1. What Is Huntingtons Disease HDA Online provides news of fund raising events, health care information and details of research into curing huntingtons disease Huntington's disease, which is often called HD, is an Huntington's disease usually develops in adulthood and can cause A high calorie diet can prevent weight loss and improve http://www.hda.org.uk/charity/whatishd.html

The information contained on this page is available as a Fact Sheet which you can download from our Fact Sheet page. H untington's disease, which is often called HD, is an hereditary disorder of the central nervous system. It used to be known as Huntington's Chorea or HC. Huntington's disease usually develops in adulthood and can cause a very wide range of symptoms. The disease affects both men and women. Page Sections: What causes Huntington's disease? The early symptoms of Huntington's disease How Huntington's disease progresses What treatment and help is available? What causes Huntington's disease? Huntington's disease is caused by a faulty gene on chromosome 4. The gene, which produces a protein called Huntingtin, was discovered in 1993. In some way - which is not yet understood - the faulty gene leads to a damage of the nerve cells in areas of the brain, including the the basal ganglia and cerebral cortex. This leads to gradual physical, mental and emotional changes.

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4. Huntingtons Disease can be helpful at all stages of the disease in maintaining make recommendations thatinvolve positioning issues, feeding techniques, diet consistency changes http://www.asha.org/speech/disabilities/Huntington-Disease.cfm

www.ASHA.org Huntington's Disease 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 Problems with communication and cognition vary in nature and severity from person to person. Although there are commonalties, no two people with HD are exactly alike, and as the disease progresses, the variability continues. The following list summarizes problems that people with HD may experience at different stages of the disease. In many cases, a person with HD will experience the same areas of difficulty throughout the course of the disease, with severity varying from stage to stage.

5. Huntington's Scene In New Zealand Website Huntingtons Disease New The Huntington A comprehensive look at the topic huntingtons chorea huntingtons disease huntingtons disease Menu PM Need advice on diet http// neuro www. http://redirect-west.inktomi.com/click?u=http://homepages.ihug.co.nz/~ghtaylor/&

6. Huntington's Scene In  New Zealand Website Huntingtons Disease New Zealand The Huntington's disease Scene In This site last updated Being such small community groups we operate within small budgets and limited resources. huntingtons disease New Zealand. Key NZ Site Resources . Genes Generations.Book. diet Book . Huntington's and Me http://www.geocities.com/graham_tay

The Huntington's Disease Scene In New Zealand Site Maintained by Graham Taylor Graham Taylor This site last updated About the Associations Auck BOP Wgtn ... Young Peoples Pages Canadian Resources Introduction to HD Publications Research Education ... International HDA Addresses Member Countries Huntingtons Disease New Zealand Key NZ Site Resources National Annual Camp forYoung People from HD Families Newsletter Diet Book ... Naturapathic Medicines and Therapies 21-22 September NZ Research Neurological Foundation Brain Bank By Alison Gray. By Alison Gray Studies by Richard Faull and his team at Auckland University International Research News Being such small community groups we operate within small budgets and limited resources. We acknowledge the generosity of the Huntingtons Society of Canada (HSC) for making considerable content publicly available on their web site and contribute to making the New Zealand site as informative as possible. Such co-operation is a feature of the Huntingtons world-wide community network. Whilst every effort will be made to keep the information on this site accurate and up to date, ‘The Huntington’s Scene In New Zealand’ [HSNZ], those responsible for compiling it will not be liable for any loss or damage arising directly or indirectly from the possession, publication or use of or reliance on information obtained from the Web Site, and reserves the right to make changes without notice. Accordingly, all HSNZ and third party information is provided "As Is".

7. HDLighthouse.org diet particularly if you are concerned about Huntington's disease. Jerry LampsonPosted to HDL 07 Dec 2002. $500,000,000 Market For huntingtons' disease http://hdlighthouse.org/treatment-care/index.shtml

8. Huntingtons Disease PM; Need Some Good Advise (11/19/98) 950 PM; Need advice on diet and vitamins HDFetal Cell Transplant (2/9/98) 1033 PM; Any information on huntingtons disease. http://neuro-www.mgh.harvard.edu/forum/HuntingtonsDiseaseMenu.html

Huntingtons Disease Menu This is a webforum to discuss and comment on Huntingtons Disease. Click here to Enter a new Neurology WebForum article... This Web Forum is not moderated in any sense. Anyone on the Internet can post articles or reply to previously posted articles, and they may do so anonymously. Therefore, the opinions and statements made in all articles and replies do not represent the official opinions of MGH and MGH Neurology. Neither is MGH or MGH Neurology responsible for the content of any articles or replies. No messages are screened for content. - Very Important Message! - Please Click Here to Read Current Posts: Oct 10, 1997 to Present Useful Websites can be found and posted here! Hurt by insensitvity (1/14/00) 3:54 AM Exam Project!!! (1/11/00) 5:59 PM Chorea (1/8/00) 7:41 AM ... Good to be back (10/14/97) 9:59 PM IMPORTANT: If this page seems to be missing recently added documents, click the "Reload Page" button on your Web Browser to update the menu. Return to the main Neurology WebForum Page. These forums are maintained by the Department of Neurology at Massachusetts General Hospital John Lester - Webspinner

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12. OhioHealth - Health Topics Brain Characteristics of the huntingtons disease include onset ranges from 35 an advancedcase of Wilson's disease may require a copper metabolism and a diet low in http://www.ohiohealth.com/healthtopics/brain/degen.htm

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1Up Health Health Topics A-Z Home Contact Us ... Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Topics A-Z Reference A B C D ... Z Topics Beginning with "H" H. flu meningitis , see Meningitis - H. influenzae H. influenzae meningitis, see Meningitis - H. influenzae H2 Receptor antagonists H2O, see Water in diet Haemophilus influenzae B conjugate vaccine , see Hib - vaccine Haemophilus influenzae type B (Hib) vaccine, see Hib - vaccine Hageman factor assay, see Factor XII assay Hair - dry Hair - excessive on females Hair - oily, see Oily hair Hair bleach, see Hydrogen peroxide overdose Hair bleaches or lighteners Hair dyes and tints Hair follicle infection, see Furuncle Hair loss Hair loss in men, see Male pattern baldness Hair loss in women, see Female pattern baldness Hair removal agents, see Depilatories Hair spray lacquer Hair straighteners Hair tonic Hairball, see Bezoar Hairy cell leukemia Hairy leukoplakia, see Leukoplakia Hairy nevus, see

14. Fwd: [DOEWatch] USES AND ABUSE OF GENOMIC INFORMATION those that are tested for huntingtons disease before manifestation of the human frame,in diet, and in the cause and prevention of disease. Attributed to http://lists.essential.org/med-privacy/msg00362.html

Date Prev Date Next Thread Prev Thread Next ... Thread Index Fwd: [DOEWatch] USES AND ABUSE OF GENOMIC INFORMATION To med-privacy@essential.org Subject : Fwd: [DOEWatch] USES AND ABUSE OF GENOMIC INFORMATION From weeethistle@yahoo.com Date : Fri, 9 Jul 1999 08:09:04 -0700 (PDT) http://mail.yahoo.com To doewatch@onelist.com Subject : [DOEWatch] USES AND ABUSE OF GENOMIC INFORMATION From Magnu96196@aol.com Date : Thu, 8 Jul 1999 20:18:10 EDT Delivered-To : mailing list doewatch@onelist.com List-Unsubscribe Mailing-List : list doewatch@onelist.com; contact doewatch-owner@onelist.com http://dailynews.yahoo.com/headlines/sc/story.html?s=v/nm/19990629/sc/health_ http://dailynews.yahoo.com/headlines/sc/story.html?s=v/nm/19990629/sc/health http://www.onelist.com Try ONElist's Shared Calendar to organize events, meetings and more! DOEWatch List A Magnum-Opus Project - The real Natl. Sec. Directive Subscribe online: http://www.onelist.com/subscribe.cgi/doewatch Prev by Date: meanwhile, back in Iceland (fwd) Next by Date: Fwd: [DOEWatch] Human Genome Promise Prev by thread: meanwhile, back in Iceland (fwd)

15. AlzheimerSupport.com benefit for AD comparable to that already found in huntingtons disease, ALS and Alzheimerdisease is Added to the Growing List of dietRelated Chronic http://www.alzheimersupport.com/articles/2000_08/1485.cfm

Alzheimer Support .com World's Largest Alzheimers site! Products Alzheimer's: Understanding Treatment Support: Chat MessageBoards Caregiving Doctor Referral ... Contact Us Free Catalog Creatine May Offer Protection to Alzheimers Patients by Deborah Cooper AlzheimerSupport.com 08-02-2000 - Creatine, a dietary supplement better known in the athletic world than in neuroscience, may have protective benefits for people with Alzheimer’s. According to a study in the June 15 issue of the Journal of Neuroscience, mice that were fed creatine experienced significant protective effects on their brains. Creatine is a naturally-occurring compound that affects energy metabolism. According to Ethan Signer, Professor Emeritus of Biology at MIT, neurodegenerative diseases in general are often accompanied by deficiencies in energy metabolism. “It is possible that supplementation with creatine might in principle compensate for that deficiency.” He noted that there have been previous studies indicating lowered activity of creatine metabolic enzymes in Alzheimer affected brains. The team of scientists drawn from several leading US research institutes, including Harvard Medical School and Cornell University, tested creatine on mice who were artificially given the gene for the neurological disorder Huntington’s disease.

16. Untitled lack of exercise, eating an improper diet, and smoking of survival over a killer diseaseby changing a single gene that contains huntingtons disease or another http://www.msu.edu/~smitht23/PAPER2.HTM

If I was Howard I would be completely opposite from him. I would change my ways because I would want to live as long as possible. I would start an exercise program, stop smoking immediately, try to eat healthier, and visit the doctor regularly. If you can delay or stop a disease from killing you, you should take all the necessary steps for prevention. If I could better my chances of survival over a killer disease by changing my ways, I would follow a regimented program endorsed by my doctor. If you exercise regularly this greatly reduces the risk of heart disease. Although you have a genetic family background of the disease, you can greatly prevent it by aerobic activity like walking 12-15 miles a week to get your blood flowing. This provides more oxygen in your blood that goes to your heart. The environment that you live and work in can play a major role in heart disease. If your environment is stressful, it can lead to high blood pressure. High blood pressure is also caused by being overweight. Exercise can lower high blood pressure. It is also very helpful to eat a healthy diet. In a healthy diet you need low cholesterol and low saturated fat levels. Both saturated fat and cholesterol contribute to clogged arteries which lead to heart attacks. The clogged arteries won't let vital nutrients and oxygen get to the heart. Arteriosclerosis is the hardening of or blocking of the blood vessels. If you lower your cholesterol, the chances of a heart attack decrease, "That means you can cut your risk in half by decreasing your blood cholesterol by 25 percent!" (Heart attack counterattack 98) If you smoke you put yourself at the greatest risk for a heart attack.

17. The Following Links Will Provide More Information About HD And homepages.ihug.co.nz/~ghtaylor/index.html ABOUT huntingtons disease GENERAL INFORMATIONThese of care, children HD, driving, swallowing diet, living with http://www.ahda.com.au/Pages/links.html

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19. Commonly Asked Questions Is there a special diet required for sufferers Where to Find Help The Huntington'sdisease Society of America at www.hdsa.org The huntingtons disease Society of http://endoflifecare.tripod.com/juvenilehuntingtonsdisease/id188.html

Juvenile-HD Commonly Asked Questions Home INDEX Page What Is Huntington's? Commonly Asked Questions 10 The Most Commonly Asked Questions Advocacy/Donations/Press Info Clinical Definitions-Terminology Facing HD~Family Handbook ... INDEX Page Commonly asked questions about HD 1. What is Huntington's Disease? Huntington's Disease (HD) also called Huntington's Chorea is an inherited disorder of the central nervous system. It causes progressive deterioration with varying symptoms which may include involuntary movements, speech impairment, and intellectual and emotional changes. Symptoms usually appear between the ages of 30 and 45, although they may appear earlier or later. 2. How does the disease get its name? The disease is named after Dr. George Huntington, an American physician, who was the first to publish a precise description of the symptoms and course of the disease in an article written in 1872. 3 Who Is Affected? HD is hereditary. Each child of a parent who has HD has a 50/50 chance of inheriting the gene and is said to be at risk. Huntington's Disease affects both genders as well as different races and ethnic groups throughout the world.

20. Netn.net/lpage Health allergies general nutrition health nutrition healthy special diet recipes heart, heartdisease, hemophilia, herpes, huntingtons disease, immunology, infertility http://www.netn.net/21113.htm

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