Click here for our response to the Coronavirus Pandemic (COVID-19) including information from the U.S. Department of Homeland Security on blood donation being permitted during Stay at Home directives. 

Click here for care provider and self-referrals for convalescent plasma donors for those that had a positive molecular test (also called PCR or polymerase chain reaction) and are fully recovered from COVID-19.  Email patientservices@mvrbc.org or call 833-610-1025 with questions.

you can make a difference

Did you know?

  • Sickle cell disease is the most common hereditary disorder and currently affects more than 70,000 Americans, predominantly people of African, Middle Eastern, Grecian, Indian, and Latin American descent. Reference
     
  • Sickle cell disease is estimated to occur in 1 in 500 African Americans and 1 in 1,000 to 1,400 Hispanic Americans. 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

Stories

Ashley

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

See all Stories

Stories

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.

See all Stories

Stories

Quinn

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.

See all Stories

Stories

Valerie

Valerie was diagnosed with sickle cell anemia at 2 years old. She explains what it is like to have sickle cell anemia and how blood transfusions save her life.

See all Stories