The APS Type 1 Foundation is pleased to share this advocacy opportunity with you. Rare Disease Week on Capitol Hill brings together rare disease community members from across the country to be educated on federal legislative issues, meet other advocates, and share their unique stories with legislators. While the EveryLife Foundation for Rare Diseases had hoped to host this event in-person, for the safety of all advocates, Rare Disease Week will be going virtual for 2021. Click Here to learn more and register.
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