Donor diversity helps save lives!

Most patients in the United States who suffer from sickle cell disease are Black or of African descent. Blood from donors who share the same race or ethnicity is more likely to be compatible for the special transfusion needs required by these patients. Therefore, having a diverse group of donors is crucial to ensure that patients in local hospitals receive blood that closely aligns with their own. Just as your blood type depends on your parents' blood types, being a match with relatives and those with a similar ancestry can be highly beneficial to patients who require multiple transfusions throughout their lifetime.

Donate blood and be a part of this life-changing cause. Schedule your appointment, and let's make a positive impact in the lives of those affected by sickle cell disease in our community. Your generous blood donation can provide hope and support to patients in need.

What is sickle cell disease?

Approximately 100,000 Americans have sickle cell disease. People who inherit a sickle cell gene from one parent and a normal gene from the other are known to have a sickle cell trait. Having sickle cell trait does not mean having sickle cell disease. Individuals with sickle cell trait typically live a normal life, but they may pass on the trait to their children. If the child receives a trait gene from each parent, he/she can be born with sickle cell disease. The disease impacts the African American and Hispanic populations the most, but can be seen internationally in many different geographic areas.

Sickle cell disease causes red blood cells to form in a crescent or sickle shape instead of the usual round shape. These misshapen cells can block blood flow and cause pain and damage to organs.

In sickle cell disease, the abnormal red blood cells break down much faster than normal ones. This leads to chronic anemia, causing tiredness, yellowing of the skin and eyes (jaundice), and a higher risk of infections. People with sickle cell disease often need regular blood transfusions. These transfusions help by replacing the sickled cells with healthy ones, which can prevent complications like severe anemia and organ damage.