MPS II – Hunter Syndrome

The story of Cath

My son was diagnosed with Mucopolysaccharidosis II (Hunter Syndrome) at the age of 6 – a progressive, incurable, life-limiting condition. Thank you for all the research that has been done, which has enabled some treatment to be available to slow the disease and some of it’s effects. With the new research we are hopeful that a cure may be found for MPS II and for other MPS diseases. Thank you to GOSH and Evelina, London. For more info: