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Huntington's Disease Huntington s disease is a genetic disorder (inherited due to a faulty gene) which diet suffers through difficulty in eating and decreased appetite, http://www2.netdoctor.co.uk/diseases/facts/huntingtons.htm
Extractions: The UK's leading independent health website Search NetDoctor NetDoctor.co.uk Home News and features News Newsletter Features Encyclopaedia Diseases Examinations Medicines Premium services SMS services StayQuit thediet Health centres ADHD Allergy and asthma Children's health Depression ... All health centres Discussion and support Discussion forums Support groups Services Ask the doctor Find a hospital Search Medline Test yourself Information About NetDoctor Commercial opportunities NetDoctor.com Huntington's disease Written by Dr Linda Appai-Kubi , King's College Hospital and Guy's King's ST. Thomas's School of Medicine, London and Dr K Ray Chaudhuri , King's College Hospital and Guy's King's ST. Thomas's School of Medicine, London Huntington's disease (HD) was described by George Huntington (1850-1916) who was born in Long Island, New York. He described this disorder in his only known written article called 'on chorea'. Huntington's disease is a genetic disorder (inherited due to a faulty gene) which usually affects people in their 40s and 50s. It primarily affects the brain, with a gradual loss of control of movement, memory and mental ability. HD is also associated with personality changes and depression as well as other mental illnesses. There is currently no cure for HD, although many strategies may be used to improve the quality of life for sufferers and their carers.
School Report Kids writing that report for school on Huntington s disease? What ways arethere of dealing with this disease (therapy, drugs, diet, etc.)? http://www.kumc.edu/hospital/huntingtons/school_report.html
Extractions: Kids writing that report for school on Huntington's disease? Want to find all the answers on the net? Want me to write your report? Don't become on the information superhighway!. Read what is on the other pages at this site and look at the questions and answers below. They have been sent to me by some of your fellow students in the US and world wide wanting help on their school papers. You can also post questions to me and I may answer them and place your questions on this page too! Just remember your teachers can search the web and find this page also. If you copy my answers word for word that is plagiarism and you will eventually be caught. Copying my words is just as bad as writing your report on frogs straight out of the Encyclopedia Britannica. Your teachers can spot the difference between my writing and yours! By the way, if you write to me, please use your own Email account and make certain that your Email address is correct, otherwise, you might not get that A that we so richly deserve. In cases where the Email fails, I will try to post your questions and my answers on this page in a timely fashion. Goldie DuBorg a very nice woman whose husband and child have passed away from Huntington's disease, has voluntered to be available for anyone who wants to learn what the firsthand experience of Huntington's disease is like.
Tube.html feeding techniques, diet consistency changes, and education of the person withHD, Medical Center and by the Huntington s disease support groups. http://www.kumc.edu/hospital/huntingtons/tube.html
Extractions: There are many interventions and strategies that can help to preserve swallowing and to lessen the risk of choking. If all attempts fail to improve swallowing, alternative methods of feeding such as tube feeding will be discussed with families. The task of deciding what is best can be difficult and emotional. This issue usually arises when a person with HD is in the end stages of the disease. However, this issue should be discussed well in advance by the person with HD, their family and the health care provider. By the late stages of HD, the person is often unable to meet nutritional needs, tends to become dehydrated, or aspirates all possible food consistencies, often reflected by frequent bouts of pneumonia. Because of the choking the eating process may have become unpleasant. Tube feeding is a method of providing nutrition to people who cannot sufficiently obtain calories by eating or to those who cannot eat because they have difficulty swallowing. Tubes which transport nutritional formulas can be inserted into the stomach (G-tubes), through the nose and into the stomach (NG-tubes), or through the nose and into the small intestine (NJ tubes). The NG and NJ tubes are considered to be temporary and the G tube is considered more permanent but it can be removed. With all tube feeding approaches, if a person is able, he/she may continue eating and drinking while the tube feeding provides the consistent caloric intake needed for weight maintenance or gain. Thus oral intake can be continued for more pleasurable sensations, such as small bites of a favorite food.
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Extractions: There are genetic disorders caused by the accidental duplication of a (A threadlike body in the cell nucleus that carries the genes in a linear order) chromosome , as in (A congenital disorder caused by having an extra 21st chromosome; results in a flat face and short stature and mental retardation) Down syndrome and (Click link for more info and facts about Klinefelter's syndrome) Klinefelter's syndrome , or repeated duplication of part of a chromosome as in (Click link for more info and facts about Fragile X syndrome) Fragile X syndrome
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Ben Is Coping With Huntington's Disease Health information, from nutrition vitamins to weight loss, diets diet pills . I don t know if they work for Huntington s disease. http://health.jdwebpages.com/freelance-health-and-fitness-articles/ben-is-coping
Market Wire: Doctor Takes On Creatine Controversy During the winter season, they sometimes consumed an allmeat diet. disorders such as Lou Gehrigs disease, huntingtons disease, and Parkinsons disease. http://www.findarticles.com/p/articles/mi_pwwi/is_200109/ai_mark09031470
Extractions: Save a personal copy of this article and quickly find it again with Furl.net. It's free! Save it. Controversy is swirling around the use of the popular supplement creatine. Parents, athletes, and coaches are concerned about its widespread use and long-term consequences. There is now little doubt, when you study the scientific literature and talk to athletes, that creatine improves athletic performance. Athletes participating in sports that require short-term explosive muscle contraction such as football, baseball and wrestling appear to benefit the most. Scientific studies confirm that creatine increases muscle mass, strength, explosive power, and stamina. As a result, creatine has become the supplement of choice for athletes across the country. Arecent study found that 48% of Division 1 NCAA male athletes take or have taken creatine. Last year, an estimated six to eight million pounds were consumed in the United States. Although creatine has been widely used in the U.S. since 1992, some still caution that it has not been used long enough to determine any possible long-term side effects. Others are opposed to creatine supplementation purely for philosophic reasons. They believe that supplements are contrary to the rules, spirit and significance of sports.
Huntington's Disease - Diet Issues Huntington s disease (HD) is an inherited disease of the brain that affects thenervous system. Common complications include problems with eating and http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Huntingtons_disea
Huntington's Disease Explained Huntington s disease (HD) is a disease of the brain that affects the nervous system.It is an inherited condition Huntington s disease diet issues. http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Huntingtons_disea
Huntington's Disease Person was placed on a finely chopped diet (regular consistency was too hard Huntington s disease is a devastating illness that affects every aspect of http://www.asha.org/public/speech/disorders/Huntington-Disease.htm
Extractions: @import url( /styles/importmenuP.css ); Skip to: content navigation Our site's pages are optimized for Web browsing software that supports current Web standards, as established by the World Wide Web Consortium (http://www.w3c.org/) . Content is accessible from older or less standards-compliant technologies, but its presentation will not be identical to visitors with standards-compliant software. Read more on our site's changes and accessiblity. Find a Professional Shop My Account Guest Login Search for: Advanced Search Home Site Location: Home For the Public Disorders and Diseases Based on a brochure developed by Lynn Rhoades, M.S., CCC-SLP for the Huntington's Disease Society of America ( www.hdsa.org ) with financial support of the American Speech-Language-Hearing Association. Why Communication and Swallowing Symptoms Arise As brain cells become depleted in Huntington' s Disease (HD), problems may develop in the following three areas: motor control (movement); cognition (thinking); and behavior. Speech and swallowing problems arise when the centers of motor or cognitive control are affected that cause muscle weakness or discoordination, chorea, and problems with memory, sequencing, new learning ability, reasoning, and problem solving. Typically, speech and language functions are primarily controlled in the left side of the brain and swallowing function is controlled in the brainstem (at the base of the brain). Cognitive function is believed to be controlled in the right side of the brain. HD typically begins in the caudate nucleus and putamen, which are located in the central part of the brain (core), and spreads to these other control centers, causing communication and swallowing problems as the disease progresses. Communication
HD Information The Huntington s disease Advocacy Center s (HDAC) HD Frequently Asked Questions The benefit of a high caloric diet has been beneficial to all in our http://endoflifecare.tripod.com/kidsyoungadults/id6.html
Extractions: The patient with moderate Huntington's disease, like any person suffering from a chronic disease, can become an easy target for abuse. This can be a result of the mental changes that he or she has undergone, the caregivers inability to adapt fast enough, or the fact that the patient with Huntington's disease is an easily identified victim. The abuse can be either way. A caregiver can abuse the patient and the patient can abuse the caregiver and the rest of the family. The section on behavior has information on working with the behavioral changes associated with Huntington's disease. A practical guide for individuals, families and professionals coping with HD Jane S. Paulsen, PhD, 2000. A must-read for anyone who deals extensively with an HD-affected individual; ex plains not only the behavior challenges created by HD, but their origin in the HD-affected brain. By understanding the basis of these behaviors, Dr. Paulsen is able to suggest effective ways of dealing with and preparing for them. The book also covers environmental, individual and health factors that contribute to behavior problems. Problem-solving tips and techniques are given for behaviors arising from communication difficulties, memory problems, cognitive break
