Spot the signs

Think Rare, Think MPS supports earlier recognition of the signs and symptoms of MPS diseases by engaging with healthcare professionals.

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For healthcare professionals

We want to give you the tools to be able to learn about MPS, Fabry and related diseases in order for children with the condition to receive a faster diagnosis.

Find out about the diseases

Resources

Find out more about our resources

E-learning

Coming soon

Publications

View our latest publications here

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The MPS Society is committed to bringing about change in the diagnostic journey of children affected by these rare conditions. The Think Rare, Think MPS campaign supports earlier recognition of the signs and symptoms of MPS diseases by engaging with and educating the healthcare professionals most likely to see a patient with MPS in the early stages of the disease. #Spotthesigns

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Think Rare, Think MPS

To find out more about our Think Rare, Think MPS campaign, please read our blog post below. 

Resources for professionals

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You might also be interested in

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Treatments

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

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Clinical trials

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

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If you need further information or have something you want to share with healthcare professionals get in touch.