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Conclusion on muscular dystrophy
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Conclusion on muscular dystrophy
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According to the MediLexicon Medical Dictionary, muscular dystrophy is defined as a general term for a number of hereditary, progressive degenerative disorders affecting skeletal muscles, and often other organ systems (Staff). Basically what that means is that muscular dystrophy is a genetic disorder that is passed down that affects the skeletal muscles and other organs by slowly breaking them down. Since it is genetic, it is not contagious and you cannot catch it from someone who has it. MD weakens muscles over time, so children, teens, and adults who have the disease can gradually lose the ability to do the things most people take for granted, like walking or sitting up. Someone with MD might start having muscle problems as a baby or their symptoms might start later. Some people even develop MD as adults (Clark, 2010). There are several types of MD, most of them affecting mostly teens including Duchenne muscular dystrophy, becker muscular dystrophy, emery-dreifuss muscular dystrophy, limb-girdle muscular dystrophy, facioscapulohumeral muscular dystrophy, myotonic muscular dystrophy, and congenital muscular dystrophy. Duchenne muscular dystrophy (DMD) is the most common type. This is caused by a problem with the gene that makes a protein called dystrophin. This protein helps muscle cells keep their shape and strength (Clark, 2010). If this protein does not form properly the person gradually becomes weaker due to their muscles breaking down. This is a disease that only affects boys and symptoms are usually noticeable between the ages of two and six years old. It is a very rapid progressing disease. Children with this disease are often bound to a wheelchair around the age of twelve. Children may also need to see a lung and heart sp... ... middle of paper ... ...all the time. Even public transportation can be difficult and maneuvering around public places that may not designed to best accommodate handicapped people. I think people can live independently for the most part with MD but they are going to need more help than normal from friends and family to accomplish some of the smaller tasks and some of the larger tasks. Works Cited Staff, M. C. (n.d.). Muscular dystrophy. Retrieved from http://www.medilexicon.com/medicaldictionary.php?t=27542 Clark, A. (2010, July). Muscular dystrophy. Retrieved from http://kidshealth.org/teen/diseases_conditions/bones/muscular_dystrophy.html Benaroch, R. (2013, 03 30). Understanding muscular dystrophy-- the basics. Retrieved from http://www.webmd.com/children/understanding-muscular-dystrophy-basics Occupational therapy guidelines. (n.d.). Retrieved from http://www.myotonic.org/node/193
DMD also known as muscular dystrophy is muscular disease that occurs on young boys around age four to six. Muscular dystrophy is genetically transmitted disease carried from parent to offspring. This disease progressively damages or disturbs skeletal and cardiac muscle functions starting on the lower limbs. Obviously by damaging the muscle, the lower limbs and other muscles affected become very weak. This is ultimately caused by the lack dystrophin, a protein the body produces.
It is hard to live with disability, because everyday things become a challenge. U.S. Census Bureau report from 2008 states that 3.3 million non-institutionalized Americans over age 15 years use wheelchairs. The reason why there are so many people with disabilities is that U.S. spent decades at war. This is why mobility industry is rethinking the products it provides to support a growing demographic. Vantage Mobility International (VMI) and Braun Ability are two leading industry players that spent decades converting wheelchair vans from companies such as Chrysler , Toyota , and Honda into wheelchair-accessible modes of transportation.
Duchenne Muscular Dystrophy, also known as DMD, is the most common form of muscular dystrophy. Muscular dystrophy is a condition that is inherited, and it is when muscles slowly become more and more weak and wasted. Duchenne muscular dystrophy is a form of muscular dystrophy that is very rapid and is most commonly found in boys. In muscle, there is a protein named dystrophin. Dystrophin is encoded by the DMD gene. When boys have Duchenne muscular dystrophy, they do not produce enough dystrophin in their muscles. This causes weakness in their muscles. Parents can tell if their child has duchenne muscular dystrophy by looking for various symptoms.
In Jessica Shea’s article “The Invisible Crutch”, a few items that she listed are taken for granted by nondisabled people but could apply to Sharon and Karen. “9. If I ask to speak to someone ‘in charge’, I can be relatively assured that the person will make eye contact with me and not treat me like I am stupid’ (Shea, p. 40) is the first example. While the last part does not always apply to nondisabled people, it certainly applies to the disabled. In the account of Sharon, she was talked to like she was stupid by medical staff and her own family. This is a very common thing the disabled have to deal with. My grandfather deals with this on a daily basis and he works in the IT department at Colorado State University. The next example is, “19. My daily routine does not have to be carefully planned to accommodate medication or therapy schedules” (Shea, p. 40). Nondisabled individuals can plan their day however they see fit according to work, prior engagements, or hobbies. For disabled people—maybe even Sharon—therapy and medications are a normal part of their day. Going without them means being in high amounts of pain, falling behind on progress made in therapy, or risking their health in general. There is a lot that the nondisabled take for granted whether it is realized or
What comes into one’s mind when they are asked to consider physical disabilities? Pity and embarrassment, or hope and encouragement? Perhaps a mix between the two contrasting emotions? The average, able-bodied person must have a different perspective than a handicapped person, on the quality of life of a physically disabled person. Nancy Mairs, Andre Dubus, and Harriet McBryde Johnson are three authors who shared their experiences as physically handicapped adults. Although the three authors wrote different pieces, all three essays demonstrate the frustrations, struggles, contemplations, and triumphs from a disabled person’s point of view and are aimed at a reader with no physical disability.
Physiological Basis of disease: DMD is the commonest and most serious form of the dystrophies. The gene responsible for dystrophin which, when absent, causes DMD. Amount of dystrophin correlates with the severity of the disease (i.e., the less dystrophin present, the more severe the phenotype). Since the gene is on the X chromosome, it primarily affects males, and females who are carriers have milder symptoms ( www.nlm.nih.gov/medlineplus/ency/article/000705.htm).
THE ROLE OF OCCUPATIONAL THERAPY IMPROVING INDEPENDENCE FOR ADULTS WITH A LEARNING DISABILITY IN THEIR LOCALITY
A severely disabled person may have to deal with much pain in their lives, but
Lou Gehrig's disease is often referred to as Amyotrophic lateral sclerosis (ALS), this is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons come from the brain to the spinal cord and from the spinal cord to the muscles throughout the entire body. The progressive degeneration of the motor neurons in ALS would eventually leads to their death. When the motor neurons die, the ability of the brain to initiate and control muscle movement is also lost. With voluntary muscle action progressively affected, for this reason patients in the later stages of the disease may become totally paralyzed (Choi, 1988).
Emery-Dreifuss muscular dystrophy is a rare form of muscular dystrophy characterized by early onset contractures of the elbows, achilles tendons and post-cervical muscles with progressive muscle wasting and weakness It is also associated with heart complications like cardiomyopathy and arrhythmia which in both cases can lead to death. Cardiomyopathy is a heart disease which affects the muscles of the heart. In cardiomyopathy is muscles get rigid, enlarged or thick. They also sometimes changed by scar tissues. On the other hand arrhythmia is a disorder with the rhythm or rate of heartbeat. The heart can beat fast, which is called tachycardia or it could be beating too slow, which is called bradycardia. Emery-Dreifuss muscular dystrophy is characterized by early onset of contractures and humeroperoneal distribution. Humeroperoneal refers to effects on the humerus and fibula. The genes known to be responsible for EDMD encode proteins associated with the nuclear envelope: the emerin and the lamins A and C.
Some range from neuromuscular disorders to myopathies. Polymyositis is an example of a group of diseases that involves inflammation of the muscles or associated tissue, such as blood vessels that supply the muscle. Another type of disorder is muscular dystrophy which affect the muscle fibers. There are even metabolic muscle disorder that interfere with the chemical reactions involved in drawing energy from food. Whereas, neuromuscular junction disorders impaired transmission of the nerve signals to the muscles. Some disorders affect the nerve cells that supply the muscles. This disorder is known as a motor neuron disorder, commonly known as amyotrophic lateral sclerosis
People who suffer from Dementia lose their ability to do a daily task. They are unable to do shopping, prepare meals, deal with bills and money. They can forget to lock the door, turn off the cooker or water. They may have difficulties with their mobility and coordination. Person who has a disability experiences this same problem.
The first historical account of muscular dystrophy was identified by Sir Charles Bell in 1830. He wrote about a disease that caused weakness in boys that progressively got worse. In 1836 another scientist whose name is unknown reported about two brothers who developed muscle damage, generalized weakness. Also damaged muscle was replaced with fat and connective tissue. At the time the symptoms were thought to point to tuberculosis. During the 1850s reports of boys with progressive muscle weakness became more and more common. There were also reports of these boys losing the ability to walk and dying at an early age. In the next decade French neurologist Guillaume Duchenne gave and in depth account of 13 boys who had the most common ...
 Mild, chronic depression has probably existed as long as the human condition, although it has been referred to by various different names. The DSM-III replaced the term “neurotic depression” with dysthymic disorder--which literally means ‘ill-humored’-and it was added to the Diagnostic and Statistical Manual of Mental Disorders, 1980
As a young child, I remember how my grandfather's disability affected my life. I don't think that I even knew what the purpose of his wheelchair was. To me, it was just a toy, just another toy that my cousins and I could play with.