If two people with cystic fibrosis were to have children then the kids would also have it. Also, cystic fibrosis is a pretty nasty disease. It's where the mucus that protect organs etc becomes thick and sticky and the person with it often ends up with serious lung diseases or intestinal infections which can be dangerous, painful and expensive. But it's the parents who are the ones choosing whether they want this for there children.
Good Question. The answer is cystic fibrosis is not contagious, however, people with cystic fibrosis tend to carry bacterial infections that can cause serious issues to other people with CF, so infection control procedures should be used when two or more cystics are around each other. General population folks need not fear of getting cystic fibrosis from others - it's a hereditary disease.
There is no evidence to show that it will be detremental to the Cistic Fibrosis its self, as long as you maintain your treatment regime there should not be a problem with you using them in moderation.
I have cystic fibrosis,and i think the best are (if you mean sports) ice skating,rollerblading,bike riding.If you/youre relative or child has cystic fibrosis and it's a good case then basketball maybe? I personally do all that stuff,but if the person is interested in music they should learn some musical instrument maybe?Like piano,violin,guitar.And if good case then drums maybe?
Other CF's and people with Chest Infections. And extremeexercise and low fat diets!
People with Cystic Fibrosis are encouraged to eat more than twice the number of calories a normal person should eat. Hence, they can eat 4,000 calories a day - steak, burgers, chips - without worry about fat or cholesterol. I should know, I've been doing it for 20 years. It's one of the only perks.
Cystic fibrosis does not make you sterile but Diabetes can do it if you don't take care of yourself. But there is nothing that says you are sterile just because you are a Diabetic. Considering you have these two conditions you should probably speak to your doctor first and discuss the risks. Some people have Diabetes more severe than others.
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 ;)
Cystic fibrosis is noncommunicable, so in that respect there is no concern. If you want to have children then there is about a 50% chance your kids will have CF, there is genetic screening to determine if your also a carrier, thus raising the chance. CF is most common in white Europeans especially of German descent. With early identification and tratment the outlook for a long life for CF patients is better than ever.
All kinds of people. If you have recently suffered from measles or chicken pox you can easily catch it just stay away from pets and farm animals and you should be fine!
Cystic fibrosis is a genetic disorder that affects the mucous membranes of the body. The ones that are most vulnerable are in the lungs, so a health care assistant should be sure that they, themselves, are not sick so they do not spread anything, particularly a respiratory infection to them.
You should know the answer to this yourself. You said you are in the 90s that means that you are 90% of predicted.
You should consult a physician.
Yes, I would see a doctor, you might have poly-cystic fibrosis.
The parents will both have a specific gene defect. If they do there is then a 1 in 4 chance of them having a child with cf. so if you are considering having children you should have a blood test to find out if you are a carrier of the gene causing cf. hope that helps.
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
You need to interact with them more.He was learning how to interact with the computer.
DefinitionCystic fibrosis is an inherited disease that causes thick, sticky mucus to build up in the lungs and digestive tract. It is one of the most common chronic lung diseases in children and young adults, and may result in early death.See also:Cystic fibrosis - nutritional considerationsNeonatal cystic fibrosis screeningCauses, incidence, and risk factorsCystic fibrosis (CF) is caused by a defective gene which causes the body to produce abnormally thick and sticky fluid, called mucus. This mucus builds up in the breathing passages of the lungs and in the pancreas, the organ that helps to break down and absorb food.This collection of sticky mucus results in life-threatening lung infections and serious digestion problems. The disease may also affect the sweat glands and a man's reproductive system.Millions of Americans carry the defective CF gene, but do not have any symptoms. That's because a person with CF must inherit two defective CF genes -- one from each parent. An estimated 1 in 29 Caucasian Americans have the CF gene. The disease is the most common, deadly, inherited disorder affecting Caucasians in the United States. It's more common among those of Northern or Central European descent.Most children with CF are diagnosed by age 2. A small number, however, are not diagnosed until age 18 or older. These patients usually have a milder form of the disease.SymptomsBecause there are more than 1,000 mutations of the CF gene, symptoms differ from person to person.Symptoms in newborns may include:Delayed growthFailure to gain weight normally during childhoodNo bowel movements in first 24 to 48 hours of lifeSalty-tasting skinSymptoms related to bowel function may include:Belly pain from severe constipationIncreased gas, bloating, or a belly that appears swollen (distended)Nausea and loss of appetiteStools that are pale or clay colored, foul smelling, have mucus, or that floatWeight lossSymptoms related to the lungs and sinuses may include:Coughing or increased mucus in the sinuses or lungsFatigueNasal congestion caused by nasal polypsRecurrent episodes of pneumonia. Symptoms in someone with cystic fibrosis include: FeverIncreased coughingIncreased shortness of breathLoss of appetiteMore sputumSinus pain or pressure caused by infection or polypsSigns and testsA blood test is available to help detect CF. The test looks for variations in a gene known to cause the disease. Other tests use to diagnose CF include:Immunoreactive trypsinogen (IRT) test is a standard newborn screening test for CF. A high level of IRT suggests possible CF and requires further testing.Sweat chloride test is the standard diagnostic test for CF. A high salt level in the patient's sweat is a sign of the disease.Other tests that identify problems that can be related to cystic fibrosis include:Chest x-ray or CT scanFecal fat testLung function testsMeasurement of pancreatic functionSecretin stimulation testTrypsin and chymotrypsin in stoolUpper GI and small bowel seriesTreatmentAn early diagnosis of CF and a comprehensive treatment plan can improve both survival and quality of life. Follow-up and monitoring are very important. If possible, patients should be cared for at cycstic fibrosis specialty clinics, which can be found in many communities. When children reach adulthood, they should transfer to a cystic fibrosis specialty center for adults.Treatment for lung problems includes:Antibiotics to prevent and treat lung and sinus infections. They may be taken by mouth, or given in the veins or by breathing treatments. People with cystic fibrosis may take antibiotics only when needed, or all the time. Doses are usually higher than normal.Inhaled medicines to help open the airwaysDNAse enzyme replacement therapy to thin mucus and make it easier to cough upFlu vaccine and pneumococcal polysaccharide vaccine (PPV) yearly (ask your health care provider)Lung transplantis an option in some casesOxygen therapy may be needed as lung disease gets worseTreatment for bowel and nutritional problems (see: Cystic fibrosis - nutritional considerations) may include:A special diet high in protein and calories for older children and adults (see: Cystic fibrosis nutrional considerations)Pancreatic enzymes to help absorb fats and proteinVitamin supplements, especially vitamins A, D, E, and KYour doctor can suggest other treatments if you have very hard stoolsCare and monitoring at home should include:Avoiding smoke, dust, dirt, fumes, household chemicals, fireplace smoke, and mold or mildewClearing or bringing up mucus or secretions from the airways. This must be done one to fours times each day. Patients, families, and caregivers must learn about doing chest percussion and postural drainage to help keep the airways clearDrinking plenty of fluids. This is particularly true for infants, children, in hot weather, when there is diarrhea or loose stools, or during extra physical activityExercising two or three times each week. Swimming, jogging, and cycling are good options. Avoid contact sports, scuba diving, and endurance activities such as marathonsSupport GroupsFor additional information and resources, see: Cystic fibrosis support groupExpectations (prognosis)Most children with cystic fibrosis are fairly healthy until they reach adulthood. They are able to participate in most activities and should be able to attend school. Many young adults with cystic fibrosis finish college or find employment.Lung disease eventually worsens to the point where the person is disabled. Today, the average life span for people with CF who live to adulthood is approximately 35 years, a dramatic increase over the last three decades.Death is usually caused by lung complications.ComplicationsThe most common complication is chronic respiratory infection.Bowel problems, such as gallstones, intestinal obstruction, and rectal prolapseCoughing up bloodChronic respiratory failureDiabetesInfertilityLiver diseaseor liver failure, pancreatitis, biliary cirrhosisMalnutritionNasal polyps and sinusitisOsteoporosisand arthritisPneumonia, recurrentPneumothoraxRight-sided heart failure (cor pulmonale)Calling your health care providerCall your health care provider if an infant or child has symptoms of cystic fibrosis.Call your health care provider if a person with cystic fibrosis develops new symptoms or if symptoms get worse, particularly severe breathing difficulty or coughing up blood.Call your health care provider if you or your child experiences:Fever, increased coughing, changes in sputum or blood in sputum, loss of appetite, or other signs of pneumoniaIncreased weight lossMore frequent bowel movements or stools that are foul-smelling or have more mucusSwollen belly or increased bloatingPreventionThere is no way to prevent cystic fibrosis. Screening those with a family history of the disease may detect the cystic fibrosis gene in 60 - 90% of carriers, depending on the test used.ReferencesBoat TF, Acton JD. Cystic fibrosis. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics.18th ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 400.Farrell PM, Rosenstein BJ, White TB, et al. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic fibrosis consensus report. Journal of Pediatrics. Aug 2008;153(2).Stallings VA, Stark LF, Robinson KA, Feranchak AP, Quinton H. Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: Results of a systematic review. Journal of the American Dietetic Association. May 2008;108(5).Yankaskas JR, Marshall BC, Sufian B, et al. Cystic fibrosis adult care: consensus conference report. Chest. 2004;125(1 suppl):1S-39S. Review.Mogayzel PJ Jr, Flume PA. Update in cystic fibrosis 2009. Am J Respir Crit Care Med. 2010 Mar 15;181(6):539-44.Tuchman LK, Schwartz LA, Sawicki GS, Britto MT. Cystic fibrosis and transition to adult medical care. Pediatrics. 2010 Mar;125(3):566-73.Borowitz D, Robinson KA, Rosenfeld M, et al. Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. J Pediatr. 2009 Dec;155(6 Suppl):S73-93.
Someone please answer
Don't interact with customers if the employee is sick! Its bad for business.
Herbs have the potential to interact with any prescription medication, as well as with other herbs. So, persons wishing to take digestive enzymes should consult a physician.
persons considering taking white willow preparations should first consult a physician or registered pharmacist, as white willow interacts with a number of nonprescription as well as prescription medications.
Some cholinesterase inhibitors should be used with caution in persons with asthma or lung disease, as cholinesterase inhibitors may interact with theophylline, a drug commonly used to treat both conditions.
No, methadone at high doses should not interact with penicillin.
side effects include drowsiness, decreased libido, fatigue, and especially worsening of asthma, breathing difficulty if you have pre-existing lung conditions such as COPD/bronchitis/pneumonia/Cystic Fibrosis. Beta blockers should be used only sparingly in heart failure, because of the vulnerability to enter into pulmonary edema.
It depends on the institution how superiors and subordinates should interact with each other. In most situations, it would be good to have a mutual respect.