The latest on the Foundation and research into Mitchell Syndrome
Morars in Missouri
Why would anyone leave Puerto Rico to visit St. Louis, Missouri, in the dead of winter? Because of the world-class medical care available for Mitchell Syndrome children.
Retrospective Natural History Study of Mitchell Syndrome Now in Process (January 2024 Newsletter)
Retrospective Natural History Study of Mitchell Syndrome in Process
New Scientific Advisor Added
Welcome Dr. Kevin Glinton from Baylor College of Medicine and Texas Children’s Hospital to our Scientific Advisory Team.
Happy Halloween from The Mitchell and Friends Foundation
Happy Halloween from The Mitchell and Friends Foundation!
Four Years and 100 Big Ones Later
Four years after Mitchell Herndon’s passing on Oct. 2, 2019, we are honored and grateful to be able to continue to support the Miller Lab and their efforts to understand Mitchell Syndrome, and identify a cure.
VP Michele Herndon Pursuing New Opportunities with Old Friends at the UDNF
VP Michele Herndon Pursuing New Opportunities with Old Friends at the UDNF
First Ever Mitchell Syndrome Summit
The First Ever Mitchell Syndrome Summit was held on June 1-2 at Houston Methodist Hospital in Texas.
Lab Work Beginning
In this month’s newsletter, we share a fundraising update and exciting developments on the research front as we seek to find a cure for Mitchell Syndrome.
Increased Awareness Leads to Early Diagnosis of Mitchell Syndrome
Increased Awareness Leads to Early Diagnosis of Mitchell Syndrome
The Inaugural Rare Diseases Symposium at Wash U
The Inaugural Rare Diseases Symposium at Washington University
Michele and Dr. B Making the (Grand) Rounds
The story of Mitchell Syndrome is a story of community, collaboration, and courage.
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.