Mighty Member since November 2015
Melissa is a lawyer by profession, a writer by passion, and an advocate by necessity. She is a mom to three boys, one with Hunter Syndrome. She lives outside Nashville, Tennessee where she writes at melissajhogan.com on her back porch. She founded Project Alive, now a leading multi-million-dollar Hunter syndrome research and advocacy foundation, and currently consults on clinical trial design and patient outcomes. She has also lived with the chronic pain of CRPS for 10 years.