Doctor insights on: Can you play sports with cystic fibrosis
Yes: Lung transplantation is a very important treatment option for people with cystic fibrosis that is severely limiting their physical ability. If successful, and it usually is, lung transplantation can offer a person with cystic fibrosis a renewed chance to regain the ability and energy to do many activities that others without this condition take for granted, including some sports. ...Read moreSee 2 more doctor answers
It may be easier to exercise earlier in your pregnancy than during the last three months (third trimester) of pregnancy. Choosing safe exercises for you and your baby is important because some positions, as your weight and balance change, may become uncomfortable or have potentially harmful effects. After 20 weeks of pregnancy, you should not do exercises that require lying flat on your back, because this position may make ...Read more
Art around what age do the obvious symptoms of cystic fibrosis set in? I'm worried of the disease although I played football for 5 years since 7th gra
CF worry: Hi KennethH, typically CF is diagnosed in infants and children. However, about 7% of cases can present in adulthood. These tend to be less of the typical disease and more likely to develop diabetes, GI symptoms, and even infertility. Adults are more likely to have normal pancreatic function, unusual genetic mutations and equivocal sweat chloride tests. If you are worried, talk to your doctor. ...Read moreSee 2 more doctor answers
PFTs with albuterol:
An additional comment:
children with CF can participate in sports if they are able to do so. Obtaining a lung function test with and without a bronchodilator to determine whether there is treatable reactivity of the airway may be useful. This can be discussed with your doctor. ...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
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
Get tested: Testing for cystic fibrosis starts with a sweat test. If that is abnormal, genetic testing in the blood is used to confirm the diagnosis by finding the specific genetic mutations. In general, people with CF have recurrent pulmonary infections and abdominal discomfort/diarrhea due to fat malabsorption. ...Read moreSee 1 more doctor answer
Cystic fibrosis is a risk factor for:: Aspergillosis, Brain abscess, Bronchiectasis, Collapsed lung, Hypertriglyceridemia, Pulmonary Aspergillosis, Sinusitis, Mucocele, Sputum, Phlegm, Rectal prolapse, Acute sinusitis, Vitamin A deficiency, Vitamin K deficiency, Vitamin E deficiency, Vitamin D deficiency. ...Read more
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
CF and environment: Depending on the severity of your cf, leading an active healthy lifestyle outside is not a fantasy. Common sense will dictate avoidance germs by simple hand hygiene (wash, wipe, alcohol base hand gels). Knowing your CF treatment plan as per your pulmonologist/specialist is important for slowing down the progression/maintaining a more resilient defense against bacterial/chronic lung infection. ...Read moreSee 1 more doctor answer
About 1 in 25: The likelihood of being a carrier for CF depends on your ethnic background. Among whites it is about 1 in 25 or 30 and in hispanics 1 in 45 or so. It is lower in african americans and asians. If there is a known person in your family with CF that will increase the risk of being a carrier. CF was only known as a disease in 1938, so before that babies died of pneumonia or diarrhea, not cf. ...Read more
Genetic disorder: Cystic fibrosis is a genetic disorder involving lungs & digestive tract, causing recurrent lung infections due to thick inspissated mucus & poor growth in majority of patients due to malabsorption. Treatment involves inhaled respiratory therapies to prevent lung disease & pancreatic enzymes to enable absorption of nutrients. Average life expectancy is near 40 years, new therapies being developed. ...Read moreSee 1 more doctor answer
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