Resources All of the sites listed here are my personal recommendations, no paid advertising or endorsements. Medical Information and Research Fibromyalgia Research Blog Billed as "the latest in fibromyalgia research, news, and clinical trials", this site really delivers. All the fibro news condensed down, and then links if you want to read further about any of the stories. Fibromyalgia Network Fibromyalgia Network is the US Fibro group with the most advanced definition of FMS, in my opinion. Their "Basic Info" pages give an excellent overview of FMS diagnosis, symptoms and treatments. For access to articles and more, you will need to become a paying member. I think it's worth it because this organization does not endorse any particular product or single point of view. They also do excellent advocacy. Holtorf Medical Group (Torrance, CA) I refer to Dr. Holtorf's explanation of FMS in my site. Check out the website for his medical practice to get a deeper understanding of his protocol. Fibro Talk Huge site is a one-stop-shop for FMS info of all kinds. Psychological and Emotional Support Christopher Maier, MA, Psychotherapist and Counselor If you live in the Denver, CO, Metro area and are looking for a therapist or counselor, I highly recommend Christopher Maier. He understands chronic illness and traumatic experiences and has useful techniques for helping live a joyous and meaningful life. Online CFS support groups and library of articles The online support group is one of the best experiences I ever had. This group teaches realistic, achievable, empowering skills to get the most out of your life with chronic illness. For the $25 cost of the 6-week support group, you get a great book full of useful techniques. Also, the site has many practical articles on various issues and how to cope. Personal Sites, blogs, etc. My Own Blog My own blog, devoted to the psychological impact of chronic illness. My goal is to offer analysis of the issues we go through, tell the truth about what I go through, offer empathy and illness to others affected by illness, and coping mechanisms that work for me. Chronic Town A good writer and a great friend, Rebecca blogs about living with sarcoidosis (yuck.) Bunny's Myspace Blog Bunny is young, creative, introspective, and she has E.D.S. Laura Hillenbrand's article The author of "Seabiscuit" has Chronic Fatigue. I never say that everyone should do something, but in this case, I think everyone should read her essay. Various personal stories about CFS&FM "Personal Testimonials" from a variety of CFS and FMS patients - a young child, a severely depressed person, upscale professionals, people in various stages of recovery. Each story is unique. But You Don't Look Sick Hilarious, empowering slogans and stories. The site is overwhelming and confusing for me to navigate, though. Check out the sections called "Sick Humor" (pun intended) and the online store. Support Systems & Partners Share The Care Share The Care is a system designed to put together a practical support system for cancer patients. My friends and I modified this idea to create Team Fabulous. Letter to those WITHOUT Chronic Illness The wonderful Ricky Buchanan has written this "Open Letter To Those Without Chronic Illness" which you can print out and hand to the people in your life. Her whole site, notdoneliving.net, is full of interesting resources and observations. CFIDS Family Resources The CFS/FM Online self-help course has a great section of articles about improving communications within families affected by a fatiguing illness. Spiritual Resources (Christian and Other - noted below) Christian - Rest Ministries Rest Ministries is a great resource center. They have daily prayer meditations illuminating Bible passages for people struggling with chronic illness and pain. Also resources to help church groups and other Christians be compassionate towards the chronically ill and to help effectively.

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