After serving as a volunteer for several months, Jeannie officially joined the MitoAction team in January 2018. Although she had never heard of mitochondrial disease until she started working for MitoAction, Jeannie has dedicated herself to learning about this rare disease so she can help MitoAction continue to expand the ways in which we serve the Mito community. Jeannie oversees the day-to-day operations of MitoAction, as well as the Marcel’s Way Family Fund, scholarships, Matthew Harty Camper Fund, MitoSocials, and MitoPlaydates.
“I couldn’t be happier to be a part of the MitoAction team! I truly love all that we do and feel so fortunate to be a part of something that touch- es the lives of so many people.”