The MSUD Family Support Group is a 501(c)(3) non-profit organization with no paid staff. Annual Support Group membership fees and donations are used for expenses such as: funding a biennial Symposium for families and health care providers, printing and providing updated information to those with MSUD and their families, funding research, and developing educational material for the public. Additional funds are needed for research in the fields of genetics, diet, related behaviors, on-going studies for improved treatment and MSUD related biochemistry.

If you would like to mail-in your donation to us Click here to print the donation form.

Click the 'Donate' button to make an online donation. Thank you for your generous support.

Updates To Nutrition Management Guidelines

The Nutrition Management Guideline for MSUD was first published in 2014. Since that time, there have been reports of new research and experiences that have prompted updates of the guideline.

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Galen Carrington Classic MSUD age 27

Galen Carrington is a 27 year old Indiana resident who has classic MSUD. He underwent liver transplantation 5 years ago at Children’s Hospital

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MSUD Awareness Day

Now more than ever before we are hearing about National Awareness Days which are set by organizations or the government to bring attention to issues of importance.

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Indigo Charlie Mays - Variant MSUD Age 4

Meet our girl Indigo Charlie Mays. After a smooth pregnancy and delivery, she was born on July 21st, 2013 in Seattle, WA.

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20th Annual White Horse Beach Charity Golf Tournament

On July 29, 2017 Charlie O’Rouke and his committee held the 20th Annual White Horse Beach Charity Golf Tournament.

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Cambrooke Foods Hosts Local Event

Cambrooke has been doing cooking demonstrations, social meet ups and educational events for patients, their families and the clinician’s that support them for many years.

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A Child's Life

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