xmrv-bloggerama-day.blogspot.com
XMRV-Bloggerama-Day: I have a problem with Trine Tsouderos's reporting on XMRV: 2 of 3
http://xmrv-bloggerama-day.blogspot.com/2011/03/i-have-problem-with-trine-tsoudeross_27.html
Sunday, March 27, 2011. I have a problem with Trine Tsouderos's reporting on XMRV: 2 of 3. Part 1 of 3. Okay, after one “loser-length” post, here we are with another. On the web chat’s comments I copied into the previous post? I can say that a phone message I left on her voicemail following her web chat on XMRV last June was not returned, and that while I had left one comment on the Tribune site on one of her pieces at some point last year, a second was not posted, for whatever reason. I realize this and...
livingwithchronicfatiguesyndrome.wordpress.com
My ME Treatments- A January 2014 Update | Living With Chronic Fatigue Syndrome
https://livingwithchronicfatiguesyndrome.wordpress.com/2014/01/29/my-me-treatments-a-january-2014-update
Living With Chronic Fatigue Syndrome. Just another WordPress.com weblog. Laquo; One Thousand Paper Cranes. My ME Treatments- An August 2014 update. My ME Treatments- A January 2014 Update. January 29, 2014 by cfssufferer. A lengthy period of time has again passed between my blog entries. This article will hopefully inform readers of the different treatments I have trialled over the past few months. The Neuroimmune Disease Alliance funded a trial of Moringa Oleifera on ME/CFS patients, to be run by the Op...
biomedicalmecfs.blogspot.com
Biomedical ME/CFIDS: May 2011
http://biomedicalmecfs.blogspot.com/2011_05_01_archive.html
Sunday, May 15, 2011. Are Singh and Bateman Afraid of Proof of Principle Studies? 8220;Our findings do not support an association between CFS and MLV-related. Off-label use of antiretrovirals. For the treatment of CFS does not seem justified at present. Dr Ila Singh et al. Http:/ jvi.asm.org/cgi/content/abstract/JVI.00693-11v1. And how can they, in scientific honesty and in good conscience, keep claiming to refute the study they refuse to actually replicate? Is it about your patent applications. Composit...
livingwithchronicfatiguesyndrome.wordpress.com
Oxymatrine | Living With Chronic Fatigue Syndrome
https://livingwithchronicfatiguesyndrome.wordpress.com/2009/11/03/oxymatrine
Living With Chronic Fatigue Syndrome. Just another WordPress.com weblog. Laquo; My Abnormal Blood Tests. November 3, 2009 by cfssufferer. The White Tiger brand contains 200mg of oxymatrine per tablet. My dosing structure is flexible based on any reaction to the oxymatrine however at the moment stands at:. 100mg each day for 2 weeks. The tablet is to be taken with water before or with meals. 100mg 2x a day for 2 weeks. 200mg at am and 100mg at pm for 2 weeks. I must stress that it is imperative to slowly ...
livingwithchronicfatiguesyndrome.wordpress.com
An ME Update- August 2013 | Living With Chronic Fatigue Syndrome
https://livingwithchronicfatiguesyndrome.wordpress.com/2013/08/05/an-me-update-august-2013
Living With Chronic Fatigue Syndrome. Just another WordPress.com weblog. Laquo; Nimodipine- The Results. One Thousand Paper Cranes. An ME Update- August 2013. August 5, 2013 by cfssufferer. It has been a lengthy period since my last blog. This entry will attempt to outline my ME related journey from the past 6 months. In a previous blog entry here. There exists a plethora of ME treatments that I have lined up and ready to trial. The one prohibiting factor for testing these treatments involves the wei...
livingwithchronicfatiguesyndrome.wordpress.com
June | 2015 | Living With Chronic Fatigue Syndrome
https://livingwithchronicfatiguesyndrome.wordpress.com/2015/06
Living With Chronic Fatigue Syndrome. Just another WordPress.com weblog. Archive for June, 2015. Ten years of M.E. On June 23, 2015 13 Comments. Today marks an anniversary for me with this illness. A decade ago to the day, my first symptoms emerged, although they were relatively mild at the time. This is my journey…. I have spent the last ten years of my life living with Myalgic Encephalomyelitis. Specialised testing ascertained that the blood wasn’t flowing freely around my brain and my immune system wa...
xmrv-bloggerama-day.blogspot.com
XMRV-Bloggerama-Day: I have a problem with Trine Tsouderos's reporting on XMRV: 1 of 3
http://xmrv-bloggerama-day.blogspot.com/2011/03/i-have-problem-with-trine-tsoudeross.html
Friday, March 25, 2011. I have a problem with Trine Tsouderos's reporting on XMRV: 1 of 3. For nearly a year now, I have had a problem with the reporting of Trine Tsouderos on a topic that I follow, mostly because of its relevance to me (and many other people) personally. Soearlier this week the Chicago Tribune had a web chat conducted by reporter Trine Tsouderos and Dr. Paul Offit, on the subject of vaccine safety and the various controversies involved. Are there more issues with vaccines- not necessari...
toadlily-gamer.blogspot.com
Failure to Thrive: Advocacy
http://toadlily-gamer.blogspot.com/p/advocacy.html
It is (ME/CFS) like some great constricting snake that denies its victims the final convulsion.". A CFS patient feels the same or worse than congestive heart failure. The same or worse than late stage AIDS." Nancy Klimas. A CFS patient feels every day significantly the same as an AIDS patient feels two months before death.". Dr Mark Loveless, AIDS and CFS researcher, in a statement to congress on CFS Awareness day, May 12th, 1995. Whittemore-Peterson Institute on Facebook. Hillary Johnson (Osler's Web).