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Fibromyalgia research essays
Fibromyalgia research essays
Fibromyalgia research essays
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Fibromyalgia (FM) affects approximately 2-6 percent of the population. FM can affect anyone of any age, but it is more common in women over 50 years old. It’s a very complex disease and the cause is unknown. People who suffer from FM report symptoms which include pain, fatigue, and trouble sleeping and morning stiffness. These symptoms can interfere with a person’s daily life and can ultimately lead to physical disability which could possibly result in depression. The management of FM does not cure the disease and some may not be suitable for all patients so many patients decide to self-manage. Some FM patients use pharmacologic and non-pharmacologic methods to help reduce symptoms, but the most used strategies out of 31 were resting, distraction, …show more content…
heat, nutritional supplements and medication. Non-pharmacological methods may ease the symptoms in chronic FM which may result in control over the disease. Medications are also prescribed for symptoms such as pain, sleep and depression. Studies have shown that adults over the age of 50 that suffer from FM, on average took 5-7 medications with almost half taking analgesic, antidepressant or antianxiety medication. However, the number of medications has fallen in the past year. Hallberg and Carlsson categorized symptom management strategies during a study of Swedish women with FM. The five themes are: self-initiated activities, professional treatments, escape behaviors, resignation and passivity. Self-initiated strategy included exercising, prayer, planning and distraction. Professional treatment included a psychotherapy, acupuncture, and physiotherapy and ultrasound therapy. Escape behaviors were things such as alcohol, pain medications and avoiding interactions. Reflecting hopelessness and lack of control was resignation and passivity simply included self-care strategies. Studies were conducted to determine if a person with and without FM showed differences in their abilities.
Participants had to meet certain criteria. They set up an interview day with the first hour being the section of the workshop that contained personal results such as scores on lower body strength and problem solving. Next they attended three 30-minute sessions that gave them information on topics such as nutrition and stress management. There were a group of participants that participated in the actual interview. They were taken to a private room where they sat at a table. Questions were asked and the person being interviewed would respond with an answer. The interview started with questions such as how life was living with FM and then questions became more detailed such as how to maintain …show more content…
symptoms. All together eight women participated in the study, one Hispanic and the rest Caucasian. The mean of the ages was 61 and all attended some type of school. All participants had been diagnosed with FM for six+ years. Two women claimed to have a fair/poor health status, which the rest reported good/very good health status. The women talked of their FM and symptoms, but strategies to manage life were also discussed. They claimed that over a period of time, they have developed things that help them live a “normal” life. The strategies included pacing/planning, focusing on the mind-body-spirit/distraction, avoiding pain attributable to extreme sensitivity, social support, pushing themselves/putting on the mask, and medications as background. Pacing/Planning included planning ahead, balancing activities and allowing others to help them with tasks. Changes in their environment had to be made and the way they do things. Avoid cold water and cold weather, using a shower chair, frequent use of a heating pad. Most women claimed that taking a warm bath or hot shower helped them along with continuously moving. Focusing on the mind-body-spirit/distraction included things such as meditation and listening to music. One woman claimed that breathing techniques helps her manage FM. Doing things to keep the mind occupied provides temporary relief. Avoiding pain attributable to extreme sensitivity to touch pretty much means that it hurts for someone to touch you. Avoiding peoples’ touch will help decrease the pain. Of course social support is a big deal. The women claimed that getting together with others that suffer from FM is extremely helpful because they are the only ones that truly understand. Women also reported that a person that suffers from FM has to push their self to accomplish daily things. And medications were also reported as a strategy to maintain symptoms. One woman said that she didn’t think she would be able to survive without her medication. The studies did show that strategies for coping with FM can be developed. I feel like this article is very informative.
Fibromyalgia runs in my family and growing up my little cousin would always cry and would not play with me and I never really understood why. I picked this disease because it runs in the family and I don’t know when I’ll run into it again. I learned ways that could possibly help with the symptoms which I will share with my family. The studies they conducted on the woman were a wonderful thing. It taught me a lot and now I understand a little better the things that have went on with my
cousin.
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.
Fibromyalgia seems to affect mostly women, although men and children can also get it. It is estimated by the that about three to six percent of the U.S. population has fibromyalgia.(Source 4) Yet another source states that it is three to six million people in the U.S. or as many as one in fifty Americans. (Source 1) All of these sources agree that women make up to eighty or ninety percent of fibromyalgic patients.
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...
Fibromyalgia is most common among women aged 20 to 50, child-bearing age. The goal of the treatment of fibromyalgia is to relieve pain and other symptoms, and to try and help the patient cope with these symptoms. The first type of treatments offered may involve ; some physical therapy, an exercise and fitness program, and trying stress-relief methods, like light massages or/and relaxation techniques. If these treatments don't work, you could ask your doctor to take the next step of treatment which would be to prescribe an antidepressant or muscle relaxant. These prescriptions aim to improve sleep and pain tolerance.
Fibromyalgia, also known as fibromyalgia syndrome and fibromyositis, is a chronic pain disorder that affects people physically, socially, and mentally. It can affect any area of the body and affects multiple areas. This disorder is most common in women, but it can also affect men and children of all ethnic groups. Most people are diagnosed between the ages of twenty and fifty. People who have Rheumatoid Arthritis, Lupus, or Spinal Arthritis have an increased risk of developing Fibromyalgia. This disorder cannot be transmitted from person to person.
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).
2. When you ask someone to participate, explain the basic nature of the study. You
Any learning that occurs should focus on treatments, tests, and minimizing pain and discomfort as they improve they can shift their focus of learning (Kitchie, 2014, p.127). I will continue to provide a meeting location that is both comfortable and private. In the emotional aspect of M.M. and her family I will try to identify moments when members feel emotionally supported as it sets the stage for a teachable moment (Miller & Nigolian, 2011, p.56). I will also discuss with each member their previous coping strategies that used that have been successful and to encourage them to find a way to build on and strengthen these qualities. Using teaching methods that are interactive and allow patients equal contributions and participation can help promote health compliance (Habel, 2005,
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
Myofascial Release (MFR) is defined as a hands-on soft tissue stretching technique that involves manipulating the muscles and the fascial covering.1 MFR is performed by a trained professional who applies a gentle yet progressive stretch where-by the amount of time for which the technique is applied, the direction in which the stretch is applied, and the force with which it is applied are all dependent upon the patient’s physical response to the treatment.2,3 Ultimately, it is what the therapist feels, the end-feel, that guides the treatment through a series of stretches and manipulations attempting to reach maximum relaxation of tight tissues.2 Due to muscles and fascia being interconnected throughout the entire body, MFR is thought to be a whole body treatment.2 This theory explains why, often times, a therapist might treat an unaffected area and provide relief in the area of the patient’s complaint.2 Furthermore, this also explains why a treatment session to one area may cause symptoms to surface in an unrelated area.2 For these reasons, it is very important for therapists to set appropriate expectations regarding the treatment and the effects thereof.2
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
Due to time restrictions, panel members were normally unable to meet in advance, so they build up their own self-sufficient interview questions. Although the principal chaired the interviews, they were rarely conceded out in an identical manner and there was no high level of uniformity with the questions. No official scoring system was used...
Life story interview/ project was design for you to get to know a random stranger or a close friends. You would asked general questions about the person life, school, work and family, therefore many will open up to you but a lot of people would not. Before you did the interview you had taken a NIH certification make sure you understand how to do the interview. You had recorded it, transmitted it, coded it and then present it to the class. Once everything was done you learned something new about this person or you may look at their cultural a different way.
The module composed of seven classical themes, consisting of topics such as Gibbs cycle, language for debates, changing NHS culture, mind maps, leadership for academic skills, communicating in difficult situations, health education, presentation skills, etc. A presenter’s appearance
Introduce yourself and the objectives of today’s workshop. Acknowledge that you appreciate participants giving up their personal time to be here. Ask each person to stand, state her name, what position she advises, and the name of her favorite superhero. Each person in this room has different experiences and comes from a different place. We are all different and unique.