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Walks, Blood Drives Among Activities Marking Sickle Cell Awareness Month
From walks to blood drives, a host of activities and efforts are marking this year’s National Sickle Cell Awareness Month, observed annually each September.
For its part, Nationwide Children’s Hospital, which has a Comprehensive Sickle Cell and Thalassemia Program, is reminding people of the importance of being tested for the sickle cell trait, which affects 1 in 13 African-American babies. Although the trait doesn’t usually cause illness, if both parents have it, there’s a 25 percent chance the couple’s child will be born with sickle cell disease (SCD).
Elsewhere, the Sickle Cell Disease Association of America is asking supporters, particularly those of African descent, to donate blood this month. The inherited disease affects red blood cells via an abnormal version of hemoglobin, the protein that carries oxygen throughout the body. The altered hemoglobin is known as hemoglobin S, or sickle hemoglobin, because it causes normally oval-shaped red blood cells to assume a sickle shape, often resulting in blood flow blockages.
people & placesCayenne Wellness CenterCayenne Wellness Center and Children’s...
people & placesDebra FigginsDebra Figgins is a Sickle Cell Educator....
news & eventsSickle cell disease is complex on its own, but black men with the illness battle its stigmas and stereotypes tooDoctors didn’t expect Marqus Valen...
videos & visualsIU Nurse Invents Medical Device for People With Sickle Cell Diseasehttps://www.youtube.com/watch?v=TjE3Urth...
news & eventsWebinar Series: Sickle Cell Science: Path to Progress – Sickle Cell Disease Care in the Emergency Department: ...To commemorate Sickle Cell Awareness Mon...
Community CenterSickle Cell Hospital ChatterHospital Chatter is an online facebook g...
videos & visuals4 Transition Stages of Sickle Cell Disease and Tips for Each Stagehttps://www.onescdvoice.com/wp-content/u...
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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.