Pat Furlong of Parents Project Muscular Dystrophy on the World Orphan Drug Congress USA

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One of the advocacy leaders in the rare disease community is Pat Furlong, President of Parents Project Muscular Dystrophy (PPMD).

This April, Ms Furlong will be speaking at the upcoming World Orphan Drug Congress USA in Washington D.C. In this exclusive interview with Rare Disease Report, Ms Furlong explains why she thinks this is one of the most important rare disease conferences in the world.

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