The Fibromyalgia "pressure points" test is a trap; a hoax. (ISDA's new quiet campaign)



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Subject: The Fibromyalgia "pressure points" test is a trap; a hoax.
(ISDA's new quiet campaign)

Date: Oct 28, 2008 4:27 AM

http://www.actionlyme.org/index.htm

IDSociety.org's new Fibromyalgia campaign

You may say to yourself, Now that Rove and the neocons have been
exposed - in a
real sense; they have no balls and no brains - will we now hear from
the AMA loud
and clear that they were duped by Yale, et al about "Lyme Disease?"
Will
the FDA grow a pair and admit they did nothing for 9 years after the
Dearborn Hoax
was exposed and didn't want to admit that they were had, too, about
the "No-OspA-B
in the standard" hoax?

Will the Corrupticut legislature, and in particular, the Democrat
Speaker of the
House, James Amann, admit he obstructed the truth about Lyme as a
cause of MS because
he was afraid his personal income as a fundraiser for the MS Society
would decrease
when the funding instead went into the prevention of MS through the
prevention of
the advanced stages of Borreliosis or Relapsing Fever?

Will the sick people of this nation and the AMA catch on to the fact
that IDSA's
new campaign is to sell Fibromyalgia (rather than continue to confront
their own
Lyme lies head-on), when the test for Fibromyalgia is itself a hoax?
No one has
this many "pressure points" from inflamed nerve roots or nerve root
ganglia
from Borreliosis, the basis of 90% of Fibromyalgia (FM) and Chronic
Fatigue Syndrome
cases. (See the graphics in the OspA-Permanente page)

The Fibromyalgia "pressure points" test itself is a hoax. MDs know no
one could possibly have that many "pressure points." The test for
Fibromyalgia
is itself a test for hypochrondria. People may be sick with a Lyme-
like syndrome,
but they answer YES to most of the pressure-points test in order to
get any diagnosis
at all.

This is IDSA's new campaign; they're quietly pushing Fibromyalgia
diagnoses
and treatments which in many cases is to get people addicted to pain
meds and then
suddenly cut them off for the fun of watching these FM patients squirm
and beg and
go berserko looking for pain meds, which is a behavior they can then
blame the victim
for, and then diagnose as "CRAZY." This is done on behalf of
insurance
companies of course, since they don't pay for "CRAZY" long term
disability.

IDSA knows what they're doing. MDs and patients and more importantly,
the people
who are supposed to investigate insurance fraud - the USDOJ -
certainly don't
give a shot. They never did.

I personally did not have too many pressure points (seen by Dr. Peter
Manu at UConn,
who tried to diagnose "not enough sex" in 1989) and I am a totally
honest
person; I never got a diagnosis of FM, although as you can see from my
EMGs, I have
had plenty of nerve root pain, as most of the nerves in my neck are by
and large,
half gone. My neck and upper back are now numb to the touch.

People need to be aware of the FM "pressure points" trap.

Another nearly important aspect of Lyme/FM misdiagnoses is that no one
should ever
fall for the brain or the pain candy. You end up in more pain, since
these anesthetics,
psych meds and pain meds work in the exact same way. They're
transporter or
receptor blockers, and as such, toxic for many people. You end up
with a chemical
equilibrium imbalance with an up-regulation in the transporter or
receptor that
has been blocked in order to compensate to what is natural for you.

It is completely untrue that people have "chemical imbalances" in the
brain (the Biopsychiatry theory) that need to be "treated" with brain
anesthetics. There are either bad people or good people and the way
to tell a bad
or a vain person is in the nature of their speech, usually. Vain
people always
act in self-interest or are braggarts, and most certainly all liars
are evil.

So, stay away from FM diagnoses and any kind of pain meds other than
anti-inflammatories
for Lyme.

Take it from the BigPharma chemist who solved the Lyme crymes.

And watch the Psychiatric_MumboJumbo movie about scientific hoax of
psychiatry and
the problem with brain damage from psychotropics
http://www.actionlyme.org/Psychiatric_MumboJumbo.wmv


There is more data and more links to the science which prove that
all psychotropics are brain damaging on the homepage at the present
time.

It is highly advisable that you save the links to medline and verify
independently. More brain damage and misdiagnoses is IDSA's new
quiet campaign. They're quietly pushing Fibromyalgia, since that
has the least science behind it, and once hooked on pain meds,
you will go crazy, since psychotropics are all brain damaging, just
like street-drugs.


Kathleen
.



Relevant Pages

  • ~*Online WACOC News 2006 June 26*~
    ... Fibromyalgia pain isn't all in the patients' heads, new brain study ...
    (alt.med.fibromyalgia)
  • ~*Online WACOC News 2007 April 14*~
    ... FM ME-itits CFIDS PIV-5 GWI MCS PPS SV40 LYMES ALS SCLERODERMA LUPUS ... Potential Animal Virus Identified in Patients with Chronic ... RES: Accelerated Brain Gray Matter Loss in Fibromyalgia Patients: ...
    (alt.med.fibromyalgia)
  • RE: Fibromyalgia Can No Longer Be Called The Invisible Syndrome
    ... degree of pain you are suffering at the time. ... -> Fibromyalgia Can No Longer Be Called The 'Invisible' Syndrome ... -> syndrome, however, have shown above-normal cerebral blood flow (brain ...
    (alt.med.fibromyalgia)
  • Re: FMS a Neurodegenerative Disorder?
    ... statistics. ... into the positive direction when looking for gray matter depletion. ... 100 MRI brain scans done here and find 20 with reduced grey matter. ... with fibromyalgia. ...
    (alt.med.fibromyalgia)
  • Re: Steph please, prognosis
    ... between the (I forget now - but between two brain lobes) ... Chest x-ray - small cluster of abnormal cells in the right upper lung. ... The pain meds issue; he'd had chronic pain from other causes for years and both ...
    (sci.med.diseases.cancer)