Subpoena the vaccine manufacturers for this data

Subpoena the vaccine manufacturers for this data

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Subject: Subpoena the vaccine manufacturers for this data

Date: Apr 11, 2008 2:24 PM

"Groovy," I say to the CDC.
Then from whence comes the neurologic adverse events listed in the MMR
monographs?
* w w w .actionlyme.org/HOWE BBC SCIENCE EVIDENCE.htm

How about we subpoena the vaccine manufacturers for this data??


We know where they come from.
Not all vaccines are for all children and children need to be pre-
screened for immune
competence to the vaccine antigens and the carriers, and they also
need to be in
perfect health (no new viral infections).

Of course, there is more data on my website which shows the clipouts
from the Immune
Deficiency Diseases textbook, which show some pictures of children
injured by vaccines
and there is "NO INFLAMMATION."
Recall that the CDC has recently again stated that the only kind of
disease there
is, inflammatory, so we know, for certain, the CDC is full of horse
manure.

The CDC has a long history of participating in and generating manure:
* w w w .actionlyme.org/CRYMEDISEASE CHP3.htm

AND, to my knowledge, we have never seen the CDC's Tuskegee Bad Blood
Program
results in full. Naturally we Lyme victims would like to see it,
since we want
to know what is in store for us!
* w w w .actionlyme.org/index.htm

My ActionLyme co-researcher/nurse, Barb Fitzmaurice died in the summer
of 2005 and
she had previously revealed to me that as a support group leader for
Lyme Disease
she noticed that people dropped off in their 50s. And then later did
herself.

I think before the CDC utters another blast of explosive diarrhea at
us on vaccines,
we should be allowed to see the Bad Blood results.

Kathleen M. Dickson


=======================
* w w w .nytimes . com /2008/04/11/health/policy/11vaccine.html? r=1&adxnnl=1&oref=slogin&adxnnlx=1207937544-fxEyyfrgjQIpsdEOXWdzRg&pagewanted=print

The New York Times
April 11, 2008
Public Forum to Address Safety Issues on Vaccines
By GARDINER HARRIS

WASHINGTON -- In the midst of yet another controversy about whether
vaccines cause
autism, the federal government will hold its first ever public meeting
on Friday
to discuss a governmentwide research agenda to explore the safety of
vaccines.

The meeting is intended to help defuse years of criticism from vaccine
skeptics
that the government is hiding what it knows about vaccine safety or
failing to investigate
the issue diligently.

But the gathering is unlikely to appease the government's many critics
in part because
the latest notion to grip vaccine skeptics -- that vaccinations trigger
or worsen
something called mitochondrial dysfunction, which in turn causes
autism -- will remain
largely unaddressed.

"I think there could be real frustration," Dr. Bruce Gellin, director
of the National
Vaccine Program Office, which is coordinating the meeting, said in an
interview
Thursday.

Indeed, Margaret Dunkle, senior fellow at the Center for Health
Services Research
and Policy at George Washington University, said government experts
needed to take
into account the latest controversy.

"If they just talk about the same old issues and don't reflect what we
now know
and the concession the government has made, that would be a huge
disappointment,"
Ms. Dunkle said.

Ms. Dunkle's niece, Hannah Poling, of Athens, Ga., was 19 months old
and developing
normally in 2000 when she received five shots against nine infectious
diseases.
She became sick and later developed autism.

Her parents sued, and late last year government lawyers agreed to
compensate the
family on the theory that vaccines may have aggravated an underlying
mitochondrial
disorder. When news of the government settlement became public,
vaccine skeptics
said the government had finally conceded that vaccines cause autism.

Government officials and researchers said they had conceded no such
thing.

"The Poling case has changed the media coverage of mitochondrial
disorders but has
added nothing to the discussions of what causes or doesn't cause
autism," Dr. Edwin
Trevathan, director of the National Center on Birth Defects and
Developmental Disabilities
at the Centers for Disease Control and Prevention, said in an
interview Thursday.

On Friday, many of the main players involved in this debate --
including Hannah's
mother and her grandparents, prominent vaccine skeptics and some of
the government's
top vaccine researchers -- will all be in the same room to discuss
research priorities.

The meeting is the result of a 2005 report by the Institute of
Medicine, which suggested
that the disease control agency might engender more trust among
skeptics if it included
them in its research planning.

At the time, vaccine skeptics were lobbying to have greater access to
the agency's
Vaccine Safety Datalink system, a huge set of health records assembled
by large
managed care organizations. The agency uses the system to conduct
epidemiological
studies to measure whether vaccines or their components cause common
problems.

Such studies, for instance, have found no link between the combined
measles, mumps
and rubella vaccine and autism, and they have found no link between a
once-common
vaccine additive, thimerosal, and autism.

In the face of such studies, vaccine skeptics have increasingly
demanded clinical
research, not epidemiological studies, to determine whether small
groups of children
may somehow be more susceptible to vaccine injuries than the general
population.
Such subsets of children might get lost in large epidemiological
studies, they say.

But that kind of clinical research is generally undertaken or
underwritten by the
National Institutes of Health, not the disease control agency.

The issues raised by the Poling case "can't go very far tomorrow
because it's really
not in C.D.C.'s lane," Dr. Gellin said.

No decisions are expected to come out of Friday's meeting; rather, it
would allow
researchers to hear the public's priorities.

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