Think Rare, Think MPS
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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.
Funding opportunities
Find out about the diseases

Spot the signs
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

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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