PHYSICIAN’S ADVANCED WARRANTY OF VACCINE SAFETY FILLABLE PACKET PRINTER FRIENDLY

MEMORANDUM OF AGREEMENT

From:

Physician’s Name: DEA Number:
Degree and Field of Specialty:
Licensed State of Practice: License Number:

To:

Patient’s Name:
Parent/Guardian’s Name:

Subj: PHYSICIAN’S ADVANCED WARRANTY OF VACCINE SAFETY

Ref: (a) CDC Immunization Schedule

Encl: (1) CDC Vaccine Excipient and Media Summary (with component table)

(2) Reference Citations (electronic copy available)

(3) Clinical Reasoning Compilation (printed copy of Encl 2’s citations)

I, (Physician’s name)_________________________, have given careful consideration to the potential risks and benefits of all medical procedures, recommendations, and treatments for which I prescribe or administer to my patient. Upon this, it is my responsibility to thoroughly, honestly, and without bias explain these potential risks and benefits to my patient prior to any form of treatment for their consideration and informed consent. Pursuant to Ref (a) in accordance with Encl (1) through (3), and in order to dispel any reasonable doubt surrounding the safety of vaccines, I have counseled the patient before granting Physician’s Advanced Warranty of Vaccine Safety. (If Physician does NOT wish to grant Physician’s Advanced Warranty of Vaccine Safety, Attachment A must be completed.)

This request is made on behalf of (Patient’s name)_________________________, in my recommended pursuance of Ref (a). I have thoroughly examined and determined my patient meets all prerequisites prior to the administration of immunizations to include: length of gestation at birth, recommended weight, manufacturer’s contraindication exceptions, family history, hereditary predisposition to autoimmune disease, and the potential for increased risk of injury due to underlying genetic factors that may have yet to be identified in my patient. There are certain medical concerns that exist to justify my recommendation of the following vaccinations for my patient’s protection:

RISK FACTOR:	VACCINATION:

INFECTIOUS DISEASE, IMMUNITY, AND INDIVIDUALIZED HEALTH

I, (Physician’s name)_________________________, have personally taken the time to thoroughly study:

The historical data surrounding individual infectious diseases that I vaccinate my patients to include: mortality rate, disease patterns, pathological mutations, antibiotic resistance, and disease decline dates vs. introduction of corresponding vaccines.1
Prevention, treatment options, and alternatives to vaccinations recognizing the importance of diet, lifestyle, and sanitation/hygiene’s role in regard to disease susceptibility and the increased odds of complications in infected individuals. This also includes the encouragement of breastfeeding when possible.3
The importance of gut health’s role in the immune system and the link between poor gut health and increased susceptibility to neurological and immunological disorders.4
The field of Epigenetics examines how nongenetic factors have an influence on gene expression and points to each patient’s health as “individualized”. Therefore, individual susceptibility to vaccine injury is determined not only by hereditary predisposition, genetic disorders, or gender and age, but also through a variety of factors to include, but not limited to: diet, sleep patterns, geographic location, environmental toxin exposure, cultural influence, occupation, etc., suggesting that each patient may have a different response to vaccine ingredients, and may not tolerate the rigorous vaccine schedule as recommended.5
The subset of Th1 vs. Th2 cell response in relation to vaccine-induced immunity vs. natural exposure to pathogens.2
Glutathione’s role in immune/inflammatory response, detox capabilities, and the increased risk of injury due to depletion, with special consideration to acetaminophen's role in depletion.2,5

I have explained this information to my patient thoroughly. (Physician/Patient Initials)____/____

EXCIPIENT AND MEDIA SUMMARY

I, (Physician’s name)_________________________, have reviewed the Vaccine Excipient

and Media Summary listed in Encl (1) and understand its entirety. I am aware of the following:

Vaccines contain growth mediums derived from a variety of animal species and human fetal cell lines. On January 11, 2018, Stanley Plotkin, a prominent figure in vaccinology, stated in a 9-hour long disposition, that 76 aborted fetuses, all with a gestational age of 3 months or older, were used for experimentation and ultimately 2 fetuses were used in the development of vaccines. The fetal cell line components of vaccines has shown that foreign fragmented DNA is present and biologically active within the cultures. Genetic engineer and President of the biomedical research organization Sound Choice Pharmaceutical Institute (SCPI) Theresa Deisher Ph.D., warns that injecting human fetal DNA contaminants bears the risk of causing two well-established pathologies and additionional concerns surrounding contaminants of the MMR vaccine specifically.2

Insertional mutagenesis: The ability of the fetal human DNA used in vaccines to incorporate into the host’s DNA causing mutations.2
Autoimmune disease: The ability of human fetal DNA used in vaccines to trigger the host’s immune system to attack it’s own body.2
The concern that Human Endogenous Retrovirus K (HERVK) is a contaminant in the MMR vaccine, which can reactivate and integrate within the host, noting autoimmune diseases have been associated with HERVK.2

Referenced Text1-13 can be found in Enclosure (2).

Carcinogens like polysorbate 80 and formaldehyde are used in the manufacturing of certain vaccines, and the chemical glyphosate was found to contaminate many vaccines on the market.6
Common allergens are used in the makeup of several vaccines to include components of dairy, soy, nut, egg, and gelatin, and may trigger an anaphylactic response in my patient, and could result in possible lifelong or life threatening allergies to any of these components.
Some vaccines contain antibiotics, noting the implications of antibiotic overuse and the threat posed by antibiotic resistance recognized by the medical community.
Several vaccines contain heavy metals which have been identified as neurotoxins i.e. forms of aluminum, mercury (thimerosal), and other such adjuvants to stimulate an immune response. Scientific evidence correlates exposure to heavy metals and early immune response with severe neurological/immunological damage and points to these ingredients as less effective than antigen immune response.7
The crucial difference between injection vs. ingestion vs. inhalation of such toxins and how they affect the body accordingly.8
The negative impact of heavy metals on healthy gut flora.9
Certain polymorphisms in the MTHFR gene is linked to hypersensitivity to heavy metals.7
The manufacturer’s insert line 13.1 of vaccines on the market stating the lack of studies involving “Carcinogenesis (initiation of cancer formation), Mutagenesis (production of genetic mutations), and Impairment of Fertility” and acknowledge the implications of these ingredients in relation to the potential health concerns listed in line 13.1, also taking into consideration increasing rates of these corresponding health concerns in our population (refer to manufacturer’s package insert of recommended vaccine in custody for patient example).

Refer to Encl (1) for a list of ingredients contained in the vaccinations to be administered and read the Open Letter from Dr. Theresa Deisher to Legislators Regarding Fetal Cell DNA in vaccines with patient.2

I have explained this information to my patient thoroughly. (Physician/Patient Initials)____/____

TRAUMATIC BRAIN INJURY (TBI) AND AUTISM SPECTRUM DISORDER (ASD)

“Pediatric TBI patients and ASD patients share several underlying pathophysiologic changes that contribute to these symptoms and cause increased susceptibility for sensory processing dysfunction, seizures, and gastrointestinal disorders”. Studies suggest that genetically susceptible patients could react to certain ingredients in vaccines in a way that could trigger or worsen these symptoms.4,5,6,7
The increased prevalence of ASD is not solely attributed to population growth or advancements in diagnostic technology, nor purely influenced by genetics, and therefore suggests that susceptibility to vaccine injury due to epigenetic influence should be considered and explored.5
Studies show that TBI and ASD individuals often have gastrointestinal issues and that heavy metals, like those in vaccines, have been shown to worsen gastrointestinal health.5,7
Studies show aluminum content in the brains of autistic individuals is exceedingly high.7
The CDC states “some children with an ASD seem to develop normally until around 18 to 24 months of age and then they stop gaining new skills, or they lose the skills they once had” further suggesting the capability of regression through epigenetic influences.5
Certain factors are attributed to an increased prevalence of ASD and should be considered as a cautionary predisposition or early indicator for diagnosis. These factors include, but are not limited to:

Referenced Text1-13 can be found in Enclosure (2).

Assisted Reproductive Technology (ART), i.e. fertility issues resulting in Intracytoplasmic Sperm Injection (ICSI) or In Vitro Fertilization (IVF), including fetal progesterone exposure. The CDC states, “overall, children conceived using ART were

about two times more likely to be diagnosed with ASD compared to children conceived without using ART”.5

Non-genetic factors such as gestational complications, premature birth, fetal exposure to medications or chemicals, and Twin/Multiple Pregnancy i.e. more that one child per birth.5
Head Circumference or accelerated cranial growth can in some cases be an early indicator for children with ASD.5
Undiagnosed, pre-existing genetic conditions have been noted to trigger adverse reactions from vaccines such as fever, seizures, and encephalitis, resulting in brain injury symptoms that display clinical features of ASD. The precedent case of Hannah Poling, was the first case in which federal authorities conceded the connection between her autistic symptoms and vaccines. “The panel said that Hannah had an underlying cellular disorder that was aggravated by the vaccines, causing brain damage with features of autism spectrum disorder (ASD)”. Due to the lack of neonate diagnostic testing in regards to such genetic vulnerability prior to the administration of routine vaccinations, noted adverse reactions could presumably result in serious or life long brain injury and present as symptoms similar to that of ASD.5
Methylenetetrahydrofolate Reductase (MTHFR) causes genetic polymorphisms and affects a significant portion of the population. This defect has been linked to an increased risk of neurological disorders and ASD and is often undiagnosed in infants before receiving vaccinations.5
The use of acetaminophen based products, such as Tylenol, before or after the administration of vaccines and it’s possible link to ASD.5

HISTORICAL VACCINE SAFETY CONCERNS

I, (Physician’s name)_________________________, acknowledge the following:

That contamination risks are possible and have been historically documented.9
That at a practice level, contamination can occur in multi-dose vials or to any vaccination not stored or administered as prescribed.
That risk of contamination at a manufacturing level is possible.
A compilation of incidents, but not limited to those listed, are recorded from 1955-2013 and can be found on the CDC web page for “Historical Vaccine Safety Concerns”.9

I have taken the following steps to assure the vaccines used in my practice hold no risk of contamination:

Referenced Text1-13 can be found in Enclosure (2).

VACCINE ADVERSE EVENT REPORTING SYSTEM (VAERS), NATIONAL VACCINE INJURY COMPENSATION PROGRAM (VICP), AND INFANT MORTALITY RATE (IMR)

I, (Physician’s name)_________________________, have personally taken the time to thoroughly

investigate reports made to VAERS. It is my understanding that according to the CDC, “Healthcare providers are required by law to report any conditions on the Reportable Events Table (RET)10 to VAERS, and are strongly encouraged to report clinically significant or unexpected events following

vaccination”. I have familiarized myself with the Vaccine Injury Table (VIT)10 in reference to proper reporting. I have also taken the following into account:

VAERS recognizes that “underreporting” is an issue and refers to “the fact that VAERS receives reports for only a small fraction of actual adverse events” and goes on to say that “fewer than 1% of vaccine adverse events are reported”. Further suggesting, an influx in injury events would be expected with proper clinician awareness and education of what to report and the general process of reporting.10
From October 1, 1988, to May 1, 2019, there have been 19,328 injury cases reported to VICP, including 1,301 deaths.10
As of May 1, 2019, the National VICP, has paid more than $4B due to injury and death, with only 6,551 cases compensated for and 11,324 cases dismissed.10
If only 1% of injury/death is reported and then partially compensated for, using conversion mathematics, VICP statistics subsequently could be projected at 1,932,800 injury cases, 130,100 deaths, and an estimated payout of over $400,000,000,000 in the same recorded timeframe.
The United States has an IMR of 5.8 per 1,000 live births according to the CDC, comparably higher than that of most other developed countries worldwide.11
The United States also list SIDS as one of the leading causes of infant death.11
IMR has been shown to regress against the number of vaccines given.11
Infarix, specifically, has SIDS listed under section 6.2 Postmarket Experience11 (refer to manufacturer’s package insert of recommended vaccine in custody for patient example).

Refer to VICP Data website link, listed in Encl (2), with patient for current report.10

I have explained this information to my patient thoroughly. (Physician/Patient Initials)____/____

CONFLICTS OF INTEREST

I, (Physician’s name)_________________________, have personally taken the time to thoroughly educate myself surrounding the following conflicts of interest in regards to vaccine safety:

Senior Scientist at the CDC, William Thompson, Ph.D., went on record stating the purposeful cover-up of a CDC study which showed a causal relationship between the MMR vaccine and autism in African American boys, as well as children with isolated cases of autism.
While employed as the Director of the CDC, Brenda Fitzgerald resigned after it was discovered she held tobacco and healthcare stock, (including Merck, one of the vaccine manufacturers on the market), which implicates personal financial gain from her actions while in office.12
Former CDC Director Julie Gerberding, who increased the vaccination schedule while in office, left her position to work for Merck and also held substantial stock in the vaccine manufacturing company, implicating personal financial gain from her actions while in office.12
In 1986 the National Childhood Vaccine Injury Act (NCVIA) was passed to remove liability from the manufacturers due to subsequent injury.12

Referenced Text1-13 can be found in Enclosure (2).

U.S. Law regards vaccines as “unavoidably unsafe” referencing to the Bruesewitz v. Wyeth case. This case concluded that “if the injury or death resulted from side effects that were unavoidable even though the vaccine was properly prepared and was accompanied by proper directions and warnings” (Bruesewitz v. Wyeth, 2011), it was therefore deemed “unavoidable” and leaves the manufacturer free of liability as per the NCVIA.12
The CDC largely relies on its own Immunization Safety Office to conduct safety testing to determine possible side effects and adverse reactions. In comparison to the FDA’s set standards for most other drugs released to the market, vaccines lack long term studies and do not go through rigorous safety protocols like randomized double-blind inert placebo-controlled studies, both in regard to individual vaccines and the entire recommended schedule synergistically.
Vaccine manufacturer Merck has a questionable past surrounding critical safety concerns:

Merck has been in federal court since 2010 over alleged fraudulent MMR vaccine efficacy claims.12
Merck’s once FDA approved product Vioxx killed an estimated 60,000 people.12
Merck is suspected to have manipulated dozens of academic documents that were published in medical literature to promote Vioxx under false pretenses.12

Vaccine manufacturer Sanofi’s Dengvaxia has been linked to multiple fatalities of children in the Philippines. The rush to produce, sell, and distribute the vaccine resulted in criminal charges.12
The FDA approved the use of Dengvaxia in at risk regions despite critical safety concerns.12
Monsanto’s Glyphosate (the chemical found in several vaccines in an independent study) herbicide Roundup lost several lawsuits with billions of dollars paid out for its link to cancer.6,12
The FDA has historically approved products lacking adequate long term safety and efficacy studies. This negligence has allowed products that have directly contributed to the degradation of health and substantial loss of life, including Vioxx and the opioid-crisis.12

I have explained this information to my patient thoroughly. (Physician/Patient Initials)____/____

EFFICACY

I, (Physician’s name)_________________________, have personally taken the time to analyze some historical data in regards to vaccine efficacy:

Historical outbreaks with traced disease genotypes to the viral lines in vaccinations.13
The theory of “Herd Immunity” being largely flawed due to a variable of factors.13
The ability for “outbreaks” to occur in highly vaccinated populations.13
The ability of infectious transmission from “vaccine shedding”.13
Disease mortality rates vs. reported vaccine injury/death rates. Example: VICP data from measles related vaccines alone display 1,189 injuries and 82 deaths that were reported from 10/01/1988-5/01/2019, taking into consideration the VAERS’s admittedly low reporting system of only 1% of cases filed. If the data serves as a representation of 1%, it could be projected that reports would exponentially jump, at this conversion rate injury could have been projected as 118,900 injuries and 8,200 deaths in this time period, which is exponentially higher than the limited number of measles deaths per thousands of cases reported in the same time frame according to CDC disease mortality statistics.10
Manufacturers have made fraudulent claims in regards to efficacy.12

I have explained this information to my patient thoroughly. (Physician/Patient Initials)____/____

Referenced Text1-13 can be found in Enclosure (2).

CONCLUSION

Upon review of Encl (1) through (3), I, (Physician’s name)_________________________, warrant that the ingredients found in vaccines are safe for injection and effective against the risk factors I have presented. The vaccinations provided in my practice pose no substantial risk and are deemed safe and effective as recommended per Ref (a).

Upon granting Physician’s Advanced Warranty of Vaccine Safety to my patient, I have provided:

The basis of my professional opinion, explained in Attachment A.
The peer-reviewed studies/medical data used to base my opinion, listed in Attachment B.
My refutation of the data presented within Encl (3), delineated in Attachment C.

MEMORANDUM OF AGREEMENT

(If Physician does NOT grant Physician’s Advanced Warranty of Vaccine Safety, Attachment A must be completed.)

I, (Physician’s name)_________________________, do hereby grant Physician’s Advanced Warranty of Vaccine Safety to (Patient’s name)_________________________. I issue this document of my own free will. In doing so, I understand that I relinquish any legal statute, limitation, or liability at the local, state, or federal level that would otherwise apply to my practice with a personal responsibility to the well being of my patient. I issue this warranty to its full capacity after consultation with competent legal counsel whose name is ____________________________, an attorney admitted to the Bar in the State of ____________________________.

_________________________________ (Signature of Physician) Date:________________

Witness: ___________________________________ Date: ____________

(Notary Seal Here If applicable)

Notary Public: ______________________________ Date: ____________

Copy to: Patient

Attachment A: Refusal of Memorandum of Agreement

ATTACHMENT A: REFUSAL OF MEMORANDUM OF AGREEMENT

From:

Physician’s Name: DEA Number:
Degree and Field of Specialty:
Licensed State of Practice: License Number:

To:

Patient’s Name:
Parent/Guardian’s Name:

Subj: PHYSICIAN’S ADVANCED WARRANTY OF VACCINE SAFETY

I, (Physician’s name)_________________________, do NOT grant Physician’s Advanced Warranty of Vaccine Safety to (Patient’s name)_________________________. I understand that the safety concerns addressed within this warranty are some of the most common concerns that have been documented in both the medical and scientific communities. In refusing to grant this warranty, I understand that I have not adequately provided enough information for my patient to make an informed decision for consent prior to any medical procedures, recommendations, and treatments for which I may prescribe or administer.

_________________________________ (Signature of Physician) Date:________________

Witness: ___________________________________ Date: ____________

Copy to: Patient

REFERENCE CITATIONS

Informed consent over body autonomy is right that can affect one’s health, safety, and the pursuit of happiness. With the interest of sanctity of human life, public health, and speciological health in mind, the following clinical reasoning has been provided, but is not limited to the below citations in support of the text references1-13.

With due diligence to sound scientific and medical evidence, the following references are largely compiled of peer-reviewed studies, published documents to medical journals, or from other reputable sources, along with a few mainstream media coverage stories pertinent to the information referenced. Due to the immense amount of data, these references will be listed as hyperlinks or can be viewed in a compiled PDF version here: https://drive.google.com/file/d/1g5Q2rALo2fd_N5ZH4T1pTv9P0vaa6zw9/view?usp=sharing

All direct source hyperlinks are listed in blue. Please note that the studies listed below are only a miniscule portion of the available information that is available in respect to these topics. The studies chose to support this endeavor are best suited for the evidence presented, but in no way represents the total insurmountable evidence that supports these topics. The resources cited are listed as supporting evidence in regards to clinical reasoning and have not funded or endorsed their inclusion or recognition for the purpose of this document.

HISTORICAL DISEASE DECLINE DATA

https://europepmc.org/abstract/med/413067
https://www.cdc.gov/healthywater/drinking/history.html
https://www.cdc.gov/nchs/data/vsus/vsrates1940_60.pdf
https://www.cdc.gov/nchs/data/vsushistorical/mortstatsh_1905.pdf

IMMUNE RESPONSE

FETAL CELL LINES

TH1/TH2 RESPONSE

GLUTATHIONE

Enclosure (2)

PREVENTION AND ALTERNATIVE TREATMENT

MEASLES

ROTAVIRUS

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1632402/

WHOOPING COUGH

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1562195/

PNEUMONIA

https://www.ncbi.nlm.nih.gov/pubmed/23925826

PNEUMOCOCCAL MENINGITIS

https://www.ncbi.nlm.nih.gov/pubmed/24903161

MUMPS

https://www.ncbi.nlm.nih.gov/pubmed/24225020

GUT HEALTH AND NEUROLOGICAL DISORDER CONNECTION

GENETICS AND VACCINE INJURY

EPIGENETICS AND DISEASE

MTHFR AND AUTISM

MTHFR AND PSYCHIATRIC DISEASE

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218441/

GENETIC HYPERSENSITIVITY TO VACCINES

https://www.tellmegen.com/en/results/pharmacologic/hypersensitivity-to-vaccination/

TRAUMATIC BRAIN INJURY (TBI) AND AUTISM SPECTRUM DISORDERS (ASD)

INFERTILITY

PREMATURE BIRTH

GESTATIONAL FACTORS

TWIN/MULTIPLE BIRTHS AND NONGENETIC INFLUENCE

https://www.ncbi.nlm.nih.gov/pubmed/21727249

Enclosure (2)

HEAD CIRCUMFERENCE

REGRESSION INTO AUTISTIC STATE

GENETIC TRIGGER FACTORS

ACETAMINOPHEN USE

INCREASED RATES AND DIAGNOSIS

TBI AND ASD ASSOCIATION

COMPENSATED VICP CASES RELATING TO AUTISM

CARCINOGENS

POLYSORBATE 80

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC539316/
https://www.ncbi.nlm.nih.gov/pubmed/14967540

GLYPHOSATE

https://people.csail.mit.edu/seneff/2017/SamselSeneff_Glyphosate_VI_final.pdf

Enclosure (2)

FORMALDEHYDE

https://www.accessdata.fda.gov/scripts/publications/search_result_record.cfm?id=49121

ADJUVANTS AND HEAVY METALS

HEAVY METALS AND GUT HEALTH

ALUMINUM AND AUTISM

ALUMINUM TOXICITY

https://www.sciencedirect.com/science/article/pii/S0946672X17300950?via%3Dihub
https://www.ncbi.nlm.nih.gov/pubmed/25243176
https://www.ncbi.nlm.nih.gov/pubmed/23932735
https://www.ncbi.nlm.nih.gov/pubmed/25699008
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214894/
https://www.ncbi.nlm.nih.gov/pubmed/29079320
https://www.jpands.org/vol21no4/miller.pdf

MTHFR AND MERCURY

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413404/

MERCURY TOXICITY

AUTOIMMUNITY

NEUROLOGICAL DISORDERS LINKED TO VACCINES

https://yaledailynews.com/blog/2017/02/21/vaccines-linked-to-mental-disorders-by-yale-study/

INJECTION VS. INGESTION

https://www.ncbi.nlm.nih.gov/pubmed/19740540

HISTORICAL VACCINE SAFETY CONCERNS

https://www.cdc.gov/vaccinesafety/concerns/concerns-history.html

VAERS

COMPENSATION DATA

https://www.hrsa.gov/vaccine-compensation/data/index.html

UNDERREPORTING ISSUE

https://healthit.ahrq.gov/sites/default/files/docs/publication/r18hs017045-lazarus-final-report-2011.pdf

REPORTING INJURY

SIDS AND INFANT MORTALITY RATE (IMR)

Enclosure (2)

https://www.ncbi.nlm.nih.gov/pubmed/22531966?fbclid=IwAR1oKqa6Fs677AU4x-zc8-06_TZhK4uAssIjiV3z21IsUdkzysQRHPsRo2I

SIDS

https://www.ncbi.nlm.nih.gov/pubmed/17654772
https://childrenshealthdefense.org/news/the-plausible-connection-between-vaccines-and-sids/

INFARIX PACKAGE INSERT

https://www.fda.gov/files/vaccines%2C%20blood%20%26%20biologics/published/Package-Insert---INFANRIX.pdf

CONFLICTS OF INTEREST

REMOVAL OF MANUFACTURER’S LIABILITY

https://www.congress.gov/bill/99th-congress/house-bill/5546

UNAVOIDABLY UNSAFE

https://www.supremecourt.gov/opinions/10pdf/09-152.pdf

ORGANIZATIONAL MISTRUST AND FALSIFIED DATA

FALSIFIED DATA

https://www.ncbi.nlm.nih.gov/pubmed/19478950

ORGANIZATIONAL MISTRUST

OPIOID CRISIS

MANUFACTURERS

MERCK

VIOXX

MMR VACCINE

https://www.huffingtonpost.ca/lawrence-solomon/merck-whistleblowers_b_5881914.html

SANOFI

DENGVAXIA

Enclosure (2)

BAYER/MONSANTO

GLYPHOSATE

https://www.cbsnews.com/news/jury-awards-couple-2billion-monsanto-roundup-weed-killer-cancer-lawsuit-trial-today-2019-05-13/

EFFICACY, HERD IMMUNITY, AND TRACEABILITY

EFFICACY

HERD IMMUNITY

TRACEABILITY AND VIRAL SHEDDING

***ELECTRONIC COPY AVAILABLE***

FORM WITH HYPERLINKS FOR ONLINE STUDY ACCESS: https://docs.google.com/document/d/1xzWb8dkJqNPAc53MrVeefQJWjkQxc17BfKxfm_MNPuY/edit?usp=sharing
PRINTER FRIENDLY FILLABLE WARRANTY PDF (with enclosure 1 and 2 included):

https://drive.google.com/file/d/1infLHvpuQBQGw3vdUNke21QFS4qOgnCZ/view?usp=sharing

ENCLOSURE (1) PDF: https://drive.google.com/file/d/1EyJ0-1NaoSL5ATHusPmYEnLKmSh2gSqQ/view?usp=sharing
ENCLOSURE (3) PDF

https://drive.google.com/file/d/1g5Q2rALo2fd_N5ZH4T1pTv9P0vaa6zw9/view?usp=sharing

Enclosure (2)

Well cited, pertinent literary pieces, but not limited to the below, are as follows:

The Vaccine-Friendly Plan by Paul Thomas M.D. & Jennifer Margulis Ph.D.
Dissolving Illusions by Suzanne Humphries M.D. & Roman Bystrianyk
Plague by Judy Mikovits Ph.D. & Kent Heckenlively
Vaccines: A Reappraisal by Richard Moskowitz M.D.
Miller’s Review of Critical Vaccine Studies by Niel Z. Miller
Crooked: Man-Made Disease Explained by Forrest Maready
How to End the Autism Epidemic by J.B. Handley

Well cited, pertinent websites, but not limited to the below, are as follows:

Pertinent statements from medical professionals:

1. Dr. Nancy Banks - http://bit.ly/1Ip0aIm

2. Dr. Russell Blaylock - http://bit.ly/1BXxQZL

3. Dr. Shiv Chopra - http://bit.ly/1gdgh1s

4. Dr. Sherri Tenpenny - http://bit.ly/1MPVbjx

5. Dr. Suzanne Humphries - http://bit.ly/17sKDbf

6. Dr. Larry Palevsky - http://bit.ly/1LLEjf6

7. Dr. Toni Bark - http://bit.ly/1CYM9RB

8. Dr. Andrew Wakefield - http://bit.ly/1MuyNzo

9. Dr. Meryl Nass - http://bit.ly/1DGzJsc

10. Dr. Raymond Obomsawin - http://bit.ly/1G9ZXYl

11. Dr. Ghislaine Lanctot - http://bit.ly/1MrVeUL

12. Dr. Robert Rowen - http://bit.ly/1SIELeF

13. Dr. David Ayoub - http://bit.ly/1SIELve

14. Dr. Boyd Haley PhD - http://bit.ly/1KsdVby

15. Dr. Rashid Buttar - http://bit.ly/1gWOkL6

16. Dr. Roby Mitchell - http://bit.ly/1gdgEZU

17. Dr. Ken Stoller - http://bit.ly/1MPVqLI

18. Dr. Mayer Eisenstein - http://bit.ly/1LLEqHH

19. Dr. Frank Engley, PhD - http://bit.ly/1OHbLDI

20. Dr. David Davis - http://bit.ly/1gdgJwo

21. Dr. Tetyana Obukhanych - http://bit.ly/16Z7k6J

22. Dr. Harold E Buttram - http://bit.ly/1Kru6Df

23. Dr. Kelly Brogan - http://bit.ly/1D31pfQ

24. Dr. RC Tent - http://bit.ly/1MPVwmu

25. Dr. Rebecca Carley - http://bit.ly/K49F4d

26. Dr. Andrew Moulden - http://bit.ly/1fwzKJu

27. Dr. Jack Wolfson - http://bit.ly/1wtPHRA

28. Dr. Michael Elice - http://bit.ly/1KsdpKA

29. Dr. Terry Wahls - http://bit.ly/1gWOBhd

30. Dr. Stephanie Seneff - http://bit.ly/1OtWxAY

31. Dr. Paul Thomas - http://bit.ly/1DpeXPf

32. Several Doctors - http://bit.ly/1MPVHOv

33. Dr. Richard Moskowitz - http://bit.ly/1OtWG7D

34. Dr. Jane Orient - http://bit.ly/1MXX7pb

35. Dr. Richard Deth - http://bit.ly/1GQDL10

36. Dr. Lucija Tomljenovic - http://bit.ly/1eqiPr5

37. Dr. Chris Shaw - http://bit.ly/1IlGiBp

38. Dr. Susan McCreadie - http://bit.ly/1CqqN83

39. Dr. Mary Ann Block - http://bit.ly/1OHcyUX

40. Dr. David Brownstein - http://bit.ly/1EaHl9A

41. Dr. Jayne Donegan - http://bit.ly/1wOk4Zz

42. Dr. Troy Ross - http://bit.ly/1IlGlNH

43. Dr. Philip Incao - http://bit.ly/1ghE7sS

44. Dr. Joseph Mercola - http://bit.ly/18dE38I

45. Dr. Jeff Bradstreet - http://bit.ly/1MaX0cC

46. Dr. Robert Mendelson - http://bit.ly/1JpAEQr

47. Dr. Theresa Deisher - https://m.youtube.com/watch?feature=youtu.be&v=6Bc6WX33SuE

48. Dr. Sam Eggertsen - https://m.youtube.com/watch?v=8LB-3xkeDAE

49. The Highwire with Del Bigtree, who regularly features medical professionals and leading scientists - https://www.youtube.com/channel/UCq6oOuhSx7ESreh6m9LGy6Q

50. PhD Toxicologist Ashley Everly - https://www.youtube.com/watch?v=P_a74DvnbMg

51. Dr. Andrew Wakefield - https://youtu.be/c1soitiMelY

Pertinent Documentaries:

1. Vaccination - The Silent Epidemic - http://bit.ly/1vvQJ2W

2. The Greater Good - http://bit.ly/1icxh8j

3. Shots In The Dark - http://bit.ly/1ObtC8h

4. Vaccination The Hidden Truth - http://bit.ly/KEYDUh

5. Vaccine Nation - http://bit.ly/1iKNvpU

6. Vaccination - The Truth About Vaccines - http://bit.ly/1vlpwvU

7. Lethal Injection - http://bit.ly/1URN7BJ

8. Bought - http://bit.ly/1M7YSlr

9. Deadly Immunity - http://bit.ly/1KUg64Z

10. Autism - Made in the USA - http://bit.ly/1J8WQN5

11. Beyond Treason - http://bit.ly/1B7kmvt

12. Trace Amounts - http://bit.ly/1vAH3Hv

13. Why We Don't Vaccinate - http://bit.ly/1KbXhuf

14. Vaxxed: From Cover-Up to Catastrophe - https://vaxxedthemovie.com

“Freedom is lost from an uninterested, uninformed, and uninvolved people.” - Thomas Jefferson