Tag Archives: Vaccinations

Truth comes out: 2009 H1N1 flu pandemic ‘deaths’ of children were actually caused by MRSA

 

November 07, 2011

by: S. L. Baker

naturalnews.com

(NaturalNews) Remember two years ago when every news show featured hysterical reports about the so-called H1N1 pandemic and how the supposed killer flu was striking down healthy kids? True, many previously healthy children became critically ill, developing severe pneumonia and respiratory failure. And some tragically died after being diagnosed with H1N1. But was that really the accurate explanation of what caused their death?

According to the largest nationwide investigation to date of the flu in children who became critically ill, scientists from Children’s Hospital Boston have found another reason to explain the severity of the youngsters illness. It turns out that it most likely wasn’t H1N1 alone that caused healthy children to become so ill many died.

Instead, these kids were unknowingly infected with something else. That additional infection, the superbug known as methicillin-resistant Staphylococcus aureus (MRSA), spiked the risk for flu-related deaths 8-fold in children who were otherwise believed to be totally healthy before they became ill.

Learn more:http://www.naturalnews.com/034081_flu_pandemic_MRSA.html#ixzz1d4PEkfIz

 


Girls Now Hitting Puberty at 7 Years Old!!!

And you still dont see anything wrong with vaccinations, fluoride, BPA or processed foods…

Obama Implements CODEX ALIMENTARIUS By Executive Order– Establishing the National Prevention, Health Promotion, and Public Health Council

By Barbara H. Peterson

survivingthemiddleclasscrash

June 14, 2010

We knew that CODEX was right around the corner, and here it is, live and in color. Barry Soetoro, AKA Barack Hussein Obama, Imposter in Chief, on June 10, 2010, issued an Executive Order – Establishing the National Prevention, Health Promotion, and Public Health Council. In short, the CODEX council. The entire Executive Order is attached, but please read this part and understand just what it is saying:

“Section 6 (g) contains specific plans to ensure that all prevention programs outside the Department of Health and Human Services are based on the science-based guidelines developed by the Centers for Disease Control and Prevention under subsection (d) of this section.”

In other words, ALL prevention programs, even those outside of the umbrella of the Department of Health and Human Services, must align with CDC guidelines, which are “science-based.” What do we take for prevention? Herbs and vitamins. Herbs that you grow in your backyard and vitamins that are not approved by your doctor do not fall under these “science-based” guidelines, and are not allowed. Therefore, this will effectively open the door to outlawing ALL disease prevention practices that use herbs and vitamins not prescribed by a doctor, and implement CODEX ALIMENTARIUS right here in the good old U.S.A. Thank you, Semra Orhon Hughes, for the heads up!

Here is the entire Executive Order:

The White House

Office of the Press Secretary

For Immediate Release

June 10, 2010

Executive Order– Establishing the National Prevention, Health Promotion, and Public Health Council

EXECUTIVE ORDER

ESTABLISHING THE NATIONAL PREVENTION, HEALTH PROMOTION, AND PUBLIC HEALTH COUNCIL

By the authority vested in me as President by the Constitution and the laws of the United States of America, including section 4001 of the Patient Protection and Affordable Care Act (Public Law 111-148), it is hereby ordered as follows:

Section 1. Establishment. There is established within the Department of Health and Human Services, the National Prevention, Health Promotion, and Public Health Council (Council).

Sec. 2. Membership.

(a) The Surgeon General shall serve as the Chair of the Council, which shall be composed of:

(1) the Secretary of Agriculture;

(2) the Secretary of Labor;

(3) the Secretary of Health and Human Services;

(4) the Secretary of Transportation;

(5) the Secretary of Education;

(6) the Secretary of Homeland Security;

(7) the Administrator of the Environmental Protection Agency;

(8) the Chair of the Federal Trade Commission;

(9) the Director of National Drug Control Policy;

(10) the Assistant to the President and Director of the Domestic Policy Council;

(11) the Assistant Secretary of the Interior for Indian Affairs;

(12) the Chairman of the Corporation for National and Community Service; and

(13) the head of any other executive department or agency that the Chair may, from time to time, determine is appropriate.

(b) The Council shall meet at the call of the Chair.

Sec. 3. Purposes and Duties. The Council shall:

(a) provide coordination and leadership at the Federal level, and among all executive departments and agencies, with respect to prevention, wellness, and health promotion practices, the public health system, and integrative health care in the United States;

(b) develop, after obtaining input from relevant stakeholders, a national prevention, health promotion, public health, and integrative health-care strategy that incorporates the most effective and achievable means of improving the health status of Americans and reducing the incidence of preventable illness and disability in the United States, as further described in section 5 of this order;

(c) provide recommendations to the President and the Congress concerning the most pressing health issues confronting the United States and changes in Federal policy to achieve national wellness, health promotion, and public health goals, including the reduction of tobacco use, sedentary behavior, and poor nutrition;

(d) consider and propose evidence-based models, policies, and innovative approaches for the promotion of transformative models of prevention, integrative health, and public health on individual and community levels across the United States;

(e) establish processes for continual public input, including input from State, regional, and local leadership communities and other relevant stakeholders, including Indian tribes and tribal organizations;

(f) submit the reports required by section 6 of this order; and

(g) carry out such other activities as are determined appropriate by the President.

Sec. 4. Advisory Group.

(a) There is established within the Department of Health and Human Services an Advisory Group on Prevention, Health Promotion, and Integrative and Public Health (Advisory Group), which shall report to the Chair of the Council.

(b) The Advisory Group shall be composed of not more than 25 members or representatives from outside the Federal Government appointed by the President and shall include a diverse group of licensed health professionals, including integrative health practitioners who are representative of or have expertise in:

(1) worksite health promotion;

(2) community services, including community health centers;

(3) preventive medicine;

(4) health coaching;

(5) public health education;

(6) geriatrics; and

(7) rehabilitation medicine.

(c) The Advisory Group shall develop policy and program recommendations and advise the Council on lifestyle-based chronic disease prevention and management, integrative health care practices, and health promotion.

Sec. 5. National Prevention and Health Promotion Strategy. Not later than March 23, 2011, the Chair, in consultation with the Council, shall develop and make public a national prevention, health promotion, and public health strategy (national strategy), and shall review and revise it periodically. The national strategy shall:

(a) set specific goals and objectives for improving the health of the United States through federally supported prevention, health promotion, and public health programs, consistent with ongoing goal setting efforts conducted by specific agencies;

(b) establish specific and measurable actions and timelines to carry out the strategy, and determine accountability for meeting those timelines, within and across Federal departments and agencies; and

(c) make recommendations to improve Federal efforts relating to prevention, health promotion, public health, and integrative health-care practices to ensure that Federal efforts are consistent with available standards and evidence.

Sec. 6. Reports. Not later than July 1, 2010, and annually thereafter until January 1, 2015, the Council shall submit to the President and the relevant committees of the Congress, a report that:

(a) describes the activities and efforts on prevention, health promotion, and public health and activities to develop the national strategy conducted by the Council during the period for which the report is prepared;

(b) describes the national progress in meeting specific prevention, health promotion, and public health goals defined in the national strategy and further describes corrective actions recommended by the Council and actions taken by relevant agencies and organizations to meet these goals;

(c) contains a list of national priorities on health promotion and disease prevention to address lifestyle behavior modification (including smoking cessation, proper nutrition, appropriate exercise, mental health, behavioral health, substance-use disorder, and domestic violence screenings) and the prevention measures for the five leading disease killers in the United States;

(d) contains specific science-based initiatives to achieve the measurable goals of the Healthy People 2020 program of the Department of Health and Human Services regarding nutrition, exercise, and smoking cessation, and targeting the five leading disease killers in the United States;

(e) contains specific plans for consolidating Federal health programs and centers that exist to promote healthy behavior and reduce disease risk (including eliminating programs and offices determined to be ineffective in meeting the priority goals of the Healthy People 2020 program of the Department of Health and Human Services);

(f) contains specific plans to ensure that all Federal health-care programs are fully coordinated with science-based prevention recommendations by the Director of the Centers for Disease Control and Prevention; and

(g) contains specific plans to ensure that all prevention programs outside the Department of Health and Human Services are based on the science-based guidelines developed by the Centers for Disease Control and Prevention under subsection (d) of this section.

Sec. 7. Administration.

(a) The Department of Health and Human Services shall provide funding and administrative support for the Council and the Advisory Group to the extent permitted by law and within existing appropriations.

(b) All executive departments and agencies shall provide information and assistance to the Council as the Chair may request for purposes of carrying out the Council’s functions, to the extent permitted by law.

(c) Members of the Advisory Group shall serve without compensation, but shall be allowed travel expenses, including per diem in lieu of subsistence, as authorized by law for persons serving intermittently in Government service (5 U.S.C. 5701-5707), consistent with the availability of funds.

Sec. 8. General Provisions.

(a) Insofar as the Federal Advisory Committee Act, as amended (5 U.S.C App.) may apply to the Advisory Group, any functions of the President under that Act, except that of reporting to the Congress, shall be performed by the Secretary of Health and Human Services in accordance with the guidelines that have been issued by the Administrator of General Services.

(b) Nothing in this order shall be construed to impair or otherwise affect:

(1) authority granted by law to an executive department, agency, or the head thereof; or

(2) functions of the Director of the Office of Management and Budget relating to budgetary, administrative, or legislative proposals.

(c) This order is not intended to, and does not, create any right or benefit, substantive or procedural, enforceable at law or in equity by any party against the United States, its departments, agencies, or entities, its officers, employees, or agents, or any other person.

BARACK OBAMA

THE WHITE HOUSE,

June 10, 2010

http://www.whitehouse.gov/the-press-office/executive-order-establishing-national-prevention-health-promotion-and-public-health

(C) 2010 Barbara H. Peterson

“provide recommendations to the President and the Congress concerning the most pressing health issues confronting the United States and changes in Federal policy to achieve national wellness, health promotion, and public health goals, including the reduction of tobacco use, sedentary behavior, and poor nutrition;”

And all this will be under our “Obese” Surgeon General!
We really want our health controlled by someone who cant control their own!
Cant believe this one went by me last week!!



The American Cancer Society Runs With the Money and Away from the Cure, Part I

June 14, 2010

by: Tony Isaacs

NaturalNews.com

(NaturalNews) The American Cancer Society (ACS) was back in the news this month when they disputed the findings of the President’s Cancer Panel on the role of toxins in causing cancer. Though the new report echoes what other experts have maintained for years, the ACS went out of its way to attack the report and downplay the role of toxins. Many critics have questioned the ACS’s apparent conflicts of interest due to numerous ACS ties to chemical industries’ influence and donations.

Critics note that the ACS condemnation of the toxins report is far from the first time the Society has taken a stance that benefits those it has ties to while disputing expert reports and studies. Indeed, the ACS dispute of the report is merely the latest in a long line of controversial stances that appear to be self-serving and against the public interest.

Another example is the ACS’s continued support of mammograms. Concerns over the safety and efficacy of mammograms have been widely reported dating all the way back to 1977, including several notable studies supporting such concerns. In spite of those studies and concerns, the ACS has remained a staunch supporter of mammograms. Notably, the ACS has strong ties to the mammography industry.

Last year the Journal of the American Medical Association (JAMA) reported that mammograms increased “the burden of low-risk cancers without significantly reducing the burden of more aggressively growing cancers and therefore not resulting in the anticipated reduction in cancer mortality”. After the JAMA paper, it was initially reported that the ACS would finally change their stance on mammograms – as they once did with tobacco after years of stonewalling. However, the pro-mammogram interests in the ACS apparently won out and such reports were later denied.

As Dr. Len Lichtenfeld, deputy chief medical officer of the American Cancer Society stated: “We are not redoing or rethinking our guidelines at this time, nor are we going to restate our guidelines to emphasize the inadequacies of screening.”

Although the ACS annually pleads poverty, it actually takes in more money than any other US charity and has huge cash reserves, property and other assets. Further, despite public promises to do everything to “wipe out cancer in your lifetime,” the ACS has failed to make its voice heard in Congress and regulatory agencies. Instead, the ACS has repeatedly rejected or ignored opportunities and requests from Congressional committees and other agencies and groups to provide scientific testimony critical to legislate and regulate a wide range of occupational and environmental carcinogens.

The scope of the ACS failure to act is illustrated by increases in a wide range of cancers, including:

Non-Hodgkin’s lymphoma has increased 76 percent mostly due to phenoxy herbicides and phenylenediamine hair dyes.

Testicular cancer has increased by 49 percent due to pesticides, harmful ingredients in personal care products and estrogen residues in meat.

Malignant melanoma has increased by 168 percent due to the use of toxic sunscreen products that fail to block long wave ultraviolet light.

Thyroid cancer has increased by 124 percent due in large part to ionizing radiation.

Childhood leukemia has increased by 55 percent due to ionizing radiation, domestic pesticides, nitrite preservatives in meats and parental exposures to occupational carcinogens.

Ovarian cancer (mortality) for women over the age of 65 has increased by 47 percent in African American women and 13 percent in Caucasian women due largely to genital use of talc powder.

Breast cancer has increased 17 percent due to a wide range of factors including birth control pills, estrogen replacement therapy, ingredients in cosmetics and personal care products, and mammogram and other diagnostic radiation.


The Beautiful Truth Trailer

This movie is a MUST see…

Its life saving information!

You have to WANT to help yourself.


Recalled children’s Tylenol products were knowingly contaminated, says FDA


by Mike Adams, the Health Ranger

NaturalNews.com

(NaturalNews) The other day I wrote a story about the massive recall by McNeil Consumer Healthcare, a subsidiary of Johnson & Johnson, of its infants’ and children’s line of Tylenol products. An FDA inspection report found these drugs to be contaminated with dangerous bacteria (they did not disclose the actual type) as well as “foreign materials” that were visible as “dark or black specks”. But a recent story published by USA Today has revealed that McNeil actually knew about the bacterial contamination and kept shipping the products anyway.

Only the drug industry could get away with this type of careless, reckless behavior with nothing more than a slap on the wrist from the FDA. In fact, the FDA did not even require McNeil to issue a recall after discovering the problem; McNeil did so voluntarily over “theoretical concerns” that were expressed by Deborah Autor, an FDA official who was quick to emphasize that the risk to consumers from the tainted products “is remote”.

So let me get this straight. An FDA report finds that a pharmaceutical company is knowingly using contaminated raw materials to make children’s and infants’ medicines in a factory that is failing to maintain its equipment, properly train its employees and correctly measure and weigh drug ingredients, and FDA officials consider the problem to be “theoretical”?

Can you imagine what would happen if an herbal product manufacturer were found to engage in the same behavior? The FDA would pounce on them, seize their products, issue a public warning and probably fine the company for its reckless behavior. But when Big Pharma pulls the same stunt, it’s just business as usual.

To the FDA, it’s all just “theoretical”

My favorite part about this is the FDA’s reliance on the word “theoretical” to try to imagine that somehow no actual safety problem existed. According to my thesaurus, some other words for theoretical include unsubstantiated and hypothetical. In other words, the FDA is saying it does not actually believe that a real risk even exists!

And yet FDA Commissioner Margaret Hamburg, at the same time as the agency is saying there really is no risk and that the whole thing is just a hypothetical situation, advises parents to “discontinue using any of the name-brand products being recalled.”

Overdosing on acetaminophen, especially in children, is a serious issue. The Mayo Clinic website warns parents that overdosing on the drug, even a little bit, can lead to “life-threatening liver problems.”

The FDA report specifies that McNeil’s had not been properly formulating the drug dosages in its children’s and infants’ medicines, which is part of the reason for the recall. Improper concentrations of active ingredients in these products potentially puts millions of children at risk. But apparently this is no big deal to the FDA which sees it as nothing more than a “hypothetical” problem.

Yet, just prior to its expression of “theoretical” concern in the current recall, FDA officials met with McNeil back in February to express “serious concerns” about the company’s poor manufacturing processes and failures to follow good manufacturing practices. So which is it?

This kind of double-speak is typical of the FDA when a case involves a beloved drug company. If this had been a supplement that was “hypothetically” thought to be contaminated (even if conclusive evidence revealed there was no threat at all), health food stores everywhere would be ordered to strip it from their shelves. But when drug company negligence leads to the contamination of children’s medicines with bacteria, unknown particles and improper drug dosage levels, the FDA leaves it to the company to “voluntarily” recall their own products. There will probably be no fine levied against the company, either.

The FDA may not even hold McNeil responsible for its gross negligence

According to a recent Los Angeles Times article, the FDA has not even decided what corrective action it is going to take. According to the story, “options range from sending a warning letter to seeking criminal penalties.”

So in essence, the options include doing nothing or actually holding McNeil responsible for putting the lives of millions of children at risk. To me, only one of these is a really a viable option. But based on the FDA’s track record in dealing with McNeil (and all other drug companies, for that matter), the agency is likely to just sweep the whole thing under the rug.

Never mind that a warning letter had already been sent to a McNeil plant in Puerto Rico several months ago over wooden shipping pallet chemicals that had been found in other McNeil drugs, causing 70 people to became ill with digestive problems. When it comes to regulating drug companies, the FDA has a very short memory.

Can any children’s medicines be trusted?

Johnson & Johnson is one of the world’s largest companies, and is consistently rated by both Harris Interactive’s National Corporate Reputation Survey and Barron’s Magazine as being one of the top, most well respected companies in the world.

If the world’s most respected company, a “family company”, is operating a subsidiary that is knowingly manufacturing contaminated children’s medicines in factories that are in violation of numerous safety protocols, what does that say about the entire drug industry? If the safety and quality of children’s medicines from one of the world’s most respected companies cannot be trusted, then what over-the-counter medicines can you really trust?

Most children’s medicines are filled with chemical toxins anyway

Bacterial contamination and poor manufacturing procedures are not the only problems with popular over-the-counter (OTC) children’s medicines. Even if McNeil had been operating up to proper standards, many of its children’s formulations are still filled with questionable chemical ingredients like aspartame, high-fructose corn syrup, sucralose (Splenda), artificial colors and preservatives, and even parabens, all of which are approved by the FDA for use in children’s and infants’ formulas. (Seriously.)

The shocking truth is that, even in their approved and “safe” forms, most OTC children’s medicines are nothing more than dangerous chemical cocktails being peddled as medicine. They’re filled with so much harmful garbage that they can hardly be considered beneficial. Most of them are outright useless. These OTC children’s medicines are the quackery of modern medicine.

Back in 2004, I wrote a story about a U.K. study which found that children’s cough syrup is medically ineffective. In tests, it proved to be just as effective as corn syrup at alleviating a cough, so basically it did nothing at all.

Most cough syrup is composed primarily of corn syrup anyway, so it is no surprise that the stuff causes the same effect on the body — basically just a sugar overload.

Pharmaceutical drugs are almost never a good choice for children. Not only do the active ingredients cause serious side effects and liver problems, but the chemical additives make them even more harmful. I think if more parents became informed about what’s really in children’s medicine, they would never willingly give it to their children.

All these things really just illustrate the FDA’s corruption and behind-the-scenes protection of drug company interests. Even when a serious problem arises above and beyond the known risks, the agency acts as if it is no big deal. The health and well-being of millions of children is put at risk but it’s all just make-believe to the FDA.

To them, all risks and side effects of pharmaceuticals are merely “theoretical.” But in their (warped) minds, the dangers of herbs and vitamins are all “very real!”

It raises a very important question: How many children need to be harmed or even killed by the Big Pharma / FDA conspiracy before the American people will demand real FDA reform?

If Parents out there are not in a uproar about this…

I don’t know what will do it for you?

Children are innocent and have no way to protect themselves,

its your responsibility!


The 10 Biggest Health Care Lies In America

Wednesday, April 21, 2010

by Mike Adams, the Health Ranger

Editor of NaturalNews.com

(NaturalNews) Mainstream health care isn’t based on “health” or “caring.” It’s actually based on an engrained system of medical mythology that’s practiced — and defended — by those who profit from the continuation of sickness and disease. This system of medical mythology might also simply be called “lies”, and today I’m sharing with NaturalNews readers the top ten lies that are still followed and promoted under mainstream health care in America today.

Lie #1) Vaccines make you healthy

Vaccines have emerged as the greatest and most insidious mythology yet fabricated by western medicine. The idea that vaccines protect you from infectious disease is blatantly false in the long term because this year’s flu shot actually makes you more susceptible to next year’s influenza (http://www.naturalnews.com/028538_s…).

On top of that, even the theoretical short-term effectiveness of vaccines is dwarfed by the far more effective protection offered by vitamin D and other immune-modulating nutrients. (http://www.naturalnews.com/027385_V…)

Lie #2) Pharmaceuticals prevent disease

The big push by Big Pharma is now focused on treating healthy people with drugs as if pharmaceuticals were nutrients that could somehow prevent disease. This is the new push with cholesterol drugs: Give ‘em to everyone, whether they have high cholesterol or not!

But pharmaceuticals don’t prevent disease, and medications are not vitamins. Your body has no biological need for any pharmaceuticals at all. People who believe they need pharmaceuticals have simply been the victims of “fabricated consent” engineered by Big Pharma’s clever advertising and P.R. spin.

Lie #3) Doctors are experts in health

Doctors don’t even study health; they study disease. Modern doctors are taught virtually nothing about nutrition, wellness or disease prevention. Expecting a doctor to guide you on health issues is sort of like expecting your accountant to pilot a jet airliner — it’s simply not something he or she has ever been trained in.

That’s not to say doctors aren’t intelligent people. Most of them have high IQs. But even a genius can’t teach you something they know nothing about.

Lie #4) You have no role in your own healing

Doctors, drug companies and health authorities all want you to believe that your health is determined by their interventions. If you believe them, you have virtually no role in your own health or healing — it’s all managed by their drugs, their screening, their surgeries and their interventions.

Lie #5) Disease is a matter of bad luck or bad genes

Western medicine wants you to believe in the mythology of spontaneous disease — disease that strikes without cause. This is equivalent to saying that disease is some sort of voodoo black magic and that patients have no way to prevent disease through their own diets or lifestyle choices.

It’s funny, actually: Western medicine claims to be driven by scientific, rational thinking, and yet the entire industry still fails to acknowledge that chronic disease always has a cause and that most of the time, that cause has everything to do with nutritional deficiencies, exposure to toxic chemicals and a lack of exercise.

Disease is almost never a matter of bad luck or bad genes.

Lie #6) Screening equals prevention

Western medicine doesn’t believe in disease prevention. Rather, the industry believes in screening while calling it prevention. But screening isn’t prevention by even the wildest stretch of the imagination. In fact, virtually all the popular screening methodologies actually promote diseases.

Mammography, for example, emits so much radiation that it causes breast cancer in tens of thousands of women each year (http://www.naturalnews.com/027558_m…). Imaging dyes used in radiological scans can cause horrific side effects, and psychiatric “disorder” screening is little more than a thinly-disguised patient recruitment scheme disguised as medicine.

Real prevention of disease must involve disease prevention through nutrition, patient education about the causes of disease and lifelong changes in eating habits. Yet western medicine teaches absolutely none of these things. Heck, it doesn’t even believe in such ideas.

Lie #7) Health insurance will keep you healthy

This is a favorite lie of those who recently pushed for the Big Pharma-sponsored health care reform that has swept across America. The lie supposes that merely having health insurance will provide some sort of magical protection against disease. But in reality, health insurance doesn’t make you healthy! It is only YOU and your choices about foods, exposures to toxic chemicals, pursuit of exercise and time in nature that can make you healthy.

Health insurance is, in effect, a wager that you will get sick. How does gambling on your sickness provide any protection whatsoever for your health? It doesn’t. Personally, I’d rather bet on health than sickness, and the way to do that is to invest in nutritional supplements, organic produce, superfoods, physical fitness and non-toxic personal care products.

Lie #8) Hospitals are places of health and healing

If you want to stay healthy or get healthy, a hospital is the very last place you want to find yourself: They are unhappy, unhealthy places that are infested with antibiotic-resistant superbugs. Hospitals usually serve disease-promoting foods and lack health-enhancing sunlight, and potentially deadly mistakes with pharmaceuticals or surgical procedures now appear to be frighteningly common in U.S. hospitals.

Certainly, emergency rooms in hospitals play an important role in urgent care for injuries and accidents — and emergency room physicians do an amazing job saving lives — but for people with chronic, degenerative disease, a hospital is a very dangerous place to be. Unless you really need immediate critical care, try to avoid hospitals.

Lie #9) Conventional medicine is “advanced” state-of-the-art medicine

Even though doctors and health authorities try to pass off western medicine as being “advanced” or “modern,” the whole system is actually pathetically outdated and stuck in the germ theory of disease. Western medicine has yet to even acknowledge the role of nutrition in preventing disease — something that has been scientifically documented for at least the last several decades. Western medicine fails to acknowledge mind-body medicine and hilariously believes the mind plays virtually no role in healing.

Neither does western medicine acknowledge the bio energy field of living systems, nor that organ transplants carry memories, nor that living food is qualitatively different from dead food. Seriously: Conventional doctors still believe that dead food is exactly the same as living food! (And the USDA food pyramid still makes no distinction between the two…)

“Modern” medicine isn’t so modern, it turns out. It is, in fact, hopelessly outdated and desperately needs to upgrade its approach to health and wellness if it hopes to survive the next hundred years.

Lie #10) More research is needed to find “cures”

This lie is especially hilarious because western medicine does not believe in any “cure” for any disease. They aren’t even looking for cures! This lie has been repeated since the 1960′s, when cancer scientists claimed they were only a few years away from curing cancer. Today, four decades later, can you think of a single major disease that western medicine has cured? There aren’t any.

That’s because drug companies make money from sick people, not cured people. A patient cured is a patient lost. It is far more profitable to keep patients sick and pretend to “manage” their disease through a lifetime of pharmaceuticals. So when drug companies and disease non-profits claim to be searching for a “cure,” what they’re really doing is taking your money to fund more drug research to patent more medications that don’t actually cure anything.

Remember this the next time you’re asked to donate to some search for “the cure.” The cures already exist in nutrition, herbal remedies and naturopathic medicine, but Big Pharma and the conventional medicine cartel isn’t interested in real cures — they only want to promote the idea of a cure while pumping patients full of drugs that don’t cure anything.

Beyond the ten lies

When it comes to western health care, there are more than 10 lies, of course, but these big 10 lies are perhaps the most relevant to your own health decisions. By avoiding being suckered in by these lies, you can take charge of your own health and avoid the health care scam by staying healthy!

Staying healthy isn’t as difficult as you think, and it doesn’t require health insurance or disease screening. It only requires making informed, intelligent decisions about what to eat, what to put on your skin and how to get more sunshine and physical exercise. Once you do these basic things, you’ll find that you are no longer held victim by a western medicine health care system based on lies and outdated medical mythology.

It’s time for a revolution in medicine… a revolution that finally advances past the mental roadblock of a system of medical mythology stuck in the 1940′s. Don’t get me wrong, 1940′s medicine was great in the 1940′s. But this is no longer the 1940′s, and the germ theory of disease is hopelessly outdated when it comes to the primary diseases that are striking the population today. Yet the profiteers of our dishonest, outmoded health care system are doing everything in their power to keep us all stranded in the past, a past based on treating the body like a chemical battleground and attacking every disease with a patented pharmaceutical.

That whole approach to health care is so far outdated that it’s hilarious it can still be pushed with a straight face. No wonder doctors only spend an average of two minutes with patients these days. That’s the limit of how long they can hold their faces without breaking out in laughter at how stupid this whole “treat the symptoms and forget the causes” approach to health care really is. Even they know it! That’s why most doctors actually eat superfoods and take vitamins themselves, even if they never dare suggest it to patients.

True fact: It is illegal in every U.S. state for a doctor to recommend any vitamin, nutrient or food for the prevention or treatment of any disease. Doing so can cause a doctor to have his medical license permanently revoked. How crazy and outdated is that?


20 Ways ObamaCare Will Take Away Our Freedoms

www.fireandreamitchell.com

With ObamaCARE now passed, containing the Cornhusker Kickback, Gator-Aid, the Lousiana Purchase, and other shady deals, Investors Business Daily gives up 20 ways that ObamaCARE will take away our freedoms. IBD’s sections described below are taken from HR 3590 as agreed to by the Senate and from the reconciliation bill which takes out the Cornhusker Kickback and Gator-Aid as displayed by the Rules Committee.

1. You are young and don’t want health insurance? You are starting up a small business and need to minimize expenses, and one way to do that is to forego health insurance? Tough. You have to pay $750 annually for the “privilege.” (Section 1501)

2. You are young and healthy and want to pay for insurance that reflects that status? Tough. You’ll have to pay for premiums that cover not only you, but also the guy who smokes three packs a day, drink a gallon of whiskey and eats chicken fat off the floor. That’s because insurance companies will no longer be able to underwrite on the basis of a person’s health status. (Section 2701).

3. You would like to pay less in premiums by buying insurance with lifetime or annual limits on coverage? Tough. Health insurers will no longer be able to offer such policies, even if that is what customers prefer. (Section 2711).

4. Think you’d like a policy that is cheaper because it doesn’t cover preventive care or requires cost-sharing for such care? Tough. Health insurers will no longer be able to offer policies that do not cover preventive services or offer them with cost-sharing, even if that’s what the customer wants. (Section 2712).

5. You are an employer and you would like to offer coverage that doesn’t allow your employers’ slacker children to stay on the policy until age 26? Tough. (Section 2714).

6. You must buy a policy that covers ambulatory patient services, emergency services, hospitalization, maternity and newborn care, mental health and substance use disorder services, including behavioral health treatment; prescription drugs; rehabilitative and habilitative services and devices; laboratory services; preventive and wellness services; chronic disease management; and pediatric services, including oral and vision care.

You’re a single guy without children? Tough, your policy must cover pediatric services. You’re a woman who can’t have children? Tough, your policy must cover maternity services. You’re a teetotaler? Tough, your policy must cover substance abuse treatment. (Add your own violation of personal freedom here.) (Section 1302).

7. Do you want a plan with lots of cost-sharing and low premiums? Well, the best you can do is a “Bronze plan,” which has benefits that provide benefits that are actuarially equivalent to 60% of the full actuarial value of the benefits provided under the plan. Anything lower than that, tough. (Section 1302 (d) (1) (A))

8. You are an employer in the small-group insurance market and you’d like to offer policies with deductibles higher than $2,000 for individuals and $4,000 for families? Tough. (Section 1302 (c) (2) (A).

9. If you are a large employer (defined as at least 101 employees) and you do not want to provide health insurance to your employee, then you will pay a $750 fine per employee (It could be $2,000 to $3,000 under the reconciliation changes). Think you know how to better spend that money? Tough. (Section 1513).

10. You are an employer who offers health flexible spending arrangements and your employees want to deduct more than $2,500 from their salaries for it? Sorry, can’t do that. (Section 9005 (i)).

11. If you are a physician and you don’t want the government looking over your shoulder? Tough. The Secretary of Health and Human Services is authorized to use your claims data to issue you reports that measure the resources you use, provide information on the quality of care you provide, and compare the resources you use to those used by other physicians. Of course, this will all be just for informational purposes. It’s not like the government will ever use it to intervene in your practice and patients’ care. Of course not. (Section 3003 (i))

12. If you are a physician and you want to own your own hospital, you must be an owner and have a “Medicare provider agreement” by Feb. 1, 2010. (Dec. 31, 2010 in the reconciliation changes.) If you didn’t have those by then, you are out of luck. (Section 6001 (i) (1) (A))

13. If you are a physician owner and you want to expand your hospital? Well, you can’t (Section 6001 (i) (1) (B). Unless, it is located in a country where, over the last five years, population growth has been 150% of what it has been in the state (Section 6601 (i) (3) ( E)). And then you cannot increase your capacity by more than 200% (Section 6001 (i) (3) (C)).

14. You are a health insurer and you want to raise premiums to meet costs? Well, if that increase is deemed “unreasonable” by the Secretary of Health and Human Services it will be subject to review and can be denied. (Section 1003)

15. The government will extract a fee of $2.3 billion annually from the pharmaceutical industry. If you are a pharmaceutical company what you will pay depends on the ratio of the number of brand-name drugs you sell to the total number of brand-name drugs sold in the U.S. So, if you sell 10% of the brand-name drugs in the U.S., what you pay will be 10% multiplied by $2.3 billion, or $230,000,000. (Under reconciliation, it starts at $2.55 billion, jumps to $3 billion in 2012, then to $3.5 billion in 2017 and $4.2 billion in 2018, before settling at $2.8 billion in 2019 (Section 1404)). Think you, as a pharmaceutical executive, know how to better use that money, say for research and development? Tough. (Section 9008 (b)).

16. The government will extract a fee of $2 billion annually from medical device makers. If you are a medical device maker what you will pay depends on your share of medical device sales in the U.S. So, if you sell 10% of the medical devices in the U.S., what you pay will be 10% multiplied by $2 billion, or $200,000,000. Think you, as a medical device maker, know how to better use that money, say for R&D? Tough. (Section 9009 (b)).

The reconciliation package turns that into a 2.9% excise tax for medical device makers. Think you, as a medical device maker, know how to better use that money, say for research and development? Tough. (Section 1405).

17. The government will extract a fee of $6.7 billion annually from insurance companies. If you are an insurer, what you will pay depends on your share of net premiums plus 200% of your administrative costs. So, if your net premiums and administrative costs are equal to 10% of the total, you will pay 10% of $6.7 billion, or $670,000,000. In the reconciliation bill, the fee will start at $8 billion in 2014, $11.3 billion in 2015, $1.9 billion in 2017, and $14.3 billion in 2018 (Section 1406).Think you, as an insurance executive, know how to better spend that money? Tough.(Section 9010 (b) (1) (A and B).)

18. If an insurance company board or its stockholders think the CEO is worth more than $500,000 in deferred compensation? Tough.(Section 9014).

19. You will have to pay an additional 0.5% payroll tax on any dollar you make over $250,000 if you file a joint return and $200,000 if you file an individual return. What? You think you know how to spend the money you earned better than the government? Tough. (Section 9015).

That amount will rise to a 3.8% tax if reconciliation passes. It will also apply to investment income, estates, and trusts. You think you know how to spend the money you earned better than the government? Like you need to ask. (Section 1402).

20. If you go for cosmetic surgery, you will pay an additional 5% tax on the cost of the procedure. Think you know how to spend that money you earned better than the government? Tough. (Section 9017).


Heath Insurers Get What They Wanted…

Health overhaul promises pain, gain for businesses

Matthew Perrone, AP Business Writer

Monday March 22, 2010, 5:47 pm EDT

WASHINGTON (AP) — When historians write the book on how President Barack Obama’s health care overhaul became law, they’ll need to leave space for some unlikely advocates: lobbyists for the drug, insurance and hospital industries.

Last summer, executives from those groups visited the WhiteHouse and pledged to do their part to help pay for the health bill. By signing on to the effort early and agreeing to absorb some of the costs, they were able to help shape its final form.

Only time will tell how smart that trade-off was for the industries, but a quick look at the bill passed by the House late Sunday shows it was far from their worst-case scenario:

A government-run health care plan that would compete against private insurers? Never made it out of the Senate.

Price controls on Medicare’s prescription-drug program that would squeeze drug industry profits? Quietly dropped from consideration last fall.

Cuts in payments to hospitals serving Medicare patients? Trimmed to modest levels and delayed until 2014.

Health care stocks have risen over the past year with the broader market, with insurers seeing the biggest gains. The Standard & Poor’s health care index has gained 30 percent since the market bottom last March and is just 12 percent from its 2007 peak.

And stocks of insurance companies are way up over the past year — even beyond the gains in the broader market.

The bill headed for Obama’s desk offers insurers both opportunities and challenges:

“You’ll continue to see premium rates go up because there are so many aspects of the system that are still increasing prices,” said Dan Mendelson, president of consultant Avalere Health.

“We The People” were told how bad Health insurance Companies were

and how they had to be stopped…

When in reality, they were the ones lobbying for this bill to be passed…

do you see why now?

Like they say just because a cars headlight is broken… you dont restore the entire car!

Sure, They heath industry needed change…

but NOW we have Socialized Medicine…

Good job folks’…

You reap what you sow.


MASS VACCINATIONS FOR HAITIANS

Mass vaccination planned in Haiti, death toll continues way up

PORT-AU-PRINCE, Feb. 2 (Xinhua) — As fear for post-disaster epidemics haunts, doctors from some countries and international organizations are orchestrating vaccination efforts against diseases that may spread in the tent cities of quake-hit Haiti.

Children are main vaccination targets and vulnerable adults will also get vaccine shots in temporary residence areas which are mostly large tents in open places.

So far there is no evidence that contagious diseases have broken out in the makeshift camps, but diseases caused by poor hygiene, like skin rashes and respiratory complaints are plentiful.

Red Cross officials worry about a potential cholera outbreak.

Cuban doctors have started vaccinating children in a clinic at the Silvia Cattor Stadium in the Haitian capital.

“The Cuban brigade is working alongside the Pan-American Health Organization, the World Health Organization and UNICEF on delivering vaccines for immune responsive infections,” said Adelaide Grau Varela, a member of the Henry Reeve Cuban Medical Brigade that has already vaccinated about 3,100 people against tetanus-diphtheria at the stadium.

UNICEF began collaboration with Cuban doctors on Monday to deliver vaccines to temporary residence areas where children are exposed to infectious diseases.

“We are aiming to reach 500,000 children in the quake area with vaccines,” said Kent Page, senior UNICEF communications officer. “We will be expanding to three or four other sites this week. Because of the living conditions in the makeshift shelters a major disease outbreak would spread like wildfire. This is a preventative measure to save children’s lives.

Again… Its always “for the Shildren”. Instead of working on living quarters and providing a clean environment… they are so eager to VACCINATE. I said this would happen a month ago… wait, No, I said “INOCULATE”.


Propaganda Alert! Doctor in MMR-Autism Scare Ruled Unethical

By Eben Harrell / London Friday, Jan. 29, 2010

TIME.com

In 1998, Andrew Wakefield, a gastroenterologist at London’s Royal Free Hospital, published a study in the prestigious medical journalLancet that linked the triple Measles, Mumps and Rubella (MMR) vaccine with autism and bowel disorders in children. The study – and Wakefield’s subsequent public statements that parents should refuse the vaccines – sparked a public health panic that led vaccination rates in Britain to plunge.

Wakefield’s study has since been discredited, and the MMR vaccine deemed to be safe. But now medical authorities in the U.K. have also ruled that the manner in which Wakefield carried out his research was unethical. In a ruling on Jan. 28, The General Medical Council, which registers and regulates doctors in the U.K., ruled that Wakefield acted “dishonestly and irresponsibly” during his research and with “callous disregard” for the children involved in his study. (See the year in health 2009.)

After the finding, Wakefield, who now heads an autism research center in Austin, Texas, described the decision as “unfounded and unjust.” He added that he had “no regrets” over his work.

Despite this, the effects of the media frenzy surrounding Wakefield’s research — a study found that MMR was the most written about science topic in the U.K. in 2002 — continue to be felt in Britain. Vaccination rates among toddlers plummeted from over 90% in the mid-1990s to below 70% in some places by 2003. Following this drop, Britain saw an increase in measles cases at a time when the disease had been all but eradicated in many developed countries. In 1998, there were just 56 cases of the disease in England and Wales; by 2008 there were 1,370.

Despite assurances from various health bodies that Wakefield’s study was seriously flawed, he still has a dedicated following among parents concerned about a rise in autism rates in the U.K. and U.S. — the cause of which has so far baffled health experts. Wakefield is now the Executive Director of the Thoughtful House autism center in Texas, which the Times of London recently claimed receives millions of dollars in donations each year. At the ruling in London, Wakefield was flanked by a small group of supporters, some of whom shouted in protest as the ruling was read out. Speaking after the hearing, Wakefield remained unbowed, and addressed his supporters directly: “It remains finally for me to thank parents whose loyalty has been extraordinary, and I want to reassure them that the science will continue in earnest.”

I’m not posting this article because I believe Dr. Wakefield was wrong… he was right.

I’m posting this to show you how far Big Pharma will push their propaganda to discredit someone and destroy their character for opposing their inoculations.


“We must make this the decade of vaccines,” -Bill Gates

Gates Makes $10 Billion Vaccines Pledge

ALEXANDER G. HIGGINS | 01/29/10 02:04 PM

Associated Press

DAVOS, Switzerland — The Bill and Melinda Gates Foundation will donate $10 billion over the next decade to research new vaccines and bring them to the world’s poorest countries, the Microsoft co-founder and his wife said Friday.

Calling upon governments and business to also contribute, they said the money will produce higher immunization rates and aims to make sure that 90 percent of children are immunized against dangerous diseases such as diarrhea and pneumonia in poorer nations.

“We must make this the decade of vaccines,” Bill Gates said in a statement. “Vaccines already save and improve millions of lives in developing countries. Innovation will make it possible to save more children than ever before.”

Gates said the commitment more than doubles the $4.5 billion the foundation has given to vaccine research over the years.

The foundation said up to 7.6 million children under 5 could be saved through 2019 as a result of the donation. It also estimates that an additional 1.1 million kids would be saved if a malaria vaccine can be introduced by 2014. A tuberculosis vaccine would prevent even more deaths.

“Vaccines are a miracle,” said Melinda Gates. “With just a few doses, they can prevent deadly diseases for a lifetime.”

Margaret Chan, head of the World Health Organization, called the Gates contribution unprecedented and urged governments and private donors to add to the initiative.

We all know that Mr. Gates is a known Eugenicist… and that vaccinations are the reason for the dumbing down of our society… Why not dumb down the rest of the world now that they have gotten the US and UK out of the way?

Did you know that birth control and vaccinations are readily available in 3rd World countries? Yet these same people have no access to clean drinking water… priorities huh?


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