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All Vaccines May Be Contaminated With At Least One Animal Retrovirus Family, All Are Associated With Cancers, Autism & More

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Written by By Judy A. Mikovits, PhD. In collaboration with The World Mercury Project

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Chronic inflammatory diseases have been skyrocketing in incidence in the past quarter century. The details explaining how retroviruses in today’s biological therapeutics including vaccines are contributing to autoimmune, neuroimmune disease and cancer are complex. Although I’ve spent my adult lifetime studying how retroviruses contribute to these diseases, paring down the complexities into basics is a daunting task.

In our book, Plague, Kent Heckenlively and I detailed the science and cover up surrounding my team’s 2009 discovery of a new family of human retroviruses related to mouse leukemia viruses, associated not only with cancer but with Autism Spectrum Disorders and Chronic Fatigue Syndrome. In Plague, my coauthor and I detail the science behind the discovery. Scientific research is not simply a study set in a defined space or time, but a lifetime of detailed observation and learning—a lifetime of forming hypotheses and modifying those hypotheses as technology and learning inform new discovery. Science is never settled as we learn each day and discover things that were once considered impossible.

However, science in the 21st century is more complex than ever in human history. Kent Heckenlively is a sixth-grade science teacher. In order to tell my story in a way everyone could understand, who better than a sixth-grade science teacher to help explain the intricacies? Or so we thought. The reviews of Plague include one from a doctor who said the science was “too complex.” As this is such a critical topic in human heath, I want to make it as simple as possible so that everyone can understand.

What are retroviruses?

Retroviruses are classified in a group of RNA viruses called RNA tumor viruses. They are called “retro” because they only have an RNA genome and function differently than other viruses.  In most viruses, DNA is transcribed (or written) into RNA, then RNA is translated into protein. Retroviruses, on the other hand, work differently.  A retrovirus works by reverse transcribing, that is “writing backwards” into DNA by using an enzyme only retroviruses encode called, “Reverse Transcriptase” (RT). The DNA form of the virus is called a provirus. The provirus is then inserted into the DNA of the host using another enzyme encoded exclusively by retroviruses called “Integrase”. (IN). Integrase cuts open the DNA and then pastes the provirus into the cellular DNA where the provirus lives for the life of the cell.

In addition to RT and IN, retroviruses encode a few other key genes important to make a virus particle called a virion. The envelope gene called env and gag encode the proteins that form an envelope and capsid, which surrounds the RNA genome. The RNA genomes of retroviruses are between seven and twelve thousand bases (7-12 kilobases, kb). The human genome contains approximately three billion base pairs. (RNA is single stranded, while DNA is double stranded, hence “base pairs.”)

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A retrovirus virion is approximately 100 nanometers (nM) in size and can only be seen by an electron microscope. The electron micrograph (EM) of the gamma retrovirus we isolated from human blood in 2009 is shown below:

EM of Gamma Retrovirus

Importantly, the provirus cannot be made into an infectious viral particle without using the machinery of a dividing cell. This is illustrated in the dark parts of the membrane of the cell where the virus is budding out of the cell taking the lipids from the cell membrane to complete the virion.

Here, there, and everywhere 

Essentially, all animals have retroviruses integrated in their genomes. Birds, monkeys, cows, pigs, cats, dogs, mice and fish all have retroviruses encoded in their genomes; even plants have retroviruses. Vertebrate genomes harbor thousands of endogenous retrovirus (ERV) elements that display a structure close to that of the integrated proviral form of exogenous retroviruses (gag-, pol-, and env-related regions flanked by 2 LTRs) but the genes are mutated so that they are thought not to be able to produce and release infectious particles. That is, ERVs most likely are the remnants of past infections of the germline by ancestral retroviruses which have been crippled by the immune system of the host. This means that the retroviral genes are defective and no longer release infectious particles. As much as 15% of the human genome is made up of ERV human retroviruses.

In animals, exogenous retroviruses are responsible for some of the deadliest diseases known. Yet, it wasn’t until 1980 when Poiesz and Ruscetti isolated the first human disease-causing retrovirus, then called Human T-cell Leukemia Virus as it was shown to cause an aggressive cancer called Adult T-cell leukemia (ATL). In fact, when my mentor and colleague of 35 years, Frank Ruscetti, joined the National Cancer Institute (NCI) in 1975 to study human disease causing exogenous retroviruses, he was told by NCI scientist John M. Coffin not to bother as they did not exist.

Although retroviruses have been an important part of human evolution as the placenta evolved from ancestral retroviral envelope genes 25-40 million years ago, envelope genes from both exogenous and endogenous retroviruses, aberrantly expressed in humans, have been shown to be responsible for the development of many chronic diseases. The incidence rates of these diseases are skyrocketing in 21st century America and include prostate cancer, breast cancer, leukemia lymphoma, multiple sclerosis, and amyotropic lateral sclerosis (Lou Gherig’s disease).

Expression and mode of development 

Many factors are important in the development of diseases associated with retroviruses. The expression and mode of transmission are keys to disease development. We have learned a great deal about the types of diseases from 40 years of study of the mechanisms of disease development from animal and human retroviruses. The two main modes of retrovirus transmission are shown schematically below:

Retrovirus transmission

In mitotic transmission, the provirus is dormant or defective and the integrated proviral form of exogenous retroviruses (gag-, pol-, and env-related regions flanked by 2 LTRs) are not expressed. In this case only the daughter cells carry the retroviral genes and if not expressed these endogenous or exogenous retroviral genes remain dormant for years and do not usually contribute to disease until much later in life as the immune system weakens. During infectious transmission, the complete virion is produced with many thousands of virions infecting many neighboring cells and spreading from person to person—both cell free and cell associated—via blood and body fluids. Infectious transmission of HIV drove the AIDS epidemic of the 80s and 90s including transmission from infected cells in a contaminated blood supply and the activation of dormant retroviruses by heavy metals, co-infections and inappropriate vaccination of HIV infected individuals.

Xenograft approaches commonly used since the 1950s in studies of human cancer, autoimmune, and neuroimmune disease promote the evolution of novel retroviruses with pathogenic properties. We now appreciate that it is the use of xenograft technologies in the development of vaccines and biological drugs and genetically modified organisms (GMOs) that have accelerated the spread of animal retroviruses into humans, a process known as zoonosis, whereby an animal retrovirus jumps species, learning to evade immune mechanisms of humans and thereby causing disease. 

The rotavirus vaccine’

Looking at the excipient list of vaccines, we can quickly see that every vaccine may be contaminated with at least one animal retrovirus family, all of which have been associated with cancers, chronic liver disease, AIDS, ALS, ME/CFS and autism.

As just one example among hundreds of retrovirus contamination of vaccines, take a look at the history of the rotavirus vaccine. In 2010, the Food and Drug Administration (FDA) convened a panel of experts to review findings that rotavirus vaccines given to infants in the U.S., Rotateq, produced by Merck Pharmaceuticals and Rotarix produced by Glaxo Smith Kline, are contaminated with pig viruses. Rotarix, an orally administered rotavirus vaccine, contained nucleic acids from porcine circovirus-1 (PCV1) virus and RotaTeq has been shown to contain nucleic acids from both PCV1 and PCV2, a pathogen in pigs that is associated with wasting and immunodeficiency. While acknowledging that the entire short and long-term risks from the porcine circoviruses PCV1 and PCV2 are as yet unknown, the advisory panel decided that “the benefits of the vaccine trumps its risks.”

While the technology to detect genetic contaminates in vaccines was not available until relatively recently, the dangers of generating new viruses and bacteria that can cause diseases were foreseen by the pioneers of genetic engineering. Horizontal gene transfer (HGT) refers to the direct uptake and incorporation of genetic material from unrelated species, in this instance from adventitious viral contaminants in live viral vaccines, into a human host or a host-related bacterium such as those colonizing the gut.

Unlike chemical pollutants which break down and become diluted out, retroviral nucleic acids are infectious, they can invade cells and genomes, multiply, mutate and recombine indefinitely. Potential hazards of HGT of free nucleic acids include the generation of new viruses and bacteria that can cause disease, spreading drug and antibiotic resistance genes among viral and bacterial pathogens making infections untreatable, random insertion into genomes of cells resulting in harmful effects including cancer and reactivation of dormant viruses, present in all cells and genomes, which may cause disease.

Research demonstrates that the pathogenic potential of PCV Type 2 to cause an AIDS-like disease in pigs is unleashed when there is simultaneous immune system activation (e.g. concurrent vaccination) in these animals. Thus, the concurrent inoculation of rotavirus vaccine contaminated with PCV Type 2 DNA sequences along with DTaP, Hib, PCV, IPV and Hep B, as currently recommended by ACIP, provides a high-risk scenario for disease in humans.

PCV Type 2 is a lymphotropic virus that infects primary lymphoid tissues. Its detection in lymphoid tissue of exposed (vaccinated) children should be the focus of urgent investigations, yet relatively few people are aware of the risks. Such tissue is available in the form of intestinal biopsies from children with a variety of conditions including autism. Lymphatic tissue is also available from rhesus macaques exposed to the current vaccine schedule as part of ongoing safety studies. These tissues should be screened using the same metagenomic and pan-microbial array technology used by Victoria et al to identify adventitious sequences in vaccines.

Every cell line or animal tissue used to manufacture any biological including vaccines must first be cleared of all endogenous viruses in order to prevent the zoonotic transmission of retroviruses to humans and make them safe. Receiving one or two injections of an adventitious retrovirus likely does little damage to a healthy immune system. However, the aggressive vaccine schedule currently in place means that the number of retroviruses injected into infants, children, and teenagers—including at vulnerable/immune compromised times in their lives—is unknown.  Combining vaccines, each of which could be carrying HERVs, BLVs, Foamy Viruses, EBV, mycoplasma and potentially more while the immune system is already crippled by mercury, aluminum, polysorbate 80 and formaldehyde is a dangerous and even deadly practice.

Where do we go from here? 

In the past two decades, my research team and others have identified viral sequences proteins and isolated viruses similar to mouse leukemia viruses, mouse mammary tumor viruses, bovine leukemia viruses, simian immunodeficiency viruses, gibbon ape leukemia viruses from human blood, saliva, cells, and cell lines. As we detail in chapter five of Plague, the scientific community failed to heed the 1953 warning of Dr. G. Stuart, when he spoke to the World Health Organization. He was talking about the yellow fever vaccine at that time. He stated:

Two main objections to this vaccine have been voiced, because of the possibility that (i) the mouse brain employed in its preparation may be contaminated with a virus pathogenic for man although latent in mice … Or may be the cause of a demyelinating encephalomyelitis; (ii) the use, as an antigen, or a virus with enhanced neurotropic properties may be followed by serious reactions involving the central nervous system.

In 1996, Dr. John Coffin, that same virologist who told Dr. Frank Ruscetti not to bother studying disease causing human retroviruses because they didn’t exist, warned against transplanting cells from animals into humans to improve the functioning of the immune system of HIV-AIDS patients. According to Dr. Coffin:

The infection is a virtually inevitable consequence of xenotransplantation and this is a very serious worry because the animals that have been chosen for doing this — the baboon and the pig — are both known to carry endogenous viruses, replication competent, but very poorly studied, that are capable of infecting human cells.

And yet, in 2017, vaccines which Coffin, the FDA, and the CDC admit are contaminated with avian retroviruses, mouse retroviruses, pig retroviruses, bovine leukemia viruses, monkey retroviruses and human endogenous retroviruses are mandated by law to be injected into infants and the elderly. As Dr. Sherri Tenpenny wrote more than a decade ago:

If shots that contain stray viruses were only given once in a lifetime, perhaps they would be of little consequence. But flu shots are now recommended – even required – for everyone, from infants to the elderly. Could retroviruses and other viruses be incorporated into the human genome without detection, leading to health problems throughout life?…The risk from avian contaminant viruses has substantially increased since 2004, when the influenza vaccine was added to the pediatric schedule, now starting at six months of age. Extra doses of flu vaccine were administered to children and adults during the bird flu and swine flu pandemic scares, the results of which may not be known for years. Are viruses from chickens and cows being incorporated into the human genome?

We extend Dr. Tenpenny’s alarming questions with knowledge of another family of exogenous human retroviruses, the murine related retroviruses which have now been confirmed in more than 6% of Americans and most likely entered humans via vaccines, and a contaminated blood supply causing the very diseases Dr. Stuart hypothesized. We ask, “Can the MMR vaccine containing avian/chicken retroviruses recombine with mouse sequences passed down from our parents (found in their polio vaccines) to produce a hybrid retrovirus or hybrid sequences?

Are we altering the genes of future generations in unknown ways through vaccines?

What’s coming through that needle canindeed, be deadly.

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Awareness

10 Vegan Body Builders That Are Changing The Way People View Protein

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In Brief

  • The Facts:

    Many body builders and athletes have a vegan diet. Several studies are pointing towards the possibility that plant based protein might actually be a better option than protein from meat.

  • Reflect On:

    Next time somebody asks you where you get your protein from, if you're vegetarian or vegan, now you can tell them. Why are we so conditioned to believe that meat is required for building muscle?

I’m not vegan. I used to identify with this label, but now I just do my absolute best to focus on a primarily plant-based diet. I really don’t like the labels for myself, but have no problem with people who choose to use them. Despite of this, it still drives me absolutely bonkers to hear this phrase, directed at me, or any person who chooses to follow a vegan or plant-based diet, “Where do you get your protein?” It literally makes me cringe, and I will not rest until every person on this planet knows that almost all foods contain protein… and how come no one ever asks the gorilla or the ox where they get their protein?!

Anyways… people often shy away from the idea of limiting their meat consumption or giving it up entirely because they believe that in order to be strong and lean they absolutely need protein from animal sources. Fortunately, for the sake of the animals and our health, this actually couldn’t be farther from the truth. There are plenty of vegan bodybuilders and athletes, many of which have claimed that their performance actually enhanced after cutting out animals and animal products from their diets. Here are the top 10 vegan bodybuilders.

Related CE Article:  Plant Based Protein Vs. Protein From Meat: Which One Is Better For Your Body

9 Things That Happen When You Stop Eating Meat

1. Jon Venus

Jon is a popular vegan bodybuilder who shares his mission and message through his large online community via YouTube and Instagram. He has a ton of videos, workout plans, recipes and online guidance. One look at him will get you inspired to try out this lifestyle, and he proves that going vegan doesn’t mean sacrificing strength or muscles.  You can follow Jon on his journey, here.

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2. Brian Turner

Brian has a large following on YouTube, and he’s here to “relate, teach a bit and have fun with you guys” through his videos. He’s been bodybuilding for over 9 years, and has figured out a way to stay in shape while following a strict vegan diet. On his YouTube channel you can find anything from workout videos, recipe videos to acne videos!

3. Derek Simnett

Derek Simnett is a personal friend of us here at CE.  We have watched his journey unfold over the years and it has been incredible to see. TRULY authentic in his message and lifestyle, Derek is living proof that you can not only achieve big results on a plant-based diet, but you can do A LOT without lifting much weight. His primary mode of training is calisthenics. Check out his stuff here. He is also on YouTube.

4. Nimai Delgado

Once again, we have a very fit and healthy YouTube vegan bodybuilder, Nimai Delgado, an International Federation of BodyBuilding and Fitness (IFBB) Pro. He documents his journey with the IFBB on his YouTube channel and shares tips and tricks with his followers, including his workout routine. He beliefs in maintaining strength and flexibility, and not necessarily just gaining more muscle mass for aesthetic purposes. Definitely check out his YouTube channel to learn more about how this lifestyle could work for you as well!

5. Torre Washington

Torre has been Vegan since 1998! He is a bodybuilder that gets 100% of his vitamins, nutrients and PROTEIN from his diet, he doesn’t believe in supplements. Aside from his hugely successful YouTube channel, Torre also has an extremely resourceful website that can offer you much support on your path towards a fit, vegan lifestyle! Check it out here.

6. Arvid Beck

Arvid is a Vegan bodybuilder from Germany. His decision to become vegan was based largely around his moral and ethical decisions. Nevertheless he is a bodybuilding champion, redefining what it means to be a gladiator! You can check out more of Arvid’s journey here.

7. Samantha Shorkey

Samantha has a popular health and fitness blog called Jacked on the Beanstalk where she shares her secrets to success, including fitness, meal plans coaching and why she decided to adopt a vegan lifestyle and how it has helped her become so successful. Samantha was awarded her pro card in July 2014 after winning first place in the overall bikini title at the 2014 INBF South Western Natural Championships in Austin Texas. This put her on the map as the first-ever VEGAN WNBF bikini pro.

8.  Crissi Carvahlo

Crissi is a vegan fitness model, online trainer and coach, director of the Vegan Fitness International group, designer at Vegan Fitness body, Chef at Vegan Fitness body, author of Vegan Fitness Food For A lean Healthy Body ebook, and so much more! Crissi became vegan at age 38 and now makes it a huge part of her message intertwining it with the knowledge she has gained about health and fitness throughout the years. Check out her website here.

9. Ryan Nelson

Ryan is an athlete, animal lover and vegan food fanatic! Ryan is also a sponsored Posha Green super-heavyweight bodybuilder. Ryan aims to inspire others to set and achieve their goals in the weight room the classroom, sports and in real life. Ryan stands as a testament to the health benefits of a healthy vegan diet! On his website he offers online coaching and nutrition programs. Check it out!

10. Patrik Baboumian

Patrick smashes all types of stereo-types as an Iranian born, German and vegan strongman competitor. Patrick is known as a gentle giant as his concern for the well-being of animals has inspired him to become a vegan and promote this diet through his success.

Conclusion

Now, I don’t want to hear it. I believe I’ve provided you with enough information that you will no longer be asking,“Where do you get your protein?”

Much Love

We Need Your Support...

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

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Alternative News

Roll Up Your Sleeves Folks: 271 New Vaccines in Big Pharma’s Pipeline

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“No vaccine manufacturer shall be liable…for damages arising from a vaccine-related injury or death.” – President Ronald Wilson Reagan, as he signed The National Childhood Vaccine Injury Act (NCVIA) of 1986, absolving drug companies from all medico-legal liability when children die, become chronically ill with vaccine-induced autoimmune disorders or are otherwise disabled from vaccine injuries. (That law has led directly to an expected reckless, liability-free development of scores of new, over-priced, potential block-buster vaccines, now numbering over 250. The question that must be asked of Big Medicine’s practitioners: How will the CDC, the AMA, the AAFP and the American Academy of Pediatrics fit any more potentially neurotoxic vaccines into the current well-baby over-vaccination schedule?)

PhRMA (the Pharmaceutical Research and Manufacturers of America),  the pharmaceutical industry’s trade association and powerful lobbying group, says that 

“today, more than 7,000 medicines are in development globally, all of which have the potential to help patients in the United States and around the world.  According to another data source, there are 3,400 medicines in development today just in the United States, an increase of 40 percent since 2005.” (http://phrma.org/pipeline#sthash.TnxVihsT.dpuf)

PhRMA also says that today 

“the 271 vaccines in development span a wide array of diseases, and employ exciting new scientific strategies and technologies. These potential vaccines – all in human clinical trials or under review by the Food and Drug Administration (FDA) – include 137 for infectious diseases, 99 for cancer, 15 for allergies and 10 for neurological disorders.” (http://phrma.org/press-release-medicines-in-development-vaccines#sthash.rI4cQ6Tg.dpuf)

Whenever the FDA signals that it is ready to grant marketing approval for a new vaccine or drug, the first step for the pharmaceutical company’s marketing department is to promote an “educational” advertising campaign designed to instill fear in parents (and their pediatricians) about the horrible illnesses (albeit previously unknown, benign or rare) that even us doctors hadn’t yet recognized as being significant up until recently, most of us physicians have gone along with the fear-mongering that makes our practices busier while it also makes billions of dollars in profits for some unworthy CEO or Wall Street investment banker, hedge fund manager or mutual fund investor – all at the expense of America’s precious and vulnerable children who are at high risk of being sickened along the way.

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The TV commercials, medical journal articles and drug representatives will be trying to educate us about a new, unaffordable vaccine that will somehow be squeezed into an already crowded and potentially deadly group of shots that America’s already at-risk-of-vaccine-injuries infants will now be receiving at their next well-child (perhaps soon to become chronically ill).check-up.

 Recognizing this, and so as not to overload the already over-loaded well-child inoculation schedule, perhaps he CDC (the Big Pharma-subsidized and vaccine cheerleader Centers for Disease Control and Prevention) will be adding shots to the in-hospital and irrational Hepatitis B shot that it recommends be given on day one – when vulnerable mothers are too exhausted and emotionally confused to give truly informed consent.

Many state legislatures are, as we speak, considering (or have already passed laws) criminalizing the previously legal parental right of refusing vaccinations on the basis of religious or philosophical beliefs. That is happening right now in Wisconsin’s Republican-dominated legislature, Minnesota’s split GOP/DFL legislature, and California’s Democratic Party-dominated legislature – where it is already signed into law by Democrat Jerry Brown. These poorly informed – and heavily bribed politicians don’t realize that their legislative efforts will be blindly forcing unsuspecting patients to submit to every new blockbuster vaccine that successfully emerges from the pipeline. Talk about making decisions on the basis of partial information or propaganda from sociopathic corporate entities! Attention, Senators Al Franken, Amy Klobuchar and other assorted legislators. Are you listening to the real science or to the corrupted, pseudoscience of Big Pharma?

Below is a list of 146 new vaccines that were in the pipeline as of 2010. The list, PhRMA proudly tells us, is now up to 271 new vaccines as of 2013. For a full listing of these vaccine trials, go to: http://phrma.org/sites/default/files/pdf/infectiousdiseases2010%20%281%29.pdf

For parents whose infants’ brains and bodies are immunologically and developmentally immature, be aware that your children may be forced to suffer untested-for and therefore unacknowledged long term neurological, autoimmune and chronic illness adverse effects. Parents need to be aware that if their infant dies, is sickened or is made chronically ill by vaccine ingredients, they, as protective parents, will be forbidden to sue the guilty drug company (or the doctor that administered them) for appropriate damages.

Parents and grandparents of children need to be aware of the fact that many of these new vaccines will be containing contaminants (such as unfilterable viral particles, bacterial particles, monkey kidney cell fragments, human fetal cells, squalene (in anthrax and some experimental swine flu vaccines), peanut oil (a likely cause of the epidemic of peanut allergies), formaldehyde and even foreign DNA fragments) as well as known neurotoxic additives such as formaldehyde and aluminum (and perhaps even mercury), all of which are known genetic toxins and known causes of  (sometimes subtle and sometimes not-so-subtle – but always preventable) brain damage, vaccine-induced epilepsy, autoimmune disorders, the so-called, but erroneously labeled “shaken baby syndrome” (now increasingly understood to represent a vaccine-induced encephalitis), SIDS (sudden infant death syndrome), dementia, autism spectrum disorders, mitochondrial toxicity, damage to the brain’s microglial and astroglial cells (the brain’s immune system), etc.

NOTE: Much of the information in this column is derived from easily accessible books and websites, including Make an Informed Vaccine Decision for the Health of Your Child by Mayer Eisenstein, MD, JD, MPH; The Sanctity of Human Blood: Vaccination is Not Immunization, by Tim O’Shea,  DC; Screening Sandy Hook, Causes and Consequences by Deanna Spingola (an online e-book); the writings and lectures of Russell Blaylock, MD; Immunologist J. Barthelow Classen, MD; Harold E Buttram, MD, Dr Sherri Tenpenny, Dr Suzanne Humphries, Dr Kenneth Stoller, Dr Andrew Wakefield, Dr Mark Geier, and Dr Joseph Mercola, and the following two articles: http://www.vaccines.net/vaccine-induced-immune-overload.pdfhttp://www.globalresearch.ca/vaccine-induced-immune-overload-and-the-epidemic-of-chronic-autoimmune-childhood-disease/5431013.

A List of 146 of the 271 Vaccines in Big Pharma’s Developmental Pipeline (as of 2010)

 (NOTE: The corporations that have the largest financial interest in the success of the trials is listed in bold letters.)

sanofi pasteur prevention of Clostridium difficile

ACE BioSciences prevention of traveler’s diarrhea caused by Campylobacter jejuni

ACE BioSciences prevention of traveler’s diarrhea caused by Escherichia coli

sanofi pasteur diphtheria, tetanus, pertussis Phase III DTP vaccine

Aeras Global tuberculosis

Novartis Vaccines prevention of influenza A infection (H5N1 subtype)

Antigenics treatment of herpes simplex virus

BioSante Pharmaceuticals anthrax Phase I/II vaccine

Intercell USA anthrax

KaloBios Pharmaceuticals Pseudomonas aeruginosa infections

Aduro BioTech treatment of hepatitis C 

Emergent BioSolutions anthrax vaccine

AlphaVax prevention of influenza virus infections in the elderly

DynPort Vaccine botulism vaccine

Inviragen Chikungunya virus vaccine

Celldex Therapeutics cholera vaccine (live attenuated)

ChronTech Pharma hepatitis C (DNA vaccine)

Virionics prevention and treatment of hepatitis C

Vical prevention of cytomegalovirus (DNA vaccine)

AlphaVax prevention of cytomegalovirus infections

Hawaii Biotech prevention of dengue fever

GlaxoSmithKline prevention of dengue fever (tetravalent)

Acambis mild to severe dengue fever

sanofi pasteur DTP-Hep B

sanofi pasteur diphtheria, tetanus, pertussis, polio, hepatitis B, polio, Hib

Dynavax treatment of hepatitis B

Crucell prevention of Ebola virus infections

Vical prevention of Ebola virus infections

GenPhar Ebola virus vaccine

GlaxoSmithKline prevention of infectious mononucleosis (Epstein-Barr virus)

BioSolutions Escherichia coli infections

Celldex Therapeutics prevention of cholera, Escherichia coli infections

Protein Sciences prevention of influenza virus infections in adults and children

sanofi pasteur influenza virus infections (new mass production method)

sanofi pasteur prevention of influenza virus (intradermal micro-injection)

Protein Sciences influenza virus infections

GlaxoSmithKline rotavirus infections in infants

GlaxoSmithKline prevention of cytomegalovirus (recombinant vaccine)

GlaxoSmithKline influenza virus (trivalent, thimerosal-free) for children ages 3-17

GlaxoSmithKline prevention of influenza virus

GlaxoSmithKline prevention of Streptococcus pneumoniae

GlaxoSmithKline prevention of diphtheria, tetanus, pertussis, Haemophilus infections, hepatitis B, meningococcal group C infections, poliomyelitis (infants)

GlaxoSmithKline prevention of Haemophilus and pneumococcal infections

GlaxoSmithKline prevention of Haemophilus and pneumococcal infections

GlaxoSmithKline prevention of influenza virus infection in children

GlaxoSmithKline prevention of influenza A virus (H1N1 subtype) for children and infants

GlaxoSmithKline staphylococcal infections 

MedImmune influenza A virus (H5N1 subtype) intranasal

Novavax prevention of influenza A virus infection

Hawaii Biotech prevention of West Nile virus infection

Novartis Vaccines helicobacter pylori

Pfizer hepatitis B (DNA)

Emergent BioSolutions hepatitis B

GenPhar hepatitis B

Novartis Vaccines treatment of hepatitis C

GlaxoSmithKline hepatitis E (recombinant)

Dynavax prevention of hepatitis B

Pfizer treatment of herpes simplex virus infections (DNA vaccine)

AuRx prevention and treatment of herpes simplex virus infections

sanofi pasteur diphtheria, tetanus, pertussis, hepatitis B, polio, Hib

Intercell prevention of influenza virus seasonal influenza

Novartis Vaccines prevention of herpes simplex virus infections

Acambis prevention of encephalitis virus

Bavarian Nordic smallpox vaccine

sanofi pasteur influenza A virus (H1N1 subtype) in adolescents, children and infants

CSL Behring prevention of influenza A virus (H1N1 subtype) for the elderly

Baxter Healthcare prevention of influenza A virus (H1N1 subtype)

Vical prevention of influenza A virus (DNA – H1N1 subtype)

Baxter Healthcare prevention of influenza A virus (H5N1 subtype)

DynPort Vaccine influenza virus

Antigen Express influenza virus infections H5N1 vaccine

Novavax prevention of influenza virus (particle vaccine)

Dynavax prevention of influenza virus infections

Vaxin influenza virus infections (intranasal)

Abbott Laboratories prevention of influenza virus (cell culture-derived)

Intercell prevention of Japanese encephalitis in children

Novartis Vaccines malaria vaccine (U.S. Naval Medical Research Center)

Vical malaria vaccine

BioSante Pharmaceuticals prevention of malaria (U.S. Naval Medical Research Center)

GenVec malaria vaccine (U.S. Naval Medical Research Center)

Crucell malaria vaccine 

Sanaria malaria vaccine

GenPhar Marburg virus (DNA vaccine)

MedImmune parainfluenza virus infections in children and infants

MedImmune prevention of respiratory syncytial virus infections in infants

MedImmune prevention of parainfluenza virus infections in children and infants

MedImmune prevention of influenza virus (quadrivalent) for adolescents and children

sanofi pasteur Neisseria meningitidis A, C  in toddlers 9 months-12 months

GlaxoSmithKline prevention of Neisseria meningitidis groups C and Y, Haemophilus influenzae type B, and tetanus toxoid

sanofi pasteur meningitis in infants

Novartis Vaccines meningococcal group B infections vaccine group B

Novartis Vaccines meningococcal group A, C infections in children

Novartis Vaccines meningococcal group A, C infections in infants

GlaxoSmithKline prevention of malaria (recombinant vaccine)

NanoBio prevention of influenza virus (intranasal)

GlaxoSmithKline prevention of influenza virus inactivated split-trivalent vaccine

GlaxoSmithKline prevention of Neisseria meningitidis groups A, C in children

LigoCyte Pharmaceuticals norovirus infections (intranasal)

Novartis Vaccines prevention of influenza virus

Protein Sciences prevention of influenza A pandemic (H5N1 subtype)

Meridian Biosciences parvovirus infections

Crucell prevention of influenza virus infections

Pfizer meningococcal group B infections (meningococcal “plague” vaccine)

DynPort Vaccine Yersinia infections (injectable)

Baxter Healthcare prevention of seasonal influenza virus

GlaxoSmithKline prevention of influenza A virus (“pre-pandemic”)

Pfizer prevention of pneumococcal infection in the elderly (Prevnar 13 Adult™)

sanofi pasteur rabies vaccine

BioSante Pharmaceuticals ricin poisoning (“biodefense” vaccine)

Soligenix ricin poisoning

sanofi pasteur prevention of rotavirus infections

Bharat Biotech prevention of rotavirus infections

Emergent BioSolutions anthrax (Fast Track) “protective antigen” vaccine

Inhibitex staphylococcal infections

Vical prevention of severe acute respiratory syndrome (SARS) coronavirus infections

Emergent BioSolutions shigella infections

GlaxoSmithKline prevention of herpes simplex virus infections

PharmAthene anthrax (“protective antigen” – rPA)

BioSante Pharmaceuticals staphylococcal infections (“biodefense” vaccine)

Nabi Biopharmaceutical prevention of staphylococcal aureus infections

GlaxoSmithKline prevention of staphylococcal aureus infections

Nabi Biopharmaceutical prevention of streptococcal B infections

Emergent BioSolutions prevention of streptococcal infections

Novartis Vaccines prevention of streptococcal infections

sanofi pasteur prevention of meningitis and pneumonia (tetravalent)

Inviragen treatment of dengue fever

Intercell USA prevention of traveler’s diarrhea due to E. coli (“patch” technology)

GlaxoSmithKline tuberculosis

Aerus Global TB prevention of tuberculosis in young children

GlaxoSmithKline prevention of  tuberculosis in adults

sanofi pasteur prevention of tuberculosis

DynPort Vaccine tularemia

Emergent BioSolutions prevention of typhoid (live typhoid organisms – oral vaccine)

Novartis Vaccines prevention of typhoid fever

Celldex Therapeutics typhoid fever

Merck prevention of herpes zoster (shingles)

Merck hepatitis B in infants

Merck human papillomavirus infections

Merck staphylococcal infections

GlaxoSmithKline prevention of varicella zoster virus

VaxInnate prevention of influenza A virus

VaxInnate influenza A virus infections in elderly patients

VaxInnate prevention of influenza A virus (H1N1 subtype)

Inovio Pharmaceuticals human papillomavirus infections

Inovio Pharmaceuticals prevention of influenza A virus (H5N1 subtype)

Xcellerex prevention of yellow fever


Dr Gary G. Kohls is a retired physician from Duluth, MN, USA. In the decade prior to his retirement from medicine, he had spent the last decade practicing what could best be described as “holistic (non-drug) mental health care”. Dr Kohls has been actively involved in peace, justice and nonviolence issues for much of his adult life and, since he retired, he has written a weekly column for the Duluth Reader, an alternative newsweekly magazine (www.readerduluth.com). His columns mostly deal with the dangers of American fascism, corporatism, militarism, racism, malnutrition, psychiatry and other movements that threaten American democracy and civility.

This work is reproduced and distributed with the permission and request of GreenMedInfo LLC. Want to learn more from GreenMedInfo? Click here http://www.greenmedinfo.com/greenmed/newsletter.”

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Awareness

Las Vegas Man Unable to Speak, Walk, See or Breathe Just Days After Getting Flu Shot

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In Brief

  • The Facts:

    A few days after getting a flu vaccine, Shane Morgan fell ill with a disease in which a person’s nerves are attacked by the immune system, causing paralysis and, in extreme cases, death.

  • Reflect On:

    How much 'evidence' do we need that the Pharmaceutical Industry is not an advocate for human health? Can we see our way out of this system of deception?

It is starting to seem like we can write a new story every few days about someone having an adverse reaction to the flu vaccine. As I mentioned in an article from last week, ‘After Getting Flu Shot, New York State Senator Gets Sick For Two Weeks, Then Dies,’ the latest flu vaccine is being suspected of actually delivering a dangerous strain of the flu that is resistant to vaccines.

And whether or not Las Vegas’ Shane Morgan had a highly adverse reaction to the vaccine itself or actually contracted this strain of flu, it is very clear in his and his wife’s mind that his adverse reaction was caused by the flu shot. Here’s what happened, according to this Las Vegas Review-Journal article:

On Nov. 2, Shane and Monique, 31, who live in North Las Vegas and are new parents to 8-month-old Briar, got their flu shots. They were planning to see Shane’s 23-year-old daughter, Sidnee Nutter, and her 4-month-old, and Nutter requested the whole family get vaccinated to protect her infant. They typically didn’t get vaccinated, but they happily obliged.

“The only reason I took this was because I didn’t want to lie to my daughter,” Shane said. In the days that followed, Shane fell ill. He was weak and achy; he had a fever and a sore throat. By Nov. 14, he asked his wife to take him to the hospital. “That’s when we really started getting worried,” Monique said. His arms and legs were going numb.

Soon after he was admitted to the hospital, he ‘was sedated and intubated, unable to breathe on his own.’ Now, two weeks later he still ‘can’t walk. His left eye is paralyzed and shut. Tubes protrude from his neck.’

Diagnosis

The doctors have made a diagnosis of ‘Guillain-Barre syndrome.’ More on this disease from the article:

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He may have months of recovery left from the rare disease, in which a person’s nerves are attacked by the immune system, causing paralysis and, in extreme cases, death. The cause of the disease that affects one or two in a million isn’t known, according to the Centers for Disease Control and Prevention. But the disease can creep up after a bout of diarrhea, a respiratory infection or an infection from Campylobacter jejuni bacteria.

In rare cases, people come down with Guillain-Barre after having the flu or getting a flu shot, though the CDC can’t show a causal effect.

So let’s go over this slowly. The Western Medical Establishment has put a fancy name to a symptom, a person’s immune system going out of whack, and called it a disease. Of course, the CDC will say it doesn’t know what causes this disease; they are only willing to offer a few conditions which precede the onset of the disease, including having the flu or getting the flu shot. Again, this admission with the disclaimer that ‘the CDC can’t show a causal effect.’ And why? Is it perhaps because that would give someone direct grounds to sue Big Pharma?

What has the CDC really done here? They have concocted a fancy hyphenated name to de-couple immune system degradation from the introduction of pathogens into the body that would seem logically to be the cause of that immune system degradation. For an organization that prides itself on their research and commitment to objective science, they certainly pull the ‘we don’t know the cause’ rabbit out of the hat whenever it serves the purposes of Big Pharma.

Are Anti-Viral Vaccines Actually Delivering A Toxic Virus?

You may have seen in my earlier article ‘Researcher Jailed After Uncovering Deadly Virus Delivered Through Human Vaccines‘ that respected researcher Dr. Judy Mikovits had isolated a murine leukemia virus, essentially a mouse virus, in examining patients who had a variety of serious diseases such as cancer, motor-neuron disorders and chronic fatigue syndrome (CFS). It was later suggested that this mouse virus likely had been transmitted to these people through vaccines. She explains how vaccines could become infected by this mouse virus when the vaccines are being made:

What we were doing to attenuate, to make the virus less pathogenic, less toxic, is we were passing them through mouse brains, so we were passing them through the brains of mice, and every scientist who works with these viruses, and worked at the National Cancer Institute recognized the possibility that if you put human tissue and mouse tissue together the possibility is that you’re going to pick up a virus that is silent, in the mouse, that is it doesn’t hurt the mouse, but it kills the human, or causes serious disease in the human.

As discussed in that article, the very possibility that people could start to believe that vaccines are transmitting a toxic virus to those who are injected with the vaccine was such a threat to the Big Pharma’s vaccine industry that she was immediately pressured into discrediting her own study, and in refusing to do so she was immediately jailed, and told that she would be ‘destroyed.’ Such is the fate of people who look too deeply and honestly into the true causes of many of our diseases and illnesses.

Flu Strains Getting More Dangerous

The business of vaccination is certainly a huge money-making venture, such that Big Pharma continues to be willing to put out the many fires that are brought on by honest researchers as well as a population getting more sick and diseased in lock step with the increase in the proliferation of vaccines. One of those fires is the clearly documented notion that the ubiquity of the flu vaccine is the actual cause of new deadlier strains of the flu that are more resistant not only to vaccines but to the protective mechanisms of our immune system.

If you consider the fairly straightforward idea that vaccines are working against our immune system and thus are degrading our natural immunity to diseases, then it stands to reason the logical step to take would be the complete cessation of all flu vaccination in our society. My bet is that it would not be long before we would see an increase in the health in the general population, the dying off of many strains of the disease, and an increase in ‘natural immunity’ to diseases in general that parents are able to pass on to their offspring. In the video below, researcher Dr. Andrew Wakefield explains the idea of ‘natural herd immunity’ very cogently:

As far as vaccines go, I would not argue that there is absolute, definitive proof that vaccines are harmful to the average person–and that is because proper, objective testing is not being undertaken. But far more sinister than proper testing not being undertaken due to costs or proper scientific mechanisms is the indisputable fact that Big Pharma, with the CDC in their pocket, care absolutely nothing about human health. Everything they do is based on the metric of profit. They do not want the causes of human disease to be found whenever that would force them to remove pharmaceuticals from human consumption, and are willing to try to convince us that they simply ‘don’t know’ the cause of certain diseases, that they are complicated, mysterious. It’s an embarrassment.

Hypothetical Statement

Doctors and advocates in the mainstream will continue to say whatever they can, spin things in whatever way necessary, to make it seem like, despite the evidence, it’s still a good idea to take the flu vaccine. In fact, their continued livelihood depends on it. Here is the typical example from that same article:

While adverse reactions to the flu vaccine happen, it’s still considered the standard to protect against the flu, which can be dangerous and deadly, said Dr. Fermin Leguen with the Southern Nevada Health District. “The likelihood of people developing Guillain-Barre after the flu shot are very small compared to the risks of developing the flu itself,” Leguen said. “Events like this are unfortunate … but it’s a very rare condition.”

So rather than saying, ‘Shane Morgan had a serious adverse reaction to the flu vaccine and we are going to find out why so it doesn’t happen again,’ the medical establishment would hypothetically say something more like this:

‘Shane Morgan has somehow contracted Guillain-Barre syndrome. We don’t know how it got it, maybe he always had that condition and it just got triggered somehow. While sometimes people come down with Guillain-Barre after having the flu or getting a flu shot–in rare cases, it must be noted over and over again–we can’t show a causal effect. So we will treat his Guillain-Barre syndrome using our pharmaceutical wizardry, and if he survives, we expect to be treated as heroes for saving him.’

Suffice it to say that, simply on the basis of their motives and those of the industry, nothing they say can really be trusted, including the fact that they can’t show a causal effect.

The Takeaway

I personally became much healthier and much more resistant to illness when I consciously moved away from allowing pharmaceutical products to enter my body. My 4-year old son is bright, healthy, energetic, and has neither taken any vaccines nor has ever been seen by a Western doctor. And I am soundly convinced that this is a part of the reason for his good health. When we see that the Western Medicine Establishment has overly complicated and obfuscated ‘health’ to suit their own nefarious agenda and purposes, then we come to realize that completely stepping away from this industry and their synthetic products is what is really best for our health.

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