Wanted Influenza – Last Seen July 2020

Provisional Mortality Statistics

Provisional deaths data for measuring changes in patterns of mortality during the COVID-19 pandemic and recovery period.

Reference period Jan 2020 – May 2021.

Check the full report here

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The following article posted on Spectator Australia The past two years have seen the trust many Australians’ have in their institutions brought to an all-time

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  1. COVID VACCINES – DIRE WARNINGS in this Paper by Seneff & Nigh – damage from these vaccines is potentially catastrophic and transgenerational – and now they have targets on our children.
    The rats will be scurrying from an exploding ship when the population learn the true facts of these shocking experimental covid vaccines – please read these papers – I note today, that already as at 16.9.2021 23,751,922 of these experimental jabs have been coerced/forced on Australians and being mandated for ever increasing population sectors – this grossly violating universal informed consent codes.
    Also Paper from Classen Immunotherapies.

    PLEASE READ THESE PAPERS AS OUR POLITICIANS are incapable of (allegedly) independent and unbiased research as their extreme pro-vaccination lobby involvement/stance proves and allegedly throughout the entire Australian Government Vaccinations Policy is rife with Conflicts of Interest -it’s shocking and they are answerable to no one. Likewise – who in the hell allowed mainstream media empires to be calling the shots and virtual mouthpieces for Pharmaceutical Industry (allegedly) – WRONG WRONG WRONG. They all have to be stopped. Read the Papers – the DIRE WARNINGS.


    Worse Than the Disease? Reviewing Some Possible
    Unintended Consequences of the mRNA Vaccines
    Against COVID-19
    Stephanie Seneff and Greg Nigh
    Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge MA, 02139, USA, E-mail:
    [email protected]
    Naturopathic Oncology, Immersion Health, Portland, OR 97214, USA
    Operation Warp Speed brought to market in the United States two mRNA vaccines, produced by Pfizer and
    Moderna. Interim data suggested high efficacy for both of these vaccines, which helped legitimize Emergency Use Authorization (EUA) by the FDA. However, the exceptionally rapid movement of these vaccines through controlled trials and into mass deployment raises multiple safety concerns. In this review we first describe the technology underlying these vaccines in detail. We then review both components of and the intended biological response to these vaccines, including production of the spike protein itself, and their potential relationship to a wide range of both acute and long-term induced pathologies, such as blood disorders, neurodegenerative diseases and autoimmune diseases. Among these potential induced pathologies, we discuss the relevance of prion-protein-related amino acid sequences within the spike protein. We also present a brief review of studies supporting the potential for spike protein “shedding”, transmission of the protein from a vaccinated to an unvaccinated person, resulting in symptoms induced in the latter. We finish by addressing a common point of debate, namely, whether or not these vaccines could modify the DNA of those receiving the vaccination. While there are no studies demonstrating definitively that this is happening, we provide a plausible scenario, supported by previously established pathways for transformation and transport of genetic material, whereby injected mRNA could ultimately be incorporated into germ cell DNA for transgenerational transmission. We conclude with our recommendations regarding surveillance that will help to clarify the long-term effects of these experimental drugs and allow us to better assess the true risk/benefit ratio of these novel technologies.
    Full Paper >

    COVID-19 RNA Based Vaccines and the Risk of Prion Disease
    Classen Immunotherapies, Inc., 3637 Rockdale Road, Manchester
    MD 21102, E-mail: [email protected]
    J. Bart Classen, MD*
    Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARSCoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing. In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients. The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations. In the current analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified. Two GGΨA sequences were found. Potential G Quadruplex sequences are possibly present but a more sophisticated computer program is needed to verify these. Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration.
    The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases.
    The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit.
    Full Paper >

    and >
    See Australian influenza vaccines information and the ATROCIOUS list of damaging/destructive side effects
    FLUADQUAD Influenza virus vaccine for 65 years and over
    List of damage/ side effects – ABSOLUTELY ATROCIOUS !!
    The most common adverse events were local reactions, myalgia, and headache.[Ref]
    Very common (10% or more): Tenderness (89%), erythema/redness (76.4%), pain (73.8%), induration (58.4%), swelling (56.8%), injection-site pruritus (46.9%), itching (28%), bruising (18%), injection-site ecchymosis (14.9%), mass (11%)
    Common (1% to 10%): Reaction, hemorrhage
    Postmarketing reports: Cellulitis, injection site inflammation, injection site sterile abscess[Ref]
    Very common (10% or more): Crying abnormal (41.2%), malaise (38%), fever (16%)
    Common (1% to 10%): Chest tightness
    Rare (less than 0.1%): Death
    Postmarketing reports: Hot flashes/flushes[Ref]
    Very common (10% or more): Myalgia (40%)
    Common (1% to 10%): Chills/shivering, back pain
    Postmarketing reports: Muscle weakness, arthritis, arthralgia, myasthenia[Ref]

    Nervous system
    Very common (10% or more): Headache (40%), drowsiness (37.7%), lethargy (14%)
    Common (1% to 10%): Migraine
    Postmarketing reports: Neuralgia, paresthesia, convulsions (including febrile seizures), encephalopathy, neuritis or neuropathy, transverse myelitis, Guillain-Barre syndrome, abnormal gait, dizziness, hypoesthesia, hypokinesia, tremor, somnolence, syncope, facial or cranial nerve paralysis, encephalopathy, limb paralysis, confusion, paralysis (including Bell’s Palsy), vertigo, exacerbation of symptoms of mitochondrial encephalomyopathy (Leigh syndrome), meningitis, eosinophilic meningitis, vaccine-associated encephalitis[Ref]
    Very common (10% or more): Runny nose/nasal congestion (58%), cough (15%), upper respiratory tract infection (13%)
    Common (1% to 10%): Sore throat, cough, oropharyngeal pain, rhinorrhea, wheezing, pharyngolaryngeal pain, nasopharyngitis
    Postmarketing reports: Rhinitis, laryngitis, dyspnea, dysphonia, bronchospasm, throat tightness, pharyngitis, epistaxis[Ref]
    Very common (10% or more): Vomiting (15%), nausea (14.9%) diarrhea (13%)
    Postmarketing reports: Dysphagia, abdominal pain, swelling of the mouth, throat, and/or tongue[Ref]
    Very common (10% or more): Loss of appetite (33.3%), decreased appetite (21%)[Ref]
    Very common (10% or more): Irritability (54%)
    Postmarketing reports: Insomnia[Ref]
    Postmarketing reports: Allergic reactions including anaphylactic shock, serum sickness, and death; Stevens-Johnson syndrome[Ref]
    Common (1% to 10%): Infection, influenza-like illness
    Postmarketing reports: Cellulitis[Ref]
    Common (1% to 10%): Facial swelling
    Postmarketing reports: Pruritus, urticaria, rash, angioedema, sweating, flushing, pallor, rash, erythema multiforme[Ref]
    Common (1% to 10%): Reddened eyes
    Postmarketing reports: Eye pain, photophobia, conjunctivitis, eye irritation, eye swelling, eyelid swelling, ocular hyperemia[Ref]
    Postmarketing reports: Transient thrombocytopenia, lymphadenopathy[Ref]
    Frequency not reported: Pleuropericarditis with effusions
    Postmarketing reports: Tachycardia, pericarditis, vasculitis, vasodilation/flushing[Ref]
    Postmarketing reports: Vasculitis with transient renal involvement[Ref]
    Common (1% to 10%): Dysmenorrhea[Ref]
    1. “Product Information. Fluarix 2014-2015 (influenza virus vaccine, inactivated).” GlaxoSmithKline, Research Triangle Park, NC.
    2. “Product Information. FluLaval Quadrivalent 2015-2016 (influenza virus vaccine, inactivated).” GlaxoSmithKline, Research Triangle Park, NC.
    More >


    FLUARIXTETRA – Influenza Virus Vaccine for babies 6 months and up to 65 years
    List of damage/side effects – ABSOLUTELY ATROCIOUS !!
    Extensive list including >
    Nervous system
    Very common (10% or more): Headache (40%), drowsiness (37.7%), lethargy (14%)
    Common (1% to 10%): Migraine
    Postmarketing reports: Neuralgia, paresthesia, convulsions (including febrile seizures), encephalopathy, neuritis or neuropathy, transverse myelitis, Guillain-Barre syndrome, abnormal gait, dizziness, hypoesthesia, hypokinesia, tremor, somnolence, syncope, facial or cranial nerve paralysis, encephalopathy, limb paralysis, confusion, paralysis (including Bell’s Palsy), vertigo, exacerbation of symptoms of mitochondrial encephalomyopathy (Leigh syndrome), meningitis, eosinophilic meningitis, vaccine-associated encephalitis[Ref]
    More >

    gsk Fluarix Tetra – Inactivated split influenza vaccine
    Product Information leaflet
    More Product Information and warnings

    FLUQUADRI – Influenza Virus Vaccine for babies 6 months up to 65 years


    More Product Information/Warnings/Damage/Side Effects

    Confidential Report to Authorities from Glaxo Smith Kline 16 Dec. 2011
    Extract from Natural Health website >
    Confidential files from GlaxoSmithKlein detail heartbreaking connection between SIDS and childhood injections
    by: Sara Middleton, staff writer | July 8, 2021
    SIDS AND CHILDHOOD INJECTIONS (NaturalHealth365) Sudden infant death syndrome (SIDS) is a heartbreaking tragedy that touches thousands of American families every year. Boston Children’s Hospital defines the “sudden and unexplained death of a baby younger than 1 year old,” SIDS is yet to be fully understood, and its exact causes are unknown.
    But despite what fact-checkers claim, there is evidence to suggest a causal link between childhood injections and SIDS, at least in some cases. Indeed, a 2011 confidential report from billion-dollar pharmaceutical company GlaxoSmithKline shares some of this evidence in great detail – along with hundreds of other troubling drug side effects.
    Confidential files from major Big Pharma company detail thousands of adverse effects, including 13 cases of SIDS, following routine childhood injections
    The files are part of GlaxoSmithKline’s (GSK) Biological Clinical Safety and Pharmacovigilance report on their drug known as Infanrix Hexa – a combined Diptheria Tetanus and Acelluar Pertusis, Hepatitis B, inactivated Poliomyelitis and Haemophilus influenza type B shot. Children are expected to receive 3 doses of Infanrix Hexa – at age six weeks, 3 months, and 5 months.

    The report, released to the public by the Italian Court of Justice Nicola Di Leo, contains over 1,200 pages of adverse side effects reported in children and infants following routine injections. Notably, the data included in this report spans just two years – from October 2009 to October 2011.
    “In the reporting period,” writes one medical doctor in his analysis of the report, “one must conclude that Infanrix Hexa vaccine could have been responsible for at least 69 [infant] deaths.” Referring directly to the GSK data, Dr. Jacob M Puliyel says it points to “a clear relationship of ‘sudden death’” and the shots. He notes:
    42 deaths occurred within the first three days post-jab
    16 deaths occurred between day 3 and day 5
    3 deaths occurred between day 6 and 8
    2 deaths occurred between day 9 and 11
    2 deaths occurred in all the remaining 10 days post-jab
    “The fact that rate of deaths decreases rapidly and continuously as time elapses after the day of immunization,” Dr. Puliyel says, “is clear that the deaths are related to the [injection] episode.” The babies who died as a result of these injections passed away of SIDS or other complications, including meningitis, sepsis, and severe hypoxic-ischemic encephalopathy (cerebral palsy leading to quadriplegia and microcephaly).
    In some situations, a family history of post-jab death was also evident. For example, while discussing the case of a 2 month-old girl who died 24 hours after receiving Infanrix Hexa, GSK notes that the “subject’s brother died 2 years ago” also after getting an injection.
    More shocking admissions can be found throughout the GSK report. A warning to anyone who wants to read it: many details are graphic and may be disturbing. More > https://www.naturalhealth365.com/sids-linked-to-childhood-injections-3895.html

    See the 2011 Confidential Report from billion dollar pharmaceutical company Glaxo Smith Kline shares files detailing thousands of adverse effects – NOTABLY, this data included in this Report spans JUST TWO YEARS from Oct. 2009 to Oct, 2011. CONFIDENTIAL GSK REPORT HERE >


    Contraindications – warnings and precautions- adverse reactions Sanofi Pasteur

    Search Vaccine Ingredients more here > https://www.procon.org/?s=vaccine%20ingredients

    I will continue to show this particular link hereunder of an allegedly damaging infant vaccine (which has since been ‘discontinued/withdrawn from use’) and it is alleged that it confirms the damage done previously to so many !! and the authorities and their interests, allegedly continued to deny any autism link also and other damage and allegedly all those people in Governments/Pharmaceutical Industries and their interests have allegedly destroyed the careers and lives over the alleged denials/cover up/lies/deception/greed/untouchable power and control. Again a reminder of more that has never been in mainstream media > THIS VACCINE HAS BEEN DISCONTINUED (but I remain horrified at (allegedly) the number of babies who were vaccine injured/sickened/died as a result) >

    Adverse events reported during post-approval use of Tripedia vaccine include idiopathic thrombocytopenic purpura, SIDS, anaphylactic reaction, cellulitis, autism, convulsion/grand mal convulsion, encephalopathy, hypotonia, neuropathy, somnolence and apnea.
    You can access the Vaccine Package Insert for this now discontinued vaccine by clicking on the link hereunder.- and NOTE Package insert – Page 11 some of the damage/side effects SIDS, AUTISM etc., from Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed Tripedia – This vaccine has now been discontinued.
    LINK HERE for Sanofi Pasteur product information 13 pages >
    Link package Information leaflet DPT vaccine which has now been discontinued

    May, 2020 Chief Health Officer, Jeannette Young, Queensland Health, the Queensland Premier and her Team, allegedly have forced Footballers against their Will which is allegedly, a blatant, brazen, reckless/wilful and negligent gross violation of Medical Ethics/INFORMED CONSENT/NUREMBERG CODE, to be forced to have flu vaccinations or any other vaccination or Medical Treatment INFORMED CONSENT – also From March, 2020 anyone involved in aged care ie working there, residents, visitors – it was allegedly mandated to have flu vaccinations and staff allegedly forced to have the Covid Jabs – you have now seen in this Paper from many independent sources the truth about the Covid jabs and also the flu vaccination information (and much more) and not the alleged misinformation and propaganda from the people in Governments and their massive interests.
    GUNPOINT MEDICINE – (allegedly) gross violation of Nuremberg Code and the rights of Informed Consent.
    REMEMBER to see the atrocious damaging side effects from FLU VACCINES previously in this Research Paper and the Covid Vaccines.

    Vaccination Policy – No Jab No Pay No Play Policy – (allegedly) Gunpoint Medicine – Gross Violation of Informed Consent/Nuremberg Code

    Australia forces/mandates vaccinations with it’s No Jab No Pay No Play Vaccination Policy allegedly initiated by Murdoch Media Empire/Tony Abbott/Malcolm Turnbull/Scott Morrison and ors. from 2016 (and in 2020 forced/mandated flu vaccinations in aged care etc. – See where Lawyers request Australian States remove the UnlawfulMandatory Flu Vaccination https://www.vaccinationdecisions.net/lawyers-request-australian-state-governments-remove-the-unlawful-mandatory-flu-vaccination/

    Citizens questioning the Australian Government’s vaccination policy are being ignored and even censored. Big Pharma is controlling taxpayer-funded vaccination policy now. Click on the YouTube link in the above picture to see Elizabeth Hart’s presentation Big Pharma’s hijacking of ‘over’-vaccination policy – Conflicts of interest and lack of transparency and accountability, presented at the 2018 Sydney Vaccination Conference – The Censorship of the Vaccination Debate in Australia Today.
    This presentation examines the influence of powerful individuals such as Bill Gates and Rupert Murdoch, and the network of conflicted academics involved in industry-funded vaccine trials who are also influencing vaccination policy, particularly Terry Nolan, the former Chair of the Australian Technical Advisory Group on Immunisation, and Robert Booy, the Head of Clinical Research at the National Centre for Immunisation Research and Surveillance and Chair of the industry-funded Immunisation Coalition.
    There are also conflicts of interest in the evaluation and regulation of vaccine products. The Therapeutic Goods Administration assesses and registers vaccine products using manufacturer supplied data. The TGA is funded by industry for this service. The TGA’s role as the evaluator and regulator of vaccine products is compromised by its reliance on industry funding, the TGA has a conflict of interest.
    See more in the presentation Big Pharma’s hijacking of ‘over’-vaccination policy – Conflicts of interest and lack of transparency and accountability. https://www.youtube.com/watch?v=atKeooIrHE8
    Transcript of presentation: Conflicts of interest in vaccination policy. https://elizabethhart.files.wordpress.com/2018/07/conflicts-of-interest-in-vaccination-policy-e-hart.pdf
    Presentation also accessible on Facebook. https://www.facebook.com/nojabnopaynoway/videos/1761991957172323/
    Extensive information continued >

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