"The vaccine-induced magnetism hinges around the possibility that a 👉graphene-like compound👈 was used as an adjuvant to increase the rate of uptake of the mRNA.
"But how could this have happened since neither graphene or graphene oxide are magnetic? The answer is that both graphene and graphene oxide, can conduct enough electricity across the cell membranes to magnetise nearby superparamagnetic particles such as ferritin and magnetite to cause a widespread magnetisation of people receiving the vaccine. It's just as the iron core of an electromagnet becomes magnetised when an electric current is passed through the coil of wire wound around it.
This means that a transmembrane strand of graphene or graphene oxide (from the vaccine) could carry a huge electric current and be likely to magnetise any superparamagnetic materials such as ferritin or magnetite that may be close by.
This effect could spread like wildfire across the membrane as each magnetized particle magnetizes its neighbours and then to those of the next cell, so that the magnetic effect increases and
Ultimately, it could spread to all parts of the body via the bloodstream, starting with the blood cells themselves, including those white cells needed for our immune system, then the veins, then the heart, followed by the lungs and finally the brain. Wherever It goes, it could wreak havoc with cell permeability and have all sorts of biological effects, including heart failure, premature Alzeimer's disease and, when the mitochondria are affected, chronic fatigue.
Another effect is that membrane damage to our sensory cells could make them hyperactive and send false signals to the brain to give symptoms very similar to electromagnetic hypersensitivity (EHS) resulting in headaches whenever we use a mobile phone, pins and needles when straying too close to a WiFi router dizziness and nausea, to name but a few.
Perhaps the most serious danger is if you have an MRI scan, when the extremely powerful magnet in the machine would try to pull these magnetised particles out of your body and, in the case of the brain or spinal cord scan, immediate and possibly permanent damage could result. When other parts of the body are scanned, the results may be less noticeable in the short term, but become apparent later as an unexplained "idiopathic" illness.
Dr Andrew Goldsworthy Lecturer and Biological Safety Officer (retired) Imperial College London"
@Not_On_The_Beeb
https://www.notonthebeeb.co.uk/post/imperial-college-london-dr-andrew-goldsworthy
"But how could this have happened since neither graphene or graphene oxide are magnetic? The answer is that both graphene and graphene oxide, can conduct enough electricity across the cell membranes to magnetise nearby superparamagnetic particles such as ferritin and magnetite to cause a widespread magnetisation of people receiving the vaccine. It's just as the iron core of an electromagnet becomes magnetised when an electric current is passed through the coil of wire wound around it.
This means that a transmembrane strand of graphene or graphene oxide (from the vaccine) could carry a huge electric current and be likely to magnetise any superparamagnetic materials such as ferritin or magnetite that may be close by.
This effect could spread like wildfire across the membrane as each magnetized particle magnetizes its neighbours and then to those of the next cell, so that the magnetic effect increases and
Ultimately, it could spread to all parts of the body via the bloodstream, starting with the blood cells themselves, including those white cells needed for our immune system, then the veins, then the heart, followed by the lungs and finally the brain. Wherever It goes, it could wreak havoc with cell permeability and have all sorts of biological effects, including heart failure, premature Alzeimer's disease and, when the mitochondria are affected, chronic fatigue.
Another effect is that membrane damage to our sensory cells could make them hyperactive and send false signals to the brain to give symptoms very similar to electromagnetic hypersensitivity (EHS) resulting in headaches whenever we use a mobile phone, pins and needles when straying too close to a WiFi router dizziness and nausea, to name but a few.
Perhaps the most serious danger is if you have an MRI scan, when the extremely powerful magnet in the machine would try to pull these magnetised particles out of your body and, in the case of the brain or spinal cord scan, immediate and possibly permanent damage could result. When other parts of the body are scanned, the results may be less noticeable in the short term, but become apparent later as an unexplained "idiopathic" illness.
Dr Andrew Goldsworthy Lecturer and Biological Safety Officer (retired) Imperial College London"
@Not_On_The_Beeb
https://www.notonthebeeb.co.uk/post/imperial-college-london-dr-andrew-goldsworthy
Not On The Beeb
IMPERIAL COLLEGE LONDON - DR ANDREW GOLDSWORTHY ON VACCINE INDUCED MAGNETISM
ENGLISH ITALIAN SPANISH HIGHLIGHT: "...Wherever It (the magnetism) goes, it could wreak havoc with cell permeability and have all sorts of biological effects, including heart failure, premature Alzeimer's disease and, when the mitochondria are affected…
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Popular German Newspaper Bild Offers Apology to Children about Telling Them to Stay Home or they Would Kill Grandma
Recent progress of graphene oxide as a potential vaccine carrier and adjuvant
Wanjun Cao et al. Acta Biomater. 2020 Aug.
"..there is an urgent need to develop new all-purpose adjuvants because some adjuvants approved for human use have limited functionality. Graphene oxide (GO), widely employed for the delivery of biomolecules, excels in loading and delivering antigen and shows the potentiality of activating the immune system. However, GO aggregates in biological liquid and induces cell death, and it also exhibits poor biosolubility and biocompatibility. To address these limitations, various surface modification protocols have been employed to integrate aqueous compatible substances with GO to effectively improve its biocompatibility. More importantly, these modifications render functionalized-GO with superior properties as both carriers and adjuvants. Herein, the recent progress of physicochemical properties and surface modification strategies of GO for its application as both carriers and adjuvants is reviewed."
https://pubmed.ncbi.nlm.nih.gov/32531395/
Wanjun Cao et al. Acta Biomater. 2020 Aug.
"..there is an urgent need to develop new all-purpose adjuvants because some adjuvants approved for human use have limited functionality. Graphene oxide (GO), widely employed for the delivery of biomolecules, excels in loading and delivering antigen and shows the potentiality of activating the immune system. However, GO aggregates in biological liquid and induces cell death, and it also exhibits poor biosolubility and biocompatibility. To address these limitations, various surface modification protocols have been employed to integrate aqueous compatible substances with GO to effectively improve its biocompatibility. More importantly, these modifications render functionalized-GO with superior properties as both carriers and adjuvants. Herein, the recent progress of physicochemical properties and surface modification strategies of GO for its application as both carriers and adjuvants is reviewed."
https://pubmed.ncbi.nlm.nih.gov/32531395/
PubMed
Recent progress of graphene oxide as a potential vaccine carrier and adjuvant - PubMed
Vaccine is one of the most effective strategies for preventing and controlling infectious diseases and some noninfectious diseases, especially cancers. Adjuvants and carriers have been appropriately added to the vaccine formulation to improve the immunogenicity…
Nano coronavirus recombinant vaccine taking graphene oxide as carrier
The invention belongs to the field of nano materials and biomedicine, and relates to a vaccine, in particular to development of 2019-nCoV coronavirus nuclear recombinant nano vaccine. The invention also comprises a preparation method of the vaccine and application of the vaccine in animal experiments. The new corona vaccine contains graphene oxide, carnosine, CpG and new corona virus RBD; binding carnosine, CpG and neocoronavirus RBD on the backbone of graphene oxide; the CpG coding sequence is shown as SEQ ID NO 1; the novel coronavirus RBD refers to a novel coronavirus protein receptor binding region which can generate a high-titer specific antibody aiming at the RBD in a mouse body, and provides a strong support for prevention and treatment of the novel coronavirus.
https://patents.google.com/patent/CN112220919A/en
The invention belongs to the field of nano materials and biomedicine, and relates to a vaccine, in particular to development of 2019-nCoV coronavirus nuclear recombinant nano vaccine. The invention also comprises a preparation method of the vaccine and application of the vaccine in animal experiments. The new corona vaccine contains graphene oxide, carnosine, CpG and new corona virus RBD; binding carnosine, CpG and neocoronavirus RBD on the backbone of graphene oxide; the CpG coding sequence is shown as SEQ ID NO 1; the novel coronavirus RBD refers to a novel coronavirus protein receptor binding region which can generate a high-titer specific antibody aiming at the RBD in a mouse body, and provides a strong support for prevention and treatment of the novel coronavirus.
https://patents.google.com/patent/CN112220919A/en
Google
CN112220919A - Nano coronavirus recombinant vaccine taking graphene oxide as carrier
- Google Patents
- Google Patents
The invention belongs to the field of nano materials and biomedicine, and relates to a vaccine, in particular to development of 2019-nCoV coronavirus nuclear recombinant nano vaccine. The invention also comprises a preparation method of the vaccine and application…
AUGUST 2020: Recent progress of graphene oxide as a potential vaccine carrier and adjuvant
"Our work describes the surface modification of graphene oxide and for the first time summarizes that functionalized graphene oxide serves as a vaccine carrier and shows significant adjuvant activity in activating cellular and humoral immunity.
In the future [OUR CURRENT PRESENT], 👉it is expected to be introduced into vaccine research👈 [VIOLATION OF NUREMBERG CODE RIGHT HERE] to improve the efficacy of vaccines."
https://www.sciencedirect.com/science/article/abs/pii/S1742706120303305?via%3Dihub
"Our work describes the surface modification of graphene oxide and for the first time summarizes that functionalized graphene oxide serves as a vaccine carrier and shows significant adjuvant activity in activating cellular and humoral immunity.
In the future [OUR CURRENT PRESENT], 👉it is expected to be introduced into vaccine research👈 [VIOLATION OF NUREMBERG CODE RIGHT HERE] to improve the efficacy of vaccines."
https://www.sciencedirect.com/science/article/abs/pii/S1742706120303305?via%3Dihub
OFFICIAL INTERIM REPORT IN ENGLISH (UNIVERSITY OF ALMERIA).pdf
1.2 MB
GRAPHENE OXIDE DETECTION IN AQUEOUS SUSPENSION
OBSERVATIONAL STUDY IN OPTICAL AND ELECTRON MICROSCOPY - Prof. Dr. Pablo Campra Madrid
Doctor of Chemical Sciences and Bachelor of Biological Sciences
ESCUELA SUPERIOR DE INGENIERIA
UNIVERSIDAD DE ALMERÍA, SPAIN
OBSERVATIONAL STUDY IN OPTICAL AND ELECTRON MICROSCOPY - Prof. Dr. Pablo Campra Madrid
Doctor of Chemical Sciences and Bachelor of Biological Sciences
ESCUELA SUPERIOR DE INGENIERIA
UNIVERSIDAD DE ALMERÍA, SPAIN
Toxicity of graphene-family nanoparticles: a general review of the origins and mechanisms
"several typical mechanisms underlying GFN toxicity have been revealed, for instance, physical destruction, oxidative stress, DNA damage, inflammatory response, apoptosis, autophagy, and necrosis."
https://particleandfibretoxicology.biomedcentral.com/articles/10.1186/s12989-016-0168-y
"several typical mechanisms underlying GFN toxicity have been revealed, for instance, physical destruction, oxidative stress, DNA damage, inflammatory response, apoptosis, autophagy, and necrosis."
https://particleandfibretoxicology.biomedcentral.com/articles/10.1186/s12989-016-0168-y
SpringerLink
Toxicity of graphene-family nanoparticles: a general review of the origins and mechanisms
Particle and Fibre Toxicology - Due to their unique physicochemical properties, graphene-family nanomaterials (GFNs) are widely used in many fields, especially in biomedical applications....
Safety Assessment of Graphene-Based Materials: Focus on Human Health and the Environment
Collectively, these studies have shed light on the biodistribution and fate of some GBMs following various administration routes. Overall, there is evidence that various GBMs are able to cross physiological barriers, reaching secondary organs distant from the point of entry.
Several studies have been published on the biodistribution of GBMs following i.v. injection. Qu et al. studied i.v. injection of GO [GRAPHENE OXIDE] suspended in PBS or GO dispersed in 1% Tween 80-PBS and noted a higher accumulation in lungs for GO-PBS (lateral dimension: 300–1000 nm).(89) In contrast, accumulation in the liver was higher for GO-PBS-Tween 80 when compared to that for GO-PBS. Even though these conclusions were based only on the blackness of organs following treatment and observation of brown/black matter in histological sections, the results support the idea that better colloidal stability helps the GO sheets to pass through lung capillaries more easily. GO sheets functionalized with poly(sodium 4-styrenesulfonate) (lateral dimension: 300–700 nm, thickness: 1–4 nm) and labeled with the fluorescent Cy7 dye were used to assess biodistribution using whole-body live imaging.(90) When organs were harvested at 24 h, fluorescence was found only in the liver and bladder. Fourteen days after injection, there was obvious macroscopic presence of materials in the lungs, liver, and spleen, which all appeared black in comparison to corresponding organs from PBS-treated animals. Materials were still present in these organs after 180 days, as evidenced by black matter in histological sections. In a recent study, nonlabeled PEGylated rGO (lateral dimension: ∼1 μm, thickness: 4–9 nm, C/O ratio: 3.7) was evaluated for its biodistribution after i.v. injection using Raman spectroscopy.(87) Most materials were found in the liver and spleen at the earliest time point of 3 days, in agreement with other studies, but transiently increased in the brain at days 7 and 14 days before decreasing by day 21."
https://pubs.acs.org/doi/10.1021/acsnano.8b04758#
Collectively, these studies have shed light on the biodistribution and fate of some GBMs following various administration routes. Overall, there is evidence that various GBMs are able to cross physiological barriers, reaching secondary organs distant from the point of entry.
Several studies have been published on the biodistribution of GBMs following i.v. injection. Qu et al. studied i.v. injection of GO [GRAPHENE OXIDE] suspended in PBS or GO dispersed in 1% Tween 80-PBS and noted a higher accumulation in lungs for GO-PBS (lateral dimension: 300–1000 nm).(89) In contrast, accumulation in the liver was higher for GO-PBS-Tween 80 when compared to that for GO-PBS. Even though these conclusions were based only on the blackness of organs following treatment and observation of brown/black matter in histological sections, the results support the idea that better colloidal stability helps the GO sheets to pass through lung capillaries more easily. GO sheets functionalized with poly(sodium 4-styrenesulfonate) (lateral dimension: 300–700 nm, thickness: 1–4 nm) and labeled with the fluorescent Cy7 dye were used to assess biodistribution using whole-body live imaging.(90) When organs were harvested at 24 h, fluorescence was found only in the liver and bladder. Fourteen days after injection, there was obvious macroscopic presence of materials in the lungs, liver, and spleen, which all appeared black in comparison to corresponding organs from PBS-treated animals. Materials were still present in these organs after 180 days, as evidenced by black matter in histological sections. In a recent study, nonlabeled PEGylated rGO (lateral dimension: ∼1 μm, thickness: 4–9 nm, C/O ratio: 3.7) was evaluated for its biodistribution after i.v. injection using Raman spectroscopy.(87) Most materials were found in the liver and spleen at the earliest time point of 3 days, in agreement with other studies, but transiently increased in the brain at days 7 and 14 days before decreasing by day 21."
https://pubs.acs.org/doi/10.1021/acsnano.8b04758#
ACS Publications
Safety Assessment of Graphene-Based Materials: Focus on Human Health and the Environment
Graphene and its derivatives are heralded as “miracle” materials with manifold applications in different sectors of society from electronics to energy storage to medicine. The increasing exploitation of graphene-based materials (GBMs) necessitates a comprehensive…
Reproductive and Developmental Effects of Graphene-Based Materials
"Pregnant women, fetuses, and neonates are among the most vulnerable populations and therefore warrant particular attention in regard to GBM hazard assessment. In pregnancy, major physiological changes occur that are expected to affect particokinetics and subsequent biological effects. Likewise, developing fetuses and neonates are more susceptible to toxic effects of xenobiotics than adults due to ongoing organogenesis, physiological changes, or immaturity of the immune system. To date, it is unknown whether GBMs can reach the placental barrier or reproductive organs.
First indications that nanoparticles may interfere with pregnancy and fetal health came from epidemiological studies showing that maternal exposure to air pollution (in particular, to particulate matter <2.5 μm) during pregnancy was associated with adverse birth outcomes such as low birth weight and preterm birth (reviewed in ref (199)). As a consequence, research on the placental transfer of nanoparticles and the impact on reproductive and developmental systems was intensified
...when small rGO [GRAPHENE OXIDE] was injected in late gestation, this resulted in abortions, malformed fetuses, and death of pregnant mice.
Thus, based on these observations, the toxicity of rGO should be seriously considered in progestational (drawing near pregnancy) females, although the rGO-exposed mice could still produce healthy offspring depending on the administered dose.(203) Developmental toxicity of GBMs has also been described in other species including zebrafish and chicken,(204,205) but because these models lack a mammalian maternal–placental–embryonic/fetal relationship, their predictive value for human developmental and reproductive toxicity assessment is limited.
These observations underscore the need for further studies on the long-term consequences of GBMs on placenta functionality and maternal–fetal health. It is pertinent to note that rGO has been suggested to induce a transitory decrease in the tightness of the blood–brain barrier in rats; rGO was systemically injected in the latter study, and the relatively large size (average size: 342 nm) of the material was apparently not an obstacle for its entry into the brain.(213) Overall, a better understanding of potential interferences of GBMs with placental, reproductive, and developmental functions will be imperative for the sustainable and safe use of GBMs, not least as reproductive and developmental toxicity has been reported for other carbon-based nanomaterials.(209,214) For studies on placental translocation and effects of GBMs, human models (e.g., ex vivo placenta perfusion, placental explant cultures, or placental microtissues) are available to complement in vivo studies and to avoid uncertainties in the extrapolation of results due to species-specific differences in placental structure and function.(215)
Finally, in addition to direct effects of GBMs on reproductive and developmental systems, the indirect consequences of GBMs on maternal and placental tissues and the release of mediators deserves attention as the creation of a hostile environment in the womb may increase the risk for pregnancy complications and the development of diseases later in life."
https://pubs.acs.org/doi/10.1021/acsnano.8b04758#
"Pregnant women, fetuses, and neonates are among the most vulnerable populations and therefore warrant particular attention in regard to GBM hazard assessment. In pregnancy, major physiological changes occur that are expected to affect particokinetics and subsequent biological effects. Likewise, developing fetuses and neonates are more susceptible to toxic effects of xenobiotics than adults due to ongoing organogenesis, physiological changes, or immaturity of the immune system. To date, it is unknown whether GBMs can reach the placental barrier or reproductive organs.
First indications that nanoparticles may interfere with pregnancy and fetal health came from epidemiological studies showing that maternal exposure to air pollution (in particular, to particulate matter <2.5 μm) during pregnancy was associated with adverse birth outcomes such as low birth weight and preterm birth (reviewed in ref (199)). As a consequence, research on the placental transfer of nanoparticles and the impact on reproductive and developmental systems was intensified
...when small rGO [GRAPHENE OXIDE] was injected in late gestation, this resulted in abortions, malformed fetuses, and death of pregnant mice.
Thus, based on these observations, the toxicity of rGO should be seriously considered in progestational (drawing near pregnancy) females, although the rGO-exposed mice could still produce healthy offspring depending on the administered dose.(203) Developmental toxicity of GBMs has also been described in other species including zebrafish and chicken,(204,205) but because these models lack a mammalian maternal–placental–embryonic/fetal relationship, their predictive value for human developmental and reproductive toxicity assessment is limited.
These observations underscore the need for further studies on the long-term consequences of GBMs on placenta functionality and maternal–fetal health. It is pertinent to note that rGO has been suggested to induce a transitory decrease in the tightness of the blood–brain barrier in rats; rGO was systemically injected in the latter study, and the relatively large size (average size: 342 nm) of the material was apparently not an obstacle for its entry into the brain.(213) Overall, a better understanding of potential interferences of GBMs with placental, reproductive, and developmental functions will be imperative for the sustainable and safe use of GBMs, not least as reproductive and developmental toxicity has been reported for other carbon-based nanomaterials.(209,214) For studies on placental translocation and effects of GBMs, human models (e.g., ex vivo placenta perfusion, placental explant cultures, or placental microtissues) are available to complement in vivo studies and to avoid uncertainties in the extrapolation of results due to species-specific differences in placental structure and function.(215)
Finally, in addition to direct effects of GBMs on reproductive and developmental systems, the indirect consequences of GBMs on maternal and placental tissues and the release of mediators deserves attention as the creation of a hostile environment in the womb may increase the risk for pregnancy complications and the development of diseases later in life."
https://pubs.acs.org/doi/10.1021/acsnano.8b04758#
ACS Publications
Safety Assessment of Graphene-Based Materials: Focus on Human Health and the Environment
Graphene and its derivatives are heralded as “miracle” materials with manifold applications in different sectors of society from electronics to energy storage to medicine. The increasing exploitation of graphene-based materials (GBMs) necessitates a comprehensive…
GRAPHENE OXIDE: Bridging Nanosafety and Medicine: Intravenous Administration
Radioactivity was detected in the stomach and intestine but not in any other major organs at 4 h. The signal was no longer detectable at 24 h, suggesting no intestinal adsorption of PEGylated GO.
Importantly, in both studies, a large amount of radioactivity was observed in the bladder at early time points. These results suggested that a large amount of i.v.-injected GO sheets had undergone renal glomerular filtration, as confirmed by the transient presence of radiolabeled GO sheets in kidneys and the detection of GO sheets in the urine.
Single- to few-layer GO sheets (lateral dimension: 100–400 nm with DOTA, thickness: 2–10 nm) were found to accumulate in both liver and spleen, with a decrease of radioactivity from 1 to 24 h in the liver and an increase in the spleen.(95) Whereas the amount in the liver was, on average, higher than that in the spleen at 1 h, it was higher in the spleen compared to the liver at 24 h.
https://pubs.acs.org/doi/10.1021/acsnano.8b04758#
Radioactivity was detected in the stomach and intestine but not in any other major organs at 4 h. The signal was no longer detectable at 24 h, suggesting no intestinal adsorption of PEGylated GO.
Importantly, in both studies, a large amount of radioactivity was observed in the bladder at early time points. These results suggested that a large amount of i.v.-injected GO sheets had undergone renal glomerular filtration, as confirmed by the transient presence of radiolabeled GO sheets in kidneys and the detection of GO sheets in the urine.
Single- to few-layer GO sheets (lateral dimension: 100–400 nm with DOTA, thickness: 2–10 nm) were found to accumulate in both liver and spleen, with a decrease of radioactivity from 1 to 24 h in the liver and an increase in the spleen.(95) Whereas the amount in the liver was, on average, higher than that in the spleen at 1 h, it was higher in the spleen compared to the liver at 24 h.
https://pubs.acs.org/doi/10.1021/acsnano.8b04758#
ACS Publications
Safety Assessment of Graphene-Based Materials: Focus on Human Health and the Environment
Graphene and its derivatives are heralded as “miracle” materials with manifold applications in different sectors of society from electronics to energy storage to medicine. The increasing exploitation of graphene-based materials (GBMs) necessitates a comprehensive…
Scientists identify natural SARS-CoV-2 super immunity against 23 variants
https://www.news-medical.net/news/20210705/Scientists-identify-natural-SARS-CoV-2-super-immunity-against-23-variants.aspx
https://www.news-medical.net/news/20210705/Scientists-identify-natural-SARS-CoV-2-super-immunity-against-23-variants.aspx
News-Medical.net
Scientists identify natural SARS-CoV-2 super immunity against 23 variants
The antibodies are capable of neutralizing a wide range of SARS-CoV-2 variants even at sub-nanomolar concentrations. In addition, the combinations of these antibodies reduce the risk of generating escape mutants in vitro. The study is published in the journal…
Forwarded from Mike Yeadon
Important: just out, updated treatment guidelines for COVID-19.
Do not be frightened of this virus. It represents a serious heath threat almost exclusively to those towards the end of their lives (because of advanced age & pre-existing illnesses).
It’s the most treatable respiratory viral illness ever.
That your government has suppressed this information is murder. They did it knowing it’s effects.
The most frightening aspect of this ‘crisis’ is governments tyrannical responses & their idiotic & ever changing ‘advice’.
It’s not advice, though, if it?
Not when you can be arrested & fined for going against illogical & unproven ‘measures’.
I urge you to state publicly “I am no longer comfortable with what’s going on. I’m questioning what the dickens is going on. Why are voices who also dispute Govts position almost always immediately smeared & censored. Something bad is happening & I’m scared”.
You do that and many people, grateful for your courageous lead, will follow with doubts if their own.
Do this often enough & govt will stop stripping us of out rights.
Remain quiet & the end of free humanity is imminent.
Best wishes
Dr Mike Yeadon
Do not be frightened of this virus. It represents a serious heath threat almost exclusively to those towards the end of their lives (because of advanced age & pre-existing illnesses).
It’s the most treatable respiratory viral illness ever.
That your government has suppressed this information is murder. They did it knowing it’s effects.
The most frightening aspect of this ‘crisis’ is governments tyrannical responses & their idiotic & ever changing ‘advice’.
It’s not advice, though, if it?
Not when you can be arrested & fined for going against illogical & unproven ‘measures’.
I urge you to state publicly “I am no longer comfortable with what’s going on. I’m questioning what the dickens is going on. Why are voices who also dispute Govts position almost always immediately smeared & censored. Something bad is happening & I’m scared”.
You do that and many people, grateful for your courageous lead, will follow with doubts if their own.
Do this often enough & govt will stop stripping us of out rights.
Remain quiet & the end of free humanity is imminent.
Best wishes
Dr Mike Yeadon
Forwarded from Mike Yeadon
The chief midwifery person is in receipt of money from the BMGF.
She’s pushing Covid19 vaccination in pregnancy despite there being clear evidence of a threat to reproductive health.
It’s just revolting.
She’s pushing Covid19 vaccination in pregnancy despite there being clear evidence of a threat to reproductive health.
It’s just revolting.
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Recall last year that anyone even suggesting “chipping people” (I recall Ian Brown’s Little Seed, Big Tree foresaw that) was called a conspiracy theorist.
I’d invite any of those idiots to defend this by Israel (rather, their notorious PM, Netanyahu).
Anyone?
Mr Brown? How the dickens did you know?
Everything in your song has happened or been suggested already & we’re nowhere near the horrible middle of this.
Mike Y
I’d invite any of those idiots to defend this by Israel (rather, their notorious PM, Netanyahu).
Anyone?
Mr Brown? How the dickens did you know?
Everything in your song has happened or been suggested already & we’re nowhere near the horrible middle of this.
Mike Y
Forwarded from Deleted Account
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Forwarded from Not On The Beeb - Stuff the BBC forgot to tell you... (Mark Playne)
In 1912 the Titanic sinks with 1,502 fatalties making instant world headlines.
In 2021, the experimental 'vaccine' roll out kills 1,517 Brits and the BBC brush the numbers under a carpet.
The social media giants censor anyone daring to publish the numbers shown below.
Stats obtained directly from the UKs government's official MHRA website.
CURRENT 30th July MHRA Yellow Card Reporting of adverse events, which only includes data up until 21st July 2021
* Pfizer - 20.4million people - 33.3m doses - Yellow Card reporting rate - 1-in-215 people impacted
* Astrazeneca - 24.7m people - 47.9m doses - Yellow Card reporting rate - 1-in-110 people impacted
* Moderna - 1.3m people - 1.6m doses - Yellow Card reporting rate - 1-in-118 people impacted
Overall 1-in-140 people experience a Yellow Card Adverse Event.
The industry expected 1 in 10 people to have a reaction, meaning real numbers could be 14X higher.
To learn about the unexpected and unrecorded side effect of vaccine-induced magnetism see more at www.notonthebeeb.co.uk/magnetism
Reports (total people reporting injury)
95,040 (Pfizer) + 224,252 (AZ) + 10,990 (Moderna) + 958 (Unknown)
Total = 331,240 (on average having about three of the below reactions)
Fatalities
466 (Pfizer)
1018 (AZ)
8 (Moderna)
25 (Unknown jab)
Total = 1,517
Acute Cardiac
4020 (Pfizer) + 8814 (AZ) + 320 (Moderna) + 30 (Unknown)
Total = 13,184
Myocardial Infarction & Heart Failure
208 (Pfizer) + 467 (AZ) + 11 (Moderna) + 6 (Unknown)
Total = 692
Anaphylaxis
437 (Pfizer) + 793 (AZ) + 27 (Moderna) + 1 (Unknown)
Total = 1258
Blood Disorders - 8707 (Pfizer) + 7202 (AZ) + 646 (Moderna) + 38 (Unknown)
Total = 16,593
Infections - 6341 (Pfizer) + 17,575 (AZ) + 518 (Moderna) + 84 (Unknown)
Total = 24,518
Herpes - 1479 (Pfizer) + 2390 (AZ) + 51 (Moderna) + 13 (Unknown)
Total = 3,933
Head pain
19,629 (Pfizer) + 82,697 (AZ) + 1716 (Moderna) + 213 (Unknown)
Total = 104,255
Migraines
- 2164 (Pfizer) + 7857 (AZ) + 197 (Moderna) + 26 (Unknown) Total = 10,244
Eye Disorders
- 4407 (Pfizer) + 13,339 (AZ) + 339 (Moderna) + 45 (Unknown) Total = 18,130
Blinded
81 (Pfizer) + 266 (AZ) + 9 (Moderna) + 3 (Unknown)
Total = 359
Deaf
- 167 (Pfizer) + 342 (AZ) + 10 (Moderna)
Total = 519
Psychiatric Disorders
5224 (Pfizer) + 16,555 (AZ) + 620 (Moderna) + 69 (Unknown) Total = 22,468
Skin Disorders
19,044 (Pfizer) + 49,260 (AZ) + 5553 (Moderna) + 188 (Unknown)
Total = 74,045
Spontaneous Abortions - 197 + 7 stillbirth/foetal death (Pfizer) + 167 + 3 stillbirth (AZ) + 16 + 1 foetal death (Moderna) + 1 (Unknown)
Total = 381 + 11
Facial Paralysis incl. Bell’s Palsy - 612 (Pfizer) + 811 (AZ) + 37 (Moderna) + 5 (Unknown)
Total = 1,465
Nervous System Disorders - 47,255 (Pfizer) + 170,969 (AZ) + 4904 (Moderna) + 551 (Unknown)
Total = 223,679
Strokes and CNS haemorrhages - 467 (Pfizer) + 1892 (AZ) + 13 (Moderna) + 6 (Unknown)
Total = 2,378
Guillian Barre Syndrome
- 38 (Pfizer) + 362 (AZ) + 2 (Moderna) + 5 (Unknown)
Total = 407
Loss of balance - 7443 (Pfizer) + 23,850 (AZ) + 1067 (Moderna) + 80 (Unknown)
Total = 32,440
Tremors
-1133 (Pfizer) + 9581 (AZ) + 109 (Moderna) + 36 (Unknown)
Total = 10,859
Pulmonary Embolism
313 (Pfizer) + 1471 (AZ) + 8 (Moderna) + 8 (Unknown)
Total = 1,800
Deep Vein Thrombosis
197 (Pfizer) + 1087 (AZ) + 7 (Moderna) + 8 (Unknown)
Total = 1,299
Respiratory Disorders
11,516 (Pfizer) + 26,785 (AZ) + 824 (Moderna) + 93 (Unknown) Total = 39,218
Seizures - 629 (Pfizer) + 1808 (AZ) + 79 (Moderna) + 8 (Unknown)
Total = 2,524
Paralysis
- 256 (Pfizer) + 693 (AZ) + 25 (Moderna) + 4 (Unknown)
Total = 978
Vertigo/Tinnitis -
2367 (Pfizer) + 6074 (AZ) + 207 (Moderna) + 19 (Unknown)
Total = 8667
Muscle & Tissue Disorders - 32,555 (Pfizer) + 96,523 (AZ) + 3444 (Moderna) + 323 (Unknown)
Total = 132,845
Reproductive/Breast - 13,599 (Pfizer) + 15,366 (AZ) + 1688 (Moderna) + 94 (Unknown)
Total = 30,747
See source here
Read more and share off-telegram with this link
In 2021, the experimental 'vaccine' roll out kills 1,517 Brits and the BBC brush the numbers under a carpet.
The social media giants censor anyone daring to publish the numbers shown below.
Stats obtained directly from the UKs government's official MHRA website.
CURRENT 30th July MHRA Yellow Card Reporting of adverse events, which only includes data up until 21st July 2021
* Pfizer - 20.4million people - 33.3m doses - Yellow Card reporting rate - 1-in-215 people impacted
* Astrazeneca - 24.7m people - 47.9m doses - Yellow Card reporting rate - 1-in-110 people impacted
* Moderna - 1.3m people - 1.6m doses - Yellow Card reporting rate - 1-in-118 people impacted
Overall 1-in-140 people experience a Yellow Card Adverse Event.
The industry expected 1 in 10 people to have a reaction, meaning real numbers could be 14X higher.
To learn about the unexpected and unrecorded side effect of vaccine-induced magnetism see more at www.notonthebeeb.co.uk/magnetism
Reports (total people reporting injury)
95,040 (Pfizer) + 224,252 (AZ) + 10,990 (Moderna) + 958 (Unknown)
Total = 331,240 (on average having about three of the below reactions)
Fatalities
466 (Pfizer)
1018 (AZ)
8 (Moderna)
25 (Unknown jab)
Total = 1,517
Acute Cardiac
4020 (Pfizer) + 8814 (AZ) + 320 (Moderna) + 30 (Unknown)
Total = 13,184
Myocardial Infarction & Heart Failure
208 (Pfizer) + 467 (AZ) + 11 (Moderna) + 6 (Unknown)
Total = 692
Anaphylaxis
437 (Pfizer) + 793 (AZ) + 27 (Moderna) + 1 (Unknown)
Total = 1258
Blood Disorders - 8707 (Pfizer) + 7202 (AZ) + 646 (Moderna) + 38 (Unknown)
Total = 16,593
Infections - 6341 (Pfizer) + 17,575 (AZ) + 518 (Moderna) + 84 (Unknown)
Total = 24,518
Herpes - 1479 (Pfizer) + 2390 (AZ) + 51 (Moderna) + 13 (Unknown)
Total = 3,933
Head pain
19,629 (Pfizer) + 82,697 (AZ) + 1716 (Moderna) + 213 (Unknown)
Total = 104,255
Migraines
- 2164 (Pfizer) + 7857 (AZ) + 197 (Moderna) + 26 (Unknown) Total = 10,244
Eye Disorders
- 4407 (Pfizer) + 13,339 (AZ) + 339 (Moderna) + 45 (Unknown) Total = 18,130
Blinded
81 (Pfizer) + 266 (AZ) + 9 (Moderna) + 3 (Unknown)
Total = 359
Deaf
- 167 (Pfizer) + 342 (AZ) + 10 (Moderna)
Total = 519
Psychiatric Disorders
5224 (Pfizer) + 16,555 (AZ) + 620 (Moderna) + 69 (Unknown) Total = 22,468
Skin Disorders
19,044 (Pfizer) + 49,260 (AZ) + 5553 (Moderna) + 188 (Unknown)
Total = 74,045
Spontaneous Abortions - 197 + 7 stillbirth/foetal death (Pfizer) + 167 + 3 stillbirth (AZ) + 16 + 1 foetal death (Moderna) + 1 (Unknown)
Total = 381 + 11
Facial Paralysis incl. Bell’s Palsy - 612 (Pfizer) + 811 (AZ) + 37 (Moderna) + 5 (Unknown)
Total = 1,465
Nervous System Disorders - 47,255 (Pfizer) + 170,969 (AZ) + 4904 (Moderna) + 551 (Unknown)
Total = 223,679
Strokes and CNS haemorrhages - 467 (Pfizer) + 1892 (AZ) + 13 (Moderna) + 6 (Unknown)
Total = 2,378
Guillian Barre Syndrome
- 38 (Pfizer) + 362 (AZ) + 2 (Moderna) + 5 (Unknown)
Total = 407
Loss of balance - 7443 (Pfizer) + 23,850 (AZ) + 1067 (Moderna) + 80 (Unknown)
Total = 32,440
Tremors
-1133 (Pfizer) + 9581 (AZ) + 109 (Moderna) + 36 (Unknown)
Total = 10,859
Pulmonary Embolism
313 (Pfizer) + 1471 (AZ) + 8 (Moderna) + 8 (Unknown)
Total = 1,800
Deep Vein Thrombosis
197 (Pfizer) + 1087 (AZ) + 7 (Moderna) + 8 (Unknown)
Total = 1,299
Respiratory Disorders
11,516 (Pfizer) + 26,785 (AZ) + 824 (Moderna) + 93 (Unknown) Total = 39,218
Seizures - 629 (Pfizer) + 1808 (AZ) + 79 (Moderna) + 8 (Unknown)
Total = 2,524
Paralysis
- 256 (Pfizer) + 693 (AZ) + 25 (Moderna) + 4 (Unknown)
Total = 978
Vertigo/Tinnitis -
2367 (Pfizer) + 6074 (AZ) + 207 (Moderna) + 19 (Unknown)
Total = 8667
Muscle & Tissue Disorders - 32,555 (Pfizer) + 96,523 (AZ) + 3444 (Moderna) + 323 (Unknown)
Total = 132,845
Reproductive/Breast - 13,599 (Pfizer) + 15,366 (AZ) + 1688 (Moderna) + 94 (Unknown)
Total = 30,747
See source here
Read more and share off-telegram with this link
Not On The Beeb
MAGNETISM | Not On The Beeb
Since the start of time, no plant, animal or human has ever been magnetic.
Since the vaccination rollout, people are now showing clear and proven magnetic properties.
Since the vaccination rollout, people are now showing clear and proven magnetic properties.
This is important if & when an alleged health crisis by variants occurs.
If it’s real & severe & sometimes lethal side effects of vaccination, then potentially those agents found useful against SARS-CoV-2 might save your life.
So get memorising
Mike
If it’s real & severe & sometimes lethal side effects of vaccination, then potentially those agents found useful against SARS-CoV-2 might save your life.
So get memorising
Mike
Forwarded from YKIchannel
The link below shows a Directory of doctors prescribing outpatient anti-COVID-19 Therapy (incl. e.g. the use of Ivermectin or Hydrochloroquine).
The Netherlands are not in this list, but the European countries France, Spain, Portugal, Italy, the UK, Ireland and Austria are included, as well as Hungary, Poland, the Czech Republic, Slovakia, Bulgaria and Macedonia.https://www.exstnc.com/ UK
SUPER33
SUPER33 - Huat Heng Ong Cai Sen Lai Liau Exstnc
Super33 si situs yang ho lu lang hoki dan jackpot jumbo karena dewa cai sen lai khi ini situs, so u lang came join tong kim mai kok tan.
Forwarded from Mike Yeadon
YouTube
Ambulatory Treatment of COVID-19. Peter McCullough, MD
Recorded 10/11/2020
Background: Pathophysiological Basis and Rationale for Early Outpatient Treatment of SARS-CoV-2 (COVID-19) Infection"
https://www.amjmed.com/article/S0002-9343(20)30673-2/fulltext
Slides from video: https://aapsonline.org/mccullough…
Background: Pathophysiological Basis and Rationale for Early Outpatient Treatment of SARS-CoV-2 (COVID-19) Infection"
https://www.amjmed.com/article/S0002-9343(20)30673-2/fulltext
Slides from video: https://aapsonline.org/mccullough…