Cystic Fibrosis Research

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Cystic Fibrosis Research: Cystic Fibrosis (CF) is a complicated genetic disease that causes you to produce extra-thick, sticky mucus. If you or your loved one is fighting this disease, they may require medicines as part of their treatment routine. In the United States, the congenital respiratory disease Cystic Fibrosis (CF) affects about 30,000 children and adults, and 40,000 suffers worldwide according to the cystic fibrosis foundation. About 1000 new cases are diagnosed each year. In 2014, some research, pharmaceutical, and technology breakthrough have helped shed new light on the respiratory disease and continue to inform treatment strategies with the ultimate goal of improving the quality of life for patients and one dying during…show more content…
A 2014 study published in Annals of Internal Medicine reports that the life expectancy for a child born and diagnosed with cystic fibrosis (CF) in 2010 is now 37years for female and 40years for males ,with the mortality rate if it continues to decrease at the rate observed between 2000 and 2010 as reported by the authors. As the life expectancy is improving in the United States according to some media report, the disease is beginning to emerge in other countries, specifically Asia. It occurs mostly among Caucasians of Northern European descent with a rate of 1 in 2,500, according to CDC statistics reported by the American Lung Association. With these reports, native Indians have begun to study and diagnose the disease in their own population. Researchers in India believed increased globalization has contributed to the spread of genetic diseases such as cystic fibrosis…show more content…
It has being used by patient’s with cystic fibrosis over 20years. The Vest uses high frequency chest wall oscillation (HFLWO) technology to dislodge mucus from the bronchial walls, and mobilize secretions and mucus from the smaller to larger airways where it can be cleared by coughing or suctioning. Cystic Fibrosis is a debilitating respiratory disease for both the child, the parents or caregivers and as a result needs constant and aggressive treatment as well as love and caring with ongoing research. On line community is a recommended place for patients and their caregivers to get advice, share stories and also learn more about the right treatments. References: Journal for Respiratory care Practitioners, September 1, 2014, retrieved from GCU, NRS -430V. Cystic Fibrosis Foundation on Line Community Contact: 1-888-756-9963. Hassan S. Alorainy, BSrc, RRT, King Faisal Specialist Hospital and Research Center, Ryadh, Saudi
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