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Crohn's disease conclusion
Crohn's disease conclusion
Crohn's disease conclusion
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For almost two years I have been fighting illness. my senior year I found out I have Crohn's disease, a lethal, incurable condition that causes inflammation of the digestive tract. This disease has kept me hospitalized on and off since August last year. At one point the doctors were deliberating different ways of treatment, including surgery and heavy doses of medication, due to me showing no signs of improvement under my current course of treatment. During testing to see if I could try a type of medication that would interrupt the nerve signals from my stomach so I would no longer suffer from extreme pain the doctors found a new issue. This medication tends to make any pre-existing heart conditions worse so we just wanted to cover our bases
Working as an oncology nurse has been a life changing experience. I have grown not only as a nurse, but also as a person. My eyes have been opened to the value of life, and not just life itself, but the precious thing that is a healthy life. I cannot count the number of patients from the beginning of my nursing career until now that have told me, “Well, I just didn’t think my symptoms were a big deal” or “The doctor told me I needed additional tests but it didn’t seem important at the time and I didn’t have any money”. The lack of patient education and provider follow-up in situations such as these is disheartening to observe. Experiences I have had with patients combined with their life stories have fueled my desire to become a family nurse
Amy Widener is a real estate agent, mother of two, and a sepsis survivor. In 2013 Amy was in the best shape of her life. She had just finished a Disney half marathon and was reaping the benefits of her intense training, little did she know that that training was going to save her life. One night she woke up with extreme abdominal pain and was rushed to the emergency room where she learned that she had a kink in her intestines. They performed emergency surgery and released her after a little bit of recovery. Instead of Amy’s pain getting better with recovery after her surgery, it got worse. This resulted in subsequent trips to the E.R. only to be sent home with more and more antibiotics. Two months after her surgery she went into the emergency
Being diagnosed with a chronic illness is a life-altering event. During this time, life is not only difficult for the patient, but also for their loved ones. Families must learn to cope together and to work out the best options for the patient and the rest of the family. Although it may not be fair at times, things may need to be centered on or around the patient no matter what the circumstance. (Abbott, 2003) Sacrifices may have to be made during difficult times. Many factors are involved when dealing with chronic illnesses. Coping with chronic illnesses alter many different emotions for the patients and the loved ones. Many changes occur that are very different and difficult to get used to. (Abbott, 2003) It is not easy for someone to sympathize with you when they haven’t been in the situation themselves. No matter how many books they read or people they talk to, they cannot come close to understanding.
When someone first finds out they have Crohn’s disease, they will probably feel overwhelmed. There are so many questions. Will I be able to work, travel and exercise? Should I be on a special diet? Could my medications have side effects? How will Crohn’s disease change my life? The better informed they can become, the more equipped they will be to be an active member in your healthcare (Crohn’s & Colitis Foundation of America, 2009).
For my Brown Bag Assignment my participant, JR, was found within my family. I was aware JR took daily medications due to his recent heart bypass surgery in June 2015 and met with him. JR is 62 years old and takes seven medication daily. My participant, JR had heart bypass surgery, exactly 4 bypasses, on June 1, 2015, due to 90% of his coronary arteries being blocked. For about two weeks prior to the surgery, he could not walk, felt very dizzy, fatigue, and weak. His legs even gave out and he fainted. He then decided to go to the doctors, got lab work done and found out about his coronary arteries were blocked. If he did not have this surgery, he would have died. This eight-hour surgery was a huge reality check for him. After this surgery, he completely changed his lifestyle by not smoking, not drinking, eating healthy and going on walks. Prior to this surgery, JR had and still has type 2 diabetes, high blood pressure, and high cholesterol for about five years now. As I was talking to him, it was clear that he knew all his medication very adequately especially when to take it, why he takes it and how to take it. He is also fully aware of healthy lifestyle choices. As we were talking I gave some advice to help continue his healthy lifestyle.
Celiac Disease is an inflammatory disease that destroys the lining of the small intestines and prevents the absorption of nutrients and vitamins into the system. The patients' health suffers; their digestive system is unable to process gluten foods that contain wheat, barley, and oats. The cause of this disease is unknown; however, environmental factors and a genetic predisposition are suspected.
Baumgart, Daniel C. , and William J. Sandborn. "Crohn's Disease." The Lancet Volume 380: 1590-1605. Web. 12 May 2014.
It has been 9 months since my diagnosis, and I am still learning coping mechanisms and pain management. Not everything is 100% though. In a perfect world it would be, but also in a perfect world there would be no disease or sickness. I can only hope for the best and continue living life as I have been for the last 28 years. There may be many changes in my life, some are worse than others, and instead of viewing them as disadvantages I will see them as a metamorphosis. At the end of this journey, I will emerge a stronger person who can withstand fire and brimstone, so to speak. For now I will continue to smile and walk through live with my head held high, even though my body is a battlefield filled with constant aches and pains.
I chose to discuss a chronic illness that has actually affected my family, rather than an illness that could affect a patient of mine. My mother-in-law has been diagnosed with cancer multiple times. The first time, was when my husband was 16 years old. She was diagnosed with a rare liver cancer. She was put on a waiting list
Ulcerative Colitis is a chronic inflammatory bowel disease (IBD) of the large intestine (colon). Ulcerative colitis only affects the colon, it causes the colon to become inflamed and develop ulcers along the lining of the large intestine. Patients can develop colorectal cancer (bowel cancer) from having extensive ulcerative colitis. Cells and proteins in a healthy immune system protect people from the infection. Patients suffering from ulcerative colitis dysplasia have an abnormal immune system. The body may mistake food or other materials as invading/foreign substances and will send in white blood cells into the lining of the intestines (colon). Ulcerations along with chronic inflammation are serious symptoms
Crohn’s disease – is the chronic inflammatory disease of the gastrointestinal tract. In 1932, gastroenterologist Burrill Bernard Crohn described the granulomatous inflammation of the ileum, which was called terminal ileitis. Later on, it was discovered that terminal ileitis is only one of the forms of the Crohn’s disease. The nature of the Crohn’s disease is still unclear. It is an autoimmune disease: the body suddenly begins to produce antibodies to its own cells. According to Lashner, “The annual incidence of Crohn’s disease ranges from 1 to 10 cases per 100,000 people annually depending on
1. Outline the causes, incidence and risk factors of the identified disease and how it can impact on the patient and family (450 words)
When I was 17, I entered into a local basic emergency medical technician class and fell in love with working in emergency medical services. I spent 5 very fulfilling years working and also volunteering as an EMT and went on to graduate from the paramedic program at St. Mary Medical Center in Hobart, Indiana. Prior to the class, I had fallen ill and worked with several doctors in an effort to find a diagnosis for a condition that was affecting my hands and feet. The effects at the time were minimal, but were exacerbated by the many hours required working on ambulances and in the hospital to complete paramedic clinicals. Immediately following graduation from the paramedic program, I became wheelchair bound. For about a year while in the wheelchair, doctors continued to work toward a diagnosis while my condition worsened. Eventually, doctors started to prepare me for the possibility of losing both of my legs. I spent a lot of time researching my symptoms before finally finding my own diagnosis. My legs were saved and I am happily back on my feet; however, I can no longer work on ambulances due to a poor immune system and there will always be the possibility that I could become
Right there and then I felt what it was like to have state anxiety. The fear of not performing again was petrifying. So needing more answers I took my news and went to doctor who had more knowledge about my situation. Reaching out to DuPont hoping to get clarity, they just agreed with my last doctor and on top of it they wanted to mediate me. With this medication it would thin my blood and I would have greater chances of passing out. I couldn’t agree with them, I begged my mom to take me somewhere else. I couldn’t handle the stress of the medication on my body. Then later that month we took the news from DuPont and ended up at Johns Hopkins. They specialized with kids who had heart problems and analyzed the diagnosis with a different approach. They thought it was rare that at such a young age I would be experiencing this dramatic of a heart defect. From there they started doing genetic testing to see if they could pin point anything that could cause this defect. After 6 months of research and genetic testing I got a call back from my doctor to come in and discuss their findings. I was diagnosed with Marfans Syndrome
Currently, my health and wellness are both a big question mark. Last fall, I was diagnosed with multiple medical issues and have had traumatic events that have affected my physical and mental health. My IBS causes sometimes constant or sudden pain throughout my abdomen that has kept me awake at night on many occasions; my plantar fasciitis causes pain in my feet and knees that can even keep me from walking.