What is sickle cell anemia.

A mother of in central Africa has had no health problems her ideal life. She has four beautiful children in her lifetime. Her first child of eight years old catches malaria; he sweats in his quiet every night, experiences the chills, is plagued with the fever, and has periodic attacks. To make matters even worse he has developed the condition known as splenomegaly which causes an enlargement of the spine that cripples him to his end when he dies of anemia. The second child, a daughter, is born with the familial condition known as sickle cell anemia. throughout this childs life she experiences ulcers up and down her legs, many fevers, and attacks that seem to be the unbearable pain a human can wear without passing out. She will never be around broad enough for her seventeenth birthday. Her last two children live considerable and healthy lives. Over time Mother Nature has fix a side door around malaria, but she has unleashed demolition with his sickle, causing peoples red blood cells not to function correctly in carrying oxygen, causing terrible side effects and death.

For a long time little was known of blood diseases. great deal in central Africa were experiencing pain and dieing from an unknown killer. In 1956, Dr. Vernon Ingram and Dr. Paulings tested the blood of patients in central Africa.



Surprisingly there were primal differences between the hemoglobin of the some patients (Silverstein 17). Hemoglobin is made up of chains of amino acids, like proteins; these chains are folded and looped in a complicated structure(Johnson 325). In club to bar up the bonds of hemoglobin and change it into mixture of shorter amino acids, Dr. Ingram utilise enzymes and other chemicals. By organizing these fragments of sections, it is possible to work out a map to the...

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