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Where to Learn More About Hunter Syndrome

Advocacy Groups

The UK National MPS Society

The Society of Mucopolysaccharide Diseases (MPS Society) is the only registered UK charity providing professional support to individuals and families affected by MPS and related Lysosomal Storage Diseases throughout the UK.
visit MPSSociety.co.uk


Additional Resources for Rare Diseases

EURORDIS

EURORDIS is a non-governmental patient-driven alliance of patient organizations representing more than 510 rare disease patient groups in 48 countries.
visit EURORDIS.org

This information should not be used in place of advice from your GP or other healthcare professional. If in doubt please contact your doctor for advice.

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MPS Day 2017

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