All vaccinated children in the Western hemisphere are carriers of what is known as MRSA (Methicillin-resistant Staphylococcus aureus/anti-biotic resistant super-bug), due to cross-infection primarily from the routine administering of the Pneumococcal (PCV) Vaccine – in combination with post vaccination anti-biotic & anti-viral drug treatment.
Alongside the sheer number of vaccines administered to young babies, it is an accumulative assault which strips children of their natural anti-biotic resistance whilst infecting them with a host of bacteria.
Please see this section for further reading on the real dangers of vaccines, we have published many articles on the subject. If you are unaware of the many dangers of vaccinations, here is yet another reason to BECOME AWARE of the many health issues they present. Including turning your immune system against itself, changing your DNA and making everyone resistant to antibiotics.
There are ways to treat these Superbugs naturally, so be sure to read the section on how to cure them. Not with more chemical tablets and vaccines, but naturally and cheaper.
With excerpts from Vaccine Resistance Movement, these findings are covered up and hidden from the public eye:
The largest superbug is known as MRSA (Methicillin-resistant Staphylococcus aureus) also known as the antibiotic resistant super-bug, due to cross-infection primarily from the routine administering of the Pneumococcal Conjugate Vaccine (PCV) Vaccine – in combination with post vaccination anti-biotic & anti-viral drug treatment, an accumulative assault which strips a child of his/her natural anti-biotic resistance whilst infecting them with a host of bacterial serotypes.
Which can leave children highly vulnerable to: Middle ear infections, high-grade seizures, Pneumonia, Myocarditis (inflammation of the heart muscle), Endocarditis (inflammation of the inner lining of the heart valves), Osteomyelitis (acute or chronic inflammatory process of the bone), Toxic Shock Syndrome (TSS), Bacteremia (presence of viable bacteria in the circulating blood) & Septicemia (blood poisoning), Meningitis (inflammation of the membranes/meninges surrounding the brain & spinal cord, usually due to the spread of an infection), and even sudden death.
The current generation have literally become unwitting hosts to a form of bacterial roulette, an ideal breeding ground for the proliferation & weaponizing of bacterial infections.
Vaccinating babies destroys their immune system
The road-map leading to most neurological & neuro-developmental disorders traces back to the earliest vaccines administered when they were babies, like HEP B, DTaP, PCV, RV, HIB, IPV, MMR. Which is a huge assault on the babies developing immune system.
As terrible as this sounds, “Timing is the key” here. A premature breach of the delicate, under-developed “electrical grid network” designed to protect the baby’s brain & nervous system (Myelin Sheath, Blood-Brain Barrier, Meninges) will leave the babies brain vulnerable for ever.
According to the CDC’s ‘Recommended Immunization Schedule for Persons Aged 0 Through 6 Years—United States (2012) by 15 months, the average child has received a whopping 25 injections including:
3 doses of Hepatitis B, Rotavirus, HIB (Haemophilus Influenzae Type b), IPV (Inactivated Polio Vaccine) & Hepatitis A, 4 doses of DPT (Diphtheria, Pertussis, Tetanus) & PCV (Pneumococcal Conjugate Vaccine), 1 dose of Varicella & Meningococcal and 2 doses of MMR (Measles, Mumps, Rubella). Natural defences? Not a chance.
Is the PCV vaccine even worse than the MMR?
It turns out the hidden dangers of the PCV Vaccine may, in fact, supersede those of the MMR series, which is terrifying, seeing as the MMR vaccine has already been proven to be a deadly vaccine.
There are a number of critical reasons as to why the PCV vaccine could be worse; chiefly timing & the extreme nature of bacterial build-up impinging on the under-developed Immune system in babies.
The PCV Vaccine, PREVNAR (Pneumococcal 7-valent Conjugate Vaccine: Diphtheria CRM197 Protein – manufactured by Pfizer/Wyeth) was introduced in 2000 as part of the standard immunization program throughout the West.
It’s later version PCV13 (Pneumococcal 13-valent Conjugate Vaccine [Diphtheria CRM197 Protein]), approved by the FDA on February 24, 2010, is typically administered to babies in 4 stages (2, 4, 6 & 12-15 months) and further given to adults 19-64 with varying chronic conditions (lung, heart, liver or kidney disease; asthma, diabetes, alcoholism/smokers, HIV/AIDS, cancer, damaged/absent spleen).
In the United States in particular, ‘Since 2000, several reports have documented the presence of MRSA infections in previously unaffected outpatient populations…a dramatic shift in the microbial flora of soft tissue infections has occurred recently in the United States.
Popovich et al. in 2008 reported data from 2000-2006 in Chicago’s Stroger Hospital/Rush University Medical Center that showed a stable rate of hospital acquired strains of MRSA infections, but a rapidly increasing rate of community acquired strains of MRSA seen in the hospital from 24% between January 2000 and June 2003 to 49% between July 2003 and December 2006.‘
According to the CDC it is ostensibly designed to project against “blood infections, pneumonia, and meningitis, mostly in young children…deafness and brain damage.”
This increase coincides precisely with the release of the first Pneumococcal (PCV) Vaccine on the market – ‘PCV7, containing the 7 most common pneumococcal serotypes causing invasive infections in children in North America was licensed in the US and recommended for routine use in infants in 2000.’
In Queensland, Eastern Australia, in 2000 to 2006, population-based surveillance of antibiotic resistance patterns of MRSA strains causing infections among inpatients demonstrated an increase from 71 to 315 cases/1 million accrued patient-days for non-MDR (i.e., resistant to at least one non-β-lactam antibiotic and susceptible to ciprofloxacin)-resistant strains.
A similar large increase was documented among outpatients during this period, from 52 to 490 cases/1 million outpatient visits, suggesting a rapid dissemination of the non-MDR MRSA strains.’
There were increasing levels of antimicrobial resistance and epidemiological changes in the hospital-associated MRSA strains isolated in this facility between 2000 and 2005.
Having the flu when vaccinated is deadly
A recent study by the Centers for Disease Control and Prevention (CDC) found that of the 36 children who died from the pandemic H1N1 from April to August (2009), six had no chronic health conditions. But all of them had a co-occurring bacterial infection. The most common co-occurring infection that causes flu-related deaths is staphylococcus aureus.
A third of the population carries it, most in their nose, or on their skin. The flu causes upper respiratory damage, which allows the staph to make its way into the lungs.’ Said Dr. Joseph Mercola
Too many antibiotics
Clearly society has reached its saturation point with the widespread over-use of antibiotics; which has given rise to the emergence of ‘multi drug resistant staphylococci’, potentially the greatest of threats to our natural immunity, in terms of its resilience in the environment & virulence in the human host. ‘
Spontaneous chromosomal mutations have also played a role in the emergence of clinically important resistance ‘…’It’s possible MRSA will become untreatable by mainstream medicine.
MRSA is treatable
Yet, we at Healing Oracle know this to not be true. MRSA and other superbugs are treatable and using natural products.
We contacted MD Simon Fermun, who said: “I find it sad and shameful that we are unable to deal with superbugs in hospitals. Indeed, it is the medical profession in general that should be held accountable for this increase in superbugs.
There are ways of dealing with MRSA and Candida Aura. You need not lose a limb, or a life if we use such things as; Ozone treatment, maggot therapy, MMS topical spray, Hydrogen Peroxide and GCMaf to repair the immune system and kill the pathogens. MMS can kill up to 99% of all known pathogens. And this is to name just a few of the natural tools we have available. By reverting to chemistry and the drug business, we are losing the war.”
Cannabis oil is also a wonderful healer and cannot be underestimated for natural treatments and cell regeneration, as we stated with the case of arthritis, cannabis has the unique power to work with the human body and to repair damage via the endocannabioid system.
GcMAF is an essential human protein our bodies naturally make to destroy cancer. All 5 billion healthy humans make their own GcMAF. A human makes 10,000 – 100,000 cancer cells a day, but your GcMAF, which has six attacks on cancer, destroys them every day.
Bacteria is able to swap Genomes to avoid detection
Bacteria that cause childhood pneumonia and meningitis have evolved to evade vaccines by swapping bits of their genome with other bacteria, according to a new study.
Vaccines that protect against these so-called pneumoccoccal infections are designed to recognise a material on the outer surface of a bacterium’s cell called polysaccharide.
Each of more than 90 kinds, or “serotypes”, of these bacteria have a different polysaccharide coating.
In 2000, a vaccine that targeted seven serotypes proved highly effective when introduced in the United States. The same formula – which also prevented transmission from children to adults – was adopted in Britain. Over time, however, the vaccine worked less well, so researchers led by Rory Bowden at the University of Oxford set out to discover why. Combining cutting-edge genetic analysis with epidemiology, which examines how disease spreads, they found that the deadly pathogens escaped detection by swapping genes with other, slightly different, bacteria. Remarkably, the exchanged genetic material came from precisely that part of the genome responsible for making the cell’s coating – the area targeted by the vaccine. The bacteria, in other words, had kept their virulence intact but changed their outward appearance.
The researchers identified several such “recombined” serotypes resistant to the vaccine, and one in particular that had spread across the US from east to west over several years. They also observed – for the first time outside a laboratory – that the bugs could swap several parts of their respective genomes at once.
“This is of particular concern, as recombination involving multiple fragments of DNA allows rapid and simultaneous exchange of key regions of the genome within the bug, potentially allowing it to quickly develop antibiotic resistance,” the researchers said.
In both the US and Britain, the original vaccine has been replaced with a new one that targets 13 rather than seven of the telltale serotypes. But the scientists caution that the bacteria will continue to morph into new forms.’
Science is creating the problem
This reformulating or “morphing” nature of the Staphylococcus aureus-type pathogen is indicative of years spent being sliced and re-spliced in top Level Bio-laboratories; while overcoming the body’s natural anti-biotic defenses through prolonged incubation in the host species – increasingly compromised generation to generation by the over-use of Prescription anti-biotics and vaccine derived heavy metal/excipient/virus & bacterium “sludge” toxicity.
Vaccinations are very rarely blamed
Whenever a child dies, in the days/weeks/months following vaccination, Medical authorities routinely obfuscate the evidence, shifting the blame AWAY from the Vaccine itself, to what is termed “comorbidities” alluding to a pre-existing medical condition, or complications inherent to that case-file.
The Vaccine Industry doesn’t want you to know that vaccines cause the very signature disease/disorder they claim to protect you against; albeit a more virulent “transforming” strain of the primary pathogen.
A virulent pathogen that is currently the most common cause of infections in hospitalized patients. S. aureus infection can involve any organ system. The success of S. aureus as a pathogen and its ability to cause such a wide range of infections are the result of its extensive virulence factors.
MRSA is a Gram-positive bacterium that is resistant to methicillin (a member of the penicillin family) and many other β-lactam antimicrobials; β-lactam antimicrobials include penicillins and cephalosporins.
The description “methicillin-resistant” was first used in 1961, based on the discovery of a human Staphyloccocus aureus infection in the United Kingdom that was resistant to methicillin.1
Since that time, MRSA has emerged as a significant problem worldwide, and the term has evolved to include resistance to additional β-lactam antimicrobials. Currently, the term MRSA is often used to describe multi-drug resistant Staphylococcus aureus.’
Invasive Pneumococcal Disease after Routine PCV in Children in England and Wales: ‘Sixty-two children died, including 4 with multiple comorbidities who died several weeks after recovering from IPD; their deaths were attributed to complications of chronic liver disease (2 children), Escherichia coli septicemia (1 child), and group A streptococcal septicemia (1 child).
The IPD-attributable case-fatality rate (CFR) was, therefore, 4.4% (58/1,332); almost one third (18/58 [31.0%]) of children who died had comorbidities.
Seven (12.1% [1 with comorbidity]) died at home; 8 (13.8% [6 with comorbidities]) died on the way to the hospital; 12 (20.7% [6 with comorbidities]) died in the emergency department; and 31 (53.5% [5 with comorbidities]) died in the intensive care unit.
One toddler, in whom Staphylococcus aureus meningitis had developed
at 7 months of age, died of pneumococcal meningitis at 13 months of age, and
IRAK-4 mutation was subsequently diagnosed at postmortem examination.
On the other hand, meningitis (aOR 6.43, 95% CI 3.36–12.3, p<0.001) and presence of comorbidities (aOR 2.70, 95% CI 1.35–5.38, p = 0.005) were significantly associated with death.‘ Emerging infectious Diseases – Shamez N. Ladhani, Mary P.E. Slack, Nick J. Andrews, Pauline A. Waight, Ray Borrow, and Elizabeth Miller 01/2013
Note: ‘a higher proportion of children with comorbidities had been previously vaccinated with >1 PCV7 dose (22/44 [50.0%] vs. 69/204 [33.8%])…‘
Post Influenza vaccinations
The routine administering of Prescription Drugs (Vancomycin & Oseltamivir aka Tamiflu) post influenza, led to serious adverse interactions, which not only hastened the critical conditions of those who sought hospital care, but may, in fact, have triggered the premature deaths of most, if not all children who succumbed to 2009’s laboratory produced “novel” strain of H1N1 (2 parts Swine Flu, 1 part Human Flu, 1 part Avian Flu).
The truth is the body is being systematically targeted & broken down from all sides, creating a perfect storm of toxicity which has derailed the inherent functionality of our natural immunity generation to generation; thereby opening the door to widespread ill health. Western medicine, however they spin its so called “progress”, continually offers the antithesis of a natural solution.
It is no longer a coincidence to suggest a correlation between “natural vs. manufactured (prescription)” anti-biotic/anti-viral breakdown in the body and“natural vs manufactured (prescription)” anti-biotic/anti-viral resistance overload proliferating in the environment.
Approximately 2 out of every 100 people carry a strain of staph that is resistant to these antibiotics. We have reached the saturation point as a species; with the continued oversight of Western Allopathic Medicine, focusing solely on treating (and thereby exacerbating) symptoms rather than seeking out and remedying the underlying cause.
‘Children with pre-existing neurologic conditions and immune compromise were at increased risk of pH1N1-associated death after PICU
Vaccines have made the flu more deadly
“There’s more risk for MRSA (methicillin-resistant Staphylococcus aureus) to become invasive in the presence of flu, or other viruses. These deaths in co-infected children are a warning sign. This is especially alarming given the rising rates of MRSA infections being carried widely among children.
It is not common in the U.S. to lose a previously healthy child to pneumonia. Unfortunately, these children had necrotizing pneumonia eating away at their tissue and killing off whole areas of the lung. They looked like immunocompromised patients in the way MRSA went through their body.
“It’s not that flu alone can’t kill – it can – but in most cases children with flu alone survived…The more antibiotics we take, the more we colonize ourselves with antibiotic-resistant organisms such as MRSA.” Said Adrienne G. Randolph, MD, Division of Critical Care Medicine at Children’s Hospital Boston
During the 2009 H1N1 influenza pandemic, many previously healthy children became critically ill, developing severe pneumonia and respiratory failure, sometimes fatal.
The largest nationwide investigation to date of influenza in critically ill children, led by Children’s Hospital Boston, found one key risk factor: Simultaneous infection with methicillin-resistant Staphylococcus aureus (MRSA) increased the risk for flu-related mortality 8-fold among previously healthy children.
Moreover, almost all of these co-infected children were rapidly treated with vancomycin, considered to be appropriate treatment for MRSA. All of the children died.
While most of the children critically ill with H1N1 had one or more chronic health conditions that increased their risk, such as asthma, neurologic disorders, or compromised immune systems, 251 children (30 percent) were previously healthy.
Among these otherwise healthy children, the only risk factor that was identified for death from influenza was a presumed diagnosis of MRSA co-infection in the lung – which increased the risk for mortality 8-fold (P<0.0001).
88 percent of the children admitted to the ICU received Tamiflu (oseltamivir) during their stay, but only 6 percent had received it prior to hospital admission…The study also found that most of the MRSA co-infected children who died had received vancomycin promptly at or before ICU admission.’ Children’s Hospital, Boston
88 percent of the children admitted to the ICU received Tamiflu (oseltamivir) during their stay
The dangers of Tamiflu
The manufacturing process for oseltamivir (Tamiflu) includes other complicating factors, such as the potentially dangerous use of sodium azide, a highly reactive chemical (also used to make automobile air bags inflate). Many companies, including Roche, contract out that step in the production process.‘ William H. Frist, M.D., Senate Majority Leader/United States Senate
Tamiflu is under examination
Developed to treat swine flu, TamifluSideEffects: ‘Allergic reactions sometimes leading to shock, Asthma, Bronchitis, Chest infection, Conjunctivitis, Dermatitis, Diarrhoea, Difficulty sleeping, Dizziness, Ear infection, Ear problems, Erythema multiforme, Headache, Hepatitis, Indigestion, Liver problems, Lymphadenopathy, Nausea, Nose bleed, Rash or rashes, Runny nose, Sinusitis, Stevens Johnson syndrome, Urticaria, Vomiting.
‘A teenage girl left disabled by the swine flu treatment Tamiflu did not even have the virus, it was revealed today. Samantha Millard, 19, became critically ill after suffering a severe allergic reaction to the tablets, which she took on the advice of the controversial NHS helpline.
Within 72 hours of taking three pills, doctors put her on life support.’
Vancomycin is also under examination: ‘Treatment failures of vancomycin in patients with MRSA infections have been reported despite in vitro susceptibility. These failures have led to the utilization of vancomycin doses higher than those approved by the FDA. Higher doses are being administered to achieve goal vancomycin trough concentrations of 10-20 μg/mL recommended by several Infectious Diseases Society of America (IDSA) endorsed clinical practice guidelines.
Three published studies have suggested that there is a significant association between increased vancomycin and the destruction of kidney cells
Almost all of these co-infected children were rapidly treated with vancomycin, considered to be appropriate treatment for MRSA (methicillin-resistant Staphylococcus aureus).’
Note: ‘88 percent of the children admitted to the ICU received Tamiflu (oseltamivir) during their stay…’
Note: ‘…detection of an increased number of A(H1N1) viruses with resistance to oseltamivir (Tamiflu)…high-level resistance to oseltamivir in N1-containing influenza viruses‘
Note: ‘Three published studies have suggested that there is a significant association between increased vancomycin through concentrations and nephrotoxicity (the quality of being destructive to kidney cells).’
Note: ‘Independent risk factors for BSI (blood stream infection) among colonized patients were admission from a long-term care facility, infection of an additional body site, and exposure to vancomycin. Independent risk factors for death were immunosuppression and VRE BSI.’
Note: ‘The 66 patients with vancomycin MICs of ≥1.5 mg/liter had a 2.4-fold increase in failure compared to patients with MICs (Minimal Inhibitory Concentration – the lowest concentration that is able to inhibit growth of the bacteria) of ≤1.0 mg/liter…a vancomycin MIC of ≥1.5 mg/liter was independently associated with failure.’
Note: ‘37% mortality was attributed to bacteremia due to vancomycin-resistant enterococci.’
Superbug resistance is escalating within the clinical setting and community at large. Innovative antibiotic strategies are still lacking within the pharmaceutical industry to keep pace with the growing resistance, with a glaring absence of any novel class of antibacterial drug in the United States for decades.
Most new antibiotics are chemical modifications of existing drugs and are quickly outsmarted by the bacteria in the environment. Clinicians are challenged by some strains of bacteria which are resistant to essentially all available antimicrobial agents.
The dangers of Prevnar
‘”I had a baby that was perfectly healthy, happy, okay until she got a shot, until she got her vaccine. Thirty, forty hours later, she’s in the hospital having seizures that they can’t stop. You’re not going to tell me it’s not related to the vaccine somehow. It’s hard, it’s very hard. I’m not angry, I’m mad. I guess I’m a little bitter about losing a child. I’m not a little… I’m a lot bitter.”
Said Ray Graves, father of baby Hayley – who slipped in and out of a coma for 45 days after receiving Prevnar7 (Pneumococcal 7-valent Conjugate Vaccine/Diphtheria CRM197 Protein: Prevnar®), until she died in September, 2001. Tremors shook her little body almost the entire time.
According to Dr. Erdem Cantekin, a medical researcher, one of the leading US experts on earaches, not only are federal regulators issuing bad information, they are also not revealing some of Prevnar’s dangerous side effects.
Cantekin says a study by the vaccine’s manufacturer shows seizures happened four times more often in infants given vaccines with Prevnar than children in a control group. “It [Prevnar] is an ineffective and toxic vaccine. I think the FDA approval of this vaccine is an act of irresponsibility. I think the FDA is following their regular course. They ignore the warnings until many people die, and then it becomes such a public outrage and public problem, they say, ‘Oops, we will take this thing off the market.‘”
Japan who have a different approach to mandating vaccines, have a higher life expectancy rate than the USA and has exercised a unilateral ban on Prevnar following the sudden deaths of several children attributed to the shot, ‘Japan’s health ministry said Monday that the children, ranging in age from six months to two years old, died after receiving one of the vaccines or a combination of them. The ministry said the suspension will be in place pending the outcome of an investigation into the deaths; results could be released Tuesday. The deaths were reported between March 2 and 4 (2011)
Based on data acquired from the ongoing Vaccine Adverse Events Reporting System (VAERS) Prevnar has been directly linked to ‘28,317 adverse reactions since it was approved in 2000, including 558 deaths, 555 life threatening conditions, 238 permanent disabilities, 2,584 hospitalisations, 101 prolonged hospitalisations, 8,166 emergency room cases and 16,155 “not serious”’.
Long-term adverse reactions to PCV Vaccine include:
- An increase in the incidence of pneumonia caused
by bacteria NOT covered by these vaccines
2. An increase in middle-ear infections due to bacteria not linked to pneumonia
3. The emergence of “superbugs” (MRSA) that are resistant to vaccines.
Dutch babies die after PCV vaccine: ‘The PCV vaccine, which is supposed to protect infants and young children against pneumonia, was recently linked to three unexplained infant deaths in the Netherlands. On 5 November 2009, the Dutch government announced that three babies died within two weeks – between one and 11 days – of receiving the vaccine. This is the Prevnar pneumonia conjugate vaccine or PCV, commonly called PCV vaccine, made by drug giant Pfizer.
The response of the Dutch government is hard to comprehend and to accept. Initial press reports sait it banned ONE BATCH of the vaccine but later reports clarified that Pfizer “quarantined” the batch, which contained about 110,000 doses. One would expect that when something as serious as this happens, the health authorities concerned would, at the very least, suspend its vaccination programme pending the results of further investigations. But no. The vaccination programme continued with other batches of the same PCV vaccine.
Source: Vaccine resistance Movement
Love and Light
Amanda Mary Jewell and The Healing Oracle team
Love and Light
The Healing Oracle Team
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