Inside the Labyrinth: Osler's Web Updates

Lies and the Lying Liars Who Tell Them (with apologies to Senator Al Franken) Copyright (C) by Hillary Johnson 2009 All Rights Reserved

August 7, 2009

Tags: Christine Heim, Emory University

We’re in a whole lot of trouble, people. I’m sorry, but it’s bad. There’s no easy way to break this and one shouldn’t even try because this requires real speak.

Appreciation and hats off to Craig Maupin’s excellent summary on July 30 (posted on Co-Cure) of an editorial in a journal called, “Future Neurology.” The five-page (including citations) editorial was penned by a former CDC-employee (Senior Scientist, 2001-2006), now employed in the psych dept. at Emory University. Her name is Christine Marcelle Heim; she reveres Sigmund Freud and she even has a breathy German accent to complement that veneration. You can write to her at cmheim@emory.edu.

Thank you Mr. Maupin, once again, for putting it out there. You are not an army of one. You are not alone. You get it, and I suspect there are thousands of others who get it, too, people who are so discouraged and ill and lacking a voice they can only acknowledge the purport of Heim’s pretend-authority—and roll over in despair.

Christine Heim cut her teeth in the Centers for Disease Control and Promotion “CFS” program, the little propaganda mill run by Bill Reeves at the agency in Atlanta. She’s a graduate of that pogrom—I mean, program. If there was any doubt that she is a mouthpiece for the CDC’s attack strategy, the first sentence in her competing interests disclosure is, “The work discussed in this editorial was supported by the CDC (Atlanta, Ga., USA).”

She is a psychologist and a member since 1988 of the American Psychosomatic society. She put in her time with Wm. Reeves, thereby copping enough CDC swagger to allow her to make the short trip from 1600 Clifton Road to Emory and be awarded an associate professor title and tenure. Emory is lousy with CDC émigrés; the money’s better; it’s more prestigious. Just a quick turn to the right and a ten minute walk—and a demonstrated commitment to CDC pod-speak—will get you there. Heim carried the CDC mission statement into the department of psychiatry, whose shrinks and hangers-on, as the redoubtable Mary Schweitzer noted in her July 19 blog post, “Political Psychiatry vs. Medical Theories of Illness in ME and CFS," “…have received more CFS consulting contracts from CDC than any other single group of researchers.”

Allow me a big digression here: I would amend Schweitzer’s excellent observation to name two more beneficiaries of CDC largesse: let us never forget Abt Associates, the Haliburton of “chronic fatigue syndrome.” Abt has been clowning around purporting to collect “data” on CFS since 1988.

And let us also never forget the Bechtel of “CFS: the CFIDS Association of America, its director Kim McCleary, and its lobbyist, Tom Sheridan. The latter two don’t qualify as researchers, of course; they qualify as the principal enablers of Reeves and his strategies given that they a) coddled and protected Reeves from public disapprobation and possibly arrest for more than a decade and b) put their backs into the job of keeping the agency’s lies front and center in the media after accepting $4.5 million in a no-bid contract by the CDC to do so. Is it coincidence that the two websites Heim apparently feels worthy of listing at the end of her editorial for additional information about her child abuse+stress theory of “chronic fatigue syndrome” are the CAA and the Centers for Disease Control?

Back to Heim: By my count, she is the third member from the CDC “cfs” shop to make that quick stroll over to Emory. Reeves was the first. James Jones—formerly a respectable clinician researcher in this field in the early 1980s, now a shadow of a man mouthing Reeves-like-like pod-speak—was the second. There may be more before this reign of terror ends.


Heim’s editorial is, as I read it, a formal-if-gently stated declaration of war on people who suffer from myalgic encephalomyelitis. It is more a declaration of war even than the agency’s 2006 press conference, hosted by Kim McCleary, wherein Kim introduced, one by one, agency quacks with whom she’s had such cozy relations over the years and invited them to unveil their comprehensive “cfs” strategy. By then, after years of trial and error, the agency seemed to have finally settled upon a lie that they hoped would stick to the wall like well-cooked pasta: blame the pandemic on ill-defined genetic “predispositions” to being unable to handle stress, and the equally vague, scientifically unquantifiable “child abuse.”

In other words, cast the outbreak in such a way that all blame falls on people who have this “illness” (pod-speak doesn’t allow the word disease) or their abusive parents, link its origins to psychiatry and simultaneously assure the public that, although “real”—at least in the minds of those who suffer—and costly, “chronic fatigue syndrome” is the last thing they need to worry about. Obesity? Certainly. Swine Flu? For sure!

Heim’s editorial will receive greatly less publicity than the 2006 blow-out press conference. It’s highly unlikely that the Associated Press or the New York Times will feel obliged to describe it. In my view, its significance is hardly diminished, however. I read it as a comprehensive preview of the government’s strategic operating plan for the foreseeable future. It has the leaden feel of policy, of mission accomplished, and not in the ironic sense that the Bush administration’s premature announcement about its effort in Iraq came to represent. Read Heim’s treatise and weep.

Anyone who thought, for instance, that the request by that little committee in Washington for new “leadership” at CDC would somehow actually lead to new leadership—in the sense of a new day wherein upper-level agency staff actually ingest the massive accretion of scientific data about “cfs” and belatedly bear down on isolation of the pathogen causing this disease—may have to get a grip.


Heim’s piece is as much a roadmap as it is a clever piece of propaganda. She hews to the government lies on everything from excessive prevalence rates (2.5 percent) to excessive under-diagnosing—“less than 20 percent” and claims people are ill an “average duration” of 5-7 years. (If only!) Some of her sentences seemed ripped from the CDC website, the CAA website, or the agency’s 2006 press release. Like the agency pods who spawned her, she predictably employs that irritating phrase that’s part of the fake-compassion sentence that inevitably pops up whenever we are in pod-speak territory: “cfs” confers suffering and debilitation upon the (sic) “affected individuals.”

Do we hear this peculiar phrase, about how the disease imposes its burden of suffering on the (sic) “affected individuals,” when the topics are diseases like cancer, heart failure, COPD, AIDS or lupus? Isn’t that implied, as in, who else would the disease cause to feel debilitated? The cockatoo? The guy who reads the water meter? Call me a nit-picker, but the phrase seems to broadcast a message that one must feel sorry for “cfs” sufferers--even if (wink, wink) it’s all in their heads. Someone please furnish an example where this odd turn of phrase appears in discussions of other diseases and prove me wrong. I would be happy to concede this point.

And if you read Heim, that IS the message. Her arguments swing between the 1930s relic Hans Selye, who invented the concept of “stress," and the 19th century relic, Sigmund Freud, who invented the concept of female hysteria.

Heim points out that “some people” believe “cfs” is a “classic manifestation of Freud’s concept of hysteria…the unconscious simulation of organic disorders…” “Some people” being perhaps herself, the pods at CDC, and that charmer Peter Manu in Connecticut. She adds, helpfully, “Of note, Freud thought that hysteria is brought about by an infantile traumatic experience.” This is important to Heim, because the new, post-Osler’s CDC has become a towering monument to the childhood sex-abuse=CFS mantra. (When I started covering this story in 1986, the theory was just a gleam in their collective eye; they began by creating questionnaires, never actually administered, which focused quite intensely on bed-wetting histories.)

Heim conveniently avoids noting that Freud denied the reality of much of the sexual abuse adult women told him that they experienced in their childhoods. His grounds? He refused to believe sexual abuse of female children could be so widespread. Ergo, it was all in their heads.

Heim shows little interest in science that has come civilization’s way since Hans Seyle invented stress. Stuff like penicillin, artificial hearts, organ transplantation, stem cell research, MRI’s, CAT scans, anti-viral drugs, immunology. Heim so conveniently ignores developments in modern medicine, even her citations at the end of the paper were published years ago, and in the case of one, published by none other than Hans Seyle in 1949! A little writerly advice to Heim: I would not try to make my readers feel more confident about my argument by referencing a sixty-year-old paper.

Heim fails to cite a single study having to do with biological abnormalities in “cfs,” but there are papers on stress, childhood abuse, and even one about stress in baby rats and their mothers. Awesome. Her referenced authors include a few from the UK’s toxic shrink lobby, one from Canada’s denialist in chief—an old hack from way back named Irving Salit—and some authored by Heim and her colleagues at CDC.

Grasping the depraved agenda in Heim’s piece requires almost sentence by sentence deconstruction in order to demonstrate how much is being covered up rather than revealed.

Take this line, wherein she argues on behalf of the disease being a psychiatric problem because, “To date, more than 4,000 research studies have failed to identify a unanimous cause of CFS..” Her figure is actually fairly representative, if a tad understated, of the number of papers which have in fact demonstrated a multitude of grave biological abnormalities. She might have stated that these 4,000 papers all find serious abnormalities, but one can easily imagine how inconvenient to her argument such information would be. Indeed, not only would her career at Emory be in jeopardy, she would be committing an unforgivable act of disloyalty to staff at the Centers for Disease Control next door, who prepped her for her post at Emory. As we know, a critical piece of the agency’s marketing strategy is wrapped up in maintaining the lie that there are no biological abnormalities in “cfs.”

“High rates of psychiatric comorbidity have been reported for cases with CFS,” she lies in order to buttress the child abuse+stress=cfs explanation for the disease.

Check out this paragraph:

“Psychological or behavioral factors contributing to the development or maintenance of CFS include inactivity, avoidance behavior, anxiety sensitivity and stress…Behavioral interventions, such as cognitive-behavioral and graded exercise, are among the most effective treatments for CFS, perhaps providing the strongest support for the importance of psychological factors in CFS.”

I won’t drag you through Heim’s piece paragraph by paragraph, but will quote a choice line from her concluding paragraph, in which she exalts “modern developmental neuroscience” as the “key to CFS.”

“ …Insights from this line of research may help to overcome the prevailing rejection of the idea that psychological factors may play a role in CFS…Perhaps patients and advocacy groups fear to be labeled with the stigma of ‘simulating’ symptoms, as initially suggested by Freud…”

You bet, Chris! Fear doesn’t even cover it. Chris, can you say, “Cover up?”

Lastly, I would add that we are unfortunate to be suffering from an appallingly severe infectious disease during a period when the entire nation, indeed, Western culture, has come under the spell of a kind of neo-Christian Science. Should we blame Bernie Siegle and his wildly popular books in the 1980s about curing cancer with optimism? Do we look to the pompous Depak Chopra, or the quackish Dr. Weill, who have popularized the notion that vibrant health is within anyone's control if they think the right thoughts and eat the right food?

In this era of unconscionable scientific behavior on the part of our own government, it seems nearly every malady but cancer and HIV disease, the only two that appear to be unassailable, can be blamed on personality failings--or simply personality--but none more so than the grotesquely named "chronic fatigue syndrome." Indeed, it is the premier model for this distorted thinking; it's not only driving the movement, it's become the primary focus of the movement.

The CDC has had 26 years to bury reality under a barrage of propaganda. A generation has passed, a period during which collective memory of what actually occurred has dimmed. At the beginning of the 1980s the number of "cfs" cases was so small the disease went unmentioned in the medical literature. By the late 1980s, the emergence of "cfs" was an intensely debated and reported phenomenon due to the astonishing numbers of people affected. An entirely new generation of people diagnosed with "CFS" in recent years may not even appreciate the degree to which they've been maligned and victimized. They may not even understand that if the CDC had done it's due dilligence twenty-five years ago, there is a reasonable possiblity their lives would NOT have been ruined by so-called "cfs" at all, because preventative measures would have been initiated long ago.


What is fearful to me is not anything Heim has to say--because it's nonsense. I fear that the agency will increasingly be able to get away with this propaganda because the collective memory will begin to forget, if it hasn't already, how this all began.



My citation (and inspiration):
Craig Maupin's post to Co-Cure, July 30, 2009

"The following is a summary and a link to a recent editorial from one
of the principal voices of the CDC's Emory collaboration. (Future
Neurology July 2009, Vol. 4, No. 4). Dr. Christine Heim is a psychiatrist
and expert in stress/anxiety disorders. She was brought onboard the CDC's
efforts at Emory around 2002. The CDC has promised CFS advocates that they
would do more to use their position to educate researchers, clinicians, and
the public on CFS.


In her editorial, Dr. Heim explains the CDC program and the CDC's
conceptualization of CFS. Some of her main points revolve around a staple
of introductory-level psychiatry texts, how past experiences affect the
brain and neuroendocrine system.

"It must be demonstrated that early adverse experience is a risk factor for
CFS and: second, that this risk factor is associated with the cardinal
biological features of CFS." She encourages readers to conceptualize CFS
as a plastic encephalopathy -- "the causes of CFS are most likely to be
found at the brain level". Stress/trauma leads to brain deregulation,
which leads to low levels of the stress hormone cortisol. This biological
model is the same seen in post-traumatic stress disorders and, to some
extent, anxiety disorders.

Heim also covers the demographics of the CDC's CFS research
subjects:

"First and foremost, the condition is very common with up to 2.5 percent of
the population suffering from CFS in the USA. CFS affects four-times more
women than men, and most cases are middle aged individuals. The average
duration of CFS is cases identified form the population is 5-7 years."

According to Heim, an abusive and neglectful childhood environment
has been the best predictor of who will suffer from CFS. She bases this
claim on the research subjects who have been enrolled in CDC studies:
"Emotional neglect and sexual abuse were the best predictors of CFS....
Childhood trauma was further associated with CFS symptom severity and with
depression, anxiety and post-traumatic disorder (PTSD) symptoms".

She talks about what she feels is the importance of research into
subgroups of CFS. However, she is clear that future "subgroups" will lead
to the "same clinical picture".

In her final conclusion, Heim cites Freud and contends that
neuroscience will build a bridge of understanding and cooperation between
psychiatry and CFS patient groups who, she believes, have an irrational fear
of non-biological approaches to CFS research/treatment:

"In conclusion, adopting a developmental neuroscience perspective has
significant potential to advance our understanding of CFS. Insights from
this line of research may help overcome the prevailing rejection of the idea
that psychological factors may play a role in CFS, at least for a proportion
of cases. Perhaps patients and advocacy groups fear to be labeled with the
stigma of 'simulating' symptoms, as initially suggested by Freud.
However, modern neuroscience clearly demonstrates that experience shapes
biology (and vice versa), and, in this way, can create 'real' organic
symptoms."





Comments

  1. August 7, 2009 11:05 PM EDT
    Best predictor eh - and exactly how much of the variance does a "history of childhood trauma/abuse" predict? Read the studies - it' so small it's not predication at all.
    - Ken Davis - OT, Counsellor, PWC
  2. August 8, 2009 1:59 AM EDT
    Thank you for your blog article in which you draw attention to Christine Heim’s piece which outlines a ‘new’ perspective on CFS. I agree that it reveals a lot of the US Center for Disease Control (CDC)’s philosophy.

    First, I cannot believe that US patient groups are not going to back to Congress ‘claiming their money back’. In the last few years we have gone from a prevalence of around 0.4% of the population to an ever-growing 2.5%. I really think the CDC have overplayed their hand. By going with this 2.5% estimate it is clear they are studying a heterogeneous group of fatigued persons. The fact that Heim claims a high rate of psychiatric co-morbidity shows something is awry with their direction. While people continue to suffer, the CDC pursue their academic agenda.

    I have to laugh that Heim raises the issue of sub-classifying CFS patients. How long have patient advocates been saying this? Why do we have to keep waiting for this happen? Answer: until we inflate the population by 10-fold. Seriously, why can’t the post-infective, sudden-onset patient group be studied? Its not that hard. Except if you don’t want to find something tangible wrong, of course.

    Despite protestations to the contrary by the CDC, their new criteria checklist is clearly far more inclusive than anything before. (Leonard Jason has shown this.) How is this helping? How can the US Government be happy with this direction?

    So now the CDC’s neuropsychiatric paradigm has been laid out more clearly than ever before. We need to retrain our brains. Don’t get me wrong, there may be something in it. But it’s not the main event. Its not the heart of the matter. Will US policy-makers see that the Emperor has no clothes?

    A bio-psychosocial approach that is only concerned with the biology of stress is really just a psychosocial one.



    Paul Leverenz

    Chairman, ME/CFS Australia

    www.mecfs.org.au
    - Paul Leverenz
  3. August 8, 2009 4:28 AM EDT
    I do despair at the peer-review system when this level of quasi-religious belief is published under the auspices of 'future neurology'. Is no-one in medical science disciplines exercising critical faculties? Or is the belief in 'the power of the mind' the equivalent of a warm milky drink, and practitioners of 'future neurology' are sleeping through the peer review process?
    - Angela Kennedy
  4. August 8, 2009 9:43 AM EDT
    I truly believe that a huge percentage of the psychosomatic paradigm is based on CFS. People misdiagnosed using the 'Oxford' and 'Empirical' definitions and whom actually suffer from Depression/Anxiety disorders/PTSD muck up the emotional/psychiatric profiles of CFS patients in the medical literature, while correctly diagnosed CFS patients taking part in biomedical research provide the biological abnormalities shown. When the two are incorrectly combined, voila!
    - Tate Mitchell
  5. August 8, 2009 10:07 AM EDT
    Hillary,

    I share your feelings of outrage, especially after reading that editorial.

    The CFIDS Association has announced that they have switched to another lobbying firm. I hope Tom Sheridan is not used as a scapegoat for all the failures in lobbying for CFS. I got to know him well enough to trust his professional ethics. He would do what his clients wanted him to do, even if he thought it was the wrong thing to do. That happened early on in CFS lobbying after the CFIDS Association took over.

    The CFIDS Association has been in control of CFS lobbying for a very long time, and Kim McCleary has been in control of the CFIDS Association. Good or bad, right or wrong, it's Kim's responsibility.

    I note with additional dismay that Kim has used the 4 million prevalence figure from the newly bastardized CDC CFS definition, and that it is now used on the CFIDS Association web site.

    - Roy S
  6. August 8, 2009 11:01 AM EDT
    Great Job of investigating what's been allowed to go on and I agree Kim Must Go just as Reeves Must Go! The CDC and CAA's history of ignoring over the over 4000 biomedical research by qualified world wide researchers and their ignoring validated research by the National CFIDS Foundation researchers and not speaking up to the public about the research makes one wonder how far they thought they could get by doing so. It's past time for the world to know what a shame all this has been! Never in my lifetime did I ever think the CDC, NIH, WHO would go against the human race of those who are sick and it was a very rude awakening to say the least!
    - Diana Saba Disabled Retired Nurse
  7. August 8, 2009 12:30 PM EDT
    I gave upon the "CFIDS" Association (CAA) over a decade ago. On Kim - longer than that. I wonder if there is a way to call attention to the no-bid contract - maybe an IG? The CAA is corrupt and must not continue to represent us.

    Thanks for a succinct discussion of this incremental excrement.
    - Pat Blankenship
  8. August 8, 2009 3:58 PM EDT
    Thank you for putting this together. I hope you will write an article about the CDC and all this history someday, and I am looking forward to the updated OW. I did not realize the CFIDS Assoc was tainted in all of this. Where should we give money, if not to them?
    - Anne Ursu
  9. August 8, 2009 6:26 PM EDT
    Let's see: "no biological basis for cfs"...that's the point, the whole enchilada (sorry, I'm in TX)!This is exactly the reason 'cfs' doesn't belong under the criminal cabal of Reeves, et al. Exactly why a lawsuit or Congressional Inquiry must be begun immediately.
    Ok, so those with cancer must have had terible childhoods, right? If not, however did their immune systems become so weak that it allowed cancer viruses to take hold? Hmmm-cancer is AIYH? Rheumatoid Arthritis, Lupus, MS, Lymphoma?..On and on. The facts are: any illness can find a subset of abused and traumatized patients. Just because you have cancer does not mean you cannot get M.E. Just because you have COPD does not mean you cannot get M.E. Just because...well, you get the idea.
    I have no doubt some subset of 'cfs', even M.E. patients have had traumatic childhoods; that makes them no different than in any other disease. No disease state makes one immune from M.E., either.
    There is no scientific basis for this junk propaganda. BTW, the Future Science Group, which publishes 'Future Neurology" is based in London...ring any CBT/GET bells? They publish "original research plus commentary and analysis from international opinion leaders..." My Q. is: since when is Heim an international anything? She is a mushroom spoored by Reeves. I intend to write the their Editorial Commissioner of Future Neurology: Victoria Lane (with CC to Laura Dormer, at: info@futuremedicine.com. Join me, if you will.

    The CAA has also been complicit in this debacle, and I think they should be sanctioned, nay, banned from being a 501c3 non-profit org representing patients. The millions they received from the CDC explicitly denied their original mission of researching CFIDS (Chronic Fatigue Immune Dysfunction Syndrome), much less M.E, so they specifically denied the legitimacy of the disease and the suffering of their patients who supported them, sometimes at great hardship (which I know as a previous SG leader).
    I am also deeply saddened by the news that Katrina Berne, PhD (author of Running on Empty) is on their Board. She who so concisely listed the neurological and immunological symptoms/damage found in patients. Has she bought into the CDC/CAA charade? I am appalled.

    Pat, incremental excrement, indeed!

    - kathryn stephens
  10. August 9, 2009 4:58 AM EDT
    One of the leading clinicians, Dr. Peterson, has data he's collected for many years that points to a large percentage of his patients that are now developing very rare forms of cancer. This apparently has gotten the attention of some cancer researchers and are associated with the new Whittemore Inst.

    How can this news not be shouted from every noteworthy organization such as the CAA if they were indeed our "advocates."

    - Nancy Henson
  11. August 9, 2009 4:10 PM EDT

    News from Truckee.
    (Anyone remember something strange happening in Truckee, a long time ago?)
    I was discussing the situation with another "local" last night, who told me her doctor has over twenty cases of lymphoma in his "small town" practice.
    He told her "We have a cancer cluster here"
    Which is exactly what Susan Wormsely predicted after seeing the cytometry results from Dr Cheney and Dr Petersons patients, so many years ago.
    How odd it is, that independant researchers can make accurate predictions for the future... while the CDC apparently can't even figure out what happened in the past?
    -Erik Johnson
    Incline Village survivor
    - Erik Johnson
  12. August 10, 2009 12:58 PM EDT
    Thanks Hillary for continuing to speak up about this.

    All research has been ignored. Though periodically there will be announcements of things that were discovered decades ago as if it were "news," I guess to try to keep donations coming. There were studies of the cancer connection over a decade ago - a cancer researcher, can't remember his name, but there was a comprehensive study published on members of a symphony orchestra (this was probably in Osler's Web).

    The CAA has been an impediment all along. But they are damn good at running a business - ME (as "cfs") is just the commodity. Great at spin and playing all sides. As Roy just commented - they denounce the new emperic def but still promote the figures. Patients have a hard time getting around them.

    At one of the CFSAC meetings when the CDC contract first came up - which was announced after the fact - I asked why the CAA got it. Reeves went ballistic, knocked over a chair and said "because they asked" and publicly accused me of infighting and attacking the CAA. It was so bad that I complained to HHS about his unprofessional behavior. Now even Reeves admits that their contract was a failure.

    CDC has ignored all research but their own. CAA has gone along and ironically they have ignored even some good research that they themselves funded. It is not about research, it is about politics. This "all we need is research" is at this point absurd. We reached critical mass long ago, but has gone nowhere.

    One of the reasons that things have gotten this bad is that in nearly all illnesses it is the patient groups who push and demand and educate. There are no credible, effective groups in the US (other than a few state groups). There are long lists of "organizations," but anyone can file proper paperwork and come up with a few names and promote themselves. And periodically jump in and take credit, no matter how much of a stretch or untrue it is. That's all it takes and there is no recourse of revoking their status, no matter how "bad" these groups are. But we don't have to support them. Most have come to the realization that as a good rule off thumb and stopped supporting "CFIDS" groups and mainly support ME groups.

    We cannot not afford to ignore the obvious and pretend - or allow ourselves to be attacked for being "negative" by speaking honestly about the situation. It has become an easy way to hijack and shut down dialogue - which has allowed this to continue - research being ignored, phony organizations, broadening definitions, PR substituting for science etc. The CAA will never object - they'll commend anything for which they receive money.


    Jill


    - Jill McLaughlin
  13. August 22, 2009 10:04 PM EDT
    Hillary might have upset quite a few people, but she's right on, not only for ME but in the bigger picture. If one watches the "debate" on the Lyme guidelines, you'll see the same psychiatric-history crap at work. If you read about PTSD treatment for today's gulf war vets, some beliefs being advocated are far from "evidence-based"... That all physical diseases are the body's way of manifesting the mind's subconscious upon us? I kid you not.

    At least Bernie Siegel said it while giving himself wiggle room; hey, when you need a medical doctor, you need one. Unfortunately, in Britain you can only see a psychiatrist for ME; otherwise, you're sectioned, as they say there.

    Give www.sophiaandme.org.uk some of your time. It's downright Orwellian, but it's real - and don't think it can't happen here. It already has, to Ryan Baldwin in North Carolina, and others. (Difference being, Sophie Mizra shortly died after her release from the ward - with a herpes spinal infection.) A common thread - or threat - is the influence of the U.K.'s psychiatric cabal of Simon Wessely, Peter White, etc. whose psycho-somaticism will keep public and private insurers rich. 'Same Peter White presented at the herpes virus conference in Baltimore last year, where one can hear Dr. Nancy Klimas cozy up to him, almost like FDR shaking hands with Uncle Joe. Why? Maybe because 'same Peter White is working with Emory/CDC on their five-year plan for CFS.

    Consider too, that Emory has its own voice through CNN in Atlanta, and you realize we really have more than ourselves to fight for. If the cabal gets their way, more Americans will be getting sick from a lot of things, denied care, and die while big shots kick back and collect.

    - Warbler512
  14. September 1, 2009 11:13 PM EDT

    The insurance industry issue is surely the big one - even more for you in the US than us here but Wessely et al are being brought over to your shores to help them out.

    Professor Michael Sharpe, who is one of the staunch Wessely crew, drew up UNUM's "Chronic Fatigue Management Plan" and he is unequivocal, (i) "Diagnosis: Neurosis with a new banner" and (ii) "UNUM stands to lose millions if we do not move quickly to address this increasing problem." UNUM Provident are, on my side of the Pond (UK) very big players in the medical insurance business.

    It is also the case here that many private medical insurers will not pay out any benefits for psychological illness. I don't know how things stand in the US, but I would guess that you need extra cover for psych illness. Lots of sick people? Easy - label them as nutters, give them a few "therapy" sessions and, when they fail to improve, say that the problem is self-inflicted and they are uncooperative. Problem solved.

    Incidentally, they get us coming and going, since Wessley and Sharpe (amongst others) are employed by the insurers to "assess" people who are claiming for ME/CFS, and then employed again to use the CBT/GET programme that will make great improvements in health for anyone who is really co-operating. This on top of running their propaganda machine.

    This machinery is also useful to governments, who don't want to waste their money on the "undeserving sick" (to quote Sharpe again).

    Obviously there are egos at work here - Simon Wessely is astonishingly pleased with himself - but the ready reception that this garbage gets can be explained by anyone who has seen "All the President's Men" - "follow the money."

    Philippa

    - Philippa Sutton

RUBBER MEETS ROAD

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Response from the Centers for Disease Control to Osler’s Web upon its publication in 1996:

“…Tom Skinner, a spokesman for the CDC, said his agency has gotten numerous inquiries about the allegations raised in Ms. Johnson’s book but is neither investigating them nor commenting on them.

‘We have not reviewed her book, and will not comment on her book and are not going to,’ Skinner said.”

Dave Parks, Birmingham News, Birmingham, Alabama