Treatments and research

Through medical research and clinical trials, we know we will find innovative ways in which to cope with living with MPS, Fabry or a related disease.
The MPS Society shares knowledge, expertise and works in partnership and collaboration with other patient organisations, medical authorities and scientific institutions across the world, in order to facilitate progress towards research and better treatment for those living with one of our conditions.

Current treatments for MPS, Fabry and related diseases consist largely of Enzyme Replacement Technology (ERT) and Hematopoietic Stem Cell Transplantation (HSCT).

Parents and patients are encouraged to talk to their expert clinician to discuss whether there are any clinical trial opportunities. 

Contact the support and advocacy team

Our helpline is open 9-5pm Monday-Friday: 0345 389 9901 or you can email: advocacy@mpssociety.org.uk
Out of hours support line: open 5pm-10pm Monday-Friday and weekends: 07712 653 258 

We are the only registered charity providing professional support to individuals and families affected by MPS, Fabry or a related disease in the UK.

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Registered Charity No.1143472 & SCO41012. Registered Company No. 7726882  

Images and stories may not be reproduced without express written permission. © 2019 Society for Mucopolysaccharide Diseases

MPS House, Repton Place, White Lion Road, Amersham, Buckinghamshire, HP7 9LP

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0345 389 9901