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Tag Archives: Facebook
About Doctors and Facebook Friends
Ampligen Hope My next blog entry was reserved for my recent medical tests and appointments, but I am still processing all those and haven’t come out yet from under the mountain of new information. I also haven’t recovered to my … Continue reading
Posted in Understanding ME/CFS
Tagged Ampligen, CFS, Chronic Fatigue S, Dr. Dan Peterson, Facebook, Hemispherx, Incline Village, Lake Tahoe, MCS, ME, ME/CFS, Myalgic Encephalomyelitis, Nannies, Sleep, tilt table test, VO2 max
23 Comments
Voices From The Shadows—World Premiere and Panel Discussion
“Voices from the Shadows,” a one-hour documentary about the commonplace abuse and neglect of gravely ill ME patients, including children, by the British government and medical establishment, most notably psychiatrists, and the misportrayal of ME* by the media, premiered on … Continue reading
Posted in Advocacy, ME/CFS Treatment, ME/CFS: The Science, Understanding ME/CFS
Tagged AIDS, at-risk register, B., Berkeley Graduate School of Journalism, Canadian Consensus Criteria, cancer, CDC, CFS, child protection conference, child protection proceedings, child-in-need plan, chronic cough syndrome, Chronic Fatigue Syndrome, Criona Wilson, David Poore, David Tuller, definition, Depression, derogatory, disbelief, disease name, Documentary, East Germany, editors, emphysema, Facebook, fatigue, fear, foster care, Fukuda Criteria, G93.3, ganglionitis, General Medical Council, GMC, Graded Exercise Therapy, Greg Crowhurst, heart disease, HGRV, hostility, human rights, I do not want to be an example of what a mental hospital can do to an ME patient., infection of dorsal root ganglia, infections, International Consensus Criteria, Jose Montoya, Josh Biggs, Judy Mikovits, Kay Gilderdale, Lenny Jason, Linda Crowhurst, London, Lynn Gilderdale, major depressive disorder, major illness, Malcolm Hooper, malingerers, ME, ME/CFS, media coverage, medical arrogance, Medical Curriculum, Medical Research Council, mental hospital, Mill Valley Film Festival, MRC, MUBI, Munchhausen Syndrome by Proxy, Myalgic Encephalomyelitis, Naomi, Natalie Boulton, National Catastophe, neurological disease, New York Times, Nigel Speight, NIH, Norwich, October 8, Online Streaming, organic medicine, Oxford Criteria, Panel Discussion, police state, psychiatrists, research money, researchers, retroviral research, San Rafael, sectioning, Smith Rafael Film Center, solicitor, Sophia Mirza, Stalinism, Stanford University, stigma, Tina Caskey, toxoplasmosis, Trailer, tribunal, trivializing, UK, United Kingdom, United States, US, Voices from the Shadows, waiting list, Wessely, wheelchair, WHO, World Premiere, XMRV, Young ME Sufferers Trust, yuppie flu, Zoe Elton
15 Comments
Please vote for the Whittemore Peterson Institute on Facebook
Thanks to all of you who have voted for the Whittemore Peterson Institute (WPI) during round 1 of the Chase Community Giving program a few weeks ago. WPI finished strong in fifth place and won $25,000. Today, round 2 starts … Continue reading
Posted in Advocacy
Tagged CFS, Chase Community Giving, Facebook, ME/CFS, Whittemore Peterson Ins, WPI, XMRV
1 Comment
Facebook users, please help finding a cure by spending 2 minutes. Thank You!
For my next post, I had planned to say a little bit about what ME/CFS is and what it’s like to live with it because, while I envision this blog to address current events, discoveries, controversies, etc., in the ME/CFS … Continue reading
Posted in Advocacy
Tagged CFS, Chase Community Giving, Count ME In, Facebook, ME/CFS, Whittemore Peterson Institute, WPI, XMRV
3 Comments
