-Caveat Lector-   <A HREF="http://www.ctrl.org/">
</A> -Cui Bono?-

 -------- forwarded message --------
 From: "Roy L. Beavers" <[EMAIL PROTECTED]>
 To:   emfguru <[EMAIL PROTECTED]>
 Date: Thu, 27 Jan 2000
 Subj: US NIH "spins" another possibly EMF related issue. (Maisch)..

 Hi everybody:

 I have held on to this long message for a few days -- thinking we
 might get a "break" in the flow of good messages ... but the storms
 in the U.S. seem to have resulted in an INCREASE......

 The value of the following message is two-fold:  (1) Some EMF
 research has pointed to a possible connection between CFS and
 EMF....  That possibility deserves to be a part of the following
 effort....  But (2) even more, I am very uncomfortable at the
 behavior of NIH that is being reported below.....!!!  It looks like
 another case where America's RICH health bureaucracy is serving the
 cause of its pharmaceutical **patron** industries.....!!!

 Be sure you read down to the statements by Dr. Schweitzer......!!!

 Is there no shame in any of our governmental bureaucracies???
 Answer:  Not in the Clinton Administration.....!!!  They are
 responsive to three motivations:  politics, politics, politics.....
 And the large $$$$$$$ political contributions which are essential
 to the perpetuation of their remaining in power under America's
 corrupt system......  "Where is Donna Shalala?" asks one of the
 writers below???...... She is right in the middle of the political
 $$$$$$$$, that's where she is.......

 Cheerio.....

 Roy Beavers (EMFguru)
 [EMAIL PROTECTED]

 ..It is better to light a single candle than to curse the darkness..
                  NEW!!! Website... http://emfguru.com
 ................People are more important than profits..............


 ---------- Forwarded message ----------
 From: Don Maisch <[EMAIL PROTECTED]>
 To:   [EMAIL PROTECTED]
 Date: Thu, 27 Jan 2000
 Subj: US NIH spins another  possibly related issue.

 Dear Roy

 I thought you would find this interesting.  There may be a secret
 agenda in the NIH's attempts to keep CFS classified a form of
 psychiatric illness.  Could it be that the US government is well
 aware of the Russian research that clearly identifies EMR exposure
 as a causitive factor immune system dysfunction, with symptoms
 remarkably similar to "CFS", and is trying to do a cover up?


 Regards

 Don



 Press Release from "The CFIDS/M.E. Information Source":
     http://www.cfids-me.org/index.html#NIH

 _________________________________________________

              For Immediate Release

 The NIH has secretly put together what they are calling a "State of
 the Science" conference to help inform NIH decision-makers about
 the current status of research on CFS.  The only "experts" they
 have invited are Stephen Straus (of NIH), Mark Demitrack (of Eli
 Lilly), Simon Wesseley (from the UK), and Michael Sharpe (also from
 the UK).  All are strongly biased in favor of the belief that
 CFS/M.E. is caused by "stress" and is a form of psychiatric illness
 they call "functional somatization;" Straus and Demitrack recommend
 SSRI's (Prozac) and "stress reduction," Wessely recommends
 traditional psychiatric talking therapy, and Sharpe recommends
 "cognitive behavior therapy;" all four recommend exercise.  These
 are the only therapies any of the four acknowledges as valid.

 Such a narrow perspective can only result in the further
 development of a strongly biased picture of CFS/M.E.  This meeting
 is not insignificant; NIH has stated that the intention is to
 "teach" NIH decision-makers "about CFS."  The meeting will have a
 strong influence on future NIH policy towards the disease, research
 funding, and the plight of patients.  As Jon Sterling (former
 president of the NJ CFS Assoc. and current patient representative
 on the CFSCC) stated in a formal letter of protest, "the view of
 these 'experts' would take us back to 1991 in terms of scientific
 progress in CFS research."

 It is both perplexing and shocking that NIH ignored the expertise
 of the three official medical representatives to the CFSCC (the
 Congressionally-chartered Chronic Fatigue Syndrome Coordinating
 Committee of the U.S. DHHS) in both the planning and outcome of the
 meeting.  Perplexing in that the idea for such a meeting originated
 within the CFSCC, but NIH took command and explicitly rejected any
 input from the body that is supposed to be coordinating DHHS policy
 on CFS; shocking that any effort at a true "survey of the science"
 would deliberately exclude these three highly-respected
 researchers:  Dr. Anthony Komaroff (Harvard), Dr. Peter Rowe (Johns
 Hopkins), and Dr. Nancy Klimas (Miami).  The NIH has relented and
 will permit them to attend (though they informed them too late for
 Komaroff to be able to be there) -- but Rowe and Klimas will be
 permitted there only as "observers," not as "participants."

 Recipients of NIH external grants for CFS research in the past
 five years were also deliberately excluded.  When asked why, NIH
 responded that "they would be prejudiced."  One wonders, then, why
 Straus and Demitrack have been included, because they have been
 beneficiaries of internal NIH grants for years -- and unlike
 external grants, internal grants are given without competition or
 the requirement of professional peer review.  Indeed, it has been
 years since Straus has won an external NIH grant to study CFS.
 If the experts chosen by peer review for NIH grants are viewed as
 so unprofessional as to be able to discuss their research in
 perspective,  why have Straus -- who also has his own research
 agenda -- and Demitrack -- who not only shares Straus's research
 interests, but is himself external to NIH -- been included?
 Why have two British researchers been brought in?  What on earth
 is going on?

 Bluntly speaking, Stephen Straus has had influence on the U.S.
 government's interpretation of CFS far beyond any accomplishments
 in the way of research; he is a virologist, but his one foray
 into a virological cause of CFS (what he once called Chronic
 Epstein-Barr) turned into a highly-publicized failure.  Since then,
 his focus has solely been on psychological causation -- well
 outside his own area of expertise.  Ironically, Straus and
 Demitrack's last published research found patients with CFS/M.E.
 to have below- normal levels of cortisol, when a theory of
 psychological causation should have produced the finding of above-
 normal levels.  Straus has thus ignored even the results of his own
 research when it has contradicted his beliefs about this disease.
 To include only Straus, his research partner, and two allies
 from the United Kingdom in their personal battle to focus on
 psychological causes as the sole basis of CFS, is grossly
 insulting to the entire CFS/M.E. community -- both patients and
 professionals.

 The bulk of published peer reviewed research on CFS today occurs
 not in psychiatry, but in the fields of neurology, cardiology,
 immunology, endocrinology, and biochemistry -- as a quick search of
 Medline will confirm.  To repeat:  none of these fields have been
 included in NIH's so-called "State of the Science" meeting.  Given
 the recent uproar over misspending at the U.S. Centers for Disease
 Control, it is stunning that NIH would so blatantly disregard the
 wishes not only of the CFS/ME research and patient community,
 but the U.S. Congress and DHHS's own Chronic Fatigue Syndrome
 Coordinating Committee (CFSCC).

 The medical representatives on the CFSCC, explicitly excluded from
 this conference, have substantial peer-reviewed publications and
 are on the faculty of highly-regarded medical schools:  Dr. Anthony
 Komaroff of Harvard has numerous publications demonstrating
 neurological damage in CFS; Dr. Nancy Klimas of Miami has a
 substantial publication record in the immunology of AIDS and CFS;
 and Dr. Peter Rowe, a cardiologist at Johns Hopkins, counts among
 other peer reviewed publications the only complete research article
 on CFS that has appeared in the prestigious Journal of the American
 Medical Association, an essay demonstrating the role of
 dysautonomia (autonomic nervous system dysfunction) in CFS, which
 was published in JAMA in the fall of 1995.  Dr. Klimas also manages
 one of three federally-funded CFS research clinics; the other two
 were also ignored.

 Dr. Benjamin Natelson and his staff at the New Jersey CFS Clinic
 have produced numerous peer-reviewed publications in the fields of
 biomechanics, neurology, and immunology; Dr. Dedra Buchwald's CFS
 clinic in Seattle, Washington, has produced important research on
 demography and genetics; she is currently working on a study of
 twins to isolate the genetic makeup of patients with CFS.  None of
 these researchers are proponents of the theory that CFS can best be
 described as "functional somatization;" indeed, Natelson's group
 has published several studies demonstrating that psychological
 causation cannot explain the symptoms of CFS/M.E. (none of which is
 referred to in Straus's work).

 To see the breadth of scholarly research in the field of CFS that
 has been excluded from NIH's conceptualization of CFS, you can
 find the following on the web:

 + Abstracts of the most recent AACFS Research Conference held in
   Boston, MA, October 1998
     http://www.cfids-me.org/aacfs

 + "Report from Second World Conference on CFS and Related
   Disorders" held in Brussels, Belgium, September 1999
      http://www.sonic.net/melissk/brussels1.html

 + Proceedings of the 1999 Sydney ME/CFS Conference in Australia.
      http://www.ahmf.org/conf99.htm

 See also the CFIDS/M.E. Information Page:
      http://www.cfids-me.org/

 particularly these sections:
 + Diagnosing and Treating CFIDS/M.E. and Fibromyalgia
      http://www.cfids-me.org/index.html#Diagnosis
 + Medical Research and References
      http://www.cfids-me.org/index.html#medical
 + General Information about CFIDS/M.E.
      http://www.cfids-me.org/index.html#Info


 The CFIDS/M.E. community is asking that the NIH postpone this
 meeting immediately, and start over by cooperating with the
 Congressionally-chartered CFSCC (Chronic Fatigue Syndrome
 Coordinating Committee of DHHS).  We also want to know how this
 could possibly have happened.  Why have a committee to coordinate
 policy on a "seriously debilitating" (according to the CDC)
 condition such as CFS if the policymakers are going to completely
 ignore the expertise represented on that committee?

 In particular, why is a single NIH researcher permitted to exercise
 such control over scholarly information and research funding,
 particularly when he has demonstrated such outright disdain for any
 research that might conflict with his own preconceptions of
 psychological causation?  Dr. Straus recently left his position at
 NIAID and whatever connection he had to CFS research to become
 the new director of the Office of Complementary and Alternative
 Medicine.  Why should he continue to retain such control over the
 way policy is decided -- particularly given that there already
 exists an interagency committee with nationally-recognized experts
 whom one would have presumed would have been the FIRST researchers
 contacted?

 In May the Department of Health and Human Service's Office of
 Inspector General confirmed CFS advocate's longstanding insistence
 that the CDC was diverting CFS funding to other projects without
 informing Congress.  CDC apologized, and has been left to proceed
 as if everything is okay now.  Yet the chief researcher in charge
 of CFS at the CDC informed the CFSCC in November that he has no
 intention of ever finishing the projects that Congress had asked of
 the CDC that were abandoned because of the false lack of funds.
 Demographic studies of the prevalence of CDC among adolescents,
 minority groups, and its effects upon pregnancy, were thrown out
 and will not be resumed.  Why is this okay?

 Now the NIH puts together a meeting in secret that is in direct
 defiance of the Congressionally-chartered CFSCC, limiting
 involvement to the same internal investigator and his allies
 who have dominated CFS funding at the NIH for over 15 years.
 Has nothing changed?  Why is this okay?

 Where is Donna Shalala in all of this?  Where are our congressional
 representatives, who chartered the CFSCC in the first place?

 The time is ripe for a high-quality investigative report by a good
 news bureau.  Since the powerful health bureaucracies of DHHS show
 no signs of policing themselves, it is time for the press to take
 up its role as the traditional guardians of the public's right to
 know.  What is the reason behind this continued insistence on
 "psychological causation," as evidence mounts in other research
 areas to the contrary?

 The "State of the Science" meeting is scheduled for the Hubert
 Humphrey Building (DHHS headquarters) in Washington, D.C., all day
 Monday, February 7.  The public has the right to attend.  We hope
 that representatives of the U.S. and international press will be
 there.

 On Tuesday, February 8, the CFSCC will meet at the same place --
 the Hubert Humphrey Building (DHHS headquarters) in Washington, DC.
 It is important that representatives of the press attend this
 meeting to report back to the public why the NIH should be
 listening to the experts in this federally-chartered committee.

 Further information on this crisis can be found on the website of
 the CFIDS Association of America at:
      http://www.cfids.org/advocacy/sos.html


 Mary M. Schweitzer, Ph.D.
 The CFIDS/M.E. Information Source
 http://www.cfids-me.org/
 mailto:[EMAIL PROTECTED]



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