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 myasthenia gravis (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 myasthenia gravis. It also gives you sources of information that can help you
find a doctor in your local area specializing in treating myasthenia gravis. Collectively, the material presented in Part I is a complete primer on basic research topics for patients with myasthenia gravis. Part II moves on to advanced research dedicated to myasthenia gravis. 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 myasthenia gravis. 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 myasthenia gravis or related disorders. The appendices are dedicated to more pragmatic issues faced by many patients with myasthenia gravis. 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 myasthenia gravis
.
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http://www.filesonic.com/file/1390302604/The_Official_Patient_s_Sourcebook_on_Myasthenia_Gravis.pdf
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