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When Treatments & Trials for Rare Disorders Exclude Malaysia

Catherine Jayasuriya, Founder & Executive Director, Coalition Duchenne | Nadiah Hanim Abdul Latif, President, Malaysia Rare Disorders Society

23-Jul-25 16:00

When Treatments & Trials for Rare Disorders Exclude Malaysia

About 95% of rare disorders don’t have a treatment for it, and even in cases where treatment is available or a clinical trial is being conducted, not everyone across the world has equal access to it. That’s what’s happening now in the context of Duchenne Muscular Dystrophy. Here to help us dive into this and why equitable access to treatments matter, we speak to Catherine Jayasuriya, Founder & Executive Director, Coalition Duchenne, and Nadiah Hanim Abdul Latif, President, Malaysia Rare Disorders Society.

Image Credit: Catherine Jayasuriya

Produced by: Lim Sue Ann

Presented by: Lim Sue Ann


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Categories:  managing diseasemedical advances

Tags:  the bigger picturehealth & livingrare diseaserare disordersduchenne muscular dystrophyhealth equity





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