----------------------------------------------
------------------------------------------------------------------
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.
Those who have this condition usually have a shortened life. In the past, men and women with this were not expected to live beyond 50. Advancements in medicine have led to better disease management and now the life span is approximated at 70 years old, although some people live beyond that. A key to management of the disease is knowledge.
Organizations or charities for children strive to provide money that can be placed toward more research and studies on this disease. These funds are also used to bring new awareness to the public by way of educational resources and other information. Essentially, the goal is to educate children, parents and others about managing this disorder until a cure is found.
Many complications can come of this disease. Sufferers are likely to have leg ulcers, opiod intolerance, infarction, bacterial infections, stroke and many other problems. Most of these issues can be prevented or treated easily when a person maintains a healthy lifestyle and gets regular care from a doctor. Some treatments that are commonly issued to these patients: penicillin and folic acid, bone marrow transplants, acute chest crisis, hydroxyurea, transfusion therapy, bone marrow transplants and more.
These charities usually put the money they collect toward a variety of programs. Their efforts are typically focused on research, public information, advocacy and education. It is highly recommended that individuals do research on the organization or charity before putting forth a donation. Although most are doing honest work, there are some that are not. These groups all strive to find a cure for the disease and support those with it as much as possible.
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 crucial that children with this receive proper care on a regular basis. Guardians are expected to share all questions or concerns with health care providers. As children get older, education about this disease is recommended. Charities do their part to make resources available to people around the world as they strive to raise funds to get a cure.
Those who have this condition usually have a shortened life. In the past, men and women with this were not expected to live beyond 50. Advancements in medicine have led to better disease management and now the life span is approximated at 70 years old, although some people live beyond that. A key to management of the disease is knowledge.
Organizations or charities for children strive to provide money that can be placed toward more research and studies on this disease. These funds are also used to bring new awareness to the public by way of educational resources and other information. Essentially, the goal is to educate children, parents and others about managing this disorder until a cure is found.
Many complications can come of this disease. Sufferers are likely to have leg ulcers, opiod intolerance, infarction, bacterial infections, stroke and many other problems. Most of these issues can be prevented or treated easily when a person maintains a healthy lifestyle and gets regular care from a doctor. Some treatments that are commonly issued to these patients: penicillin and folic acid, bone marrow transplants, acute chest crisis, hydroxyurea, transfusion therapy, bone marrow transplants and more.
These charities usually put the money they collect toward a variety of programs. Their efforts are typically focused on research, public information, advocacy and education. It is highly recommended that individuals do research on the organization or charity before putting forth a donation. Although most are doing honest work, there are some that are not. These groups all strive to find a cure for the disease and support those with it as much as possible.
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 crucial that children with this receive proper care on a regular basis. Guardians are expected to share all questions or concerns with health care providers. As children get older, education about this disease is recommended. Charities do their part to make resources available to people around the world as they strive to raise funds to get a cure.
0 comments:
Post a Comment