Surely if Mikovits is wrong ,as seems increasingly likely...
To someone who hasn't been following the XMRV research closely, then I agree that it would seem increasingly likely that Mikovits is wrong.
But 'likely wrong' or 'maybe wrong', or 'probably wrong' is not the same as 'wrong' and the Mikovits' original study has not been disproved.
But to many of us who have been following very closely, we can see that the Original Science study still stands strong, for many different reasons.
You talk as if all scientists except her are corrupt or part of some conspiracy.
I see you are new to the forum RedRuth. Welcome.
From your posts, it does show that you are not aware of the history of ME/CFS and the way the disease and patients have been treated by governments and the scientific establishment and some scientists over many many years.
If you had been at the receiving end of this treatment, then maybe you would not have made the comments that you have made, and would understand that there is politics at play in the world of CFS/ME.
We have also seen politics at play in the scientific community with XMRV.
So you'll have to forgive us if we sometimes get cranky when we see the scientific establishment attempting to shut down the cutting-edge research of a decent and very competent scientist because her results happen to displease them.
Science have issued a statement (see below) saying, in effect, that the jury is still out with XMRV and ME/CFS, so in which case, why have they asked for a retraction? Is that good science?
"The U.S. National Institutes of Health is sponsoring additional carefully designed studies to ascertain whether the association between XMRV and CFS can be confirmed. Science eagerly awaits the outcome of these further studies and will take appropriate action when their results are known."
http://www.sciencemag.org/content/early/2011/05/31/science.1208542.full.pdf
Addition:
Hi, Bob, thanks for the reply. I only have an academic interest - my sister thought she had CFS and asked me to look into the XMRV story for her as I'm a scientist. I have to say that I'm pretty taken aback by some of the comments here about scientists, it's pretty shocking really. I'm entirely agnostic about XMRV though I have to say from what I've read, it seems unlikely that it's the cause of CFS.
Thanks RedRuth, for sharing your background, and welcome to the forum.
There is so much more to the story of ME and XMRV than is probably apparent from the posts that you have read.
We have very good reason to be suspicious of many in the medical profession, and of many scientists.
I won't go into details here, because I'd be writing for at least a week, if I tried to summarise the history now!