Patient Stories

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Patient Story

Braxton’s Time to Thrive

Braxton was born with 7q11.23 duplication syndrome, a genetic disorder that can cause a variety of neurological issues, developmental delays, and other conditions.

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Patient Story

Sydney’s Story

Sydney was diagnosed with a rare genetic disorder called Urea Cycle Disorder / Ornithine Transcarbamylase deficiency (UCD/OTC) at just one year old.

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