Friday, July 13, 2018

A Vaccine for Meningitis is Causing Epidemic of Diabetes!

Image result for diabetes images

Tom McLachlan
It was the high incidence of diabetes from the HiB vaccines which banned the shot forever from Finland. We still give 4 doses to our kids. And what is the incidence of childhood diabetes in the US in the last 10 years?
An Australian National Health and Medical Council information sheet on Hib vaccines advises that Hib meningitis can cause brain damage with later learning difficulties and behavioural disorders (
Fungal meningitis is not contagious
Parasitic meningitis is not
Non-infectious meningitis is not
Viral meningitis.. The enteroviruses that cause viral meningitis can spread through direct contact with saliva, nasal mucus, or feces. They easily spread through coughing and sneezing but you are unlikely to develop meningitis as a complication
Bacterial meningitis is contagious but is less contagious than the germs that spread cold and flu. Meningococcal bacteria can’t survive outside the body for long, so you are unlikely to get it from being near someone who has it.
Frederick R. Klenner, M.D. of North Carolina has seen cures of diphtheria, staph and strep infections, herpes, mumps, spinal meningitis, mononucleosis, shock, viral hepatitis, arthritis and polio using high doses of vitamin C (Journal of Preventive Medicine, Spring, 1974).
Dr Cathcart
"This disease is made more deadly because of the "acute induced scurvy" involved. This means that intravenous sodium ascorbate and later bowel tolerance doses of ascorbic acid should be administered along with the appropriate antibiotic. Not only does the ascorbate broaden the spectrum of activity of the antibiotics against bacteria and works synergistically with the antibiotic, but it avoids allergic reactions to the antibiotic. The susceptibility of sick people to allergic reactions is because of the up-regulation of the immune system while you are sick. This up-regulation is caused by free radicals. If the free radicals are neutralized by massive doses of ascorbate, the immune system, as far as allergic reactions are concerned, is down-regulated so that allergic reactions to the antibiotics do not occur. However, unlike steroids that universally down-regulate the immune system, ascorbate up-regulates the ability of white cells to kill viruses and bacteria......The incidence of meningitis "surges" after the flu because the acute induced scurvy induced by the flu decreases the ability of the body to fight off the meningitis bacteria."
"The matron was convinced that the diagnosis was meningitis so she prepared a lumbar puncture. I had however, seen this problem before. Lumbar punctures performed by me had been negative and the infants died....the trauma of inserting a needle..might result in a haemorrage that might cause spinal cord paralysis. So I decided to give an injection of vitamin C..I probably gave as many as 6 injections, each 100mg. After half an hour Mary was normal. It was hard to believe, but I had performed a miracle!...I found that any viral infection, including measles and hepatitis, could be dramatically 'cured' by administering Vitamin C intravenously in big doses--provided that treatment was commenced early."---Dr Kalokerinos MD (Medical Pioneer of the 20th century p175)
"Meningitis is not a transmissible disease, we do not "catch" it from one another. My first lesson in vaccine propaganda is when I learned, back in the forties, that the "epidemics" of meningitis amongst military recruits were not epidemics but clusters, and the second thing I learned was that only the freshly vaccinated recruits "caught" meningitis. The mess sergeant didn't, the drill sergeant didn't, only the recruits did. Not even the girls who worked at the base exchanges and service clubs, with whom the recruits played kissy face "caught" meningitis - only the freshly vaccinated recruits "caught" it.......In over thirty years of clinical practice I have never seen an infectious hepatitis "caught" by another member of a household and believe me when I say I really looked high and low for one of those. If I found one I would look for a source of the poisoning, not for a germ or a virus"---Daniel H Duffy Sr. DC
Cases of meningitis and septicaemia have fallen from about 4,000 a year in the late 1990s to 2,446 last year following the introduction of a vaccine against meningitis C in November 1999. But in a bizarre twist the number of deaths rose last year by 17 per cent from 317 to 370 and is not far below the level before the vaccine was introduced. [Media September 20, 2004] Meningitis vaccinations 'blamed' for rise in deaths
"When I was in high school, my parents had me vaccinated for meningitis. Following my meningitis vaccination, I ended up in the hospital with a major infection that attacked every area of my system. My parents told me that for the first two days that I was hospitalized I did not even recognize them. The doctors performed a lumbar puncture on me. This procedure involved freezing my mid-section so the doctors could insert a large needle into the pit of my spinal cord to withdraw fluid for testing. Their diagnosis was meningitis. I remained hospitalized for three weeks. They did not want to even consider that my meningitis vaccination could have caused my nearly fatal disease." Vaccine Safety Manual by Neil Z. Miller. (p.337)
"When notifications of meningitis (from MMR vaccine) from physicians were included; when the vaccine records of hospital cases of meningitis were included; when cross linkage of vaccine records from laboratory reports (4 laboratories) was performed and included the figure was increased to 1 in 11,000. It should be noted that in the case of one particular laboratory, this was 1 in 4,000. "----- Paul Shattock and Dawn Savery, Autism Research Unit, University of Sunderland, Sunderland, UK
"When I heard about the 14 year old boy who died of group C meningitis I remember wondering how soon beforehand he had had his BCG vaccination (another vaccine with a ‘live’ organism)."---DrJayne L M Donegan
"Every time you hear of the tragic death of an infant, carried off in the first weeks of life by ‘viral meningitis’, you have the right to suspect that BCG is at work, even if the autopsy confirms a viral diagnosis. My wife lived through this tragedy in a major Swiss hospital where she worked. The autopsy of the child revealed the tubercular nature of the ‘viral’ meningitis following a BCG inoculation, but all the assistants and nurses had received very clear instructions to say nothing or risk terrible consequences. As with all secret societies, the law of silence is absolute among doctors!"--Dr Jean Elmiger (Rediscovering Real Medicine ISBN 1862041997)
"The use of Hib vaccines has displaced haemophillus as a cause of disease and death, but other organisms like the far more serious, and more untreatable pneumococcus or other bacterial meningitis types have risen to take the place of Hib as causes of meningitis."---Hilary Butler
"In Minnesota, a state epidemiologist concluded that the Hib vaccine increases the risk of illness when a study revealed that vaccinated children were *five times* more likely to contract meningitis than unvaccinated children."
"hib is not a disease but a type of bacteria---defined by lab hard to see if there is any disease decline.......Primary motive was to combat "invasive bacterial infections", but no evidence this has been achieved. 3 major types of "ibi"--hib, pneumococcal, and meningococcal. ..decline in hib infections appears to have been accompanied by an increase in the other two.... there appears to be no evidence of a decrease in invasive bacterial disease overall.... in aus notifications of meningococcal disease in 1995 was highest since 1979...this rise occurred in parallel with the fall in hib disease, so what savings in illness have there been?, there seems to be no demonstration savings in illness in children, on top of this there seems to be an association between dpt vacc and invasive hib disease."--Greg Beattie
"The Government was last night accused of a cover-up over the safety of its mass meningitis immunization programme after The Observer obtained confidential documents that show at least 11 people have died after injections to prevent the disease."--Media Aug 2000
"Classen's data and other published data indicates the following vaccines are associated with an increased risk of diabetes (increased risk): hepatitis B (50%), hemophilus (25%), tetanus (20%), diphtheria (9%), pertussis (25%), mumps- rubella (23%). These findings are supported by a case control study performed in Europe. The cumulative effect of all these vaccines on diabetes is tremendous."--PRNewswire
"I have published many articles linking vaccines and diabetes. In one study, a clinical trial on the hemophilus vaccine, I showed that the risk of the vaccine exceeds the benefit. This is published by the British medical Journal."--Bart Classen
"Four of the medical experts advising the Government on whether the new meningitis C vaccine is safe have links to one or more of the drug companies that produce it......Professor Janet Darbyshire, a member of the Government's Committee on Safety of Medicines, had received support for academic research from US firms Wyeth and Chiron, who produce the two main meningitis products being used on children in Britain....three members of the Joint Committee on Vaccination and Immunisation had declared interests in vaccine manufacturers...Dr David Goldblatt of the Institute of Child Health, has served on an expert advisory panel for Wyeth and received research grants from Wyeth and North American Vaccines, which produces a third meningitis C drug to be introduced this year. Another, Professor Keith Cartwright of the University of Bristol, received funding from the drug industry to 'evaluate candidate meningicoccal vaccines'. "--Martin Bright and Tracy McVeigh, Sunday Observer, UK September 3, 2000
The aim of this retrospective study was to evaluate the incidence and the characteristics of spontaneously reported aseptic meningitis (AM) in France following mumps vaccination with monovalent or multivalent vaccines containing the Urabe strain. Fifty-four cases of AM were reported to the regional drug surveillance centres or to the manufacturer from the time each vaccine was launched up until June 1992. Twenty cases were associated with the time off administration of a monovalent mumps vaccine and 34 with a trivalent measles, mumps and rubella vaccine (MMR). A mumps virus was isolated in four cases in the cerebrospinal fluid and an Urabe-like strain was characterised twice by polymerase chain reaction (PCR).
A probable mumps origin was assumed in 17 other cases where the patients presented with other clinical or biological signs of mumps infection. The clinical outcome of AM was always favourable. The global incidence of mumps vaccine-associated AM was 0.82/100,000 doses, which is significantly lower than the incidence in the unvaccinated population. Even considering that the actual incidence of AM is much higher when assessed by active surveillance studies, the risk/benefit ratio of mumps vaccine remains in favour of vaccination. The incidence of mumps vaccines containing Jeryl Lynn (ROR Vax et Imu ORR) associated with AM needs to be evaluated. PMID: 9164005, UI: 97306738.…
Saturday, March 5, 2011
Four infant deaths trigger vaccines halt
Kyodo News
The health ministry has decided to suspend the use of two types of publicly subsidized vaccines following the deaths of four children.
Municipal governments were notified of the decision.
The two types are the Hib vaccine, which prevents bacterial meningitis, and a vaccine against streptococcus pneumonia.
There have been no reports so far from the doctors who treated the children that there is a causal relationship between the vaccines and the deaths, according to the Health, Labor and Welfare Ministry.
The ministry is planning to assemble a panel of experts this week after consulting with other doctors to examine the cases, according to officials.
The ministry is expected to let the vaccinations resume if the panel decides the two vaccines don't pose serious safety concerns.
The four children were a 3-month-old girl in Kawasaki who died Feb. 20, a 2-year-old boy in Takarazuka, Hyogo Prefecture, who died Tuesday, a 1-year-old girl in Nishinomiya, also in Hyogo, who died Wednesday, and a 6-month-old girl in the city of Kyoto who died Friday.
The doctors of the children described the causal relationship between the vaccines and their deaths as either unclear or impossible to evaluate. Some had underlying illnesses and others did not.
All four children were administered a vaccine against streptococcus pneumonia made by Pfizer Inc., and all except the girl in Nishinomiya received ActHIB, an Hib vaccine made by Sanofi Pasteur Inc.
In addition, all except the boy in Takarazuka received a mixed vaccine against diphtheria, whooping cough and tetanus on the same day they received other vaccines.
The streptococcus pneumonia vaccine has been administered to an estimated 1.10 million people in 2.15 million doses since it went on sale in February 2010. The Hib vaccine has been administered to an estimated 1.55 million people in 3.08 million doses since its launch in December 2008.
Japan, known for being notoriously slow to accept new vaccines, approved the Hib vaccine in 2007, 20 years after the United States did so. Approval for the streptococcus pneumonia vaccine came in 2009, compared with 2000 in the U.S.
An increasing number of people are believed to be receiving these vaccines because of a subsidy program launched last November in which the government agrees to shoulder half the cost of vaccination if municipal governments organize and subsidize vaccination programs.
by What Doctors Don't Tell You (Volume 10, Issue 9)
Children who receive multiple doses of the Haemophilus influenzae b (Hib) vaccine are at increased risk of developing type I juvenile-onset diabetes, according to new American research.
When researchers in Baltimore compared children who had received four, one and no doses of the vaccine, the cumulative incidence of diabetes per 100,000 in the three groups was 261, 237 and 207 at age 7 and 398, 376 and 340 at age 10, respectively. This works out to be that the greatest increased risk is among children who receive the full quotient of the vaccine.
The incidence of diabetes among US children aged five to 10 had been stable in the 10 years prior the introduction of the vaccine.
The increased risk of diabetes - which is just one of the potential adverse effects of the Hib jab - certainly exceeds the benefits of the vaccine, say the Baltimore research team. The Hib vaccine has been estimated to prevent approximately seven deaths, and between seven and 26 cases of severe disability per 100,000 children who have been immunised (BMJ, 1999; 319: 1133).
* In another study, scientists have found that the routine vaccination of newborns with the hepatitis B vaccine increases the risk of fever (Arch Dis Child, Fetal and Neonatal Edition, 1999; 81: F206-7). A before-and-after study showed a link between the launch of the vaccination programme in Israel and the number of babies with unexplained fever in the first three days of life. As yet, the scientists do not know what significance this finding has for the short- or long-term health of the infants.
Can Hib Vaccine Cause Asthma?
by Heidi White
Can the Haemophilus influenzae type b (Hib) vaccine cause asthma or allergy? I am not aware of any human studies that have specifically looked at the effect of Hib vaccine on asthma. However, a Swiss study1 found that invasive Hib infection (epiglottitis) could possibly be linked to an increase in the rate of asthma and allergies (OR 4.8). There may be a few explanations for this. Firstly, the treatment of a Hib infection with antibiotics, such as cephalosporins (eg cefotaxime or ceftriaxone), may by itself increase the risk of asthma.2 And secondly, cell wall components from the Hib bacteria may also be a cause of asthma.
If invasive Hib infection is able to cause asthma then it may also be possible that the Hib vaccine could also have a similar effect. Animal studies have provided various mechanisms for why this could occur:
a) A nasal Hib vaccine has been shown to stimulate Th1 and Th2 cells in mice.3 If the Th2 side of the immune system is over stimulated, then this can increase the risk of asthma and allergy.
b) Hib vaccination in rats has been shown to enhance histamine levels with a corresponding increase in the number of eosinophils.4-7 Eosinophils (white blood cells, used to fight infection) will proliferate and accumulate in the airways under stimulation by interleukin-5 (IL-5), a cytokine produced by Th2 cells. Eosinophil accumulation is also evident in the dermis of the skin seen in people with atopic dermatitis (eczema).
c) Hib vaccination in rats has been shown to cause increased bronchoconstriction in response to histamine, possibly due to an increased reactivity of the para-sympathetic/cholinergic pathways.7,8
d) Studies in guinea-pigs have shown that Hib vaccination may impair the beta (b ) 2-adrenergic system by causing a blocking or desensitization of b 2 receptors, or by reducing the number of b 2 receptors in the lung.9-13 Inhibition of b receptors can lead to increased bronchoconstriction. It is thought that the polysaccharide component of the bacterial cell wall may be responsible for this effect.14 HibTitre vaccine contains purified polysaccharide (PRP), from the capsule of the Hib bacteria, which is linked to a diphtheria carrier protein. PedvaxHIB vaccine contains PRP linked to a meningococcal protein.
It would be interesting to see the results of a human study that specifically examines the effects of Hib vaccine on the incidence of asthma and allergy.
Heidi White
Hospital Pharmacist
September, 1999.
1. Muhlemann K et al. Risk factors for invasive Haemophilus influenzae disease among children 2-16 years of age in the vaccine era, Switzerland 1991-1993. The Swiss H. Influenzae Study Group. Int J Epidemiol 1996 Dec;25(6):1280-5
2. Farooqi IS, Hopkin MH. Early childhood infection and atopic disorder. Thorax 1998 November; 53: 927-932
3. Kurono Y et al. Nasal immunization induces Haemophilus influenzae-specific Th1 and Th2 responses with mucosal IgA and systemic IgG antibodies for protective immunity. J Infect Dis 1999 Jul;180(1):122-32
4. Nijkamp FP et al. Facilitation of histamine release in the Haemophilus influenzae vaccinated experimental animal. Br J Pharmacol. 1980 Jan; 68(1):147P
5. Raaijmakers JA, Terpstra GK, Kreukniet J. Mast cells as a possible source of Haemophilus influenzae-induced changes in plasma and lung histamine levels. Int Arch Allergy Appl Immunol 1980;61(3):352-7
6. Terpstra GK, Raaijmakers JA; Kreukniet J. Comparison of vaccination of mice and rats with Haemophilus influenzae and Bordetella pertussis as models of atopy. Clin Exp Pharmacol Physiol 1979 Mar-Apr;6(2):139-49
7. Terpstra GK et al. Effects of Haemophilus influenzae vaccination on the (para-)sympathic- cyclic nucleotide-histamine axis in rats. Ann Allergy 1979 Jan; 42(1):36-40
8. Schreurs AJ, Nijkamp FP. Bronchial hyper-reactivity to histamine induced by Haemophilus influenzae vaccination. Agents Actions 1984 Oct; 15(3-4): 211-5
9. Terpstra GK, Kreukniet J, Raaijmakers JA. Changes in beta-adrenergic responses as a consequence of infection with micro-organisms. Eur J Respir Dis Suppl 1984;135:34-46
10. Schreurs AJ, Terpstra GK et al. The effects of Haemophilus influenzae vaccination on anaphylactic mediator release and isoprenaline-induced inhibition of mediator release. Eur J Pharmacol 1980 Apr 4;62(4):261-8
11. Schreurs AJ, Versteeg DH, Nijkamp FP. Involvement of catecholamines in Haemophilus influenzae induced decrease of beta-adrenoceptor function. Naunyn Schmiedebergs Arch Pharmacol 1982 Sep; 320(3):235-9
12. Schreurs AJ, Terpstra GK, Raaijmakers JA, Nijkamp FP. Effects of vaccination with Haemophilus influenzae on adrenoceptor function of tracheal and parenchymal strips. J Pharmacol Exp Ther 1980 Dec;215(3):691-6
13. Nijkamp FP et al. Inhibition of effects of isoprenaline and adrenaline by Haemophilus influenzae vaccination. Br J Pharmacol. 1980 Jan; 68(1):146P.
14. Schreurs AJ, Verhoef J, Nijkamp FP. Bacterial cell wall components decrease the number of guinea-pig lung beta-adrenoceptors. Eur J Pharmacol 1983 Jan 28; 87(1):127-32
Beware of HIB vaccine
by Dr Robert Mendelsohn MD
Just as with the older vaccines, the best advice I can give parents is to carefully read the prescribing information before permitting the doctor to use this new Hemophilus influenza b vaccine.
You then will learn that, in addition to the active agent or germ, the vaccine injection also contains lactose, thimerosal (a derivative of mercury) and sodium chloride. You might ask your doctor whether any studies have shown that the injection of these materials——sugar, mercury and salt——is safe. I know of none.
Be sure that your doctor has a second syringe available if he gives your child the shot. The prescribing information states that an epinephrine (adrenaline) injection should be available for immediate use if an anaphylactoid (shock—like) reaction should occur. Also, be sure he takes a careful history and performs a physical examination on your child, since any febrile illness (one that is accompanied by a fever) or active infection is reason to delay the vaccine.
If you decide to have the doctor inject the vaccine, watch that he injects it in the right place. The vaccine should be given under the skin (subcutaneously) and not intradermally (between the layers of the skin), intravenously or intramuscularly. The safety and efficacy of these other routes of administration have not been evaluated.
Where has the vaccine come from? Has it been sitting on a table or in a drawer? The prescribing information says the Hib vaccine should be refrigerated upon receipt and should be stored when not in use at 35 to 46 degrees Fahrenheit. Be sure the vaccine is taken out of the refrigerator and not out of the freezer, since the prescribing information carries the warning——DO NOT FREEZE.
If you can, determine when the doctor mixed the vial of vaccine with the vial of diluting fluid, since, after mixing, the vaccine is stable for only 30 days when stored as directed. The date of mixing (reconstitution) should be recorded on the label of the vial containing the vaccine. Look at the label before the shot is given to make sure the expiration date has not passed.
Since the Hib vaccine first was introduced a few years ago, I have been warning people about the tendency of doctors to use a new medicine as fast as they can before all the adverse effects are known. Now, the darker side of this new vaccine, designed to prevent children from getting meningitis, is beginning to surface.
In an article entitled, "Meningitis Risk Seen from Use of Vaccine" (St. Paul Pioneer Press Dispatch, April 21, 1987), Minnesota state epidemiologist Michael Osterholm reported that, instead of protecting children from meningitis, the Hib vaccine increases the risk of illness. Speaking to physicians and health experts from around the United States who were gathered at the National Institutes of Health, Osterholm reported that a study of children who had received the Rib vaccine since its introduction in 1985 showed they faced a fivefold increase in the risk that they Will be infected by the Hemophilus influenza type b bacteria (against which the vaccine is supposed to protect them). This Minnesota study found the vaccine has an effective rate of minus 86 percent, meaning the number of infected children grew. In Minnesota, many doctors have stopped administering the vaccine until they get a definitive response from the FDA.
In contrast, the original study of children in Connecticut, Pittsburgh, and Dallas which was done by Dr. Eugene Shapiro of the Yale University School of Medicine, found the vaccine to be effective 89 percent of the time. The most startling revelation is that Shapiro excluded Minnesota from his study (even though that study used the same methodology) because the state’s results were so far out—of—line from the other areas examined. I hope every reader of this Newsletter, whether in the United States or in Canada, is aware of the almost uncontrollable tendency of researchers to throw out findings that don’t agree with their preconceived conclusions!
In view of this important news, every parent whose doctor recommends the Hib vaccine must ask the doctor if he knows what’s happening in Minnesota.
The authoritative Centers for Disease Control publication, Morbidity and Mortality Weekly Report, reported in its August 21, 1987 edition that invasive Hib disease was occurring in children who previously had been vaccinated with that immunizing agent.
When the vaccine was introduced in 1985, the FDA asked its manufacturers to conduct post—marketing studies. As a result, the FDA, CDC, vaccine manufacturers and individual vaccine investigators have received spontaneous reports of these vaccine failures.
The word "spontaneous" is important. It indicates that government agencies and vaccine manufacturers have depended on passive surveillance in their search for adverse effects.
"Passive surveillance" is the epidemiological term used when there is only voluntary, spontaneous and therefore spotty reporting of adverse effects by patients and doctors to the government or drug companies. In contrast, "active surveillance" refers to a situation in which the company making the drug" or vaccine and the government’s health and watchdog agencies make an effort to check up on the patients to determine the extent of adverse effects.
For example, in active surveillance, a vaccine manufacturer or the FDA might keep a file card on each person who was given the vaccine during field trials. Then at some point——days, weeks, months or even years later—each vaccinee and his family would be contacted, examined and closely questioned to determine both the efficacy and safety of the vaccine.
As you can see, from the scientific standpoint, active surveillance is vastly superior to passive surveillance. However, not too unsurprisingly, vaccine manufacturers are quite resistant to the idea of active surveillance. They claim it is too expensive, too time—consuming, etc.
I often have felt that a more basic reason for opposition to active surveillance is vaccine manufacturers’ fears of what such a scientific study might turn up. But even with inadequate, slapdash and sloppy passive surveillance, bad news about the Hib vaccine has surfaced. Investigators at the Northern California Kaiser Permanente Health Plan and the Minnesota Department of Health have reported some cases of invasive Hib disease during the one—week period following vaccination.
Last year, one investigator suggested in the New England Journal of Medicine that these vaccine failures might be due "to an inability to induce an appropriate antibody response." Translating this into English, the vaccine might not work.
The CDC says further investigation is necessary to evaluate the meaning of Hib cases found soon after vaccination. They warn that physicians should be aware that "cases may occur in the week after vaccination, prior to onset of the protective effects of the vaccine."
I will not argue with the CDC that physicians should be aware of the vaccine failure. But just in case your physician does not have time to read this weekly government publication, I think it important that patients get the message directly.
Loss of speech after Hib vaccine
Letter WDDTY April 2001
in 1992, immediately following a then new vaccination against Haemophllus influenzae type b (Hib) infection, my two-year-old granddaughter became unresponsive and regressed until she lost all understanding and speech.
She was finally diagnosed with the extremely rare childhood disintegrative disorder Heller’s syndrome.
An Australian National Health and Medical Council information sheet on Hib vaccines advises that Hib meningitis can cause brain damage with later learning difficulties and behavioural disorders (
On hearing of US reports of an elevated risk of Hib disease in the week following Hib vaccinations, I sought as much information as possible. Through the US Freedom of Information Act (as WDDTY suggested), I was able to obtain adverse reports for 1988—90, when the vaccine given to my granddaughter was first used in the US. The reports showed clustering of meningitis on day two following vaccination, with an unexpected involvement of the MMR vaccine.
There are 140 serious outcome reports, with 24 cases of meningitis. Five meningitis cases occurred on day two following vaccination and one on day four; nine are classed as ‘no drug effect’ and nine had undefined timing. The ‘no drug effect’ cases must be vaccine failures, occurring at least a month, but up to two and a half years, after vaccination.
If the five day-two meningitis cases represent ‘background’ disease, there should have been comparable reports for all seven days of the week following vaccination. It seems most unlikely that ‘background’ disease cases could be so concentrated on day two.
Seven of the 140 serious outcome children also received MMR vaccine, probably representing those who missed this shot at one year of age. Three of these seven children had day-two meningitis. It is most unlikely that the involvement of MMR in day-two meningitis is a chance occurrence.
If no one can say which braindamaging illness caused a particular child’s autistic regression, greatest suspicion must fall on the most common illness with features consistent with parents’ experiences.—BG, Canberra
Parents demand answers as children fall ill after meningitis jabs
(Western Daily Press, June 12, 2000)
Case 1
Father's fears over tot's reaction
TERRY Meredith’s daughter has never been an angel but the change in her behaviour since having the meningitis C vaccination has left him worried about the long-term effects.
Amy, who is almost three, has been acting differently since her injection two weeks ago.
"The day she had the jab she went absolutely loopy. It was like she was on Ecstasy or something," he said.
"She is normally boisterous but she has been particularly bad since the injection. Her behaviour has deteriorated and she has been violent towards her mother and her 13-month-old sister Stacey. We have had to discipline her and tell her off more than ever before."
Mr Meredith, who lives in Tidenham, near Chepstow, said friends had also reported strange behaviour among their children since the injections.
"One of our friends has a little boy and he has gone stubborn and is shouting and has been violent, he said.
"Two others have also said they have seen a marked change in their children’s behaviour since they had it.
"Amy has never been as good as gold, but since the day she had it she has been hyperactive," he said.
"We all want to know whether any damage has been done, if it is temporary and whether something should be done about it."
He said the family’s experience had put them off taking their children for any more injections.
Case 2
Black-outs ‘not treated seriously’
KEVIN and Nicola Hall say they are still waiting for an explanation of their daughter’s sudden illness.
In the weeks after her vaccination at Norton Hill School in Midsomer Norton, near Bath, Rebecca suffered ten blackouts, severe headaches and other symptoms.
The 12-year-old collapsed two hours after receiving her injection at the 1,250-pupil school on March 29.
She was taken to Royal United hospital and kept under observation for a night.
But since then she has collapsed at school on two other occasions and reported to the nurse seven times with headaches, dizziness and weakness.
She has also been sent home from school ten times and advised not to take part in PE lessons after collapsing on the playing field twice.
Mr Hall said he wanted to know if she had suffered any lasting damage.
"Before she had the vaccination she was fit and healthy but the doctor and paediatrician are treating it as if it is a migraine and giving her tablets," he said.
"She has not had a history of migraines and there is no history of it in the family and from what we know her symptoms are not even the same.
"I don’t feel her case has been treated seriously. We certainly want the health authorities to be more aware of the side effects that some people are having.
"I am not in favour of the immunization programme being stopped but we don’t want these side effects being treated as if is just a migraine."

This is NOT Normal Childhood!

Image result for crying baby images

Parents are saying,
"My child does not have any appetite"
"My child is refusing milk; both breast and cow's milk"
"My child vomits if given milk"
"My child vomits if given food"
"My child is always suffering from colds"
"My child is not growing properly"
"My child is obese though his appetite is weak"
"My child is always asking for food, yet eats very little"
"Fever at the slightest opportunity"
"Very hyper, I cannot control my child"
"My child is unreasonable, obstinate and headstrong."
"My child is always crying for absolutely no reason."
"My child is listless, does not have any energy"
"Always suffering from ear infections and sinus"
"My child is interested only in sugar and throws tantrums if he is not given sugary drinks every day."
"My child will not eat anything except junk food."
Doctors are saying;
"All of these are normal in childhood"
Autism, cancers, obesity, paralysis, tuberculosis, neurological disorders, depression, hyperactivity, attention deficit, tantrums.
This is NOT normal childhood.

54% of American Kids Have A Diagnosed Chronic Illness
by Michael Suede • August 29, 2017

Here’s the stats breakdown.  Pretty shocking stats.
Beth Lambert discusses the state of chronic illness among children in America today. Some researchers are projecting that autism will impact 1 in 2 kids, 80% of boys, by 2025.  If we go by more modest models looking at the 13% growth rate of autism and projecting it forward, you still end up with 1 in 4 children by 2033.
Lambert notes that autism effects boys 4 to 1 over girls, which leads her to wonder how many boys will be left that don’t have autism or a neuro-behavioral disorder to carry on our society.
Lambert suggests inflammatory diets as being the link that’s causing the rise in all of these chronic childhood illnesses.  Animal products are the primary driver of inflammation in our western diets.
Be sure to check out Dr. Michael Kalper, Dr. Garth Davis, and Dr. Michael Greger’s lectures as well.

Results: We found a diverse group of children who suffered with serious, multiple chronic conditions, and who accessed comprehensive, multidisciplinary care. Most children had neuromuscular conditions (54%), cardiovascular conditions (46%), and cancer (30%). A majority (56%) had multiple CCCs. Children with CCCs received comprehensive care including hospital inpatient (67%), primary (82%), ancillary (87%), and other acute care services (83%).
According to the U.S. Surgeon General, about 20% of American children suffer from a diagnosable mental illness during a given year. Further, nearly 5 million American children and adolescents suffer from a serious mental illness (one that significantly interferes with their day-to-day life).
Which Mental Illnesses Are Most Common in Children?
Children can suffer from the following mental illnesses:
  • Anxiety disorders: Children with anxiety disorders respond to certain things or situations with fear and dread, as well as with physical signs of anxiety (nervousness), such as a rapid heartbeat and sweating.
  • Disruptive behavior disorders:Children with these disorders tend to defy rules and often are disruptive in structured environments, such as school.
  • Eating disorders: Eating disordersinvolve intense emotions and attitudes, as well as unusual behaviors, associated with weight and/or food.
  • Elimination disorders: These disorders affect behavior related to the elimination of body wastes (feces and urine).
  • Affective (mood) disorders: These disorders, including depression, involve persistent feelings of sadness and/or rapidly changing moods.
  • Schizophrenia This is a serious disorder that involves distorted perceptions and thoughts.
  • Tic disorders : These disorders cause a person to perform repeated, sudden, involuntary and often meaningless movements and sounds, called tics.
  • ADHD (attention deficit hyperactivity disorder): Children with this disorder are hyperactive and have trouble controlling their impulses and paying attention. ADHD is the most commonly diagnosed mental disorder in children.

Are you aware of animal cells in vaccines?

Vaccine Animal Cells: Bird, Pig, Cow, Dog, Monkey, Mouse, Worm & Insect DNA Used in Vaccines

Vaccine animal cells are widely used by Big Pharma in the making of their concoctions. Bird, pig, cow, dog, monkey, mouse, worm & insect DNA can all be found in various vaccines.

Vaccine animal cells

are a disturbing but frequently overlooked aspect of the whole vaccination issue. Fortunately, there has been a wide-growing awareness of the many toxic ingredients and adjuvants used in vaccines (see here for a list of the top 10). While people rightly object to substances such as mercury, MSG, aluminum and formaldehyde, how much attention has been placed upon vaccine animal cells? Did you even know that many vaccines use animal DNA to grow and culture the bacterium or virus being vaccinated against? Today’s vaccines have been made from a variety of animal cells, including but not limited to DNA from birds (chicken cells are very common), cows, pigs, dogs, monkeys, worms and other insects. This information alone makes many people shudder. The vaccine packaging label often states that these cells are there only in trace amounts, but they are present nonetheless. What are the implications of this? How many people are having reactions due to taking a vaccine with cells of an animal to which they are already allergic?

Bird Cells

Chickens and their embryos have long been used in the production of vaccines. Thomas Rivers and others at the Rockefeller Institute for Medical Research (see here for Rockefeller influence on Western medicine and Big Pharma) popularized the method in the 1920s and 1930s. Numerous vaccines use chicken DNA such as the influenza (flu) vaccine, the MMR vaccine, the rabies vaccine and the yellow fever vaccine.

Pig Cells

Next up is pig DNA. Zoster (Shingles – Zostavax) contains “hydrolyzed porcine gelatin”, while the rotavirus (Rotarix and RotaTeq) vaccines contain “porcine circovirus type 1 (PCV-1)”.

Vaccine animal cells include fetal cow serum (cow blood), harvested from abattoirs like this one pictured above.

Cow Cells

A large number of vaccines (e.g. the adenovirus vaccine, the MMR vaccine, the rotavirus vaccine and the varicella [chickenpox] vaccine) are made from fetal bovine serum, i.e. cow blood. The cow blood serum is used as a substrate or nutrient broth for viruses to grow in cells. Anyone with any feeling at all for animals is going to shudder at how this cow blood is collected. The Humane Research Australia site describes the serum harvesting process like this:
“After slaughter and bleeding of the cow at an abattoir, the mother’s uterus containing the calf fetus is removed during the evisceration process (removal of the mother’s internal organs) and transferred to the blood collection room. A needle is then inserted between the fetus’s ribs directly into its heart and the blood is vacuumed into a sterile collection bag. This process is aimed at minimizing the risk of contamination of the serum with micro-organisms from the fetus and its environment. Only fetuses over the age of three months are used otherwise the heart is considered too small to puncture.
Once collected, the blood is allowed to clot at room temperature and the serum separated through a process known as refrigerated centrifugation.”
This goes to show that concerns about vaccine animal cells don’t have to be limited to concern about your own health or the health of your family, but rather wider issues such as animal welfare. Do you really want to be participating in a manufacturer-consumer chain with end products made like this?

Dog Cells

Hold on, because this list of vaccine animal cells is going to get more gross and disgusting as we progress. Since many people eat eggs, pork, diary and steak, perhaps the thought of injecting yourself with chicken embryos, porcine cells and cow blood isn’t that bad (for some). But what about dog DNA? Where do you draw the line? In late 2012, the FDA approved the seasonal influenza vaccine, Flucelvax, manufactured by Novartis. Flucelvax is mass-produced using the Madin Darby Canine Kidney (MDCK) cell line as a vaccine substrate. MDCK are kidney cells from untested dogs, originally derived from a female cocker spaniel in 1958.

Vaccine animal cells also include those from the African Green Monkey, pictured here.

Monkey Cells

From dog to monkey … while dog cells in vaccines are a relatively new concoction, monkey cells have been around awhile, at least since the days of the polio vaccine when Sabin and Salk were engaged in a great race to see who could produce a better polio vaccine. From my point of view, they both failed in the end, since many became ill from the polio vaccines (some of which were infected with SV40 or Simian Virus 40, a cancer-causing monkey virus – see the conclusion of this article).
Natural News recently highlighted how the ACAM2000 smallpox vaccine is grown and cultured in African Green Monkey kidney (vero) cells. The vaccine insert label contained the following warning:
Vaccine WARNINGS related to the vaccine using African Green Monkey kidney cells
Not surprisingly, this vaccine is known to cause extremely serious and even deadly side effects at a shockingly high rate. Here’s the WARNING box from the vaccine insert sheet, linked above:
See full prescribing information for complete boxed warning
Myocarditis and pericarditis (suspect cases observed at a rate of 5.7 per 1000 primary vaccinees (95% CI: 1.9-13.3)), encephalitis, encephalomyelitis, encephalopathy, progressive vaccinia, generalized vaccinia, severe vaccinial skin infections, erythema multiforme major (including STEVENS-JOHNSON SYNDROME), eczema vaccinatum resulting in permanent sequelae or death, ocular complications, blindness and fetal death, have occurred following either primary vaccination or revaccination with live vaccinia virus smallpox vaccines. These risks are increased in certain individuals and may result in severe disability, permanent neurological sequelae and/or death [see Warnings and Precautions (5)].”
The aforementioned page on the CDC website states that other vaccines contain African Green Monkey kidney cells, including the polio vaccine (IPOL by Sanofi Pasteur), DTaP-IPV (Kinrix) and DTaP-HepB-IPV (Pediarix).

Mouse DNA is part of the many types of vaccine animal cells.

Mouse Cells

From primates we now go on to smaller mammals: mice. Vaccine animal cells include rodent cells. Vaccines such as the Japanese encephalitis (JE) vaccine and the rabies vaccine used to contain mouse brain cells. They have been used in many Asian countries. Other vaccines that either include or used to include mouse DNA are the inactivated mouse brain vaccine (IMB), suckling mouse brain vaccine (SMB), JE virus vaccine (Beijing-1) and acute disseminated encephalomyelitis vaccine (ADEM).

Some vaccine animal cells are those derived from the armyworm, pictured above.

Worm Cells

Flucelvax is a great vaccine to take if you want a full dose of vaccine animal cells. Not only does it contain dog DNA, but also worm DNA! That’s right: the Flucelvax flu shot has worm ovary cells from the armyworm spodoptera frugiperda. The FDA approved the Flublok vaccine in 2013. The worm cells are from an insect cell line called “expresSF+®”. The vaccine package insert for Flublok also states it may contain other viruses like the baculovirus:
“Each 0.5 mL dose of Flublok may also contain residual amounts of baculovirus and host cell proteins (≤ 28.5 mcg), baculovirus and cellular DNA (≤ 10 ng) …”

Insect Cells

Finally, to top it all off, we have more insect cell lines being used in vaccines. In 2007, a company known as Protein Sciences Corporation developed a patented influenza vaccine produced from caterpillar eggs:
“A flu vaccine made in insect cells instead of chicken eggs is safe and at least as effective as standard shots, a study reports. Scientists say the experimental vaccine marks an advance toward the development of a faster method of making flu vaccine.
In today’s Journal of the American Medical Association, John Treanor of the University of Rochester, N.Y., tested an experimental vaccine made by using an insect virus, baculovirus, to produce virus proteins in cells taken from caterpillars.”

Conclusion: Is It Really Good for Human Health to Inject Ourselves with Bacteria- and Virus-Containing Animal Cells?

The question of whether it’s truly good for the health for humans to take infected animal cells into their bloodstreams needs to be thoroughly examined. The immune system of the human body is designed to recognize foreign substances as invaders – and kick into gear to defend the human organism against them. Are we helping or harming the body by putting animal cells (foreign DNA particles and fragments) straight into our blood? Yes, many people eat animal flesh and animal products in the form of beef, fish, chicken, dairy products and eggs, but digesting these in our stomach is a very different thing than having them directly injected into our bloodstream. Even the mainstream medical site The History of Vaccines admitted that vaccine animal cells are not ideal:
“… using animals in vaccine development – particularly live animals – is not ideal. Research animals are costly and require extensive monitoring, both to maintain their health and to ensure the continued viability of the research. They may be carrying other bacteria or viruses that could contaminate the eventual vaccine, as with polio vaccines from the mid 20th century that were made with monkey cells and eventually found to contain a monkey virus called SV40, or Simian Virus 40 …”
The article goes on to claim that the monkey virus SV-40 or SV40 (found in polio vaccines) was found to not be harmful to humans. This claim is highly dubious. As I mentioned in the article Cause of Cancer Explained? Widespread Monkey Virus SV-40 From Old Polio Vaccines Could Be One of the Factors, there may well be a connection between SV40 and cancer. The reason is that many viruses can be reactivated through stress, a toxic environment and a lowered immune system. Bernice Eddy was a bacteriologist at the NIH and was told to safety test the Salk polio vaccines in 1955. She discovered faulty batches and found that the vaccine virus wasn’t dead but was still alive and able to breed. When she tried it on her monkeys, they became paralyzed. To her credit, she then tried to delay the release of the vaccine … unsuccessfully. Afterwards, millions of Americans were injected with contaminated polio vaccines.
What do you think? Do you believe that injecting yourself with vaccine animal cells can really lead to good health? Post your comment below.
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Makia Freeman is the editor of alternative media / independent news site The Freedom Articles and senior researcher at, writing on many aspects of truth and freedom, from exposing aspects of the worldwide conspiracy to suggesting solutions for how humanity can create a new system of peace and abundance.