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What is the relationship between sickle cell anemia and the risk of corona infection?

Sickle cell disease (SCD) is a genetic condition that affects millions of people worldwide, and living with this condition in times of COVID-19 is not easy and extra precautions must be taken.

People with sickle cell disease are more susceptible to COVID-19 because they are immunocompromised, so they should be careful during the pandemic, making sure they follow protocols including social distancing, hand washing, etc. A little caution, awareness, and daily management can help avoid risks.

What is sickle cell disease?


According to healthsite, in sickle cell disease, normally elastic red blood cells (erythrocytes) become hard and sticky and acquire a sickle or crescent shape. Sickle-shaped RBCs clump together and attach to the walls of blood vessels, cutting off the blood and oxygen supply to the Various body parts or organs resulting in organ damage or even stroke.

The disease is caused by a mutation in the gene that controls the production of red blood cells, sickle cells carry a type of hemoglobin that contributes to the formation of the characteristic sickle, while a person who carries the sickle cell gene may be a carrier without symptoms, sickle cell disease appears in those who inherit Two sickle cell genes, one from each parent a 'carrier'.

Some complications for a person with sickle cell anemia include anemia, pain, slow growth, vision problems, reduced immunity, gallstones and stroke.

Pain management


Pain management is a very important aspect of sickle cell disease. Patients with this condition should keep in touch with their doctor regularly and find out how they can relieve their pain. This can be through medications or other treatments. There may be certain things that can cause pain and should be avoided. As with any other case, there is no one-size-fits-all even in an SCD. Find out what works best for you and manage your condition accordingly in consultation with your doctor.

Symptom management


While it is a chronic condition, it is possible for people to live a full life and carry on most of their daily activities with proper management. Most treatment methods for this condition aim to relieve pain and other side effects incidentally. Just as with any other condition, there are few What people with sickle cell anemia should keep in mind to prevent symptoms from getting worse.