Thursday, May 15, 2008

RSM and Stand back a minute !



Yes, some strong words, but just read Greg's article and you will see why.....


By: Greg Crowhurst,
14th May 2008

A Cartesian reflection on the RSM letter to Jan van Roijen (which was send to my and I assume many others as well as a standard reply full of bullshit, but just read what Greg says about it. And everybody who has been wishing me a speedy (!!!!) recoverey, MUCH APPRECIATED


On April 28 2008 there was a one-sided, closed, psychiatrically biased conference, in London, on CFS. The RSM believes, in a letter to Jan van Roijen, that all the content was evidence-based and of high scientific quality; an extraordinary
claim to make given that the conference was claiming that ME no longer exists.


Peter White is reported to have referred in his opening speech, to the philosopher Descartes; It is a particularly alarming statement, because it could be inferred to mean that the split between psychiatry and the biomedical reality of ME cannot be safely used to protect people with ME anymore from the
involvement of psychiatry in the treatment of their illness:

'The ME-CFS debate may be remembered in future more as one of the tipping points for the rejection of Cartesian dualism than for diseases that lie within'.


Actually Descartes, if he had been present at the Conference, might well have responded to this statement by exclaiming - wow, hold on, stand back a minute !


He has very much indeed to contribute to the current ME debate.

A gifted mathematician as well as a brilliant philosopher, Descartes is the person who invented analytic geometry and the graph (those two familiar lines on a graph, the Cartesian co-ordinates, are named after him).

Far more importantly, Descartes laid out a sound method for acquiring certain knowledge about the world; so sound in fact that he built the basis upon which modern science would subsequently be constructed; a basis that seems to have been
thoroughly shattered by the psychiatric lobby in their treatment of ME.

It is indeed instructive to consider the nature of Cartesian dualism and how one might set about overcoming it.

By truth or by fantasy? That, in relation to the psychiatric lobby, is the all-important question.

Is it by paying rigorous attention to the physical/medical research and experience of people with ME, or is it about plucking an hypothesis seemingly out of the air?

Descartes provides the answer.
Time and time again, this wonderfully bold, easy to read writer stresses the importance of disciplined, critical rationality.

A scientist, he stated, should analyse the world uncontaminated by any dogma or propaganda. Can that be safely said of the psychiatric lobby and their relationship with the Medical Insurance Industry?

Descartes would most certainly advise the psychiatric lobby to pay great attention to the facts, like the 4000 published clinical studies on ME, which they apparently ignore: like severe ME patient's personal experience of pain, numbness, spasms and other serious neurological and physical symptoms, which
can be perceived clearly and distinctly and analysed in quantitative terms, using experiment and hypothesis, which they ignore.

Psychiatrys perennial problem it seems is its "relatively underdeveloped status as a science" (KW Fulford, AY Smirnov and E Snow 1993*) leaving it with an undue reliance upon consensual definition, rather than hard science, to determine disorders; a consensus that critics say, more often than not, is determined by GlaxoSmithKlines or UNUM's billions of dollars.

Consensus is not necessarily truth.

The original term "Chronic Fatigue Syndrome", for example, rather than arising out of careful Cartesian analysis was simply the working title of a study that was developed in the 1980s on the basis of some cluster outbreaks in the USA thought to be due to Epstein Barr Virus.

The trouble is this throwaway title stuck with the most awful consequences.

The criteria of CFS, according to Lajla Marks (2007)were never meant to cover ME.

Inconceivably, although the World Health organisation classified Myalgic Encephalomyelitis in 1969 in their international classification of diseases (ICD) as a neurological disease, listed in ICD-10, code G93.3 under "Other diseases in the brain", in the USA they just kept on focussing upon "fatigue" and ignoring the neurological and neurocognitive symptoms, which are the main symptoms in ME, states Marks.

Even in their revised criteria, Fukuda et al in 1994, in the USA, chose not to "include the characteristic neurological and neurocognitive symptoms, described
by Ramsay and others before him - symptoms that were of vital significance for the understanding of the disease and for further research and treatment."

Today, CFS is being forcefully promoted, rather than ME.

ME, according to a report on the RSM Conference, no longer exists; yet what has reputedly eradicated ME from the world, apart from the propaganda of the psychiatric lobby?

Nothing it seems, as physical government backed research for it does not exist.

There has been no programme of medical eradication or vaccine development, for example, which is the usual course to eradicate a serious disease.

The fears of a further outbreak of epidemic proportion have been silenced and argued away, based on opinion rather than biomedical science - how can you have an epidemic of psychiatric mental health issues? It is not the same thing at all.

No risk there then.

People with real neurological ME are today cleverly excluded from the ME now called CFS clinics, categorically because they have neurological symptoms, which are purported to no longer exist, except in a historical sense.

Descartes would, presumably, be shaking his head in some bewilderment. (and be violently sick of so much psycho stupidity , my addition............)

Departments of Neurology across the land, who should know better, are often so heavily influenced by psychiatric propaganda that they refuse to validate neurological ME so that the patients reality becomes a torment of real physical, yet completely unexplored, unexplained, untreated and invalidated
symptoms.

People with real ME are not included in the data that
would prove that GET and CBT do not work for ME,
because they are excluded under the psychiatric-
based criteria.

CFS excludes neurological symptoms from its criteria
and focuses upon fatigue, a symptom not necessarily
present and actually post -exertional in nature in
true ME. Tiredness and deconditioning come no
where near this, as a definition of what an ME
sufferer experiences.

Yet the psychiatric lobby have taken the name ME,
incorporated it into CFS, accepted the funding to help
the people, then in reality denied them access by
denying their neurological disease.


In business this would be deemed a successful
hostile take-over.

It can be safely reasoned then that Descartes would
not have been behind the take over of a valid
biological disease by psychiatry, especially one that
is based on not a shred of solid empirical evidence

Negated and excluded, people with severe ME are
left, under the psychiatric lobby's influence with no
viable option or alternative. The psychiatrists have
occupied the central ground of ME and excluded
people with ME from it at the same time.


It is not too hard to imagine what Descartes
might have to say about this deadly state of
affairs.

He might well draw the psychiatric lobby’s attention
to how the study of "Myalgic Encephalomyelitis"
(ME), has always been based on clinical findings of
signs of dysfunction in the Central Nervous System
(CNS) and over the years has been shown, without
the slightest doubt, to be a physical disease.

He would probably ask, alongside Margaret Williams
(2004),: Can White really be looking at patients with
ME / ICD-CFS or is he looking at those with a primary
complaint of the "Wessely School" construct,
namely, one end of a continuum of "medically
unexplained fatigue"?


It is not too hard to imagine Descartes agreeing
wholeheartedly with Dr Derek Englander's, March 22
2008 letter to the Daily Telegraph on the RSM
Conference, citing as arrogant, how obscurity over
the cause of ME has been masterfully used by
psychiatrists to claim that the disease is a
manifestation of a psychiatric condition, leading to
an imagined problem.


Such a clever take over from such a simple
statement, as this severe ME sufferers poem
shows:


But then there is the psychiatric lobby
who have intentionally set out to negate my reality
based on nothing more than whim and whimsy
fabrication and aggrandisement,
without the slightest hint of evidence-based integrity.
Yet still in their arrogance
they persecute and deny me
And all the thousands like me
too ill to properly engage in the world or make truth
of their existence known,
too ill to fight their corner.
Yes, my life is bizarre and disturbed and certainly it
feels unreal,
but it is not half as insane and unreal
as the emptiness
at the centre of their argument.

Linda Crowhurst 2008



The lesson appears to be, abandon rigourous
Cartesian rationality at your peril.

People with the WHO defined neurological disease
ME, caused by an enterovirus, especially those who
have more recently become ill now face decades of
suffering from a supposedly non illness, without
validation, treatment or hope of a cure and without
appropriate and proper medical tests or care.



Under the psychiatric lobby’s influence there is:
* No way out for people with neurological ME.
* No valid tests.
* No valid treatments.
* No hope.
* No acknowledgement of their suffering.
* No alleviation of symptoms.
* No biomedical consultation.
* No development of an appropriate biomedical
service.
* Only intense suffering, hopelessness and even
death.

And all of this because of psychiatrys irrational grip .

Forget Descartes dualism of mind and body too soon
and you create a living hell for people too ill to
speak up, too poor to mount campaigns.

It is true that we are indeed approaching a tipping point.

The tipping point must be the primacy of the
individual severe ME patients experience; which will
rid ME once and for all of psychiatry’s influence and herald in a long overdue era of proper recognition, biomedical treatment and sound clinical research.

Cogito ergo sum.: I think therefore I am; Descartes
powerful affirmation of human experience and being,
equips us to critically view the tragic psychiatric
supremacy that devastates so many ME patients
lives, and perceive the power-game that is being
played out, because it affirms the reality and validity
of the persons experience, which the psychiatric
lobby fails to do .

As for resolving any mind/body dualism (the
Cartesian split), the psychiatric lobby, on such flimsy
foundations, is not very likely to achieve this most
holy of grails.

References

KW Fulford, AY Smirnov and E Snow (1993) Concepts
of disease and the abuse of psychiatry in the USSR
University Department of Psychiatry, Warneford
Hospital, Oxford.

The British Journal of Psychiatry 162: 801-810 (1993)
http://bjp.rcpsych.org/cgi/content/abstract/162/6/801?ck=nck

Marks L (2007) What is ME?
http://mesite.dk/WhatIsME.htm

Williams M (2004) Paradoxical Proliferation of
Professorial Psychiatry?
http://www.meactionuk.org.uk/Paradoxical_Proliferation_of_Professorial_Psychiatry.htm

PS: the original cartoon with almost the SAME wording appeared in the TIMES at the end of last year I think, just see for yourself:

2 comments:

Anonymous said...

Thank you for posting Gregs brilliant work!

The thing I really don't understand about the pschiatric lobby's hijacking of ME is their aversion to any form of treatment other than CBT and GET. I found this page by searching Google:

http://www.primarypsychiatry.com/aspx/SearchResults.aspx?st=c&search=4

This seems to indicate that psychiatric problems are a complication of neurological disorders and treatment for the underlaying neurology has to go hand-in-hand with the psychiatric treatment.

Why then, is this not the case for ME? (Other than complete misdiagnosis and faulty assumptions on the part of the psychiatrists themselves.)

It seems to show a basic failing in the psychiatric treatment of ME even by basic psychiatric methodology (right or wrong).

Ho hum.

Anonymous said...

thanks from me too for posting this article from greg and linda.

those two have done more than most with their continuous efforts to promote the truth and reality of severe m.e. and all that surrounds this illness - with all they have written and their videos on youtube.

they have done so with courage, compassion, clarity and integrity - to the benefit of the rest of us.

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