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Leeds Marathon for MPS Society -10th of May 2026

Julie williams is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)
In memory of Oliver Stevens

MPS Society Awareness Week 2026 · 11 May 2026 to 17 May 2026 · Start fundraising for this event

MPS Society Awareness Week 2026
Campaign by The Society For Mucopolysaccharide Diseases (The MPS Society) (RCN 1143472 (England & Wales), SC041012 (Scotland))
Our MPS Awareness Week runs from 11-17 May this year and we're encouraging everyone to wear blue, share our posts and donate or fundraise to help us continue to support those with MPS conditions.

Story

I'm raising awareness and funds for the MPS Society. This small charity supports families affected by rare, genetic conditions.

The MPS society provides support to families affected by rare genetic conditions. They raise money & awareness of these conditions through fundraising, information, research & support

MPS conditions are a family of rare, life limiting lysosomal storage disorders that can affect both children & adults.

Just recently we lost a dear friend - Oliver to MPS hunters syndrome, In his mid twenties.The MPS is a small charity but is currently supporting over 1800 families who are living with this condition & we want to raise awareness & funds to support them.

Donation summary

Total
£415.00
+ £101.25 Gift Aid
Online
£415.00
Offline
£0.00

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