Understanding Sickle Cell Disease 
In the State of Connecticut

Get the FAQs about Sickle Cell Disease

Understanding Sickle Cell Disease 

Sickle Cell Disease (SCD) is a genetic disease of the red blood cells. It is characterized by painful episodes, lower resistance to infections, organ damage, anemia, joint degeneration, strokes, and other health problems. SCD occurs when a child inherits a hemoglobin gene that sickles from both parents. In this case, the child is born with the disease.

 

Sickle Cell Trait (SCT) occurs when a child inherits a normal hemoglobin gene and a sickle gene. This results in a carrier of the sickle cell gene. SCT is harmless. The concern about the trait is that this abnormal gene can be passed to a child. 

HOSPITAL VISITS

A Person with Sickle Cell Disease has an average of 5.6 more hospital encounters annually with 20% having 11 or more encounters annually.

HOSPITAL ENCOUNTERS

Hospital encounters for Sickle Cell Disease increased 24% from

2011-2015 

CONNECTICUT #s

In Connecticut, nearly 

40,000 people carry the

Sickle Cell Trait.

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2019 SCDAA-CT : WOW! Creative Design Group