The Society for Mucopolysaccharide Diseases (The MPS Society) is the only UK charity supporting individuals and families affected by MPS and related diseases. These are progressive, life limiting genetic conditions.
Since 1982 we have provided support to children, adults and their families affected by MPS and related diseases, funding research into treatments and actively trying to raise awareness about this rare group of diseases.
Registered as a charity in England and Wales, Charity No. 1143472
Charity registered in Scotland, Charity No. SC041012
Registered company limited by guarantee in England and Wales, Company No. 7726882