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A small Johns Hopkins Children’s Center study of children and teens with cystic fibrosis (CF) shows that simple exercise, individually tailored to each patient’s preference and lifestyle, can help improve lung function and overall fitness. Frequent lung infections, breathing problems, and decreased lung function are the hallmark symptoms of CF, a genetic disorder marked by a disruption in the body’s ability to transport chloride in and out of cells that leads to the buildup of thick mucus in the lungs and other organs.
The Johns Hopkins team designed exercise regimens that fit easily into each patient’s daily life because rigidly structured high-intensity exercise routines are hard to sustain over time.
The researchers asked 58 children with CF, ages 6 to 16, to describe their daily routine and preferred physical activities. Based on their answers, the patients received individual exercise recommendations, including going for a stroll, taking a dance class, playing basketball in the driveway, or playing with a Wii™.
Researchers compared the patients’ lung function and exercise tolerance before and after the two-month program. The exercise tolerance test consisted of walking multiple 10-meter (roughly 33 feet) intervals. After completing the exercise programs, patients were able to perform seven more 10-meter walking intervals, on average, than they were before completing the exercise regimen.
All children showed small bumps in pulmonary function tests, but children who increased their exercise capacity by 10 or more walking intervals showed even more noticeable improvement (5 percent or more) in lung function scores.
To read more of this article click http://www.bmedreport.com/archives/27302
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