The latest on the Foundation and research into Mitchell Syndrome
Announcing a New Research Partnership
Matt and Michele Herndon, Founders of The Mitchell and Friends Foundation, announce a new research partnership with Washington University School of Medicine.
Mitchell Syndrome Meet-Up
As the number of children diagnosed with Mitchell Syndrome slowly grows, we want the M&F Foundation to be a place where parents and caregivers can connect with each other in a group setting—for support and advice. This past Tuesday night—and for the first time ever—that happened.
New Discoveries on Rare Disease Day
As we add new friends to the Mitchell and Friends network, we’re also learning more about the Syndrome these families are battling.
First Official Board Meeting
The inaugural meeting of The Mitchell and Friends Foundation included old friends, a big vision, and fresh cookies.