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Over time, damage to the lungs can cause severe breathing problems.
Respiratory failure is the most common cause of death in people who have CF.
As treatments for CF continue to improve, so does life expectancy for those who have the disease.
Today, some people who have CF are living into their forties or fifties, or longer.
If the disease is mild, symptoms may not show up until the teen or adult years. As the disease gets worse, you'll have more severe symptoms more often.
The symptoms and severity of CF also vary over time. Lung function often starts to decline in early childhood in people who have CF.
You and your doctor may be able to treat your interstitial cystitis (IC) with lifestyle changes, bladder training, physical therapy, medicines, bladder hydrodistention, bladder instillation, surgery, or a combination of these treatments.
No research consistently links certain foods or drinks to interstitial cystitis (IC), although many people find that certain foods and drinks can make their IC symptoms worse, such as alcohol, caffeine, and high-acid foods.
This content is provided as a service of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), part of the National Institutes of Health.
Cystic fibrosis (SIS-tik fi-BRO-sis), or CF, is an inherited disease of the secretory (see-KREH-tor-ee) glands.
Secretory glands include glands that make mucus and sweat.
This can upset the balance of minerals in your blood and cause many health problems.
Examples of these problems include dehydration (a lack of fluid in your body), increased heart rate, fatigue (tiredness), weakness, decreased blood pressure, heat stroke, and, rarely, death.
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The thick, sticky mucus also can block tubes, or ducts, in your pancreas (an organ in your abdomen).