How do you know if you are at risk of getting cystic fibrosis? It can affect males and females and people from all ethnic groups. The disease is most common in Caucasians. Cystic fibrosis is the most common inherited disease among American Caucasians. Caucasians who have ancestors that came from Northern Europe are most susceptible to getting cystic fibrosis.
The thick mucus that is clinging to the linings of the air passages and lungs must be dislodged and removed. There are several ways removing the mucus. Many have been used since the disease was first diagnosed and named in the 1940's. New treatments are being discovered every year and the average life span of a CF patient has risen from 16 to the late 30's.
One of the most classic methods of dislodging the thick mucus is called chest percussion. This involves tapping on the chest and the back. This seems a cruel way to ease the suffering of a cystic fibrosis patient but has been effective. The parent of a CF child is taught how to tap the chest and back to loosen the mucus and without hurting the child. Another method is to change the patient's position as often as possible.
There are many mutations of the cystic fibrosis gene. Some will have more severe symptoms than others born with cystic fibrosis. Scientists estimate that as many as one of every 3600 Caucasian babies born in the United States this year will be born with cystic fibrosis. In comparison, there will be one of every 17,000 African American babies born with the disease, and only one of every 90,000 Asian babies will be born with cystic fibrosis.
In severe cases of cystic fibrosis a doctor may prescribe an oxygen machine. These are used for patients who have damaged lung capacity from the damage mucus has done to the lungs. This condition could be potentially life threatening and a constant supply of oxygen may help. There are many types of oxygen machines on the market including portable oxygen tanks you can take with you when you go out. No longer is a patient confined to his or her house with a big green oxygen tank sitting next to them. There are machines that provide a constant flow of oxygen. It can be set in one room of the house but have long enough hoses to allow the patient to freely roam in their home.
Sometimes, a medical doctor may recommend a lung transplant. The conditions need to be just right for the patient to be put on a list for a potential lung transplant. A lung transplant will not cure cystic fibrosis! Candidates for lung transplants should not have severe damage to other parts of their body, have cancer, are obese, have HIV, or are susceptible to a major psychiatric illness. Patients who do not have these severe complications can be considered for a lung transplant. Nicholas Pipens
The thick mucus that is clinging to the linings of the air passages and lungs must be dislodged and removed. There are several ways removing the mucus. Many have been used since the disease was first diagnosed and named in the 1940's. New treatments are being discovered every year and the average life span of a CF patient has risen from 16 to the late 30's.
One of the most classic methods of dislodging the thick mucus is called chest percussion. This involves tapping on the chest and the back. This seems a cruel way to ease the suffering of a cystic fibrosis patient but has been effective. The parent of a CF child is taught how to tap the chest and back to loosen the mucus and without hurting the child. Another method is to change the patient's position as often as possible.
There are many mutations of the cystic fibrosis gene. Some will have more severe symptoms than others born with cystic fibrosis. Scientists estimate that as many as one of every 3600 Caucasian babies born in the United States this year will be born with cystic fibrosis. In comparison, there will be one of every 17,000 African American babies born with the disease, and only one of every 90,000 Asian babies will be born with cystic fibrosis.
In severe cases of cystic fibrosis a doctor may prescribe an oxygen machine. These are used for patients who have damaged lung capacity from the damage mucus has done to the lungs. This condition could be potentially life threatening and a constant supply of oxygen may help. There are many types of oxygen machines on the market including portable oxygen tanks you can take with you when you go out. No longer is a patient confined to his or her house with a big green oxygen tank sitting next to them. There are machines that provide a constant flow of oxygen. It can be set in one room of the house but have long enough hoses to allow the patient to freely roam in their home.
Sometimes, a medical doctor may recommend a lung transplant. The conditions need to be just right for the patient to be put on a list for a potential lung transplant. A lung transplant will not cure cystic fibrosis! Candidates for lung transplants should not have severe damage to other parts of their body, have cancer, are obese, have HIV, or are susceptible to a major psychiatric illness. Patients who do not have these severe complications can be considered for a lung transplant. Nicholas Pipens
