WORLD HEALTH ORGANIZATION reversed itself on Covid Vaccines for Pregnant Moms
The Auto Immune diseases take about four months to begin kicking in. Save that cash influencers. You are going to need it to pay your doctor bills.
"It is essential to #educate the #media on the importance of providing context when reporting on anti-vaccine #sentiment, to make sure that people do not form an erroneous impression that this is the dominant viewpoint." [p 5]
"It is therefore important to focus on building trust in #COVID19 vaccines before people form an opinion against them. This should involve using trusted messengers…"
"Some people may try to compare the #risk of getting infected with that of taking a new vaccine, and determine that between the two, the #risk of #COVID19 is #lower."
"Making vaccine uptake “visible” to others… enabling ways for people to #signal that they have received the vaccine, either on #socialmedia, in news #media or in person, can contribute to making the #socialnorm more salient." [p 5] pic.twitter.com/eUKqBnrp6k
So Joe Rogan has taught us that you can't express an opinion about COVID-19 vaccines unless you're a doctor or medical expert, unless your opinion is that they're awesome and everyone should get them, in which case you don't need any knowledge whatsoever to express your view.
She is brilliant, hilarious, and writes better than anyone I have ever read.
This morning her newsletter zeroed in on the conservative males who have reported they will NOT be getting vaccinated. She also linked to a stupefying article written by Talia Lavin.
“As the petals drop to the pavement and shots slip into arms, we’re rolling inexorably toward Hot Vaxxed Girl Summer. We, the immunized, survivors of the plague, are supposed to emerge from our Covid quarantines without hesitancy. The problem with this is that I was never Hot in the first place and this Summer is no different.
…So many people have died this year, millions, and I have survived to take into my body a miraculous shot that is the very flower of medical science, a code written in my genome to lock out the great threat. And I, imbibing this, have the temerity to not even be sexy. If Vaxxed Girl Summer is meant to be a kind of pan-cultural Rumspringa I ought to be someone that transcends schlubhood under its thrilling aegis. And yet…
She finished the article with these stunning words:
…I never learned how to be flat enough, silent enough, to be all winking, passive chrome. During the pandemic I was lucky enough to be cloistered; this privileged solitude left me alone with a mind that wouldn’t stop buzzing, alone with a body that kept manufacturing its own insistent and extraneous desires. I know that there are many women who excel at both the labor of performed femininity.
Who lust and take with grace, and who are as skilled in attaining their own pleasure as they are at giving pleasure away. Still, after this wearing year, a year of morgue-trucks and uncertainty and pain, I am still a woman unskilled at womanhood, not new to its arts but still humbler than an apprentice: A supplicant at the door of the temple.
The world calls me out into the light of Hot Vaxxed Girl Summer, to be warm and poised and lush, but the spring is still cold and I am frightened and frozen at the threshold. Each step I take from an isolation in which my body, being alone, had no locus of comparison, is a step back into a world of all-too-familiar shame.
Forgiving myself for every untoward fold and hair, every lemurish attempt at eyeliner, every clumsy waddle on thighs like boiled dumplings, forgiving myself for being me, or even just for being, is its own ongoing labor.
Having survived through a plague I want to live every inch of my survival, the world my oyster and I, its irritant little pearl, the gem at the lip of the mantle, to be plucked out and buffed to shining nacre.
Instead I’m the oyster, all slime in the throat, eating grit. Still, I lived. My body allowed me to hide and survive and, surely, for this it has earned a little grace.
Penelope, the wife of Odysseus, undid her weaving each night to ward off suitors and buy herself time. I too have much to unthread each time I close my door on the world.
From the poor material of myself, I have to spin patience and a little kindness. Hot Vaxxed Girl Summer is coming, and all I can do is set my fat hands to the loom.”
Talias tweet is a perfect example of why society should never allow twenty something mockingbird journalists to frame the important issues of the day with their perfect prose.
They do not know anything, about anything important. These oversized children are naively trusting yet arrogant enough to laugh and mock those of us who understand the science of the dreaded shed.
Heck, I read about shedding 32 years ago when I was training to become a Childbirth Educator and learned that the only documented cases of polio in recent years were diagnosed in men who changed their childrens diapers after they received the polio vaccine.
Communicable.
Contagious.
Spreads from person to person through saliva, sweat, urine, and feces.
The vaccinated patient sheds for weeks after getting the shot.
I know this.
The Pharma companies know this.
Talia and her twitter tribe obviously do not.
As per her question of what percentage of the population knows about shedding?
The educated side. The side that knows to avoid those who were recently vaccinated over concerns of having the dreaded cytokine storm or cascade of symptoms that in some leads to death.
There is a reason I will be staying home from church now that the vaccine is widely being given to members of my congregation. As someone who has lived with anaphylactic allergies since I was a baby, I now wonder if I will ever go out in public again.
Pfizer knew during the drug trials for the Covid shot that shedding was causing miscarriages in the women with ties to the vaccine trial participants.
Here is what just this small portion of the Pfizer document is saying:
1. If a man who was not vaccinated touches a vaccinated woman, or breathes any of the air she breathes, (in other words, walks by her in the office) and he then has sex with his wife, his wife can have an adverse event and she should avoid having children.2. If a woman who was never vaccinated gets exposed to a woman who was vaccinated, she can:
A: miscarry, B: spontaneously abort, C. poison a baby via her breast milk D: Have babies that have congitive difficulties.
This is universal, and very bad. Here is a small section of text I translated to English:
8.3.5.3. Occupational Exposure
“An occupational exposure occurs when a person receives unplanned direct contact with a vaccine test subject, which may or may not lead to the occurrence of an adverse event. These people may include health care providers, family members, and other people who are around the trial participant.
When such exposures happen, the investigator must report them to Pfizer saftey within 24 hours of becoming aware of when they happened, regardless of whether or not there is an associated secondary adverse event. This must be reported using the vaccine secondary adverse event report form. SINCE THE INFORMATION DOES NOT PERTAIN TO A PARTICIPANT INVOLVED IN THE STUDY, THE INFORMATION WILL BE KEPT SEPARATE FROM THE STUDY.”
TO CLARIFY: Vaccine study participants become super spreaders of something, they don’t say what it is, but it triggers secondary adverse events in people that never had the vax, when they are exposed to people who did have the vax.
THIS IS SO BAD that right here, in this little bit of quoted text, it warns that un-vaccinated men who have been exposed to a woman who was vaxxed will then pass whatever is in the vax to another woman.
Even the relatively small portion of the document I have put below here says the vax triggers spontaneous abortions and reproductive problems when un-vaccinated people are exposed to the vaccinated and that breast milk from a vaccinated mom can harm the infant. And if anyone does not believe it, then click the link above and wade through that enormous and intentionally confusing document. It’s for real folks, the vax is indeed the kill shot.
Do not permit the vaccinated to come anywhere near you, it is now official.
Here is a small portion of this huge document, straight from pfizer:
Terms:
Study intervention – A vaccine test subject. AE – Adverse event in someone who got the vax. SAE: An adverse event in someone who was exposed to someone who got the vax. EDP: Exposure during pregnancy8.3.5. Exposure During Pregnancy or Breastfeeding, and Occupational Exposure Exposure to the study intervention under study during pregnancy or breastfeeding and occupational exposure are reportable to Pfizer Safety within 24 hours of investigator awareness. 8.3.5.1. Exposure During Pregnancy An EDP occurs if:
* A female participant is found to be pregnant while receiving or after discontinuing study intervention.
* A male participant who is receiving or has discontinued study intervention exposes a female partner prior to or around the time of conception.
* A female is found to be pregnant while being exposed or having been exposed to study intervention due to environmental exposure. Below are examples of environmental exposure during pregnancy:
* A female family member or healthcare provider reports that she is pregnant after having been exposed to the study intervention by inhalation or skin contact.
* A male family member or healthcare provider who has been exposed to the study intervention by inhalation or skin contact then exposes his female partner prior to or around the time of conception.
____
If this vax is not shedding into other people, why would contact between vaccinated and un-vaccinated be an event worth noting?
If this vax is not shedding, then WHY does a guy who has been around a vaccinated woman, even if he did not touch her or have sex, need to worry about getting a different woman pregnant?
____
That’s not all, the following is detailed, and far worse.
The investigator must report EDP to Pfizer Safety within 24 hours of the investigator’s awareness, irrespective of whether an SAE has occurred. The initial information submitted should include the anticipated date of delivery (see below for information related to termination of pregnancy).
* If EDP occurs in a participant or a participant’s partner, the investigator must report this information to Pfizer Safety on the Vaccine SAE Report Form and an EDP Supplemental Form, regardless of whether an SAE has occurred. Details of the pregnancy will be collected after the start of study intervention and until 6 months after the last dose of study intervention.
* If EDP occurs in the setting of environmental exposure, the investigator must report information to Pfizer Safety using the Vaccine SAE Report Form and EDP Supplemental Form. Since the exposure information does not pertain to the participant enrolled in the study, the information is not recorded on a CRF;
however, a copy of the completed Vaccine SAE Report Form is maintained in the investigator site file. Follow-up is conducted to obtain general information on the pregnancy and its outcome for all EDP reports with an unknown outcome. The investigator will follow the pregnancy until completion (or until pregnancy termination) and notify Pfizer Safety of the outcome as a follow-up to the initial EDP Supplemental Form.
In the case of a live birth, the structural integrity of the neonate can be assessed at the time of birth. In the event of a termination, the reason(s) for termination should be specified and, if clinically possible, the structural integrity of the terminated fetus should be assessed by gross visual inspection (unless preprocedure test findings are conclusive for a congenital anomaly and the findings are reported).
Abnormal pregnancy outcomes are considered SAEs. If the outcome of the pregnancy meets the criteria for an SAE (ie, ectopic pregnancy, spontaneous abortion, intrauterine fetal demise, neonatal death, or congenital anomaly), the investigator should follow the procedures for reporting SAEs. Additional information about pregnancy outcomes that are reported to Pfizer Safety as SAEs follows:
* Spontaneous abortion including miscarriage and missed abortion;
* Neonatal deaths that occur within 1 month of birth should be reported, without regard to causality, as SAEs. In addition, infant deaths after 1 month should be reported as SAEs when the investigator assesses the infant death as related or possibly related to exposure to the study intervention.
Additional information regarding the EDP may be requested by the sponsor. Further follow-up of birth outcomes will be handled on a case-by-case basis (eg, follow-up on preterm infants to identify developmental delays). In the case of paternal exposure, the investigator will provide the participant with the Pregnant Partner Release of Information Form to deliver to his partner. The investigator must document in the source documents that the participant was given the Pregnant Partner Release of Information Form to provide to his partner.
8.3.5.2. Exposure During Breastfeeding An exposure during breastfeeding occurs if: * A female participant is found to be breastfeeding while receiving or after discontinuing study intervention.
* A female is found to be breastfeeding while being exposed or having been exposed to study intervention (ie, environmental exposure). An example of environmental exposure during breastfeeding is a female family member or healthcare provider who reports that she is breastfeeding after having been exposed to the study intervention by inhalation or skin contact.
The investigator must report exposure during breastfeeding to Pfizer Safety within 24 hours of the investigator’s awareness, irrespective of whether an SAE has occurred. The information must be reported using the Vaccine SAE Report Form.
When exposure during breastfeeding occurs in the setting of environmental exposure, the exposure information does not pertain to the participant enrolled in the study, so the information is not recorded on a CRF. However, a copy of the completed Vaccine SAE Report Form is maintained in the investigator site file.
An exposure during breastfeeding report is not created when a Pfizer drug specifically approved for use in breastfeeding women (eg, vitamins) is administered in accord with authorized use. However, if the infant experiences an SAE associated with such a drug, the SAE is reported together with the exposure during breastfeeding.
Here’s the clear part of this, that everyone can understand:
8.3.5.3. Occupational Exposure An occupational exposure occurs when a person receives unplanned direct contact with the study intervention, which may or may not lead to the occurrence of an AE. Such persons may include healthcare providers, family members, and other roles that are involved in the trial participant’s care.
The investigator must report occupational exposure to Pfizer Safety within 24 hours of the investigator’s awareness, regardless of whether there is an associated SAE.
The information must be reported using the Vaccine SAE Report Form. Since the information does not pertain to a participant enrolled in the study, the information is not recorded on a CRF; however, a copy of the completed Vaccine SAE Report Form is maintained in the investigator site file.
I WILL TRANSLATE THAT TO ENGLISH:
An occupational exposure occurs when a person receives unplanned direct contact with a vaccine test subject, which may or may not lead to the occurrence of an adverse event. These people may include health care providers, family members, and other people who are around the trial participant.
When such exposures happen, the investigator must report them to Pfizer saftey within 24 hours of becoming aware of when they happened, regardless of whether or not there is an associated secondary adverse event. This must be reported using the vaccine secondary adverse event report form.
SINCE THE INFORMATION DOES NOT PERTAIN TO A PARTICIPANT INVOLVED IN THE STUDY, THE INFORMATION WILL BE KEPT SEPARATE FROM THE STUDY.
Dr. Tenpenny is an integrative medicine physician in Cleveland, OH who has studied the vaccine problems for over 20 years – read 1000s of mainstream medical scientific papers and has put in over 40,000 hours of study on these issues
Certificate of Vaccine Identification Artificial Intelligence COVID-19 is an acronym for Certificate of Vaccine Identification 19 (19 ==> 1 for A and 9 for I, thus AI)
This “vaccine” is not a vaccine, but an exceptionally well-designed genetic modification killing tool
It can cause full blown autoimmune disease anywhere from 2 years and up to 20 years after injection !!!
This “vaccine “ permanently alters host immune system
Not only does shot NOT stop host from getting sick, the antibody (AB) itself turns on host’s body creating havoc & massive auto-immune disease
Governments around the world are saying NO to mRNA vaccines because they are a form of MASS MURDER = GENOCIDE
Remember that genocide is absolutely a key part of the Deep State Plan
Spike protein AG presented to host immune system in 1 of 2 ways Pathway 1 – CELL-MEDIATED IMMUNITY Spike protein fragment antigen (AG) binds MHC-1 receptor in ER & then MCH-1 Protein Complex leaves ER as vesicle to be exocytosed at plasma membrane This MCH-1 Protein Complex then binds to and activates cytotoxic T-cells Pathway 2 – Antibody-Mediatedy IMMUNITY Remainder of article discusses this pathway
How Shot Works
Spike protein mRNA created from viral DNA spike protein sequence via revverse transcriptase
Spike protein mRNA transcribed by ribosomes to create spike protein
mRNA codes for the spike protein on corona viruses (37 corona viruses out there for at least 60 years, but only 7 infect humans)
WHAT SHE SAYS ABOUT TRANSFECTION DOES NOT MAKE SENSE TO ME, AS TRANSFECTION IS INTRODUCTION OF FOREIGN DNA OR RNA ????
Host DNA is indirectly, not directly, affected
Spike protein binds to ACE receptor to gain entry into host cell to begin to replicate
It takes up to six weeks for this spike protein to be fully expressed & for re-exposure problems to surface
Then, host immune system generates AB against spike protein
The problem is that the AB against spike protein is a non-neutralizing AB, that it, it is NOT made against the entire virus, but only the spike protein
Spike protein antibody (AB) is a non-neutralizing antibody (unlike measles, mumps, chickenpox, shingles, etc. antibodies)
An antibody (AB) has 2 Fab fragments and 1 Fac fragment in the shape of a “Y” (which is creepy in an of itself ==> Family Y)
Fab fragments bind to antigen to neutralize it and make it go away With this shot, the Fac fragment causes alot of problems
FAc fragment can bind to tissue in the lungs, Eosinoophils, Basophilss, other receptors that can cause anaphalatic shock, can cause direct modification of macrophages, can cross react with human tissues to cause autoimmune disease via molecular mimicry
A key problem is B cell sensitization – the AB generating B cells retain memory of the AB forever (Memory B cells
We have no idea how long the spike protein will last in host
We have no idea how long the AB will last in host
We have no idea how long the B cells will continue to be active
For the rest of host’s life, host may be suseptible to autoimmune disease, shock, allergies & death from this injection
10 Mechanisms by which this Injection Can Cause Harm (Dr. Tenpenny can only cover a few in this video)
PEG – Polyethelene Glycol
The coding around the mRNA is unstable, so they had to encase it in a lipid bubble (liposome)
The lipid bubble contains PEG
Humans have been sensitized (i.e. primed or made allergic to) to PEG via many, many products over the decades
In 1960, about 2% of population was sensitized to PEG
In 2021, about 70-72% of population is now sensitized to PEG
PEG reaction can cause an acute allergic reaction and/or anaphalactic shock & death
PEG is in Moderna & Pfizer shots
Concept of “Re-Exposure” or Antibody Dependent Enhancement
There are many folks who have taken the shot and say “Look at me, I’ve had no problems !!!”
Well, the problem comes when that person is re-exposed to any of the corona viruses
The anti-spike AB can then set up autoimmune disease
Anti-spike AB can bind to spike protein, AG-AB complex internalized in macrophages (MP), RNA of virus released inside MP then causes
OVERWHELMING infection (MUCH WORSE than had you never had the shot)
They have been trying to develop ABs against corona virus since 2005 because the flu, a corona virus, has a large burden of disease WW and there are corona viruses other than flu that also have a large burden of illness (so getting a corona virus vaccine is desireable)
Scientists have NEVER been able to get their studies (ABs against the full virus) past the safety studies on rats, rabbits, ferrets, hamsters & monkeys). These animals all got extremely sick or died on re-exposure to corona virus. Failure on both safety & efficacy.
These evil, Cabal, DS scientists are very smart & have almost unlimited money to spend on their genocidal projects
With COVID vaccine, they did not even bother with animal studies, and went straight to humans
AG-AB complex Can Cross BBB
Can converts two proteins in the brain and cause them to malfunction
When these two proteins are corrupted, one can lead to ALS and one to Frontal Temporal Lobe Degeneration (Alzheimers Dementia)
Covid Vaccine linked to infertility (placental protein deviously & malevolently contained in shot causes generation of Anti-placenta AB)
Mechanism of Cytokine Storm
Macrophages (MPs) are the little garbage eaters of the immune system
Two types of macrophages (MP): MP1 & MP2
MP1 is active on initial infection
When MP1 attacks pathogen, cytokines are released
Cytokines are proinflammatory & cause fever & call in NK cells
As infection begins to resovle, MP2 come in like fire fighters to quell & calm the hot inflammatory soup & then begin to clean up debris
MP1 ==> increased cytokines (what you want in initial infection)
MP2 ==> decreased cytokines (also what you want to resolve initial infection)
The Anti-spike AB inactivates MP2s by binding by the FAc fragment to the MP2 cells ==> fire fighters CANNOT show up because they are inactivated So the cytokine storm goes on and on and on
The OFF SWITCH has been deactivated – “There is an ON SWITCH, but NO OFF SWITCH”
New J&J Shot
We have very little information on this shot
Spike protein is inserted into an adenovirus (> 100 different strains for adenovirus) to gain entry into host
Some adenoviruses turn on ONOCGENES that can cause cancer
Autoimmune Disease & the “Vaccine”
A well-know immunologist tested the Anti-spike AB on 55 tissue types to determine cross reactivity
The Anti-spike AB cross reacted with 28 of the tissue antigens
Thus, you can see how a plethora of autoimmune diseases can take hold.
Hundreds of Sx can look different, but underlying pathology is that the Anti-spike AB, via molecular mimicry, interacts with up to 28 different tissue AGs in multiple organ systems
VAERS (Vaccine Adverse Event Reporting System)
As of 2/18/21 VAERS has over 1000 reported deaths
This is about 10% of what is out there, so 10,000 – 100,000 deaths are possible just SO FAR
> 19,0000 adverse events reported
This is about 10% of what is out there, so 190,000 to 1,000,000 adverse events are possible just SO FAR
In the next 4-18 months, we can expect to see massive injury & major death from these shots
FDA & CDC have violated 3 areas of Federal Law to allow the Emergency Use Authorization for the “Vaccine”
Given a 99.91 % Survivability of COVID , “Vaccine” is much less “effective” & this is part of Emergency Use Authorization criteria being violated
Other Effective Treatments that can also PREVENT infection
HCQ, Zinc, Ivermectin, High Dose Vitamin C & High Dose Vitamin D
I wonder how many thousands of dollars this influencer was paid to create this propaganda? (I balanced it out with a Jennifer Hudson song and some headlines).
Click to Watch!
My heart is aching with these outrageous numbers of side effects from the vaccine, especially knowing that so many people never report to anyone what happened to them.
The European database of suspected drug reaction reports is EudraVigilance, which also tracks reports of injuries and deaths following the experimental COVID-19 “vaccines.”
Here is what EudraVigilance states about their database:
This website was launched by the European Medicines Agency in 2012 to provide public access to reports of suspected side effects (also known as suspected adverse drug reactions). These reports are submitted electronically to EudraVigilance by national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorisations (licences) for the medicines.
EudraVigilance is a system designed for collecting reports of suspected side effects. These reports are used for evaluating the benefits and risks of medicines during their development and monitoring their safety following their authorisation in the European Economic Area (EEA). EudraVigilance has been in use since December 2001.
This website was launched to comply with the EudraVigilance Access Policy, which was developed to improve public health by supporting the monitoring of the safety of medicines and to increase transparency for stakeholders, including the general public.
The Management Board of the European Medicines Agency first approved the EudraVigilance Access Policy in December 2010. A revision was adopted by the Board in December 2015 based on the 2010 pharmacovigilance legislation. The policy aims to provide stakeholders such as national medicines regulatory authorities in the EEA, the European Commission, healthcare professionals, patients and consumers, as well as the pharmaceutical industry and research organisations, with access to reports on suspected side effects.
Transparency is a key guiding principle of the Agency, and is pivotal to building trust and confidence in the regulatory process. By increasing transparency, the Agency is better able to address the growing need among stakeholders, including the general public, for access to information. (Source.)
Their report through April 24, 2021 lists 8,430 deaths and 354,177 injuries following injections of four experimental COVID-19 shots:
A Health Impact News subscriber in Europe ran the reports for each of the four COVID-19 shots we are including here. This subscriber has volunteered to do this, and it is a lot of work to tabulate each reaction with injuries and fatalities, since there is no place on the EudraVigilance system we have found that tabulates all the results.
Since we have started publishing this, others from Europe have also calculated the numbers and confirmed the totals.
Here is the summary data through April 24, 2021.
Total reactions for the experimental mRNA vaccine Tozinameran (code BNT162b2,Comirnaty) from BioNTech/ Pfizer: 4,524 deaths and 151,306 injuries to 24/04/2021
11,191 Blood and lymphatic system disorders incl. 40 deaths
7,372 Cardiac disorders incl. 522 deaths
50 Congenital, familial and genetic disorders incl. 3 deaths
4,183 Ear and labyrinth disorders incl. 3 deaths
112 Endocrine disorders
4,629 Eye disorders incl. 6 deaths
33,33 Gastrointestinal disorders incl. 227 deaths
103,813General disorders and administration site conditions incl. 1459 deaths
214 Hepatobiliary disorders incl. 16 deaths
3,338 Immune system disorders incl. 20 deaths
10,160 Infections and infestations incl. 527 deaths
3,950 Injury, poisoning and procedural complications incl. 89 deaths
7,595 Investigations incl. 168 deaths
2,564 Metabolism and nutrition disorders incl. 91 deaths
53,714 Musculoskeletal and connective tissue disorders incl. 47 deaths
150 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 7 deaths
65,745 Nervous system disorders incl. 425 deaths
192 Pregnancy, puerperium and perinatal conditions incl. 7 deaths
80 Product issues
6,008 Psychiatric disorders incl. 63 deaths
938 Renal and urinary disorders incl. 66 deaths
994 Reproductive system and breast disorders incl. 1 death
13,954 Respiratory, thoracic and mediastinal disorders incl. 523 deaths
16,171 Skin and subcutaneous tissue disorders incl. 35 deaths
438 Social circumstances incl. 6 deaths
124 Surgical and medical procedures incl. 8 deaths
8,220 Vascular disorders incl. 165 deaths
Total reactions for the experimental mRNA vaccine mRNA-1273 (CX-024414) fromModerna: 2,283 deaths and 17,625 injuries to 24/04/2021
839 Blood and lymphatic system disordersincl. 16 deaths
1,278 Cardiac disorders incl. 231 deaths
7 Congenital, familial and genetic disorders incl. 2 deaths
378 Ear and labyrinth disorders
23 Endocrine disorders incl. 1 death
570 Eye disorders incl. 3 deaths
3,857 Gastrointestinal disorders incl. 80 deaths
12,513 General disorders and administration site conditions incl. 1012 deaths
77 Hepatobiliary disorders incl. 3 deaths
476 Immune system disorders incl. 3 deaths
1,449 Infections and infestations incl. 118 deaths
803 Injury, poisoning and procedural complications incl. 44 deaths
1,087 Investigations incl. 60 deaths
515 Metabolism and nutrition disorders incl. 47 deaths
5,669 Musculoskeletal and connective tissue disorders incl. 47 deaths
48 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 8 deaths
7,489 Nervous system disorders incl. 244 deaths
50 Pregnancy, puerperium and perinatal conditions
8 Product issues
862 Psychiatric disorders incl. 31 deaths
299 Renal and urinary disorders incl. 23 deaths
106 Reproductive system and breast disorders incl. 1 death
2,198 Respiratory, thoracic and mediastinal disorders incl. 197 deaths
2,163 Skin and subcutaneous tissue disorders incl. 19 deaths
162 Social circumstances incl. 6 deaths
109 Surgical and medical procedures incl. 13 deaths
1,166 Vascular disorders incl. 74 deaths
Total reactions for the experimental vaccine AZD1222(CHADOX1 NCOV-19) from Oxford/AstraZeneca: 1,579 deaths and 184,833 injuries to 24/04/2021
5,319 Blood and lymphatic system disorders incl. 64 deaths
7,374 Cardiac disorders incl. 199 deaths
76 Congenital, familial and genetic disorders incl. 2 deaths
5,011 Ear and labyrinth disorders
155 Endocrine disorders incl. 2 deaths
7,922 Eye disorders incl. 5 deaths
56,473 Gastrointestinal disorders incl. 62 deaths
141,042General disorders and administration site conditions incl. 495 deaths
248 Hepatobiliary disorders incl. 13 deaths
1,837 Immune system disorders incl. 7 deaths
10,631 Infections and infestations incl. 99 deaths
4,341 Injury, poisoning and procedural complications incl. 18 deaths
9,798 Investigations incl. 21 deaths
6,977 Metabolism and nutrition disorders incl. 18 deaths
82,522 Musculoskeletal and connective tissue disorders incl. 16 deaths
144 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 4 deaths
111,873Nervous system disorders incl. 244 deaths
108 Pregnancy, puerperium and perinatal conditions
52 Product issues
9,514 Psychiatric disorders incl. 12 deaths
1,745 Renal and urinary disorders incl. 11 deaths
2,076 Reproductive system and breast disorders
15,824 Respiratory, thoracic and mediastinal disorders incl. 171 deaths
23,168 Skin and subcutaneous tissue disordersincl. 10 deaths
364 Social circumstances incl. 3 deaths
383 Surgical and medical procedures incl. 12 deaths
8,706 Vascular disorders incl. 91 deaths
Total reactions for the experimental COVID-19 vaccine JANSSEN (AD26.COV2.S) from Johnson & Johnson: 44 deaths and 413 injuries to 24/04/2021
11 Blood and lymphatic system disorders
45 Cardiac disorders incl. 10 deaths
1 Congenital, familial and genetic disorder
20 Ear and labyrinth disorders
1 Endocrine disorder
20 Eye disorders
109 Gastrointestinal disorders incl. 1 death
235 General disorders and administration site conditions incl. 14 deaths
3 Hepatobiliary disorders
18 Immune system disorders
44 Infections and infestations incl. 2 deaths
34 Injury, poisoning and procedural complications incl. 1 death
61 Investigations
19 Metabolism and nutrition disorders incl. 1 death
95 Musculoskeletal and connective tissue disorders incl. 1 death
232 Nervous system disorders incl. 3 deaths
3 Product issues
45 Psychiatric disorders
11 Renal and urinary disorders
5 Reproductive system and breast disorders
80 Respiratory, thoracic and mediastinal disorders incl. 3 deaths
50 Skin and subcutaneous tissue disorders
5 Social circumstances
3 Surgical and medical procedures
96 Vascular disorders incl. 8 deaths
This is public information funded by the European Medicines Agency (EMA), and anyone can use the EudraVigilance system and verify this data.
Denmark and Norway have completely suspended use of the AstraZeneca experimental COVID-19 shots.
A statement issued by the Norwegian Institute of Public Health stated that the AstraZeneca COVID “vaccine” is more dangerous than COVID itself, especially for young people.
The EMA continues to recommend it. They did, however, add a safety warning to the J&J shots, due to fatal blood clots. (Source.)
The report covers data collected from December 9, 2020, through April 21, 2021, for the three experimental COVID “vaccines” currently in use in the U.K. from Pfizer, AstraZeneca, and Moderna.
They report a total of 1,047 deaths and 725,079 injuries recorded following the experimental COVID injections.
685 of the 1,047 deaths followed AstraZeneca COVID injections, and 573,650 of the 725,079 injuries followed AstraZeneca COVID injections.
Two countries, Norway and Denmark, have now completely halted injections of COVID shots by AstraZeneca, with the Norwegian Institute of Public Health stating that the AstraZeneca experimental shots are associated with a higher risk of injury and death than the COVID-19 virus. See:
Other European countries have also temporarily halted the AstraZeneca shots while they review safety data, but the UK has never halted injecting people with the shot causing fatal blood clots, and the reported events of death and injuries following AstraZeneca shots.
The UK Medicines and Healthcare products Regulatory Agency concludes:
Vaccines are the best way to protect people from Covid-19 and have already saved thousands of lives. Everyone should continue to get their vaccination when asked to do so unless specifically advised otherwise.
As with all vaccines and medicines, the safety of COVID-19 vaccines is being continuously monitored .
Cases of an extremely rare specific type of blood clot with low blood platelets continue to be investigated.
Click to view Laura-Lynn Tyler Thompson interviews Dr. Charles Hoffe who offers an explanation for why pregnant mothers are having miscarriages after getting the Covid Vaccine
Contact me if you have had a Covid Vaccine reaction around your fertility. I am compiling cases of miscarriage, breastfeeding issues, menstruation problems, and infertility on my blog. If you are willing to share your story, it might help other people.
I am so amazed by the brave doctors who are risking EVERYTHING to get the truth out. And the indie journalists who are documenting their claims. Laura-Lynn Tyler Thompson interviews Dr. Charles Hoffe.
Contact me if you have a Covid Vaccine story to tell…
Comments by Brian Shilhavy Editor, Health Impact News
Charles Hoffe has been a medical doctor for 28 years in the small, rural town of Lytton in British Columbia, Canada. The town is comprised of many indigenous groups and the “First Nations.”
When Dr. Hoffe was given 900 doses of the Moderna experimental COVID-19 injections, he administered the doses through the Lytton Medical Clinic to those who wanted them.
He chose not to inject himself.
Dr. Hoffe reports that the result of injecting 900 people among the indigenous First Nations community was that 2 people went into anaphylactic shock, one person died, and several others have suffered what appear to be permanent disabilities. He relates how one of his patients is in so much pain now, that she prefers death to life.
By contrast, no one in the community died or became permanently disabled due to the COVID-19 virus for the past year.
Dr. Hoffe reported these adverse reactions by email to the medical personnel in his community who were responsible for the roll-out of the Moderna shots, which included pharmacists, nurses, and doctors in his area, a total of about 18 people he says.
His email expressed grave concern over the side effects he was seeing, and he asked if perhaps they should pause the injections for a while.
He reports that within 48 hours he received a very stern rebuke from his superiors at the Interior Health Authority accusing him of causing “vaccine hesitancy” and that they were going to report him to BC College of Physicians and Surgeons.
They forbade him from saying anything negative about the Moderna shots by issuing a gag order against him.
Dr. Hoffe explains that this is a method of intimidation that is being used against other doctors who have become too afraid to speak out, because the College of Physicians and Surgeons has great authority to shut down doctors’ careers, or heavily fine them.
As he continued to see more injuries the following week, he became very angry about his gag order. He was told that if he had any concerns about the injections that he had to contact the medical health officer in charge of the Moderna roll out.
He did, but when he did not receive a reply, he decided to write an open letter directly to Dr. Bonnie Henry, British Columbia Provincial Health Officer, in direct defiance of his gag order since he made it public.
Here is a copy of the letter.
Dr. Charles D. Hoffe, BSc, MB, BCh, LMCC Lytton Medical Clinic Lytton BC V0K 1Z0
5 April, 2021
Dr. Bonnie Henry, British Columbia Provincial Health Officer Ministry of Health 1515 Blanchard Street Victoria, BC, V8W 3C9
Dear Dr. Henry,
The first dose of the Moderna vaccine has now been administered to some of my patients in the community of Lytton, BC. This began with the First Nations members of our community in mid-January, 2021. 900 doses have now been administered.
I have been quite alarmed at the high rate of serious side-effects from this novel treatment. From this relatively small number of people vaccinated so far, we have had:
Numerous allergic reactions, with two cases of anaphylaxis.
One (presumed) vaccine induced sudden death, (in a 72 year old patient with COPD. This patient complained of being more short of breath continually after receiving the vaccine, and died very suddenly and unexpectedly on day 24, after the vaccine. He had no history of cardiovascular disease).
Three people with ongoing and disabling neurological deficits, with associated chronic pain, persisting for more than 10 weeks after their first vaccine. These neurological deficits include: continual and disabling dizziness, generalised or localized neuromuscular weakness, with or without sensory loss. The chronic pain in these patients is either generalised or regional, with or without headaches.
So in short, in our small community of Lytton, BC, we have one person dead, and three people who look as though they will be permanently disabled, following their first dose of the Moderna vaccine. The age of those affected ranges from 38 to 82 years of age.
So I have a couple of questions and comments:
Are these considered normal and acceptable long term side-effects for gene modification therapy? Judging by medical reports from around the world, our Lytton experience is not unusual.
Do you have any idea what disease processes may have been initiated, to be producing these ongoing neurological symptoms?
Do you have any suggestions as to how I should treat the vaccine induced neurological weakness, the dizziness, the sensory loss, and the chronic pain syndromes in these people, or should they be all simply referred to a neurologist? I anticipate that many more will follow, as the vaccine is rolled out. This was only phase one, and the first dose.
In stark contrast to the deleterious effects of this vaccine in our community, we have not had to give any medical care what-so-ever, to anyone with Covid-19. So in our limited experience, this vaccine is quite clearly more dangerous than Covid-19.
I realize that every medical therapy has a risk-benefit ratio, and that serious disease calls for serious medicine. But we now know that the recovery rate of Covid-19, is similar to the seasonal flu, in every age category. Furthermore, it is well known that the side effects following a second shot, are significantly worse than the first. So the worst is still to come.
It must be emphasised, that these people were not sick people, being treated for some devastating disease. These were previously healthy people, who were offered an experimental therapy, with unknown long-term side-effects, to protect them against an illness that has the same mortality rate as the flu. Sadly, their lives have now been ruined.
It is normally considered a fundamental principal of medical ethics, to discontinue a clinical trial if significant harm is demonstrated from the treatment under investigation.
So my last question is this: Is it medically ethical to continue this vaccine rollout, in view of the severity of these life altering side-effects, after just the first shot? In Lytton, BC, we have an incidence of 1 in 225 of severe life altering side-effects, from this experimental gene modification therapy.
I have also noticed that these vaccine induced side effects are going almost entirely unreported, by those responsible for the vaccine rollout. I am aware that this is often a problem, with vaccines in general, and that delayed side-effects after vaccines, are sometimes labelled as being “coincidences”, as causality is often hard to prove. However, in view of the fact that this is an experimental treatment, with no long-term safety data, I think that perhaps this issue should be addressed too.
Furthermore I have noticed, that the provincial vaccine injury reporting form, which was clearly designed for conventional vaccines, does not even have any place to report vaccine injuries of the nature and severity that we are seeing from this new mRNA therapy.
It is now clearly apparent with medical evidence from around the world, that the side-effect profiles of the various gene modification therapies against Covid-19, have been vastly understated by their manufacturers, who were eager to prove their safety.
Thank you for attention to this critically urgent public health matter.
Yours sincerely,
Dr. Charles Hoffe
The IH (Interior Health) responded to his letter publicly and it was published in the Ashcroft Cache Creek Journal as they tried to do “damage control” and attack Dr. Hoffe.
IH says COVID-19 vaccines safe despite claims of Lytton physician
Doctor makes unsubstantiated claims about serious side effects of Moderna vaccine
by BARBARA RODEN
Interior Health (IH) is reassuring Lytton and area residents about the safety of COVID-19 vaccines, after a physician in that community shared a letter in which he claimed that the death of a Lytton resident was linked to the Moderna vaccine.
In a letter to Provincial Health Officer Dr. Bonnie Henry dated April 5, Dr. Charles Hoffe claimed that there had been “numerous” allergic reactions — including two cases of anaphylaxis — among people in Lytton and area who had received the Moderna vaccine. He also claimed that three people were exhibiting “ongoing and disabling” neurological deficits.
Hoffe also claimed that the death of a 72-year-old patient with COPD, 24 days after the man was vaccinated, was “presumed” to be vaccine-induced. The physician did not produce any evidence to prove that any of the events resulted from the vaccine.
“It has been a challenge for us to investigate this thoroughly and take reports seriously,” says Dr. Carol Fenton, Medical Health Officer with IH. In a written statement issued on April 14, Fenton says that “There have been no deaths or lasting adverse reactions connected to the Moderna/Pfizer vaccines, or any COVID-19 vaccine, in Lytton, Interior Health, or B.C. at this time.”
The statement adds that IH knows unequivocally that the vaccines are safer than COVID-19 itself, and that the vaccines have been demonstrated to be safe and effective through all levels of clinical trials.
“There is a detailed process to review all adverse effects following immunizations, and all serious events are recorded and reported to the provincial and national level to monitor for safety signals that may be missed at the local level. With the information we have from the vaccine roll-out so far, the COVID-19 vaccines are very safe.”
Fenton tells the Journal that while there will always be some variations between medical practitioners, when it comes to the safety of vaccines it is important to look at consensus-based reports from those who are trained in the field.
“These people are the experts of the experts,” she says. “I can answer most vaccine questions, but I don’t consider myself to be an expert in vaccines. The decisions and analyses are defined by people with the skills and expertise to parse through the information we have.”
The immunization clinics being run by IH have trained vaccinators on site to monitor for and respond to allergic and anaphylactic reactions, which are rare, but can occur with any vaccine or medication.
“The safety of people in Lytton, Nlaka’pamux, and Northern St’at’imc Nations and all communities is the top priority, and our recommendation is that all individuals should get immunized when they are eligible,” says the statement. (Full article here.)
So basically the same as what we are seeing around the rest of the world when honest doctors come forward and report the truth.
The health authorities lie. No science, no statistics, just an appeal to authority. “We know what we are talking about, but this doctor does not.”
A local and independent talk show host in Canada, Laura-Lynn Tyler Thompson, tracked down and interviewed Dr. Hoffe. The original show is an hour long and on her Facebook Page, as well as her Bitchute Channel.
We have extracted the 30 minute interview with Dr. Hoffe, and it is on our Rumble channel, and will also be on our Bitchute channel.
Dr. Hoffe has served the members of his community for 28 years, and he had a wonderful reputation among his patients, with glowing online reviews.It is being reported now on some social media sites that his patients are being told he is no longer available to meet with them.