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The Life Span of Sickle Cell Patients Is Twice as Long as The Average Person

One such health issue is sickle cell disease (SCD). Sickle cell disease (SCD) is a congenital red blood cell abnormality termed after the crescent shape of red blood cells. SCD affects millions of people worldwide. Around 100,000 people in the United States have congenital illnesses.

Famous people who had or have SCD include jazz artist Miles Davis and former NFL running back Tiki Barber.

The sickle-shaped cells result in blockages known as vaso-occlusion, which impedes the correct flow of blood and thus oxygen throughout the body.

Miles Davis, a jazz musician, and former NFL running back Tiki Barber are two famous people who have had SCD.

People with SCD encounter numerous obstacles, including acute pain episodes, stroke, and organ damage, with a national median life expectancy of 42–47 years. The sickle cell disease podcast clearly explains how SCD, a hereditary, lifelong blood illness, is characterized by hard and sickle-shaped red blood cells that adhere to blood vessels, limit blood flow, and have just one FDA-approved treatment. Some people may have limited access to proper care.

However, according to a new study published today in Blood, the Journal of the American Society of Haematology (ASH), some persons with moderately symptomatic SCD can live long lives with adequate disease treatment, including strong family support and strict adherence to medication and appointments.

The four-case study analysis details the outcomes of four women with milder variants of SCD who have outlived the U.S. median of 47 years for women with the condition, lasting as long as 86 years.

“Their healthy lifestyles most likely contributed greatly to their longevity.” All of the women were nonsmokers who drank little to no alcohol and had a normal BMI.

I would frequently come out to the waiting room and find these ladies talking with other SCD patients, and I could tell that they gave others hope, that just because they have SCD does not mean they are doomed to die by their 40s — that if they take care of themselves and live close to those who can help keep them well, there is hope for them to live long full lives.” says a doctor.

Some sickle cell disease patients may benefit from stem cell transplantation. Bone marrow contains stem cells. A bone marrow transplant from a healthy, matched sibling would be ideal for an SCD patient. However, only around 15% of patients have a relative who fits the requirements. And bone marrow transplants are still dangerous, with as high as 5% fatality rates. Several sickle cell disease podcasts emphasize the significance of African American blood donations in helping persons with sickle cell illnesses who may require one or more blood transfusions. You can find more videos and podcasts on sickle cell disease on getting healthy.

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