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The 'mask'arade continues.......

Discussion in 'Educating Doctors' started by Jack Kruse, Nov 26, 2020.

  1. Study in Italy: 94% of vaccinated patients had abnormal blood

    The use of dark-field microscopic analysis of fresh peripheral blood on a slide was once widespread in medicine, allowing a first and immediate assessment of the state of health of the corpuscular components of the blood. In the present study we analyzed with a dark-field optical microscope the peripheral blood drop from 1,006 symptomatic subjects after inoculation with an mRNA injection (Pfizer/BioNTech or Moderna), starting from March 2021. There were 948 subjects (94%of the total sample) whose bloodshowed aggregation of erythrocytes and the presence of particles of various shapes and sizes of unclear origin one month after the mRNA inoculation.In 12 subjects,blood was examined with the same method before vaccination, showing a perfectly normal hematological distribution. The alterations found after the inoculation of the mRNA injections further reinforce the suspicion that the modifications were due to the so-called “vaccines”themselves. We report 4 clinical cases, chosen as representative of the entire case series. Further studies are needed to define the exact nature of the particles found in the blood and to identify possible solutions to the problems they are evidently causing


    In the present study, blood samples of 1,006 symptomatic subjects after one or more anti-COVID mRNA injections from Pfizer/BioNTech or Moderna were analyzed under an optical microscope in the dark-field. Of the 1,006 cases, 948 (94.23% ) showed various alterations in their blood. Aggregation of erythrocytes were highlighted and exogenous point-like and self-luminescent particles in the dark-field were detected. The luminescence of those particles was markedly higher than that of oxygenated red blood cell walls. The particulate infiltrates, whatever they may consist of, gave the appearance of a starry sky at night.


    A Web of Science search for “graphene AND covid” produced 190 hits and “graphene AND vaccine” turned up 124 hits on July 30, 2022. However, a search for “graphene oxide” generated 133,756 dating from 1995 to the present. Taking account of the findings of Ou et al. (2016), showing that “graphene-family nanomaterials” have been associated with “physical destruction, oxidative stress, DNA damage, inflammatory response, apoptosis, autophagy, and necrosis” on account of their stressful impact on “toll-like receptors- . . . , transforming growth factor β- (TGF-β-) and tumor necrosis factor-alpha (TNF-α)”, if the mRNA concoctions by Pfizer and Moderna do contain the suspected graphene materials, they are implicated as disease causing in the recipients of those vaccines.


    In conclusion, such abrupt changes as we have documented in the peripheral blood profile of 948 patients have never been observed after inoculation by any vaccines in the past according to our clinical experience. The sudden transition, usually at the time of a second mRNA injection, from a state of perfect normalcy to a pathological one, with accompanying hemolysis, visible packing and stacking of red blood cells in conjunction with the formation of gigantic conglomerate foreign structures, some of them appearing as graphene-family super-structures, is unprecedented. Such phenomena have never been seen before after any “vaccination” of the past. In our collective experience, and in our shared professional opinion, the large quantity of particles in the blood of mRNA injection recipients is incompatible with normal blood flow especially at the level of the capillaries. As far as we know, such self-aggregation phenomena have only been documented after the COVID-19 mRNA injections were first authorized, then, mandated in some countries, and now are still being widely distributed in more than 12.3 billion doses (Bloomberg.com, 2022). Further studies are needed to determine the precise nature and purposes of the foreign particles found in the blood drops of about 94% of the mRNA recipients we have studied. Where do they come from and why are they in these injections?

    Last edited: Sep 19, 2022
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  2. JanSz

    JanSz Gold

    This Russian doctor did dark-field microscopic analysis of my blood.
    It was 20 years ago or more.

    How do you feel about this type of analysis now?

  3. @JanSz - knowing your "conditions" - may I suggest you askJack for a recommendation for a "decentralized quantum" MD whose specialty is in cancer.
    JanSz likes this.
  4. Jack Kruse

    Jack Kruse Administrator

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  7. Clinicians should be aware of subacute thyroiditis as a possible thyroid-related side effect of an inactivated SARS-CoV-2 vaccine.

    Case Report: Subacute thyroiditis after receiving inactivated SARS-CoV-2 vaccine (BBIBP-CorV) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9355607/

    Pi L, Lin J, Zheng Y, Wang Z, Zhou Z. Case Report: Subacute thyroiditis after receiving inactivated SARS-CoV-2 vaccine (BBIBP-CorV). Front Med (Lausanne). 2022 Jul 22;9:918721. doi: 10.3389/fmed.2022.918721. PMID: 35935798; PMCID: PMC9355607.

    Key paragraph:

    “As there are many proteins originated from or similar to the pathogen virus in the inactivated virus vaccines, molecular mimicry seems to play a potential role in the development of inactivated SARS-CoV-2-vaccine-related subacute thyroiditis. Spike (S) protein is an immunodominant antigen of SARS-CoV-2, which is also the target of neutralizing antibodies (8, 15, 17). A previous study has proven that there is similarity between S protein and various self-tissue proteins in human (18). It has also been shown that thyroid peroxidase (TPO) sequences share homology and similarity with sequences in S protein, which to extent supported another finding that human monoclonal antibodies against SARS-CoV-2 S protein react with TPO (19). Furthermore, by comparing immunogenic epitopes of SARS-CoV-2 with human proteins, Lyons-Weiler found a high degree of homology with various tissues including thyroid gland (20). In addition, a pilot study further implied that proinflammatory cytokines could increase the expression of angiotensin-converting-enzyme-2 (ACE-2), the receptor for cellular entry of SARS-CoV-2, which might facilitate the entering of SARS-CoV-2 into thyroid and contribute to the understanding of pathogenesis in subacute thyroiditis after SARS-CoV-2 infection or vaccination (21).”

    Author’s conclusion:

    “Inactivated SARS-CoV-2 vaccine may be a causal trigger leading to subacute thyroiditis. Clinicians should be aware of subacute thyroiditis as a possible thyroid-related side effect of an inactivated SARS-CoV-2 vaccine.”

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  9. JanSz

    JanSz Gold

    My 1 cent.
    Get these tests:

    TSH, T4, FT4, T3, FT3, RT3
    Thyroid Peroxidase (TPO) Ab
    Antithyroglobulin Ab

    Thyroiditis is a general term that refers to “inflammation of the thyroid gland”. Thyroiditis includes a group of individual disorders causing thyroidal inflammation but presenting in different ways. For example, Hashimoto’s thyroiditis is the most common cause of hypothyroidism in the United States.

    John Schumacher likes this.
  10. ND Hauf

    ND Hauf Pleb

  11. As of Oct 12th 2022, FDA informs Pfizer that -

    FDA is revising the following Fact Sheets: (releases by court order)

    1) Fact Sheet for Recipients and Caregivers About the Pfizer-BioNTech COVID-19 Vaccine and the Pfizer-BioNTech COVID19 Vaccine Bivalent (Original and Omicron BA.4/BA.5) to Prevent Coronavirus Disease (COVID-19) for Use in Individuals 5 Through 11 Years of Age;

    2) Fact Sheet for Healthcare Providers Administering Vaccine (Vaccination Providers): Emergency Use Authorization (EUA) of Pfizer-BioNTech COVID‑19 Vaccine to Prevent Coronavirus Disease 2019 (COVID-19) Primary Series For 5 Through 11 Years of Age Dilute Before Use;

    Table 3 continues to “require” / authorized: page 18

    This authorization also covers the use of the licensed COMIRNATY (COVID-19 Vaccine, mRNA) product when used to provide a third primary series dose at least 28 days following the second dose to individuals 12 years of age or older who have undergone solid organ transplantation or who are diagnosed with conditions that are considered to have an equivalent level of immunocompromise. - Page 19

    From page 26: Section F. –

    Pfizer Inc. will report to Vaccine Adverse Event Reporting System (VAERS):
    · Serious adverse events (irrespective of attribution to vaccination);
    · Cases of myocarditis;
    · Cases of pericarditis;
    · Cases of Multisystem Inflammatory Syndrome in children and adults; and
    · Cases of COVID-19 that result in hospitalization or death, that are reported to Pfizer Inc.

    These reports should be submitted to VAERS as soon as possible but no later than 15 calendar days from initial receipt of the information by Pfizer Inc.

    Question: What motive will hospitals have for reporting adverse effects from an injection when "they" don't even track the "effects" positive/negative to most of the prescriptions sold each and every day?

    Source: https://www.fda.gov/media/150386/download
    Last edited: Oct 31, 2022
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  12. Jack Kruse

    Jack Kruse Administrator

  13. Merry Christmas

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  14. upload_2022-12-24_16-7-14.png

    Attached Files:

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  15. caroline

    caroline New Member

    Merry Christmas from ES Johan to you and your beautiful family....

    See you again ....... soon hopefully
    Johan Lindstrøm likes this.
  16. Dr. @Jack Kruse - for your review:

    Dr. @Jack Kruse - As you may or may not know, I do not have the money to purchase time with you whether on a Q&A, consult, nor a "Farm-membership". The Silver-level purchase is the best I can do. So, I have no idea if you can afford the time from your schedule to dialog at this lower "level" of membership.​

    One of the most common tactics the medical industry uses to defend against the scrutiny of bad medical practices is to accuse those who question those practices (and thus make the public reluctant to receive them) of “killing their patients!” (under the logic that the treatment is so safe and effective that causing the public to avoid it equates to murder). Although I am used to seeing inflammatory approaches like this being used to silence debates, I was nonetheless quite taken aback by the WHO’s recent tweet (watch it; it’s only 52 seconds long):

    COVID is not novel.

    Reported May 7th 2004: "The global outbreak of severe acute respiratory syndrome (SARS) in 2003 resulted in more than 8000 cases and 774 deaths."

    This PBC article - published online 2004 May 7. doi: 10.1002/path.1560 “Organ distribution of severe acute respiratory syndrome (SARS) associated coronavirus (SARS‐CoV) in SARS patients: implications for pathogenesis and virus transmission pathways” –

    From the SARS‐CoV vaccine, its viral material can be found in lung, trachea/bronchus, stomach, small intestine, distal convoluted renal tubule, sweat gland, parathyroid, pituitary, pancreas, adrenal gland, liver and cerebrum. It is also now being found in oesophagus, spleen, lymph node, bone marrow, heart, aorta, cerebellum, thyroid, testis, ovary, uterus or muscle. The pathological changes found in these organs are caused directly by the cytopathic effect mediated by local replication of the SARS‐CoV vaccine, resulting in potential systemic failure(s).

    We know nature uses viruses to edit our genome;
    however, SARS is not natural, it was developed and patented (7279327) by the CDC on 19th April 2002.
    We also know the vaccine formulated SARS-CoV-2 spike protein S1 Receptor-Binding Domain (SPIKE) is designed to enhance the permeability of cells with the encapsulated engineered virus.

    Since this viral code is transformative, as the article above reports, its mutations are what concerns me. The symptoms "medically" maybe "less than" previous mutations; however, the imprint onto the human genome is permanent. What seems most interesting to me is what the human immune system "learned", or should I say did not learn - do to the formulation described above and how the human cell did not respond.

    May I introduce COVID & IL-10.
    • IL-10 on CD8+ T cells is depended on the strength of the antigenic signal, as CD8+ T cells recognizing different LCMV epitopes appear to have different IL-10 inhibition thresholds. <- This is where the COVID code sequence has been successful by limiting (reducing) or eliminating the CD8+T cell recognition antigenic signal.
    • Since the sequenced code of the COVID virus has shown the capacity to infect human cells without the detection of the CD8+ T cell recognition, the IL-10 response is not activated "well enough" to the invasion.
    • Thus, the editing of the human mRNA occurs without hindrance
    • The cell's replication code is permanently written, reducing the cell's future cells' response to this specific virus
    • All future cells will have a decrease response to COVID infection
    • The question is -> Is that a good thing?
    • What was the COVID code designed for...

    CRISPR is laying down patents to counter the damaged genes from SARS COVID-19 injections.

    Will only the wealthy survive?
    Last edited: Jan 31, 2023
  17. 5G Canary

    5G Canary Gold

    It isn’t about health or wealth... it’s about wisdom. Think of wisdom like a muscle... that is the muscle to strength each day. Because it needs to become huge in the next two years. Who is programming you? Nature or technology?

  18. Jack Kruse

    Jack Kruse Administrator

    Glad someone gets it
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