Rare Disease Day is an annual global observance held on the last day of February — February 28 in 2026 — bringing together patients, advocates, researchers, and healthcare professionals committed to improving diagnosis, care, and access to treatment.

For millions of families, the search for answers is long and uncertain, Rare Genomics Institute (RG) works to change that by funding genomic sequencing and advancing research that help identify potential variants and diagnoses.

Your support helps RG accelerate discovery, connect patient with research institutions, and bring clarity and hope to families navigating rare disease journeys.