Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 I did get something from a local allergy specialist called a staph toxoid vaccine which I found brilliant- yet it wore off quick.Apparently there's a couple of different versions of this and I think it's big vetenary medicine more than human medicine. There's a company in switzerland BERN pharmaceuticals that make this- I think.It's also sometyhing that comes in different grades or strengths again the one I got isn't necessarily the one that they talk about in the study. Actually to give you an idea of the vaccine I put subdermally- while flaring/feeling miserable it stopped me almost after 10 minutes.Th effect sort of lasts the day and the preceeding days aren't as bad. More later I'm out the door. tony > Hey Tony, I found that study you posted about the therapeutic use of > PST [purified staph toxin] totally fascinating. > > I was wondering if you could elaborate on a few things: > > 1) I easily found multiple references to the PST experiments, but > not to the initial findings that gave rise to them, which I think is > where a lot of your excitement came from. Can you help point me to > more documentation on just what the Newcastle researchers found that > was different in CFS patients? What was that test they used, that > was telling us docs weren't sure how to interpret? I'd like > to know as much about that as possible. > > 2) Readings gave me the impression that PST was widely used in > Russia, and that this had something to do with a prevalence of abx- > resistant staph - are you familiar with that side of it? I found > references to it being used for atopic dermatitis, as well as CFS > and FM - anything else? > > 3) It seems kinda unfortuante that the PST CFS/FM studies relied so > heavily on a psychiatric assessment, the Comprehensive > Psychopathological Rating Scale, to determine improvements. Any idea > why things more directly relevant to the diagnoses, like tender > point sensitivity, exercise tolerance, physical stamina, cognitive > performance, etc weren't used? > > 4) I found references to one of the Newcastle guys > saying " antibiotics are useless in these patients. " What do you make > of that statement? It seems like that assessment led directly to the > use of PST, but I'd like to know more on how they arrived at it. > > 5) Do you know if PST is still in wide clinical use in Russia? Has > it ever made into clinical use anywhere else? > > I know, lots of questions. But that's what happens when I read > something interesting. I wanna know more. > > The highest-priority question is my first one, about the testing > that lead up to this. Where the heck is the documentation for that? > Did I just miss it? > > Thanks much, > > S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Tony, and the group, Staph toxoid has been studied by a group in Sweden for treating CFS for several years, and they have had some success, but they have to keep doing it. Again, I think it's a case of not getting the immune system to the point where it can take over and hold off the bugs. It would be interesting to know how these people would have responded if their glutathione had been built up at the same time they were given the staph toxoid. Here is the abstract of their most recent paper: Eur J Pain. 2002;6(6):455-66. Treatment with staphylococcus toxoid in fibromyalgia/chronic fatigue syndrome--a randomised controlled trial. Zachrisson O, Regland B, Jahreskog M, Jonsson M, Kron M, Gottfries CG. Psychiatry Section, Institute of Clinical Neuroscience, Goteborg University, Goteborg, Sweden. olof.zachrisson@... We have previously conducted a small treatment study on staphylococcus toxoid in fibromyalgia (FM) and chronic fatigue syndrome (CFS). The aim of the present study was to further assess the efficacy of the staphylococcus toxoid preparation Staphypan Berna (SB) during 6 months in FM/CFS patients. One hundred consecutively referred patients fulfilling the ACR criteria for FM and the 1994 CDC criteria for CFS were randomised to receive active drug or placebo. Treatment included weekly injections containing 0.1 ml, 0.2 ml, 0.3 ml, 0.4 ml, 0.6 ml, 0.8 ml, 0.9 ml, and 1.0 ml SB or coloured sterile water, followed by booster doses given 4-weekly until endpoint. Main outcome measures were the proportion of responders according to global ratings and the proportion of patients with a symptom reduction of > or =50% on a 15-item subscale derived from the comprehensive psychopathological rating scale (CPRS). The treatment was well tolerated. Intention-to-treat analysis showed 32/49 (65%) responders in the SB group compared to 9/49 (18%) in the placebo group (P<0.001). Sixteen patients (33%) in the SB group reduced their CPRS scores by at least 50% compared to five patients (10%) in the placebo group (P< 0.01). Mean change score on the CPRS (95% confidence interval) was 10.0 (6.7-13.3) in the SB group and 3.9 (1.1-6.6) in the placebo group (P<0.01). An increase in CPRS symptoms at withdrawal was noted in the SB group. In conclusion, treatment with staphylococcus toxoid injections over 6 months led to significant improvement in patients with FM and CFS. Maintenance treatment is required to prevent relapse. Publication Types: Clinical Trial Randomized Controlled Trial PMID: 12413434 [PubMed - indexed for MEDLINE] Rich > > I did get something from a local allergy specialist called a staph > toxoid vaccine which I found brilliant- yet it wore off > quick.Apparently there's a couple of different versions of this and > I think it's big vetenary medicine more than human medicine. There's > a company in switzerland BERN pharmaceuticals that make this- I > think.It's also sometyhing that comes in different grades or > strengths again the one I got isn't necessarily the one that they > talk about in the study. > Actually to give you an idea of the vaccine I put subdermally- while > flaring/feeling miserable it stopped me almost after 10 minutes.Th > effect sort of lasts the day and the preceeding days aren't as bad. > More later I'm out the door. > tony > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Yep, Rich, this is the study Tony shared with us that got it the discussion started. It's a shame the effects are so temporary, but very interesting that they occur at all. I had the same thought you did, that it would have been interesting to see it combined with glutathione or its precursors. Mostly, I would like to understand better how it works. Not a true vaccine, since it doesn't develop immunity - but what exactly IS it doing? > > > > I did get something from a local allergy specialist called a staph > > toxoid vaccine which I found brilliant- yet it wore off > > quick.Apparently there's a couple of different versions of this > and > > I think it's big vetenary medicine more than human medicine. > There's > > a company in switzerland BERN pharmaceuticals that make this- I > > think.It's also sometyhing that comes in different grades or > > strengths again the one I got isn't necessarily the one that they > > talk about in the study. > > Actually to give you an idea of the vaccine I put subdermally- > while > > flaring/feeling miserable it stopped me almost after 10 minutes.Th > > effect sort of lasts the day and the preceeding days aren't as bad. > > More later I'm out the door. > > tony > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 I truly think it helps you cope with thge toxins. I feel the failure of any therapy in fibro/cfs falls at the feet of the hammering your body has endured while not being treated often for several years.If you walked up to a healthy cow in the field and walked up to a human in a shopping mall the cow is closer to pristine than the battered human. So therpy in the animal model may not relate nicely to the battered human model. Frequently the battered human model is carrying a mouth full of multiple infection sites due to lifestyle choices, high sugar, high fat, processed foods with additives, coagulating blood. The cow would be the better candidate to treat because it's never as far from baseline health/habits as many humans may be. > > > > > > I did get something from a local allergy specialist called a > staph > > > toxoid vaccine which I found brilliant- yet it wore off > > > quick.Apparently there's a couple of different versions of this > > and > > > I think it's big vetenary medicine more than human medicine. > > There's > > > a company in switzerland BERN pharmaceuticals that make this- I > > > think.It's also sometyhing that comes in different grades or > > > strengths again the one I got isn't necessarily the one that > they > > > talk about in the study. > > > Actually to give you an idea of the vaccine I put subdermally- > > while > > > flaring/feeling miserable it stopped me almost after 10 > minutes.Th > > > effect sort of lasts the day and the preceeding days aren't as > bad. > > > More later I'm out the door. > > > tony > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 I'll attempt to recall whjat I remember about the cfs newcastle stuff.The urine metabolites that they observed using I think gas chromotography, just basically sophisticated lab equipemnt- enabled them to screen for pain markers and depression markers.When you pee the inflammation/toxins tell a lot of stories in your urine. The urine is not the same once you cross over into autoimmune.A simple explanation I suppose, but looking for markers is informative. The screwed bowel flora, a move away from beneficial E coli which in most number 80%- to 40% in the ill, followed closely by alpha haemolytic streptococcus an oral only bacteria, then high number's of enterococcus possably a food chain demented bug. High levels of vancomycin resistant enterococcus appear in supermarket chickens.(1 in 10). So basically you have slime and post nasal drip often that your not even aware of that keeps the stomach and bowel under the pump from sinus oral flows that just keep the toxic bacteria eroding and dementing your whole bowel flora.People are alway's trying to add the supplements yet DON " T ADDRESS THE SINUS PROBLEM. You can't colonise the gut correctly when an all day drip can add up to a bucket load of slime. The other finding was the toxic molecule produced by coagulase negative staph that was just shy of a staph areus toxic molecule. They also realise that these staph produce toxic shock toxins, delta toxins. It's basically a study totally focused on sinus bacteria flowing into screwed bowel flora bacteria and toxin expression of bacteria causing pain and many irregularioties in the body showing up as screwd urine markers not like normal folk. tony > Hey Tony, I found that study you posted about the therapeutic use of > PST [purified staph toxin] totally fascinating. > > I was wondering if you could elaborate on a few things: > > 1) I easily found multiple references to the PST experiments, but > not to the initial findings that gave rise to them, which I think is > where a lot of your excitement came from. Can you help point me to > more documentation on just what the Newcastle researchers found that > was different in CFS patients? What was that test they used, that > was telling us docs weren't sure how to interpret? I'd like > to know as much about that as possible. > > 2) Readings gave me the impression that PST was widely used in > Russia, and that this had something to do with a prevalence of abx- > resistant staph - are you familiar with that side of it? I found > references to it being used for atopic dermatitis, as well as CFS > and FM - anything else? > > 3) It seems kinda unfortuante that the PST CFS/FM studies relied so > heavily on a psychiatric assessment, the Comprehensive > Psychopathological Rating Scale, to determine improvements. Any idea > why things more directly relevant to the diagnoses, like tender > point sensitivity, exercise tolerance, physical stamina, cognitive > performance, etc weren't used? > > 4) I found references to one of the Newcastle guys > saying " antibiotics are useless in these patients. " What do you make > of that statement? It seems like that assessment led directly to the > use of PST, but I'd like to know more on how they arrived at it. > > 5) Do you know if PST is still in wide clinical use in Russia? Has > it ever made into clinical use anywhere else? > > I know, lots of questions. But that's what happens when I read > something interesting. I wanna know more. > > The highest-priority question is my first one, about the testing > that lead up to this. Where the heck is the documentation for that? > Did I just miss it? > > Thanks much, > > S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Thanks much, Tony! This is a nice, clear, explanation. I think the question that remains, that really needs to be answered to help people get these cultures done, is why: a) We have the Newcastle guys saying " antibiotics are useless with these patients " We have Tarello (who seems to be looking at blood, not gut flora or unite metabolites, though maybe he did those too) saying arsenic works like a charm but 3 years of antibiotics got him and his wife nowhere. In other words, where you went with these findings, to culturing and treating with abx based on what cultures reveal, is not where either of these researchers seem to have ended up. Why is that? S. > > Hey Tony, I found that study you posted about the therapeutic use > of > > PST [purified staph toxin] totally fascinating. > > > > I was wondering if you could elaborate on a few things: > > > > 1) I easily found multiple references to the PST experiments, but > > not to the initial findings that gave rise to them, which I think > is > > where a lot of your excitement came from. Can you help point me to > > more documentation on just what the Newcastle researchers found > that > > was different in CFS patients? What was that test they used, that > > was telling us docs weren't sure how to interpret? I'd > like > > to know as much about that as possible. > > > > 2) Readings gave me the impression that PST was widely used in > > Russia, and that this had something to do with a prevalence of abx- > > resistant staph - are you familiar with that side of it? I found > > references to it being used for atopic dermatitis, as well as CFS > > and FM - anything else? > > > > 3) It seems kinda unfortuante that the PST CFS/FM studies relied > so > > heavily on a psychiatric assessment, the Comprehensive > > Psychopathological Rating Scale, to determine improvements. Any > idea > > why things more directly relevant to the diagnoses, like tender > > point sensitivity, exercise tolerance, physical stamina, cognitive > > performance, etc weren't used? > > > > 4) I found references to one of the Newcastle guys > > saying " antibiotics are useless in these patients. " What do you > make > > of that statement? It seems like that assessment led directly to > the > > use of PST, but I'd like to know more on how they arrived at it. > > > > 5) Do you know if PST is still in wide clinical use in Russia? Has > > it ever made into clinical use anywhere else? > > > > I know, lots of questions. But that's what happens when I read > > something interesting. I wanna know more. > > > > The highest-priority question is my first one, about the testing > > that lead up to this. Where the heck is the documentation for > that? > > Did I just miss it? > > > > Thanks much, > > > > S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 wrote: " The other finding was the toxic molecule produced by coagulase negative staph that was just shy of a staph areus toxic molecule. " If you've read Ritchie Shoemaker's theories on Coag Neg Staph, how does this relate? Are you saying that the staph areus produces toxins as bad as the coag neg staph? What urine tests are done to show auto-immune problems that follow these staph infections and toxin buildup? I'm tuning in late here, and I will read more, but is the use of PST like homeopathy/energy medicine? Thanks! > > Hey Tony, I found that study you posted about the therapeutic use > of > > PST [purified staph toxin] totally fascinating. > > > > I was wondering if you could elaborate on a few things: > > > > 1) I easily found multiple references to the PST experiments, but > > not to the initial findings that gave rise to them, which I think > is > > where a lot of your excitement came from. Can you help point me to > > more documentation on just what the Newcastle researchers found > that > > was different in CFS patients? What was that test they used, that > > was telling us docs weren't sure how to interpret? I'd > like > > to know as much about that as possible. > > > > 2) Readings gave me the impression that PST was widely used in > > Russia, and that this had something to do with a prevalence of abx- > > resistant staph - are you familiar with that side of it? I found > > references to it being used for atopic dermatitis, as well as CFS > > and FM - anything else? > > > > 3) It seems kinda unfortuante that the PST CFS/FM studies relied > so > > heavily on a psychiatric assessment, the Comprehensive > > Psychopathological Rating Scale, to determine improvements. Any > idea > > why things more directly relevant to the diagnoses, like tender > > point sensitivity, exercise tolerance, physical stamina, cognitive > > performance, etc weren't used? > > > > 4) I found references to one of the Newcastle guys > > saying " antibiotics are useless in these patients. " What do you > make > > of that statement? It seems like that assessment led directly to > the > > use of PST, but I'd like to know more on how they arrived at it. > > > > 5) Do you know if PST is still in wide clinical use in Russia? Has > > it ever made into clinical use anywhere else? > > > > I know, lots of questions. But that's what happens when I read > > something interesting. I wanna know more. > > > > The highest-priority question is my first one, about the testing > > that lead up to this. Where the heck is the documentation for > that? > > Did I just miss it? > > > > Thanks much, > > > > S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Most people are doing the 2 doxy a day recommended by the fda type treatments(mostly failure). I believe in the multi therapy with best choice, and understanding you have area's so damaged they need long hard therapy similar to tuberculosis to chisel away at them. Also I advocate IV hard therapy because it's encephalitis/meningitis that alway's gets serious treatment. Do you understanbd what upto 80 grams of penicillin a day looks like? Compare that to 1 gram of ceftriaxone or if your lucky 2 grams. Who's trying to get an infection out seriously, the guy that's dosing meningitis/blood poisioning levels or the 2 doxy a day mild improvement dudes.Can you see where the pharmaceutical literature doesn't stack up? Tarello and newcastle are doing recommended stuff yet the literature is what's incorrect and why you see I'm a little twisted in my beliefs. An egs. I often quote is my cousins run in wityh his strep throat episodes, once yearlky and maybe sometimes twice yearly. A whole box of amoxacillin doesn't cut it, one jab in the ass and he's good to go an hour later.The medicalk literature mostly doesn't stack up, I also observe this with all the patients that supposedly do this that and the otherand they were like labratory rats that got well and my friends hunt them down and there not there? Again tarello does the fda recommende 2 doxy a day and gets knowhere on an infection this size. His arsenical therapy distributes thru tissue like no other therapy.His animal models again are different than us. I think of a cow and how it would be fit for consumption, if they dissected us we would fail to pass all the consumption tests. What do we have as an option? I know that it's an engrained bone eroding soft tissue destroying infection opf the hiughest magnitude- I just adopt ideologies like TUBERCULSOS attack into my line of thinking because I know our infection to be larger than this. > > > Hey Tony, I found that study you posted about the therapeutic > use > > of > > > PST [purified staph toxin] totally fascinating. > > > > > > I was wondering if you could elaborate on a few things: > > > > > > 1) I easily found multiple references to the PST experiments, > but > > > not to the initial findings that gave rise to them, which I > think > > is > > > where a lot of your excitement came from. Can you help point me > to > > > more documentation on just what the Newcastle researchers found > > that > > > was different in CFS patients? What was that test they used, > that > > > was telling us docs weren't sure how to interpret? I'd > > like > > > to know as much about that as possible. > > > > > > 2) Readings gave me the impression that PST was widely used in > > > Russia, and that this had something to do with a prevalence of > abx- > > > resistant staph - are you familiar with that side of it? I found > > > references to it being used for atopic dermatitis, as well as > CFS > > > and FM - anything else? > > > > > > 3) It seems kinda unfortuante that the PST CFS/FM studies relied > > so > > > heavily on a psychiatric assessment, the Comprehensive > > > Psychopathological Rating Scale, to determine improvements. Any > > idea > > > why things more directly relevant to the diagnoses, like tender > > > point sensitivity, exercise tolerance, physical stamina, > cognitive > > > performance, etc weren't used? > > > > > > 4) I found references to one of the Newcastle guys > > > saying " antibiotics are useless in these patients. " What do you > > make > > > of that statement? It seems like that assessment led directly to > > the > > > use of PST, but I'd like to know more on how they arrived at it. > > > > > > 5) Do you know if PST is still in wide clinical use in Russia? > Has > > > it ever made into clinical use anywhere else? > > > > > > I know, lots of questions. But that's what happens when I read > > > something interesting. I wanna know more. > > > > > > The highest-priority question is my first one, about the testing > > > that lead up to this. Where the heck is the documentation for > > that? > > > Did I just miss it? > > > > > > Thanks much, > > > > > > S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 I think the toxin staph areus produces which causes ACUTE ILL HEALTH is just shy of the mark when you look at this new toxin coagulase negative staph produces that the newcastle team studied in the sinus issues.It's basically a 25 molecule toxin just shy of the 26 molecule staph areus toxin.I just read this yerars ago and this is a vague overview. I know that everything they did they did it according to all the correct protocols as opposed to tarello a single operator that just shared his own experiences and did what the merck manual and examples of animal disease and arsenicals had to offer. > > > Hey Tony, I found that study you posted about the therapeutic use > > of > > > PST [purified staph toxin] totally fascinating. > > > > > > I was wondering if you could elaborate on a few things: > > > > > > 1) I easily found multiple references to the PST experiments, but > > > not to the initial findings that gave rise to them, which I think > > is > > > where a lot of your excitement came from. Can you help point me > to > > > more documentation on just what the Newcastle researchers found > > that > > > was different in CFS patients? What was that test they used, that > > > was telling us docs weren't sure how to interpret? I'd > > like > > > to know as much about that as possible. > > > > > > 2) Readings gave me the impression that PST was widely used in > > > Russia, and that this had something to do with a prevalence of > abx- > > > resistant staph - are you familiar with that side of it? I found > > > references to it being used for atopic dermatitis, as well as CFS > > > and FM - anything else? > > > > > > 3) It seems kinda unfortuante that the PST CFS/FM studies relied > > so > > > heavily on a psychiatric assessment, the Comprehensive > > > Psychopathological Rating Scale, to determine improvements. Any > > idea > > > why things more directly relevant to the diagnoses, like tender > > > point sensitivity, exercise tolerance, physical stamina, > cognitive > > > performance, etc weren't used? > > > > > > 4) I found references to one of the Newcastle guys > > > saying " antibiotics are useless in these patients. " What do you > > make > > > of that statement? It seems like that assessment led directly to > > the > > > use of PST, but I'd like to know more on how they arrived at it. > > > > > > 5) Do you know if PST is still in wide clinical use in Russia? > Has > > > it ever made into clinical use anywhere else? > > > > > > I know, lots of questions. But that's what happens when I read > > > something interesting. I wanna know more. > > > > > > The highest-priority question is my first one, about the testing > > > that lead up to this. Where the heck is the documentation for > > that? > > > Did I just miss it? > > > > > > Thanks much, > > > > > > S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2005 Report Share Posted July 28, 2005 Interesting that someone has markers in the urine, I could smell a difference in my urine when I was feeling miserable. Kind of a soft fruity vanilla peach odor to it. I was wondering about this for a while. I'm feeling better and my urine has the more normal urine smell. This is a very qualitative observation. I was Bowen positive for Lyme. You could see the L form spheres of Lyme in the WBC/Monocytes? flourese in the photos they sent. > > Hey Tony, I found that study you posted about the therapeutic use > of > > PST [purified staph toxin] totally fascinating. > > > > I was wondering if you could elaborate on a few things: > > > > 1) I easily found multiple references to the PST experiments, but > > not to the initial findings that gave rise to them, which I think > is > > where a lot of your excitement came from. Can you help point me to > > more documentation on just what the Newcastle researchers found > that > > was different in CFS patients? What was that test they used, that > > was telling us docs weren't sure how to interpret? I'd > like > > to know as much about that as possible. > > > > 2) Readings gave me the impression that PST was widely used in > > Russia, and that this had something to do with a prevalence of abx- > > resistant staph - are you familiar with that side of it? I found > > references to it being used for atopic dermatitis, as well as CFS > > and FM - anything else? > > > > 3) It seems kinda unfortuante that the PST CFS/FM studies relied > so > > heavily on a psychiatric assessment, the Comprehensive > > Psychopathological Rating Scale, to determine improvements. Any > idea > > why things more directly relevant to the diagnoses, like tender > > point sensitivity, exercise tolerance, physical stamina, cognitive > > performance, etc weren't used? > > > > 4) I found references to one of the Newcastle guys > > saying " antibiotics are useless in these patients. " What do you > make > > of that statement? It seems like that assessment led directly to > the > > use of PST, but I'd like to know more on how they arrived at it. > > > > 5) Do you know if PST is still in wide clinical use in Russia? Has > > it ever made into clinical use anywhere else? > > > > I know, lots of questions. But that's what happens when I read > > something interesting. I wanna know more. > > > > The highest-priority question is my first one, about the testing > > that lead up to this. Where the heck is the documentation for > that? > > Did I just miss it? > > > > Thanks much, > > > > S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2005 Report Share Posted July 28, 2005 That fruity smell is frequently pseudonomads in my culture plates. But there's no way known on the planet that your good when your violently ill, on carefull observation half the inside of your bladder is showing up in your urine.I just get so pissed off when the crap that is fed to people is gobbled up like gospel.When you get ill you can feel the inflammation/TOXINS in your urine even-IT'S JUST NO LONGER THE SAME WHEN YOU CROSS THE LINE INTO ILL HEALTH. > > > Hey Tony, I found that study you posted about the therapeutic > use > > of > > > PST [purified staph toxin] totally fascinating. > > > > > > I was wondering if you could elaborate on a few things: > > > > > > 1) I easily found multiple references to the PST experiments, > but > > > not to the initial findings that gave rise to them, which I > think > > is > > > where a lot of your excitement came from. Can you help point me > to > > > more documentation on just what the Newcastle researchers found > > that > > > was different in CFS patients? What was that test they used, > that > > > was telling us docs weren't sure how to interpret? I'd > > like > > > to know as much about that as possible. > > > > > > 2) Readings gave me the impression that PST was widely used in > > > Russia, and that this had something to do with a prevalence of > abx- > > > resistant staph - are you familiar with that side of it? I found > > > references to it being used for atopic dermatitis, as well as > CFS > > > and FM - anything else? > > > > > > 3) It seems kinda unfortuante that the PST CFS/FM studies relied > > so > > > heavily on a psychiatric assessment, the Comprehensive > > > Psychopathological Rating Scale, to determine improvements. Any > > idea > > > why things more directly relevant to the diagnoses, like tender > > > point sensitivity, exercise tolerance, physical stamina, > cognitive > > > performance, etc weren't used? > > > > > > 4) I found references to one of the Newcastle guys > > > saying " antibiotics are useless in these patients. " What do you > > make > > > of that statement? It seems like that assessment led directly to > > the > > > use of PST, but I'd like to know more on how they arrived at it. > > > > > > 5) Do you know if PST is still in wide clinical use in Russia? > Has > > > it ever made into clinical use anywhere else? > > > > > > I know, lots of questions. But that's what happens when I read > > > something interesting. I wanna know more. > > > > > > The highest-priority question is my first one, about the testing > > > that lead up to this. Where the heck is the documentation for > > that? > > > Did I just miss it? > > > > > > Thanks much, > > > > > > S. Quote Link to comment Share on other sites More sharing options...
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