Idiopathic pulmonary fibrosis or IPF is a progressive lung disease. There is no known cause of IPF. Symptoms include shortness of breath, cough, fatigue, mild fevers, muscle pain, clubbing fingers, and ankle swelling. Treatment of idiopathic pulmonary fibrosis is directed at managing symptoms. The life expectancy is about 2 to 5 years. Read more: What Is Idiopathic Pulmonary Fibrosis (IPF)? Article
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10 Smart Exercises for People With COPD: Pictures See SlideshowRelated Disease Conditions
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Is Pneumonia Contagious?
Pneumonia is inflammation of the lung usually caused by bacterial or viral infection (rarely, also by fungi) that causes the air sacs to fill with pus. If inflammation affects both lungs, the infection is termed double pneumonia. If it affects one lung, it is termed single pneumonia. If it affects only a certain lobe of a lung it's termed lobar pneumonia. Most pneumonias are caused by bacteria and viruses, but some pneumonias are caused by inhaling toxic chemicals that damage lung tissue.
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Chronic Cough
Chronic cough is a cough that does not go away and is generally a symptom of another disorder such as asthma, allergic rhinitis, sinus infection, cigarette smoking, GERD, postnasal drip, bronchitis, pneumonia, medications, and less frequently tumors or other lung disease. Chronic cough treatment is based on the cause, but may be soothed natural and home remedies.
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Pulmonary Fibrosis
Pulmonary fibrosis is scarring throughout the lungs. Pulmonary fibrosis can be caused by many conditions including chronic inflammatory processes, infections, environmental agents, exposure to ionizing radiation, chronic conditions, and certain medications. Symptoms include shortness of breath, coughing, and diminished exercise tolerance. Treatment options are dependent on the type of pulmonary fibrosis; lung transplant and/or medications are options.
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Pneumonia
Pneumonia is inflammation of the lungs caused by fungi, bacteria, or viruses. Symptoms and signs include cough, fever, shortness of breath, and chills. Antibiotics treat pneumonia, and the choice of the antibiotic depends upon the cause of the infection.
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Pneumococcal Pneumonia
Second Source article from Government
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Cystic Fibrosis
Cystic fibrosis is a disease of the mucus and sweat glands. Cystic fibrosis is an inherited disease. The outcome of the disease leaves the body malnourished, with bulky and fouls smelling stools, vitamin insufficiency, gas, painful or swollen abdomen, infertility, susceptible to heat emergencies, and respiratory failure. There is no cure for cystic fibrosis, treatment of symptoms is used to manage the disease.
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Sarcoidosis
Sarcoidosis, a disease resulting from chronic inflammation, causes small lumps (granulomas) to develop in a great range of body tissues and can appear in almost any body organ. However, sarcoidosis most often starts in the lungs or lymph nodes.
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Smoking (How to Quit Smoking)
Smoking is an addiction. More than 430,000 deaths occur each year in the U.S. from smoking related illnesses. Secondhand smoke or "passive smoke" also harm family members, coworkers, and others around smokers. There are a number of techniques available to assist people who want to quit smoking.
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Lung Anatomy
The lungs are primarily responsible for the exchange of oxygen and carbon dioxide between the air we breathe and the blood. Eliminating carbon dioxide from the blood is important, because as it builds up in the blood, headaches, drowsiness, coma, and eventually death may occur. The air we breathe in (inhalation) is warmed, humidified, and cleaned by the nose and the lungs.
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Is a Cough Contagious?
There are many types of coughs: for example, dry cough, wet cough, a barking cough, whooping cough, stress induced cough, acute cough, and chronic cough. Cough is a symptom of an underlying condition or disease. Treatment of cough as a symptom is generally with OTC lozenges and liquids. The cause of the cough will be necessary to treat.
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Scleroderma
Scleroderma is an autoimmune disease of the connective tissue. It is characterized by the formation of scar tissue (fibrosis) in the skin and organs of the body, leading to thickness and firmness of involved areas. Scleroderma is also referred to as systemic sclerosis, and the cause is unknown. Treatment of scleroderma is directed toward the individual features that are most troubling to the patient.
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Interstitial Lung Disease (Interstitial Pneumonia)
Interstitial lung disease refers to a variety of diseased that thicken the tissue between the lungs' air sacks. Symptoms of interstitial lung disease include shortness of breath, cough, and vascular problems, and their treatment depends on the underlying cause of the tissue thickening. Causes include viruses, bacteria, tobacco smoke, environmental factors, cancer, and heart or kidney failure.
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Pulmonary Hypertension
Pulmonary hypertension is elevated pressure in the pulmonary arteries that carry blood from the lungs to the heart. The most common symptoms are fatigue and difficulty breathing. If the condition goes undiagnosed, more severe symptoms may occur. As pulmonary hypertension worsens, some people with the condition have difficulty performing any activities that require physical exertion. While there is no cure for pulmonary hypertension, it can be managed and treated with medications and supplemental oxygen to increase blood oxygen levels.
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What Is Bronchiectasis?
Bronchiectasis has three types: cylindrical bronchiectasis, saccular or varicose bronchiectasis, and cystic bronchiectasis. Causes of bronchiectasis include infection, environmental exposure, drug or alcohol abuse, and alpha-1 antitrypsin (congenital). Symptoms of bronchiectasis include shortness of breath, fatigue, chronic cough, bloody sputum, and wheezing. Treatment for bronchiectasis includes antibiotics and possibly surgery.
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How Long Can You Live With Cystic Fibrosis?
The life expectancy of patients with cystic fibrosis has improved over the last 50 years. The improved chances of survival are due to advances in early diagnosis, supportive care, nutritional care, and infection control.
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Can You Get Cystic Fibrosis at Any Age?
Cystic fibrosis is classically a disease of childhood that progresses into adulthood. If you have a genetic defect related to cystic fibrosis (CF), you are more likely to be born with cystic fibrosis. The symptoms might appear later, and hence, the age at diagnosis varies widely.
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Asbestos (Exposure Dangers, Testing, Symptoms)
Asbestos is a mineral fiber that is found in soil and rock. Asbestos exposure occurs when asbestos fibers are disturbed and released into the air then and inhaled. Inhaling asbestos fibers causes three lung diseases; asbestosis, lung cancer, and noncancerous lung disease. In asbestosis, the asbestos fibers scar the lungs. Asbestosis and lung cancer have the same symptoms of cough and shortness of breath.Asbestosis progresses slowly, frequently even 20 to 40 years after asbestos exposure. Asbestos exposure include can come from a variety of products, for example, drinking water due to the decay of asbestos cement in water mains and erosion of natural deposits (which increases your risk of developing benign intestinal polyps), insulation, vinyl floor tiles, some paints and patching compounds, oil and coal furnaces and doors, heat-resistant fabrics, and automobiles brakes and clutches. Some uses of asbestos are banned; however, most are not. Examples of products banned from using asbestos are commercial, corrugated, and specialty paper, flooring felt, and artificial fireplace embers that contain asbestos. Examples of products not banned from using asbestos include vinyl flooring, clothing, roof and non-roof coatings, friction materials, and some car components.Cancers of the larynx, throat, kidney, esophagusand gallbladder have been linked to asbestos exposure. Treatment is dependent upon the type of condition related to asbestos exposure.
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Can You Live a Long Life With Cystic Fibrosis?
How long can you live with cystic fibrosis? Learn the signs of cystic fibrosis and what to do if someone you know has cystic fibrosis.
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Cystic Fibrosis Life Span
Cystic fibrosis (CF) is a progressive disease that needs daily care. Though a patient needs to take medications lifelong, most people with cystic fibrosis are usually able to attend school and work. The improvement in screening and treatments mean that people with CF now may live into their mid- to late 30s or 40s, and some are living into their 50s.
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