The latest on the Foundation and research into Mitchell Syndrome
Thankful for Caregivers
This Thanksgiving, we are thankful for the many caregivers in our community who help care for Mitchell Syndrome patients.
WashU Lab Tour and Family Conference
WashU Lab Tour and Family Conference in St. Louis, Missouri
August 2024 Newsletter
August 2024 Newsletter: The Lajaunie Lab Tour, Meet Andrea, and a Special Invitation from Matt and Michele Herndon, and their dog
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.