Think Rare Program

Recognise MPS Early. Change a life forever.

Mucopolysaccharidosis (MPS) is often misdiagnosed, resulting in treatment delays that profoundly impact a patient’s future. The MPS Learning Zone equips frontline pediatricians and GPs with practical tools to detect early signs, initiate appropriate referrals, and ensure timely intervention. Access expert-led webinars, essential resources, and clinical insights — all in one place, designed to help you Think Rare in every consultation.

MPS – Recorded Webinars

Learn about MPS on-demand from
Recorded Webinars

Browse our library of recorded webinars and key takeaways from past sessions. Learn at your own pace with real-world case studies and diagnostic strategies from international MPS specialists.

View All MPS Webinars
Our MPS Resources

Access Pediatric Research
& Clinical Resources

Our resource library ensures access to expert insights, reports, and case studies designed to enhance pediatric care worldwide.

All Resources
MPS – Speakers

Meet the Experts behind
the MPS Think Rare Program

Our faculty brings together pediatric specialists, rare disease researchers, and clinicians at the forefront of MPS education. Their combined expertise fuels our mission to promote earlier diagnosis and improve care.

Program Supporters

Supported by Our Partners in Care

The MPS Resource Centre is independently developed and managed by EiP regarding content, topics and speakers appointed. Unrestricted grants are sought to support EIP activities, and Sanofi has provided an unrestricted grant to partially support EIP's work on the misdiagnosis of metabolic disorders.

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