Sickle-cell anemia or the sickle-cell disease is a disorder of the blood where red blood cells are shaped abnormally. This can lead to a host of health problems, including those that are lethal. Sickle cell charities for kids are meant to raise money to put toward awareness, research and other important programs.
People that have this condition usually have a life that is shortened. In the past, males and females were not thought to live past 50 years of age. There have been advancements in medicine that have made for better disease management and now people with this are expected to live much longer. In fact, some live to 70 years old or beyond. A key to managing this being knowledgeable.
Charitable organizations for children with this problem aim to earn funds to increase medical studies for this disease. They are also designed to bring about awareness to all. This is often done by organizing educational resources so that sufferers, including children, are able to learn more about this disorder and how best to keep it in control.
There are a lot of complications that can come on as a result of this disease. Sufferers are more likely to have a stroke, bacterial infections, leg ulcers, decreased immune systems, opiod intolerance, cholelithiasis, infarction and priapism and more. Most of these problems are preventable or easily treated amongst those who take care of themselves. Some of the most common treatments needed by sufferers of sickle cell include: penicillin and folic acid, malaria chemoprophylaxis, transfusion therapy, bone marrow transplants, vaso-occlusive crises, acute chest crisis and hydroxyurea.
Charities may use donations for a variety of purposes. Typically these are used to fund programs and benefits as they relate to education, public information, advocacy and research. It is essential to look a the background of the organizations prior to offering contributions. Make sure the donations are going where they are said to go. Most of these groups share the goal of finding a cure for this inherited condition so that children do not have to live with it or pass it on.
The first written records of this date back to the 1800s. It was in the 1900s that a lot of information was brought to light about this. The condition afflicts people of all kinds, thought it seems dominant and those who have ancestors from East India, Mediterranean countries, Middle Eastern countries and Africa.
Diagnosis is usually done at birth through a blood test, which is routine for newborn screening. A child that tests positive on this screen will received a second blood test, known as hemoglobin electrophoresis, to confirm this diagnosis. Children that have this disease are more likely to get an infection or other complications, which is why early diagnosis and treatment is important as a preventative measure.
It is important that children receive regular care for this problem. Guardians should always share any concerns or questions with professionals. As the child gets older, educating them about their disease is important. Charities are doing their part to make these services more available around the world, while still raising money to put toward research to find a cure.
People that have this condition usually have a life that is shortened. In the past, males and females were not thought to live past 50 years of age. There have been advancements in medicine that have made for better disease management and now people with this are expected to live much longer. In fact, some live to 70 years old or beyond. A key to managing this being knowledgeable.
Charitable organizations for children with this problem aim to earn funds to increase medical studies for this disease. They are also designed to bring about awareness to all. This is often done by organizing educational resources so that sufferers, including children, are able to learn more about this disorder and how best to keep it in control.
There are a lot of complications that can come on as a result of this disease. Sufferers are more likely to have a stroke, bacterial infections, leg ulcers, decreased immune systems, opiod intolerance, cholelithiasis, infarction and priapism and more. Most of these problems are preventable or easily treated amongst those who take care of themselves. Some of the most common treatments needed by sufferers of sickle cell include: penicillin and folic acid, malaria chemoprophylaxis, transfusion therapy, bone marrow transplants, vaso-occlusive crises, acute chest crisis and hydroxyurea.
Charities may use donations for a variety of purposes. Typically these are used to fund programs and benefits as they relate to education, public information, advocacy and research. It is essential to look a the background of the organizations prior to offering contributions. Make sure the donations are going where they are said to go. Most of these groups share the goal of finding a cure for this inherited condition so that children do not have to live with it or pass it on.
The first written records of this date back to the 1800s. It was in the 1900s that a lot of information was brought to light about this. The condition afflicts people of all kinds, thought it seems dominant and those who have ancestors from East India, Mediterranean countries, Middle Eastern countries and Africa.
Diagnosis is usually done at birth through a blood test, which is routine for newborn screening. A child that tests positive on this screen will received a second blood test, known as hemoglobin electrophoresis, to confirm this diagnosis. Children that have this disease are more likely to get an infection or other complications, which is why early diagnosis and treatment is important as a preventative measure.
It is important that children receive regular care for this problem. Guardians should always share any concerns or questions with professionals. As the child gets older, educating them about their disease is important. Charities are doing their part to make these services more available around the world, while still raising money to put toward research to find a cure.
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