Support the
Genomics Access Precision Program (GAPP)
Bridging Discovery and Treatment for
Children with Rare Diseases
The Genomics Access Precision Program (GAPP) is transforming what happens after a child receives a rare disease diagnosis. By bringing together leading researchers, geneticists and clinicians, GAPP helps families move beyond diagnosis by identifying personalized and intersectional treatment options, connecting them to promising therapies and clinical trials, and providing expert guidance every step of the way.
GAPP is a collaboration between the Center for Precision Medicine and Genomics Research and the Division of Genetics and Metabolism within Children’s National. GAPP creates a powerful bridge between scientific discovery and patient care. Your support will help expand access to life-changing genomic expertise, accelerate research-driven treatment strategies, and bring hope to children and families facing rare diseases.
To learn more about endowments, naming opportunities or additional ways to give, please contact, Kerri Yoder Hubbard, Associate Vice President, Children's National Foundation: KYoder@childrensnational.org.