How long is a person with CF expected to live?

Today, the average life span for people with CF who live to adulthood is about 44 years. Death is most often caused by lung complications.
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How long can you live with CF?

Not only are there more of us with CF, but we are now living longer. Based on the 2021 CF Foundation Patient Registry data, the current life expectancy for CF patients born between 2017 and 2021 is 53 years — a substantial jump from a decade ago when the life expectancy was 38.
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What is the oldest person with CF?

The oldest person in the United States diagnosed with CF for the first time was 82. Those who are not diagnosed with CF until later in life generally suffer from colds, sinus infections, pneumonia, stomach pains, and acid reflux. They may also have trouble gaining or keeping on weight.
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Can you live past 40 with cystic fibrosis?

Currently, about half of people with cystic fibrosis will live past the age of 40. Children born with the condition nowadays are likely to live longer than this.
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Can you live to 70 with cystic fibrosis?

Some people will live longer. In fact, some people with CF are living into their 70s.
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Can people with CF have kids?

Most women with CF are able to become pregnant and achieve a normal pregnancy. Your obstetrician should be able to help you understand your reproductive health to help you make the right family planning decisions.
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What is end stage cystic fibrosis?

Common symptoms at the end of life include dyspnea, fatigue, anxiety, anorexia, pain, and cough (see Fast Facts #27, 199, 200). Care providers must balance benefit versus burden of disease-specific treatments such as nebulized medications, NIPPV, and chest physiotherapy.
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Is CF painful?

People with cystic fibrosis are at higher risk of developing a dangerous thinning of bones. They may also experience joint pain, arthritis and muscle pain.
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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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What is the cause of death for 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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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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Why does CF shorten life span?

Cystic fibrosis (CF) shortens life by making the lungs prone to repeated bacterial infections and associated inflammation. UNC School of Medicine researchers have now shown for the first time that the lungs' bacterial population changes in the first few years of life as respiratory infections and inflammation set in.
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What gender is most affected by cystic fibrosis?

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 you fully recover from cystic fibrosis?

There's currently no cure for cystic fibrosis, but it's possible to help control the symptoms, prevent or reduce complications, and make the condition easier to live with. A person with cystic fibrosis will be supported by a team of healthcare professionals at a specialist cystic fibrosis centre.
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Is cystic fibrosis hard to live with?

Despite the fact that there is currently no cure for cystic fibrosis, there are treatments that improve patients' quality of life and life expectancy. In fact, children with CF tend to remain healthy when medicated until adulthood, but as lung function declines, the patient often becomes disabled.
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What is the average age of death?

For women and men, life expectancy of 79.1 years and 73.2 years reflects a long-apparent, significant gap.
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Can 2 CF patients be together?

That's why it's important for people with CF to stay at least 6 feet away from others with CF and anyone with a cold, flu, or infection. 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.
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Is cystic fibrosis curable if caught early?

There is no cure for cystic fibrosis, but treatment can ease symptoms, reduce complications and improve quality of life. Close monitoring and early, aggressive intervention is recommended to slow the progression of CF , which can lead to a longer life.
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Can CF patients get new lungs?

Lung transplantation is a surgical option for people with cystic fibrosis who have advanced lung disease. Lung transplantation can extend and improve your quality of life, but it involves an extensive evaluation and dedication to living the lifestyle required to keep your new lungs healthy.
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How does someone with CF feel?

Several people shared that CF feels like a cold that never goes away, which makes sense considering this diagnosis affects the lungs. Many folks named coughing and congestion as symptoms they deal with every day. “If they think a cold is bad, imagine having one all the time.
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Does CF cause brain damage?

Cystic fibrosis (CF) patients present with a variety of symptoms, including mood and cognition deficits, in addition to classical respiratory, and autonomic issues. This suggests that brain injury, which can be examined with non-invasive magnetic resonance imaging (MRI), is a manifestation of this condition.
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What age do CF 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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What happens if CF is not treated?

CF causes thick mucus that clogs certain organs, such as the lungs, pancreas, and intestines. This may cause malnutrition, poor growth, frequent respiratory infections, breathing problems, and chronic lung disease. There is no cure for CF.
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What happens to CF patients after lung transplant?

Although you will not have cystic fibrosis in your lungs after the transplant, you will have CF everywhere else. You will need to continue receiving treatment to manage your CF in your other organs. Of course, if anything comes up between visits, contact your CF care team immediately.
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Are all men with CF infertile?

While 97-98 percent of men with cystic fibrosis are infertile, they can still enjoy normal, healthy sex lives and have biological children with the help of assisted reproductive technology (ART).
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