Judy is definitely sticking around. She was on a video with some European researchers and doctors talking about Rituximab and she and her mentor are involved in an ME/CFS study with Frank Rice, I believe it is, looking for pathogens.
it would be interesting to hear abit more about her current work.Judy is definitely sticking around. She was on a video with some European researchers and doctors talking about Rituximab and she and her mentor are involved in an ME/CFS study with Frank Rice, I believe it is, looking for pathogens.
Yeah I'd like to know what her direction is now? I'd think it has to be with viruses.it would be interesting to hear abit more about her current work.
I think even her initial research before she found xmrv??? she noticed the immune dysfunction that to her looked like a retrovirus. Its possible it could be another retrovirus or some type of stealth adapted virus from ebv/cmv etcYeah I'd like to know what her direction is now? I'd think it has to be with viruses.
I am curious as too what ARVs you are refering to as their are many?She stands by all her work on :
XMRVs MIKOVITS/RUSCETTI :
viruses very different to :
XMRV SILVERMANN which is the virus that Lipkin and the other negative authors reduced their testing scale to.
The smart crowd have worked it all out. It's all documented by articles,video,sound and common sense observations in mainstream n second stream media,such as no third decisive samples being given in the Lipkin study, for instance. Great power he had if he couldnt power his own study.Delusional..
We are at the breaking point.
Breaking through the semantics and old tricks.
And the band plays on.......There was never any contaminations at the essential cut-off periods of the critical laboratory stages. And there were two labs also anyway where she worked. Again, the negative papers and Lipkin s definitive negative all went after the wrong viruses....no matter their prestige or their names THEY MESSED UP.
And messed with peoples lives too...
Trash in. Garbage out. If Mikovits had not been sent to jail then she n Ruscetti could have worked to fine tune their discovery instead of everybody just guessing n presuming n assuming what they had found originally as xmrv silvermann...daft.
I just wish all these non ME ers would leave the scene. These fake CFS ers. Patients. Bogus scientists too pretending n mixing n messing up with fake experimental protocols and not doing it right for the real patients for the real rv.
Just leave us alone. We have a RV. It isnt funny. Just go away. Stop messing.
The inconvenient truth is that arv s cure real ME. The cost to society is huge. Just testing everybody is a huge bill to foot. Then the arv meds. But only about 15% of those diagnosed need continuous follow up testing n treating. Only 15% have it n need treatment for it.
85% of the patients need other treatments for their persisting symptoms,however real n undefined they are. ME is NOT on their spectrum.
Im not ruling out retroviruses playing a role in cfsme but what you are saying is just your opinion. Even judy mikovits said that xmrv has a possible association with cfsme. As for 5/6ths dont have ME, that just shows you are plucking numbers out of thin air. Im sure you dont know everyone's medical history.Five sixths of people on this forum and other forum(s) dont have ME. And dont need arv's. They have Wessely/Lipkin CFS..
End of Story.
So in response to this I would agree that their are people on these forums that do not have ME. To give a stat I dont think that is even possible.Five sixths of people on this forum and other forum(s) dont have ME. And dont need arv's. They have Wessely/Lipkin CFS..
End of Story.
Do you have a link to the video I would like to hear a bit about her theories etc.?Judy is definitely sticking around. She was on a video with some European researchers and doctors talking about Rituximab and she and her mentor are involved in an ME/CFS study with Frank Rice, I believe it is, looking for pathogens.
Maybe preface your comments with "it is my opinion" or "I believe".Five sixths of people on this forum and other forum(s) dont have ME. And dont need arv's. They have Wessely/Lipkin CFS..
End of Story.