People with cystic fibrosis typically take a significant number of pills daily, often ranging from 20 to over 30, depending on their specific health needs and treatment regimen. These medications may include pancreatic enzyme supplements, antibiotics, vitamins, and medications to manage lung function. The exact number can vary widely among individuals based on their age, severity of the disease, and additional health conditions. Regular consultation with healthcare providers is essential to tailor the treatment plan effectively.
There is no cystic fibrosis centre in pakistan But Agha khan hospital karachi is best to diagnoseand treat cystic fibrosis patients .Almost all the medications of cystic fibrosis are available in Pakistan.
1 in every 8000
Unfortunately, cystic fibrosis cannot be cured by prayer. If it could be cured by prayer, the disease would have disappeared a long time ago, because there are a great many people praying all the time. We have a great abundance of prayer, in this world. But we still have cystic fibrosis.
go to www.cdc/gov.com :D hope i helped
The person who has Cystic Fibrosis has it for life.
cystic fibrosis
Cystic fibrosis is widely recognized as a lung disease, but it is actually a disease that affects many parts of the body. So yes. it can:) hope this is helpful
Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). http://www.cff.org/
Deaths from Cystic Fibrosis: 485 deaths (NHLBI 1999)Death rate extrapolations for USA for Cystic Fibrosis: 484 per year, 40 per month, 9 per week, 1 per day, 0 per hour, 0 per minute, 0 per second. Note: this extrapolation calculation uses the deaths statistic: 485 deaths (NHLBI 1999)45 people died from cystic fibrosis in Australia 2000 (Australia's Health 2004, AIHW)Source(s):RRT
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.
It is estimated that 70,000 to 100,000 people worldwide have cystic fibrosis. CF is a genetic disorder that primarily affects the lungs and digestive system, causing a range of symptoms and complications. Early diagnosis and treatment are essential for managing the condition.
The long-term prognosis for someone with cystic fibrosis varies greatly from person to person. Genetic mutations, modifier genes, environmental factors, and, to some degree, luck can all influence the progression of the disease. Many people with cystic fibrosis live into their 20s, 30s, and beyond but there are some that do not. There are exciting new drug therapies in the pipeline that have the ability to change cystic fibrosis from a life-shortening disease to a completely manageable disease. For instance, the drug Kalydeco is considered a functional cure for a certain subset of the CF population.