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MPS Society

The MPS Society is a UK-based charity dedicated to transforming lives through support, research, and awareness for individuals affected by MPS, Fabry, and related lysosomal diseases. It provides professional support, patient resources, advocacy, and funding for research into treatments and cures. The organization offers a range of support services including mental health, bereavement, and community support, and actively engages in research, clinical trials, and policy advocacy. It maintains a website with extensive resources, publishes reports and educational materials, and collaborates with healthcare professionals and research institutions. The Society aims to improve diagnosis, treatment, and quality of life for patients and families affected by these rare conditions.
About Us
Contact Information
Conditions We Support

Mucopolysaccharidosis

  • Mucopolysaccharidosis IV (Morquio syndrome)
  • Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)
  • Mucopolysaccharidosis I (Hurler Syndrome)
  • Mucopolysaccharidosis II (Hunter Syndrome)
  • Mucopolysaccharidosis III (Sanfilippo Syndrome)
  • Mucopolysaccharidosis VII (Sly syndrome)

Fabry Disease

    If you've been diagnosed with any of these conditions, we're here to help.

    Link to this page

    Link to this page on PatientGroups.ai