FAQ'S about Sickle Cell Disease

What is sickle cell disease (SCD)?

Sickle cell disease is a genetic blood disorder where red blood cells become rigid and crescent-shaped, leading to various complications.

How is SCD inherited?

Sickle cell disease is inherited through autosomal recessive genes, meaning both parents must carry the trait for a child to be affected.

What are the symptoms?

Symptoms include pain, anemia, fatigue, and increased susceptibility to infections.

How is it diagnosed?

Diagnosis involves blood tests, including hemoglobin electrophoresis, to identify abnormal hemoglobin.

Can SCD be prevented?

Genetic counseling and testing can help identify carriers, but complete prevention involves avoiding having children with another carrier.

Is there a cure?

As of now, there is no cure, but treatments focus on managing symptoms and preventing complications.

Does SCD affect all races equally?

SCD is more common in certain populations, including people of African, Mediterranean, Middle Eastern, and Indian descent.

How does SCD affect pregnancy?

Pregnancy in women with SCD requires careful monitoring due to potential complications for both the mother and the baby.

Can SCD be managed with medication alone?

Medications, including hydroxyurea, can help manage symptoms, but a comprehensive approach often involves various interventions.

Are there support groups for individuals with SCD?

Yes, there are support groups and organizations that provide resources and community for individuals and families affected by SCD.