"Recently the government's vaccine court conceded the case of Hannah Poling,
admitting that vaccines triggered her regression into autism by exacerbating
mitochondrial dysfunction"
Read what it "says" rather than what you want it to mean.
IOW it is "mitochondrial dysfunction" that was the *cause* and a vaccine
the *trigger* for that cause, regardless of Mercury or Aluminum content,
therefore, the "mercury" was neither cause nor trigger...further indicated
by other studies of both vaccinated and unvaccinated control subjects where
mercury levels were the same in both from environmental loads [And Aluminum
is completely unavoidable, being the 3rd most common element on the planet]
If mitochondrial dysfunction is common to monkeys [IOW, not necessarily a
dysfunction FOR "monkeys" but part of their common genetic structure ], a
human vaccine would naturally trigger more Autistic signs, proving nothing
about "humans", but much about susceptible genetic conditions that both
humans and monkeys can have.
If anything, it all means "Don't vaccinate monkeys", they won't commonly
tolerate it.... OR..... certain uncommon children who share that condition
with a common monkey.
The common factor that contains ALL the other conditions in *humans* is the
effects of a given *vaccine* COUPLED WITH "mitochondrial dysfunction".
The next question is: Since eliminating toxins made
absolutely-no-difference, does going *unvaccinated* eliminate Autism?
That does NOT mean that toxins shouldn't be eliminated for other reasons
not relevant to "Autism". That's another "stand alone" consideration.
If catching the disease that the vaccine prevents has the same effect as
the vaccine, then the answer is no...BUT..everyone else being vaccinated
will interrupt a disease vector and that childs odds of ever contracting
that disease will be greatly diminished.
Therefore NOT vaccinating *certain* people will prevent Autism BY
vaccinating other people.
Therefore, the answer to the problem of CAUSE [vs triggers ] is to develop
genetic screening tests to determine who should and who shouldn't be
vaccinated.
Studying "mitochondrial dysfunction" in both humans AND monkeys will lead
to those tests being possible...and that IS relevant.
Blaming non triggers won't do a danged thing but make screamers feel
justified about not using their heads and make people who can add two and
two together and not wind up with minus 12 shake theirs in dismay.
Knowing what triggers what, in who, can lead to avoiding triggers, EVEN
IF actual *causation* can't be avoided.
Plus "mitochondrial dysfunction" is most likely hereditary as a
combination of recessive genes, so who should and shouldn't replicate could
be an important factor in not visiting the likelihood of Autism on their
children.
Do YOU care enough about children to make good strong ones? Or would you
rather just blame the problems that weak ones have on the irrelevant while
NOT doing what CAN be done.
It, like cycle cell anemia, could probably be eliminated from the gene
pool by screening, parental self control and wise choices..but since when
were the majority of parents acting wisely when having children any more
than insisting [despite very strong evidence to the contrary ] on blaming
the wrong thing for a problem and being surprised when eliminating that
...does NOTHING to change ANYTHING, yet still insist that's IT.
Obviously, some would prefer a scape goat to barbecue, over a solution
that requires considered responsible action on their own parts where
something can "actually be done" when making ANY sort of noise cannot solve
the wrong problem.
An easy way out, to total failure and helplessness.....but gee, mindless
anger expressed "feels like" work and golly, it IS work..digging a below
sea level ditch to the ocean.
If you get there you'll drown, but at least you got tired and sweaty with
lots of other people in that ditch for the right company.
..or consuming electricity made by Mercury [by the annual tons ] spewing
power plants, for that matter ....while worrying madly about how many Tuna
Fish sandwiches you eat. [ Proven beyond a reasonable doubt to be
****Irrelevant***** to Autism rates, but still a nasty toxin.]
..or being stuck with a gas guzzler because you didn't notice the
inevitable future and didn't buy the small car when you could have, then
can't because you didn't, so its' the Automakers fault for not making
something that doesn't sell when NO automaker can do that and stay in
business to sell anything at all.
That's like avoiding speeding cars by stepping in front of trains and
blaming tracks for injuries while ignoring the differences in mass and
inertia common to both situations...and attacking "the powers that be
physics" by going SPLAT ...very loudly in protest.
OK, apply all efforts to being right over solving a serious problem.
If it doesn't work, do it harder to someone else. [Earth Motto]
Good luck..have fun with that.
I'll be quitely watching where I walk.
"To date, the CDC has
conducted no safety testing on the possible harmful effects of simultaneously
administering multiple vaccines to infants,...[tests that might actually
tell something have yet to be developed and tests that say nothing are
pointless.
and has steadfastly refused to
state a preference for mercury-free vaccines to be given to children and
pregnant
women." [Rather than telling the truth in deference to reactionaries, that
removing Mercury made no difference at all to Autism rates and the
environmental load is many many times that of what's in a vaccine,
completely swamping out any effect from removing them, even if there was a
difference. IOW They wisely kept their mouths shut in the face of the
irrelevant as, true or not, saying anything at all will trigger a blame
fest and know NOTHING congress might wind up with control over
not-know-enough CDC]
Ode
At 06:21 AM 6/15/2008 -0700, you wrote:
This one's for Ode,
INFANT PRIMATES GIVEN VACCINES ON U.S. CHILDREN'S IMMUNIZATION SCHEDULE
DEVELOP BEHAVIORAL SYMPTOMS OF AUTISM
_http://www.nationalautismassociation.org/press051908.php_
(http://www.nationalautismassociation.org/press051908.php)
GROUNDBREAKING RESEARCH PROVIDES EVEN MORE SCIENCE SUPPORTING THE THEORY
THAT VACCINES CAN AND DO CAUSE AUTISM
Nixa, MO - A primate model for autism using the U.S. children's
immunization schedule was unveiled at the International Meeting For Autism
Research
(IMFAR) this weekend. The research underscores the critical need for
studies into
vaccine safety and the immune and mitochondrial dysfunction of autistic
children. The National Autism Association (NAA) questions why the
government hasn'
t undertaken these vital studies and why researchers have had to depend on
private money to perform this critical science that will surely impact the
health of millions of children worldwide.
While the authors and organizations associated with this study are
withholding comment until publication, University of Pittsburgh's Dr.
Laura Hewitson,
Ph.D., described at the IMFAR meeting how vaccinated animals, when compared
to unvaccinated animals, showed significant neurodevelopmental deficits and "
significant associations between specific aberrant social and non-social
behaviors, isotope binding, and vaccine exposure."
Researchers also reported at the scientific meeting that "vaccinated animals
exhibited progressively severe chronic active inflammation whereas unexposed
animals did not" and found "many significant differences in the GI tissue
gene expression profiles between vaccinated and unvaccinated animals."
Gastrointestinal issues are a common symptom of children with regressive
autism.
NAA calls for the NIH to conduct large scale, non-epidemiological studies
into the biomedical symptoms surrounding young children and all vaccines,
including those containing the mercury-based preservative thimerosal and
other
additives like aluminum.
This request for further research echoes that of Dr. Bernadine Healy, Former
NIH Director in a CBS interview earlier this week. "I think public health
officials have been too quick to dismiss the hypothesis as 'irrational,'
without sufficient studies of causation... without studying the
population that got
sick," Healy said. "I have not seen major studies that focus on 300 kids who
got autistic symptoms within a period of a few weeks of the vaccines."
Recently the government's vaccine court conceded the case of Hannah Poling,
admitting that vaccines triggered her regression into autism by exacerbating
mitochondrial dysfunction. "The recent Poling case and this new research
provide further evidence that the CDC has fallen down on their job to protect
children from harm. The biomedical research to date suggests that parental
reports of regression following vaccination is not only plausible, but
likely in
certain individuals," said Scott Bono, NAA Chairman. "To date, the CDC has
conducted no safety testing on the possible harmful effects of simultaneously
administering multiple vaccines to infants, and has steadfastly refused to
state a preference for mercury-free vaccines to be given to children and
pregnant
women. It's time for HHS and Congress to step in and take vaccine safety
away from the CDC."
On June 4th, parents of vaccine-injured children will rally for toxin-free
immunizations in Washington, DC. For more information visit
_www.nationalautism.org_ (http://www.nationalautism.org/) .
----- Original Message ----- From: "Ode Coyote" <odecoy...@alltel.net>
To: <silver-list@eskimo.com>
Sent: Saturday, June 14, 2008 9:32 AM
Subject: Re: CS>Dental Mercury Victory....FDA MUST classify fillings
How are people screwing up your genes?
What I was suggesting was the value and wisdom of preventing already
screwed up genes from being passed down.
Ode
And I don't think *anyone* has the right to screw up my genes without my
knowledge and consent. But it is being done, on purpose anyway.
Sometimes I wonder why I bother voting, except maybe to be heard from.
kathryn
On Jun 13, 2
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