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Our campaign is now complete. 406 supporters helped us raise £5,042.00

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Closed 28/02/2018
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Closed 28/02/2018

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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.

Story

As the autumn leaves begin to glow, why not get out and walk, toddle or roll to show support and raise vital funds for the MPS Society.  Create an event, small or large, a casual stroll or full blown hike! Let’s get out there in the fresh air – you know you want to –before the cold sets in! We want you to post here or make a pledge about your event and link your sponsors! So for starters three of our fabulous fundraisers, Sophie, Helen and Amanda, have pledged that they will challenge the rest of the MPS Team to walk on the 31st October from Chalfont and Latimer in Buckinghamshire - Get in touch if you want to join them for only £5 per person

Help The Society For Mucopolysaccharide Diseases (The MPS Society)

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Donation summary

Total
£5,041.10
+ £938.25 Gift Aid
Online
£4,856.10
Offline
£185.00
Direct
£110.00
Fundraisers
£4,746.10

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