Rarebase

Rarebase Remarks Episode #1 – Lynsey Chediak: Never give up

Jan 24, 2022

Rarebase Team

Lynsey Chediak is Rarebase’s Head of Impact and Patient Experience. She was born with a rare genetic bone and joint disease called arthrogryposis. Formerly, she led the inaugural precision medicine portfolio at the World Economic Forum. She is also the Founder and CEO of a rare disease patient advocacy non-profit, working to increase patient engagement across pediatric hospitals in the USA.

In Episode #1 of Rarebase Remarks, Lynsey shares her own experience with rare disease, her many professional contributions to the community, and her goals at Rarebase.

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Rarebase Remarks Episode #1 – Lynsey Chediak: Never give up

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