Saskia Harrison
100k for Rare Disease UK
Fundraising for Genetic Alliance UK - Rare Disease UK
1 in 17 people will live with a rare disease in their lifetime, but despite the numbers, it can be an incredibly isolating experience.
I’d be honoured if you would consider sponsoring me, no matter how small the amount, to walk 100k for Rare Disease UK and Syndromes Without A Name (SWAN UK) to help families living with rare diseases and to fund research into future treatments
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