National Organization for Rare Disorders’ Post

What does #HealthEquity for EVERYONE in the #RareDisease community look like? Who has been left out and needs to be included? What changes need to be made now? Our 2024 Living Rare Forum panelists discussed it: https://lnkd.in/ecKyM2c4 Featuring speakers from Dreamsickle Kids Foundation,Inc, Hemophilia Foundation Southern California, and more.

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