant she would die before teenage years.

Anabelle had the bone marrow transplant and endured months of medical treatment,  seeing this and her parents go through it , was heartbreaking.  Sadly on Christmas day 2012, when they believed they were over the worst, Anabelle aged just 22 months died at Southampton General Hospital from an infection.

MPS 1 is so rare that it occurs in 1 in 100,000 newborns.  Please help me raise money to help other families who are affected by this rare disorder and hopefully find a cure so they don't have to go through what my brother, sister-in-law and the whole family has been through.

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Donation summary

Total
£225.00
+ £51.25 Gift Aid
Online
£225.00
Offline
£0.00

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