Our platform and DNA sequencing is free to any rare disease patient, anywhere on the planet.
Wherever you are, we are here to help you.
You (and your care team) can use our platform to look across all known research in minutes - create a personalized visual health journey and get information on every treatment, drug, or gene known to science.
Your personal data will never be shared, ever.
But you will get notified if we ever find a better clinical trial, treatment, or care path that works for your unique needs.
Unsure if you have a rare disease?
Start with Ubie's AI powered symptom checker!
Symptom clusters are often not specific enough for doctors to pinpoint a rare disease. And no doctor can know the intricate details of every rare disease. A full genome sequence can be a rare disease patient's best hope for pinpointing their specific condition.
TMA believes that rare disease patients deserve the best healthcare available. Often that means needing a full genetic sequencing - and we're happy to be the first company in the world to offer free whole genome sequencing + analysis to rare disease patients.
If you are (or represent) a patient in need of WGS, please sign up. We are currently prioritizing patients with pediatric epilepsy, neuromuscular disorders, and lipid storage disorders.
Regardless of whether you are eligible today, we encourage you to sign up to the waitlist - we're scaling up fast and will be working hard to help everyone that needs it.
