In Vaccinegate: Initial results on Infanrix Hexa chemical composition, Corvelva a scientific research group reported their findings on the Infanrix Hexa vaccine, the first of many vaccines they are testing and the results are shocking. Continue reading
What if I were to tell you that there were 40 deaths in the Gardasil trails. This fact is clearly stated in the Manufacturer Merck’s prescribing information sheet . Of these deaths 21 occurred in the vaccine group and 19 in the aluminium adjuvant group. But you didn’t hear this from the mainstream media, did you?
Aluminium found in granulomas and lymph nodes of sheep after vaccination. A wake-up call like no other!
This week’s episode of The Highwire with Del Bigtree featured a shocking new Vaxxed vs Unvaxxed Study. Del interviews Professor Lluis Lujan from the Department of Animal Pathology, Veterinary Faculty, University of Zaragoza, one of the authors of Cognition and behavior in sheep repetitively inoculated with aluminum adjuvant-containing vaccines or aluminum adjuvant only.
The Australian experience
Australia has its own special but scandalous place in the history of HPV vaccines now distributed to teenagers in over 130 countries. Australia might be regarded as the birthplace of Gardasil for it was Professor Ian Frazer and the late Jian Zhou who first produced an HPV virus-like particle at the University of Queensland. Australia was also one of the first countries to offer Gardasil to girls in 2007 even though cervical cancer is rare with 1.7 deaths per 100,000 Australian women. Continue reading
In 2014 the U.S. Food and Drug Administration approved Gardasil 9 for use in males and females aged 9 through to 26 years. And as the US market for Gardasil declines there is a new customer base for this dangerous vaccine.
On October 5 2018 the FDA approved Gardasil 9 for use in women and men aged 27 through 45 years. This is a very strange move owing to the fact that for the last ten years the FDA had denied Merck’s request to expand the Gardasil market to adults. Continue reading
When the Australian Government announced its free whooping-cough (pertussis) vaccine for every pregnant woman in the country I was shocked. I had not thought that pregnant women would be targeted for vaccination. But little did I know there were more to come. Continue reading
The introduction of the infant hepatitis B vaccination program began in the state of Victoria on 1 May 2000.
The decision to vaccinate newborns was required as a condition of funding to public hospitals in the state of Victoria under the policy and funding guidelines, issued by the Acute Health Division of the Department of Human Services.
I could not believe this could happen and note that this unethical practice has been in place for 18 years with no sign of it ending. The addition of the hepatitis B vaccine to the infant vaccination schedule meant infants were and still are given four doses of the vaccine: one shortly after birth, and subsequent doses at 2, 4, and 6 months.
When the news broke about this new vaccine for infants I expected some dissent but of course there was no mainstream media analysis and so who really knew of the latest development to over vaccinate our children. At the time I presented a women’s health program on community radio 3CR where I provided some analysis of the issue followed by writing an article that was published in Birth Matters: The Journal of the Maternity Coalition Inc where I expressed my displeasure providing additional information such as the clear directive issued that all health professionals have a legal duty to implement this National Health and Medical Research Councils (NHMRC) policy seen as a major step towards the reduction of acute hepatitis B infection.
Universal hepatitis B immunisation
The statement titled Universal hepatitis B immunisation appeared in NEXUS (Vol 6 Issue 2, November 2000), a publication of the Nurses Board of Victoria. It stated:
In a follow up edition of Birth Matters, the midwives had their say on the hepatitis B addition to the infant vaccination schedule.
MIPP midwives (Midwives in Private Practice) are particularly concerned about the administration of the first dose, for babies who are not in contact with carriers of the disease. The concerns are around informed consent, possible side effects, and storage of the vaccine. MIPP members report that they have informed their clients about the availability of the vaccine, and recommend that those parents who wish their child to have the ‘birth’ dose arrange to have it given at a hospital or by a general practitioner. It is important to note that babies who do not receive the ‘birth dose’ but receive the three subsequent doses will be fully immunised.
The birth dose?
That is a very interesting point: Why are children given four doses when three doses is what is needed for so-called ‘immunisation’. Why are babies given the vaccine at birth? Is this because there is a ‘captive audience’ so to speak. The mums and babies are hospitalised so let’s get them used to having their baby injected with vaccines on the schedule starting with hepatitis B.
The virus infection is generally caused by either unprotected sexual contact or contact with infected blood.
It is apparent that the vast majority of infants born in Australia today would have absolutely no risky behaviours which would leave them susceptible to Hepatitis B infections.
Why was hepatitis B put on the vaccination schedule?
According to the National Vaccine Information Center
The primary reason that the CDC recommended hepatitis B vaccination for all newborns in the United States in 1991 is because public health officials and doctors could not persuade adults in high risk groups (primarily IV drug users and persons with multiple sexual partners) to get the vaccine.
There is no need to give this vaccine to children except maybe if they are at risk due to an infected mother or other person so infected. Vaccines are not harmless as is evident by examining their contents.
Hepatitis B surface antigen recombinant (yeast) vaccine.
The infant dose is (0.5 ml) containing:
Hepatitis B surface antigen. Adsorbed on 250 micrograms of aluminium hydroxide.
Produced in yeast cells (Saccharomyces cerevisiae) by recombinant DNA technology
The final vaccines also contain sodium phosphate – dibasic dihydrate, sodium phosphate – monobasic dihydrate, sodium chloride, and water for injection and traces of polysorbate 20.
Not something you really want to have injected into your newborn child, is it?
An independent review of the VAERS (Vaccine Adverse Events Reporting System – the national database maintained in the US to track and study vaccine reactions) data; publications by governmental, pro-vaccine, and anti-vaccine groups; and a sample of the medical literature leads to the following conclusions:
For most children, the risk of a serious vaccine reaction may be 100 times greater than the risk of hepatitis B.
Overall, the incidence of hepatitis B in the U.S. is currently about 4 per 100,000 and even less for a young child.
In Australia the risk is even lower where:
The overall notification rate of newly acquired hepatitis B decreased from 1.2 per 100,000 in 2009 to 0.7 per 100,000 in 2013.
Adverse events from the vaccine
There are 25,000 reports related to hepatitis B vaccine according to Vaers about one-third of which were serious enough to lead to an emergency room visit, hospitalization, or death. It is often assumed that only 10% of reactions are reported. So the real damage is not known.
A paper published in Neurology 2009 by Mikaeloff Y, Caridade G, et al called Hepatitis B vaccine and the risk of CNS inflammatory demyelination in childhood stated:
The Engerix B (hepatitis B) vaccine appears to increase this risk particularly for confirmed multiple sclerosis in the longer term
They reported that children with a confirmed diagnosis of multiple sclerosis were significantly more likely to have received the Engerix brand of vaccine.
Time for action
Recently it was suggested to me by a fellow critic of this particular vaccine that surely the hepatitis B given at birth is the most unnecessary and unethical and if there was any vaccine that we could use as an example of the burdensome, ever increasing schedule and the damage such vaccines are doing to young lives then this is the one.
We must educate young parents that once their child is born he/she will be given a hepatitis B shot. We need to forewarn them that this vaccine comes with real risks.
Remember we are not ‘pro-choice’ we are ‘anti-vaccine’ – Dr Heather Wolfson
Such a powerful video and an amazing couple who are anti-vaccine and proud of it.
One Doctor’s Surprising Answer to the Epidemic of Autoimmunity and Chronic Disease
Thomas Cowan, MD, argues for a direct causal relationship to a corresponding increase in the number of vaccines American children typically receive―approximately 70 vaccine doses by age eighteen. The goal of these vaccines is precisely what we’re now seeing in such abundance among our chronically ill children: the provocation of immune response.
Thomas Cowan’s latest book is one I can’t wait to read. I want to understand all about autoimmunity and how our increasing insane vaccine schedule is implicated.
Cowan begins his book with a description of how when he was growing up he never heard of children with chronic illness or of children who took prescription medicines.
Many of us had horrible diets, yet chronic disease among children was relatively unknown. No one had ever heard of autism, let alone a family member with autism.
I have to agree with his childhood recollections. Children with cancer or an autoimmune disease was unheard of in 1950s Australia.
In his work as a medical practitioner Thomas Cowan has had the experience of treating vaccinated children, partially vaccinated children and the unvaccinated. He writes that he rarely saw an unvaccinated child with any chronic illness however the same could not be said for those who were vaccinated many of whom were suffering from asthma, eczema, seizures and gut problems. This state of affairs he believes:
corresponded with the introduction in the late 1980s to the mid 1990s of certain adjuvants and excipients, as well as the introduction of ever more vaccines.
During his practice he has treated many children who had childhood infectious diseases such as whooping cough, chicken pox, rubella, mumps and measles. These children recovered well and did not develop complications.
1 in 2.5 children have an allergy
1 in 6 children has a developmental disability
1 in 9 children has attention-deficit/hyperactivity disorder ADHD
1 in 11 children has asthma
1 in 13 children has severe food allergies
1 in 36 children has autism
He calls it ‘a national emergency’.
How did we get to such a state where we have so many sick children?
Cowan writes that the cause is environmental requiring us to do something about it. The problem as he sees it stems from the huge drop in infectious disease which ‘train the immune system’.
In writing Vaccines, Autoimmunity and the Changing Nature of Childhood Illness Cowan wanted to explain the nature of disease.
when we get sick there is a very certain sequence of events that happens: We are fine, then we get a fever, or we get hot then we get snot, and then we get better
In an interview with Dr Joseph Mercola he explains that he often wondered why disease follows this progression. His curiosity led to his researching the nature of fever along with the working of the cell and why our bodies follows this sequence of events in relation to disease.
Once you realise the wonder of this sequence of the events you can understand what happens when something is done to interfere with nature which Cowan describes as ‘thwarting of the sequence’. This is what happens in the context of vaccines leading to chronic disease. Vaccines cause a distortion in the immune response and increases the risk of cancer.
What happens inside the body of a child who gets a new viral disease.
When a new virus enters the body it distorts the cells whereupon the body begins its attack and produces a cell mediated immune response. This system consists of white blood cells which attack the infected cells, chewing them up and spitting them out – this is ‘snot’. This process takes about 5-10 days and over this time we consider the person affected ‘sick’ and all the while the virus has promoted a cell mediated response which clears the body of the virus and dead cells and rejuvenates the cells.
The humoral system which responds by making antibodies to the virus is also activated taking place after the cell mediated response. If the child meets a particular virus again then he/she will not get sick. This production of antibodies takes place around 6-8 weeks after the infection. ‘It is almost a 100% fool proof system’, says Cowan.
These are the two parts of our immune system.
When we vaccinate there is no cell mediated immune response. Vaccines provoke an antibody reaction but because there is no cell mediated response the immunity wears off and boosters are required. Adjuvants such as aluminium are required to stimulate this antibody reaction.
Such as Graves’ disease, inflammatory bowel disease, multiple sclerosis, psoriasis, rheumatoid arthritis, and systemic lupus erythematosus.
these diseases are characterised by an excessive antibody reaction
In autoimmunity there is non specific activation of the humoral immune system caused by the adjuvants such as aluminium. Vaccines stimulate humoral antibodies without a prior cell-mediated response.
There has never been until about the 1940s a situation where you have the stimulation of one without the other. So that’s what happens with vaccines, the whole point of a vaccine is to stimulate the humoral immunity, the humoral antibodies without a prior cell-mediated response.
It is not enough to just put the antigen in a vaccine along with saline. To make the vaccine stimulate humoral immunity, that is to produce antibodies, adjuvants such as aluminium or other irritants such as formaldehyde and mercury are necessary for the immune system to react. These are neurotoxins and should have no place in the human body.
The diseases that are characterized by suppressed cell-mediated immunity and heightened humoral immunity, you’re talking things like asthma, allergies, eczema and autoimmune diseases including Crohn’s, colitis, MS [multiple sclerosis], Sjogren’s syndrome, Hashimoto’s, etcetera. All of these are characterized by increased antibody production – that is what we mean by an autoimmune
Cowan states that the the fastest growing type of diseases are autoimmune diseases. Autoimmune diseases are soaring globally and together affect as many as one in five Americans today. Thomas Cowan’s Vaccines, Autoimmunity and the Changing Nature of Childhood Illness explains how our wonderful immune system has been ravaged by vaccines and includes chapters on treatment and diet protocols for autoimmune disease.
A must-read book on vaccines and autoimmunity and a history lesson on natural immunity that we all need to read and share.