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What is Cystic Fibrosis?

Cystic Fibrosis (CF) is a genetic disorder that causes a malfunction in the body system responsible for producing sweat, saliva, tears and mucus. People with CF produce thick and sticky mucus within the lungs and airways and the digestive system. This impairs digestive functions of the pancreas and traps bacteria in the lungs resulting in recurrent infection and damage to the lungs over time. There is currently no cure but advances in care and treatment are helping people manage their CF.

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What is cystic fibrosis (CF)?

Cystic fibrosis is a genetic condition, which means that it is something you are born with. Cystic fibrosis is known to cause your lungs to produce extra-thick, sticky mucus. This mucus builds up and clogs your airways.

Even before symptoms present, people with cystic fibrosis develop mucus that is thicker and stickier than normal.

Helpful tips on how to help your patients stay ahead of CF

 

  • Encourage, eating well, being active and establishing treatment routines which may help them manage their CF
  • Eating a high-calorie, high-fat diet is important to help make sure CF patients are getting the nutrients they need from food
  • Exercising as often as they can, helps CF patients manage lung function
  • Patients that partner with their CF Care Team helps them develop a treatment routine that works best for them
  • Supporting patients to make time every day for their Bronchitol and other cystic fibrosis treatments
  • Encourage patients to discuss their treatment plan with you as their doctor or their Care Team to find the right balance to fit their personal needs

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