why cant cystic fibrosis patients dating each other

Daisy Keller, 23 years old


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Cystic fibrosis is a serious inherited disease which mainly affects the lungs and pancreas but can involve other organs. Symptoms usually begin in early childhood and include persistent cough, wheeze, repeated chest infections, difficulty absorbing food and general ill health. Treatments include antibiotics, physiotherapy, medicines for thinning mucus, pancreatic enzyme replacements and other therapies. Cystic fibrosis is a condition which mainly affects the lungs and pancreas but can affect other parts of the body, including the liver, nose and sinuses and sweat glands. Normally, cells in these parts of the body make mucus and other watery juices and secretions. In people with cystic fibrosis, these cells do not function correctly and make mucus and secretions which are thicker than normal. This can cause various symptoms and problems which are described below.

In this week's episode of Grey's Anatomy the docs of Seattle Grace Mercy West put an end to a relationship for the sake of the physical health of both parties involved. Ricky and Julia have cystic fibrosis and were thus a danger to each other's well-being. It made for powerful drama, but is it based in fact? Cystic fibrosis, or Why cant cystic fibrosis patients dating each other, is an inherited disease caused by a defective gene.

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This copy is for your personal non-commercial use only. Cystic fibrosis is known as a devastating disease that causes severe respiratory problems and interferes with digestion because of thick mucous in the lungs. As of this week, the roughly 4, CF patients across the country, their families and friends have a new way to connect. A social network launched by the non-profit Cystic Fibrosis Canada will help them find one another and converse via video-chat, instant message or online forums. Stagg was diagnosed at the age of 14, much later than most cases, which are identified in the first few years of life. It was around the time medical authorities discovered that gatherings of CF patients put them at risk, bringing an end to summer camps for children with the disease and other group activities. The network will allow patients to share information about therapies, recipes and research in a Canadian context. Relatives planning to have children and going through genetic testing for CF will be able to find one another, as well as parents of children struggling with the illness.

Cystic fibrosis CF is an inherited disease that causes the body to produce mucus that's extremely thick and sticky. The mucus is thicker than normal because CF affects cells in the epithelium pronounced: In a person who does not have CF, the epithelial cells produce a thin, watery mucus that acts like a lubricant and helps protect the body's tissues. In someone with CF, however, the thicker mucus doesn't move as easily. This thick, sticky mucus clogs passages in many of the body's organs and infection sets in.

Although cystic fibrosis is a rare disease, in some schools there may be more than one person with CF present. Germs are a major concern for people with CF, but there are steps you can take to help students and faculty with CF lower the risk of cross infection. Medical studies show that people with CF are at particular risk of spreading certain germs among others with the disease. This is known as cross-infection. In people with CF, thick, sticky mucus that clogs the lungs also allows germs to thrive and multiply. This buildup makes them more susceptible to developing lung infections. Despite significant progress in treating CF , infections remain a serious problem and can lead to worsening lung disease and death.