According to Innovative Hematology, Marion and Lake counties have the highest rates of sickle cell disease patients in Indiana. Photo by Adobe Stock.

By Terri Dee
Indiana News Service

INDIANAPOLIS — The Centers for Disease Control and Prevention report the life-shortening blood disease sickle cell anemia affects about 100,000 Americans, mostly people of color.

And many individuals with the illness do not get the important screenings and treatments.

Sickle cell disease causes normally healthy, round, and flexible blood cells to become “C” or sickle-shaped and stick to small blood-vessel walls.

This blockage prevents blood and oxygen flow to the arms, legs, and internal organs. Around 1,700 Hoosiers, mostly women of color, are impacted by the disorder.

Lisa Hoffman, grants and team manager with Innovative Hematology, said she would like to see better public awareness about the inherited disease.

“I would like to think it’s not an issue about race, but 87% of the people in Indiana that have sickle cell are Black or African American,” said Hoffman. “There are other diseases that affect predominantly white folks, and those diseases seem to get a bit more attention.”

Patient education is essential for addressing sickle cell anemia complications. The blockages cause repeated episodes of severe pain, organ damage, infections, or sometimes a stroke.

Innovative Hematology indicates that 52% of sickle cell anemia patients in Indiana are female, and 48% are male.

One barrier to care is insufficient or no insurance coverage, which affects disease management. Another is a lack of medical providers with knowledge of detecting the illness. This can lead to a misdiagnosis or prescribing an ineffective treatment plan.

Hoffman said family members in dual roles as caregivers often do not get needed support. And other factors can present additional burdens for a patient.

“If you’re a single mom and you have sickle cell disease and you are having a pain crisis and really should go to the hospital,” said Hoffman, “you face a lot of barriers – such as, who’s going to watch my child? How am I going to get there?”

The Indiana Statehouse hosted 174 attendees for Sickle Cell Advocacy Day Monday, Feb. 3, to raise the voices of those in the community who are affected by the painful disorder.

Hoffman said she wants legislators to extend health care services beyond age 21 for individuals with this specific condition.