Sickle Cell Anemia Symptoms

When the sickle cells go through they can block up blood vessels and cause severe pain, fatigue, paleness, rapid heart rate, shortness of breath, and/or yellowing of eyes and skin. This can also start in early childhood and cause you to have a low number of red blood cells. This disorder can affect major organs such as lungs, kidneys, spleen, and brain. Anemia can cause shortness of breath, fatigue and Delayed growth development. The severity of the pain varies from person to person. The pain is usually medium to

People with sickle cell anemia also may have bouts of pain in the chest, stomach, arms, legs, or other parts of the body. This is caused by sickle cells blocking blood flow through the blood vessels. Feeling tired and having trouble fighting

If you have and unhealthy diet or if you are dehydrated or you get it genetically. Your symptoms are dizziness, tired or weak felling, thirsty a lot more often or thronging up also you your skin or white parts of eyes turn yellow, you get a lot of pain in your lower back, legs, arms abdomen, and chest, tempter change, stress, high altitude can also bring on Sickle Cell Disease. To help find out if you have Sickle Cell Disease you can get a bone marrow tests or a blood test, and a couple ways to help get rid of the disease you could get a bone marrow transplant or a blood transfusion. To live with it would be awful you have to get a lot of medical treatment and sometimes you don’t make it. The Sickle Cell Disease usually happens in African

Sickle cell anemia can cause numerous symptoms, which the severity of this can vary between individuals. Symptoms that might vary from person to person that change over time, include anemia, episodes of pain, frequent infections, delayed growth, vision disorder, acute chest syndrome, and more. Indeed, of each symptom; anemia, sickle cell breaks red blood cell faster and die living people without enough red blood cells. Sickle cell anemia usually dies in 10 to 20 days while normal live for about 120 days before it replaced. Episodes of pain is a major symptom of this disease and the most common reason for people to get hospitalization; Pain develops when sickle-shaped red blood cells block blood flow through tiny blood vessels to the chest,

Sickle-cell Anemia is a genetic disorder that causes sever pain in the lower back, legs, arms, abdomen, and chest. Red blood cells carry oxygen to the body. The body uses oxygen to make energy. Inside the red blood cell is a protein called hemoglobin, which hooks on to the oxygen. People with sickle-cell anemia have abnormal hemoglobin known as hemoglobin S. Hemoglobin S changes the blood cells into the shape of a sickle. These abnormal sickle cells stick to the blood vessel walls causing blockages. These blockages do not allow blood to flow. This is what causes the pain. People get sickle cell disease when a parent has a mutated hemoglobin gene. Their child has a chance of inheriting the sickle-cell trait or getting sickle-cell Anemia.

Physical Development – Due to the low levels of red blood cells, this hinders the delivery of oxygen and nutrients to organs, tissues and cells. People with Sickle Cell Anemia will have a lower than average height and weight than those with normal hemoglobin. This lower than average height and weight continues until late adolescence. Many children with sickle cell anemia will also experience puberty at a later stage at around 13-14 years of age for girls and 13½-14½ years of age for boys, rather than the average age of puberty for children who are unaffected by sickle cell anemia

Last semester in clinical, there was a patient with sickle cell anemia and he automatically sparked an interest in me. The patient was quite young and was in so much pain that he could not even bear to be touched by the nurse and reported a pain level of 8. Before my encounter with this patient, I did not know much about sickle cell anemia and decided to do some research on this disease. In my research, I learned that a majority of these patients go through acute pain episodes that occur chronically. After learning this and thinking about the young boy in the hospital, I wanted to discover more about how the pain in these patients are managed and controlled.

Sickle cell anemia can produce mild to severe symptoms and complications. Anemia symptoms are tiredness, irritability, dizziness, lightheadness, a fast heart rate, difficulty breathing, pale skin color, jaundice, slow growth and delayed puberty. Hand-foot syndrome which is usually the first symptom of sickle cell anemia is the swelling of the hands and feet (“Facts About Sickle Cell Disease,” 2016). The signs and symptoms can vary from person to person and change over time in sickle cell anemia (https://www.nhlbi.nih.gov/health/health-topics/topics/sca/signs). Over time sickle cell anemia can worsen. (“Facts About Sickle Cell Disease,” 2016)

Sickle cell is a blood disease. People with sickle cell anemia have crescent moon shaped blood cells that are hard and sticky. When the Sickle cells move through blood tubes, they can clog blood flow and break apart. This can cause main, damage, and a low blood count. The symptoms of the disease are not life threatening, however are not enjoyable. Sickle cell anemia can cause you to experience dizziness, headaches, and shortness of breath. Your skin may also turn more yellow or pale than it usually is. Sickle cell is an inherited disease. It is an unpreventable disease that you are born with. If you have a sickle cell gene, you do not have sickle cell, however your children have a 25% chance of having sickle cell anemia. This blood disorder can cause pain and discomfort but it is unlikely that your life will be in danger if you have the disease.

Have you ever wondered what could possibly hurt you more than just a simple pain that goes away less than a second? Have you ever wondered what could be worse than a headache or stomachache? Many of you complain about simple pain because you know it will go away. Temporary is a word that doesn’t exists for me and many others that are like me. That pain that some of you never image is Sickle Cell Anemia. Kids and Adults that suffer from sickle cell experience variety of issues. One of those issues is acute chest syndrome. Acute chest syndrome is a life threating lung related complication. Some symptoms of it are chest pain, a cough, fever, and shortness of breath. Another issue that people suffer from is Chronic Pain. Pain can occur anywhere

Approximately, two million Americans carry the sickle cell trait. 72,000 people are affected by sickle cell anemia in the U.S., most of whose ancestors had come from sub Saharan Africa, Spanish speaking regions, and Mediterranean countries such as Turkey, Greece, and Italy. In Hispanic American births, one in every thousand people acquire sickle cell anemia. The symptoms created by the blockage of blood flow can vary from patient to patient. Some have milder symptoms than others. Physicians use Hand-foot syndrome on patients to determine the disease. Sickle cells that clog small blood vessels in the hands and feet are one characteristic of the disease. Symptoms the patient suffers are swelling of the hands, feet and various joints. The pain

SCD Signs and symptoms often don't appear until an infant is at least four months old and may include several indications. First, Anemia sickle cells are weak. They die and split up easily, leaving you without a great supply of red blood cells. The major symptoms of SCD are Episodes of pain which occur at chest, abdomen, joints and bones. The pain might differ in intensity and can last for a couple hours to a couple weeks. Moreover, Hand-foot syndrome with swollen hands and feet might be the first indications of SCD in babies. Some people faced vision troubles because the small blood vessels that supply your eyes might stop and this can destroy the retina — the part of the eye that handle visual pictures.

A 4-year-old male of African American/Tunisian descent presented with pain of the hands, feet, and upper right quadrant of the abdomen following 3 hours of moderate to heavy physical exertion. Upon physical examination the boy presented with an enlarged spleen. Pre-screening indicates signs of sickle cell anemia (SCA). Patient’s mother reports no family history; however, paternal aunt passed away at an early age.

Sickle cell anemia is an anemia that is inherited and mostly affects people whose heritage can be traced back to places where malaria was prevalent. There are approximately 100,000 Americans that have the disease and many more with the trait. Several of my family members are afflicted by this medical condition that causes red blood cells to take on an irregular shape.

The genetic disease sickle cell anemia is a very fascinating disease. I was glad and beyond astonished on how this genetic disease was discovered, described, treated, and all the obstacles the carrier had to weave through each and every day. Sickle cell anemia is actually carried on the 11th chromosome. Chromosome 11 codes for the beta subunit of the hemoglobin protein. As a result, since the chromosome is damaged it cannot produce hemoglobin for the cell causing the cell to form into a “C” or sickle shape, hence the name sickle cell anemia. Sickle cell can cause hand-foot syndrome which is swelling of your hands or feet, very common in infected newborns. You can also experience episodes of pain. It is the most common symptom to deal with.