Sickle Cell Knowledge and Information Network
It was great meeting you at the SCDAA Convention.
Here you will find our poster, two ways to try SickleCellPedia, a short form to stay in touch, and how to work with us if you run a community organization or see patients.
Try SickleCellPedia
Free, multilingual, and available any hour. Ask it anything about sickle cell disease and it tells you where its answers come from.
Stay in touch
Our mission
Make useful and reliable information about sickle cell universally accessible.
People live with sickle cell disease every day, yet most see a specialist rarely, and many never do. Reliable information in their own language, at the moment they need it, helps them recognize danger signs, use treatments well and arrive in clinic with better questions.
Two ways to work with us
Non-profits and community organizations
Add SickleCellPedia to your platform
We provide SickleCellPedia to all non-profit organizations on a pay-what-you-can basis: your website, your WhatsApp line, your members. If you are interested in incorporating it in your platforms, write to us.
Medical providers
Join the SickleCellPedia PRO waitlist
SickleCellPedia PRO is a clinical decision-support tool for healthcare professionals, with mandatory citations and credential-based access. In development, expected Q4 2026. Register your interest to be among the first to try it.
Sign up for the PRO waitlistFeedback?
Anything about SickleCellPedia, the poster or SCKIN. We read every message.