The MPS Society's 2024 team of runners will be raising money to help us support our members who are affected by MPS, Fabry and related lysosomal diseases by taking part in the TCS London Marathon on 21st April 2024.
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On 21st April 2024 I will be running the London Marathon, in memory of a close family friend who sadly lost his battle earlier this year with a genetically rare disease called Fabry.
I will be running on behalf of the MPS Society, a small charity that supports families affected by rare genetic conditions.
Any donations/shares go a long way and are greatly appreciated!
The MPS Society's 2024 team of runners will be raising money to help us support our members who are affected by MPS, Fabry and related lysosomal diseases by taking part in the TCS London Marathon on 21st April 2024.
The MPS Society provides professional support to children, adults and families affected by MPS, Fabry and related Lysosomal Storage Diseases and funds research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions.