The latest on the Foundation and research into Mitchell Syndrome
From Russia with Love
What is St. Louis but a gateway through which new connections can be made? It was a joy meeting a fellow Mitchell Syndrome family, all the way from Russia.
Holiday Update from The Mitchell and Friends Foundation
Anyone who has lost a loved one knows that holidays are the worst. There's always an empty space at the table or a stocking left on the wall--or a holiday photo from years past--to trigger your grief.
2022 Trivia Night Wrap-Up
Our First! Ever! Mitchell and Friends Trivia Night was a team effort, a ton of fun, and an all around success.
$25,000 Raised
Thanks to your generosity, The Mitchell and Friends Foundation has reached the first leg of its $150,000 race.
Scientific Advisory Team Announced
Meet the doctors and scientists who were key in helping identify Mitchell Syndrome and continue to fight for greater awareness and possible treatments.
Michele on the Move
Michele Herndon, Vice-President of The Mitchell and Friends Foundation, attends the World Orphan Drug Congress USA and a meeting of the Undiagnosed Diseases Network in Boston.
Remembering Henry
Remembering Henry, who passed away from Mitchell Syndrome on June 6, 2022.
Senator Blunt Discusses Mitchell Syndrome
In a recent Senate Appropriations Hearing, Senator Roy Blunt from Missouri challenges the National Institutes of Health to maintain funding for the Undiagnosed Diseases Network (UDN). As an example of the good work being done at the UDN, he shares the story of Mitchell Herndon, diagnosed with Mitchell Syndrome at the UDN site at Baylor in 2017.
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.