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Melissa Hogan

Project Alive
Melissa Hogan is the President of Project Alive, the leading research and advocacy foundation for the rare disease Hunter Syndrome (MPS II). She also serves as a Patient Representative to the FDA and on the boards of several rare disease organizations. Prior to her son’s diagnosis with Hunter Syndrome in 2009, Ms. Hogan practiced as a corporate attorney with a focus on health care law, and later as a strategy consultant. Ms. Hogan is also a member of the DIA2015 Patient Fellow class.

My Speakers Sessions

Tuesday, June 20

2:00pm CDT