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Understanding Sickle cell

Microscopic view of sicke cells causing anemia disease.

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There are many kinds of diseases that are associated with blood. Some are contagious diseases. Others are developed within the body because of lifestyle or unhealthy habits. On the other hand, there are also such diseases that are inherited, and one of these diseases is sickle cell.

What Is Sickle Cell Disease?

Sickle cell disease or SCD is a red blood cell disorder that is passed on from parents to children. This red blood cell is identified as sickle hemoglobin or hemoglobin S. There are many people with abnormal hemoglobin such as hemoglobin S, but the most common type of SCD is hemoglobin SS or sickle-cell anemia.


Our body tissues require oxygen, and this is being supplied by our hemoglobin or red blood cells throughout our body. Since hemoglobin has a round shape, it becomes flexible enough to easily flow through blood vessels. It’s soft and elastic, so it can fit freely flow along with other red blood cells.

Meanwhile, sickle cell has a sickle shape similar with that of a leech. Inside the sickle cell, there are strands that form such a shape, and these stands are hard. As a result, sickle cells don’t easily flow through blood vessels. Instead, they stick to the wall and block the blood vessel. Because of this, the supply of oxygen to our tissues are slowed down or even blocked completely.

When your body tissues don’t have enough supply of oxygen, you may suffer from severe pain crises. Such pain comes without early signs or warning, and this usually ends up being sent to the hospital for immediate treatment. In some cases, it can also harm or damage organs such as lungs, heart, brain, kidneys, and liver.


SCD is only inherited from a parent as it’s not contagious nor developed overtime. Nevertheless, the probability of inheriting sickle cell disease is low because even if your parent has SCD doesn’t necessarily mean you have also inherited it. There are factors that affect the transfer of SCD such as another parent’s condition. This means that both parents should have SCD in order to pass it on to their children. If only one of the parents has SCD, the disease will not be passed down.


There are different symptoms of sickle cell disease, and they vary from one patient to another depending on health condition. Nonetheless, these are some common symptoms you should observe:

  • Eye Problems
  • Slow Growth
  • Infections
  • Swelling
  • Pain

Swelling takes place in hands and feet; however, chronic pain is usually experienced by young adults who have SCD. If not managed properly, it may lead to bone damage and ulcers. Meanwhile, vision problems happen when eyes have the lack the supply of blood as a result of sickle cell blockage.

When You Should See a Doctor

Symptoms may be a false sign or just a sign of another different disease. It’s difficult to predict until you see a doctor. Visit a doctor if you see and experience the following signs:

  • Yellow Skin
  • Frequent Fever
  • Abnormal Swelling
  • Episodes of Pain


The only cure for SCD is stem-cell transplant or bone marrow transplant. However, it has a lot of challenges to do so. Aside from the fact that it is difficult to find a donor, only those who are16 years old or below are able to undergo such an operation. Moreover, the operation is risky, and it sometimes leads to death. Nevertheless, antibiotics are administered to cure the crises or pain.



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