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NEWSLETTER
VOLUME 5, ISSUE 1
by
Dr. Deborah Baker-Racine 2004-2005
US
Senate Bill 3 will PREVENT states from banning mercury in vaccines in
addition to individuals being compensated for the harm they have experienced
as a result of innoculations.
THIS
IS A PRESS RELEASE FROM http://www.nomercury.org/
TAKE ACTION!
LET THESE SENATORS
KNOW HOW YOU FEEL ABOUT THIS. GO TO THIS SITE FOR
SUGGESTIONS ON LETTER WRITING AND FAX COMPOSTION!! www.NoMercury.org.
Dear Parent/Adovate:
Please look closely
at US Senate Bill 3. A copy of the bill is available
at http://www.nomercury.org/
Under the guise
of Protecting America in the War on Terror, US Senators Gregg, Frist,
Sessions, DeWine, Allen, Santorum, McConnell, and DeMint have introduced
S. 3 which calls for many sweeping changes in pharmaceutical product
liability, vaccine regulation, policy, research and The Vaccine Injury
Compensation Act. This directly impacts those families whose children
have suffered adverse vaccine reactions, Gulf War Veterans, and any
other veteran who suffers from adverse reactions from the multiple vaccines
given (remember the ill-fated anthrax vaccine and small-pox vaccines).
The most recent
bill introduced in the U.S. Senate (S. 3) is aimed at liability protection
of drugs and vaccines and to prevent state legislation to ban Thimerosal
(mercury) in vaccines. This bill is worse than the Eli Lilly provision
of the Homeland Security Act and is a direct gift to the pharmaceutical
companies. The pharmaceutical industry gave almost $45 million in campaign
contributions for Presidential and Congressional elections since 2002
(www.opensecrets.org) and the health care/pharmaceutical industry has
over 600 lobbyists in Washington, D.C. alone. If constituents do not
weigh in on this horrendous bill, the American people will suffer; having
their civil rights violated and state autonomy will be compromised.
It is an insult to every state elected official and every American.
This bill is being
fast-tracked and is already on the agenda at the National Vaccine Advisory
Committee meeting, scheduled for February 8, 2005 at 10:45 am: http://www.hhs.gov/nvpo/nvac/agenda.html.
It would also severely
limit the public access to any information regarding vaccine research,
vaccine production, vaccine regulations, including, but not limited
to meetings about vaccines and countermeasures for pandemics, epidemics,
etc. This bill places severe restrictions on FOIA and will impact your
ability to find out about drug/vaccine safety, regulation and policy.
The last thing this country needs is to give government the ability
to hold more closed meetings without accountability to the media/public.
Furthermore, Sec.
761 (a)(1) would preempt any state legislation regulating vaccines.
It would preempt State authority and legislation dealing with vaccines
or vaccines components, such as Thimerosal (mercury). Missouri currently
has three bills pending to ban mercury (Thimerosal) in vaccines. They
are Missouri SB 49, SB74 and HB 131. The States of Iowa and California
have already banned mercury in vaccines yet this bill will preempt such
legislation forcing states to allow vaccine manufacturers to continue
using toxic levels of mercury in vaccines (in excess of Federal EPA
safety guidelines). Numerous other states are pursuing similar legislation
such as Maryland, Nebraska, New York, Pennsylvania and Washington. Various
other states are also planning to introduce legislation banning mercury
in vaccines within the next few weeks/months, such as Ohio, Illinois,
North Carolina, Michigan, Massachusetts and Minnesota.
This horrendous
piece of Federal legislation would even prohibit the warning or informed
consent provisions for drugs, vaccines and biologics. Additionally,
this bill would prohibit punitive damages and cap compensatory damages
against any pharmaceutical company. This takes the saying to the victor
goes the spoils to a whole new and ominous level. If the FDA approves
it, the company making it is protected from liability. We have all seen
how attentive the FDA has been to protect Americans from dangerous drugs
such as Vioxx.
This cleverly crafted
legislation includes something nearly every American will understandably
want to support: raising the death gratuity for families of soldiers
killed in Iraq from $12,000 to $100,000 and increases other military
benefits. Including an unrelated but popular provision that should stand
alone legislatively seeks only to cloud the issues addressed in the
major portion of this bill's language. Every American supports increased
benefits for our soldiers and their families and that includes us. As
parents and loyal Americans, however, we believe that S. 3 has been
carefully crafted to unfairly paint parents who seek justice for vaccine
injured children into a political corner. Similar to the legislative
sleight of hand employed in the Homeland Security Bill fiasco in 2002
the sponsors of S.3 are manipulating the political process by tying
domestic programs affecting every American's health and safety to unrelated
anti-terrorism programs. In this way they are attempting to make legitimate
opposition to S. 3 politically unacceptable.
We question why
politically popular legislation supporting our troops is tied to a bill
with far-reaching provisions that affect and the safety of vaccines
given to millions of American children. Let's not confuse the issues.
We believe that by casting the vaccine safety provisions in the language
of fighting terrorism (epidemic countermeasures is S.3's new code word
for vaccines--this is truly Orwellian doublespeak) the American people
are being misled about S.3's impact on vaccine safety programs. Let's
deal with one thing at a time. Taking away the right of states to protect
their citizens from dangerous vaccine components and drugs like Vioxx
and Paxil does not translate into protecting our children--from terrorism
or anything else. All it does is give control of these matters--vaccines
and drugs--to a few powerful people who operate behind closed doors.
The vaccine safety provisions are pharma support positions, plain and
simple, and are not necessary for bio-terror defense, at least not in
this form.
It would also overhaul
The National Vaccine Injury Compensation Program to the detriment of
children and families. Other parts of this legislation are extremely
troublesome as well and you can go to No
Mercury and read the bill. This is not a benign bill--this
goes directly to counter state and parental efforts to protect children
from vaccine injuries.
Read a few excerpts
below. If this bill is as concerning to you as it is to other parents
and many members of the medical community, please contact all members
of the US Senate, particularly your Senators and members of the US Senate
Finance Committee (see their contact info below). This is not anti-terrorism--this
is Federalism gone wild!!!!
Finance
Committee
Republicans on Finance Committee
Grassley Charles R- IA
Chairman, Committee on Finance
135 Hart Senate Bldg.
Washington, DC 20510-1501
Tel: (202) 224.3744
Fax: (202) 228 0578
http://grassley.senate.gov/index.cfm?FuseAction=Contact.Home |
Hatch
Orrin R- UT
104 Hart Office Building
Washington, DC 20510
Tel: (202) 224-5251
Fax: (202) 224-6331
http://hatch.senate.gov/index.cfm?FuseAction=Offices.Contact |
Lott Trent
R- MS
487 Russell Senate Office Building
Washington, DC 20510
Phone: 202-224-6253
Fax: 202-224-2262
http://lott.senate.gov/index.cfm?FuseAction=Contact.Email |
Snowe, Olympia
R-ME
154 Russell Senate Office Buildg.
Washington DC 20510-1903
Ph 202-224-5344
Fax 202-244-1946
olympia@snowe.senate.gov |
Kyl Jon R-
AZ
730 Hart Senate Building
Washington, D.C. 20510
Phone: (202) 224-4521
Fax: (202) 224-2207
http://kyl.senate.gov/contact.cfm |
Thomas, Craig
R- WY
United States Senate
307 Dirksen Senate Office Building
Washington, D.C. 20510
Phone: 202-224-6441
Fax: 202-224-1724
http://www.senate.gov/%7Ethomas/html/contact.html |
Santorum Rick
R- PA
511 Dirksen Senate Office Building
Washington, DC 20510-3804
Phone: 202-224-6324
TTYD Number: 202-224-5024
Fax: 202-228-0604
http://santorum.senate.gov |
Frist Bill
R- TN
Office of Senator Bill Frist
509 Hart Senate Office Building
Washington, DC 20510
202-224-3344
202-228-1264 (fax)
http://frist.senate.gov/index.cfm |
Smith Gordon
R- OR
404 Russell Building
Washington, DC 20510-3704
Phone: (202)224-3753
Fax:(202)228-3997
http://gsmith.senate.gov/webform.htm |
Bunning Jim
R- KY
1717 Dixie Highway Suite 180
Fort Wright KY, 41011
Phone 859-341-6480
Fax: 859-341-6482
Jim@bunning04.com |
Crapo, Mike
R- ID
239 Dirksen Senate Office Building
Washington, DC 20510
phone 202-224-6142
FAX 202-228-1375
TDD 202-224-2806
http://www.crapoforsenate.com/contact_us.asp |
Democrats
on Finance Committee
Baucus Max
D- MT
511 Hart Senate Office Bldg.
Washington, D.C. 20510
(202) 224-2651
(202) 224-4700 (Fax)
(800) 332-6106 (from MT)
(202) 224-1998 (TDD)
http://www.senate.gov/~baucus/emailmax.html |
Rockefeller,
IV, John D. D- WV
531 Hart Senate Office Bldg
Washington, DC 20510
Ph: 202-224-6472
Fax: 202-224-7665
Email Address: senator@rockefeller.senate.gov |
Conrad, Kent
D-ND
530 Hart Senate Office Building
United States Senate
Washington, DC 20510-3403
Fax: (202) 224-7776
Online: http://conrad.senate.gov
E-mail: http://conrad.senate.gov/webform.html |
Jeffords, James
(I - VT)
728 Hart Senate Office Bldg.
Washington DC 20510
Phone: (202) 224-5141
Fax (202) 228-0776
http://jeffords.senate.gov/contact-form.html |
Bingaman, Jeff
D- NM
413 Dirksen Senate Office Building
Washington, D.C. 20510
(202) 224-5141
(202) 224-5521
TDD: (202) 224-1792
http://www.senate.gov/~jeffords/contact-form.html |
Kerry, John
F D-MA
304 Russell Bldg.
Third Floor
Washington D.C. 20510
(202) 224-2742 - Phone
(202) 224-8525 - Fax
http://kerry.senate.gov/bandwidth/contact/email.html |
Lincoln Blanche
L. D- AR
355 Dirksen Senate Building
Washington, DC 20510-0404
Phone: (202)224-4843
Fax: (202)228-1371
http://lincoln.senate.gov/webform.html |
Wyden Ron D-
OR
230 Dirksen Senate Office Building
Washington, DC 20510-3703
(202) 224-5244
fax (202-228-2717)
http://wyden.senate.gov/contact/ |
Schumer Charles
D- NY
313 Hart Senate Building
Washington, DC 20510
Phone: 202-224-6542
Fax: 202-228-3027
TDD: 202-224-0420
http://www.senate.gov/%7Eschumer/webform.html |
For GREAT
information on the dangers of vaccines contact:
Sheri Nakken,
R.N., MA, Classical Homeopath
Vaccination Information & Choice Network, Nevada City CA & Wales
UK
$$ Donations to help in the work - accepted by Paypal account
vaccineinfo@tesco.net voicemail US 530-740-0561
(go to http://www.paypal.com) or by mail
Vaccines - http://www.nccn.net/~wwithin/vaccine.htm
Vaccine Dangers On-Line course -
http://www.nccn.net/~wwithin/vaccineclass.htm
Homeopathy On-Line course - http://www.nccn.net/~wwithin/homeo.htm
ANY INFO OBTAINED HERE NOT TO BE CONSTRUED AS MEDICAL
OR LEGAL ADVICE. THE DECISION TO VACCINATE IS YOURS AND YOURS ALONE
OR
Sandy
at www.vaccinationnews.org
DID YOU
KNOW?????
These were passed
on to me...not sure how well they work..but kind of fun!
Before you head
to the drugstore for a high-priced inhaler filled with mysterious chemicals,
try chewing on a couple of curiously strong Altoids peppermints. They'll
clear up your stuffed nose.
Sore Throat? Just
mix 1/4 cup of vinegar with 1/4 cup of honey and take 1 tablespoon six
times a
day. The vinegar kills the bacteria.
Honey remedy for skin blemishes.. Cover the blemish with a dab of unpasteurized
honey and place a Band-Aid over it. Honey kills bacteria, keeps the
skin, sterile, and healing. Works overnight.
Listerine therapy
for toenail fungus... Get rid of unsightly toenail fungus by soaking
your toes in Listerine mouthwash. The powerful antiseptic leaves your
toenails looking healthy again
Great one for kids...Smart
splinter remover... just pour a drop of Elmers Glue-All over the splinter,
let dry, and peel the dried glue off the skin. The splinter sticks to
the dried glue.
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CARDIO-MAG
2.0 |
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True Magnesium
Orotate for Cardiovascular Health
Ask health-conscious
people about the mineral most important to their heart health,
and most will hit on magnesium right away. But few
people look beyond the amount of elemental magnesium in their supplements
to consider the importance of the other half of their magnesium
supplement – the chelating amino acid or anion to which it’s
bound. For instance, the widely-used magnesium oxide
has “extremely low” bioavailability (22.8%), making
it more likely to cause diarrhea; and on top of this
embarrassing side-effect, magnesium oxide is an antacid,
which can impair digestion and nutrient absorption.
But there’s more to the effects of a magnesium supplement than
its bioavailability. Because the “other half” of
one magnesium supplement is extensively documented to have profound
effects on cardiovascular health. That supplement is true,
fully-reacted Magnesium Orotate. Magnesium Orotate
is magnesium bound to orotic acid, a key intermediate in the
biosynthesis of pyrimidine nucleotides (a building block of the “letters”
of your DNA code, and of RNA, the messenger that delivers the instructions
from the DNA to the cellular machinery that assembles cellular proteins
based on DNA’s commands). Although little known and underappreciated,
decades of research and clinical trials have documented the powerful
benefits of Magnesium Orotate to the weakened heart.......READ
MORE
Researchers
find diabetes trigger, possible fix
Researchers in Boston
have pinpointed a primary trigger for the most common form of diabetes
and have uncovered evidence that simple, inexpensive aspirin-like drugs
could keep the disease that affects millions in check.
The researchers,
from Joslin Diabetes Center in Boston, discovered a genetic "master
switch" in the liver that is turned on when people become obese.
Obesity has long been linked to diabetes, but the reason, until now,
has been unknown. Joslin researchers found that once on, this switch
produces low-level inflammation, which disrupts the body's ability to
process insulin, causing type 2 diabetes.
But the researchers
took the finding one step further. Reasoning that aspirin-like drugs
are used to quell inflammation, they successfully used the drugs, called
salicylates, to eliminate the symptoms of type 2 diabetes in mice. Human
tests are already underway in Boston, though no results have been published.
"These drugs,
among the safest drugs known, can do a surprisingly good job of toning
down this inflammation," said Joslin researcher Dr.
Steven E. Shoelson,
lead author of the paper. "These are hopeful ideas for the future."
Shoelson warned
against rushing out to get salicylates. Their effectiveness has been
proved thus far only in mice.
"No one should
go out and take these drugs," said Shoelson. He said losing weight,
exercising, and eating healthy are the obvious things to do.
Nonetheless, researchers
at Joslin were excited about their findings and are preparing federal
grant requests to fund a major, multicity trial of salicylate therapy
for type 2 diabetes. And there are indications that the drugs could
also help stave off heart disease.
"There is good
reason to believe that this could develop into a therapy for diabetes.
The evidence is quite good," said Dr. Gokhan Hotamisligil, professor
of genetics and metabolism at Harvard School of Public Health, who was
not involved in the study. "I'm fully convinced this is where the
key therapies for diabetes will emerge from."
The findings appeared
Sunday in the online version of the journal Nature Medicine. The work
was funded by the federal government and the American Diabetes Association.
About 18 million
Americans have diabetes, and most have type 2 diabetes.
In type 2 diabetes,
the body's cells become resistant to insulin, which transports sugar
from the bloodstream into cells, giving cells energy to function. In
diabetes, this feeding is blocked, causing sugar to build up in blood.
Those afflicted
grow excessively thirsty, exhausted, and confused if the condition goes
untreated, and are at high risk for heart disease, stroke, blindness,
and amputations. About three-quarters of sufferers are obese or overweight.
Shoelson's team
began the experiment seeking the biological connections between weight
gain and diabetes. They knew that the livers of obese people accumulate
fat faster than any other organ, and that many overweight diabetic patients
had high levels of proteins - particularly one called NF-kB - in their
livers that normally trigger inflammation.
They zeroed in on
it and were stunned to discover its role in diabetes.
The scientists were
able to trigger inflammation and the symptoms of diabetes in lean, previously
healthy mice by using genetic techniques to turn on the gene that makes
NF-kB.
Normally, in response
to an infection, the liver produces massive amounts of NF-kB, which
triggers a biological process that sends white blood cells to an injury
site to fight off infections, causing inflammation in the process. NF-kB
acts as a master switch, triggering this complex and life-saving reaction.
But in obese mice,
Shoelson's team found that a fatty liver - for reasons still unknown
- also flipped on NF-kB, though at far lower levels.
The proteins secreted
when this low-level inflammation occurs disrupt the body's ability to
process insulin, leading to diabetes.
"We previously
knew that in obesity, the liver becomes fatty and that it accumulates
fat faster than other organs and tissues," said Shoelson.
"But until
now, we didn't know fat in the liver could orchestrate the entire inflammatory
process that results in insulin resistance, both locally and throughout
the body."
Shoelson's team
decided to use salicylates, already used as anti-inflammatory, to try
to stop low-level inflammation and diabetes symptoms triggered by NF-kB
- and was successful. As long as the mice got adequate doses, their
diabetes was held in check. Aspirin is the best known of this family
of drugs. But Shoelson found that it would take more than 20 aspirins
daily to suppress NF-kB in human diabetics, which would cause severe
gastrointestinal bleeding.
In human trials,
Shoelson is using a milder, commercially available prescription salicylate
called salsalate, used safely by thousands to treat joint pain. He is
negotiating with the National Institutes of Health to fund a large-scale
national trial.
Another intriguing
finding emerged from the study: Within the complex cascade of biological
events triggered by NF-kB, Shoelson found that C-reactive protein levels
were elevated. C-reactive protein, or CRP, has been found to be a strong
risk marker for heart disease.
Shoelson is preparing
an experiment to test if salicylates also can reduce CRP and thus heart
disease risk.
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DID YOU KNOW?????
You've heard it
everywhere..."Drink milk....lose weight!!". The U.S. dairy
industry has created a "Healthy Weight with Milk" campaign
to boost sales. What's the evidence? Most of it came from a researcher
who has a patent on the claim that dairy foods aid weight loss.
In a new study -
the largest so far - a high-dairy diet didn't help people lose weight.
Twenty-three obese patients on 1,500 calorie diets who were randomly
assigned to consume four servings of dairy a day, lost no more weight
or body fat after six months than 22 others who consumed one serving
a day.
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WARMLY,
DR.
DEB.
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