Bronchiectasis Research Paper

Improved Essays
According to the American Lung Association, 23 million people have asthma, 13.6 million people have COPD, and an equal number still have not been diagnosed. Most have heard of asthma, COPD, bronchitis, and pneumonia. For some, these are very common lung issues; but have you ever heard of bronchiectasis? According to the American Lung Association, bronchiectasis is a chronic condition where the walls of the bronchi are thickened from inflammation and infection. Bronchiectasis is divided into two categories: cystic fibrosis bronchiectasis and non - cystic fibrosis bronchiectasis. No matter the form, this disease is long term with symptoms that need to be managed over long periods of time, causing a toll on individuals struggling with this lung disease.
Symptoms for bronchiectasis can include: pain in the chest area or back, shortness of breath, sinusitis, wheezing, fatigue, weight loss or gain, coughing with phlegm or blood, recurrent infection, and a cough that occurs over months or years and daily production of large amounts of phlegm. For some, finding
…show more content…
This much more mild form of bronchiectasis is characterized by the enlargement and scarring of the lung’s airways. Similar to cystic fibrosis bronchiectasis, the cause of the non cystic fibrosis form can be tough to discover for some, but it is usually developed because of re-occuring infections and inflammations that damage the walls and airways of the lungs. Ironically though, nearly one third of non-cystic fibrosis bronchiectasis cases are actually caused by cystic fibrosis itself. No need to fear though, when treated correctly, non-cystic fibrosis bronchiectasis is a chronic lung disease that one can learn to live a normal life with. Playing sports, owning pets, and having a family is something individuals living with this disease can look forward to. But the only way to achieve this is by staying

Related Documents

  • Improved Essays

    Bronchitis Case Study

    • 808 Words
    • 4 Pages

    In chronic obstructive lung problems are known because resistance in airflow increases and causes obstruction in the walls of lumen. Patient must have had chronic or productive cough that would last for 3 months and then happen it again for at least 2 years or more. Chronic bronchitis is also known as type B COPD or the “blue bloater,” which is diagnosed symptomatically by hypersecretion of bronchial mucus and in R.S.’s clinical findings there is definitely signs of emphysema, airway obstruction is persistent and irreversible. Q2. How would the consequences of the COPD of R.S. (identified in question 1) differ from those of emphysematous COPD?…

    • 808 Words
    • 4 Pages
    Improved Essays
  • Great Essays

    Introduction The genetic autosomal recessive disorder known as Cystic Fibrosis (CF) effects on average 1 of 28 Caucasians. The average age for patients to be diagnosed with this genetic disorder is around 2 weeks and 2 years old, there are some cases where they are find out sooner and others when they are adults. CF affect the patient’s chloride channels which causes the mucus in their lungs to thicken and pool. It can also affect the pancreas by blocking it up and not allowing it to produce digestive enzymes.…

    • 1413 Words
    • 6 Pages
    Great Essays
  • Decent Essays

    Website: http://www.wsvn.com/story/26299941/camps-take-cystic-fibrosis-patients-surfing Cystic fibrosis (CF) is a genetic-disease that causes thick, sticky mucus to build up in the lungs, digestive tract, and continues throughout other areas of the body. Cystic fibrosis has signs and symptoms that differs, depending on how bad the disease affects someone. Cystic fibrosis varies through ages, it affects infants, teenagers, and young adults, but is mostly found in white people.…

    • 378 Words
    • 2 Pages
    Decent Essays
  • Improved Essays

    My inspiration to do my project on Cystic Fibrosis dated back on Nov, 2016 when I participated Student Success Leadership Conference at Virginia Beach. One of the motivational speaker at the end of her speech played music video by One Republic “I lived”. In that video clip a teenager with cystic fibrosis was shown and explained how it feel living with cystic Fibrosis. The boy explained that having cystic fibrosis caused him to have breathing problem and he said that he felt he is breathing with a straw. As he continued explaining he said the more he tried to breathe the more he has pain.…

    • 364 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Cystic Fibrosis Part 1 Jenna Saline Kaplan University Cystic Fibrosis is a genetic condition that has an affect on many organs of the patient. This disease will ultimately lead to fatal impairment of the lungs. It is most common to see Cystic Fibrosis diagnosed from early childhood to young teens. Cystic Fibrosis is an autosomal recessive disorder in which both gene alleles must be mutated for the disease to be expressed (Ignatavicius and Workman, 2013). As every person is unique, the severity of the effects from CF will vary from person to person.…

    • 657 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Genetic Disorder Paper Cystic fibrosis is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time (cystic fibrosis foundation). It is a decease in the secretory glands, the glands that make mucus and sweat (medicine). It causes the cells in those parts to not function correctly and when needed to produce fluids, produce thick, sticky mucus in the lungs, pancreas and other organs (cystic fibrosis foundation). It builds up and blocks tubes and airways making it harder to breathe.…

    • 614 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    During the 1930’s and 40’s, the majority of children diagnosed with Cystic Fibrosis died in the first couple years of their lives. ("Prognosis") This unfortunate reality is caused by the effect of the inherited disease, Cystic Fibrosis; this sickness is caused by the build-up of excess mucus that has the potential to permanently damage one’s lungs. Cystic Fibrosis, also known as CF, Cystic Fibrosis of Pancreas, Fibrocystic Disease of Pancreas, or Mucoviscidosis, is a non-contagious genetic disease that works by producing mucus that is abnormally thick and sticky, and can ultimately kill the patient. Mucus, as most are aware of, is a slippery substance that lubricates and protects the linings of the airways, digestive system, reproductive system,…

    • 1584 Words
    • 7 Pages
    Superior Essays
  • Improved Essays

    Cystic fibrosis (CF) is a genetic and inherited disease that is life threatening. CF effects not only one’s breathing with continuous lung infections by lining the lungs with mucus, but can also trap infections by blocking the airway. The buildup of mucus effects the digestive system by preventing prevents the digestive enzyme process from breaking down food and obtaining nutrients. An infant that has been diagnosed with CF has inherited two copies of the defective CF gene, a copy from each parent as a carrier. When screening infants for cystic fibrosis, the most effective way to prevent serious lifelong complications is to diagnosis the disease early.…

    • 740 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    The Disease with No Cure Approximately 30,00 people on the united states have Cystic Fibrosis. Cystic Fibrosis is a lung disease that limits your ability to breathe overtime. There is no cure but, the disease can be controlled with treatments and a management team. In CF a gene causes a thick buildup of mucus that blocks the airways. Today the life expectancy for people with CF who live past child hood is 37 years.…

    • 969 Words
    • 4 Pages
    Superior Essays
  • Improved Essays

    Cystic Fibrosis is a life shortening disease which causes an abnormal collection of mucus in the lungs, pancreas, and other organs. “Mucus is a substance made by tissues that line some organs and body cavities, such as the lungs and nose. Normally, mucus is a slippery, watery substance. In victims of Cystic Fibrosis it becomes thick…

    • 1606 Words
    • 7 Pages
    Improved Essays
  • Improved Essays

    Emphysema is the condition in which the alveoli are destroyed due to damaging exposure. Chronic bronchitis is the inflammation of the lining of the bronchial tubes. COPD is treatable. People with the condition can control the symptoms by quitting smoking or being around harmful gases. Remission or restoring is possible if they quit smoking before the age of 35.…

    • 751 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Cystic fibrosis is a disease that is passed down in families. It is a disease that does not affect your normal life, you can still work and go to school. There have been many improvements so people are doing better longer. It does require daily care. Some common symptoms include: coughing thicker mucus, wheezing, breathlessness, lung infections, stuffy nose, exercise intolerance, and more.…

    • 144 Words
    • 1 Pages
    Improved Essays
  • Great Essays

    Introduction This case study focuses on 18 year old John who has cystic fibrosis (CF). He is the fourth child in a family of eight. The pregnancy and birth were routine and there was nothing to suggest that John had any illness but her hospitalised at 2 months and consequently received a diagnosis of CF. He returned home four weeks later with a treatment plan of physiotherapy, medication and nebulizers, which has continued all his life. Depending on his condition John may need physiotherapy and nebulizers at least twice or up to four times a day.…

    • 2133 Words
    • 9 Pages
    Great Essays
  • Improved Essays

    Cystic Fibrosis is a genetic disease that is incurable, but can be helped with treatment, and can last for a few years upto a lifetime. Its symptoms include coughing, lung infections, inability to gain weight, and fatty stools. It can cause pain in the abdomen, induce diarrhea or constipation, cause slowed growth, fatigue, and much more. Treatment is very hard to conduct as the disease varies in severity from person to person, but some common measures, such as airway cleaning, inhaling medicines, and taking pancreatic enzyme supplements, are taken. Cystic Fibrosis is affects 70,000 people worldwide, and 30,000 just in the United States.…

    • 341 Words
    • 2 Pages
    Improved Essays
  • Superior Essays

    What Is Cystic Fibrosis?

    • 1546 Words
    • 7 Pages

    Most people do not know cystic fibrosis is sometimes called “sixty-five roses.” The nickname came from a young boy who heard his mom talking about the condition on the phone. Each time she said cystic fibrosis he thought she was talking about sixty-five roses. In reality, cystic fibrosis is a devastating disease caused by a hereditary disorder which affects the exocrine glands. Around one in twenty three people in the United States carry at least one defective gene causing it to be the most common genetic defect of its severity.…

    • 1546 Words
    • 7 Pages
    Superior Essays