DISCLAIMER
The 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.compose your message
message sent
email sent successfully
Trusted Resources: News & Events
Latest announcements and gatherings
Show Love, Give Blood for National Sickle Cell Awareness Month 2023
September is National Sickle Cell Awareness Month. The Sickle Cell Disease Association of America invites you to join us for a virtual blood drive to support sickle cell warriors!
Did you know…
That blood transfusions are one of the most critical treatments for sickle cell patients, but less than 10% of Americans donate blood?
That sickle cell patients benefit most from blood transfusions from people of the same race or similar ethnicity, but only five percent of blood donors are of African ancestry?
Join us in recognizing National Sickle Cell Awareness Month and help us make a difference for SCD patients by pledging to donate blood. It takes one hour, and you could save someone’s life. Thank you for your support!
Related Content
-
people & placesKenneth Ataga, MDDr. Ataga's clinical interest is in clas...
-
Community CenterToday’s Faces of Sickle Cell Disease: Jennifer NsenkyireJennifer Nsenkyire, who is originally fr...
-
videos & visualsRoald Dahl’s Marvellous Children’s Charity “Everyone’s Business” campaignhttps://www.youtube.com/watch?v=VqdP3Sxa...
-
people & placesMaria Grazia Roncarolo, MDMaria Grazia Roncarolo, MD is the co-dir...
-
education & researchRacism and Health-Related Quality of Life in Pediatric Sickle Cell Disease: Roles of Depression and SupportIntroductions: Sickle cell disease (SCD...
-
news & eventsThe Life, Death, and Dream of a Research Diversity Crusader“We want to have a nation in which the...
-
education & researchImplementation of the NCAA sickle cell trait screening policy: A survey of athletic staff and student-athletesObjective: To describe the perspectives...
send a message
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
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.