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CF is an autosomal recessive disorder, meaning that you need to inherit the CFTR mutation from both your mother and father to have the disease.

If you only inherit one defective gene, you won't have CF but will instead be a carrier of the mutated gene.

While there is no cure for CF, there are treatments that can improve both the length and quality of one's life.

These include airway clearance techniques, inhaled antibiotics, mucus thinners, pancreatic enzymes, a high-calorie diet, and newer generation medications known as CFTR modulators. As a genetic disorder, cystic fibrosis is something you are born with.

By the 1980s, one could expect to live as long as 20 to 25 years.Cystic fibrosis is one of the more common genetic diseases, affecting roughly one in every 2,500 babies born in the United States.It is most common among Caucasian and Hispanics, and occurs less frequently in people of African or Asian descent.(CF) is an inherited, life-threatening disorder that damages the lungs and digestive tract.It is caused by a defective gene that triggers the production of thickened mucus which clogs airways and blocks the secretion of digestive enzymes.While there is no cure for cystic fibrosis, advances in treatment have extended the lifespans of those living with the disease.The aim of CF treatment is four-fold: to prevent infections, retain lung function, normalize digestion, and slow the progression of the disease.There are a few tests used to diagnose cystic fibrosis.They work either by directly detecting the CFTR mutation or indirectly measuring biological changes consistent with the disease.Death will most often be the result of respiratory failure, followed by heart failure and liver failure.Cystic fibrosis is caused by the mutation of the cystic fibrosis transmembrane receptor (CFTR) gene, which is responsible for producing the CFTR protein.