About The Society For Mucopolysaccharide Diseases (The MPS Society)
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.
www.mpssociety.org.uk
mps@mpssociety.org.uk
The Society For Mucopolysaccharide Diseases (The MPS Society) Registered charity number 1143472 and Scotland SC041012
