Comments on: XMRV: Wait for the science http://newly-nerfed.net/2010/02/08/xmrv-testing-and-questionable-ethics/ Thu, 12 Apr 2012 21:40:22 +0000 hourly 1 http://wordpress.org/?v=3.0.1 By: Lisa http://newly-nerfed.net/2010/02/08/xmrv-testing-and-questionable-ethics/comment-page-1/#comment-1241 Lisa Thu, 03 Jun 2010 06:15:10 +0000 http://newly-nerfed.net/?p=1622#comment-1241 All true. The sad thing is that critical thinking hasn't been happening re: CFIDS for decades. It's just been ignored basically. By science, by the gov't, you name it. I've been sick since 1980. Enough, you know? That's 30 years. And my son probably has it too. Wow. Way to go science, gov't, alternative meds, whatever. All true. The sad thing is that critical thinking hasn’t been happening re: CFIDS for decades. It’s just been ignored basically. By science, by the gov’t, you name it.
I’ve been sick since 1980. Enough, you know? That’s 30 years. And my son probably has it too. Wow. Way to go science, gov’t, alternative meds, whatever.

]]> By: XMRV: Wait for the science « FIGJAM http://newly-nerfed.net/2010/02/08/xmrv-testing-and-questionable-ethics/comment-page-1/#comment-1048 XMRV: Wait for the science « FIGJAM Mon, 19 Apr 2010 09:18:28 +0000 http://newly-nerfed.net/?p=1622#comment-1048 [...] Link: XMRV: Wait for the science [...] [...] Link: XMRV: Wait for the science [...]

]]> By: sue http://newly-nerfed.net/2010/02/08/xmrv-testing-and-questionable-ethics/comment-page-1/#comment-817 sue Sun, 07 Mar 2010 08:16:01 +0000 http://newly-nerfed.net/?p=1622#comment-817 i go to a lot of CFS message boards and very few patients have blindly accepted the fact that XMRV is the cause. the vast majority are skeptical. a few, like me, who are severely affected, are clinging a little harder to the hope that XMRV is "it". out of thousands of people, i have run into only one person who has tried an antiretroviral for any meaningful length of time. lets not forget that dr. mikovits of the WPI has now found the virus in over 300 samples after the study came out. she was also able to culture the virus from 95% of those who are antibody positive. the virus is very, very hard to find. sue i go to a lot of CFS message boards and very few patients have blindly accepted the fact that XMRV is the cause. the vast majority are skeptical. a few, like me, who are severely affected, are clinging a little harder to the hope that XMRV is “it”.

out of thousands of people, i have run into only one person who has tried an antiretroviral for any meaningful length of time.

lets not forget that dr. mikovits of the WPI has now found the virus in over 300 samples after the study came out. she was also able to culture the virus from 95% of those who are antibody positive. the virus is very, very hard to find.

sue

]]> By: To Get Tested For XMRV Or Not. That's The Question. — Life With ME/CFS http://newly-nerfed.net/2010/02/08/xmrv-testing-and-questionable-ethics/comment-page-1/#comment-800 To Get Tested For XMRV Or Not. That's The Question. — Life With ME/CFS Tue, 02 Mar 2010 20:24:59 +0000 http://newly-nerfed.net/?p=1622#comment-800 [...] Newly Nerfed – XMRV: Wait for the science [...] [...] Newly Nerfed – XMRV: Wait for the science [...]

]]> By: Joey http://newly-nerfed.net/2010/02/08/xmrv-testing-and-questionable-ethics/comment-page-1/#comment-727 Joey Wed, 17 Feb 2010 03:49:33 +0000 http://newly-nerfed.net/?p=1622#comment-727 Thank you, and thanks also for being one of the few medical skeptics to cover this. Thank you, and thanks also for being one of the few medical skeptics to cover this.

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