Sickle-cell disease or sickle-cell anemia are names tied to a hereditary blood disorder found in humans. Both SCD and SCA, respectively, involve red blood cells that have become rigid, abnormal and are shaped like a sickle. This sickling of cells is what reduces their flexibility and therefore heightens the risk of persons dealing with life-threatening problems. This problems is caused by mutant genes that produce both normal and abnormal hemoglobin. Sickle cell charities for kids are in operation around the globe and used to raise funds to help with medical treatments and research for those who suffer with this hereditary condition.
Those with this problem are more likely to have a shortened expectancy of life. In the past, it was under 50 years old for both women and men. Nowadays, advances in technology, knowledge and better management of sickle cell have increased the average life expectancy. Many have been known to live into the 70s and sometimes beyond then.
The charitable organizations for kids strive to bring in funds to increase the number of medical studies done on this problem. They are also meant to bring new awareness to people. This includes providing sufferers, of all ages, with necessary education resources so they can know more about the condition and the best solutions for keeping it under control.
A lot of complications can come with SCD. People with this are at a heightened risk of bacterial infections, opiod intolerance, osteomyelitis, cholelithiasis, decreased immune system, ulcers on the legs, stroke, acute papillary necrosis and more. Most of these issues can be prevented. They can also be healed with proper care and healthy lifestyle choices. Numerous options are available for managing this disorder, such as: hydroxyurea, bone marrow transplants and transfusion therapy.
Donations given to charities are used for many benefits and programs. Often they are used to provide the public with information, support medical research, advocacy, and offer professional education. It is essential that research be done on the charities to guarantee the funds are going to the correct source and there is no foul play. Most groups have the same goal of finding a cure for this disorder.
An autopsy from the 1800s is the first known recording of this condition in humans. During the 1900s, it was seen more often in people in many different regions of the world. Today, this condition affects all types of people but is most commonly seen amongst those originating from Middle Eastern and Mediterranean countries, as well as East India and Africa.
The diagnosis process is usually done at birth through a blood test common of newborn screenings. Kids testing positive will be given another test, hemoglobin electrophoresis, to verify the diagnosis. Those who have this disease are more likely to get infections and other medical complications, which is why early diagnosis and management is essential.
Children should be given regular care from a hematologist and doctor if they have this issue. There are also special clinics that specialize in care for sickle-cell patients. Health education is important for these kids as they grow older. Charities do their best to provide help to people with this all around the world and also raise money to find a cure.
Those with this problem are more likely to have a shortened expectancy of life. In the past, it was under 50 years old for both women and men. Nowadays, advances in technology, knowledge and better management of sickle cell have increased the average life expectancy. Many have been known to live into the 70s and sometimes beyond then.
The charitable organizations for kids strive to bring in funds to increase the number of medical studies done on this problem. They are also meant to bring new awareness to people. This includes providing sufferers, of all ages, with necessary education resources so they can know more about the condition and the best solutions for keeping it under control.
A lot of complications can come with SCD. People with this are at a heightened risk of bacterial infections, opiod intolerance, osteomyelitis, cholelithiasis, decreased immune system, ulcers on the legs, stroke, acute papillary necrosis and more. Most of these issues can be prevented. They can also be healed with proper care and healthy lifestyle choices. Numerous options are available for managing this disorder, such as: hydroxyurea, bone marrow transplants and transfusion therapy.
Donations given to charities are used for many benefits and programs. Often they are used to provide the public with information, support medical research, advocacy, and offer professional education. It is essential that research be done on the charities to guarantee the funds are going to the correct source and there is no foul play. Most groups have the same goal of finding a cure for this disorder.
An autopsy from the 1800s is the first known recording of this condition in humans. During the 1900s, it was seen more often in people in many different regions of the world. Today, this condition affects all types of people but is most commonly seen amongst those originating from Middle Eastern and Mediterranean countries, as well as East India and Africa.
The diagnosis process is usually done at birth through a blood test common of newborn screenings. Kids testing positive will be given another test, hemoglobin electrophoresis, to verify the diagnosis. Those who have this disease are more likely to get infections and other medical complications, which is why early diagnosis and management is essential.
Children should be given regular care from a hematologist and doctor if they have this issue. There are also special clinics that specialize in care for sickle-cell patients. Health education is important for these kids as they grow older. Charities do their best to provide help to people with this all around the world and also raise money to find a cure.
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