Melissa Hogan: Halting Hunter Syndrome

Published: Dec. 7, 2017, 1 p.m.

E78 – Founder and president of Project Alive human Melissa Hogan is dedicated to finding a cure for Hunter Syndrome. It’s one of the rarest diseases/genetic disorders in the world and her son Case was born with it, prompting Melissa to leave her attorney life behind and devote all of her time, energy and resources […]