Cystic fibrosis (CF) affects the lungs, the digestive system and other organ systems — so caring for it takes a team working together across specialties. We bring pulmonology, gastroenterology, nutrition, nephrology and other specialists together, so you don’t have to manage it alone.
There's no cure for cystic fibrosis yet, but treatment has come a long way. Our specialists stay current with the latest options, from respiratory therapies and nutritional support to newer medications. Day to day, that means helping you breathe easier, stay nourished and feel supported in your daily life. Because cystic fibrosis is lifelong, we build care around you.
All you need to get started is a referral from your primary care provider. From there, you’ll have a team that knows your cystic fibrosis and knows you.
Symptoms can vary, but common ones include:
How much cystic fibrosis affects you can vary. Some people have symptoms from birth, while others may not notice anything until their teen or young-adult years. Symptoms can also stay light for a while and build up over time. Your cystic fibrosis care team can help make sense of your symptoms and what will help most.
Cystic fibrosis affects nearly every system in the body, not just the lungs. The thick, sticky mucus that builds up in the airways — driving a cough and frequent infections — can also block ducts in the pancreas, making it harder to digest food.
Over time, cystic fibrosis can also affect the liver, intestines, sinuses, bones, kidneys and reproductive system. Because cystic fibrosis affects so many systems, regular monitoring across these areas is a core part of care.
There’s no one treatment plan for cystic fibrosis. Your care team designs a plan around your symptoms and will adjust it to your needs. However, your treatment will usually combine a few approaches, like:
Cystic fibrosis is a lifelong condition, so the care behind it should be comprehensive and consistent. Here, you have access to: