I was born on September 24, 1987 with classic MSUD to Tish and Mike Fuller. I had a liver transplant on February 3, 2006 in Pittsburgh. Through the nine years since being transplanted, my levels have remained in good standing without any problems with rejection.

I married Shawn Richards on September 1, 2012. On December 18th Shawn and I welcomed our first baby boy into the world. As I was hoping to get pregnant, I was referred to a high risk doctor. I was told that liver transplant patients are at risk for preeclampsia, liver rejection and preterm labor. Once I did become pregnant I was under constant observation throughout the pregnancy and we didn’t run into any of those complications. In the beginning I was monitored every month and then towards the end every week. We got to see our little guy grow through the ultrasound at every appointment.

Sawyer was estimated to be due on December 28th but as this was a high risk pregnancy the doctors delivered him a week and a half early. On the night of Sawyer’s arrival, my doctor was thinking I would have a C-section delivery. I was really hoping for a normal birth and was allowed to go into labor. After a total of 10 hours labor, we got to welcome Sawyer Michael into the world. It was more than what we thought when he was placed in my arms. I was overjoyed that our little boy was here and healthy. Both sides of the families were happy for his safe and healthy arrival. Sawyer was born 6:38pm in Columbus, Indiana. He weighed 6 pounds 13 ounces and measured 19.5 inches long. The day after his birth, the doctors ordered some blood work to be done to verify how my liver was doing. With luck on our side the liver numbers remained perfect.

Melvin Carruth

This letter is a tribute to my brother Melvin Carruth! We believe he is one of the oldest living African Americans with Maple Syrup Urine Disease.

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NBS-MSUD Connect: Your One-Stop Shop For MSUD Resources

NBS-MSUD Connect was launched as part of the Newborn Screening Connect patient registry (NBS Connect) in 2013 through a partnership between the Department of Human Genetics at Emory University, the Maple Syrup Urine Disease (MSUD) Family Support Group and other key stakeholders.

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Cambrooke Therapeutics

Cambrooke Therapeutics continues to expand its line of delicious and nutritious low protein foods to help improve the lives of individuals with Inborn Errors of Metabolism such as MSUD.

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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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Emory Metabolic Camp 2018 Announcement

Join us June 18-23, 2018 for the 24th Annual Metabolic Camp at Emory University in Atlanta, GA!

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From The Chairman’s Desk

As I sit here reflecting on how much the care and treatment of MSUD has changed over the years, my mind goes back to 1978 when our son Keith was born.

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MSUD Advocacy Report

Medical Nutrition Equity Act

The Medical Nutrition Equity Act (MNEA) would require all private insurance plans (state regulated or self-insured/self-funded) and federal health programs, including Children’s Health Insurance Program, Tricare, Medicaid, Medicare, and Federal Employee Health Benefit Plans, to provide coverage for formula and low-protein foods for all children and adults with MSUD.

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The MSUD Family Support Group Is Excited To Announce Their Participation In The Million Dollar Bike Ride

The MSUD Family Support Group is excited to announce their participation in The Million Dollar Bike Ride

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19th Biennial MSUD Symposium

I can’t believe that almost two years have passed and it is time for another MSUD Symposium! I am especially excited about this conference because I’ve built in extra time for social interaction.

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A Child's Life

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