This sourcebook has been created for patients who have decided to make education and Internet-based research an integral part of the treatment process. Although it gives information useful to doctors, caregivers and other health professionals, it also tells patients where and how to look for information covering virtually all topics related to huntington's disease, from the essentials to the most advanced areas of research. The title of this book includes the word official. This reflects the fact that the sourcebook draws from public, academic, government, and peer-reviewed research. Selected readings from various agencies are reproduced to give you some of the latest official information available to date on huntington's disease. Following an introductory chapter, the sourcebook is organized into three parts. PART I: THE ESSENTIALS; Chapter 1. The Essentials on Huntington's Disease: Guidelines; Chapter 2. Seeking Guidance; Chapter 3. Clinical Trials and Huntington's Disease; PART II: ADDITIONAL RESOURCES AND ADVANCED MATERIAL; Chapter 4. Studies on Huntington's Disease; Chapter 5. Books on Huntington's Disease; Chapter 6. Multimedia on Huntington's Disease; Chapter 7. Physician Guidelines and Databases; Chapter 8. Dissertations on Huntington's Disease; PART III. APPENDICES; Appendix A. Researching Your Medications; Appendix B. Researching Alternative Medicine; Appendix C. Researching Nutrition; Appendix D. Finding Medical Libraries; Appendix E. Your Rights and Insurance; ONLINE GLOSSARIES; HUNTINGTON'S DISEASE GLOSSARY; INDEX. Related topics include: Artificial insemination, Chronic Progressive Chorea, Chronic progressive hereditary chorea, Degenerative Chorea, Hereditary Chorea, Hereditary Chronic Progressive Chorea, Huntington chorea, Huntington's chorea, Huntington's disease, Very Early Onset Huntington's Disease, Woody Guthrie's Disease.
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This is a "must have" reference book for patients, parents, caregivers, and libraries with medical collections. This sourcebook is organized into three parts. Part I explores basic techniques to researching huntington's disease (e.g. finding guidelines on diagnosis, treatments, and prognosis), followed by a number of topics, including information on how to get in touch with organizations, associations, or other patient networks dedicated to huntington's disease. It also gives you sources of information that can help you find a doctor in your local area specializing in treating huntington's disease. Collectively, the material presented in Part I is a complete primer on basic research topics for patients with huntington's disease. Part II moves on to advanced research dedicated to huntington's disease. Part II is intended for those willing to invest many hours of hard work and study. It is here that we direct you to the latest scientific and applied research on huntington's disease. When possible, contact names, links via the Internet, and summaries are provided. In general, every attempt is made to recommend "free-to-use" options. Part III provides appendices of useful background reading for all patients with huntington's disease or related disorders. The appendices are dedicated to more pragmatic issues faced by many patients with huntington's disease. Accessing materials via medical libraries may be the only option for some readers, so a guide is provided for finding local medical libraries which are open to the public. Part III, therefore, focuses on advice that goes beyond the biological and scientific issues facing patients with huntington's disease.
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Though many physicians and public officials had thought that the emergence of the Internet would do much to assist patients in obtaining reliable information, in March 2001 the National Institutes of Health issued the following warning: "The number of Web sites offering" health-related resources grows every day. Many sites provide valuable information, while others may have information that is unreliable or misleading." Since the late 1990s, physicians have seen a general increase in patient Internet usage rates. Patients frequently enter their doctor's offices with printed Web pages of home remedies in the guise of latest medical research. This scenario is so common that doctors often spend more time dispelling misleading information than guiding patients through sound therapies. ... This book has been created for patients who have decided to make education and research an integral part of the treatment process. ... While this sourcebook covers huntington's disease, your doctor, research publications, and specialists may refer to your condition using a variety of terms. Therefore, you should understand that huntington's disease is often considered a synonym or a condition closely related to the following: Artificial insemination; Chronic Progressive Chorea; Chronic progressive hereditary chorea; Degenerative Chorea; Hereditary Chorea; Hereditary Chronic Progressive Chorea.
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This review is from: The Official Patient's Sourcebook on Huntington's Disease: A Revised and Updated Directory for the Internet Age (Paperback)
This book is a VERY remedial introduction to the "world wide web" and is written for someone who thinks a computer is just a typewriter hooked up to a television. And since the internet changes every second, this book was outdated before it even went to print. Don't waste your money on this book - everything inside can be found online for free.
I've purchased nearly every book on Amazon about HD, and I am very sorry to say that the body of knowledge on HD is frighteningly sparse. There really are no good books on HD unless you want to know the history of the disease or read about a particular family's struggle. For up to date medical information, the best resource, hands down, is The Huntington's Disease Lighthouse at [...].
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