Patient journeys are the key that will unlock new treatments for cancers, but critical patient data, needed by researchers and industry partners to advance medical breakthroughs, is not always accessible.
Count Me In is a direct-to-patient research initiative and discovery engine that enables patients to share their samples, medical information, experiences, and voices to contribute toward a collection of novel genomic data that is de-identified and released for researchers and clinicians to access globally, to accelerate discovery and advance treatments.
Learn how you can help to create a better future for patients everywhere.
Your journey matters
Your medical records, biological samples, and personal experiences hold clues—about which diseases will respond or become resistant to which therapies—that often can’t be found in research labs or clinical trials. Count Me In enables patients anywhere to share their information with researchers everywhere to help reveal patterns in the data.
> 13,000
Patients across the United States and Canada have registered to participate in Count Me In research projects.
> 10
Releases of data into scientific repositories across existing Count Me In projects.