Cystic Fibrosis Video Analysis

Improved Essays
Show More
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. After watching people with Cystic Fibrosis go through I decided that I am going to do my pathology paper on it for the coming semester. Compared to many existed

Related Documents

  • Great Essays

    Genetic Disorders: Cystic Fibrosis
    • 1413 Words
    • 6 Pages

    Genetic Disorders: Cystic Fibrosis

    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
    Read More
  • Decent Essays

    Cystic Fibrosis Annotated Bibliography
    • 378 Words
    • 2 Pages

    Cystic Fibrosis Annotated Bibliography

    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
    Read More
  • Improved Essays

    Cystic Fibrosis Lab Report
    • 390 Words
    • 2 Pages

    Cystic Fibrosis Lab Report

    People who are prone to delta F508 mutation tend to have more critical symptoms of cystic fibrosis because of the lack of chloride ion transport, needed to control the thin layer of mucus that can be removed by the cilia lining the lungs and organs. The lack of chloride ion transport causes a thick mucus layer that the cilia can not remove, which in result traps bacteria causing disease. The chloride channels are to let chloride out of the epithelium cells. Someone who does that have cystic fibrosis the channels will open a fair amount of times in order to keep it balanced inside and outside of the cells,…

    • 390 Words
    • 2 Pages
    Improved Essays
    Read More
  • Improved Essays

    Cystic Fibrosis Part 1 Paper
    • 657 Words
    • 3 Pages

    Cystic Fibrosis Part 1 Paper

    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
    Read More
  • Improved Essays

    How Did Medical Technology Change Canada
    • 1160 Words
    • 5 Pages

    How Did Medical Technology Change Canada

    Since the discovery of the gene, doctors have been trying to to create effective therapies to treat Cystic Fibrosis. One of the doctors who works at the Sick Kids Hospital in Toronto, and studies the cystic fibrosis gene said, “Finding the gene opened the door to unprecedented knowledge of the disease. After its discovery we were able to study and understand how the protein made by the CFTR gene worked and what happened when it didn’t, Once we figured this out, therapy that targeted defects caused by CF gene mutations could begin” (Doctor Christine Bear). The discovery of the Cystic Fibrosis gene has helped the doctors learn much more about the disease and hopefully will help them find a cure to Cystic Fibrosis in the…

    • 1160 Words
    • 5 Pages
    Improved Essays
    Read More
  • Improved Essays

    Cystic Fibrosis Research Paper
    • 413 Words
    • 2 Pages

    Cystic Fibrosis Research Paper

    In Cystic Fibrosis, symptoms start slowly. The respiratory tract (nose to lungs) and the gastrointestinal (digestive) systems are the most affected. Symptoms usually start in the gastrointestinal system. Male fertility and sweat glands are also affected. Only about fifteen percent of babies who carry the disease have meconium ileus which is sticky and thick caused by thick mucus from intestinal glands.…

    • 413 Words
    • 2 Pages
    Improved Essays
    Read More
  • Improved Essays

    Cystic Fibrosis Research Paper
    • 614 Words
    • 3 Pages

    Cystic Fibrosis Research Paper

    This is how cystic fibrosis is inherited and the tools used to test for…

    • 614 Words
    • 3 Pages
    Improved Essays
    Read More
  • Superior Essays

    Cystic Fibrosis Research Paper
    • 849 Words
    • 4 Pages

    Cystic Fibrosis Research Paper

    Cystic Fibrosis is an inherited disease of the secretory glands, glands that make up mucus and sweat. It is also known as mucoviscidosis, that affects mostly the lungs but also the pancreas, liver, kidneys and intestine. Long term issues include difficulty breathing and coughing up sputum as a result of frequent lung infections. A defect in the CFTR gene causes cystic fibrosis. This gene makes a protein that controls the movement of salt and water in and out of your body's cells.…

    • 849 Words
    • 4 Pages
    Superior Essays
    Read More
  • Improved Essays

    Cystic Fibrosis Presentation
    • 905 Words
    • 4 Pages

    Cystic Fibrosis Presentation

    Cystic Fibrosis Presentation Cystic fibrosis is genetic disorder. It is an inherited disorder that can result in a severe damage to the respiratory and digestive systems. This disorder can affect the lungs, pancreas, intestines, liver and even the sex organs. Cystic fibrosis builds up a thick and sticky mucus in the lungs and other respiratory and digestive organs in our body. For an infant to be at risk of developing Cystic Fibrosis, both parents must pass on the abnormal gene to the infant.…

    • 905 Words
    • 4 Pages
    Improved Essays
    Read More
  • Decent Essays

    Cystic Fibrosis Research Paper
    • 523 Words
    • 3 Pages

    Cystic Fibrosis Research Paper

    The most important thing to do is to know about it. Learning more about Cystic Fibrosis can help in stressful times and also when someone tries to misinform you on something you know what it actually is and tell them. Support groups also work for patients and families. As well as physical problematic symptoms, there are some that are more mental and harder to see in the parent of a child with CF. Dealing with someone in the family who has Cystic Fibrosis can cause depression or anxiety to the caretaker.…

    • 523 Words
    • 3 Pages
    Decent Essays
    Read More
  • Improved Essays

    Biological Basis And Symptoms Of Cystic Fibrosis
    • 836 Words
    • 4 Pages

    Biological Basis And Symptoms Of Cystic Fibrosis

    The biological basis and symptoms of Cystic Fibrosis.…

    • 836 Words
    • 4 Pages
    Improved Essays
    Read More
  • Improved Essays

    Cystic Fibrosis Research Paper
    • 495 Words
    • 2 Pages

    Cystic Fibrosis Research Paper

    Digestive system complication can be averted with medication with digestive enzymes for the pancreas. Physical therapy can help improve respiratory problems. To prevent infections a person with Cystic Fibrosis should not go near another person with the disease. If a person tells their doctor, their issues the right medication and help can be given and the person can live a healthy…

    • 495 Words
    • 2 Pages
    Improved Essays
    Read More
  • Superior Essays

    Advancements In Cystic Fibrosis
    • 1730 Words
    • 7 Pages

    Advancements In Cystic Fibrosis

    CF is an autosomal recessive gene disorder caused by mutations in a pair of genes located on chromosome 7.1 There are thousands of combinations of gene mutations that can lead to a diagnosis of cystic fibrosis. These are referred to as cystic fibrosis transmembrane conductance regulator (CFTR).1 Cystic fibrosis affects about 30,000 children and adults in the United States, and about 70,000 worldwide per the Cystic Fibrosis Foundation.1 Cystic fibrosis does not just affect the respiratory system, it also encompasses other body systems. These include exocrine gland function, pancreas insufficiency, high chloride concentrations in the sweat, kidneys, liver, and intestines. Cystic fibrosis patients also have abnormalities in sodium and chloride production which aids in the dysfunction of the mucociliary transport…

    • 1730 Words
    • 7 Pages
    Superior Essays
    Read More
  • Improved Essays

    Cystic Fibrosis Research Paper
    • 1065 Words
    • 5 Pages

    Cystic Fibrosis Research Paper

    When an infant has Cystic Fibrosis, the disease will be caught early in his or her life; however, the symptoms of CF may not manifest until the later teen years. There are several different warning signs that go off when one has cystic fibrosis. Some sign that CF may be developing in a young child are: constant diarrhea, greasy stools that are foul smelling; also children’s bodies may grow poorly, they have severe cough with thick mucus and frequent wheezing (Patient Education Institute). When parents kiss his or her children, normally the parents cannot taste sweat. However, children with Cystic Fibrosis normally have salty skin, which parents will notice with his or her…

    • 1065 Words
    • 5 Pages
    Improved Essays
    Read More
  • Great Essays

    Cystic Fibrosis Case Study Essay
    • 2133 Words
    • 9 Pages

    Cystic Fibrosis Case Study Essay

    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
    Read More

Related Topics

Ready To Get Started?
Discover
Company
Follow
©2024 Cram.com
Privacy Policy |  About Ads |  Site Map |  Advertise  | 
  • Cookie Settings