The latest on the Foundation and research into Mitchell Syndrome

Morars in Missouri
Matt Herndon Matt Herndon

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.

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New Scientific Advisor Added
Matt Herndon Matt Herndon

New Scientific Advisor Added

Welcome Dr. Kevin Glinton from Baylor College of Medicine and Texas Children’s Hospital to our Scientific Advisory Team.

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Four Years and 100 Big Ones Later
Matt Herndon Matt Herndon

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.

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Lab Work Beginning
Matt Herndon Matt Herndon

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.

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From Russia with Love
Matt Herndon Matt Herndon

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.

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2022 Trivia Night Wrap-Up
Matt Herndon Matt Herndon

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.

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$25,000 Raised
Matt Herndon Matt Herndon

$25,000 Raised

Thanks to your generosity, The Mitchell and Friends Foundation has reached the first leg of its $150,000 race.

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Scientific Advisory Team Announced
Matt Herndon Matt Herndon

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.

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