Allison Muedder lives in Charlotte, NC with her husband Jon and their three beautiful children (5 and under). Her background as a special educator and speech-language pathologist is being taken to a new level as she begins navigating the world of rare disease - her son Finn (3) was diagnosed with Hunter Syndrome in 2016.
Allison serves on the board of Project Alive, a non-profit focused on funding the cure for Hunter Syndrome. Despite these new challenges, Allison still enjoys a good laugh, a good organizing project, and a hard workout. She strives to live authentically and love others well with intentionality, grace and hope.