EVENT DATE: Oct 02, 2016
The Society for Mucopolysaccharide Diseases (The MPS Society) is the only UK charity providing support to individuals affected by MPS and related Lysosomal Storage Diseases, their families, carers and professionals. My nephew has recently been diagnosed with MPS which is a rare, life-limiting, progressive genetic condition caused by a shortage of a particular enzyme. There is currently no cure for MPS and related diseases and many sufferers will not reach their teenage years. Your donations will go towards research supported by the MPS society. There are now treatments for some of the diseases which, although not a cure, can help delay the progression of the disease.