Preview

Cystic Fibrosis Personal Impact

Better Essays
Open Document
Open Document
1477 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Cystic Fibrosis Personal Impact
Cystic Fibrosis: A Personal Impact
Carrie Minton
NUR/427
June 8th, 2013
Dr. Angela Lowery

Cystic Fibrosis: A Personal Impact Isabel and Anabel Stenzel, identical twins, were born with the deadly chronic disease, Cystic Fibrosis. This disease has had a huge impact on their everyday quality of life as well as their family and friends. It is a daily fight and struggle. Not giving up and continuing to be proactive about caring for themselves is key to survival. At birth the doctor said they had 10 years to live. They are now 40 years old and have accomplished so much in their lives despite the difficulties of living with Cystic Fibrosis.

Cystic Fibrosis: The science Cystic Fibrosis is a very progressive and chronic lung
…show more content…
For the majority of their lives, living with Cystic Fibrosis has been an uphill battle. Ultimately, the end result of the progression of Cystic Fibrosis is lung transplantation. They were able to keep their own lungs for around 30 years. “Lung transplantation for patients with severely advanced cystic fibrosis lung disease may be a treatment option. The tissues of the transplanted lung do not develop cystic fibrosis; however, any other involved systems remain diseased. Between 120 and 150 patients with cystic fibrosis undergo lung transplantation each year with a 5-year survival rate of about 50%” (Scott, 2013). In order to even qualify for transplantation, it had to be proven that they were vigilant with caring for themselves and were consistent with treatments and medications. It has been around 10 years since they have had their double lung transplants. So they have beat those statistics as well. There were many days when one would want to skip a treatment or cut it short and the other was there to not allow it. They attribute their health and lives to having each other. Having up to five treatments a day, growing up, gets old fast. Being vigilant in living with Cystic Fibrosis requires hours of attention everyday in order to prevent a downward …show more content…
Spending a lot of their time in the hospital setting, they decided to make the most of it. Their parents raised them to look at their disease as an opportunity and a challenge. The twins were determined to beat the odds. And beat the odds they did. Isabel and Anabel grew up with a very strong support group. Their parents were always their for them and exposed them to other kids their age struggling with Cystic Fibrosis. They talked about going to camps every summer that were specifically for kids with Cystic Fibrosis. Throughout the years, the twins have met many doctors and nurses who have helped educate and motivate them through this challenging journey. Having this illness has really opened their eyes to the fact that they still have healthy minds, to not take advantage of the time they have on this earth, and that they are more than their bodies. Accepting and letting go of the fact that they have Cystic Fibrosis and will have it forever was the first step to a motivated and positive mindset. The twins strongly believe that they can do anything they set their minds

You May Also Find These Documents Helpful

  • Satisfactory Essays

    There are many diseases in the world that affect the human body. In many cases people do not care or don’t become aware of all the diseases that can be harmful and possibly put their lives at risk. There is a great list of diseases that can impact our lives. For example, one of the diseases that I found to be sadly life changing is the Spina Bifida. Even though, the outlook for children with spina bifida has changed dramatically over the years; a study has shown that with appropriate medical care about 75% of children born with the most severe form of spina bifida will most likely live until their early adult years.…

    • 520 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    Cystic Fibrosis is a genetic disease that is passed down from both of the parents who have a copy of a defective in their DNA. There are variety of symptoms when it comes to cystic fibrosis such as: ‘Very salty-tasting skin, wheezing or shortness of breath, and male fertility ‘. There are no known cures for this genetic diseases, but there are treatments, and research that can help control this disease, and to possibly make a breakthrough discovery for a cure.…

    • 570 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Laura Hillenbrand is becoming a world sensation after writing her bestselling book, Unbroken. Sure she may seem like she is living the dream life with thousands of people buying her books every day, but what most people do not know about her is that she suffers from Chronic Fatigue Syndrome, a disease that drains all energy from the body and leaves it feeling lifeless and overly tired. The disease keeps her on bed rest for many of her days but she still finds time to write bestselling novels. She is resilient in that because even though she is living with Chronic Fatigue Syndrome, she does not let it stop her from living her life and doing what she loves. She developed the disease while on a road trip with her boyfriend and other friends. They were driving along a highway when a deer began to step into the road. The car barely missed the deer by a few inches. Later that night a meteor came streaking across the sky. She was the only one who saw it. She then became very nauseous. Her boyfriend thought she had food poisoning but he would later learn that she had developed CFS, or Chronic Fatigue Syndrome.…

    • 833 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Cystic fibrosis is a disease passed down through families, a genetic disorder, that causes thick, sticky mucus to build up in the lungs, digestive tract, and other areas of the body. Cystic fibrosis is where it affects the cells that produce mucus,sweat and digestive juices. These fluids are normally thin and slippery, but in Cystic fibrosis, a defective gene causes the fluids to become thick and sticky plugging up tubes, ducts and passageways in the human body especially in the lungs and pancreas. Its caused by a mutation in a gene that changes a protein that regulates the movement of salt in and out of cells. The affected gene, which is inherited by the child’s parent, is a recessive gene. The child has to inherit one copy of the gene from…

    • 359 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Cystic Fibrosis

    • 386 Words
    • 2 Pages

    Cystic Fibrosis (CF) is the most common life-threatening genetic disease and is a progressive, permanent disorder in which the glands making sweat, mucus and intestinal secretions don’t function correctly.…

    • 386 Words
    • 2 Pages
    Good Essays
  • Good Essays

    My Aunt Dori has always been different; however, I never truly realized how different until a few years ago. She has severe cerebral palsy. I have always known, nonetheless it did not fully sink-in until August 3, 2003. This particular day I had witnessed her having a grand-mal seizure. I remember being terribly afraid and confused. The scent of disinfectant filtered deliberately through the air. The aroma filling my nostrils gradually at first, then all at once. The hospital seemed empty, and hair-raisingly cold. Lots of concrete pillars, large windows, and white linens everywhere I looked. I was ten years old, and no one would reveal what was happening. I can remember my mother telling me with a worried smile, “Do not worry, sweetheart.…

    • 788 Words
    • 4 Pages
    Good Essays
  • Better Essays

    Cystic Fibrosis

    • 1221 Words
    • 5 Pages

    The Human Race, almost inherently, has developed quite the propensity for taking things for granted. Whether it be indoor plumbing, air conditioning, eating on a daily basis, or having clean socks to wear, you can bet we don’t appreciate it like we should. The majority of the population carries on their whole life like this; totally ignorant of how truly lucky they are. Then, there’s a small piece of the pie that is born, for lack of a better word, unlucky. Very, VERY unlucky. I just so happen to be closely related to one of these “unlucky” individuals. No, he’s not unlucky because he’s married to my sister (which I’m sure pains him on some occasion, anyway) but rather because he was born with Cystic Fibrosis, or CF, to those of us “in the know”……

    • 1221 Words
    • 5 Pages
    Better Essays
  • Good Essays

    Cystic fibrosis (CF) is the most common inherited disorder which results from mutation of cystic fibrosis transmembrane regulator (CFTR) gene. It occurs approximately in one of every 2500 live births in the white population(1) ; and characterized by abnormal thick viscous secretions in the respiratory, gastrointestinal and genitourinary tracts together with chronic suppurative endobronchial infection(2), resulting in death or lung transplantation in more than 500 patients every year in the United States(3). Incidence of CF is lower among African Americans (1in 15000)(4)and Asians (1in 32000)(5).…

    • 325 Words
    • 2 Pages
    Good Essays
  • Better Essays

    Survivor Siblings

    • 1483 Words
    • 6 Pages

    One of the most important hopes of any parent is to raise a happy and healthy child, and watch that child grow up and become an adult. What if one of those children had a disease that would one day claim his or her life? What if there was an option that could save your child’s life? To what lengths will parents go to save the life of a terminally ill child? A savior sibling is a child selected as a result of genetic screening to have some innate characteristics that will help save the life of an existing brother or sister (Saviour sibling). In 1990, Abe and Mary Ayala became the first successful publicized case in which a family sought to conceive a child (Marissa) to save another child (Anissa). Anissa was battling leukemia when her parents decided to conceive another child that was an exact bone marrow match. They gave birth to a healthy baby girl they named Marissa who at 14 months of age donated bone marrow that saved her sister’s life.…

    • 1483 Words
    • 6 Pages
    Better Essays
  • Good Essays

    Cystic Fibrosis, also called CF, is the most common life threatening disorder in the US. It is an inherited disease of the secretory glands (National Blood, Heart and Lung Institute, 2013). Affecting about 30,000 people, it is an autosomal recessive disorder due to mutations in the CF transmembrane conductance regulator (CFTR) gene (National Blood, Heart and Lung Institute, 2013). Usually diagnosed at a young age, CF causes the mucus, sweat and digestive fluids to become thick and sticky (Mayo Clinic) resulting in ducts, passageways, and tubes in the lungs and pancreas becoming plugged, causing respiratory, digestive and pancreatic problems. As of now, this disorder cannot be cured, but it can be treated. With the field…

    • 1090 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Cystic Fibrosis and Asthma

    • 1094 Words
    • 5 Pages

    There is an estimated 30,000 people in the United States that have Cystic Fibrosis (CF) and about 25 million who have asthma. CF is often confused with asthma because of their symptom similarities. CF, despite what people may think is far more severe than asthma. Most people think that CF would be easier to treat and cure because there are fewer people with it. Unfortunately, at this point there is no cure for CF. Cystic Fibrosis is far more severe than asthma because it is terminal, the treatment is vigorous, and it can cause many other life threatening issues.…

    • 1094 Words
    • 5 Pages
    Good Essays
  • Powerful Essays

    Orem's Theory

    • 7687 Words
    • 31 Pages

    EDIATRIC NURSES OFTEN observe an inconsistency in the performance of self-care in adolescents with cystic fibrosis (CF) and struggle to find ways to encourage them to engage in selfcare that is essential to their health and life. Owing to medical advances, children and youth with CF are now surviving many years longer as compared with the past. The current median life expectancy is 36.5 years (Cystic Fibrosis Foundation, 2005). In spite of impressive medical advances and increased survival rates, self-care remains to be a critical element for persons with CF. To survive and thrive, adolescents with CF not only require self-care supportive of general health and development but also self-care specific to the management…

    • 7687 Words
    • 31 Pages
    Powerful Essays
  • Good Essays

    Life’s journey can carry us on different roads and those roads can lead us to our destinies. My roads have sometimes been long and winding along the way to get to where I am today. There are more paths to travel to get to my future with each one having its own story. The road loved the best is that of being a mom to wonderful seven year old twin girls. On this particular path my heart has been softened and challenged as one of the girls was born deaf as well as blind. Taking the steps to get her what she has needed to grow successfully in life has taught lessons in faith, patience, persistence and courage. Having to be resourceful and making choices that would be best for my daughter has been tough but worth every minute. My heart longs to see the day she goes on to pursue many dreams in life along with my other daughter whom is also a great joy in my life. The desire is to portray to them…

    • 899 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Hehe

    • 955 Words
    • 4 Pages

    * Sister of Anna and Jesse. When Kate was 2, she was diagnosed with APL. She was cured but had another very serious relapse when she was 5. Her kidneys are failing and her parents wanted Anna to give her a kidney but Kate told her not to, as she wanted to die.…

    • 955 Words
    • 4 Pages
    Good Essays
  • Better Essays

    Comparative Literature

    • 2336 Words
    • 10 Pages

    Cystic Fibrosis (CF) according to Cohen 2004, is the most common fatal hereditary disease amongst children and adults. It is an autosomal recessive disorder, and most carriers of the gene are asymptomatic. The flawed gene that causes CF affects the glandular secretions by altering chloride transport across cell membranes. Thickening of bronchial secretions leads to infection and other respiratory disorders. Other mucus secreting glands, sweat glands, and glands of the pancreas are also involved, causing electrolyte imbalance and digestive disturbance.…

    • 2336 Words
    • 10 Pages
    Better Essays

Related Topics