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 the Sickle Social: Meet and greet, patient panel, & get a chance to hear from Sickle Cell experts about the future of Sickle Cell. Be sure to wear your red shirts and red face mask!
Date & Time:
Friday, June 19, 2020
Meet and greet: 5:45 PM
Sickle social: 6:00 PM to 7:00 PM
This event has ended.
Community CenterWhy You Don’t Hear Much About Sickle Cell AnymoreAbout 100,000 Americans have sickle cell...
education & researchImplementation of an Educational Intervention to Optimize Self-Management and Transition Readiness in Young Adults W...Background: The transition from the ped...
news & eventsLiving Rare, Living Stronger – NORD Patient and Family ForumRare family, we are back in person! The ...
people & placesMississippi Sickle Cell FoundationThe mission of the Mississippi Sickle Ce...
people & placesLorri BurgessLorri Burgess was the Chief Operating Of...
people & placesSickle Cell Community Advisory Council of Northern CaliforniaThe Sickle Cell Community Advisory Counc...
education & researchCaregivers and Sickle Cell DiseaseCaregivers are responsible for the physi...
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.