The latest on the Foundation and research into Mitchell Syndrome

Thankful for Caregivers
Matt Herndon Matt Herndon

Thankful for Caregivers

This Thanksgiving, we are thankful for the many caregivers in our community who help care for Mitchell Syndrome patients.

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August 2024 Newsletter
Matt Herndon Matt Herndon

August 2024 Newsletter

August 2024 Newsletter: The Lajaunie Lab Tour, Meet Andrea, and a Special Invitation from Matt and Michele Herndon, and their dog

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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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