Does CF get worse as you get older?

Cystic fibrosis tends to get worse over time and can be fatal if it leads to a serious infection or the lungs stop working properly. But people with cystic fibrosis are now living for longer because of advancements in treatment. Currently, about half of people with cystic fibrosis will live past the age of 40.
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What's the oldest you can live with cystic fibrosis?

In fact, babies born with CF today are expected to live into their mid-40s and beyond.
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At what age do cystic fibrosis symptoms start?

The signs and symptoms of cystic fibrosis generally begin to occur around 6-8 months after birth, though this can differ significantly from person to person. Symptoms tend to differ depending on age and can affect various areas of the body.
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Do people with cystic fibrosis get sick easier?

People with CF are susceptible to infections from bacteria, viruses, and fungi because abnormally thick, sticky mucus traps these germs in the airways. They also are prone to infections because their mucus and airway liquid does not have the same infection-fighting properties as normal mucus.
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Why can't people with CF be close?

For people with CF, being close to others with the disease puts them at greater risk of getting and spreading dangerous germs and bacteria. This is called cross‐infection. Not only are these dangerous germs difficult to treat, but they can also lead to worsening symptoms and faster decline in lung function.
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CF Foundation | CF Diagnosis in Adulthood



What kills people with CF?

In cystic fibrosis, Pseudomonas aeruginosa is a much-feared pathogen. The bacterium easily colonizes the lungs of people with cystic fibrosis, leading to chronic infections that are almost impossible to eradicate and are ultimately fatal.
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How long can cystic fibrosis go undetected?

In the U.S., because of newborn screening, cystic fibrosis can be diagnosed within the first month of life, before symptoms develop. But people born before newborn screening became available may not be diagnosed until the signs and symptoms of CF show up.
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Can you have CF and not know it?

While cystic fibrosis is usually diagnosed in childhood, adults with no symptoms (or mild symptoms) during their youth can still be found to have the disease.
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What triggers cystic fibrosis?

Cystic fibrosis (CF) is a genetic disease. This means that CF is inherited. Mutations in a gene called the CFTR (cystic fibrosis conductance transmembrane regulator) gene cause CF. The CFTR mutations causes changes in the body's cell's electrolyte transport system.
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Who is the longest CF survivor?

The Results: 30 Years After Transplant

Thirty years post-transplant, Paul is considered the longest-living lung transplant recipient with CF in the United States.
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Can you live to 80 with cystic fibrosis?

Some people will live longer. In fact, some people with CF are living into their 70s.
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Is there a cure for cystic fibrosis coming soon?

Currently there's no cure for rare types of cystic fibrosis, but researchers are making significant advances. Current treatments for cystic fibrosis are not suitable for all patients.
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Which parent passes down cystic fibrosis?

To be born with cystic fibrosis, a child has to inherit a copy of the faulty gene from both of their parents. This can happen if the parents are "carriers" of the faulty gene, which means they don't have cystic fibrosis themselves.
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Which parent passes cystic fibrosis?

Cystic fibrosis (CF) is a genetic disease. This means that CF is inherited. A child will be born with CF only if two CF genes are inherited - one from the mother and one from the father. A person who has only one CF gene is healthy and said to be a "carrier" of the disease.
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What is mild form of cystic fibrosis?

Atypical CF is a milder form of the CF disorder, which is associated with mutations of the cystic fibrosis transmembrane receptor gene. Instead of having classic symptoms, individuals with atypical CF might only have mild dysfunction in 1 organ system and might or might not have elevated sweat chloride levels.
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Is CF inherited from mother or father?

Genetics and Diagnosis

Cystic fibrosis is a genetic disease. People with CF have inherited two copies of the defective CF gene — one copy from each parent. Both parents must have at least one copy of the defective gene.
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What are 3 major symptoms of CF?

What Are the Symptoms of Cystic Fibrosis?
  • Chronic coughing (dry or coughing up mucus)
  • Recurring chest colds.
  • Wheezing or shortness of breath.
  • Frequent sinus infections.
  • Very salty-tasting skin.
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Can a chest xray show CF?

X-rays (radiographs) of the chest may not show early lung changes in people with CF, though x-rays may reveal small airway blockages. Advanced bronchiectasis will show up on a chest x-ray. More than 90% of people with CF show signs of chronic sinusitis on x-ray.
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How painful is cystic fibrosis?

Pain is an important part of cystic fibrosis disease in children and adults. Indeed, pain is reported in more than 60% of studies published last years. Further studies are necessary to create a specific pain assessment tool to evaluate pain and improve care.
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Does a lung transplant cure CF?

Does a lung transplant cure cystic fibrosis? No. Cystic fibrosis is a genetic condition so even though the transplanted lungs will not have CF and will never develop it, the rest of the person's body will continue to have cystic fibrosis.
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Why 5 feet apart for cystic fibrosis?

In people with CF, the mucus in the lungs can trap bacteria, causing infection. These infections can be dangerous – even life-threatening – to people with CF. This is why doctors say that patients with CF should stay 6 feet (or more) away from anyone who is sick.
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What is most common cause of death for people with CF?

Mucus in CF patients is very thick and accumulates in the intestines and lungs. The result is malnutrition, poor growth, frequent respiratory infections, breathing difficulties, and eventually permanent lung damage. Lung disease is the usual cause of death in most patients.
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Why is hygiene important for people with cystic fibrosis?

The equation is simple: Less germ exposure equals fewer infections. This is particularly important for people with cystic fibrosis (CF) who are at greater risk of developing lung infections. Thus, preventing these infections helps preserve lung function and improve quality of life for people with CF.
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Is CF more common in males or females?

Males account for slightly more than 50 percent of all cases of cystic fibrosis (CF) but generally have better outcomes than females until about age 20. After that, men and women experience roughly equal outcomes for long-term survival. Still, males with CF tend to live an average of 2 years longer than females.
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Can guys with CF have kids?

The Difference Between Infertility and Sterility

Even though the vas deferens is missing, the sperm are not. In fact, sperm production in the testicles is normal in 90 percent of men with CF and CBAVD, meaning that most men with CF can still have biological children through assisted reproductive technology (ART).
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