BLOOD SHORTAGE: URGENT/CRITICAL NEED for ALL DONATIONS & BLOOD TYPES. Click here to schedule your donation and help spread the word!

There is no deferral for COVID-19 vaccinations currently being administered in the U.S. and donors are not required to show status. Learn more about our Coronavirus Pandemic Response and COVID-19 Vaccinations. As part of the healthcare community, we are still requiring masks for donors, staff, volunteers and visitors to our facilities and blood drives but will provide updates if this changes. We will provide a mask for those who need one. Appointments are required but can be made the day of donation by contacting us at 800-747-5401.  

We're excited to announce that our organization is now officially named ImpactLife! Read more about our evolution here: 

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Sickle Cell Awareness Toolkit  Additional Resources

Did you know?

  • Sickle cell disease is the most common hereditary disorder and currently affects more than 100,000 Americans, predominantly people of African, Middle Eastern, Grecian, Indian, and Latin American descent. Reference
  • Sickle cell disease is estimated to occur in 1 of every 365 black or African-American births and 1 out of every 16,300 Hispanic-American births. Reference
  • Sickle cell disease causes the body to create abnormal hemoglobin and abnormally ‘sickle’ shaped red blood cells that causes pain and numerous health complication. 
  • More than 100 million people worldwide have the sickle cell trait. They carry only one defective gene (unlike two with sickle cell disease) and typically live normal lives. Rarely, extreme conditions such as severe dehydration and high-intensity physical activity can lead to serious health issues, including sudden death, for individuals with sickle cell trait. Reference
  • Although there is no cure for Sickle Cell Disease, blood transfusions are a critical part of treatment and can relieve the pain and complications that occur during a sickle cell crises. 
  • Thalassemia is also inherited blood disorder caused when the body doesn’t make enough hemoglobin. It is a treatable disorder that can be well-managed with blood transfusions and chelation therapy. Reference

Additional Resources



If I can do that little part, I hope you can too.

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Ashli, Aniyah and Octavia

Octavia, a phlebotomist, knows that blood donors are changing the world with each donation, but when she recently met Ashli and Aniyah heard their story, it encouraged her to spread the word about the difference a diverse donor base can make for sickle cell patients.

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Quinn was diagnosed with sickle cell disease when she was just three weeks old. But thanks to blood donors like you, she is out there living her best life, traveling the world and going to graduate school.

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