Monthly Archives: December 2013

Vaccine Information Network: Compilation on Flu Vaccines…Proof that they are worthless and dangerous

A Johns Hopkins scientist has issued a blistering report on influenza vaccines in the British Medical Journal (BMJ). Peter Doshi, Ph.D., charges that although the vaccines are being pushed on the public in unprecedented numbers, they are less effective and cause more side effects than alleged by the Centers for Disease Control and Prevention (CDC). Further, says Doshi, the studies that underlie the CDC’s policy of encouraging most people to get a yearly flu shot are often low quality studies that do not substantiate the official claims.  Read more…

Vaccine Information Network: Compilation of Videos “To Vaccinate or Not”

1229852_675119635832097_209265457_n“Your page has been a great help. I chose not to vaccinate my baby and yesterday she had her 2 month well check. When I told the nurse that I was not signing the forms to let her get vaccinated, she flipped out. Then the peds Dr. came in, did her well check then said they would no longer see my little one in their office.

There is also a vaccine-induced epidemic of diabetes, allergies, asthma, ear inflammations, ADHD and other neurological disorders as well as childhood cancers and leukemia, which is hardly surprising when one considers that babies and children whose nervous and immune systems are immature are being repeatedly and systematically poisoned with highly neurotoxic, allergenic and carcinogenic substances.  Go to Website…

INFECTIOUS DISEASE MORTALITY RATES before & after vaccines

UK-Deaths-1838-1978-CopyEngland/Wales: Combined infectious disease mortality rates 1838 – 1980

“The combined death rate from scarlet fever, diphtheria, whooping cough and measles among children up to fifteen shows that nearly 90 percent of the total decline in mortality between 1860 and 1965 had occurred before the introduction of antibiotics and widespread immunization. In part, this recession may be attributed to improved housing and to a decrease in the virulence of micro-organisms, but by far the most important factor was a higher host-resistance due to better nutrition.”-Medical Nemesis, Bantam Books, 1977

So, who is right? Here is what official government statistics of infectious disease mortality (number of deaths) show:  Read more and see graphs:

 

Black Seed: Curing Hep C & HIV (and other viruses)

Nigella Sativa, also known as ‘black seed,’ has been studied for a wide rage of health benefits, but not until recently was it discovered to hold promise as a curative agent against potentially lethal viral infections, including Hepatitis C[i] and now HIV.

 

Black Seed Extract 'Cures' HIV Patient Naturally

There are words you don’t use in medicine today, such as “cure.” But a remarkable case study in an HIV positive patient treated with black seed extract resulted in a sustained remission, indicating a safe, accessible and affordable alternative to highly toxic antiretroviral HIV drugs may already exist.

Nigella Sativa, also known as ‘black seed,’ has been studied for a wide rage of health benefits, but not until recently was it discovered to hold promise as a curative agent against potentially lethal viral infections, including Hepatitis C[i] and now HIV.

A remarkable case study published in August of this year in the African Journal of Traditional, Complementary, and Alternative Medicine described an HIV patient who after undergoing treatment with a black seed extract experienced a complete recovery, with no detectable HIV virus or antibodies against HIV in their blood serum, both during and long after the therapy ended. Green med…

STUDIES:

Effects of Nigella sativa on outcome of hepatitis C in Egypt AbstractRead abstract

Nigella Sativa Concoction Induced Sustained Seroreversion in HIV Patient. – GreenMedInfo Summary

Garlic/Black Cumin Seeds Study A combination of crushed garlic (Allium sativum) and black cumin seeds (Nigelia sativum) has been used as a traditional remedy for urinary tract infections. In-vitro antimicrobial testing suggested that the mixture of two spices in the ratio of 1:1 has antimicrobial effects on both Staphylococcus aureus and Escherichia coli specieS.

DEFINITION OF NIGELLA SATIVA:

Nigella sativa is an annual flowering plant, native to south and southwest Asia. It grows to 20–30 cm (7.9–12 in) tall, with finely divided, linear (but not thread-like) leaves. The flowers are delicate, and usually coloured pale blue and white, with five to ten petals. The fruit is a large and inflated capsule composed of three to seven united follicles, each containing numerous seeds. The seed is used as a spice.The seeds are frequently referred to as black cumin (as in Assamese: kaljeera or kolajeera or Bengali kalo jeeray), But black cumin (kala Jeera)[clarification needed] is different than Nigella sativa (Kali Jeeri).[citation needed] In south Indian language Kannada it is called [ಕೃಷ್ಣ ಜೀರಿಗೆ] “Krishna Jeerige”, but this is also used for a different spice, Bunium persicum.

Common names

In English, Nigella sativa seed is variously called fennel flower,[3] nutmeg flower,[3] black caraway,[3] Roman coriander,[3] and also called black cumin.[3] (see comment below on cumin). Other names used, sometimes misleadingly, are onion seed and black sesame, both of which are similar-looking, but unrelated.[citation needed] Blackseed and black caraway may also refer to Bunium persicum.[4]

 

Breaking News: Mayor signs bill to Ban GMOs on the Big Island of Hawaii, Kauii anti-GMO bill safe also

gmo_ban

Read more…Huffington Post (Big Island)

Some history on Kauii bill

Council overturns mayor’s veto, GMO bill SAVED-green flag!!!

VLA comment:  At one time we had a copy of the hearing on GMOs in the early day.  The Hawaiian Islands were posed to the Congress as “most important” to the Biotech companies because it is the place to grow the seed stock.  It will be very interesting to see how this turns out.  So far we can’t find the governor’s response.  HMMM!

 

 

Social Workers steal baby from mother’s womb

Woman-Pregnant-Holding-Stomach-Baby(NaturalNews) In a shocking series events British Social Workers from Essex Social services obtained a Court Order to forcibly remove a baby from its mother by caesarean section against the mothers will. Read the unbelievable story…

Sources for this article include

http://www.dailymail.co.uk
http://www.telegraph.co.uk
http://www.telegraph.co.uk
http://www.telegraph.co.uk

 

Elsevier (Sinister Evil) Medical Journals : Puts Monsanto as Associate Editor to force retraction of GMO study

antiElsevier3-320x319Fast forward to September 2012, when the scientific journal Food and Chemical Toxicology (FCT) published a study that caused an international storm (Séralini, et al. 2012). The study, led by Prof Gilles-Eric Séralini of the University of Caen, France, suggested a Monsanto genetically modified (GM) maize, and the Roundup herbicide it is grown with, pose serious health risks. The two-year feeding study found that rats fed both suffered severe organ damage and increased rates of tumors and premature death. Both the herbicide (Roundup) and the GM maize are Monsanto products. Corinne Lepage, France’s former environment minister, called the study “a bomb”.

Subsequently, an orchestrated campaign was launched to discredit the study in the media and persuade the journal to retract it. Many of those who wrote letters to FCT (which is published by Elsevier) had conflicts of interest with the GM industry and its lobby groups, though these were not publicly disclosed.

The journal did not retract the study. But just a few months later, in early 2013 the FCT editorial board acquired a new “Associate Editor for biotechnology”, Richard E. Goodman. This was a new position, seemingly established especially for Goodman in the wake of the “Séralini affair”.

Richard E. Goodman is professor at the Food Allergy Research and Resource Program, University of Nebraska. But he is also a former Monsanto employee, who worked for the company between 1997 and 2004. While at Monsanto he assessed the allergenicity of the company’s GM crops and published papers on its behalf on allergenicity and safety issues relating to GM food (Goodman and Leach 2004). Read more…

Elsevier also publishes, VACCINE journal and American Journal of Obstetrics and Gynecology (AJOG)

More on Elsevier who publishes over 1000 journals controlling the scientific community:

Elsevier funds NY Congresswoman, Carolyn Maloney to initiate sinister evil bill.. Excerpts

Feb. 2012  Monday, the publisher announced it was withdrawing its support of the Research Works Act, a proposed piece of legislation, sponsored by Congresswoman Carolyn Maloney that would have dropped the requirement that all publicly funded research be open to the public. Upon hearing the news, US Representatives Darrel Issa  and Carolyn Maloney immediately withdrew the bill, killing it.

Elsevier COVER UP & COLLUSION WITH THE CDC of 4,250% increase in abortion reports associated with the push to vaccinate pregnant women with the H1N1 untested Pandemic vaccine. Because of the successful cover up (riveting backstory) pregnant women now receive a flu shot (with no mention of the Thimerosal content) and a Tdap shot…that is 4 vaccine doses while pregnant.

 

 

Emergency Authorization Use: More on the 30 million narcolepsy-causing vaccines FDA/BARDA stockpiling for use on unwitting American Public

imageThe vaccine Pandemrix, (According to GSK, some 30 million doses of the vaccine were administered across Europe and 800 people, mostly children, developed narcolepsy) will be added to the national stockpile.The vaccine will not be available commercially; it will be placed in the U.S. government’s emergency stockpile, FDA said.

Letter of Acceptance from FDA

FDA site: GSK Influenza A (H5N1) Virus Monovalent Vaccine, Adjuvanted with ASO3.

VLA comment: This newly approved “Influenza A (H5N1) Virus Monovalent Vaccine, Adjuvanted is like Pandemrix, (Pandemrix, which has not been approved in the United States). It is also made by GSK and is almost identical in structure and has just been approved for our national stockpile. This vaccine contains the adjuvant ASO3 (contains Squalene) and (polysorbate 80) for use on the American people under Emergency Use Authorization*, so you won’t know what’s coming!  Generally unknown,  In June 23, 2011 the FDA approved Novartis FLUAD Influenza vaccine which contains a similiar adjuvant- MF596 (contains Squalene) and (polysorbate 80).

While GSK has acknowledged an association between the vaccine and the narcolepsy cases, it has said there is insufficient evidence to prove the adjuvant (ASO3) was to blame. Scientists believe AS03 may be the culprit in the narcolepsy cases though they have yet to decipher the precise nature of the association. Read article…

Read March 2013 Huffington Post…

GKS: The vaccine will be supplied in a kit consisting of one package containing 50 multidose vials of H5N1 antigen and two packages each containing 25 multidose vials of AS03 adjuvant. Since, as stated in your November 11, 2013, submission, you do not intend to market this product for commercial distribution. (Stockpiling for emergency authorization use). “Supporting the U.S. Government’s capability to help protect Americans against pandemics ranks among GSK’s most important U.S. public-health responsibilities,” said Bruce Innis, Vice President of Vaccines Development for GSK. “H5N1-related illness has thus far been rare, but life-threatening when it has occurred”.

GSK will make this vaccine available in the U.S. only if directed to by the Biomedical Advanced Development and Research Authority (BARDA) in the U.S. Department of Health and Human Services’ Office of the Assistant Secretary for Preparedness and Response. The GSK H5N1 pandemic influenza vaccine programme has been supported by a development contract (HHSO100200700029C) from BARDA. GSK’s Influenza A (H5N1) Virus Monovalent Vaccine, Adjuvanted, has also received marketing authorisation in Europe and Canada under the brand names, Pumarix™ and Arepanrix™ H5N1, respectively. Read more…

Pumarix: Glaxo’s super-charged product is the first to show it can confer protection in the event of a pandemic. European regulators have approved it under the brand name Pumarix  (contains Squalene) and (polysorbate 80)

Read more…

Some ingredients of the FDA approved vaccine (Nov. 22, 2013): ASO3, (contains Squalene) (polysorbate 80) & Thimerosal (mercury),

Division of Chemical, Biological, Radiological and Nuclear Medical Countermeasures (CBRN MCM)

Stockpiling Lifesaving MCMs
The Division of CBRN MCMs is responsible for developing and establishing stockpiles of lifesaving vaccines, drugs, and diagnostics against CBRN threats. The Project BioShield Act of 2004 established the Special Reserve Fund (SRF), a one-time appropriation of $5.6 billion (2004 – 2013) to accelerate the research, development and acquisition of MCMs against CBRN threat agents. Eight Project BioShield programs have led to the acquisition of MCMs for the Strategic National Stockpile (SNS). These include an anthrax vaccine for post-exposure prophylaxis, anthrax therapeutics, a novel smallpox vaccine, a smallpox antiviral drug, a botulinum antitoxin, and radiation countermeasures. Read more…

MUST READ…Bioshield Annual Report (2012) 

All Annual Bioshield Reports

*Emergency Use Authorization for Medical Counter-measures– Section 4 of the Act allows the HHSSecretary to issue an Emergency Use Authorization (EUA) after an emergency has been declared by the Secretary as described in the “Statutory Authority”section found on page 7. The EUA declaration justifies the use of a FDA-approved, licensed, or cleared product for an unapproved indication or an unapproved product for an indication over a specified period of time during the emergency.