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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
Wiki User
∙ 12y ago
Wiki User
∙ 9y agoScientists are trying to find a cure to cystic fibrosis. So far there are no current cure to cystic fibrosis, though temporary or not a long time, a patient with cystic fibrosis will sometimes need to stay in the hospital for a very long time.
Wiki User
∙ 15y agoVisit cff.org, they have a newsletter that is constantly being updated and placed on their page. cff stands for the Cystic Fibrosis Foundation.
Wiki User
∙ 15y agoAs of right now there is a medication going into the human trials of testing that like it is likely that it is the poteintial cure for Cystic Fibrosis!!!
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The treament for Cystic Fibrosis is?
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.
Can you get life insurance for cystic fibrosis sufferes?
I am an independent life insurance agent. We recently lost my best friends wife to cystic fibrosis. I have done much research and have found one company that will insure someone with cystic fibrosis. All of the information is on a website I have created. life4cf.com Thanks, Chris Duncan
What is a good closing statement for cystic fibrosis research paper?
Perhaps the hardest thing to deal with is the fact that there is nothing that can be done to prevent it from happening, it is simply in the DNA makeup of the individual. Cystic fibrosis is a challenging disease to live with but the treatments that have been developed are forever improving the quality of life of those diagnosed with the fatal disease. Maybe with the advancements in medicine, one day there will be a cure, but all that can be done is hope.
Why treatment with medicines does not cure cystic fibrosis?
Cystic fibrosis is a genetic disorder. You can alleviate symptoms CAUSED by the defect but to completely cure the disease the faulty gene needs to be disrupted in ALL tissues affected by it. Realistically it can only be done effectively if gene therapy is applied when the embryo of a sufferer is still a bundle of stem cells in their mother's womb, elminating need for repeat gene therapy after birth.
Neonatal cystic fibrosis screening?
DefinitionNeonatal cystic fibrosis screening is a blood test that looks for increased levels of immunoreactive trypsinogen (IRT), an enzyme produced by the pancreas. The test is performed on newborns to screen for cystic fibrosis (CF).Alternative NamesCystic fibrosis screening - neonatal; Immunoreactive trypsinogen; IRT testHow the test is performedA sample of blood is either taken from the bottom of the baby's foot of a vein in the arm. A tiny drop of blood is collected onto a piece of filter paper and allowed to dry. The dried blood sample is sent to a lab for analysis.How to prepare for the testThere is no special preparation needed.Some states include this test in the routine newborn screening tests that are done before the baby leaves the hospital.If you live in a state that does not perform routine CF screening, your health care provider will explain whether testing is needed.How the test will feelThe brief feeling of discomfort will probably cause your baby to cry.Why the test is performedChildren with CF who are diagnosed early in life and start treatment at a young age may have better nutrition, growth, and lung function. Newborn screening tests allow doctors to identify children with CF before they have symptoms.Normal ValuesNormal values vary from lab to lab. Ask your doctor or testing center for details.What abnormal results meanIt is important to remember that a positive screening test for cystic fibrosis does not diagnose cystic fibrosis. If your child's test is positive, further tests will be done to confirm the possibility of CF. Not all children with a positive screening IRT test have CF.What the risks areRisks associated with the test include:Infection (a slight risk any time the skin is broken)Anxiety over false positive testsFalse reassurance over false negative testsSpecial considerationsThe IRT level does not indicate the severity of the CF. False-positives may occur.ReferencesFarrell 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).
How long has Celine Dion been singing?
Celine has done charity work (to my knowledge) since 1983, when she taped a commercial for Cystic Fibrosis Canada. She has a personal connection, as her niece Karine was diagnosed with it.
Is the repair of cardiac muscle and nervous tissue done by fibrosis?
true
Cystic fibrosis?
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.
What is being done to help the Island Fox?
nothing is being done
What is being done about the gases in the atmosphere?
what is being done to show that there are gases in the atmosphere
What is being done to help water shortages?
nothing is being done to help
How do you know work is being done?
work is being done when you use energy
