Doctor insights on:
Cystic Fibrosis Cf Physical Therapists
Anything: Most individuals with cystic fibrosis can participate in all physicial activities. Salt supplementation is needed because of excess salt loss in CF sweat. Individuals with severe lung disease should discuss what level of activity is safe/appropriate for them with their physician. ...Read more
Physical therapists are healthcare professionals who diagnose and treat individuals with heath-related problems and injuries that limit their abilities to move and perform daily functional activities. Physical therapists create plans with techniques that help individuals restore their ability to move, reduce ...Read more
Genetic: CF is caused by mutations in the cftr gene - mostly they are inhereted from both the mother and father who are carriers (but rarely these mutations can occur spontaneously). Club feet can be caused by several circumstances - some from a generic defect, some from problems during fetal deveopment or toxic exposures. ...Read more
Recurrent pneumonias: Cystic fibrosis (CF) is a genetic disease of cftr chloride channel defect with multi-organ involvement. Pancrease (pancrelipase) and lung are particularly affected causing lung infections, asthma type symptoms, pancreatic insufficiency with malabsorption, fat solubale vitamin deficiencies and diabetes which manifest maily during teenage years. Shahzeidi, md, pulmonologist. ...Read more
Not specifically: Most CF patients that are monitored and receiving regular healthcare can not be picked out in a crowd of people of similar age. If their disease were to go unrecognized and or untreated they would appear ill. ...Read more
Depends on Lung Fx: The level of physical activity for a child with CF is an individual choice that should be made in consultation with the treating physician. However, there has been some interesting research done in australia, which suggests Hypertonic Saline (e.g., salty air) inhalation in CF patients was beneficial in maintaining lung function. Why? A doctor noticed surfers with CF tend to have better outcomes! ...Read moreSee 1 more doctor answer
I have a very mild form of cystic fibrosis and want to become a police officer. If i'm in great physical shape do you think they will consider me?
Cystic fibrosis: That question is likely covered by a written policy specific to your possible employer. Just remember that failing to reveal a medical condition prior to employment might be grounds for firing you at a later time. For example, if you have active asthma when you apply for military service, their policy is to exclude you from consideration. ...Read more
Newborn boy has a severe mutation delf508 and a 5-t gt12. Was told that he might or might not develop mild cystic fibrosis. How does mild CF manifest?
Varies: Mild CF can vary from recurrent sinus infections, recurrent pneumonia, pancreatitis, fertility problems. One may have no evidence of CF until adulthood. Sometimes the first sign is recurrent pancreatitis in the second or third decade of life. Usually growth is not impaired. ...Read moreSee 1 more doctor answer
My son has hirschsprung disease. My wife tested neg. for cystic fibrosis. Are the two related? Should I be tested for CF? I'm 32 w/no issues.
No, not related: Hirschsprung's disease is a congenital condition that leads to absence or lower numbers of nerve cells in the large intestine that are responsible for allowing the colon muscles to function, leading to constipation or inability to pass stool. Cystic fibrosis is an inherited recessive disorder of salt transport leading to thickened secretions. If your wife is negative, no need for you to be tested ...Read moreSee 2 more doctor answers
Progressive disease: Cystic fibrosis (CF) is a progressive, lifelong condition in which the glands that produce mucus, sweat, and intestinal secretions do not function properly. Thick mucus accumulates in the lungs, leading to breathing difficulty and infection. CF also impairs digestion, and affected males are usually infertile. ...Read moreSee 1 more doctor answer
Can men with atypical cystic fibrosis have children? I have 2 children, I have no symptoms of CF and I am 32 years old. Never tested for CF.
My wife & son passed california newborn screening for CF, does that mean odds are low for typical cystic fibrosis or mild form?
Newborn screening : for Cystic Fibrosis is done by Immunoreactive Trypsinogen, IRT. If othe IRT level is ^, DNA tests for CF gene mutations are done on blood on the Guthrie card. CF Foundation-accredited Care Centers in CA look for an "intermediate" sweat chloride result in young infants who do not gain wt. & have bad gas, abdominal pain & loose or hard stools &/or wheezing/coughing for > 2 wks. to diagnose CRMS. ...Read more
Should I be tested for cystic fibrosis? If wife had negative prenatal screening & my son had negative IRT/DNA test (california screening). Curious after reading about CF in adults. Feel fine. anxiety
My son & wife tested neg for Cystic Fibrosis through screening test, not sweat test. However my son has hirschsprung disease. Should I test for CF - or it's high unlikely I have it? I'm 32. Feel fine
I wouldn't: There is no relationship between Hirschprung disease and CF. If you wand to know if you are an asymptomatic carrier of CF, the tests are available. However, you don't get to age 30 without symptoms when you have the disease and your fertility would also be diminished.If your wife is not a carrier, you can not produce babies with CF. ...Read moreSee 3 more doctor answers
My 3 1/2 yr. Old with cystic fibrosis has cold/ allergy symptoms...But unusually grumpy and purple color under eyes...Allergies or CF exacerbation?
Pls see answer: There is an overlap between the symptoms of allergy and cf. Allergic symptoms tend to be associated with a particular exposure that triggers an allergic response. The discoloration under the eyes may be caused by allergies, infection, lack of sleep, iron deficiency. If the area around the eye is red and swollen, it is best to check with your doctor. Fever > 101 is not usual for an allergic resp, . ...Read moreSee 1 more doctor answer
Certainly: Cystic Fibrosis (CF) most common life-limiting genetic disorder of Caucasians, affecting approximately 30K people in the US.A, impacting mainly respiratory function. In recent years patients symptoms better controlled by genetic findings and better medications.Emotional & phys. development depend on severity, time in hospital, complications.Morb. & mort.factors afect emotional,cognitive behavior. ...Read more
As a carrier: Genetic carrier testing: more than 10 million americans are symptomless carriers of the defective CF gene. This blood test can help detect carriers, who could pass CF onto their children. To have cystic fibrosis, a child must inherit one copy of the defective CF gene from each parent. ...Read more
Yes: Yes it is possible. Presentation of cystic fibrosis varies greatly, and it is possible, depending on your specific mutation (and other factors) to present at a later age. In order to prevent late diagnoses, all states now have a newborn screen in place for cystic fibrosis. ...Read moreSee 1 more doctor answer
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