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Tammy Smith’s daughter, Precious, often got sick as a baby and she cried—a lot.
It wasn’t until Precious became so sick and nearly died that Tammy took her to a different hospital for treatment and learned that Precious had sickle cell disease (SCD). The inherited blood cell disorder causes red blood cells to morph into a crescent (“sickle”) shape and get stuck in small blood vessels. This blockage inhibits blood flow, which deprives tissues of oxygen and causes severe pain and tissue damage.
Precious received her first blood transfusion at the age of two. It was the beginning of many stays in the hospital that would prove isolating and difficult for the young family.
Here are the details of 9th Annual Walk for Sickle Cell organized by Precious Organization:
Saturday, September 18, 2021
Rock Spring Park, 2116 College Ave.
Alton, IL, USA
people & placesMatthew Karafin, MD, MSMatthew Karafin, MD, MS is the associate...
people & placesElizabeth S. Klings, MDDr. Klings is an Associate Professor in ...
news & eventsSoutheastern sickle cell conferenceSickle Cell Foundation of Georgia is org...
news & eventsKids Who Need Sickle Cell Meds Don’t Always Get ThemLess than a fifth of U.S. children with ...
Community CenterA Patient Advocate’s Take on Sickle Cell Disease: The Pain and the PromiseSeptember is National Sickle Cell Awaren...
news & eventsOrphan Drug Designation Granted for CSL Behring’s Investigational Plasma-Derived Hemopexin Therapy for Sickle ...Global biotherapeutics leader CSL Behrin...
news & eventsResearchers raise funds for phase 1 trial to test medical cannabis in sickle cell diseaseThe Sickle Cell Foundation of Georgia ...
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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.