Showing posts sorted by relevance for query vaccines. Sort by date Show all posts
Showing posts sorted by relevance for query vaccines. Sort by date Show all posts

Sunday, February 20, 2011

Vaccines ARE Germ Warfare

Vaccines ARE Part of the Dumbing Down of America

There is a vaccine for just about everything now. From the common vaccines issued during early and mid childhood, to the flu vaccines issues to adults. There are even vaccines now for HPV(Guardasil) and HIV/AIDS, and there are more and more being thought up and created everyday by the CDC/FDA think tank.

A lot of the ‘diseases’ that vaccines have been issued are in reality not diseases, but non-life threatening illnesses that can be cured with a proper diet, Vitamin D, and medicinal herbs. Many of the health conditions that we consider to be diseases, have been made so ONLY through the workings of the AMA, CDC, and FDA think tanks; So that vaccines and other dangerous pharmaceuticals can be created and marketed for the profit of Big Pharma.

We have been brainwashed to believe that we need a weakened form of a virus to prevent us from catching another virus—which is not true. Ask yourself the question: when you were vaccinated during childhood, which came first–the vaccine, or the chicken pox….I think most will answer the vaccine.

There is no definite proof that a weakened( live) virus can prevent one from becoming ill. Just about in all cases, even going back to some of the first issuing of mandatory vaccinations in Victorian England, the population was healthy pre-vaccine and became ill AFTER the vaccines were issued. The worst part of the scenario is that majority of the world’s ‘first’ and ‘second’ world populations are in a health crisis, all while after being vaccinated, yet very few seem to make the connection.

The truth is Vaccines, all made possible thanks to Edward Jenner, compromise our immune system for the duration of our lives after they are issued. Many of us who suffer from allergies, frequent colds, arthritis, etc do so because of vaccinations.

If more people knew the deadly cocktail that went into vaccines, more would protest them. Mercury, Formaldehyde, Squalene, Chick Embryonic Fluid, Aborted Fetal Tissue, are just a few of the ingredients of the macabre concoction that make up vaccines.

Vaccines have been proven time and time again to cause many of the childhood illnesses that many children suffer from which in some circumstances cause death. They have even been used as a means to cause sterilization and unwanted abortions in women in places such as Africa, Asia, and South America. And Autism has been proven beyond the shadow of a doubt to be caused by vaccines.

One thing that can be determined is that vaccines are indeed germ warfare. They took over where the smallpox blankets left, but were used against all peoples. If we learn to take back control of our health and rely on our bodies, a positive diet, natural herbs, and vitamin D; our children and ourselves will be in much better health.

UPDATE:

Since there are those who out there who still believe that those who reject vaccinations are mentally ill and would like to challenge whether or not they are safe, here are some books and articles from various websites that give more than enough evidence that vaccines cause damage instead of preventing it. And since we still need validation from ’experts’ and ‘professionals’   a lot of the commentary is from them.

http://www.bibliotecapleyades.net/vatican/esp_vatican35.htm

The Medical Mafia

http://www.whale.to/a/medical_mafia.html

Vaccination Myths

http://www.relfe.com/vaccine.html

Historical Facts About The Dangers Of Vaccines

http://www.wariscrime.com/2009/08/31/news/historical-facts-about-the-dangers-of-vaccines/

Anti Vaccine Doctors (Most important one)

http://www.whale.to/vaccines.html

National Vaccine Information Center(Very Important)

http://www.nvic.org/

CDC: Vaccine Components(Even admits parents should consult physicians before vaccine is administered)

http://www.cdc.gov/vaccines/vac-gen/additives.htm

Government Admits Vaccines Contribute To Autism

http://www.americanchronicle.com/articles/view/54119

Military & Biodefense Vaccine Project

http://www.military-biodefensevaccines.org/

Babies Die Within Hours After Being Vaccinated

http://www.infiniteunknown.net/2010/09/05/3-babies-die-within-hours-after-they-were-vaccinated/

Leonard Horowitz

http://www.whale.to/vaccines/horowitz.html

http://www.tetrahedron.org/

Bill Gates: Vaccines For Depopulation

http://www.naturalnews.com/029911_vaccines_Bill_Gates.html

h/t to  Kateri originally posted on Oct 7th 2010 at USAHitman

Monday, November 11, 2013

The Pets Most Likely to Suffer from Vaccine Adverse Reactions

Story at-a-glance

  • In the second half of a two-part interview, Dr. Becker talks with Dr. Ronald Schultz of the Rabies Challenge Fund about a variety of vaccine-related topics, including the mysterious rattlesnake vaccine, how it actually works, and for what snake in particular.
  • Dr. Becker and Dr. Schultz also discuss the Lyme disease vaccine, and under what circumstances it can prove beneficial, as well as the challenges of diagnosing leptospirosis and improvements in that vaccine in recent years.
  • Dr. Schultz also offers an excellent explanation of the various bordetella vaccines, what dogs really need them and how often, as well as what form of the vaccine he prefers. He and Dr. Becker also discuss the pros and cons of the canine influenza vaccine.
  • Dr. Becker and Dr. Schultz agree that veterinarians should discuss vaccines with pet owners before they vaccinate. And Dr. Schultz offers his view on which pets are most likely to develop an adverse reaction to vaccines.
  • Lastly, Dr. Becker and Dr. Schultz discuss the important work the Rabies Challenge Fund is doing to determine the duration of immunity conveyed by rabies vaccines. The goal is to extend the length of time between rabies vaccines to five years, then, if possible to seven years. The project is in year six of a seven-year study and depends on grassroots funding to conduct the necessary clinical trials. This week only, Mercola Healthy Pets will match every $1 donated by readers with a $2 donation, up to $30,000, to help the Rabies Challenge Fund complete its invaluable work toward reducing the number of vaccines our pets must receive during their lifetime.

Video: Dr. Becker Interviews Dr. Schultz About Vaccines (Part 2) 

Dog and Cat Vaccines are Not Harmless Preventive Medicine

By Dr. Becker – Cross-Posted at Just One More Pet

I’m back with Dr. Ron Schultz for the second half of our vaccine discussion.  Dr. Schultz heads up the Department of Pathobiological Sciences at the University of Wisconsin-Madison School of Veterinary Medicine. He’s joining me today on behalf of an important project he’s been working on for several years – the Rabies Challenge Fund. The purpose of the fund is to determine the duration of immunity conveyed by rabies vaccines, with the goal of extending the required interval for rabies boosters to five and then to seven years.

If you missed the first part of our discussion on Wednesday, I encourage you to watch that video as well. Dr. Schultz talks about core and non-core vaccines, and the benefits of the feline leukemia virus (FeLV) vaccine and why he believes every kitten should receive it (I must politely disagree on this topic). We also discuss vaccines Dr. Schultz does not recommend, why the whole topic of titering is so confusing, and whether or not he believes cats should be titer tested.

Continuing our discussion of vaccines today, the first thing I asked Dr. Schultz to talk about – because I don’t know much about it myself and get many questions about it – is the rattlesnake vaccine.

How Does the Rattlesnake Vaccine Work, and Is It Effective?

Dr. Schultz explained that the rattlesnake vaccine is actually an aid to prevent death in the event an animal is bitten by a specific type of rattlesnake. He says it does have value in that it can keep an animal bitten by a Western diamondback rattlesnake alive. But he cautions that when the vaccine is used, it’s important for pet owners to know their dog must still be treated for snake bite for two reasons. One, the snake may not have been a Western diamondback rattlesnake, in which case the vaccine offers no protection. Two, the vaccine in most cases will not prevent the venom from causing disease. What the vaccine does is buy time to get the animal treated, and it seems to work well in that regard.

I asked Dr. Schultz if he has concerns about the adjuvant used in the rattlesnake vaccine causing a reaction. He replied that unfortunately, nobody knows very much about the vaccine and in his opinion, it hasn’t been adequately tested. Most of the tests were done with rabbits, mice and other species, but not dogs. It should be tested in dogs. There’s just not a lot of research on this particular vaccine.

Dr. Schultz’s View on Lyme Disease Vaccines

Next I asked Dr. Schultz to discuss his thoughts on Lyme disease vaccines. He explained that there are several of them. There are whole killed organism vaccines of Borrelia burgdorferi, which is the bacteria that causes Lyme disease. And there’s a recombinant vaccine that contains just the important outer surface protein A component.

Dr. Schultz’s recommendation regarding Lyme vaccines depends on where the animal lives. For example, in the Madison area of Wisconsin, there’s currently about a four percent infection rate. But if you travel just 70 miles to La Crosse, there’s about a 70 percent infection rate. And in parts of Long Island, New York, there is a 90 percent infection rate.

So depending on where you live or plan to visit, your dog may have a very high risk of being infected with Borrelia burgdorferi. In high risk cases, Dr. Schultz recommends not only a tick preventive, but also the vaccine. Most of the Lyme disease vaccines are around 60 to 75 percent effective at preventing the organism from causing disease.

I asked Dr. Schultz if he has concerns about reactions from Lyme disease vaccines, and he replied that yes, there are some potential concerns. The Lyme vaccines are bacterial vaccines, and bacterial vaccines always carry a greater risk of adverse reactions, especially reactions of an immediate nature. With both leptospirosis bacterin vaccines and Lyme bacterin vaccines, the nature of the bacteria can cause adverse reactions in some animals. According to Dr. Schultz, these vaccines have the ability to stimulate the IgE antibody in animals, which is responsible for immediate or type 1 hypersensitivity reactions. So bacterins are always more likely to cause an adverse reaction than a live viral vaccine, for example.

If he were to recommend a Lyme vaccine, Dr. Schultz likes the outer surface protein A product better than the whole killed product because the former takes some of the potentially reactogenic antigens out of the formula. But even with that, the vaccine can still cause adverse reactions in some animals.

What About Leptospirosis? Is It a Bigger Threat Today Than in Years Past?

Leptospirosis (and its vaccines) is another confusing subject. There are veterinarians in the Chicago area who are promoting lepto as some kind of new, trendy infectious disease. But lepto has been around forever. Dr. Schultz agrees – there’s nothing new about leptospirosis. And he believes it’s probably no more common today than it was 40 or 50 years ago, despite the hype, which is driven in part by the really poor diagnostics used to detect the disease.

Fortunately, according to Dr. Schultz, there are better detection techniques on the horizon. The current gold standard, he says, “… is about as poor a test as you’ll ever find.” It gives false readings – false positives. Dr. Schultz says he’s seen a high number of supposed lepto cases that are NOT lepto cases thanks to poor diagnostics. Poor diagnostics have added to the general confusion surrounding lepto, and are partly why veterinarians are recommending mass vaccination against the disease.

Dr. Schultz restated that in his view, lepto is no more prevalent today than it was 40 years ago. However, the vaccine has improved tremendously in recent years, because it now contains the 4 serovars that cause lepto in the U.S. In the past, all lepto vaccines contained only 2 serovars. With the old 2-serovar vaccines, Dr. Schultz says there were as many vaccinated dogs with lepto as there were non-vaccinated dogs.

He believes today, the lepto vaccine is probably 60 to 80 percent effective in preventing disease. I asked him if the animal can still transmit or shed the bacteria. He replied there is that potential, but even the shedding is reduced with the 4-serovar vaccine.

Of course, despite the improved effectiveness of the lepto vaccine, there are still concerns about adverse reactions with the first dose, or subsequent revaccinations. Dr. Schultz explains this is another of the bacterins that is more likely to cause an adverse reaction simply as a result of the nature of the organism.

Adverse Reactions to Vaccines Can be Immediate, or They Can Develop Weeks, Months or Even Years Post-Vaccination

So we’ve established that the majority of adverse events occur with bacterin-type vaccines. These vaccines can cause all types of hypersensitivity reactions in some animals. Type 1 adverse reactions typically occur immediately after vaccination and are obviously directly linked to the vaccine.

But as Dr. Schultz goes on to explain, when we have a reaction like the development of autoimmune hemolytic anemia or another autoimmune disease in a genetically predisposed animal, it usually occurs weeks, months or even years after vaccination. Often the offending vaccine in those cases is a live viral vaccine, and it isn’t blamed for causing the disease because there’s a span of time between vaccination and development of the autoimmune disorder.

Many veterinarians will say, in response to the suggestion that a vaccine caused an autoimmune disorder, something like, “What do you mean? There’s no correlation. It was last year when the dog received that vaccine.” And even worse, both Dr. Schultz and I have seen veterinarians tell pet owners their animal’s illness couldn’t be a vaccine reaction even when the two events happen within days of each other.

Dr. Schultz’s Bordetella Vaccine Recommendation

Next I asked Dr. Schultz to talk to us about bordetella vaccines. He explained that the vaccine is available now in a variety of forms. There’s an oral vaccine, which is a live, attenuated bordetella organism. There’s the intranasal form, which is also the live organism. And there’s the injectable form, which is a killed product. Dr. Schultz says he has been able to clearly demonstrate that the live product is the most effective, whether oral or intranasal.

But one of the problems with bordetella is that it is always accompanied by other agents in causing canine infectious respiratory disease complex, otherwise known as kennel cough. There are many infectious agents involved, but the most important one from a bacterial standpoint is bordetella. From a viral standpoint, an impressive number of infectious agents can play a role.

I personally can’t see a reason to use injectable bordetella when there are other safer, non-adjuvanted and attenuated vaccines available. Dr. Schultz points out that one of the reasons the injectable is popular is that it can be used with dogs that won’t cooperate with intranasal or oral administration of the vaccine. He does a lot of work with shelters, and there are many difficult dogs in that population that must receive the vaccine by injection. Some dogs can be muzzled and given the oral vaccine, but often it’s too dangerous for shelter staff to even try to muzzle certain dogs.

In my opinion, the bordetella vaccine should only be given when a dog must be boarded. If you don’t board your dog, or if you don’t plan to have your dog in contact with other dogs (such as at shows and training classes), then my recommendation is to opt out.

However, some kennels require dogs to receive a twice-yearly schedule of bordetella revaccinations. Dr. Schultz believes if you’re taking your pet to a boarding facility that requires bordetella vaccines every six months, you should change to another facility, because the one you’re using has a ventilation or hygiene problem and not an infectious disease problem. “Don’t allow anyone to tell you that you need to get bordetella vaccine every six months. If they do, don’t go there anymore,” says Dr. Schultz.

The Canine Influenza Vaccine – Is It Really Necessary?

I also asked Dr. Schultz about the canine influenza vaccine, which is another vaccine commonly required at boarding facilities and similar businesses. He answered that he’s not sure the vaccine should be required, because canine influenza isn’t a casually transmitted virus. It’s not something the average well cared-for dog will pick up at the local dog park.

Dr. Schultz does caution, however, that if the canine influenza vaccine is to be given, it can’t be administered at the last minute. Dogs that have never received the vaccine need at least three weeks to develop immunity after being vaccinated. And two doses must be given, with a minimum of two weeks separating them. If a dog is receiving annual boosters of the vaccine, it won’t take three weeks for immunity to develop after revaccination.
Dr. Schultz explains that bordetella (as well as other bacterial diseases such as streptococcal infections) and canine influenza together can create severe disease.

Dr. Schultz mentioned that many kennels do require the canine influenza vaccine, so I asked him if that is out of concern about spreading disease, or concern about covering their bases from a liability standpoint. Dr. Schultz thinks much of it comes from a concern that if there were to be an outbreak of canine influenza, the facilities would be found at fault because they didn’t require the vaccine. Fortunately, to date there have only been a few outbreaks of canine influenza in shelters and kennels.

I agree. I feel a lot of those requirements are simply a way to bounce liability away from the business owner. And it’s up to pet owners to determine the true motivation behind the requirement if they choose to board or have their dog groomed at a facility that demands certain vaccines. And as Dr. Schultz points out, if any of the vaccines required by these businesses cause an adverse reaction in a pet, the costs (both financial and emotional) associated with the adverse event are the owner’s responsibility even though the vaccines were required by a third party.

Are Pet Owners Informed About the Potential for Adverse Vaccine Reactions?

As it stands right now, veterinarians must obtain informed consent from a pet owner when we elect not to vaccinate an animal. I asked Dr. Schultz if he believes we should also obtain informed consent TO vaccinate an animal. He replied that he definitely agrees we should. In my opinion, many in the traditional veterinary community are casual vaccinators. They aren’t informing their clients of all the potential ramifications of administering vaccines.

Dr. Schultz agrees that pet owners need to be aware, even though the number of adverse reactions is relatively small. And something he wants to re-emphasize – something that people don’t realize or think about – is that adverse reactions are genetically controlled. When Dr. Schultz talks to breeders, he tells them that if they see adverse vaccine reactions in puppies from a specific combination of mother and father dogs, they should not mate those two dogs again, because the incidence of adverse reactions will increase with each litter and potentially with litters of those litters, and so on. By continuing to mate those two dogs to each other, they will perpetuate the genetic predisposition to adverse vaccine reactions.

Dr. Schultz says, as an example, we might see allergic neuritis or paralysis develop in about 1 in 10,000 vaccinates, yet in a litter of five puppies, three of the five may develop the condition. One of them dies, and two are paralyzed. So the incidence of adverse reactions is not rare in that litter of five, because genetics plays a key role in causing the vaccine adverse reaction.

What Pets Are Most Likely to Have an Adverse Reaction to Vaccines?

There are genetic predispositions among breeds of dogs. As a Boston Terrier owner, I have concerns not just about immediate adverse reactions, but about mast cell tumors, for example. No one is studying the correlation, but I personally believe there’s a strong correlation between vaccinations and mast cell tumors.

Dr. Schultz agrees and thinks that in dogs, we should look at mast cell tumors, histiocytomas and other similar responses at vaccine injection sites. We are aware of feline injection-site sarcomas, but really, any vaccine in a dog or cat that stimulates a proliferative response in cells should be looked at. Particular individuals with a genetic predisposition turn those cells neoplastic, and the animal doesn’t have the suppressor factors necessary to control the disease (tumor) at the cellular level. It’s going to turn into a tumor.

Recognition among veterinarians has been slow in coming, but it’s coming. As Dr. Schultz points out, until fairly recently the veterinary community never considered that a vaccine could cause a lethal tumor in a young, healthy animal. He says it was a great awakening in the mid-1980s for the veterinary profession to realize the potential for adverse events following vaccination, specifically at the time, injection-site sarcomas in cats. But Dr. Schultz believes it’s important to keep in mind that these events are rare, and many veterinarians have never seen one. Other practices see six or eight a year. The frequency isn’t based on the number of cats coming into a particular practice. Which brings us back to the matter of genetic predisposition to adverse events from vaccines.

Other factors that can play a role include an animal’s nutritional status, environmental status, the type of vaccine, the stress the animal feels – all those things and more play into an animal’s immunologic response.

In terms of genetics, one example Dr. Schultz points out is the small breed dog. He says it’s not every small breed, but there are small breeds out there that are genetically predisposed to react to many vaccines. Dr. Schultz says this is a critically important point when it comes to making decisions about giving vaccinations.

If you have a small breed dog that has proven to be hypersensitive to vaccines – or is related to other hypersensitive dogs -- and that dog spends most of his time in the house on someone’s lap, what are the chances he’ll be exposed to leptospirosis? The chances are slim to none, so why would you even think about injecting that dog with a lepto vaccine? Dr. Schultz says vaccine manufacturers don’t want those animals vaccinated due to the risk of adverse reactions.

In terms of recognizing the potential dangers of certain vaccines for certain pets, breed-specific organizations seem to, and of course individual pet owners who’ve lived through horrific experiences do as well. But there are still a large number of veterinarians who seem unwilling to put the puzzle pieces together to protect potentially vulnerable patients.

Dr. Schultz replied that he’s still shocked by the number of practices that are still giving core vaccines annually. As he puts it, “If ever we could get away from this addiction to vaccination just for the sake of vaccination …”.

Dr. Schultz and the Rabies Challenge Fund

The last topic I want to discuss with Dr. Schultz today is one that is close to my heart, the Rabies Challenge Fund. I asked Dr. Schultz to describe the project and its purpose for people who aren’t familiar with it.

He responded that what he and his colleagues Dr. Jean Dodds and Kris Christine have been doing for over five years now is trying to answer the question, can be we get protection from rabies vaccines, and how long can that protection last? Right now there are rabies vaccines that carry either a 1-year or 3-year license. Many of those vaccines are actually the same product – they were just licensed differently. Dr. Schultz is looking beyond the 3-year license by conducting very difficult, very expensive studies to determine how long immunity from a rabies vaccine truly lasts.

This is the way a rabies vaccine is licensed: The USDA requires that a vaccinated group of animals be challenged with the rabies virus at three or five or seven years after the vaccine is given. There must also be a control group of dogs that are unvaccinated. When challenged, a certain percentage of that group must develop rabies to insure the challenge is viable. Of the vaccinated group, 88 percent or more must be protected in order for the USDA to license the vaccine for the number of years protection is provided.

At this time, the Rabies Challenge Fund is at five years with one of the vaccines they are testing, and at three years with the other. They are currently trying to determine whether or not the vaccines will be effective at five years. If those tests show that there should still be protection at five years post-vaccination, the next step will be to do the challenge itself.

Dr. Schultz has two years left on one of the vaccine products and four years left on the other product to determine length of immunity. The work he and his colleagues are doing with the rabies challenge is funded by dog owners. Dr. Schultz says no one is really interested in the work other than caring dog owners, which also includes a number of breed-specific clubs and organizations – basically people who want to give their dogs as few vaccines as necessary – law-abiding citizens who want their pets protected from disease, but don’t want to risk their pet’s health with unnecessary vaccinations.

How You Can Help

The Rabies Challenge Fund study is the first of its kind, and it takes a lot of money to do the work. It’s seven years of research, data collection, and publishing the results. That’s why Mercola Healthy Pets is partnering with the Rabies Challenge Fund to help raise the remainder of the money needed to not only complete the study, but to insure the research is published in a manner that will benefit the most pets.

And of course research is still ongoing. They are in year six, and have year seven still to go. The project depends on grassroots gifts for funding the costs of conducting the requisite vaccine trials. Contributions to date have come mostly from kennel clubs and private individuals. None of the money collected by the Rabies Challenge Fund goes to Dr. Schultz, Dr. Dodds, Kris Christine, or others working on their behalf. Salaries and other overhead costs are not involved, with the exception of expenses for care and testing of the study animals.

I want to extend my thanks to Dr. Schultz for talking with us today and for his work with the Rabies Challenge Fund. Extending the length of time between rabies and other vaccinations, thereby reducing the total number of vaccines animals receive during their lifetime, will be a huge benefit to the health and well being of pets.

Mercola Healthy Pets is proud to partner with the Rabies Challenge Fund to raise money to help improve the lives of animals. This week, for every $1 donated to the Rabies Challenge Fund by a Mercola Healthy Pets reader, we will donate $2, up to $30,000. I hope you’ll join us in helping RabiesChallengeFund.org fund the remaining research needed to complete their seven-year study.

Related:

Do Vaccinations Affect the Health of our Pets?

New Parasite Prevalence Maps Help Pet Owners Prepare

The dangers of vaccines are surfacing for children, people in general, and now pets: New Organization VaxTruth Fights Vaccine Damages

Sunday, February 21, 2010

Drug Companies Shift Emphasis to Vaccines

vaccinesThe extent to which the recession has cut into high-value research and development jobs in the pharmaceutical industry will be apparent soon as job losses in the industry climb to an additional 12,000.

GlaxoSmithKline (GSK), the British drugs group, will announce plans for further restructuring with the loss of 4,000 jobs, nearly half in the research and development departments.

The job attrition reflects widespread unease among drug companies about the loss of revenues from a small number of blockbuster medicines.

For example, this year GSK will lose patent protection for Seretide, an asthma treatment worth $4 billion.

GSK started reshaping its business in 2007 by focusing on three areas: vaccines, over-the-counter medicines and non-medical products, and emerging markets. GSK diverted investment away from pure research and toward products that enabled the company to catch a greater share of the consumer dollar.

However, GSK is not the first drug company to announce job cutbacks and realignment of their target markets, with a path toward vaccines. Novartis, Merck, Pfizer, Novartis, and Sanofi Pasteur are just a few of the Big Pharma members that have done this within the past two years.

And while the recession definitely played a part in this, the truth is, plans to switch to the vaccine market were already in place, long before the recession began.

Posted by: Dr. Mercola
Sources:

The Times Online February 1, 2010

The-infoshop.com

Nature.com April 1, 2009

Dr. Mercola's Comments:

If nothing else, this announcement proves what I’ve been saying all along – that, contrary to what they’d like you to believe, vaccine makers are not philanthropists just looking to do benevolent philanthropy for the world with their products.

They are businesses, first and foremost, whose primary goal is to earn profits for their stockholders.

It has become clear to me that there is a major shift occurring. It is becoming increasingly difficult to find new blockbuster drugs so the new emphasis will be on introducing more and more mandated vaccines which provide nearly unending annuities to continue to increase their revenues

You will see more and more vaccines introduced as time goes on.

The Big Picture

Please remember that collectively the drug cartels make over half a TRILLION dollars every year by selling their product. That amount of money yields enormous power and leverage and they are focused on earning even more.

And how do they do that?

By finding a product they can manufacture in massive quantities and sell to infinite numbers of people at whatever price they want to charge. For a long time, psychotropic drugs and therapeutic medicines were the yellow brick road to that Wall Street goal.

Just a few years ago drug giants like Merck, Eli Lilly, GlaxoSmithKline, and Astra Zeneca were dancing in the land of Oz with blockbusters like Vioxx, Zyprexa, Paxil, and Seroquel. But when the Emerald cities they’d built with these drugs became blighted with a cyclone of lawsuits, their profits quickly began to melt.

Add in pending expirations of patents on key products, and accusations by the European Commission that they purposely delay generic medicines by offering payments to rival manufacturers, and these companies knew they had to change the road they were on, even before the recession hit.

It’s All about the Money

The line up of Big Pharma companies that have been announcing job cutbacks and realignment of their product lines over the past two or three years is impressive:

Novartis announced in December 2007 that it planned to cut 2,500 jobs worldwide by 2010 in an attempt to save $1.6 billion. Citing expiring patents, generic competition, and increased industry costs, Novartis said that poor US pharmaceutical sales had forced this reorganization.

Noting that it had experienced “strong growth” in its vaccines and diagnostics division, Novartis said it planned to expand its presence in emerging markets in Africa, Central Asia and Southeast Asia.

Merck announced job cuts in its US sales force a month ago, saying that the cutbacks were part of its merger with Schering-Plough. In all, the newly married company plans to reduce its global workforce by 15 percent, for a savings of nearly $3.5 billion.

But even before Merck and Schering-Plough became a couple, Merck had already begun making job cutbacks, as part of its 2005 restructuring plan.

A major focus of that plan, Merck told its stockholders in 2005, would be to enter, and become a leader in, emerging markets, which “provide enormous opportunity” for Merck’s medicines and vaccines.

Saying that the company planned to rely less on US markets and more on global initiatives, Merck told Nasdaq in December 2009 that 40 percent of its job cuts would be in the US, as the company moved its market focus to worldwide ventures.

But Merck and GSK aren’t the only ones totake this route: Johnson & Johnson announced in November 2009 that it was cutting 8,000 jobs.

Pfizer said it was cutting 20,000 jobs, or 20 percent of its workforce, as part of its merger with Wyeth; Eli Lilly said it was making a 13 percent reduction totaling 5,000 jobs; Astra Zeneca it was cutting 7,000 jobs, or about 10 percent of its workforce.

But simultaneously with job cut announcements, they all have alluded to, or plainly said, emerging markets are where their new focus lies.

Of course, it’s all about the money and the bottom line – which isn’t a bad thing, since these companies are for-profit entities. But what is this thing, “emerging markets,” anyway, and how do drug companies’ desires to follow emerging markets affect the rest of the world?

Emerging Market ‘Inoculations’

The Wall Street Journal probably said it best when it called this new pharma marketing strategy emerging market inoculations.Referring to Novartis’ purchase of an 85 percent stake in a Chinese vaccine maker, and a similar investment by Sanofi Aventis, the WSJ used this term to describe the drug companies’ plans to expand production and sales in vaccines.

Emerging markets are areas of the world that are beginning to show promise as a profitable venture for many products, including vaccines. And emerging markets – primarily in developing countries in Southeast and Central Asia, and Africa – have been on vaccine makers’ radar for quite some time.

One reason that vaccine makers are interested in these parts of the world is that that’s where most of the world’s deaths from major infectious diseases occur.

World health leaders have long believed that most, if not all, of these diseases could be prevented by vaccines.

The only problem has been that, until recently, making vaccines for undeveloped countries with no money to pay for them, was not exactly a profitable goal for vaccine makers.

In 2001, an article in Tropical Medicine & International Health chastised the pharmaceutical industry for thinking too much about the bottom line, and not investing more in neglected diseases. Accusing them of being more interested on return in investment than in global health needs, the article’s author urged drug companies to re-evaluate their priorities.

It also urged national and international reorientation of public health policies:

New and creative strategies involving both the public and the private sector are needed to ensure that affordable medicines for today's neglected diseases are developed,” the article said.

The article made several suggestions as to how these new policies could come about, from a legal and regulatory standpoint, as well as from research-and-development and distribution of needed drugs for mainly third-world countries.

And Then Something Changed

Fast-forward to February 10, 2010. Suddenly, third-world countries are exactly where the previously maligned drug companies want to be. In a market study released this month, these companies said that vaccines are the new bottom line.

“The developed world has been the initial focus of vaccine makers due to the better healthcare and higher price levels,” the report said. “However, facing increasingly saturated markets in the West, companies are looking to expand into new geographies, such as Asia's emerging markets.”

You have to purchase it to see the complete study on emerging markets. But GSK has its May 2009 emerging market planposted, free, on the Internet. Listing the top 10 countries that are “big and growing fast,” GSK said these countries represent 85 percent of emerging market potential.

Emerging markets will soon outgrow developed markets by hundreds of billions of dollars, the GSK report says. One way to make that happen will be to “build and capture” the vaccine market, the report explains.

And the way to do that, it goes on to say, is through growing government attention to the public health agenda, capitalizing on birth cohorts for pediatric vaccines, and by concentrating on new vaccine products.

Say ‘Hello’ to Advance Market Commitments

So what happened between 2001, when world health leaders were criticizing drug makers for not making exactly this kind of investment, and the past couple years, when vaccine makers suddenly started beating a path to third-world countries?

I can assure you it wasn’t because the 2001 chastisement shamed them in to it. Rather, I can just about bet next week’s paycheck that it had more to do with the promise of a new bottom line – sales of vaccines through something called Advance Market Commitments – than anything else.

Between 2001 and 2005, several vaccine researchers and market developers responded to the 2001 chastisement by writing numerous articles about why drug companies were getting out of the vaccine business. Declining markets, increased costs, and regulatory issues were the top three reasons.

Fix those problems, and everybody would be happy to concentrate on vaccines for developing countries, the responses all said.

Concerned that developed countries would have little or no resources for addressing serious infectious diseases if vaccine makers continued their pull-out, the World Health Organization and the G8 – the top developed countries in the world – responded with a plan for inducing vaccine companies to stay in the business.

That plan was called Advance Market Commitments. Under AMCs, developed countries make legal, binding agreements to purchase vaccines that are needed in low-income countries. The purchase guarantees a bottom line for the manufacturers. In return, the manufacturers promise to sell those vaccines at reduced prices in the countries where they are most needed.

Dozens of New Vaccines in the Pipeline

Do an Internet search on Advance Market Commitments and you will find a whole new vaccine world you most likely didn’t know existed. Start by going to the WHO website, and by reading its August 2007 draft global policy on AMCs. The document focuses on financing and funding health research and development of drugs, vaccines and diagnostics for neglected diseases.

The WHO acknowledges in this document that private, public and not-for-profit donations and investments have helped fight neglected diseases – infections that are prevalent in mostly low-income, third-world countries. But those investments are not enough, the WHO says. And that is why AMCs are necessary, the WHO says.

It sounds like a good plan: Establish a market that heretofore was considered not profitable and, therefore, not worthy of investing in. Promise incentives to lure vaccine makers in to the research and development of new vaccines. And then, stimulate market competition through increased sales and reduction of costs in vaccine programs.

To show how well it could work, a pilot Advance Market Commitment was launched in February 2007 for pnuemococcal vaccines. In June 2009, the WHO and the GAVI announced that that plan had finally come to fruition. Now, thanks to AMCs, a $70 pneumococcal vaccine can be distributed in desperately poor countries for just $3.50.

Sounds like a win-win situation – at least for vaccine makers and the countries where the vaccine’s going.

Serious Concerns about this Program

The reason I’m wary of this plan is that legally binding, advance market commitments to purchase vaccines that are mostly needed in third world countries could backfire on developed countries that don’t need – or want – certain vaccines.

Think about it: The top neglected diseases that world health leaders want to address with AMCs besides pneumonia are HIV-AIDS, malaria, human papilloma virus (HPV), rotavirus, and tuberculosis.

And what do you see?

Standing out big and clear are HPV and rotavirus – two diseases that are relatively rare in the US and other developed countries. (There are over 100 HPVs; the new vaccines address four HPVs that cause 70 percent of cervical cancer and genital warts. In developed countries, death from cervical cancer is very rare, while in third world countries, it is a leading cause of death in women.)

Yet, these are diseases with new vaccines that, for some reason or other in the past few years, have been recommended by the US Advisory Committee on Immunization Practices for babies (rotavirus) and adolescents (HPV).

While the ACIP only recommends vaccines, states are free to do what they choose, and we all know where that leads: to mandates of vaccines that more and more people are beginning to question the need for.

And that’s why I am leery of vaccine makers who announce they’re on their way to third world countries in an effort to boost their bottom line. I don’t fault any profit-driven business for wanting to do things that will make share holders happy.

But I do question where these ventures are headed.

Many scientific journal reports have already revealed that a malaria vaccine is on the verge of being marketable. It only leaves me wondering if that will be the next one on the ACIP’s list.

So stay tuned.

Dozens of other vaccines are in the pipeline, from one for strep throat to another for simple ear infections. I promise this won’t be the last you hear of AMCs and mandated vaccines in the US – what better way is there to “guarantee” a vaccine market than through mandates to help pay for it?

If ObamaCare is forced through against the will of the American people, medical care and the dangers of uncertainty and profit first will come to the forefront for every patient and their family.

More vaccines that people don’t need or are even harmful; more questionable medications; centralized medical records that will me monitored and controlled by the government with unbelievable powers and loss of freedoms for Americans; and progressive John McCain just introduced an bill for more government regulation of natural remedies and supplements that will only help Big Pharma and reduce options for the average person.

McCain Proposes Natural Supplement Regulation Bill

Avandia Recall… Finally After Senate Report – Just Wait Until the Gov’t really controls healthcare and drugs. Avandia is suspected in the cause of 300,000 heart attacks

Related Links:

Anthrax and War: the Marketing of Disaster

Media Helps Generate Fear Among Public to Demand West Nile Virus Vaccine

Follow the Money on Vaccines

Posted: True Health Is True Wealth

Wednesday, April 4, 2012

78 percent increase in autism rates over past decade coincides with new vaccination schedules

Back in 1983, for example, the CDC recommended only ten vaccines for children from birth through six years old (http://www.cdc.gov/vaccines/pubs/images/schedule1983s.jpg). Today, that number has risen significantly to 29 vaccines and counting, many of which are now administered all at one time or in combinations like the measles, mumps, and rubella (MMR) vaccine (http://www.cdc.gov).

78 percent increase in autism rates over past decade coincides with new vaccination schedules

Jonathan Benson  -  Infowars.com  -  April 3, 2012 – h/t to MJ

The rate of autism among American children has nearly doubled over the past decade, according to a new report released by the U.S. Centers for Disease Control and Prevention (CDC), jumping from about one in 150 children back in 2000 to about one in 88 children in 2008, which is the last time official estimates were calculated. And interestingly, this steady rise in autism rates coincides directly with CDC-endorsed vaccination schedules that have also risen sharply since the 1980s.

Back in 1983, for example, the CDC recommended only ten vaccines for children from birth through six years old (http://www.cdc.gov/vaccines/pubs/images/schedule1983s.jpg). Today, that number has risen significantly to 29 vaccines and counting, many of which are now administered all at one time or in combinations like the measles, mumps, and rubella (MMR) vaccine (http://www.cdc.gov).

And yet the mainstream medical system and its allies in the government and media are willfully ignoring this glaring fact, blaming “unknown” causes and “genetics” for causing autism, which are the two most common catch-all scapegoats. And in explaining the drastic rise in autism rates over the years, the talking heads actually claim that there is no rise — the seemingly elevated autism rates are merely the result of improved autism screening methods that are now identifying more cases.



Vaccines, fluoride, MSG, GMOs, toxic chemicals, processed foods – the real causes of autism

Sadly, these laughably unscientific excuses for this epidemic condition are actually being taken seriously by many people, while the true causes of autism — vaccines, fluoridated water, monosodium glutamate (MSG), genetically-modified organisms (GMOs), toxic chemicals, and processed foods — continue to remain taboo subjects when talking about autism.

But any rational human being that takes the time to objectively investigate the science behind how autism spectrum disorders are, at the very least, spurred on by these and other toxins, will quickly realize that the ugly truth about autism is being concealed from the public. And while these factors may not cause autism symptoms in every single person that is exposed to them, they surely trigger it in many, especially when exposures are combined and persistent.

Vaccines, for instance, which the medical establishment have presumptuously declared to play absolutely no role in autism, continue to show up in independent, non-pharma-sponsored research as a cause of autism. Whether they contain thimerosal (mercury) or not, vaccines are definitively linked to neurological disorders that were largely non-existent prior to mass-vaccination campaigns.

Even the kangaroo “vaccine court” has quietly admitted this, having settled with several families whose children were injured by vaccines. Back in 2009, for instance, a vaccine court ruled that Bailey Banks, a young boy who suffered acute brain damage after getting the MMR vaccine, had indeed been injured by the vaccine. Special Master Richard Abell wrote at the time that “the MMR vaccine at issue actually caused the conditions from which Bailey suffered and continues to suffer” (http://www.ageofautism.com).

The case was one of several that has received little or no media attention, and yet it speaks volumes about the dangers associated with vaccines. It also exposes the lies of the deniers who have declared that vaccines are in no way related to autism — case closed.

And besides vaccines, fluoridated water, MSG (http://www.msgtruth.org/autism.htm), GMOs (http://www.ageofautism.com), toxic chemicals both in the environment and in the food supply, and processed foods in general have all been linked to autism spectrum disorders as well (http://www.tacanow.org/family-resources/living-in-a-toxic-world/).

Sources for this article include:

http://www.cnn.com/2012/03/29/health/autism/?hpt=hp_t1

This article was orinally published at Natural News.

Related:

Drug Companies Shift Emphasis to Vaccines

83 percent of brain injury vaccine compensation payouts were for autism caused by vaccines

More Doctors 'Fire' Vaccine Refusers

Popping the Vaccine Bubble

Wednesday, March 28, 2012

For The Record: Rockefeller Soft Kill Depopulation Plans Exposed

Jurriaan Maessen  -  Infowars.com  -  March 26, 2012

In the course of August and September 2010, I wrote several articles for Infowars on the Rockefeller Foundation’s admitted funding and developing of anti-fertility vaccines intended for “mass-scale distribution.” As the soft-kill depopulation agenda accelerates it seems all the more relevant to re-post these articles as one. I ask the great Infowars-readership to project this information out to as many people as possible. Only by countering the elite’s disinformation with genuine information do we stand a chance against their plans for humanity.

1: Rockefeller Foundation Developed Vaccines For “Mass-Scale” Fertility Reduction

In its 1968 yearly report, the Rockefeller Foundation acknowledged funding the development of so-called “anti-fertility vaccines” and their implementation on a mass-scale. From page 51 onward we read:

“(…) several types of drugs are known to diminish male fertility, but those that have been tested have serious problems of toxicity. Very little work is in progress on immunological methods, such as vaccines, to reduce fertility, and much more research is required if a solution is to be found here.

The possibility of using vaccines to reduce male fertility was something that needed to be investigated further, according to the Rockefeller Foundation, because both the oral pill and the IUD were not suitable for mass-scale distribution:

“We are faced with the danger that within a few years these two “modern” methods, for which such high hopes have been held, will in fact turn out to be impracticable on a mass scale.”

The possibility of administrating hormone preparations to reduce fertility was also mentioned, although- states the report- they have been known to “cause bleeding problems, which may limit their usefulness.”

“A semipermanent or renewable subcutaneous implant of these hormones has been suggested, but whether or not the same difficulties would result has not been determined.”

Saying that research thus-far had been too low-grade to produce any substantial results, the report was adamant:

“The Foundation will endeavour to assist in filling this important gap in several ways:

1- “Seeking out or encouraging the development of, and providing partial support to, a few centres of excellence in universities and research institutions in the United States and abroad in which the methods and points of view of molecular biology are teamed with the more traditional approaches of histology, embryology,and endocrinology in research pertinent to development of fertility control methods;”

2- “Supporting research of individual investigators, oriented toward development of contraceptive methods or of basic information on human reproduction relevant to such developments;”

3- “Encouraging, by making research funds available, as well as by other means, established and beginning investigators to turn their attention to aspects of research in reproductive biology that have implications for human fertility and its control;”

4- “Encouraging more biology and biochemistry students to elect careers in reproductive biology and human fertility control, through support of research and teaching programs in departments of zoology, biology, and biochemistry.”

The list goes on and on. Motivation for these activities, according to the RF?

“There are an estimated five million women among America’s poverty and near-poverty groups who need birth control service (…). The unchecked fertility of the indigent does much to perpetuate poverty, undereducation, and underemployment, not only in urban slums, but also in depressed rural areas.”

It wasn’t long before all the Foundation’s efforts began to have effect. In its annual report of 1988, The RF was happy to report the progress made by the Foundation’s Population Division in the field of anti-fertility vaccines:

“India’s National Institute of Immunology successfully completed in 1988 the first phase of trials with three versions of an anti-fertility vaccine for women. Sponsored by the government of India and supported by the Foundation, the trials established that with each of the tested vaccines, at least one year of protection against pregnancy could be expected, based on the levels of antibodies formed in response to the immunization schedule.”

In its 1997 review of anti-fertility vaccines, Indian based International Centre for Genetic Engineering and Biotechnology didn’t forget to acknowledge its main benefactor:

“The work on LHRH and HCG vaccines was supported by research grants of The Rockefeller Foundation, (…).”

In the 1990s the work on anti-fertility vaccines went in overdrive, especially in third-world nations, as did the funding provided by the deep pockets of the Rockefeller Foundation. At the same time, the target-population of the globalists- women- began to stir uncomfortably with all this out-in-the-open talk of population reduction and vaccines as a means to achieve it.

Betsy Hartman, Director of the Population and Development Program at Hampshire College, Massachusetts and “someone who believes strongly in women’s right to safe, voluntary birth control and abortion”, is no supporter of the anti-fertility vaccine, as brought into being by the Rockefeller Foundation. She explains in her essay Population control in the new world order:

“Although one vaccine has been tested on only 180 women in India, it is being billed there as ‘safe, devoid of any side effects and completely reversible’. The scientific community knows very well that such assertions are false - for instance, many questions still remain about the vaccine’s long-term impact on the immune system and menstrual cycle. There is also evidence on film of women being denied information about the vaccine in clinical trials. Nevertheless, the vaccine is being prepared for large-scale use.”

The Women’s Global Network for Reproductive Rights based in Amsterdam, the Netherlands, quoted “a leading contraceptive researcher as saying:

“Immunological birth control methods will be an ‘antigenic weapon’ against the reproductive process, which left unchecked, threatens to swamp the world.”

Animal rights activist ms. Sonya Ghosh also expressed concerns about the Rockefeller-funded anti-fertility vaccine and its implementation:

“Instead of giving individual women more options to prevent pregnancy and protect against AIDs and sexually transmitted diseases, the anti fertility vaccine is designed to be easily administered to large numbers of women using the least resources. If administered to illiterate populations the issues of user control and informed consent are further cause for concern.”

To avoid such debates, the Foundation has in the last couple of decades consorted to its long-practised and highly successful methods of either outright lying through its teeth or using deceptive language to hide the fact that it continues to work tirelessly toward its long-stated mission. If you think the RF and others have abandoned their anti-fertility efforts with the help of vaccines, think again or read this article.

2: Global Distribution of Rockefeller-Funded Anti-Fertility Vaccine Coordinated by WHO

In addition to the recent PrisonPlanet-exclusive Rockefeller Foundation Developed Vaccines For “Mass-Scale” Fertility Reduction- which outlines the Rockefeller Foundation’s efforts in the 1960s funding research into so-called “anti-fertility vaccines”- another series of documents has surfaced, proving beyond any doubt that the UN Population Fund, World Bank and World Health Organization picked up on it, further developing it under responsibility of a “Task Force on Vaccines for Fertility Regulation”.

Just four years after the Rockefeller Foundation launched massive funding-operations into anti-fertility vaccines, the Task Force was created under auspices of the World Health Organization, World Bank and UN Population Fund. Its mission, according to one of its members, to support:

basic and clinical research on the development of birth control vaccines directed against the gametes or the preimplantation embryo. These studies have involved the use of advanced procedures in peptide chemistry, hybridoma technology and molecular genetics as well as the evaluation of a number of novel approaches in general vaccinology. As a result of this international, collaborative effort, a prototype anti-HCG vaccine is now undergoing clinical testing, raising the prospect that a totally new family planning method may be available before the end of the current decade.”

In regards to the scope of the Task Force’s jurisdiction, the Biotechnology and Development Monitor reported:

The Task Force acts as a global coordinating body for anti-fertility vaccine R&D in the various working groups and supports research on different approaches, such as anti-sperm and anti-ovum vaccines and vaccines designed to neutralize the biological functions of hCG. The Task Force has succeeded in developing a prototype of an anti-hCG-vaccine.

One of the Task Force members, P.D. Griffin, outlined the purpose and trajectory of these Fertility Regulating Vaccines. Griffin:

“The Task Force has continued to coordinate its research activities with other vaccine development programmes within WHO and with other international and national programmes engaged in the development of fertility regulating vaccines.”

Griffin also admitted to the fact that one of the purposes of the vaccines is the implementation in developing countries. Griffin:

“If vaccines could be developed which could safely and effectively inhibit fertility, without producing unacceptable side effects, they would be an attractive addition to the present armamentarium of fertility regulating methods and would be likely to have a significant impact on family planning programmes.”

Also, one of the advantages of the FRVs over “currently available methods of fertility regulation” the Task Force states, is the following (179):

“low manufacturing cost and ease of delivery within existing health services.”

Already in 1978, the WHO’s Task Force (then called Task Force on Immunological Methods for Fertility Regulation) underlined the usefulness of these vaccines in regards to the possibility of “large scale synthesis and manufacture” of the vaccine:

“The potential advantages of an immunological approach to fertility regulation can be summarized as follows: (a) the possibility of infrequent administration, possibly by paramedical personnel; (b) the use of antigens or antigen fragments, which are not pharmacologically active; and (c) in the case of antigens of known chemical structure, there is the possibility of large-scale synthesis and manufacture of vaccine at relatively low cost.

In 1976, the WHO Expanded Programme of Research, Development and Research Training in Human Reproduction published a report, stating:

“In 1972 the Organization (…) expanded its programme of research in human reproduction to provide an international focus for an intensified effort to improve existing methods of fertility regulation, to develop new methods and to assist national authorities in devising the best ways of providing them on a continuing basis. The programme is closely integrated with other WHO research on the delivery of family planning care by health services, which in turn feeds into WHO’s technical assistance programme to governments at the service level.”

Although the term “Anti-Fertility Vaccine”, coined by the Rockefeller Foundation, was replaced by the more bureaucratic sounding “Fertility Regulating Vaccine (FRV), the programme was obviously the same. Besides, the time-line shows conclusively that the WHO, UN Population Fund and World Bank continued on a path outlined by the Rockefellers in the late 1960s. By extension, it proves that all these organization are perfectly interlocked, best captured under the header “Scientific Dictatorship”. The relationship between the WHO and the Rockefeller Foundation is intense. In the 1986 bulletin of the World Health Organization, this relationship is being described in some detail. While researching the effectiveness of “gossypol” as an “antifertility agent”, the bulletin states:

“The Rockefeller Foundation has supported limited clinical trials in China and smallscale clinical studies in Brazil and Austria. The dose administered in the current Chinese trial has been reduced from 20 mg to 10-15 mg/day during the loading phase in order to see if severe oligospermia rather than consistent azoospermia would be adequate for an acceptable, non-toxic and reversible effect. Meanwhile, both the WHO human reproduction programme and the Rockefeller Foundation are supporting animal studies to better define the mechanism of action of gossypol.

In August of 1992, a series of meetings was held in Geneva, Switzerland, regarding “fertility regulating vaccines”. According to the document Fertility Regulating Vaccines (classified by the WHO with a limited distribution) present at those meetings were scientists and clinicians from all over the globe, including then biomedical researcher of the American Agency for International development, and current research-chief of USAID, Mr. Jeff Spieler.

In 1986 Mr. Spieler declared:

“A new approach to fertility regulation is the development of vaccines directed against human substances required for reproduction. Potential candidates for immunological interference include reproductive hormones, ovum and sperm antigens, and antigens derived from embryonic or fetal tissue.(…). An antifertility vaccine must be capable of safely and effectively inhibiting a human substance, which would need somehow to be rendered antigenic. A fertility-regulating vaccine, moreover, would have to produce and sustain effective immunity in at least 95% of the vaccinated population, a level of protection rarely achieved even with the most successful viral and bacterial vaccines. But while these challenges looked insuperable just a few years ago, recent advances in biotechnology- particularly in the fields of molecular biology, genetic engineering and monoclonal antibody production- are bringing antifertility vaccines into the realm of the feasible.”

“Vaccines interfering with sperm function and fertilization could be available for human testing by the early 1990s”, Spieler wrote.

In order for widespread use of these vaccines, Spieler writes, the vaccine must conquer “variations in individual responses to immunization with fertility-regulating vaccines”.

“Research”, he goes on to say,”is also needed in the field of “basic vaccinology”, to find the best carrier proteins, adjuvants, vehicles and delivery systems.”

In the 1992 document, the problem of “variations in individual responses” is also discussed:

“Because of the genetic diversity of human populations”, states the document, “immune responses to vaccines often show marked differences from one individual to another in terms of magnitude and duration. These differences may be partly or even completely overcome with appropriately engineered FRVs (Fertility Regulating Vaccines) and by improvements in our understanding of what is required to develop and control the immune response elicited by different vaccines.”

The picture emerging from these facts is clear. The WHO, as a global coordinating body, has since the early 1970s continued the development of the Rockefeller-funded “anti-fertility vaccine”. What also is becoming clear, is that extensive research has been done to the delivery systems in which these anti-fertility components can be buried, such as regular anti-viral vaccines. It’s a mass-scale anti-fertilization programme with the aim of reducing the world’s population: a dream long cherished by the global elite.

3: On Top of Vaccines, Rockefeller Foundation Presents Anti-Fertility Substance Gossypol for “Widespread Use”

It seems there is no limit to the Rockefeller Foundation’s ambitions to introduce anti-fertility compounds into either existing “health-services”, such as vaccines, or- as appears to be the case now- average consumer-products.

The 1985 Rockefeller Foundation’s annual report underlined its ongoing dedication towards finding good use for the anti-fertility substance “gossypol”, or C30H30O8 – as the description reads.

Indeed, gossypol, a toxic polyphenol derived from the cotton plant, was identified early on in the Foundation’s research as an effective sterilant. The question was, how to implement or integrate the toxic substance into crops.

“Another long-term interest of the Foundation has been gossypol, a compound that has been shown to have an antifertility effect in men, By the end of 1985, the Foundation had made grants totaling approximately $1.6 million in an effort to support and stimulate scientific investigations on the safety and efficacy of gossypol.”

In the 1986 Rockefeller Foundation annual report, the organization admits funding research into the use of fertility-reducing compounds in relation to food for “widespread use”:

“Male contraceptive studies are focused on gossypol, a natural substance extracted from the cotton plant, and identified by Chinese researchers as having an anti-fertility effect on men. Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive. The Foundation supported research on gossypol’s safety, reversibility and efficacy in seven different 1986 grants.”

In the RF’s 1988 annual report, gossypol as a contraceptive was also elaborated upon (page 22):

“Gossypol, a natural substance found in the cotton plant, continues to show promise as an oral contraceptive for men. Because it suppresses sperm production without affecting sex hormone levels, it is unique among the experimental approaches to fertility control in men. Foundation-funded scientists worldwide have assembled an aray of information about how gossypol works, and studies continue on a wide variety of its clinical applications. Dose reduction is being investigated to reduce health risks associated with the use of gossypol.”

The following year, according to the annual report, funds were allocated to several research institutions to see how this “dose reduction” could best be accomplished without interfering with the ant-fertility effects of gossypol.

(1988- $ 400,000, in addition to remaining funds from prior year appropriations) To support research on gossypol, its safety, reversibility, and efficacy as a contraceptive for use by men (…).”

Mention is made on money allocated to the University of Texas, “for a study of gossypol’s effects on DNA replication (…).”

The last mention of gossypol in the Foundation’s annals we find in the 1994 annual report, where funds were appropriated to the University of Innsbruck of Austria “for a study at the Institute of Physiology on the molecular action of gossypol at the cellular level.”

It seems that the funded scientists have indeed found a way of “lowering the dosage” of gossypol, circumventing the toxicity of the substance, so as to suppress or even eliminate these “undesirable side-effects”, which include: low blood potassium levels, fatigue, muscle weakness and even paralysis. If these effects could be eliminated without reducing the anti-fertility effects, the Foundation figured, it would be a highly effective and almost undetectable sterilant.

Although overtly, research into and development of gossypol as an anti-fertility compound was abandoned in the late 1990s, the cottonseed containing the substance was especially selected for mass distribution in the beginning of the current decade. Around 2006 a media-campaign was launched, saying the cottonseed could help defeat hunger and poverty.

In 2006, NatureNews reported that RNA interference (or RNAi) was the way to go. On the one hand it would “cut the gossypol content in cottonseeds by 98%, while leaving the chemical defenses of the rest of the plant intact.” Furthermore, the article quoted Dr. Deborah P. Delmer, the Rockefeller Foundation’s associate director of food security, who was quick to bury any concern:

“Deborah Delmer, associate director of the Rockefeller Foundation in New York City and an expert in agricultural food safety, points out that a benefit of using RNAi technology is that it turns off a gene process rather than switching on a novel function. “So instead of introducing a new foreign protein, you’re just shutting down one process,” Delmer says. “In that sense, I think that the safety concerns should be far less than other GM technologies.”

A 2006, National Geographic article Toxin-Free Cottonseed Engineered; Could Feed Millions Study Says, quotes the director of the Laboratory for Crop Transformation (Texas A&M Universtity), Keerti Singh Rathore as saying:

“A gossypol-free cottonseed would significantly contribute to human nutrition and health, particularly in developing countries, and help meet the requirements of the predicted 50 percent increase in the world population in the next 50 years.”

“Rathore’s study”, states the article, “represents the first substantiated case where gossypol was reduced via genetic engineering that targets the genes that make the toxin.”

I bring into recollection the statement made by the Rockefeller Foundation in its 1986 annual report, which reads:

Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive.

In the 1997 Foundational report, Rathore is mentioned (page 68). A postdoctoral fellowship-grant was given to a certain E. Chandrakanth “for advanced study in plant molecular biology under the direction of Keerti S. Rathore, Laboratory for Crop Transformation, Texas A&M University, College Station, Texas.”

Compromising connections, in other words, for someone who claimed academic objectivity in regards to gossypol and its sterilizing effects. Rathore explained the workings of RNAi in a 2006 issue of the Proceedings of the National Academy of Sciences.

“Cottonseed toxicity due to gossypol is a long-standing problem”, Rathore said, “and people have tried to fix it but haven’t been able to through traditional plant breeding. My area of research is plant transgenics, so I thought about using some molecular approaches to address this problem.”

Rathore also mentioned the desired main funder of his work without actually saying the name:

“we are trying to find some partners and will probably be looking at charitable foundations to help us out in terms of doing all kinds of testing that is required before a genetically engineered plant is approved for food or feed. We are in the very early stages and have a lot of ideas in mind, but we need to pursue those. Hopefully, we can find some sort of partnership that will allow us to do them.”

He also expressed the final adaptation of the cottonseed for widespread use is something of the long term:

“(…) right now there are many hurdles when you are dealing with a genetically modified plant. But I think in the next 15 or 20 years a lot of these regulations that we have to satisfy will be eliminated or reduced substantially.”

The Foundation, as is evident from the statements of Rockefeller’s own Deborah Delmer, is more than interested. Even worse, through the process of readying gossypol for mass-distribution in food, the fulfillment of their longstanding goal of sterilizing the populous into oblivion comes into view.

4: Rockefeller Foundation Conceptualized “Anti-Hormone” Vaccine in the 1920s and 30s, Reports Reveal

Rockefeller Foundation minion Max Mason, who acted as president in the mid-1930s, on multiple occasions expressed his master’s desire for an “anti-hormone” that would reduce fertility worldwide. Now keep in mind, this is more than 35 years before the Foundation actually mentioned funding “anti-fertility vaccines” in subsequent annual reports from 1969 onward.

Having traveled far beyond the realm of rumor and speculation, research into the admitted funding of anti-fertility vaccines has uncovered more and more sinister revelations along the way.

By the mid-1930s, Mason of the Rockefeller Foundation thought that “the ultimate solution of the problem [of birth control] may well lie in the studies of endocrinology, particularly antihormones.” The Foundation’s 1934 annual report states:

“The Rockefeller Foundation has decided to concentrate its present effort in the natural sciences on the field of modern experimental biology, with special interest in such topics as endocrinology, nutrition, genetics, embryology, problems centering about the reproductive process, psychobiology, general and cellular physiology, biophysics, and biochemistry.”

“(…) research work is being conducted on the physiology of reproduction in the monkey. This work was begun at the Johns Hopkins University in 1921, and since 1923 has been continued at the University of Rochester. It involves observational and experimental studies of the reproductive cycle in certain species of the higher primates, in which this cycle closely resembles that of the human species. The effect of the various interrelated reproductive hormones is being studied.”

In the annual report of the previous year (1933), the Foundation stresses the fact that work on the reproductive hormones of primates serves to experiment on man in the future:

“(…) much work has been done in the formulation and solution of basic problems in the general biology and physiology of sex in organisms other than man. It was essential that this fundamental work on infra-man pave the way for that on man.”

In the book Discipling Reproduction by Adele E. Clarke, the roots of Rockefeller-funded “anti-hormones” is being described in some detail, pointing out that the family’s ambitions to control man’s fertility date back even further than the 1930s. Clarke writes:

“On a cold morning in 1921, George Washington Corner, a physician and fledgling reproductive scientist, awoke in Baltimore to discover that it was snowing.”

“By 1929”, Clarke writes a bit further on, “Corner had mapped out the hormonal action of progesterone, an essential actor in the menstrual cycle and subsequently an actor in birth control pills.”

The 1935 Rockefeller Foundation annual report acknowledges funding Dr. Corner’s research:

“To the University of Rochester, for research on the physiology of reproduction under the direction of Dr. G. W. Corner during the threeyear period beginning July 1, 1935, and ending June 30, 1938, there has been appropriated the sum of $9,900. Dr. Corner’s activities are concentrated on a study of the oestrus cycle, using monkeys as the experimental animals. A colony of about thirty monkeys has been maintained, and experiments have furnished information on the normal histology of the reproductive cycle, the time of ovulation, the relation of ovulation to menstruation and other anatomically detectable correlations of the oestrus cycle. Work is continuing on two main lines: normal sex reproduction in the monkey, including the histology of ovary and uterus, and, secondly, the effects of the ovarian hormone.”

Again, never forget that the Foundation in 1933 stated outright that “It was essential that this fundamental work on infra-man pave the way for that on man.”

Another essential problem which arises, of course, is how exactly the funding-mechanism worked by which Corner’s research could be made ready for mass-consumption. Clarke mentions that officially the National Research Council, an arm of the National Academy of Sciences (NAS), was the institute responsible for the task of doing so. More specific: the Committee for Research in Problems of Sex (CRPS):

“The NRC itself was founded in 1916 as an agency to inventory research toward enhanced military preparedness.”

“The NRC”, states the author, “was a prestigious organization from its inception, thanks to its early association with the NAS, the Carnegie Corporation, and the Rockefeller Foundation. Kohler (1991:109) has argued that the NRC essentially served as an intermediary between the foundations and scientists in the interwar years.(…). The NRC/CRPS itself was funded almost exclusively by Rockefeller monies, initially through the Bureau of Social Hygiene and, after 1931, through the Rockefeller Foundation.”

On the subject of so-called “current immunological contraceptive research”, Clarke channels Rockefeller-president Max Mason:

“Other lines of current immunological contraceptive research continue to seek what, during the 1930s, Max Mason of the Rockefeller Foundation called “anti-hormones”: vaccines to block hormones needed for very early pregnancy and a vaccine to block the hormone needed for the surface of the egg to function properly.”

In a February 1934 “progress report” written by Warren Weaver (director of the Natural Sciences Division of the Rockefeller Foundation) once again underlined the endgame:

“Can man gain an intelligent control of his own power? Can we develop so sound and extensive a genetics that we can hope to breed, in the future, superior men? Can we obtain enough knowledge of physiology and psychobiology of sex so that man can bring this pervasive, highly important, and dangerous aspect of life under rational control?”

The same Warren Weaver wrote a “biographical Memoir” in honor of his friend Max Mason, revealing some more interesting facts. Weaver, who describes himself as a great personal friend of Mason, gives a general description of him as Rockefeller-minion:

“He had by that time developed a consuming interest in behavioral research, and particularly in the possibility that the physical sciences, working with and through the biological sciences, could shed new and revealing light on the normal and abnormal behavior of individuals, and ultimately on the social behavior of groups of men.”

Here we have it. The blueprint for sterilizing vaccines has been first conceptualized way back in the 1920s and 1930s by social scientists of the Rockefeller Foundation. Although later the eugenic language (“anti-fertility vaccine”) was polished up with the help of some linguistic plastic surgery producing the term “immunological contraceptive”, the ultimate goal remains the same.

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Monday, August 13, 2012

Dog and Cat Vaccines are Not Harmless Preventive Medicine

The dangers of vaccines are surfacing for children, people in general, and now pets (below), See: New Organization VaxTruth Fights Vaccine Damages
Story at-a-glance
  • Vaccinosis is a condition recognized almost exclusively by the holistic veterinary community. It is not generally acknowledged by traditional veterinarians.
  • Dr. Richard Pitcairn defines vaccinosis this way: “Vaccinosis is to be understood as the disturbance of the vital force by vaccination that results in mental, emotional, and a physical change that can, in some cases, be a permanent condition.”
  • Vaccines are composed of modified live viruses, killed viruses and a number of potentially toxic substances. They also enter the body in an unnatural way (by injection) compared to real viruses. They bypass the body’s first lines of defense and are delivered directly to the blood and lymph systems.
  • Vaccine reactions, or vaccinosis, are wide-ranging. Some reactions are relatively minor, while others are life-threatening.
  • Fortunately, the traditional veterinary community is slowing becoming aware that vaccines are not the benign disease-prevention tools they were once thought to be.

Video: Vaccinosis and Your Pet

Download Interview Transcript

By Dr. Becker  -  Dr. Mercola.com – Cross-Posted at Just One More Pet

I talk a lot about vaccine dangers here at MercolaHealthyPets, and I often mention a condition called vaccinosis.

Since vaccinosis isn’t recognized by most traditional veterinarians and isn’t something many pet owners have ever heard of before, I thought it would be helpful to do a short video to explain the condition.

Vaccinosis Defined

First, let’s talk about what vaccinosis isn’t.

It isn’t an acute, often immediate adverse reaction to a vaccine. Adverse events, or hypersensitivities, whether mild (such as lethargy, flu-like symptoms, etc.), or severe (such as anaphylactic shock), that are clearly linked to a recent vaccination are widely acknowledged by the traditional veterinary community.

Unfortunately, these reactions are considered by traditional vets to be occasional aberrations of a basically safe procedure.

Vaccinosis, on the other hand, is a problem only holistic veterinarians seem willing to acknowledge. It is a reaction of a pet’s body to vaccines that have been injected without the pet having experienced a notable adverse event or hypersensitivity. These are chronic reactions to not only the altered virus contained in the vaccine, but also to the chemicals, adjuvants, and other components of tissue culture cell lines -- as well as possible genetic changes -- that can be induced by vaccines.

Dr. Richard Pitcairn, who holds a PhD in immunology, defines it this way: “Vaccinosis is to be understood as the disturbance of the vital force by vaccination that results in mental, emotional, and a physical change that can, in some cases, be a permanent condition.”

Dr. Pitcairn: Vaccines Create Chronic Disease

According to Dr. Pitcairn, vaccines intended to protect pets against acute natural diseases actually create chronic conditions with features of the disease the vaccine was supposed to prevent.

This transformation happens in the laboratory, where natural viruses are modified in order to make vaccines.

Where the natural virus would trigger a strong immune system response, the modified lab-created virus in the vaccine doesn’t elicit much of a reaction by the animal’s immune system. Instead, it creates chronic disease.

The delivery of a vaccine is also very different from how a natural disease develops in an animal’s body.
Vaccines contain a number of toxic substances, including viruses, mutated bacteria, immune irritants, foreign proteins, and chemical preservatives. All of these toxins are delivered by injection directly into the blood and lymph, bypassing the usual first line of defenses, including the skin, mucous membranes, saliva, and so forth. So not only is the virus in the vaccine unnatural, the way it enters a pet’s body is also very unnatural.

When you look at the situation from this perspective, it’s easy to see how abnormal immune reactions are triggered by vaccinations.

Your Pet’s Individual Risk of Vaccinosis

The strength and balance of every animal’s immune system is different, so there’s no way to predict – unless your dog or cat has had a reaction in the past -- how much danger your pet is in from exposure to the modified virus contained in any given vaccine or the many toxic ingredients it contains.

That’s why I strongly encourage pet owners to avoid all unnecessary vaccines and re-vaccinations.

Symptoms of Vaccinosis

Common vaccine reactions include:

  • Lethargy
  • Stiffness
  • Hair loss
  • Lack of appetite
  • Hair color change at injection site
  • Conjunctivitis
  • Fever
  • Sneezing
  • Soreness
  • Oral ulcers

More serious reactions:

  • Immunosuppression
  • Granulomas and abscesses
  • Behavioral changes
  • Hives
  • Vitiligo
  • Facial swelling
  • Weight loss
  • Allergic hypersensitivity
  • Reduced milk production (females)
  • Respiratory disease
  • Lameness
  • Allergic uveitis

Very severe illness:

  • Injection-site sarcomas (cancer)
  • Glomerulonephritis
  • Anaphylaxis
  • Myocarditis
  • Autoimmune arthritis
  • Encephalitis or polyneuritis
  • Polyarthritis
  • Seizures
  • Hypertrophic osteodystrophy
  • Abortion
  • Autoimmune hemolytic anemia
  • Congenital abnormalities
  • Immune-mediated thrombocytopenia
  • Embryotic (fetal) death
  • Thyroiditis
  • Infertility

Dog and Cat Vaccines: The Importance of Exercising Caution

Since the introduction of dog and cat vaccines, the traditional view of their use has been that they are safe and can be given as frequently as once or twice a year. This approach, tragically, has caused a tremendous amount of suffering for millions of pets.

As the truth about the dangers of vaccines slowly emerges, even traditional veterinary organizations and practitioners are acknowledging that vaccines are not the benign, “better safe than sorry” veterinary tools they were thought to be.

My recommendations for vaccinating your pet can be found in several videos, articles, and interviews here at MercolaHealthyPets. Most importantly, I don’t recommend automatic re-vaccinations at prescribed intervals for any pet.

If you believe your pet could be suffering from the negative effects of over-vaccination, I strongly recommend you work with a homeopathic or holistic vet to create a tailor-made vaccine detox program to assist your dog’s or cat’s body in recovering from vaccinosis.

Related:

Do Vaccinations Affect the Health of our Pets?

New Parasite Prevalence Maps Help Pet Owners Prepare