cystic-fibrosis


General Symptoms Of Cystic Fibrosis Throughout The Body

People often think of cystic fibrosis as only affecting the respiratory organs of the body. This the place cystic fibrosis patients experience the most severe symptoms of cystic fibrosis. The common signs of cystic fibrosis in the pulmonary and respiratory system are commonly known. Coughing, wheezing, frequent bouts of bronchitis and pneumonia, sinusitis and fleshy growths in the nose. Thick, sticky mucus that is discolored when it is brought up is a sure sign of cystic fibrosis.

Cystic fibrosis often will show up in other parts of the body and will not be as easily recognized. This disease will often show up in the digestive organs. A common sign of digestive problems is stomach cramping, pain, and excess gas. Other common signs of a possible diagnosis of cystic fibrosis are diarrhea, stools that look greasy and smell foul. In worse cases a patient may experience a bowel blockage. A patient with cystic fibrosis may have severe vomiting.

The reproduction organs may also be affected. If a child has a delayed onset of puberty and have other signs of the disease this could be a sign of cystic fibrosis. Most males with cystic fibrosis will be sterile. Women with this disease may have difficulty becoming pregnant and be aware of the dangers of passing on the mutant gene that causes cystic fibrosis.

Another part of the body that can be affected by cystic fibrosis is the blood system. Anemia may occur. Anemia is a decrease in the number or make-up of the blood cells. Bleeding disorders such as inability to clot are also associated with cystic fibrosis.

Bone and joint problems is a little known sign of cystic fibrosis. We normally think of respiratory and digestive problems when a person is diagnosed with this disease. It might be surprising to learn that CF may affect arthritis, stunt the growth of a cystic fibrosis patient, severe pain in the joints and bones, and cases of osteoporosis may be attributed to this disease.

Another unusual sign of cystic fibrosis is an enlargement of the fingertips and toes. The digits swell, this symptom is called clubbing. This symptom is not rare but is often overlooked when searching for causes of respiratory, digestive, and reproduction problems. Other miscellaneous signs of cystic fibrosis is the inability to gain weight while still having an appetite and eating a normal diet. Salty skin and sweat, and liver problems are signs that may be overlooked in a diagnosis of cystic fibrosis. This disease could be mistaken for other problems with similar symptoms. Genetic testing needs to be done to confirm the diagnosis of cystic fibrosis. Knowing your family history may help your doctor decide what is causing your distress.

If you are experiencing any problems with breathing, frequent bouts of pneumonia or upper respiratory infections, or have polyps in your sinuses, you should contact your doctor. If you are diagnosed with cystic fibrosis it is helpful to have a medical team that specializes in this disease. Educate yourself also so you will be able to contribute to your own treatment.

 

 

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Cystic Fibrosis


Are You A Carrier Of The Cystic Fibrosis Gene?

... for having the mutant gene Asian-Americans have the least risk of being a carrier; the rate for this ethnic group is 1 in 90. The Cystic Fibrosis Foundation estimated about 30,000 adults and children in the United States have cystic fibrosis. This disease severely affects several organs in the body but ... 

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Medical Problems Caused By Cystic Fibrosis

... cause rectal prolapse. This pushes the rectal tissue outside of the body. Another serious illness you may have because of cystic fibrosis is low bone density. Your body does not get enough Vitamin D and can cause rickets. Your doctor may recommend Vitamin D supplements to prevent low bone density. If ... 

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Drug Therapy For Cystic Fibrosis Patients

... adrenal gland and they may be prescribed to prevent the severity and the frequency of lung infections. The cystic fibrosis patient may also take oral nonsteroidal anti-inflammatory drugs. Ibuprofen and other similar drugs can reduce the severity of some symptoms of cystic fibrosis. There are potentially ... 

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Standard Tests For Diagnosing Cystic Fibrosis

... the liver, pancreas, and the breathing capacity of the lungs. Antibiotics will be needed to help fight infections. The heavy mucus allows bacteria, germs, and infections to stay in the system and create chronic respiratory and digestive problems. The testing done to find out if a person has cystic fibrosis ... 

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How To Recognize The Symptoms Of Cystic Fibrosis In Children

... the hospital they will be checked to be sure they have proper lung function and they will be given a diet with digestive enzymes and the vitamins they need to gain weight normally. The child will need to see their doctor at least once every three months. The child with cystic fibrosis will need daily ... 

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