Major pain in different parts of body
The symptoms for sickle cell ANEMIA are breathlessness, fatigue, chest pain, rapid heart rate, delayed growth or puberty, abdominal pain, weakness, joint pain, vomiting, fever, excessive thirst, and bloody urination. If you think you have this serious disease contact your doctor immediately!!!
What is sickle cell disease?Sickle cell disease is an inherited disorder that affects red blood cells. People with sickle cell disease have red blood cells that become hard and pointed instead of soft and round. Sickle cells cause anemia, pain and many other problems.Top2) What is sickle cell trait?If you have sickle cell trait, you have inherited the gene for sickle cell disease. Sickle cell trait does not turn into sickle cell disease. If someone has sickle cell trait and his partner has sickle cell trait they may produce a child with sickle cell disease. There are about 2.5 million people in America with sickle cell trait.Top3) If sickle cell trait is not an illness, why are people tested?Babies are tested to see if they have sickle cell disease. Teens and adults are tested mainly to see if they can have a baby with the disease.Top4) What medical problems are caused by sickle cell disease?Lung tissue damage, pain episodes and stroke. The blockage of blood flow caused by sickled cells also causes damage to most organs including the spleen, kidneys and liver.Top5) How many people have sickle cell disease?Sickle cell disease is a global health problem. In the United States it is estimated that over 70,000 people have sickle cell disease. About 1,000 babies are born with the disease each year in America.Top6) How long does a person with sickle cell disease live?The average life expectancy in America has improved. It is now in the mid 40 years of age range.Top7) Are people of African descent the only group affected?No. It is also present in Portuguese, Spanish, French Corsicans, Sardinians, Sicilians, mainland Italians, Greeks, Turks and Cypriots. Sickle cell disease also appears in Middle Eastern countries and Asia.Top8) Is there a cure?There is no universal cure for sickle cell disease. Research in gene therapy, the ultimate universal cure, is currently underway.Top9) What are some promising treatment developments?The use of hydroxyurea has shown promising results on some adult sickle cell patients. It reduces the frequency of severe pain, acute chest syndrome and the need for blood transfusions.Top10) Can people with sickle cell disease live a productive life?Yes. But like all patients with chronic disease, sickle cell patients are best managed in a comprehensive multi-disciplinary program of care and a strong extended support system.
1. Sickle Cell was the 1st genetic disorder discovered2. 1 in every 500 Black babies born have Sickle Cell However any one of any race can have sickle cell this is why in more than 40 states every single baby born is tested for sickle cell 3. Sickle Pain happen because the blood flow is blocked and the tissue is dying, the same reason that people have pain from a heart attack. So think of a crises as having heart attacks all over your body 4. Pain is not the only symptom of Sickle cell, every sickle cell champion is not in pain but blood flow can be interrupted any where even in your organs this is why the most devastating thing that this disease can do is cause a STROKE. 5. There is only 1 medication that is FDA approved To treat "Sickle Cell" (many medications treat the symptoms) but HYDROYUREA is the only medication to treat the disease.
Sickle cell trait and sickle cell disease are both genetic conditions caused by a mutation in the hemoglobin gene. Sickle cell trait means a person carries one copy of the mutated gene, while sickle cell disease means a person has two copies. The key distinction is that individuals with sickle cell trait usually do not experience symptoms, while those with sickle cell disease can have severe health issues such as pain crises, anemia, and organ damage.
Peope with sickle cell disease suffer from pain crisis in arms,legs or ,chest. Well at least my daughter do. It is painful and she has to be admitted to hospital and receive morphine and. Iv fluids to relieve pain.
C. Sickle-cell anemia
It has to do with your genitic make up. You don't have sickle cell anemia because you only have 1 of the traits on your beta hemoglobin gene. People with sickle cell anemia have two.Most of the time peolple with sickle cell trait display much milder symptoms. It is more prevolent in African Americans and woman should be monitored during pregnancy.
If you have sickle cell anemia and already know it, then it wil lbe pretty easy to tel lwhen the symptoms show themselves. I don't have it myself but people with sickle cell apparently go through a lot of pain when a sickle cell gets stuck in a blood vessel and causes a clot; there isn't a cure, just doctors can give stuff to make the pain less but not totally go awayunless maybe they knock you unconscious. Also people with sickle cell have more trouble with sports and activites since sickle cells can't carry as much oxygen as normal ones. I'm sorry, but that's all the symptoms I know...
OK i know this guy who has sickle cell and he had gotten shot once and he said that the sickle cell pain her ts more it is also like your worst headake it hurts more than breaking a bone their are no words in the English dictionary to describe it
Sickle Cell Anaemia is a genetic disorder that affects the red blood cells. The shape of the cells are changed from being round and flexible to sickle or crescent shaped. These abnormal cells can then clog the blood vessels, causing extreme pain and discomfort. These episodes are known as sickle cell crisis.
I think you mean sickle cell diseaase. Here is some more information for you that will answer your question better than I can: http://en.wikipedia.org/wiki/Sickle_cell_disease In short, sickle cell disease is a blood disorder of the red blood cells. Basically, the red blood cells have an abnormal, rigid, sickle shape (hence the name sickle cell disease).