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Candace Lerman

Candace is a rare disease patient, blogger and advocate with Immune Thrombocytopenia. She is the Volunteer Director for the Rare Disease United Foundation in Florida. Candace has done extensive work for repurposing FDA approved drugs and creating legislation for rare disease patients. She is a J.D. Candidate at Nova Southeastern University.
September 23, 2015
Immune Thrombocytopenia (ITP) is a rare, autoimmune blood disorder where the body destroys platelets.
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