Google
Trusted Resources: News & Events
Latest announcements and gatherings
Fear, Anger, SCD and #BLACKLIVESMATTER
June 10, 2020 at 6pm Eastern Time
Session #11: FEAR, ANGER, SCD AND #BLACKLIVESMATTER
*An immediate response to COVID-19 pandemic was to provide weekly online SCD & COVID-19 education/information sessions.
**These sessions allow patients to engage with their doctor, PHSSCA and other patients/family members.
***The weekly Zoom sessions are a partnership between Piedmont Health Services & Sickle Cell Agency and The SCD Enterprise, Atrium Health | Dr. Ify.
+myBinderRelated Content
-
Dr. Doris Wethers, 91, on Front Lines against Sickle Cell, DiesDr. Doris L. Wethers, who broke racial b...
-
When Actions Speak Louder Than Words – Racism and Sickle Cell DiseaseSCD is a life-threatening, inherited blo...
-
Racism and Health-Related Quality of Life in Pediatric Sickle Cell Disease: Roles of Depression and SupportIntroductions: Sickle cell disease (SCD...
-
Sickle Cell Disease: Racism in the American Health Care SystemWednesday, June 28 1-4 pm EDT Massachu...
-
Black Americans With Sickle Cell Trait At Increased Risk Of Kidney DiseaseAfrican Americans with sickle cell trait...
-
‘Every Time It’s A Battle’: In Excruciating Pain, Sickle Cell Patients Are Shunted AsideAmy Mason had toughed it out for hours o...
-
Stigmatization of Sickle Cell Disease – Selina Olwenda-Chairperson Children Sickle Cell Foundationhttps://www.youtube.com/watch?time_conti...
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.
Powered by
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.