PATIENT STORIES

Real experiences.
Real signs.
Real reasons to Check Ammonia.

These families share their experiences with hyperammonemia and urea cycle disorders to help raise awareness and support earlier recognition and treatment.

FEATURED STORY

Zoey’s Story

Zoey’s experience shows how quickly symptoms can escalate when hyperammonemia is not recognized. Her story highlights the importance of listening to symptoms, testing for ammonia, and getting the right treatment.

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MORE PATIENT STORIES
Pruitt Kruse

Pruitt

Pruitt’s journey with newborn onset OTC deficiency highlights the importance of recognizing early symptoms and checking ammonia promptly.

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Jim Stavas

Jim

Jim’s experience shows that an undiagnosed urea cycle disorder can appear unexpectedly in adulthood, especially following medical stress.

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Jennings LaRue

Jennings

Jennings’ story reminds us that a newborn who appears healthy can become critically ill very quickly from an undiagnosed UCD.

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Baine

Baine

Baine’s legacy demonstrates how awareness, family education, and genetic testing can help protect future generations.

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Elliot

Elliot

Elliot’s story underscores the importance of checking ammonia when a young person develops unexplained vomiting or neurological changes.

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Gabriela Palacios

Gabriela

Gabriela’s journey shows how finding the correct diagnosis after years of unexplained symptoms can change the course of a person’s life.

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Madelyn

 Madelyn’s story highlights the importance of checking ammonia when a newborn has unexplained vomiting and lethargy, and shares her journey of growing up with citrullinemia.


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