Wait a second!
More handpicked essays just for you.
More handpicked essays just for you.
Student essays on fibromyalgia
Fibromyalgia research paper essay
Fibromyalgia research essays
Don’t take our word for it - see why 10 million students trust us with their essay needs.
Recommended: Student essays on fibromyalgia
The treatment of Fibromyalgia should be viewed as a “team approach”. Most chronic pain does not respond to drugs and may require an aggressive use of nonpharmacological therapies or “the rehab approach”. This includes a lifestyle change, physically, mentally, and emotionally. This approach should include use of a physician, occupational therapist, physical therapist, massage therapist, chiropractor, an acupuncturist and any specialists, such as a Rheumatologist. Mondell, D. L., & Wright, P. (2005).
Psychological counseling is recommended early after receiving the diagnosis of Fibromyalgia. Mainly because it takes many years of visiting doctors and having tests results come back negative that an individual will begin to think this is “all in their head”. Then when finally a diagnosis is given like Fibromyalgia and they are told that “the cause is unknown, the treatment is unknown and there is no cure” can be hard to accept. It is recommended that the patient’s loved ones attend sessions, because they, too, will find it hard to understand the diagnosis, its effect on the patient and the recommended treatments for this syndrome. Depression is commonly associated with a patient diagnosed with Fibromyalgia. The patient has to learn that they can no longer be the “SuperMom” and may have to relinquish some of her chores to an assistant. This can lead to low self esteem, feelings of inadequacy on their role in the family unit. Talking to a professional about these feelings, reevaluating their position in life and understanding that following a good balanced diet, getting restorative sleep, and participating in a reasonable exercise program and maintaining a good outlook on life this patient can still be a successful, productive, a...
... middle of paper ...
...algia & Chronic Myofascial Pain Syndrome, A Survival Manual. Oakland, CA:New Harbinger Publications, Inc.
Guide to Fibromyalgia, www.JohnsHopkinsHealthAlerts.com , 2009
Clauw, D.J., & Wallace, D.J.(2009). Fibromyalgia, The Essential Clinician’s Guide. New York : Oxford University Press
Format: Electronic Book ; Electronic Resource
Parker, J.N., Parker, P.M., (2002). The 2002 Official Patient’s Sourcebook on Fibromyalgia. San Diego: Icon Group International, Inc. Format: Electronic Book ; Electronic Resource
Wallace,D. J. & Wallace, J.B. ,(2002). All about fibromyalgia. New York: Oxford University Press Format: Electronic Book ; Electronic Resource
Mondell, D. L., & Wright, P. (2005). Living with fibromyalgia: 4 steps to manage pain and lead a fulfilling life. New York: McGraw-Hill Format: Electronic Book ; Electronic Resource
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.
The purpose of this paper is to discuss an invisible disease call Reflex Sympathetic Dystrophy and how it impacts an individual’s life. The framework that will be utilized is the strength and empowerment perspective to show some coping mechanism to assist individual’s adjusting to the impact this disease has on their life and how to improve their everyday experience when dealing with the symptoms of this disease. This paper will also discuss four policy recommendations that could be used to improve a patients overall heath and tools to manage this life altering experience.
A long term condition not only brings the physical symptom of pain, but a number of psychological and social effects too. In 2014 the Department of Health recognised that the impact of having a long term condition can contribute to mental health problems like depression and anxiety (Department of Health, 2014). As well as finding ways to manage their physical symptoms, patients are encouraged to adopt acknowledge and address all of their health and wellbeing needs, in particular self-management at home and incorporating and educating the patient’s family and close friends as a support system (Kraaimaat and Evers, 2003). The suffering that a person with chronic pain endures not only impacts on their life, but also affects their family, time lost from employment and uses up precious healthcare resources.
Have you ever wondered why when you stub your toe on the chair in the living room, it helps tremendously to yell out an expletive or two and vigorously rub the area? I may not be able to discuss the basis for such language in this paper, but we will explore the analgesic response to rubbing that toe, in addition to the mechanism of pain and alternative treatments such as acupuncture and transcutaneous electrical nerve stimulation.
Try to build a healthy regular yoga practice, and attend the appropriate class for the symptoms you are feeling each day.
Fibromyalgia Syndrome (FMS) is a musculoskeletal illness (which causes chronic pain) and a chronic fatigue disorder. It can also change sleep patterns and cause the following: digestive disorders, chronic headaches, painful menstrual periods, temperature sensitivity, morning stiffness, numbness or tingling of extremities, and even cognitive memory problems. The name fibromyalgia comes from "fibro" in Latin meaning tissue, "my" in Greek meaning muscle, and "algia" (also Greek) meaning pain.(source 5)
Although there is no known cure for this condition despite the advent of science and technology, the good thing is that there are numerous options to offer relief for fibromyalgia patients. You must have heard about being dependent to certain types of medicines or those people who no longer respond to low dose analgesia. In this case, most patients look for natural remedies to avoid complications later on. Even top-notch medical specialists believe that the treatment and management for fibromyalgia should be a balanced and holistic approach that comes with complementary medicine, appropriate exercise and therapy.
The Diagnostic and Statistical Manuel of Mental Disorders, Fifth Edition (DSM-V), describes somatoform disorders as a group of related mental health symptoms that are characterized by a patient’s presentation of multiple, current somatic symptoms that are distressing or result in significant impairment of daily functioning. A somatic symptom is the presentation of physical illness or distress that would appear to have a medical basis but which cannot be explained by either a general medical condition, direct effect of a substance, or any other mental health disorder. Patients who suffer from somatoform disorders firmly believe that the pain they are experiencing stems from a physical problem rather than a mental one; indeed, that is a fundamental aspect of the disorder. Somatoform disorders range from a simple and persistent pain disorder to hypochondriasis, which involves persistent anxiety over the existence of a serious illness, to conversion disorder, which involves the actual loss of a bodily function from excessive anxiety over the perceived ailment. (DSM-V, 2013)
Fibromyalgia is not a new disease that has just surfaced, it has been around for a long time, it just didn’t have a name and was not recognized for what it truly was. It was...
The cause of Fibromyalgia is still unknown, but researchers believe it is linked to a disorder of central processing neurotransmitters. They believe the pain is caused by the amplification of abnormal sensory processing in the nervous system. Some studies suggest that genes are involved, but ...
Fibromyalgia is an extremely disabling condition associated with chronic widespread musculoskeletal pain and reduced pain thresholds (Wolfe et al., 2010)(Kelley et al., 2011). Observational studies have shown that over a 12 month period 25% of men and women surveyed over the age of 65 will consult a primary care physician for musculoskeletal pain (Jordan et al., 2010). Overall, between 46% and 80% of people over the age of 65 report experiencing pain on a daily basis and 15% of women and 10% of men over 50 report widespread musculoskeletal pain (Soldato et al., 2007; Thomas et al., 2004). The Centers for Disease Control and Prevention estimated in xxxx that fibromyalgia patients generated $6000 per patient per year in healthcare costs where as another recent study of administrative claims found that fibromyalgia healthcare costs may exceed $18,000 per patient annually (Wolfe et al., 1997). In a population study of ten chronic diseases, fibromyalgia was highest ranked for healthcare not received in the previous year and in long-term disability, pain, and poor self-rated health by survey participants (Kasman and Badley, 2004).
The development of Fibromyalgia and depression in one’s life is dependent on many factors. Firstly, depression can result from issues such as reacting to loss, struggles of life or personal issues related to self-esteem. Fibromyalgia can also result from similar issues as well. However, statistics show that this disorder is common in women than in men (Schmidt et al, 2010). This disorder has been linked to
It is also common that many people who have long-term health conditions can also be susceptible to depression and stress when attempting to deal with the aspects of their illness, such as being reliant on insulin injections or having to take care about what they eat and drink. As explained in an article by W.H Polonsky. (K101, Resources 3, pg19 )
After meeting with our patient twice, I believe we have set into place a relationship where the patient is very open to us about her health. This is helpful for my partner and I as an open and honest patient is beneficial as we assist them in their health. Goals for next semester include reducing our patient’s blood sugar as well as reducing our patient’s fibromyalgia pain. Our patient has expressed to us that her glucose is high but she is ok with the high number as long as she is feeling relatively healthy. We hope to give practical ways to reduce blood sugar throughout next semester so hopefully we can reduce that number by semester’s end. Our patient is going to see her physician soon, so we hope to get an update on the patient’s fibromyalgia
The symptoms of somatic symptom disorder can often be hard to notice because it is psychological and many times the pain they express may seem legit. Many people with the somatization pattern of the somatic symptom disorder will experience many long-lasting physical ailments, and these ailments typically have little to no physical basis (Comer, 2014). These people will usually go from doctor to doctor, hospital to hospital just to find some relief or even answers...