December 23, 2012

Gardasil Victims Take Legal Action Against Merck Over Miscarriage, Deadly Reactions

When one Australian woman decided to lead the charge against Gardasil maker Merck after experiencing serious adverse reactions, she soon found another 7 Victorian women with similar intentions and experiences. Naomi Snell, a resident of Melbourne, Australia, suffered an auto-immune and neurological attack after being injected with the HPV shot Gardasil. After reading about a Sydney neurologist who exposed Gardasil as a potential cause of MS-like symptoms, Snell realized that Gardasil could be behind her recent health ailments.

She made a timeline of her declining health using reports from her doctor and physiotherapist. What she found was that the events unfolded right after she had received the Gardasil vaccine. At 28 years of age, Snell lost her ability to walk, suffered from crippling back and neck pain, and experienced convulsions that put her life on hold for 2 years. The health issues started soon after receiving the HPV shot in July 2008.

I never attributed it to my vaccine so I went back for my second and third dose, Ms Snell said. My doctors said I was a case for Dr House. They were baffled.

After launching the class action lawsuit against Merck, 7 Victorian women considered joining the case after experiencing similar reactions to the Gardasil vaccine. One woman linked the Gardasil injection to her miscarriage, which occurred afterwards in her local supermarket.

Gardasil has led to thousands of adverse reactions and even death

Naomi Snell is not the first Gardasil recipient to develop adverse reactions. In fact, many before her have actually died as a result of the Gardasil vaccine.

The Gardasil vaccine has a very questionable timeline, riddled with corruption and devastating side effects. Shockingly, the HPV shot led to 3,589 harmful reactions and 16 deaths between May 2009 and September 2010 alone. Of the 3,589 adverse reactions, many were debilitating. Permanent disability was the result of 213 cases; 25 resulted in the diagnosis of Guillain-Barre Syndrome; there were 789 other “serious” reports according to FDA documents.

Merck of course makes no mention of this in their deceptive advertisements, leading consumers to think that the vaccine is safe.

 

Source: https://www.activistpost.com/2011/11/gardasil-victims-take-legal-action.html

FDA Accused of Endangering U.S. Health by Caving to Cattle Farms on Antibiotics

MANHATTAN (CN) - A supine Food and Drug Administration is allowing the use of low doses of antibiotics in animal feed to deal with cramped and unsanitary conditions on cattle farms, according to the Union of Concerned Scientists and four other groups, raising the “specter of untreatable infections” just around the corner. 


The Natural Resources Defense Council, the Center for Science in the Public Interest, the Food Animal Concerns Trust, Public Citizen, and the Union of Concerned Scientists sued the U.S. FDA and its Commissioner Margaret Hamburg, the Center for Veterinary Medicine and its Director Bernadette Dunham, and the Department of Health and Human Services and its Secretary Kathleen Sebelius.

The watchdog groups say the FDA first approved feeding of “preventative” antibiotics to healthy livestock in the 1950s. 
But in 1977, the FDA found that found that “subtherapeutic” doses of penicillin and tetracyclines - at levels too low to treat disease - contributed to development of antibiotic-resistant bacteria that could be transferred to humans.

“This litigation does not concern targeted, short-term uses of antibiotics to treat animals that are already sick,” the complaint states.

The nonprofits say that the FDA never retracted its 1977 study, and later research confirmed its findings. Drug resistance is a fact of life for virologists and public health workers, who, for example, must design new forms of influenza vaccine each year to try to counter the diseases’ ability to survive old forms of vaccines and drugs.

“The misuse and overuse of antibiotics has given rise to a growing and dangerous trend of antibiotic resistance,” the complaint states. “Increasingly, bacteria are resistant to not one but multiple antibiotics, resulting in infections that are difficult to treat, require longer and more expensive hospital stays, and are more likely to be fatal. The Institute of Medicine of the National Academy of Sciences has warned that ‘[t]he specter of untreatable infections - a regression to the pre-antibiotic era - is looming just around the corner.’”

In 1999, four of the plaintiffs submitted citizen petitions asking the FDA to withdraw its approvals for nontherapeutic uses of antibiotics in livestock if the antibiotics are also important in human medicine.

The fifth plaintiff, the Natural Resources Defense Council, joined in 2005.

The nonprofits say the FDA “unreasonably delayed ruling on” these petitions, and “has never issued a final response to either petition.”

But the scientific evidence is overwhelming, the groups say.

“Approximately 80 percent of all antibiotics used in the United States today are used in livestock. Most of these drugs are not used to treat disease. Instead, they are given to healthy animals in their feed or water, both to promote faster growth and to prevent infections that tend to occur when animals are kept in cramped, unsanitary conditions. Research has shown that the use of antibiotics in livestock leads to the development of antibiotic-resistant bacteria that can be - and have been - transferred from animals to people through direct contact, environmental exposure, and the consumption and handling of contaminated meat and poultry products.”

The FDA’s failure to act, and to respond to the petitions, violates the Administrative Procedure Act and the Food and Drug Act, the groups say. 
They want the FDA ordered to withdraw its approval of subtherapeutic uses of penicillin and tetracyclines in animal feed.

They are represented by Mitchell S. Bernard from the Natural Resources Defense Council.

 

Source: https://www.activistpost.com/2011/05/fda-accused-of-endangering-us-health-by.html

Water Fluoridation War: Government Admits Dangers, Experts Speak Out

It was only a few years ago that if you labelled fluoride as a dangerous substance, you would be laughed at and scorned.

For years, a select minority of individuals were the only ones raising the awareness of this health concern. Their cries have been and continue to be met with dissonance, despite the fact that the public’s opinion on fluoride has changed much in just a short time.

In fact, even the United States government has called for lower levels of water fluoridation following a study published in Environmental Health Perspectives, which found that increased fluoride consumption led to decreased IQ in children.

Communities are attempting to end water fluoridation, mainstream news is acknowledging its negative effects, and even a number of professional dentists have recognized the dangers of fluoride, and spoken out against its use and distribution. Most recently, the Palmer City Council of Alaska passed an ordinance repealing the town’s water fluoridation mandate.

Sodium fluoride, the voyage from rat poison to toothpaste

Mainstream dentistry and oral health has been the vehicle through which sodium fluoride, a chemical byproduct of fluorine, has been injected into our everyday lives. Said to ‘fight tooth decay’ and ‘strengthen enamel,’ it has been proliferated into nearly every form of toothpaste. Dentists also apply fluoride topically to teeth during routine visits to produce said effects. It has been added to municipal water supplies since the early 1900s, under the same premise of aiding oral health and hygiene.

Despite this, fluoride has a notoriously negative track record in terms of how it is used, and the products that use it as an active ingredient. While being used in toothpaste and various mouth washes, fluoride is also the main ingredient in many rat poisons, Prozac (an anti-depressant found to actually lead to suicide and other health conditions), and is even labeled as a toxic substance.

In fact, the safety precautions regarding sodium fluoride are quite telling themselves:

Risk and Safety Phrases.
      • R25 – Toxic if swallowed.
      • R32 – Contact with acid liberates very toxic gas.
      • R36/38 – Irritating to skin and eyes.
      • S1/2 – Keep locked up and out of reach of children.
      • S22 – Do not breathe dust.
      • S36 – Wear suitable protective clothing.
      • S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)

Of course it is important to note that there is a difference between topical fluoride exposure and internal consumption. With topical fluoride exposure, the amount of actual internal exposure can be minimal. However, many forms of fluoride exposure are through the internal digestion of the substance that has been linked to reduced IQ in major studies. Fluoride tablets have been distributed to children in public schools, leading to the complete digestion of the substance, as opposed to topical use.

For quite some time there have been a host of individuals speaking out against water fluoridation and its inclusion in foods, oral hygiene products, and as psychotropic drugs. Many foreign countries have banned its inclusion in municipal water supplies, and many U.S. states are progressively moving towards the same, as research continues to come out on the subject.

More recently, many practicing dentists have admitted that water fluoridation is a health risk, and should be stopped. This demonstrates a profound nature of humility that most doctors and large drug companies have yet to realize. If the mainstream medical establishment could own up to its shortcomings and work towards changing them, there would be nothing to fear. Sadly, in pursuit of profit, they go to great lengths to maintain the guise of authenticity, while slowly shearing the individual of their health and wealth.

 

Source: https://www.activistpost.com/2011/11/water-fluoridation-war-government.html

Emergency Stockpile of Vaccines Set Up In UK

An extra two million flu vaccines have been ordered and an emergency “shot-pile” is being set up as health officials prepare for the flu season.

Last year there were reports of local shortages with older jabs being used to fill the shortfall.

The Chief Medical Officer for England, Prof Dame Sally Davies, said the contingency supply would be used to “smooth things out”.

Pregnant women, Over 65s, Health Workers and other at risk groups are all recommended to take the jab however the jabs insert states that Pregnant women, babies and more should not take the jab due to side effects that it may cause to the development of unborn babies to young children.

Last year, 14.7 million shots were ordered. For this winter 16.7 million have been ordered and 400,000 will be kept in reserve.

For the second year running there will be no advertising campaign in England to raise awareness, unlike in Scotland and Northern Ireland, however there are posters and leaflets all over hospitals and Doctors’ surgeries across the United Kingdom.

Many Doctors recommend the jab to patients when patents visit for other reasons.

Prof Davies questioned the usefulness of adverts, saying people “listen to trusted sources, not government”, suggesting that the majority of the public do not trust the government with their health.

She is instead relying on health workers, charities and pharmacies to target those at risk.

Bags of medicine from the pharmacist will carry messages encouraging people to have the jab as “patients in at risk groups are taking medicines,” she said.

Last winter more than 600 people in the UK died as a direct result of catching flu.

‘As a direct result’ simply means that Flu has resulted in death, the person may also have had other health problems that contributed to their death.

The vaccine itself, based on advice from the World Health Organization, will again protect against swine flu (H1N1) as well as the H3N2 and Flu B strains.

These are the same three viruses as last winter, but the government’s director of immunisation, Prof David Salisbury, warned patients they would be gambling if they were not immunised again this year.

“You actually need it just as much as last year,” he said.

He warned there was no evidence that last year’s shot would still offer protection and that “it’s playing high risk stakes thinking you’re protected”. This is likely due to the lack of evidence that last year’s shot worked last year..

Prof Davies again criticised healthcare workers who did not get vaccinated, saying they were “selfish” for not protecting their patients.

Last year 35% were vaccinated, up from 26% the year before.

Prof Salisbury said there had been renewed attempts to “persuade, influence and cajole employees”, but there also needed to be improvements within hospitals to make it easier for staff to get vaccinated.

He said that at Birmingham Children’s Hospital Foundation NHS Trust, 95% of front-line staff had had the seasonal flu jab, but that figure was as low as 10% in other areas.

Statistics used refer to people with Flu-LIKE symptoms, which most of the time is not any strain of Flu at all.

There are no official statistics for side effects or deaths as a result of the vaccine, this is due to many deaths and side effects being blames on other long term health problems.

Sources:

https://www.bbc.co.uk/news/health-15016840

https://www.telegraph.co.uk/health/flu/8244076/Leftover-swine-flu-vaccines-used-to-fill-flu-jab-shortfall.html

https://www.fluadvisor.co.uk/