02/28/2026
More than 300 million people worldwide are living with a rare disease. Behind every number is a story shaped by uncertainty, resilience, and the search for answers.
For families like Kelly’s, that search can be long and complex. When traditional testing fell short, a combined Whole Genome Sequencing and RNA Sequencing approach at Baylor Genetics helped identify a FOXP4 variant linked to neurodevelopmental disorders, providing the clarity needed to guide her son Reed’s care.
Rare disease isn’t just a statistic. Families are navigating the unknown every day, while providers and researchers work tirelessly to close the diagnostic gap.
This Rare Disease Day, we’re reminded why this work matters. Learn more about Kelly and her family’s journey here: https://www.linkedin.com/pulse/mothers-strength-navigating-rare-disease-finding-answers-rjvre