Soccer fan, nurse, and actual Oxbryta patient
With sickle cell, the hemoglobin in the red blood cell releases oxygen, causing it to clump together (polymerize) and change into a sickle, or banana shape.
HEALTHY RED BLOOD CELLS
are flexible, can change shape easily, and can travel through blood vessels of any size.
HEMOGLOBIN
is a special protein inside red blood cells that helps carry oxygen throughout the body.
POLYMERIZATION & SICKLING
occur when hemoglobin inside red blood cells clumps together and causes red blood cells to change into a sickle shape.
Polymerization, which causes sickling, can cause other things to happen in the body, including serious consequences that may lead to long-term damage:
When red blood cells break down, the body does not have the amount of healthy red blood cells that it needs. This is called anemia, and this type of anemia could result in the body not having enough oxygen. Over time, lack of oxygen can damage body tissue, organs, and joints.
Polymerization and sickling weaken red blood, cells causing them to break down (hemolysis).
Sickled cells can block blood flow. When a blood vessel is partially or completely blocked, a pain crisis may occur.
Signs & Symptoms
The breakdown of red blood cells (RBCs)
Bilirubin
When there are high levels of bilirubin, yellowing of the eyes and skin may occur (jaundice).
Reticulocyte
High numbers of reticulocytes mean that the body is working to replace broken down RBCs.
Too few RBCs
Oxygen
When RBCs break down, less RBCs can deliver oxygen throughout your body.
Signs
Too few RBCs
Hemoglobin
A protein in RBCs that carries oxygen to the body’s organs and tissues.
When there are low levels of hemoglobin, you may experience anemia.
Too few RBCs
Oxygen
When your body does not have the amount of RBCs that it needs, this may mean not enough oxygen is being delivered throughout your body.
Take a look inside the red blood cell to learn more about why cells sickle and the impact sickling can have on the body.
Actual Oxbryta patient
Actual Oxbryta patient
When many people think about sickle cell, they only think about the painful crises that can put those living with sickle cell in the hospital. Many don't realize that sickle cell is more than that.
Sickle cell is a 365-day-a-year condition. That can mean living with day-to-day fatigue, yellow eyes from jaundice, and shortness of breath—all things you can easily feel and see.
But in addition, damage from sickle cell is always happening even if you don’t have pain crises or feel sick at all. Even when you feel fine, sickle cell may be causing damage. This damage can mean harm for many parts of your body.
Labs and screenings help you and your healthcare provider to proactively manage your sickle cell.
They can show if you are becoming anemic, if your blood cells are making too few red blood cells, if the red blood cells are breaking down too quickly, or if there are any other changes happening in your body.
There are some basics that can help you manage your sickle cell successfully. Be sure to see your healthcare provider regularly and establish an open dialogue so you can get the care you need.
Actual Oxbryta patient
Knowing your numbers is important
Your healthcare provider may check your lab reports for the following levels: