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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 lysosomal 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.
Contact the support and advocacy team
Our helpline is open 9-5pm Monday-Friday: 0345 389 9901 or you can email: email@example.com
Out of hours support line: open 5pm-10pm Monday-Friday and weekends: 07712 653 258
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