A genetic diagnosis gives families a path forward
One that enables clinical action and personalized care, unlocks resources and services, and connects to communities.
to answers with genetic testing*
A diagnosis shouldn't take 5 years1
The average time to receive a rare disease diagnosis is approximately 4–5 years. Genetic testing can offer clarity in just weeks.1
fewer hospitalizations2
Earlier answers can mean less reactive care
Children with developmental or intellectual delays experienced 79% fewer hospitalizations in the year after testing.2
covered patients3
Diagnosis starts with access
Coverage is available for 98%+ of people with commercial insurance who qualify for outpatient exome sequencing.3
Real families.
Real diagnoses.
Real outcomes.
Read stories from families whose genetic testing journey led to diagnosis and a clearer path forward.
What changed after your genetic diagnosis?
Share your story on social. It could be the reason another family asks a question, seeks testing, or finds answers soon.
Supported by organizations that understand your journey
Every diagnosis creates
a new beginning
Access genetic testing
Whether you’re exploring testing for epilepsy, developmental delay, or another concern, we’ll help you understand your options and connect with the right resources.

Spread the word
Too many families spend years searching for answers. Genetic testing can help turn uncertainty into action. Help spread awareness.


Because a diagnosis isn’t the end of a journey. It’s the beginning of action.

































































