SICKLE CELL DISEASE

Treatment advances bring hope to those with SCD

With proper treatment and support people with SCD can live full and enjoyable lives.

WHAT IS SICKLE CELL DISEASE?

Inherited red blood cell disorders

Red blood cells contain hemoglobin, a protein that carries oxygen. Healthy red blood cells are round and move through small blood vessels to carry oxygen to all body parts.

Abnormal hemoglobin

In someone who has SCD, the hemoglobin is abnormal, which causes the red blood cells to become hard and sticky and look like a C-shaped farm tool called a “sickle.” The sickle cells die early, which causes a constant shortage of red blood cells.

Clogged blood flow

When sickle cells travel through small blood vessels, they get stuck and clog the blood flow. This can cause pain and other serious complications such as infection, acute chest syndrome, and stroke.

DIAGNOSIS

Sickle cell anemia is diagnosed through blood testing. A blood test will demonstrate the following situations:

  • Your hemoglobin is normal.
  • You have sickle cell anemia or another sickle cell disease.
  • You have sickle cell trait (meaning you are a carrier for the disease).
  • Sickle cell disease can be identified before birth by testing a sample of amniotic fluid or tissue from the placenta.
  • Early diagnosis is important to better prevent complications.

SYMPTOMS

Possible symptoms include:

  • Skin that’s paler than normal
  • Yellowish skin, eyes, or mouth (jaundice)
  • Difficulty concentrating
  • Shortness of breath, especially during exercise
  • Dark-colored urine
  • Fever
  • Weakness
  • Dizziness
  • Confusion
  • Inability to handle physical activity
  • Enlarged spleen and liver
  • Increased heart rate
  • Heart murmur

The CDC states that SCD occurs in 1 of every 365 Black Americans. The disease occurs in 1 of every 16,300 Hispanic Americans.

About 1 in 13 Black children in the United States are born with sickle cell trait.

According to the American Society of Hematology, the condition also affects people of Middle Eastern, Asian, Indian, and Mediterranean descent.

CAN SCD BE PREVENTED?

Sickle cell anemia is an inherited blood disorder. Because it’s a genetic condition someone is born with, there is no way to prevent the disease, so scientists are constantly investigating ways that the disease can be stopped before it passes to the next generation.

The only cure for sickle cell disease is a bone marrow or stem cell transplant.

A child gets sickle cell disease (SCD) when he or she receives two sickle cell genes, one from each parent.

WHATS NEXT?

With proper treatment and support people with sickle cell disease can live full lives. Whether you are a person with an SCD diagnosis, a caregiver for a loved one with the disease, or a carrier of the trait, there are resources and support to help you on your journey.

I HAVE A SCD DIAGNOSIS

Explore more about SCD, including healthy lifestyle tips to keep you feeling well. Get recipes and exercise routines along with helpful resources for further support.

I'M A CAREGIVER FOR SOMEONE WITH SCD

Caring for a loved one with SCD can be daunting, but there is much you can do to help your loved one lead a fulfilling life.

I CARRY THE SICKLE CELL TRAIT

Whether understanding more about genetic testing, or how carrying the trait impacts family planning, there are resources to help guide you on your journey.

Learn more about YOUR HEALTH