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No. Unfortunately there is no cure for Cystic Fibrosis at this time.
Cystic fibrosis is a inherited disease where ususally by the time of 30-35 the person who has it does die.
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.
Unfortunately, cystic fibrosis cannot be cured. There is medication getting better all the time but now, the government in the UK have not funded in any cure. This means that in the UK, we may only find a cure if a devoted medical professional actually spent his own time to find the cure
Cystic fibrosis currently does not have any sort of cure. Treatment is mainly done to reduce symptoms and complications. Treatment options include antibiotics, mucus-thinning drugs, and oral pancreas enzymes.
Yes, all the time.
Unfortunately, there is none at this time. Sucks for me.
Cystic fibrosis primarily affects the respiratory and digestive systems, but it can also have implications for the urinary system. The thick mucus characteristic of the disease can lead to complications in the kidneys, such as kidney stones or urinary tract infections, due to dehydration and imbalances in salt and fluid levels. Additionally, cystic fibrosis can result in reduced kidney function over time, complicating the body's ability to regulate electrolytes and maintain fluid balance. However, the urinary system is generally less affected than other systems in cystic fibrosis.
Cystic fibrosis is a genetic condition that leads to the production of thick and sticky mucus in the lungs. This mucus can obstruct the airways, making it difficult for oxygen to pass through and enter the bloodstream. Over time, this can lead to decreased oxygen levels in the blood and difficulty breathing.
well im 7 and i have it
Cystic fibrosis has had reported incidents since the early 17th century. The poem Woe Is the Child gives a description of a child at this time period who had CF. The first clear description and medical entry for CF was made in 1938. Cystic fibrosis has had reported incidents since the early 17th century. The poem Woe Is the Child gives a description of a child at this time period who had CF. The first clear description and medical entry for CF was made in 1938.
The mucus that forms from cystic fibrosis affects the gas exchange in humans. The build up from cystic fibrosis can affect the gas exchange by increasing carbon dioxide and decreasing oxygen.