work with Montoya
look for infectious agents - plasma samples in order to look at genetic data
agents are: HHV6, Herpes simplex 1 & 2 , EBV, parvo, enterovirus, retrovirus, CMV, west nyle and about ten more
samples 285 cases and 201 controls
HHV6 - 4 cases and 2 controls
4 HHV6b and 2 HHV6a very small proportion found in CFS potential confound but pretty much meaningless
no others found
confident that everything would have been detected.
found 85% retroviruses in the pool - no conclusion that there is a relationship to disease. doesn't think it will pan out
Presently looking for agents - viruses, infections in 400 patients looking for bacteria with specific method ?
looking at fecal material - very expensive and takes a long time - this is early days - need funding
I didn't hear him say, only that's where cut off was. I missed first part though.
INteresting thing is, if someone is going to get better, that's the time frame they usually do. The long standing me/cfs docs have long said that. Now there is data to go along.
I thought he was testing for shedloads of viruses but that doesn't seem like a very long list.
I've got a special interest in HHV-6 - was that PCR coming up negative, as opposed to antibody titres? HHV-6 virus particles are supposed to hard to detect, even in tissue (since there may not be any in the particular sample you've got). Anybody got any views on the HHV-6 findings?
I was surprised he gave out so much info! Did he say anything about publication plans?
Comparing now in ME/CFS research to early year AIDS research. I've been sick for 27 years. I have been in studies from the first year on. Well now studies don'w want those who have been sick this long.
I have a knife in my heart. This isn't early. It's late. And I know many more who have been sick longer.
Why didn't he make more noise in 1997 when he published ?
Crap. I know better than to look back. Doesn't do any good.
Don't mind me. It's been a long haul, some days are harder than others.
ETA: Thank you Nielk for the updates. I got in on the call late.
How do we go about trying to get more funding for Dr. Lipkin and his colleagues? So he can pursue the microbiome work, he thinks that that's where we will find answers. He brought it up three times that he needs money to fund this project and he has enough money for 10% of the study.
It would be great if someone on this forum who isn't as brain dead as I, could put together a letter that we could copy and paste into emails to our congressman. And maybe make a list of people we could email this letter to and keep emailing them daily until we get something done. We have this great researcher who seems to be onto something and needs more money. But instead our government wants to spend our tax dollars on high end vacations, lobster dinners, catered breakfast meetings etc... Sorry just a little bitter.
How do we go about trying to get more funding for Dr. Lipkin and his colleagues? So he can pursue the microbiome work, he thinks that that's where we will find answers. He brought it up three times that he needs money to fund this project and he has enough money for 10% of the study.
Was he saying that we ought to be getting congress people to get more money for ME/CFS research for the NIH and CDC? If so, would there be any guarantee that they'd fund Lipkin to do the other 90% of the study? Is there something more direct to ask for?
Maybe we have advocates who could work with him to come up with a suitable letter, even if he was just advising rather than signing. He has a much better idea of how stuff works than we do. Does anyone have a contact? Nielk? medfeb? jspotila?