Michelle's page

Michelle Petersen is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)
“Michelle Petersen's fundraising”

on 3 August 2011

£2,254
raised
Donations cannot currently be made to this page
The Society For Mucopolysaccharide Diseases (The MPS Society)

Verified by JustGiving

RCN 1143472 and Scotland SC041012
We support affected individuals & families to raise awareness of rare conditions.

Story

Thanks for taking the time to visit my JustGiving page.

Chiara was born with a rare disease called MPS1 (Hurlers).  In her first year of life she has endured so much hospital treatment but still remains a happy, contented, loving wee Princess. She has undergone 2 bone marrow transplants and spinal fusion which will hopefully give her the quality of life she deserves.  Treatment for MPS has only the later years become available and more advanced and with the help of donations through fundraising hopefully can continue and benefit every single person affected by this horrible disease.  I personally aim in the coming months to walk, run and swim to raise lots more money for further research and help.

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So please dig deep and donate now.

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About the charity

The Society For Mucopolysaccharide Diseases (The MPS Society)

Verified by JustGiving

RCN 1143472 and Scotland SC041012
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.

Donation summary

Total
£2,253.89
+ £444.00 Gift Aid
Online
£2,253.89
Offline
£0.00

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