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Posted by / 05-May-2016 20:44

However, these tests also won't always detect a CF gene.Doctors diagnose most kids with CF by the time they are 3 years old, but if someone has a milder form of the disease, it may not be diagnosed until that person reaches the teen years.Cystic fibrosis is an inherited disease caused by mutations (changes) in a gene on chromosome 7, one of the 23 pairs of chromosomes that children inherit from their parents.

The two organs most affected are the lungs and pancreas, where the thick mucus causes breathing and digestive problems.A person with CF produces abnormal CFTR protein — or no CFTR protein at all, which causes the body to make thick, sticky mucus instead of the thin, watery kind.People who are born with CF have two copies of the CF gene.Babies are usually tested if they are born with an intestinal blockage called meconium ileus, which is more common in CF infants.Other symptoms include: People with CF get frequent lung infections that can damage their lungs over time and require strong antibiotics along with stays in the hospital.

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Because the mucus can block the path between the pancreas and the intestines, people with CF have trouble digesting food and getting the vitamins and nutrients they need from it.