SCDAA's Advocacy Update for Q3 is out now! Get the latest on recently reintroduced SCD legislation, resources on Medicaid and work reporting requirements, the Inaugural Congressional Sickle Cell Disease Caucus Briefing and more โก๏ธ buff.ly/QCGHtUo
SCDAA
@SCDAAorg
The Sickle Cell Disease Association of America (SCDAA) serves as the nation's headquarters for sickle cell disease support and advocacy & the search for a cure.
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Meet the newest members of the SCDAA board of directors! These dedicated individuals will bring new perspectives to our organization, and we are excited to see where they lead us as we continue our work on behalf of the #sicklecell community. Welcome, all, to SCDAA! ๐
โฐ TOMORROW! Don't miss our free Blood Transfusions and Iron Overload in Sickle Cell Disease webinar, presented in partnership with @ChiesiGRD.
๐ Nov. 5
๐ 12-1 p.m. ET
๐ Virtual
๐ฃ๏ธ Feat. Dr. Anish Chackochan
๐ buff.ly/rvW3kTE
๐ Nov. 5
๐ 12-1 p.m. ET
๐ Virtual
๐ฃ๏ธ Feat. Dr. Anish Chackochan
๐ buff.ly/rvW3kTE
Sickle Cell Voices Shaping Change survey responses are requested by Friday, November 13! ๐ buff.ly/DKcBf62 (for SCD warriors and caregivers only)