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Although there is no cure for cystic fibrosis, people with this condition are generally able to live normal lives. There are many tools and techniques doctors use to help manage this complicated condition and with improvement in screening and treatments, life expectancy for those with cystic fibrosis is better than ever before.
There is no cure for cystic fibrosis, but treatment can ease symptoms, reduce complications and improve quality of life. Close monitoring and early, aggressive intervention is recommended to slow the progression of CF , which can lead to a longer life.
In people with pulmonary fibrosis, especially idiopathic pulmonary fibrosis, shortness of breath can suddenly get worse over a few weeks or days. This is called an acute exacerbation. It can be life-threatening.
There are many tools and techniques doctors use to help manage this complicated condition and with improvement in screening and treatments, life expectancy for those with cystic fibrosis is better than ever before. Simply put, cystic fibrosis is a gene defect.
Pulmonary fibrosis is a life-long lung condition that worsens over time. Having pulmonary fibrosis can cause fear, depression and stress. Here are some tips that may help you cope.
MARK E. WYLAM: The life expectancy of cystic fibrosis today approaches 40 years of age, and for many, it's gonna be much greater than that, as those persons born in the last two decades have access to not only the standard cares sponsored by the Cystic Fibrosis Foundation but by the new drugs and the pipeline drugs that are in place.
Cystic fibrosis; High blood pressure in the lungs (pulmonary hypertension) Lung damage can often be treated with medication or with special breathing devices. But when these measures no longer help or your lung function becomes life-threatening, your health care provider might suggest a single-lung transplant or a double-lung transplant.
Over the past few years, new medications have been developed that can dramatically improve lung function and overall well-being for most patients with cystic fibrosis. Also, these cumulative medical advances, coupled with attentive multidisciplinary care, have helped increase the life expectancy for patients with cystic fibrosis to an all-time ...
Interstitial lung disease can lead to a series of life-threatening complications, including: High blood pressure in your lungs (pulmonary hypertension). Unlike systemic high blood pressure, this condition affects only the arteries in your lungs.
Nephrogenic systemic fibrosis can begin days to months, and even years, after exposure to an older gadolinium-based contrast agent (group 1). Some signs and symptoms of nephrogenic systemic fibrosis may include: Swelling and tightening of the skin; Reddened or darkened patches on the skin