12 activists share what they want you to know about living with a rare disease https://t.co/P3Lk3ZDnxx pic.twitter.com/GQE7YRnPdD— Mashable (@mashable) 29 February 2016
My Normal | storytelling for rare disease health
Monday, February 29, 2016
A Story of Rare Disease Activists
Celebrate the patient voice for Rare Disease Day with perspectives from activists, including My Normal founder Emma Rooney, on what it means to live with a rare disease and advocate on behalf of the community.
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