DISCLAIMERThe information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.
Trusted Resources: News & Events
Latest announcements and gatherings
Join us for a Zoom gathering as we celebrate National Sickle Cell Awareness Month.
We look forward to seeing you ONLINE and IN RED!
Date & Time:
September 28, 2021
06:00 PM – 07:00 PM
This event has ended.
people & placesSharon B. Lewis, MHHASharon B. Lewis assumed her duties as Ex...
people & placesThe Valerie FundThe Valerie Fund has pediatric sickle ce...
Community Center@juliemakaniScientist|Doctor - Sickle Cell Disease f...
news & eventsAn Introduction to the Institute for Clinical Economic Review (ICER) and Their Implications for New Sickle Cell Dise...January 16, 2020 2:00 – 3:00 PM ET W...
education & researchImproving the Quality of Care for Adolescents and Adults With Sickle Cell Disease—It’s a Long RoadThe World Health Organization defines qu...
people & placesTracee D. PattersonTracee was a Director of operations and ...
videos & visualsHow to register for oneSCDvoicehttps://www.youtube.com/watch?v=_XQN1Egx...
send a message
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.