What foods should you avoid with CF?

Dietary Restrictions
As with any diet, eating foods with empty calories (such as sugar-laden drinks) is not recommended on the cystic fibrosis diet. People with CF need to eat a balanced diet with a variety of bright-colored fruits and vegetables, whole grains, whole-fat dairy products, and healthy protein.
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What foods are good for 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 snack would you recommend for your patient with cystic fibrosis?

Cheese sticks and single servings (peel-and-eat varieties such as Gouda, cheddar, and string cheeses). Single servings of whole-milk cottage cheese. Whole-milk yogurt and yogurt drinks. Hummus in a small container and pita bread cut into triangles.
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Can people with cystic fibrosis eat fat?

People with CF need more calories than people who do not have CF, especially if they do not absorb all the food they eat. Extra calories are needed to fight infection as well. , high-fat diet, with 40 percent of total calories from fat is generally recommended.
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Does cystic fibrosis affect eating?

Cystic fibrosis is a disease that causes thick, sticky mucus to build up in your lungs and digestive tract. You need to eat high-calorie, high-protein foods throughout the day to maintain a normal weight because your disease makes it hard to get enough calories from the foods you eat.
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Diet and nutrition | My CF



What can trigger cystic fibrosis?

It's an inherited condition. A child needs to inherit one copy of the mutated gene from each parent to develop cystic fibrosis. If they only inherit one copy from one parent, they won't develop it. However, they will be a carrier of that mutated gene, so they could pass it along to their own children in the future.
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Does cystic fibrosis affect teeth?

Oral implications associated with CF include enamel hypoplasia and tooth discoloration, salivary gland involve- ment, reduced incidence of dental caries, reservoir for poten- tially pathogenic respiratory bacteria, mouth breathing, and anterior open bite associated with nasal and sinus obstruc- tion.
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What can you not do with cystic fibrosis?

Avoid activities that put you near other people with CF, to lower the risk of spreading sickness. Frequently wash your hands with soap and water. Clean and disinfect your medical equipment properly. Don't share items that come into contact with saliva (straws or utensils) with other people -- even family.
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Is coffee good for cystic fibrosis?

This characteristic of patients with CF makes consuming large quantities of caffeine an unwise choice. The diuretic properties of caffeine, which causes frequent urination, can endanger a patient who is already at risk of dehydration based on the underlying pathogenesis of their inherited disease.
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Why are cystic fibrosis patients skinny?

Malnourishment isn't funny. Many people envy the slender ones with cystic fibrosis who have pancreatic insufficiency, which is characteristic of about 85 percent of CF cases. That insufficiency makes it difficult to digest food and absorb nutrients, like fat and protein.
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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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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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Why milk is good for cystic fibrosis?

Calcium. Kids with CF, especially those with pancreatic insufficiency, are at risk for osteopenia or osteoporosis (weak, brittle bones). Dairy products are good sources of calcium (and the full-fat varieties also are good sources of fat and calories).
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Does drinking water help cystic fibrosis?

Keeping well hydrated can help to keep the mucus in the lungs thinner and make your airway clearance easier, as well as help keep food moving through your gut. There is some evidence that people with CF do not always feel thirsty when their bodies need more fluid.
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What vitamins do CF patients need?

Summary
  • People with cystic fibrosis have trouble absorbing fats, which means they have trouble absorbing vitamins that need fat to be absorbed -- A, D, E, and K. ...
  • People with CF also need to get water-soluble vitamins, which include vitamin C and the B-complex vitamins, folic acid, biotin, and pantothenic acid.
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Is gluten good for cystic fibrosis?

First, if you have both CF and celiac disease, you must follow a strict gluten-free diet to avoid damage to your small intestine.
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Why do CF patients need salt?

Sodium Chloride (Salt)

Not getting enough salt can interfere with growth; reduce appetite; and cause stomach pain, weakness, muscle cramps, nausea and headache. People with CF lose a lot of salt in their sweat, so they must eat more salty foods, especially during hot, humid weather.
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Does alcohol affect cystic fibrosis?

Alcohol may aggravate or intensify health conditions common to people with CF such as dehydration, osteoporosis, and liver disease. Drinking alcohol can increase the likelihood of pancreatitis, a painful inflammation of the pancreas.
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Is walking good for 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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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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Is cystic fibrosis 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 are the worst symptoms of cystic fibrosis?

Symptoms of CF
  • Wheezing or shortness of breath.
  • Poor growth or weight gain in spite of a good appetite.
  • Frequent greasy, bulky stools or difficulty with bowel movements.
  • Nasal polyps.
  • Chronic sinus infections.
  • Clubbing or enlargement of the fingertips and toes.
  • Rectal prolapse.
  • Male infertility.
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Does cystic fibrosis affect your appearance?

Cystic fibrosis can affect the way your body develops, looks and functions and present a number of challenges to body image.
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Do people with cystic fibrosis get tired easily?

Fatigue is one of the most common symptoms reported by people with cystic fibrosis (CF), and it causes significant distress in approximately one-third of this patient population.
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Does cystic fibrosis make you gain weight?

The sticky mucus from cystic fibrosis can block normal absorption of key nutrients and fat in the intestines, causing: poor digestion. slow growth. trouble gaining weight.
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