Google
Trusted Resources: News & Events
Latest announcements and gatherings
A Proclamation on National Sickle Cell Awareness Month, 2021
Today, 100,000 Americans live with sickle cell disease (SCD). The genetic disease, named for the sickle-shaped red blood cells it causes, leads to severe pain, serious infections, and organ damage. The severity of SCD varies, with many people facing a shortened life expectancy and a host of recurring, debilitating, and expensive health problems.
This condition also disproportionately affects Black and Brown Americans, with an estimated 1 in 365 Black Americans and 1 in 14,000 Hispanic Americans suffering from it. As President, I am committed to supporting those who have been hit the hardest by SCD. And during National Sickle Cell Awareness Month, our Nation reaffirms our commitment to improving the quality of life and health outcomes for all individuals living with SCD.
Now, therefore, I, Joseph R. Biden Jr., President of the United States of America, by virtue of the authority vested in me by the Constitution and the laws of the United States, do hereby proclaim September 2021 as National Sickle Cell Awareness Month.
+myBinderRelated Content
-
People With Sickle Cell Are Seen as Hypochondriacs or Drug Addicts. Even a Nine-Year-Old Has to Scream to Get the Ca...Nine year old Jacob has sickle cell dise...
-
Sickle Cell Anemia Treatment & ManagementThe National Institutes of Health advise...
-
Stuart H. Orkin, MDDr. Orkin is David G. Nathan Distinguish...
-
Jordin Sparks Remembers Sister Who Died of Sickle Cell Complications: ‘She Was So Strong’Last week, the American Idol winner’...
-
2021 WEPSCF Rockin’ the Red – 16th Annual EventJoin us for a Zoom gathering as we celeb...
-
Charles T. Quinn, MD, MSDr. Quinn is Associate Professor of clin...
-
Orphan Drugs for Sickle Vaso-occlusion: Dawn of a New Era of Targeted TreatmentWhile an orphan disease in the USA, sick...
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.