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The sickle cells can block the flow of blood through vessels resulting in lung tissue damage (acute chest syndrome), pain episodes (arms, legs, chest and abdomen), stroke and priapism (painful prolonged erection). It also causes damage to most organs including the spleen, kidneys and liver. Damage to the spleen makes sickle cell disease patients, especially young children, easily overwhelmed by certain bacterial infections. All The above mentiond causes will appeare if the patient not get proper medication

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14y ago
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13y ago

It depends on what type. SC and SS patients have it bad they can not participate in sports and always have to be an an appropriate temp. they have to CONSTANTLY drink water and get alot of rest .people with the trait don't really go through anything maybe alittle pain here or there every once in a blue moon but it is VERY easy to shake of no real pain occurs. SC patients have it hard but they don't have it nearly as hard as SS patients. SS patient SS are cut short because it is very hard to control SC life span is cut to short but can be if they don't take care of themselves. a SS patient that doesn't take care of themselves are SURE to die a VERY early death. there is no good cure the only possible cure is to get new bone marrow which isn't advised because there is a higher chance that you will die than anything else.

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13y ago

Sometimes, people wouldn't like living with Sickle-Cell disease. I, personally, have a friend who has Sickle Cell Leukemia, and he's been suffering with it his entire life. Some of the symptoms are:

Dizziness

Headaches

Coldness in the Hands and feet

Jaundice (a yellowish color of the skin or whites of the eyes)

Paler than normal skin or mucous membranes (the tissue that lines your nose, mouth, and other organs & body cavities).

So yes, living with Sickle-Cell Disease isn't all that great you guys.

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11y ago

There are two versions of sickle cell: sickle cell disease (which is less severe) and sickle cell anemia (which is more severe). Sickle cell disease is caused by inheritance of one allele for sickle-shaped red blood cells and often has moderate effects on a person's health. Individuals with sickle cell disease may be exercise intolerant (they get short of breath and tired faster than others), have circulatory issues that typically manifests in the capillary beds and in general they have to be a little more careful about injuries and infections because their blood cells are not all normally shaped.

Sickle cell anemia is caused by inheritance of two alleles for sickle-shaped red blood cells and can have severe effects on a person's health. Individuals with sickle cell anemia are generally exercise intolerant - they can work out some, but have to pace themselves to not use too much oxygen too fast, have true anemia in which their blood doesn't transport enough oxygen and typically have damage to their capillary beds resulting in poor circulation in the distal limbs and some organs.

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12y ago

No. Its hereditary

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Q: How would sickle cell effect the life of the person?
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Related questions

What is requires for a person to have sickle cell disease?

The person is homozygous for the trait


What effect does sickle cell anemia have on the sedimentation rate?

Describe the effect that sickle cell anemia has on the sedimentation rate!


Who does the sickle cell disease effect?

blood


Does sickle cell effect children?

yes it does


Is it safe to marry a person with sickle cell?

it is safe to marry a person with sickle cell, provided that you are not a career of the trait.


What groups get sickle cell disease?

A person can only inherit sickle-cell genes if some of their ancestors came from certain regions in Africa where the inhabitants carry sickle-cell genes. A person with one sickle-cell gene has sickle-cell trait, a milder problem. If both father and mother pass on sickle-cell genes, the child, with two genes, will have sickle-cell disease.


How does a person with one sickle cell different than two Sickle cell?

A person with one sickle cell is a "carrier". This means that they have the dormant cell in their genetic composition, and if combined with another with the "carrier" gene, they run the high risk on concieving a child with the blood disease-one who has two sickle cells. A person with two sickle cells, has the sickle cell disease and are carriers(The gene is not dormant but active). Hope this simplifies and explains it for you.


Where in the world are the most cases of Malaria and Sickle Cell anaemia?

Malaria is common in topical ad subtropical zones. The malaria has selected the people with sickle cell anaemia. Although person with sickle cell anemia can have malaria, the carrier, or the person with sickle cell trait is resistant to malaria.


If sickle-cell anemia is so destructive why hasn't the sickle-cell allele been eliminated from the population?

It is important to note that sickle-cell anemia comes in two forms. The homozygous sickle-cell anemia and the heterozygous sickle-cell trait. The difference between the two is that sickle-cell anemia has a high rate death rate at a young age (20~), and the sickle-cell trait is nearly asymptomatic.In regions such as North America, sickle-cell anemia would be selected against and would eventually leave the gene pool. The sickle-cell trait on the other hand, has little effect on the fitness of the organism, and as such will remain in the gene pool.In malaria endemic regions such as sub-Sahara Africa, sickle-cell anemia provides very high levels of immunity to malaria and the sickle-cell trait provides a slightly lesser level of immunity. Both forms of sickle-cell will increase the organisms fitness and as such, it will remain in the gene pool. Further on, the sickle-cell trait has greater fitness than sickle-cell anemia, hence, the sickle-cell trait will be selected as the fittest allele.If s is the sickle-cell allele and S is a normal allele;The relative fitness in malaria endemic regions;Ss > ss > SSSickle-cell trait > Sickle-cell anemia > NormalThe relative fitness in non-malaria endemic regions;SS > Ss > ssNormal > Sickle-cell trait > Sickle-cell anemia


If Natasha has normal blood cell but marries someone who has sickle cell trace What are the chances of them having a child with sickle cell?

If a person does not carry the Sickle cell trait and they marry some one with the trait. The child that comes from that relationship can never have sickle cell disease, however that child has a chance of having the sickle trait.


What is the ESR in a person with sickle cell anemia?

0mm


What is require for a person to have sickle-cell disease?

The person is homozygous for the trait