What is it like for someone living with cystic fibrosis?

Cystic fibrosis may cause mucus to clog lung airways, leading to difficulty breathing. The mucus also can trap bacteria, causing serious lung infections, including pneumonia. Additionally, it can cause the pancreas to stop producing digestive enzymes that help break down food and allow the body to absorb nutrients.

What are the difficulties of living with CF?

Lung infections that may come back or be difficult to treat. Malnutrition because the pancreas may not make enough enzymes to help digest and absorb nutrients from food. Mental health problems, such as depression and anxiety.

Is it hard living with cystic fibrosis?

Handling the physical limitations of cystic fibrosis, coping with a shorter life expectancy, and dealing with a sometimes lesser quality of life are all huge parts of living with this disease. It is so important to understand but, regrettably, treating mental health issues is only now becoming a big focus in CF care.

Can a person with cystic fibrosis live a normal life?

Living productive lives with cystic fibrosis

According to the CFF's Patient Registry, children with CF grow up to lead full, productive lives despite their disease. In 2017, the registry found that: 51 percent of adults with CF work in full- or part-time jobs. 42 percent of adults with CF are married or living together.

How does cystic fibrosis affect daily life?

CF causes thick mucus that clogs certain organs, such as the lungs, pancreas, and intestines. This may cause malnutrition, poor growth, frequent respiratory infections, breathing problems, and chronic lung disease.

Tara's Story - Living With Cystic Fibrosis

Is CF painful?

People with cystic fibrosis are at higher risk of developing a dangerous thinning of bones. They may also experience joint pain, arthritis and muscle pain.

How old 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.

Why can't you get close to someone with cystic fibrosis?

For people with CF, being close to others with the disease puts them at greater risk of getting and spreading dangerous germs and bacteria. This is called cross‐infection. Not only are these dangerous germs difficult to treat, but they can also lead to worsening symptoms and faster decline in lung function.

What limitations does a person with cystic fibrosis have?

What kind of limitations does someone with CF have? People with CF can live very full, normal lives. There are no limitations to their exercise, diet, or activities. However, due to the different lung infections that they can get, they should not meet or talk with other patients with CF in-person.

What is most common cause of death for people with CF?

Mucus in CF patients is very thick and accumulates in the intestines and lungs. The result is malnutrition, poor growth, frequent respiratory infections, breathing difficulties, and eventually permanent lung damage. Lung disease is the usual cause of death in most patients.

Why do CF patients have to be 6 feet apart?

The guidelines set forth physical distancing recommendations, which include the “6-foot rule”—people with CF should stay 6 feet away from anyone who is sick and any other individuals who have CF, to avoid cross-infection.

Does cystic fibrosis get worse with age?

Outlook. 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.

Can someone with cystic fibrosis kiss someone with cystic fibrosis?

Is cystic fibrosis contagious through kissing? No. Cystic fibrosis is not contagious, even via kissing, because it's a genetic disease.

Can patients with cystic fibrosis dating each other?

People with cystic fibrosis should never meet each other, as they carry bacteria within their lungs that could be harmful to each other.

Does a lung transplant cure CF?

Does a lung transplant cure cystic fibrosis? No. Cystic fibrosis is a genetic condition so even though the transplanted lungs will not have CF and will never develop it, the rest of the person's body will continue to have cystic fibrosis.

Can you drink alcohol with cystic fibrosis?

The more you drink, the greater the risk to your baby. The British Liver Trust advises people with CF-related liver disease to avoid alcohol to minimise further damage to their liver. It is important that you understand the effects of alcohol on your blood glucose levels if you have CF-related diabetes (CFRD).

Can CF guys have kids?

The Difference Between Infertility and Sterility

Even though the vas deferens is missing, the sperm are not. In fact, sperm production in the testicles is normal in 90 percent of men with CF and CBAVD, meaning that most men with CF can still have biological children through assisted reproductive technology (ART).

How long can cystic fibrosis go undetected?

However, not every case of CF presents with meconium ileus in the newborn, failure to thrive, or severe lung disease. Atypical CF is characterized by a milder form of the disease usually remaining undiagnosed for years, even into late adulthood [2].

What are 3 major symptoms of CF?

Frequent lung infections including pneumonia or bronchitis. 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.

Does CF cause brain damage?

Cystic fibrosis (CF) patients present with a variety of symptoms, including mood and cognition deficits, in addition to classical respiratory, and autonomic issues. This suggests that brain injury, which can be examined with non-invasive magnetic resonance imaging (MRI), is a manifestation of this condition.

What is a fun fact about CF?

9. While cystic fibrosis is primarily found in Caucasians, it affects other ethnicities as well: about one in 17,000 African Americans and one in 31,000 Asian Americans suffer from the disease. 10. Cystic fibrosis is considered a Mendelian disorder — a condition caused by the mutation of a single point in a gene.

What is CF belly?

What is CF belly? A large percentage of CF people have insufficient pancreatic enzymes because the pancreas is inflamed and blocked just like the lungs. Many patients are prone to late gastric emptying, GERD, SIBO, DIOS, and slow gut transit. These conditions can mask each other. This just piles onto the poop problem.

How long can a female with cystic fibrosis live?

Lung disease eventually worsens to the point where the person is disabled. Today, the average life span for people with CF who live to adulthood is about 44 years. Death is most often caused by lung complications.

How does CF affect people emotionally?

People with chronic diseases, such as cystic fibrosis, are at greater risk for developing clinical depression. When left untreated, depression can interfere with your ability to manage your CF effectively and experience a better quality of life.

Is cystic fibrosis rarely fatal?

Cystic fibrosis used to be considered a fatal disease of childhood. With improved treatments and better ways to manage the disease, many people with cystic fibrosis now live well into adulthood. Adults with cystic fibrosis experience health problems affecting the respiratory, digestive, and reproductive systems.