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.

Adjusting Protein In An Adult With MSUD

A little over a year ago, in January, Jeff was just not himself. He had limited energy, was not eating well, and often appeared slightly agitated.

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I want to help out, but I don’t know how

Have you ever wanted to help out the MSUD Family Support Group but were unsure about how to contribute? The MSUD Family Support Group is actively looking for volunteers to assist with advocacy and fundraising efforts.

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As our legislators headed home for their August break, Rare Disease Legislative Advocates got busy.

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NBS-MSUD Connect: Advancing MSUD Research And More


Rare disease registries have received attention in recent years because of the many ways in which they can benefit the rare disease community.

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MSUD Advocacy Update

Healthcare and issues facing the rare disease community have been at the forefront of national conversations over the past 6 months.

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In The Professional Journals

A Patient with MSUD: Acute Management with Sodium Phenylacetate/Sodium Benzoate and Sodium Phenylbutyrate

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A Child's Life

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