The Sickle Cell Disease Association of America, a national nonprofit membership organization that advocates for people affected by sickle cell from Harlem to Hollywood.
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You’ll Love The Sickle Cell Disease Association Of America Virtual Advocacy Training
The Sickle Cell Disease Association of America will hold its annual Advocacy Day event and offer virtual training on Tuesday, April 5, from 1 p.m. to 3:30 p.m.Continue reading
Sickle Cell Disease Association Of America Named Regina Hartfield New CEO
The Sickle Cell Disease Association of America (SCDAA) named Regina Hartfield as CEO and president effective January 14, 2022. Continue reading
Support Sickle Cell Disease Association of America From Harlem To Hollywood
Sickle Cell Disease Association of America will hold the eighth annual Walk with the Stars fundraiser, where participating teams and individuals can track their walk, run, dance, or movement steps.Continue reading
Sickle Cell Disease Association Offers Community Health Worker Training From Harlem To Hollis
Sickle Cell Disease Association of America will offer sickle cell disease community health worker training from April 12 to June 21, 2021. Continue reading
Sickle Cell Disease Association Holds 48th Annual National Convention Virtually
Sickle Cell Disease Association of America will hold its 48th annual national convention virtually this year from Tuesday, October 13, through Saturday, October 17th, 2020.Continue reading