Wednesday, November 29, 2017

Cancer Patients Lack History of Common Childhood Illnesses

Lack of history of fever, cold, common childhood illnesses observed in cancer patients,
Clinical oncologists repeatedly report that cancer patients stress in their history that they were never ill before the onset of cancer. As a result of this observation, a number of epidemiological studies have been conducted. In 1894, Laurence [42] acknowledged the fact that cancer patients have a ‘... remarkable disease-free history ...’. In 1910, Schmidt [43] confirmed these findings in observing ‘afebrile (missing fever) diathesis (constitution)’ in the case histories of 241 cancer patients. Later, in 1934 and 1935, Engel [44, 45] observed a similar finding when comparing 300 cancer patients with 300 patients not suffering from cancer. Individuals who had never experienced a febrile infectious disease were 2.5–46.2 times more likely to have developed cancer than those who had had febrile infections. In 1936, Sinek [46] reported similar results for 232 cancer patients and 2,444 controls.
In a study of 300 women with ovarian cancer, Newhouse et al. [48] correlated sociological factors and found fewer marriages and lower incidences of mumps, measles or rubella in the cancer group compared to an age-matched control group. Remy et al. [49] found an increased risk for cancer among patients who had no [odds ratio (OR) = 2.6] history of former infectious organ diseases, no history of common colds (OR = 5.7) and no history of fever (OR = 15.1).
[Source: http://www.samueliinstitute.org/File%20Library/Knowledge%20Center/Publications/meuroimmun mod.pdf ]

JE Vaccine Drive: Why in 13 districts of Odisha?

JE Vaccine Drive in 13 Districts of Odisha:

Why 13 districts? JE has been reported from only 4 districts in Odisha. There are other controversies also. Not all cases of encephalitis carry the JE virus. Other sources of encephalitis (more common than JE) are metabolic syndrome, scrub typhus, west nile virus, bacterial infection, parasites, other infectious diseases, malnourishment, pesticide poisoning, and vaccines themselves. What is being done about the other cases? The vaccine contains protamine sulfate, a compound known to cause serious allergic reactions in some people. Recently three deaths have been reported in Myanmar after this vaccine. In India also deaths and severe reactions requiring hospitalization has been reported from Bihar. Is there any screening being done? Will parents be informed about risks and their informed consent taken?

LINKS: Girl, 10, Dies After Being Administered Encephalitis Vaccine
https://www.irrawaddy.com/news/burma/girl-10-dies-administered-encephalitis-vaccine.html

Two children die in Bihar after being administered vaccine against Japanese encephalitis
http://www.hindustantimes.com/india-news/two-children-die-in-bihar-after-being-administered-vaccine-against-japanese-encephalitis-measles/story-a3pFN3Q6XQP1QSYGSuSHeN.html

Two more children in Ayeyawady region were found dead in few days after being vaccinated.A post mortem showed that acute viral infection and damage to gastrointestinal tract heart and kidney caused the death of the two children, according to the release of the ministry.
http://news.xinhuanet.com/english/2017-11/25/c_136779091.htm

Five children who died from Encephalitis vaccine came from Pinlaung township in Shan State, Tharbaung and Pathein townships in Ayeyarwady Region, Chanmyae Tharsi township in Mandalay Region and Myoethit township in Magwe Region.
https://www.mmtimes.com/news/deaths-five-children-not-related-encephalitis-vaccine-say-doctors.html


Encephalitis after vaccines:
Post-vaccination Acute disseminated encephalomyelitis ADEM has been associated with several vaccines such as rabies, diphtheria–tetanus–polio,
smallpox, measles, mumps, rubella, Japanese B encephalitis, pertussis, influenza, hepatitis B, and the Hog vaccine.
http://home.smh.com/sections/services-procedures/medlib/Pandemic/Pan_geriatrics/PanGer_73_Huynh_050309.pdf

Vaccine Failure:
In fact, out of the 12 people who were detected to be infected by Japanese encephalitis in Bhogamukh, 11 had been vaccinated. And they are not the only ones.Almost 28% of people in the state who have been infected by Japanese encephalitis had been vaccinated, said Dr Parashee Choudhury, senior medical and health officer at the state’s Infectious Disease Surveillance Program. “There is definitely a problem there too. We need more research to say what exactly is wrong.”
https://scroll.in/pulse/845647/japanese-encephalitis-continues-to-kill-in-assam-despite-immunisation-against-the-virus

Side Effects of JE Vaccine:
Nervous system side effects have included encephalitis, encephalopathy, seizures, peripheral neuropathy, transverse myelitis, cranial nerve paresis, cerebellar ataxia, behavior disorder, acute disseminated encephalomyelitis, and Bell's palsy.
https://www.drugs.com/sfx/japanese-encephalitis-virus-vaccine-nakayama-side-effects.html

Autism: Cascading effect of vaccine damage

Vaccines do not cause "autism"!!

Gina Zakharin

🚫Autism is a behavioral diagnosis. In order to receive the diagnosis of “Autism” a child must exhibit a certain number of behaviors over a certain time frame. If he or she does not do so, the diagnosis of “autism” is not warranted.
There is no blood test for “autism.”
“Autism” can’t be confirmed or “ruled-out” by laboratory analysis. It’s strictly a behavioral diagnosis.
Therefore, anything that causes physiological damage cannot directly “cause” autism.
Ergo… vaccines cannot “cause autism.”
VACCINES CAUSE OTHER STUFF
Vaccines cause encephalitis.
Vaccines cause seizures.
Vaccines cause immune system deficiencies.
Vaccines cause gastrointestinal problems.
Encephalitis causes mood swings.
Encephalitis causes extreme pain.
Encephalitis causes inattention and impulsivity.
Encephalitis causes aggression.
Encephalitis causes balance problems and difficulty relating to one’s environment.
Seizures cause mood swings.
Seizures cause inattention and impulsivity.
Seizures cause alterations in conciousness.
Immune system deficiencies cause children to have more frequent bacterial infections, such as ear infections, upper respiratory infections (URIs), sinusutis, and strep infections.
Immune system deficiencies cause children to have more frequent viral infections, such as stomatitis, “fevers of unknown origin,” “viral rashes,” hives, conjunctivitis, and gastrointestinal viruses that cause vomiting and diarrhea.
Immune system deficiencies cause children to be more vulnerable to “everything that’s going around” and to have a tougher time getting over things than their peers.
Gastrointestinal damage from vaccines causes diarrhea.
Gastrointestinal damage from vaccines causes nausea, reflux, vomiting, and the recently discovered “disease” now known as GERD (Gastro-Esophageal Reflux Disease).
Gatrointestinal damage from vaccines causes increased vulnerability to viruses and bacteria, which leads to increased administration of antibiotics, which leads to overgrowth of pathogenic yeast.
Pathogenic yeast overgrowth leads to intestinal hyperpermeability (“leaky gut syndrome”).
Pathogenic yeast overgrowth leads to constipation.
Pathogenic yeast overgrowth leads to food allergies.
Pathogenic yeast overgrowth leads to skin eruptions, “drunken, silly behavior,” inattention and impulsivity, and cravings for bread, sugar, ice cream, milk, and carbohydrates.
Vaccines CAUSE the underlying physical conditions that result in the pain, neurological damage, immune system disorders, gastrointestinal damage, and yeast overgrowth – all of which combine to produce the behavioral symptoms THAT RESULT IN THE “AUTISM” DIAGNOSIS.
Gastrointestinal damage is the most obvious result of vaccine damage.
When a previously healthy child suddenly starts having multiple episodes of watery and extremely stinky diarrhea every day, and this happens shortly after receiving vaccinations, it is notable as a “vaccine injury.” What is not so obvious is that when the child’s gut is permanently damaged, he or she is no longer able to absorb nutrients necessary to produce neurotransmitters necessary for proper brain function. So when the child develops mood swings, sleep difficulties, and learning disabilities several months later, these issues are not recognized as being related to the vaccine injury because the initial damage occurred many months earlier.
PLEASE RE-READ THE PREVIOUS PARAGRAPH.
This is why Dr. Andrew Wakefield is such a threat to the pharmaceutical industry.
Dr. Wakefield NEVER said vaccines cause autism.
Dr. Wakefield is a gastroenterologist. He saw a number of children with gastrointestinal problems who also happened to be diagnosed with autism. Dr. Wakefield reported his observations. He never claimed that the MMR “caused” autism. He merely reported that a number of children he had seen had BOTH gastrointestinal problems AND autism, and according to parental report, these issues developed within a short time of when the children received the MMR vaccine.
Again… Why is Dr. Wakefield such a threat to the pharmaceutical industry?
Hint: Not because vaccines cause autism – they don’t.
Vaccines cause gastrointestinal damage.
Gastrointestinal damage causes malabsorption of nutrients necessary for proper brain function.
Malabsorption of essential nutrients causes immune system disorders, seizures, encephalopathy, etc… and THAT’s what leads to the ultimate diagnosis of “autism.”
If Dr. Wakefield’s observations are correct, SOMEONE, SOMEWHERE will eventually draw the connection between vaccines and the domino-effect that leads to the “autism” diagnosis. From the perspective of the pharmaceutical industry, better to “nip it in the bud” now, which means discrediting Dr. Wakefield to the extent that no one will look further into the science.

HPV Vaccine Introduced in India Based on Faulty Research


Did Punjab introduce cancer vaccine based on faulty research by PGI Chandigarh?


Highlighting success of a vaccine, a research by professors at Postgraduate Institute of Medical Education and Research (PGIMER) Chandigarh gets published with allegedly incorrect data. Following this, a state government introduces the vaccine, despite the fact that it was yet to get approval of a national body that is authorised to approve it. The worst thing is that the same vaccine has been in controversy in past.
Yes, all this is happening in Punjab.
The PGIMER in Chandigarh published its research in May this year about Human Papilloma Virus (HPV) vaccine in the journal Cancer. HPV infection is a sexually-transmitted disease, much like syphilis. Based on the research, the Punjab government introduced this vaccine in the state on November 9. The vaccine was introduced in Mansa district of Punjab after the PGIMER evaluated it. However, it is not approved by the National Technical Advisory Group on Immunisation (NTAGI).
The  paper claimed that the HPV vaccine was cost-effective in India, even if it were to cost US$14 (Rs 900) for vaccinating each girl child.
The claims made in the paper have been challenged by Jacob M Puliyel from the Department of Pediatrics at St. Stephens Hospital, Delhi. He is also the member of NTAGI.
In a letter sent to the same journal, Puliyel wrote that the PGI paper has assumed 98 to 99 per cent mortality and falsely exaggerated the benefit of vaccination. The PGI researchers, according to Puliyel, used the logic that most of the cancer cases are diagnosed only at the third or fourth stage, thus, concluding that the mortality rate is quite high.
The letter points out that the authors of the PGIMER paper not only presented a faulty model, but their findings “also distort the science published by others”. The PGIMER authors claim that a paper by the Harvard School of Public Health has reported that only if the price of the vaccine is as high as $100 per dose, the cost per DALY (disability-adjusted life year) averted generally exceeds the cost-effectiveness threshold of the respective countries.”
However, an article published in Harvard College Global Health Review claimed that the vaccine is not cost-effective if it costs more than $3.30 per child, as pointed out by Puliyel in his letter.
It should be noted that this is the vaccine that was associated with deaths of tribal girls in Andhra Pradesh, in a clinical trial performed without their consent by PATH of the Bill and Melinda Gates Foundation and Indian Council Medical Research (ICMR). The trial was funded by Merck Sharp and Dohme (MSD) and Glaxo SmithKline (GSK)—the vaccine manufacturers.
This vaccine was developed to prevent infection with some strains of HPV. However, there is no study that claims vaccine’s effectiveness in preventing cancer. It is because the disease takes decades to develop while the vaccine is barely 10 years old.
Puliyel claims that use of this vaccine in adolescents has been associated with adverse impacts. This was the reason the vaccine was withdrawn from Japan’s immunisation programme. Simultaneously, a study conducted in Thailand found that it is not cost-effective.
This vaccine in India has been under controversy when it was used in an unethical trial by PATH of the Bill and Melinda Gates Foundation. 
It remains to be seen how the PGIMER reacts to this revelation about its research paper and the arbitrary move to introduce the vaccine

Friday, November 24, 2017

Excellent: Biological Mechanism of Vaccine Injury

Biological Mechanisms of Vaccine Injury

Aluminum, it turns out, plays a critical role in our understanding of the biological mechanisms of vaccine injury. In this article, I will review the scientific evidence of four major ways that vaccines can cause harm. These are (1) Vaccine-Induced Mitopathy; (2) Vaccine-Induced Persistent Gliosis; (3) Vaccine-Induced Endoplasmic Reticulum Damage, and (4) Vaccine-Induced Autoimmunity (to appear as a separate article). My intent and purpose is not and has never been to discourage anyone from accepting vaccines, nor to provide medical advice of any kind; rather, my intent is to make a clear path toward safer routes to artificial immunization and communicate the state of scientific knowledge about mechanisms of the pathophysiology of disease caused by vaccines, and how such human pain and suffering can be mitigated.

For full article (not to be missed)
https://jameslyonsweiler.com/2017/11/23/biological-mechanisms-of-vaccine-injury/

Homeopathic Immunization: Success in india


Homeoprophylaxis in India

https://www.westonaprice.org/health-topics/homeoprophylaxis-in-india/
Medical doctors are frustrated! Their hands are tied, and they can no longer practice medicine in the way they originally intended. With the advent of electronic records and innumerable insurance company requirements, doctors’ eyes are glued to the computer screen instead of free to look their patients in the eyes. Pharmaceutical companies have overtaken public media by advertising drugs for every symptom imaginable, drugs that are often accompanied by dire side effects. What happened to “First, do no harm,” and what’s happened to modern medicine?
Actually, one nontoxic and inexpensive form of medicine is alive and well. Homeoprophylaxis, also known as HP, is a safe and effective form of immune education to protect from infectious disease. In countries such as India, where HP is sanctioned by the government, doctors are able to administer HP openly and achieve outstanding results. Homeoprophylaxis costs less than pennies per person due to the fact that very little source material can produce enough HP for thousands, if not millions, of people.
HOW HOMEOPROPHYLAXIS WORKS
Homeopathic practitioners use HP in the context of both short-term prevention during epidemic disease outbreaks as well as long-term prevention of contagious infectious diseases. Samuel Hahnemann, MD, the founder of homeopathy and the very first to use homeoprophylaxis, viewed epidemics as cases of disease that “attack many people and present with very similar suffering from the same causes.”1 In epidemic situations, homeopaths often apply a principle called genus epidemicus(GE) when the epidemic has a similar and characteristic nature in multiple patients. The GE—a homeopathic medicine individually selected for a particular outbreak of an epidemic2—addresses the common symptoms of the disease.
In the case of scarlet fever (also known as scarlatina), for instance, the common symptoms might include fever, red rash and headache. Hahnemann used HP very successfully during a 1799 epidemic of scarlatina.2,3 Homeopathic Belladonna either prevented the disease altogether or, if contracted, reduced the severity significantly and prevented complications, easing recovery and alleviating any post-epidemic symptoms. Homeopathic Belladonna proved so effective that the King of Prussia mandated its use to curtail or alleviate subsequent outbreaks of scarlet fever.
A second method of achieving prophylaxis is through the use of homeopathic “nosodes” of the targeted disease. Nosodes are made in the same manner as all homeopathic medicines. Beginning with a source material—either plant, animal, mineral or disease itself in the case of nosodes—serial dilution and succussion (vigorous shaking) is applied until no molecules of the original substance remain. A dilution of 1:99 repeated twelve times results in a solution devoid of any molecules. This is labeled as 12C, referring to the potency. A high potency such as 10M repeats the dilution and succussion process ten thousand times.
HOMEOPROPHYLAXIS IN INDIA
India has a population of 1.3 billion and is governed under a parliamentary system. There are twenty-nine states and seven union territories. Homeopathy in India is under the control of the Ministry of Ayurveda, Yoga and Naturopathy, Unani, Siddha and Homeopathy (AYUSH).4 In addition, the Central Council for Research in Homeopathy (CCRH) functions as an autonomous organization within India’s government.5 The CCRH oversees standardization, clinical research and trials, training of homeopaths and public awareness.
In response to the persistence of infectious disease as a major problem, India has employed HP effectively for cholera, the H1N1 influenza virus (“swine flu”), conjunctivitis, chickenpox and mosquito-borne viral diseases such as Japanese encephalitis, dengue fever and chikungunya. Researchers at the Government Homoeopathic Medical College in Thiruvananthapuram (the capital of the state of Kerala) surveyed families during threatened dengue and chikungunya epidemics from 2003–2006 to assess the protection provided by HP.1 Of one thousand and five families surveyed in 2003, almost nine in ten took HP for prevention of dengue; of those taking HP, only 14 percent (123/869) went on to contract dengue. In a follow-up study in 2006 of the prophylactic efficacy of HP for chikungunya, the college found a comparable 82 percent efficacy.
The state of Kerala also has used HP to great effect in Alappuzha, an area full of backwaters and coconut lagoons. Though beautiful, living conditions in this area are difficult due to poor sanitation, low socioeconomic status, lack of education, limited health awareness and poor infrastructure. Epidemics can take hold and flourish due to inadequate health care facilities. Narrow canals through mangrove swamps are the roadways, so in 2013 the government started a floating homeopathic dispensary.6 This boat provides free treatment, HP and health education. The program has been such a success that two more boats were launched in 2014 and 2015!
As another example of HP’s acceptance in India, in 2016, in direct response to two cases of swine flu in Hyderabad in the state of Andhra Pradesh, India’s Homoeo Times published the following news statement:
The state government has…directed “all the people to take homoeopathy medicines in order to avoid the attack of swine flu.” The medicine is available for free at all dispensaries. The patients who already have swine flu should take homoeopathy medicines under prescription.7
FURTHER HP SUCCESS IN KERALA
Worldwide Choice is an organization that educates medical providers about HP and offers programs to families.8 In October, 2016, Worldwide Choice conducted a three-day conference in St. Petersburg, Florida, entitled “Homeoprophylaxis: The Evidence-Based Choice.” Two Indian doctors from the states of Kerala and Andhra Pradesh presented some quite remarkable information, which deserves sharing with the Weston A. Price Foundation community and beyond.
The first speaker, Dr. Mohammed Rafeeque, is a medical officer in the Department of Homeopathy for the state of Kerala. Dr. Rafeeque reported on HP as an alternative to vaccination for individuals in India. Dr. Rafeeque also discussed the need for stronger international support for the medical science of homeopathy, including more funding for research on HP, as well as standardization of methods to assess and compare HP results between countries.
Dr. Rafeeque noted that allopathic practitioners often dismiss homeopathy and HP as “untested” because of allopathic medicine’s single-minded reliance on double-blind placebo-controlled studies. However, scientific conclusions are strongest when they evaluate the totality of studies, draw on a variety of research methods, agree on established methodology, show strong effects and publish complete findings. Over the past two hundred years, homeopathy and HP have satisfied all of these requirements, including but not limited to conducting randomized controlled trials.
Questions about HP also have arisen within the homeopathic community itself. For example, classical homeopaths who interpret Hahnemann’s directives in a dogmatic manner may prefer to wait until an epidemic fully breaks out before undertaking homeopathic treatment. The rationale for this approach is that it takes time to gather evidence and determine which remedies will be most effective for a given epidemic. However, significant loss of life may occur during the interim, even though this approach may ultimately prove clinically effective. This is why Hahnemann successfully used homeopathic Belladonna to forestall scarlet fever outbreaks.
Some homeopaths also have expressed concern about administering high potencies homeoprophylactically, fearing “aggravations” or disruptions of the individual’s vital force, but this has not been observed in populations that regularly use HP. Dr. Isaac Golden, a leading expert on HP based in Australia, conducted a fifteen-year study on the safety and effectiveness of HP for prevention of childhood diseases.9 When administering a high 10M potency to healthy children, Dr. Golden detected aggravations in less than 2 percent of children. In fact, high potencies such as 10M are well suited for educating the immune system to recognize the disease in nature and repel it or mount an appropriate immune response.
In Kerala, Dr. Rafeeque was most recently charged with distributing HP to over five thousand people for prevention of chickenpox during a 2016 outbreak. The genus epidemicus (GE) of Eupatorium perfoliatum was also highly effective for preventing chikungunya. In a group that did not receive HP, 73 percent contracted chikungunya disease, while only 17 percent did so in the HP-treated group.
Dr. Rafeeque also noted that members of Kerala’s state legislative assembly take HP for prevention of epidemics. In a blog post, Dr. Rafeeque cited the late Mr. G. Karthikeyan, honorable speaker of the assembly, who said that members of the assembly “do not want empty chairs, that is why homeopathic medicine is given to all members.”10
HP FOR JAPANESE ENCEPHALITIS
The second Indian speaker at the Worldwide Choice conference was Dr. Srinivasulu Gadugu, MD, an assistant professor in the department of organon of medicine at Government Medical College in the city of Kadapa, Andhra Pradesh. Dr. Gadugu is an esteemed clinician, researcher and teacher who has received a variety of teaching and research awards and has made numerous contributions to homeopathic research and pedagogy.
Dr. Gadugu shared valuable information about the prevention of Japanese encephalitis (JE) in Andhra Pradesh. JE is an endemic disease that primarily affects children under the age of fifteen. Globally, JE is estimated to have infected ten million children over the past sixty years.11 In India, outbreaks are widespread, with many concentrated in the southern part of the country. Although less than one percent of individuals infected with JE virus develop clinical illness,12 up to thirty percent of those who do develop illness die.13 Symptoms associated with JE include headache, fever, meningeal signs, stupor, disorientation, coma, tremors, paralysis (generalized), hypertonia and loss of coordination. For patients who survive, half or more experience steady improvement while thirty to fifty percent suffer long-term neurological deficits.13
The JE virus is transmitted by Culex species mosquitoes. Water birds and pigs play a major role as amplifying hosts. Humans get infected when bitten by an infected mosquito. However, humans are “dead-end hosts,”14meaning that further spread from human to human does not take place.
Spring2017homeo
Vaccines have been available for JE since 1941, with efficacy of approximately 60 percent. Because of low production capacity and relatively high cost, the vaccines have remained out of reach for most countries. The difficulty of accessing rural areas for intervention, along with interruptions from natural catastrophes, can cause major setbacks in reaching the full population. In India, immunizing one hundred and sixty million people with vaccines in twelve territories would cost more than four hundred and sixty million U.S. dollars. To protect children in hyper-endemic districts would require eighteen million doses (costing fifty-two million U.S. dollars), followed by boosters every two years. Treatment with HP can be done for a few thousand dollars, not millions.
Dr. Gadugu described the trend toward homeopathic treatment of JE in Andhra Pradesh. Between 1993 and 1999, despite vaccination, recorded pediatric JE cases in the state numbered five thousand three hundred and eight, with a fatality rate of 28 percent. In 1999, the government sought the help of homeopaths in combating this epidemic. Dr. G. Sastry, a pioneer in public health, emphasized the need to address JE through homeopathy.
In the past, a GE remedy had been used, but without lasting effect. Dr. Sastry reassessed the disease from a holistic view and proceeded to address its tendency for recurrence. He advocated a unique way of prescribing a plant remedy, followed by a mineral remedy, followed by a disease nosode. His recommendation was that Belladonna 200C should be given on days one, two and three; Calcarea Carbonica 200C would be given on the tenth day; and Tuberculinum 10M on the twenty-fifth day to all children in the birth-to-fifteen-year age group in the month of August every year for three consecutive years.15 The project—known as BCT—was accepted and administered to twenty million children in Andhra Pradesh in 1999.
As a result of the BCT intervention, morbidity and mortality rates associated with JE fell dramatically (Figure 1), prompting the government to acknowledge the efficacy of homeopathy. In the year 2000, three hundred and forty-three cases were reported, with seventy-two deaths (21 percent), whereas in 2001 only thirty-three cases were reported with four deaths (12 percent). The next year, there were only eighteen cases and no deaths, and no cases at all in 2003 and 2004. Dr. Gadugu concluded that HP helped to check the child mortality rate from JE.
RESEARCH ON HP
Because HP is complementary to existing health care and is inexpensive and effective, it warrants further research and application. Eager to continue to test the efficacy of homeopathic Belladonna in the prevention of JE, the Indian government awarded a research grant to the department of microbiology, virology unit, at the school of tropical medicine in Kolkata. In 2010 and 2011, Dr. Bhaswati Bandyopadhyay conducted experiments on two animal models, both of which indicated that homeopathic Belladonna can play a clear role in preventing JE.16
Subsequently, the CCRH took up the task of additional in-depth research in this area. Dr. Gadugu is currently serving as co-investigator in a collaborative governmental research project funded by the CCRH, pursuing work on “Elucidation of molecular mechanism of action of Belladonna and Belladonna-Calcarea Carbonica-Tuberculinum Bovinum (BCT) during Japanese encephalitis (JE) virus infection.”17 Dr. Gadugu emphasized the need for international research collaboration regarding homeopathic epidemic control, given that epidemics do not respect borders.
TRULY SAFE AND EFFECTIVE
India’s experiences indicate that American medical personnel would do well to consider HP as a valid intervention for contagious infectious disease. Powerful corporate interests tout conventional vaccines as the only available form of protection against existing and emerging disease threats but never discuss the chemicals, adjuvants, preservatives and foreign DNA present in all vaccines. HP, on the other hand, is a natural and inexpensive solution that holds great promise. If practitioners can open their minds to being educated about HP, they will see that HP’s safety and effectiveness have been amply demonstrated worldwide.
REFERENCES
1. Anand PR, Dinesh RS, Sreejith S, Mridula G. Guidelines for epidemic management in homoeopathy. Homeo Book, September 29, 2015.
2. Taylor W. Taking the case: on the genus epidemicus. Whole Health Now, 2001.
3. Hahnemann S, Jain B. Organon of Medicine, §100 to §102. New Delhi, India, 1842.
4. National Health Portal (NHP) India. AYUSH. http://www.nhp.gov.in/ayush_ms.
5. Central Council for Research in Homoeopathy (CCRH). http://www.ccrhindia.org/index.asp.
6. Homeo Book. World’s first floating homeopathic dispensary at Kerala. December 28, 2013.
7. Homoeo Times. AP govt directed to take homoeopathy medicines for swine flu. September 2016;13(9).
8. www.worldwidechoice.org.
9. Golden I. Homoeoprophylaxis—a fifteen-year clinical study: a statistical review of the efficacy and safety of long-term homoeoprophylaxis. Isaac Golden Publications, 2004.
10. Rafeeque M. Members of Kerala State Legislative Assembly takes homoeopathic preventive medicine. Homeopathy World Community, June 23, 2012.
11. Shipra V, Gupta RD. The use of satellite data for identifying the risk of JE disease in District Gorakhpur, Uttar Pradesh, India.
12. Centers for Disease Control and Prevention [CDC]. Japanese encephalitis: symptoms & treatment.
https://www.cdc.gov/japaneseencephalitis/symptoms/index.html.
13. World Health Organization. Japanese encephalitis. Fact sheet no. 386, December 2015.
14. CDC. Transmission of Japanese encephalitis virus. https://www.cdc.gov/japaneseencephalitis/transmission/index.html.
15. Gadugu S, Nyapati SR, Sastry GLN. An open observational study on efficacy of miasmatic prescription in the prevention of Japanese encephalitis. Homeopathy 2014;103(1):78-79.
16. Bandyopadhyay B, Das S, Sengupta M, Saha C, Raveendar C, Chakravarty R, Khurana A, Ray K. Prevention of Japanese encephalitis (JE) virus infection. In: Molecular Virology, M Adoga (Ed.), pp. 111-124. InTech, 2012.
17. Central Council for Research in Homoeopathy. http://ccrhindia.org/pdf/IMR_Collaborative.pdf.
This article appeared in Wise Traditions in Food, Farming and the Healing Arts, the quarterly magazine of the Weston A. Price Foundation, Spring 2017.

Thursday, November 23, 2017

What is health?

At a class I have been asked the question, "What is health?".
Health is not being worried about the body mind complex and functioning happily without being aware of its presence. When the society starts worrying so much about disease that it does not think twice about injecting dozens of highly toxic shots as "preventives" into its young infants, then that society is sick beyond measure, beyond reason and perhaps beyond help.
Is it so difficult to prevent disease? It is not - provided one understands what disease is. Disease has very little to do with the ubiquitous bacteria and viruses. Disease is an imbalance that starts when man goes against the laws of nature. This imbalance lets loose a change in the physical sphere, taking the shape of pain and unease, sending out the signal that things are wrong. A disturbed human mind also results in a disturbed environment, thus completing the picture. The physician's duty is to alert the patient and lead him back to the state of balance. When the mind, emotions, the body, and environment fall in line once again to the basic laws, health is restored; true healing has taken place.
Except for modern medicine all the other methods of treatment recognize this basic truth. Modern medicine blatantly ignores this and adds to the imbalance by attacking symptoms (which are but the body's way to deal with the imbalance) and thereby forcing ailments that come to the surface to go deeper into the body and mind. Its highly toxic interventions also lead to toxic syndrome that the body finds very difficult to tackle. Chronic physical and mental illnesses, and organ changes result. These get accentuated with each passing generation through epigenetics. 
Do the modern medicos not realise this? They do. Modern research increasingly points towards the deviant mind being the root of ills that plague mankind. (Read, "Cure: A Journey into the Science of Mind Over Body" by Jo Marchant) However modern medicine is not geared towards good health, it thrives on sickness. The pharma industry has to grow at the rate of 25% or more annually. This cannot be achieved unless there is a 40% rise in illness every year. To the doctor thus appears the dilemma, to heal or not to heal? It is very difficult to avoid the easy life that pharmaceutical incentives offer. It is very tough to take the right decision.
I can already hear the question coming. What about epidemics? I will ask a question in return, can you show me one epidemic that is not the result of some disturbance on a mass scale? The epidemics that have reared their heads in recent memory have come after wars, after large scale immigration that led to a disturbed psyche, squalid conditions, and malnourishment. Modern epidemics can be traced to poverty, unclean conditions, lack of nourishment, erroneous surgical procedures, injudicious interventions, and increasingly impacts of dreaded toxins that have become central to our lives.
Had these not been the prime cause, and bacteria and viruses been the sole reason for disease, mankind would have been wiped off the face of the earth. We have the body's own coping ability - the immune system being central to it - an ability that has to be improved upon and not derailed with "preventive shots". The environment must be cleansed to allow life to continue upon earth. Our attitudes towards the earth and fellow beings must change. Our respect for biodiversity must transcend our urge for toxic growth.
The patients too should now start inquiring, "Do I wish to be healed or should I go from bad to worse in the name of a false science?" The sooner this question arises the better. Besides protecting the earth, we also need to protect ourselves and regain our stature as the guardians of the earth, the children of the earth. Let us stop playing with dangerous toys and sick ideas of grandeur and go back to mother nature. The mother knows what is best for us, as Sri Ramakrishna has candidly confessed.

Use of Deceptive Statistics in the Vaccine and Pharmaceutical Literature

Flu Shots, Fosamax and Pharmaceutical Fakery

BY TRANSCEND MEMBERS, 20 November 2017
Gary G. Kohls, MD | Duty to Warn – TRANSCEND Media Service
The Common Use of Deceptive Statistics in the Vaccine and Pharmaceutical Literature
For full article:
 https://www.transcend.org/tms/2017/11/flu-shots-fosamax-and-pharmaceutical-fakery/

14 Nov 2017 – Several years ago there was a temporary media buzz generated by an October 2011 article in The Lancet Infectious Disease journal, which is a pro-vaccine, pro-pharmaceutical industry medical journal that is published in Britain. The article showed that flu vaccinations were far less effective than had been previously believed. In fact, the study suggested that the trivalent flu vaccine currently being pushed at that time approached worthlessness.
The article’s principle author was Michael Osterholm, PhD, MPH, a widely published infectious disease researcher who, prior to his current faculty position at the University of Minnesota, had served in various capacities with the CDC and the Minnesota Department of Health (MDH), including a high-profile role as the MDH’s Chief of the Acute Disease Epidemiology Section. For 15 years of that association with the MDH Osterholm served as Minnesota state epidemiologist. Osterholm has published over 300 articles and is highly respected in his field.
The Disconnect Between Real, Unbiased Science and Profit-focused Corporate Propaganda
The Lancet study, in the reports that I listened to on NPR and read about in various print media reports, was deceptively reported as showing that the trivalent flu vaccines should still be regarded as “moderately effective” for flu prevention rather than being brought into question as the minimally effective vaccine that the article suggested. What could explain the disconnect between the science and the propaganda?
Seeing no sign of a public retraction from Osterholm or his co-authors about the glaring misperceptions, I began to wonder if they were even aware that they had stooped to the depths that so many other medical, psychiatric and pharmaceutical industry researchers have gone to when their articles are published in mainstream medical journals. Misleading statistics that have appeared in medical journals are also used in drug commercials and by drug sales representatives when they try to convince us physicians to prescribe their company’s synthetic drugs.
What I am talking about is the common statistical trick of the trade called the Relative Risk Reduction [RRR], a statistic that intentionally inflates embarrassingly low or even statistically insignificant results that had been obtained from dubious research studies.
What the public deserves to be informed about, but usually doesn’t receive, is the far more meaningful Absolute/Actual Risk Reduction [ARR] numbers, which, compared to the RRR, are often so small and unconvincing that any rational thinker would regard the study as a failed one. Hence, the cunning invention of the misleading RRR. I will deal with the important mathematical differences further below.
The Deceptive Relative Risk Reduction Statistic
A lot of medical research these days is done by academic scientists that may not be clinicians. The vast majority of these researchers, estimated to represent over 80% of the medical research that is currently being done, are in the employ of the for-profit drug and medical device industries. The research articles that list them as authors are frequently written by ghost-writers who are salaried by the corporations that designed and funded the study. And what should worry everybody is the fact that the self-interested corporations have exclusive control over how the research is utilized. Whoever pays the piper, calls the tune.
The researchers involved in such studies are naturally highly motivated to help rapidly get to market the products they are working on, with the additional hope that any positive results that they can generate will increase the value of any stock holdings that may be part of their compensation package. Additional contracts with the pharmaceutical company will be more likely if negatives are not found. I hasten to add that there is nothing wrong with making money in an ethical and honest manner, but a lot of medical research intentionally overstates the positives of the products that are being marketed and minimizes, or even hides, the negatives of their new drugs, vaccines or medical devices.

Toxic Vaccine Adjuvants & Ingredients

Toxic Vaccine Adjuvants & Ingredients

http://freedom-articles.toolsforfreedom.com/toxic-vaccine-adjuvants-the-top-10/

Toxic vaccine adjuvants and ingredient are not emphasized enough in the debate over the safety of vaccines. The medical establishment, which has essentially been wed to Big Pharma ever since its inception by the Rockefellers, routinely downplays the idea that these adjuvants are quite harmful. In reality, many are known carcinogens. Western medicine also tends to makes the excuse that it is a case of “benefit vs. risk”, and that the benefit outweighs the risk – but does it really, given the ton of natural alternative remedies and the fact that these adjuvants can get stuck in your body forever? I have listed 10 of the most common toxic vaccine adjuvants and ingredients below, and after reading about each one, please consider whether you think we can accurately call vaccines “good medicine”, given that these 10 adjuvants and ingredients are being injected directly into the bloodstream (thus bypassing the digestive filters) of every vaccine patient who receives them.
You can confirm that these adjuvants and ingredients are indeed being added to vaccines by looking the official lists of the CDC (Center for Disease Control) as well as other websites like this.

Toxic Vaccine Adjuvants / Ingredients #1: Mercury (Thimerosal or Thiomersal)

Mercury, which constitutes 49.7% of thimerosal (or thiomersal), has been commonly known for a very long time to be a highly toxic agent. Mercury has always been beloved by allopathy ever since its inception; in fact, the 3 main treatments of the early allopaths of the 19th century were bloodletting, surgery and the injection of toxic heavy metals like lead and mercury to purportedly displace disease! The expression “mad as a hatter” comes from the observation that the early hat makers, who used mercury in felt to make hats, became crazy through inhaling the stuff.
Numerous studies have been done on the toxicity of mercury, with evidence it leads to infertilitygastritis (a precancerous stage of gastric cancer), neurodegenerationmitochondrial abnormalitiesnephrotic syndromeapoptosis (cell death) and autism, yet the IARC (International Agency for Research on Cancer, under the auspices of the Rockefeller-created WHO) still refuses to admit mercury can cause cancer and is leaving mercury categorized as a class 2b possible carcinogen (as opposed to class 2a probable carcinogen or class 1 definite carcinogen). The study above on cell death concluded:
Mercury (Hg) is a highly toxic metal that can exert multiple adverse effects, ultimately leading to cell death. Before causing death, the Hg enters the cells and affects diverse intracellular targets.
Since thimerosal contains about 50% mercury by weight, vaccines with a ratio of 1:10,000 (or 0.01% thimerosal) have about 50 mg/L mercury, which exceeds the 0.2 mg/L hazardous waste toxicity regulatory level for mercury. According to US state and federal hazardous waste management requirements, any vaccines with this level of thimerosal which are discarded need to be treated as hazardous waste.

Toxic Vaccine Adjuvants / Ingredients #2: Aluminum

Aluminum is another metal which, like mercury, is highly harmful for human health. Aluminum is a “light” metal rather than a heavy metal like lead and mercury, but its health effects are devastating nonetheless. As a vaccine adjuvant, aluminum is normally mixed into the vaccine as a salt, e.g. as aluminium phosphate and aluminium hydroxide.
This study specifically asked the question, “Aluminum vaccine adjuvants: are they safe?” and found they were not. Other studies have implicated aluminum in the development of impaired congitive functionneurotoxicityAlzheimer’s and autism. (It should be noted, however, that it is possible to take aluminum into the body if it is tightly bound as a molecule and not suffer any ill effects, because it will pass straight through the body and not be released. An example of this is zeolite, a matrix of aluminum silicates, which is actually a spectacular health supplement that can safely remove toxins like mercury from your body.)

Toxic Vaccine Adjuvants / Ingredients #3: Human Diploid Cells (Aborted Fetuses)

Believe it or not, fetal DNA tissue in used in vaccine cultures, disguised under the name of diploid cells. A diploid cell is simply a cell with a double set if chromosomes. These cells are human cells, derived from the tissue of babies or fetuses, some of which are definitely aborted! This has being going on for over 50 years. The article Human Fetal Links with Some Vaccines admits that “Two different strains of human diploid cell cultures made from fetuses have been used extensively for vaccine production for decades. One was developed in the United States in 1961 (called WI-38) and the other in the United Kingdom in 1966 (called MRC-5).”
Many people, religious or not, are understandably opposed to allowing themselves to be injected with the tissue of dead babies. Would you want to be injected with that? There are major ethical ramifications here, not to mention grave health issues too. A study by Dr. Deisher found a connection between the injection of human diploid cells and autism. The basis of this is that when you inject something foreign into your body, your cells will either assimilate it (whereby the foreign human DNA will be transported into nuclei and be integrated into host genome, causing phenotype change) or attack it (meaning you develop an auto-immune response, leading to the auto-immune diseases of the ASD [Autism Spectrum Disorder]). Either way, residual human fetal DNA fragments in vaccines can be one of causes of autism in children. Dr. Deisher’s study concluded:
Autistic disorder change points years are coincident with introduction of vaccines manufactured using human fetal cell lines, containing fetal and retroviral contaminants, into childhood vaccine regimens. This pattern was repeated in the US, UK, Western Australia and Denmark. Thus, rising autistic disorder prevalence is directly related to vaccines manufactured utilizing human fetal cells.
I also recommend watching Clint Richardson’s fantastic documentary “Lethal Injection” where he delves into the issue of aborted diploid cells and offers further research and analysis.

Toxic Vaccine Adjuvants / Ingredients #4: Animal Cells

Almost all vaccines need something in which to grow the culture, and that normally means animal cells. All sorts of animals are used for this, including chickens, pigs, dogs, monkeys, horses, rabbits, cows and more. All these animal cells remain in trace amounts in the vaccine, as admitted by the FDA. This means that when you allow a vaccine to be injected into your body, you are allowing animal DNA into your body, which of course are foreign protein cells. Is this really a good idea for your body? Consider that:
  • many vaccines contain egg-derived albumin, which is responsible for a lot of allergic reactions according to this study;
  • pig/swine viruses were discovered in the Rotarix vaccine which the FDA suspended in 2010;
  • the polio vaccines of the 1960s, which contained monkey cells, were contaminated with a virus known as SV40 (simian virus 40). This later was shown to cause widespread cancer.
New vaccines are now being developed which contain dog cells (e.g. Flucelvax). Additionally, albumin can be human-derived, but it’s still a problem. This study concluded side effects were grossly under-reported, and there are still have concerns over the safety of it.
Marti Oakley in an article on Activist Post entitled “Vaccines: Human and Animal DNA” points out that:
Cell lines, which can be derived from aborted human babies, can last for decades and are developed from a single type of cell.  Yet it is known that after continuous culturing these lines begin to mutate into cancer-causing agents. If these cell lines do this spontaneously in the lab, what are the chances they are doing the same thing once inside the human body where the culturing never ends? … We are being injected via vaccine with bits and pieces of other human beings; with the bits and pieces of other mammals.  Whatever the intended purpose of vaccines was initially, it is apparent that too little is either known or acknowledged regarding the potential adverse side affects from co-mingling the DNA of humans and animals and the potential for viral and bacterial cross-contaminations that can and do occur.

Toxic Vaccine Adjuvants / Ingredients #5: MSG (Monosodium Glutamate)

MSG (monosodium glutamate or sodium glutamate) is the sodium salt of the glutamic acid (glutamate), which is one of the amino acids or protein building blocks. Free glutamic acid is a neurotransmitter that your brain, nervous system, eyes, pancreas and other organs need to function and start certain processes in your body. MSG has become notorious for being a hidden ingredient in many foods which creates the illusion of protein or more food being present in what you’re eating – when they’re really not. In 1959, the FDA (Food and Drug Administration) labeled MSG as “Generally Recognized as Safe” (GRAS), yet since then it has acknowledged the existence of an “MSG Symptom Complex” which describes short-term reactions to MSG. These include numerous side effects which people experience after eating MSG, such as numbness, headaches, fatigue, disorientation and heart palpitations.
Despite its GRAS rating, the FDA commissioned a study on MSG in 1995, probably because of people complaining about “Chinese Restaurant Syndrome”. This study found that MSG Symptom Complex can involve symptoms such as:
  • Burning sensation
  • Facial pressure or tightnes
  • Chest pain or difficulty breathin
  • Headache
  • Nausea
  • Palpitation
  • Numbness
  • Tingling
  • Bronchospasm
  • Drowsiness
  • Weakness
How many people are sensitive to MSG? It has been estimated up to 40%. Dr. Russell Blaylock, a board-certified neurosurgeon and author of “Excitotoxins: The Taste that Kills”, has done considerable research on MSG. He calls it an excitotoxin, meaning it overexcites your cells to the point of damage or death, causing brain damage to varying degrees, and potentially triggering or worsening amyotrophic lateral sclerosis (ALS, Lou Gehrig’s disease), Parkinson’s, and Alzheimer’s. All three diseases can develop gradually.
Why is MSG being used in vaccines? It’s being used because it is a stabilizer that prevents or slows down oxidation or damage from light. This websiteclaims that MSG is only added to some vaccines: “Glutamate is added as a nutrient to the growth medium for MMR-II and is not in the final product in significant amounts; monosodium glutamate is added to FluMist (0.188 mg/0.2 mL dose); monosodium L-glutamate is added to ProQuad (.4mg), Zostavax (.62mg) and Varivax (.5mg); and potassium glutamate is added to RabAvert (1mg).”
Still, since MSG is a known toxin with deleterious effects on human health, why do doctors willingly inject it into people?

Toxic Vaccine Adjuvants / Ingredients #6: Formaldehyde

Formaldehyde is a foul-smelling chemical used a preservative and biocide. The IARC categorizes it as a class 1 definite carcinogen, and the National Toxicology Program concluded in this study that:
Formaldehyde is known to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in humans and supporting data on mechanisms of carcinogenesis. Formaldehyde was first listed in the Second Annual Report on Carcinogens in 1981 as reasonably anticipated to be a human carcinogen based on sufficient evidence from studies in experimental animals. Since that time, additional cancer studies in humans have been published …

Toxic Vaccine Adjuvants / Ingredients #7: Antibiotics

Antibiotics are typically used in vaccine production and manufacture. Antibiotics were once the crown jewel of Western medicine, with their ability to wipe out infectious diseases, but many have long known they are a double-edged sword. Antibiotics indiscriminately kill all the bacteria in your system, helpful or harmful. This obviously destroys the balance of bacteria in your gut, which forms the basis of your immune system. Thus, antibiotics invite all sorts of future problems and disease (unless you quickly re-establish the proper balance of bacteria, e.g. with probiotics), including fungal attacks.
I have previously written about the phenomenon of antibiotic overuse. There have been many reports in the last few years that Big Pharma is no longer investing in antibiotics, because every time they invent a new antibiotic drug, the bacteria adapt to it and change. This process is fueling the rise of superbugs. The FDA states some of the antibiotics used during vaccine manufacture include neomycin, polymyxin B, streptomycin and gentamicin. Some of these belong to the aminoglycoside class of antibiotics, which include side effects such as dizziness, nausea, renal (kidney) toxicity and ototoxicity (hearing loss).

Toxic Vaccine Adjuvants / Ingredients #8: Squalene

Squalene was an experimental toxic vaccine adjuvant added to vaccines around the time of the first Gulf War. Squalene has been implicated in GWS (Gulf War Syndrome) in this study, and the DoD (Department of Defense) conveniently “lost” (read destroyed) 700,000 immunization records, which might have told us why squalene was showing up in Gulf War veterans’ blood samples. ProjectCensored.com commented:
A military lab researcher interviewed by Insight was quoted as saying, “We have found soldiers who are not sick that do not have the antibodies, and we found soldiers who never left the United States, but who got shots (administered by the military) who are sick—and they have squalene in their systems. We found people who served overseas in various parts of the desert that are sick who have squalene. And we found people who served in the desert but were civilians who never got the shots, who are not sick and do not have squalene.”

Toxic Vaccine Adjuvants / Ingredients #9: Peanut Oil #65

Peanuts are known as a very common allergen, yet despite this, there are some vaccines which contain peanut oil. It has been used for a very long time. In fact, Dr. Lawrence Palevsky writes that it has been in use since 1960, and since Big Pharma vaccine manufacturers are not required by law to list every single ingredient used in culturing vaccines, there may be no real way to now which vaccines have traces of it. He writes:
If current vaccine package inserts do not contain the specific evidence that peanut oil, or peanut meal, is contained within the final vaccine product, it does not mean that peanut antigen is not in the final vaccine product. Vaccine manufacturers use different growth media on which to manufacture the vaccines. They do not report, and I believe are not required to report, the exact ingredients in all of the growth media. Therefore, we may not know whether peanut antigen is used in the vaccine manufacturing process just by reading through the package inserts … and, it may, or may not, have anything to do with an attempt to purposely hide the information that peanut antigen is present in vaccines.
Peanut oil is far from the only adjuvant used in vaccines which is highly allergenic. Other vaccine antigens, such as those used in Hepatitis B vaccines and the HPV (Human Papillomavirus) vaccine Gardasil, are manufactured in yeast cells. Yeast proteins have been shown to cause allergic reactions in people. Do you want this stuff in your bloodstream?

Toxic Vaccine Adjuvants / Ingredients #10: GMOs

On top of all the toxic vaccine adjuvants listed above, the GMO (Genetically Modified Organism) issue also pertains to vaccines, because vaccines are now being made with genetically engineered viruses. This goes to show that, sadly, the so-called sacred precautionary principle of science is often thrown to the wind when the potential for massive profit arises. We simply do not know what effect genetically engineered viruses will have on the human body long term. What happens when foreign DNA is inserted into the body? Does it trigger undesirable changes in human cells? Does the human body treat it as foreign and attack it? Does it combine with human DNA, and if so, is the new combined DNA an enhancement or impairment? Will it transfer to future generations? We’re clearly moving into unknown and potentially very dangerous territory by allowing this stuff to be be injected into our bodies.
This study warned of the dangers of using genetically engineered viruses in vaccines:
Genetically modified (GM) viruses and genetically engineered virus-vector vaccines possess significant unpredictability and a number of inherent harmful potential hazards … Important questions concerning effects on nontargeted individuals within the same species or other species remain unknown. Horizontal transfer of genes, though lacking supportive experimental or epidemiological investigations, is well established. New hybrid virus progenies resulting from genetic recombination between genetically engineered vaccine viruses and their naturally occurring relatives may possess totally unpredictable characteristics with regard to host preferences and disease-causing potentials. Furthermore, when genetically modified or engineered virus particles break down in the environment, their nuclei acids are released … There is inadequate knowledge to define either the probability of unintended events or the consequences of genetic modifications.

Other Toxic Vaccine Adjuvants and Ingtedients

In addition the above top 10 toxic vaccine adjuvants and ingredients, it would also be wise to take note of many other possible vaccine fillers, which include:
• acetone (solvent used in fingernail polish remover)
• ammonium sulfate
• amphotericin B
• betapropiolactone
• formalin
• gelatin
• glycerol
• hydrolized gelatin
• phenol red indicator
• phenoxyethanol (antifreeze)
• potassium diphosphate
• potassium monophosphate
• polymyxin B
• polysorbate 20
• polysorbate 80
• residual MRC5 proteins
• sorbitol
• streptomycin (antibiotic)
• tri(n)butylphosphate (neurotoxin)
Investigating vaccines fully and deeply is like opening a witch’s “Pandora’s box” brew … who knows what creatures and concoctions are lurking in that syringe?
What do you think? Do you think it’s fair to call vaccines “good medicine”? Please spread this article far and wide, and let us know your opinion.
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Makia Freeman is the editor of The Freedom Articles and senior researcher at ToolsForFreedom.com, writing on many aspects of the the global conspiracy, from vaccines to Zionism to false flag operations and more, and also including info on natural health, sovereignty and higher consciousness.