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Trusted Resources: News & Events
Latest announcements and gatherings
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.
education & researchDescribing perceived racial bias among youth with sickle cell diseaseOBJECTIVES: Sickle cell disease (SCD) p...
news & eventsSickle Cell Disease: Racism in the American Health Care SystemWednesday, June 28 1-4 pm EDT Massachu...
Community CenterLiving With Sickle Cell: ‘I Don’t Know What It Means to Be Without Pain’Once a month, she undergoes a grueling p...
education & researchRacism and Health-Related Quality of Life in Pediatric Sickle Cell Disease: Roles of Depression and SupportIntroductions: Sickle cell disease (SCD...
Community Center‘Every Time It’s A Battle’: In Excruciating Pain, Sickle Cell Patients Are Shunted AsideAmy Mason had toughed it out for hours o...
news & eventsBlack Americans With Sickle Cell Trait At Increased Risk Of Kidney DiseaseAfrican Americans with sickle cell trait...
videos & visualsStigmatization of Sickle Cell Disease – Selina Olwenda-Chairperson Children Sickle Cell Foundationhttps://www.youtube.com/watch?time_conti...
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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.