How long can a person live who has just found out they have cystic fibrosis and is 37 years old?

Why does a person with cystic fibrosis feel pain?

Cystic fibrosis has no cure. However, treatments have greatly improved in recent years. Early treatment for cystic fibrosis can improve both quality of life and lifespan.

How long does cystic fibrosis last?

The person who has Cystic Fibrosis has it for life.

Can you survive with cystic fibrosis and Down syndrome?

My daughter had Cystic Fibrosis and Down Syndrome. She died a little over a year ago at the age of 10.5 years.

What is survival rate for Cystic Fibrosis?

Cystic Fibrosis is a life threatening genetic disorder. More children are living into adulthood with better treatment options. The death rate is 100 percent, when the lungs and pancreas quit functioning.

What are some facts about cystic fibrosis?

More than 1,000 different mutations in the CFTR gene have been identified in cystic fibrosis patients. The most common mutation (observed in 70% of cystic fibrosis patients) is a three-base deletion in the DNA sequence, causing an absence of a single amino acid in the protein product. About 2,500 babies are born with cystic fibrosis in the U.S. each year. More than 10 million Americans carry the cystic fibrosis gene but don't know it.

Is cystic fibrosis more common in boys or girls?

i copied the following answer from health.howstuffworks.com Unlike some other genetic conditions, cystic fibrosisoccurs equally as often in men and women. The genetic mutation for cystic fibrosis occurs on chromosome 7 and is not impacted by gender. The severity of symptoms related to cystic fibrosis, however, does vary in men and women. In particular, girls with cystic fibrosis have more difficulty with meeting growth milestones and experience more lung-related problems compared to boys. Due to these more severe symptoms, women with cystic fibrosis have shorter life expectancies than men. It is estimated that men with cystic fibrosis live four to five years longer than women with cystic fibrosis, Moreover, under the age of 20, girls have a 60 percent greater chance of dying due to cystic fibrosis complications compared to males [source: Cystic Fibrosis Worldwide]. As a result, the prevalence of male adults with cystic fibrosis is greater than the prevalence of female adults with cystic fibrosis, suggesting a male advantage with the disorder. Cystic fibrosis researchers argue that this gender difference is the result of early-onset lung infections in girls. Girls appear to develop these infections earlier in life than boys, leading to more severe cystic fibrosis complications, and even death. Girls also appear to have greater difficulty maintaining a healthy body weight after puberty compared to males, which places girls at greater risk for cystic fibrosis complications. It appears that this gender gap can narrow if girls are provided with more intensive medical care. In fact, girls and women who receive regular intravenous antibiotics, regardless of their condition, have improved survival rates [source: Cystic Fibrosis Worldwide]. As a result, countries with excellent health care, such as Scandinavian countries, do not have a difference in the survival rate of men and women with cystic fibrosis. i hope it helps:)

What is the current life span of a person with cystic fibrosis?

There is no cure for CF, and most individuals with cystic fibrosis die young: many in their 20s and 30s from lung failure. However, with the continuous introduction of many new treatments, the life expectancy of a person with CF is increasing to ages as high as 40 or 50. Lung transplantation is often necessary as CF worsens.

Do people with Cystic Fibrosis die young?

The life expectancy of individuals with cystic fibrosis has significantly improved over the years due to advancements in treatments and therapies. However, it is still considered a life-shortening disease, with most individuals living into their 30s and 40s. With proper management and care, many people with cystic fibrosis can lead fulfilling lives.

Are Purple fingertips in cystic fibrosis patience normal?

Yes, the finger nails are often bluish in patients with Cystic Fibrosis. Clubbing of the fingernails is also seen in later stages of CF. My daughter had CF for 34 years before dying of Sepsis (blood infection), 115 days after a double lung transplant.

What is an fact about the cystic fibrosis?

Cystic Fibrosis Is The UK's Most Common Life-Threatening Disease. It Affects About 7500 People In The UK. It Is An Inherited Disease. People With CF Are Recommended To Have A High Calorie And High Fat Diet. Both Parents Must Pass On The Defective Gene For Any Of Their Children To Get CF. CF Can Cause Coughing Or Whezzing , Weight Loss And More Symptoms. Most Cystic Fibrosis Patients Only Live To Be Slightly More Than Thirty Years Old.

What's Cystic fibrosis?

Cystic fibrosis is a genetic disorder which affects the lungs and pancreas. It causes the lungs to get clogged with mucus, which in turn makes the lungs a breeding ground for bacteria. In the pancreas, it blocks the pancreas from absorbing enzymes, which makes its victims prone to malnutrition. Often times, they have to take treatments such as lung therapy every day, as well as enzyme supplements on a daily basis. The average life expectancy is 37.Cystic Fibrosis is caused by a defective gene which causes a thick, sticky mucus. It builds up in the lungs and pancreas (the organ that helps to break-down food.) Cystic Fibrosis results in life-threatening lung infections and digestive problems. Symptoms are varied, but the most common are: No bowel movements in first 24 - 48 hours of life (baby!) Stools that are pale or clay colored, foul smelling or float. Infants can have salty tasting skin. Recurrent respiratory infections, such as pneumonia or sinusitis. Coughing/wheezing. Weight loss or can't gain weight normally in childhood. Diarrhea, delayed growth and fatigue.Cystic Fibrosis is the most common fatal genetic disease occurring in about 1 in 30,000 births. The gene must be inherited from both the mother and the father. Children inheriting only one copy of the gene are carriers but do not display symptoms. Average life expectancy for Cystic Fibrosis is approximately 32 years of age. There are many treatments but no cure. People with Cystic Fibrosis are at high risk of developing other conditions such as Cystic Fibrosis related Arthritis and Cystic Fibrosis related Diabetes, Liver failure and ultimately respiratory failure leading to death. Once a person with Cystic Fibrosis loses enough lung function the only other treatment is a lung transplant

Does Miley Cyrus have a tattoo on her stomach?

She has one under her left breast which says "Just Breathe". It is in memory of her friend Vanessa, who died of a lung disease called Cystic Fibrosis three years ago.