Serenity my comments were not aimed at you.
oops my fault Kati i'm sorry it was Rebecca who was askin me questions.
i will go back & edit. sorry!
Serenity my comments were not aimed at you.
...Are you saying that members here in this forum who would prefer to see a more professional demeanor on the part of our advocates have a vested interest in keeping things the way they are? Please elaborate.
Who said that, Simon Wessely?“will fall into ruin and her work will lie in the science rubble heap”
There's a strong belief that DeFreitas was done in but my take on it after reading Osler's Web and another publication was that the work simply failed. Dr. DeFreitas was unable to distinguish between well and CFS patients at the CDC and even more importantly, when the CAA gave her an opportunity to distinguish between healthy controls and doctor Bell's patients - the patients she'd originally worked on - she failed to do that as well. (Even though Hilary Johnson had that information she failed to put it in her book - it apparently didn't fit with her us against them scenario)
Neither the CDC, nor a Texas lab whose name escapes me, or a pharmaceutical firm in California that had an agreement with Wistar to produce her test, nor a group of CFS researchers, nor a Japanese group, nor the NC Foundation funded study 10 or 15 years later were able to find any evidence of that kind of retrovirus in CFS patients.
I think she just failed, unfortunately. I would note the she and Wistar also made a big splash with a similar finding in multiple sclerosis patients that was later disproved as well. This was all from a researcher that everyone agreed was quite diligent and responsible - its a tough, tough field.
now
That last study was not in the book. The book ended basically ended with both Dr. Martin and Herst labs failing miserably to distinguish CFS patients in a double blinded study set up by the CFIDS Association. Dr. DeFreitas was the third leg of the study but she had been in unable to complete her end because a hurricane wiped out her lab in Miami. That's where the book, published three or four years later ends. But I found a CFIDS Association newsletter that indicated that six months later or so Dr. DeFreitas did complete her end of the study and that she too was unable to determine who had CFS and who didn't. That was when the CAA, which had been her sole support, stop funding her. They also stopped funding Dr. Martin. They continued funding Dr. Grossberg for years in his search for a retrovirus but that never panned out either. I think its Ironic that the only group that ever funded Dr. DeFreitas search for retrovirus in CFS - and they did it for years - got so slammed afterward. Its kind of surreal to me
I do feel that Dr. Mikovits is held to a different standard than other researchers. I believe the meme that she is angry and inappropriate is being perpetuated by those with a vested interest in preserving the status quo.
The more I see, the more I believe this is the case. It just doesn't make sense that there are people who have done us intentional harm, "advocates" who (while I'm sure very professional) have done very little to help us, quacks bleeding our thin wallets dry...and yet all this - it really seems like anger - directed at one of the most unlikely targets possible. It seems like people like to go the parade of horribles route and suggest that she has, by calling the situation as she sees it, authored her own and the ME community's collective doom. This is patently absurd.
Another thing to think about is that she probably knows some things that she has, despite her hysterical and unprofessional nature (j/k), managed to keep quiet. Her cockiness is hugely reassuring to me. Anyone who knows someone with profound autism will understand, if WPI has found a solid link, that the Africa comment was not particularly inappropriate. The agony that condition causes in families cannot be overstated. Agony is agony, whether it causes death or not...as we all know.
The examples that you and Rebecca cite- CAA (I am infering McCleary and Vernon) and Dr. Klimas are women, so they don't support the charge of sexism against Dr. M. I do think some of Dr. M's statements are probably at least a stretch and are counterproductive. (She has also done more than almost any other scientist for us so overall she gets much luv from me).
The results of DeFreitas' leg was definitely in OW. I remember it clearly. I will try to find it if you would like.
He cited, in addition, thirty year old medical papers that pinned recovery speed among mono and influenza victims to "the emotional state of the patient." "If we had been aware of these studies," he said, "some of us might not have tried to reinvent the wheel" by attempting to assign the disease a virological cause...
[Retroviral causation] "doesn't make any sense because ...retroviral infection... includes progressive hematologic, immunologic and neurologic deficits in one mix or another, and those aren't really prominent features of chronic fatigue syndrome."...
[Re: DeFreitas' work] "there's really no good scientific merit to it." He further posited, "There is no current evidence for chronic infection in CFS. Therefore, broad screening of CFS patients for infections is completely unwarranted. Your patients may demand exotic screenings," he added, "but it's only confusing."...
A significant portion of the symptomology of the disease, he commented, was a result of "poor sleep hygiene" and failure to exercise: "Patients exacerbate things because they take multiple naps during the day and break up their rest periods and sleep periods. They stay in bed a lot...
The scientist was roundly applauded, with at least one audience member shouting, "hear, hear!"
[emphasis added]
If you are a researcher, and you see that CFS Europeans are testing positive for XMRV, ASD children are testing positive for XMRV, would you sit back and do nothing? Seriously?
sorry to hear about your loss Martlet.
Correlation is not causation, it isn't until a plausible mechanism is shown to have the effect that the link can be considered highly likely to be real.
The Chicago article has made the LA Times.
http://www.latimes.com/news/health/la-he-chronic-fatigue-20100614,3,5214211.story
Seattle Times
http://seattletimes.nwsource.com/text/2012093566.html
About the LA reprint:
The emails mentioned in the tribune, which I suspected had been sent as part of the interview have been labeled as part of the interview.
The emails with the worst quotations, which I suspected had text taken (with purpose) out of context has been removed.
The article looks totally different with just small changes.
I'd really like to see which context the quotes from the original article was taken from. I'll repeat what I wrote earlier, if Mikovits wanted to send out messages such as "Our continent will be like HIV Africa only worse!" without a specific context, she could have done so in other ways than to write it to Trine.