What are the best sports for cystic fibrosis?

In general, people with CF should play any sport or game they enjoy. There are very few activities to avoid. These are scuba diving, skydiving, bungee jumping, and high-intensity activities at high altitudes. Those with an enlarged liver or spleen should avoid collision sports such as football, basketball, or soccer.
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What is the best exercise for cystic fibrosis?

Children with CF should be encouraged to take part in as much physical activity as possible, ideally types of exercise that leave you out of breath, such as running, swimming, football or tennis, although there are a wide range of suitable activities.
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Can children with cystic fibrosis play sports?

Children with CF go to school and can play sports just like other kids. Many of them go to college, get jobs, marry, and have families. Your child's CF care team is there to support you and your child. That team includes your child's doctor, nurse, dietitian, and social worker.
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Can kids with CF play football?

Exercises to Avoid

Children with CF should not scuba dive, skydive, bungee jump or do high-intensity activities at high altitudes (mountain climbing). Children who have an enlarged liver or spleen should avoid collision sports such as football, basketball and soccer.
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What are the pros of cystic fibrosis?

The mutation that causes cystic fibrosis may actually serve a useful purpose: protecting against typhoid fever. The finding, reported in tomorrow's issue of Nature, may help explain why this invariably fatal inherited disease is so prevalent today.
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Cystic Fibrosis: Sports and Exercise



Is cystic fibrosis a big deal?

Cystic fibrosis is a disease that causes thick, sticky mucus to build up in the lungs, digestive tract, and other areas of the body. It is one of the most common chronic lung diseases in children and young adults. It is a life-threatening disorder.
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What activities should be avoided with cystic fibrosis?

Activities to avoid

These are scuba diving, skydiving, bungee jumping, and high-intensity activities at high altitudes. Those with an enlarged liver or spleen should avoid collision sports such as football, basketball, or soccer.
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Can you still play sports with cystic fibrosis?

Research shows that regular physical activity or exercise provides multiple benefits for people with cystic fibrosis. These benefits go beyond better lung function — keeping fit also helps you strengthen your bones, manage diabetes and heart disease and improve your mood.
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How long do CF kids live?

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. Now, almost 60% of us are older than 18.
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Does CF affect puberty?

Growing up, both men and women with cystic fibrosis may go through puberty later than many of their peers. For boys with CF, delayed puberty often stems from the impaired production of sexual development hormones.
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Can you run with cystic fibrosis?

A high sweat sodium concentration and many other issues can make exercising difficult for people with CF, but it certainly isn't an insurmountable barrier, as ultra-runner Hannah Campbell has proven.
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Does CF stunt growth?

Poor growth has long been a characteristic feature of cystic fibrosis (CF) and is significantly linked to lung function and overall health status.
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Is it hard to exercise with cystic fibrosis?

CF symptoms can make it difficult for patients to exercise, but regular physical activity can have a significant impact in improving patients' quality of life, as determined by recent studies on the topic.
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Can you build muscle with cystic fibrosis?

There is however, evidence to suggest that people with CF can still experience increased muscle strength through weights training. Muscle is gained through a combination of strength/resistance exercise and diet, which contains adequate energy and carbohydrate to fuel the exercise.
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How do you slow down cystic fibrosis?

Pulmonary rehabilitation
  1. Physical exercise that may improve your condition.
  2. Breathing techniques that may help loosen mucus and improve breathing.
  3. Nutritional counseling.
  4. Counseling and support.
  5. Education about your condition.
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What foods help cystic fibrosis?

Best foods to eat with cystic fibrosis
  • Fruits.
  • Vegetables.
  • Eggs.
  • Fish and seafood.
  • Nuts.
  • Dairy products.
  • Olive oil.
  • Dark chocolate.
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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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Does CF worsen with age?

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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Is CF considered a disability?

The Social Security Administration recognizes cystic fibrosis as a serious impairment in its Blue Book under Section 3.04. Applicants with cystic fibrosis are eligible for automatic approval of disability benefits if they suffer from poor lung function and repetitive lung infections.
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What football player has cystic fibrosis?

Valley football player Justin Lucero battles cystic fibrosis.
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Can you swim if you have cystic fibrosis?

Regular swimming can assist in mucus clearance and improve ventilatory function in children with cystic fibrosis.
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What do people with cystic fibrosis do everyday?

The average person with CF spends 2 to 3 hours each day going through their regimen of treatments when you include all treatments plus time for nutritious meals and fitness. Add in school, work, and family time and it's easy to understand why time management plays such a huge role in successfully living with CF.
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What do people with cystic fibrosis have to do everyday?

My daily treatment consists of physiotherapy, physical exercise, rest, and medication. I take bronchodilator drugs, to open the airways of the lungs, every morning and evening, and also just before a physiotherapy session. I take antibiotics every day to control persistent lung infection, both orally and by nebuliser.
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How much does it cost to live with cystic fibrosis?

Results: The mean annual health care cost for treating CF is US $15,571. Costs for patients with mild, moderate, and severe disease are US $10,151, US $25,647, and US $33,691, respectively. Lifetime health care costs are approximately US $306,332 (3.5% discount rate).
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