Nt1310 Unit 5 Nursing Case Studies

In “Am I MS?” Miriamne Ara Krummel talks about her personal journey she endured dealing with multiple sclerosis. Krummel further explains at the end how she was finally able to accept her diagnosis and to embrace it. She finds that it’s important to be open about the disease. She believes that, “it might be helpful if more people would talk about death and dying as an intrinsic part of life” (76-77).When she was first diagnosed, she had a difficult time coping with MS. In fact, she at first denied that she could possibly have MS and like her family, were hoping that it was some kind of flu, until further testings’ at the hospital proved them wrong. However, through the process she learned that she felt better as she acknowledge the disease

Multiple Sclerosis is a real life disease, that effects real life people, so why is it not portrayed on television? Nancy Mairs life with Multiple Sclerosis was one thing she could not control. Showing people what living with MS can be like was something she might be able to change.

Through studying MS, researchers are finding ways to better protect our Myelin against attacks such as through a process called remyelination. Recent studies have led many scientists to believe that CD8+ T cells, whose job is to protect good cells and kill dangerous ones, play a role in the myelin damage. However, more research is needed to learn more about MS and what causes it. Not all studies agree that DD8+ cells cause the attacks, but instead some think that they tone down the attacks. Overall, there is many answers for scientists to find. Through learning how MS happens we may be able to learn how to stop it and return the freedom and health of those

Multiple Sclerosis is when the immune system attacks the nervous system. Higgins has multiple lesions on her brain and spine and she relapses and remits which means she gets sick and then better but she never restores complete function of her brain and body. To her children, MS means “Many Scars” because she has scars on her brain and spine. Harper and Hudson are too little to understand Multiple Sclerosis but they understand that sometimes Higgins is sick and in pain. Higgins was diagnosed with Multiple Sclerosis when she was in college around twenty two years old. She was suffering from loss of vision and horrible migraines. She had a vision test, an MRI, and then a spinal tap. The MRI showed four lesions on her brain and the spinal tap confirmed the diagnosis because her spinal serum tests differently than healthy humans. Every month Higgins has an injection of medicine that is meant to help slow down the progression of her MS. Higgins also takes steroids every time she relapses and gets sick. The steroids are meant to make her feel better and send her into remission. Every three months Higgins has checkups with her doctor in Emmetsburg, Dr. Spora. If Dr. Spora notices a new lesion on her brain or spine, she sends her to the specialist in Des Moines, Dr. Hughes. Multiple Sclerosis affects Higgins on a daily basis because sometimes she can not do the

Josepha is working on a medical surgical unit with three other RNs and one LPN. There is also a male and a female patient care tech. Josepha has been a nurse for four months, and after completing two months of orientation she takes a full assignment as a registered nurse. Josepha feels that the assignments she receives are not always fair, as she tends to get the most challenging clients. In addition, she is most frequently assigned any change of shift admissions. While she understands that she is part of a team, she often feels that the consistency of the inequity of these assignments is not fair. She is self-aware of how this is affecting her. As she starts her shift today she is again assigned to the

Kayla Montgomery is worth admiring because she is still chasing her dream while being diagnosed with Multiple Sclerosis. MS blocks nerve signals which causes her legs to go numb while running in the races. Kayla is one of the fastest long distance runners in the country and is a freshman on an athletic scholarships at Nashville’s Lipscomb University. With her condition, she has no feeling whatsoever while running when her body temperature gets higher and higher. People feel as if that isn 't fair- but when Kayla gets to the finish line, it then turns into a struggle. Her coach has caught her after every one of her meets, Kayla loses control and is unable to stop her legs until her body temperature lowers back to normal.

“Define success on your own terms, achieve it by your own rules, and build a life you’re proud to live,” quoted Anne Sweeney, formerly the co-chair of Disney Media, President of the Disney–ABC Television Group, and the President of Disney Channel. In this quote, Anne wanted everyone to know that everyone has their own definitions of success and have their own ways to get their. Two ways that people define success is being happy or satisfied with what they love doing and reaching their goals after obstacles. These two features can be seen in the books, The Outliers, The Last Lecture, Chicken Soup for the Teenage Soul and the article, Catching Kayla, by Digital Sports News.

Breaking down the disease “amyotrophic lateral sclerosis” word for word can help you understand how this disease affects someone. The word “Amyotrophic” comes from the Greek language. “A” means no, “myo” refers to the muscles, and “Trophic” means nourishment. This translates to “No muscle nourishment.” When a muscle has no nourishment it wastes away and cannot be used. The word “lateral” refers to the area where the nerve cells are in the spinal cord. As this area is affected by ALS it creates scarring or hardening which is that last part of the name “sclerosis” (What Is ALS?). The symptoms of ALS include the muscles to not operate correctly in the legs, arms, face, and tongue. Eventually, a person with ALS can lose the ability to breathe too, but recent technologies have made a tubing system to allow you to breathe. ALS is all physically affected, not logical thought. People with ALS still will have the ability to gain intelligence, touch, taste, smell, hear, see, and be able to function sexually (Harvard Med School Family Health Guide). Amyotrophic lateral sclerosis is also referred

It can occur to someone that has no history in their family. It is rare order that more than one person in the family is diagnosis with this syndrome. When paitents have a bacterial or viral infection may be more likely to develop GBS, however, only a very small percentage of people who have this infection are likely to develop Guillain-Barré syndrome. In order for the immune system to fight the infection, specialized immune cells have to produce proteins called antibodies, which are able to recognize specific proteins or molecules within the bacteria or virus. Some research shows that antibodies that recognize molecules on some pathogens may also recognize proteins on the body’s own nerves. As a result, the immune system attacks the nerves, causing inflammation and damaging the axons and myelin, which can lead to the signs and symptoms of Guillain-Barré

Multiple Sclerosis is primarily a T-cell mediated immune inflammatory disease that disrupts the regular functions of our central nervous system. Our central nervous system, the brain and the spine, are responsible for many of our voluntary and involuntary movements. However, in patients with Multiple Sclerosis, the immune system attacks the myelin sheaths that protect the nerves of the CNS. After repeated attacks, the myelin sheath will fall apart, and the immune cells will continue to attack the nerves themselves, which can be irreversibly damaged. Symptoms of Multiple Sclerosis include fatigue, numbness, weakness, vision problems, depression, and walking difficulties. In the United States, more than 350,000 patients

I. I spent the early half of my childhood like any other kid, outside playing, jumping in puddles, having an excess of energy that no one could contain. Then one day all of my energy was gone. I spent my afternoons and evenings napping from severe fatigue. My family thought nothing of it, until I started getting rashes all over my body. After a few blood tests, the doctors came back with an answer. As a child one may never expect to be diagnosed with an incurable auto immune disease, let alone one that affects your day to day functioning.

Amyotrophic lateral sclerosis is a degenerative neuromuscular disorder that affects the motor neurons of the spinal cord and brain. Due to degeneration or destruction of the motor neurons, muscles throughout the body begin to become weak and waste away to the point that an individual has no muscle movement. In most cases, due to having muscle strength, a patient with ALS will succumb to their disease because of respiratory failure or dehydration and malnutrition. It is a progressive disease with a prognosis of 3 to 5 years after initial diagnosis. There is no cure for the disease as of now. This paper will discuss a more in depth look into the symptoms, diagnosis process, treatment options, medications, prognosis, and ongoing research.

Hyperacusis is found to be associated with both peripheral and central factors. Hyperacusis is often accompanied by a cochlear hearing loss, and this usually involves damage to cochlear hair cells and subsequent auditory nerve degeneration. However, annoyance, fear, and pain hyperacusis must involve central mechanisms.

DOI: 07/17/2013. This is a 25-year-old female cashier who incurred injury to her low back when she missed a step and fell off a ladder while stocking sleeping bags. MRI of the lumbar spine dated 10/03/2013 revealed broad based central disc protrusion at L4-L5; moderate discogenic edema along endplates at L4-5; and broad bulge with a central annual tear at L5-S1. CT scan of the lumbar spine dated 01/08/2014 revealed that at L3, bilateral pars interarticularis defects are seen with sclerotic margins. The vertebrae at L3-4 are normal in present on the prior MRI. The vertebrae at L3-4 are normal in alignment. At L4-3, there is 2 mm of anterolisthesis. Bilateral L4 pars interarticularis defects are seen with sclerotic margins. Office notes dated 06/28/2016

Clinical depression is a complex condition and symptoms can vary greatly from patient to patient. To complicate matters even more, it can be difficult to imagine what depression is like if you have never experienced it firsthand. Despite these issues, there are a few hallmarks and common symptoms of depression that can help you identify a possible case in yourself, a friend or family member.