Understanding Cystic Fibrosis. Cystic fibrosis is a genetic disorder. It affects the lungs and digestive system. People with CF have thick, sticky mucus in their bodies. This can make it hard to breathe and digest food. CF is caused by a change in the CFTR gene. This gene controls the flow of salt and water in and out of cells. When the CFTR gene is not working right, the body makes mucus that is thick and sticky. Common symptoms of CF include coughing, trouble breathing, lung infections, poor growth, and greasy stools. To learn more about the symptoms of CF, visit https://www.cff.org/What-is-CF/About-Cystic-Fibrosis/. Diagnosing Cystic Fibrosis. Doctors can diagnose CF by doing a sweat test. This measures the amount of salt in a person's sweat. People with CF have more salt in their sweat than people without CF. Doctors can also do a genetic test to look for changes in the CFTR gene. This is done with a blood test or a cheek swab. All babies in the United States are now tested for CF at birth. This helps doctors find and treat CF early. To learn more about newborn screening for CF, go to https://www.cff.org/What-is-CF/Testing/Newborn-Screening-for-CF/. Treating Cystic Fibrosis. There is no cure for CF yet. But there are treatments that can help people with CF feel better and live longer. These include:  Chest physical therapy to loosen mucus in the lungs Breathing treatments with medicines to open the airways Antibiotics to treat and prevent lung infections Pancreatic enzymes to...

Cystic fibrosis, a genetic disorder, affects lungs and digestion due to thick mucus. Treatments alleviate symptoms, but no cure exists.

Exploring the Advancements in Cystic Fibrosis Treatments

What is Cystic Fibrosis? Cystic fibrosis (CF) is a genetic disease. It causes thick, sticky mucus to build up in the lungs and digestive system. CF is passed down through families. You must inherit two copies of the faulty CF gene to have the disease. About 30,000 children and adults in the United States have CF. Most are diagnosed by age 2. Why Early Detection Matters. With CF, the earlier it's found, the sooner treatment can begin. This may help prevent or delay problems caused by the disease. All babies in the U.S. are now tested for CF at birth. This is done with a blood test. If the test is positive, doctors do more tests to be sure it is CF. These include a sweat test or genetic test. How Cystic Fibrosis Affects the Body. CF mainly affects the lungs and digestive system, including the pancreas. The thick mucus clogs the lungs and leads to breathing problems and infections. The mucus also blocks ducts in the pancreas. This stops digestive enzymes from reaching the intestines. Without these, the body can't absorb fats and proteins from food. Symptoms often start in infancy and childhood. They include coughing, wheezing, frequent lung infections, poor growth, and greasy stools. Treating Cystic Fibrosis. There is no cure for CF, but treatments can ease symptoms and reduce complications. The earlier treatment starts, the better. Treatments may include:  Airway clearance techniques to loosen and get rid of mucus in the lungs Inhaled medicines to open...

Cystic fibrosis affects 30,000 Americans, causing mucus buildup. Early detection and treatment are key, with ongoing research for cures.

Unlocking the Potential of Cystic Fibrosis Treatments

Cystic Fibrosis affects 30,000 people in the U.S. It causes an imbalance of salt in the body, which affects the pancreas shortly after birth, impedes proper digestion, and causes airways to fill with mucus, leaving patients vulnerable to lung infections and other problems. Patients are often small and malnourished and tend to have overly salty skin due to sweat glands not working properly. Currently, those diagnosed with cystic fibrosis have an average life expectancy of 37 years, but that could change for some patients with a new drug called Kalydeco (generic name ivacaftor), which has just been approved by the Food and Drug Administration (FDA). Kalydeco targets a genetic mutation in four to five percent of people with cystic fibrosis. It helps to keep the chloride gateway open in cells, resulting in a restored salt balance in the body and a prevention of future lung disease. This is the first time a drug is aiming at the underlying problem that causes cystic fibrosis, not simply treating the symptoms. The FDA fast-tracked Kalydeco and approved it in only three months, given its early signs of promise in clinical testing. Lindsay Shipp is a 27-year-old in San Diego, CA, who participated in a closely watched clinical trial for this experimental drug. She loves singing and dancing and dreamed of auditioning on Broadway until her lungs became so bad that she had to give it up. When Shipp took ivacaftor, her lungs cleared to the point that her physician told her during a...

New CF drug Kalydeco, targeting a specific genetic mutation, may increase life quality and expectancy for patients, showing early promise.

Cystic Fibrosis Drug Kalydeco Shows Promise

 Cystic fibrosis is a chronic disease in which the protein product of a defective gene produces thick and sticky mucus, which clogs the lungs and prevents the pancreas from helping the body break down food.   Symptoms of cystic fibrosis include:    Salty tasting skin   Persistent coughing, often with phlegm   Wheezing and shortness of breath   Lack of growth or weight gain   Difficulty with bowel movements   Frequent lung infections due to the buildup of thick mucous     Cystic fibrosis, also called CF, affects mostly the lungs and the pancreas. When mucus builds up in the lungs, it causes difficulty breathing, and as it gets stuck in the airways, it causes inflammation and possible infections. The mucus also builds up in the digestive tract and pancreas, which prevents enzymes from getting to the intestines. These enzymes are needed to break down food, and the blockage of these enzymes is what causes the difficulty with bowel movements.   CF is a genetic condition, which means it is inherited from parents; a person with CF must inherit two copies of the defective gene, one from each parent.   Cystic fibrosis affects about 70,000 people worldwide, and about 1,000 new cases are identified each year. Most children with CF are diagnosed by age 2, so receiving care from an early age is likely. Diagnosis typically happens from a test at birth, and the sweat test (testing...

Cystic fibrosis is a genetic disease causing thick mucus in lungs and digestive issues, often leading to infections and growth impediments.

What is Cystic Fibrosis?

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Exploring the Advancements in Cystic Fibrosis Treatments

Unlocking the Potential of Cystic Fibrosis Treatments

Cystic Fibrosis Drug Kalydeco Shows Promise

What is Cystic Fibrosis?

Find Providers Near You

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Exploring the Advancements in Cystic Fibrosis Treatments

Unlocking the Potential of Cystic Fibrosis Treatments

Cystic Fibrosis Drug Kalydeco Shows Promise

What is Cystic Fibrosis?

Find Providers Near You

Special Needs
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