In addition, patients often experience other respiratory symptoms like persistent coughing, wheezing, exercise intolerance, and inflamed nasal passages or a stuffy nose.Digestive symptoms including foul-smelling and greasy stools, poor weight gain and growth, intestinal blockage, particularly in newborns (meconium ileus), and severe constipation are among many other symptoms.

cystic fibrosis dating another cystic fibrosis patient-60

Carrier detection and prenatal diagnosis of CF were developed for families with a history of the disease.

Mouse models of the disease were developed in the early 1990s, but unlike humans, mice without CFTR did not exhibit typical symptoms of CF, including the lung and liver disease that cause the premature mortality seen in humans. states, newborn screening for CF is provided even without the presence of symptoms.

Note: Cystic Fibrosis News Today is strictly a news and information website about the disease.

It does not provide medical advice, diagnosis or treatment.

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For people with cystic fibrosis (CF), cross-infection poses serious health risks - people with CF grow bugs in their lungs which are usually harmless to people who don't have the condition, but can be easily transmitted from one person with CF to another and be very harmful.

There is currently no cure for CF, but research leads to new medications that helps patients improve their quality of life and life expectancy.

According to the National Institutes of Health (NIH), the current average life expectancy for CF patients in the United States who live past childhood is about 37 years.

This is one case where you should shun your parents' otherwise good advice on sharing.

Cystic fibrosis (CF) is a chronic, inherited disease that affects the secretory glands, which are responsible for the production of mucus and sweat.

is an inherited disease characterized by the buildup of thick, sticky mucus that can damage many of the body's organs.