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What are facts on cystic fibrosis?
-Doctors take a sweat test to see if you have cystic fibrosis.-About 2,500 babies are born with cystic fibrosis each year.
How can you detect cystic fibrosis?
Most babies with cystic fibrosis are diagnosed at birth from meconium ileus (stomach blockage) however if undetected at birth if a doctor is suspicious he can give the "sweat test" which measures the concentration of chloride that is excreted in sweat. for a further list of symptoms here's the cystic fibrosis website in the below related link.
What capsules do you take for cystic fibrosis?
you take creon its a capsule filled with tiny tan beads you open up the pill and swallow the beads on the inside the beads are real tiny so its easy and they have no taste so u dont hafe to worry i know cause i have cystic fibrosis
How can you find out the inheritance of cystic fibrosis?
take a genetic test - a blood or tissue sample is analysed for specific mutations
Are women beyond a particular age more likely to give birth to a baby with cystic fibrosis?
Yes but depending on your age and the risk you are willin to take
What age does cystic fibrosis occur?
it is a infection in the liver an dlungs and can kill u...... if u have exercise everyday and drink lots of fluids an have a healthy diet also u can take medicines to help treat this dissorderEdit from another person:Cystic Fibrosis is not an infection, it is an inherited genetic disorder. Nor is it restricted to the liver and lungs, as my mother has it in her uterus and ovaries. However, I believe the (incomplete) question was about what it does. Basically, it causes tissues to become hard tumors, which can continue to grow in size significantly.
How dangerous is cystic fibrosis?
It can be very deadly.For the source and more detailed information concerning your request, click on the related links section (Wikipedia) indicated directly below this answer section.
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
What are cystic fibers?
If you're talking about "fibrocystic" breasts, it means that there are small cysts in the breast tissue that react to things like how much caffeine (makes them worse) or how much fiber (makes them not as bad) you take in. If you're talking about "cystic fibrosis," that is something different.
Can a child with cystic fibrosis take vitamin supplement?
Absolutely infact its recommended that they should take vitamin E, multi-vitamins and sometimes vitamin K (helps bones). Ive been taking them for as long as i can remember and my dietician is always asking if ive taken them! Hope this helps
Is cystic fibrosis cureable?
Cystic Fibrosis can be permanently treated, but you can control it with daily breathing treatments and clapping treatments( make cupped hands and then pat yourself or the patient on the chest and in the back) which loosens the thick, sticky mucus in the lungs. Some CF patients need to take medicine. Young CF kids and teens should exercise as much as they can because it loosens the mucus. Hope this helps ;)
In what year did Albert Einstein get cystic fibrosis?
Here is an excellent candidate to show the ability of the internet to take a mischevious rumour and start furiously blowing it up to a status approaching fact. I have had this claim appear in a gullible student's essay, but I can find no evidence whatsoever being presented in favour of it. Not "I don't believe the evidence", but rather "there is NO evidence". So did Einstein have CF? Sure! As much as Shakespeare, Super Mario and Jesus did too.
