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Melissa J. Hogan
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Biography
Melissa J. Hogan, JD, is a parent to a child with a rare, genetic disease who has faced a countless number of surgeries, specialists, and as a result, medical trauma. In addition to caregiving and advocating for her son’s needs, she is a practicing attorney, specializing in the area of abuse and trauma. She also founded the leading research and advocacy foundation in Hunter syndrome, Project Alive, which has raised millions of dollars for research. She lives outside Nashville, Tennessee.