pseudo-science
We all need cheering up a bit, I’m sure.
Luckily, I found just the thing.
The New York Post reported that a former Versace model, Tom Casey, is crediting his youthful looks to drinking his own urine, and to perineum sunning (exposing your butt hole to sunshine). “I drink my own urine every morning — I call it hair of the dog!” Casey proclaimed, “the feeling is electric.” The ex-model also flushes his urine into his rectum and applies it to his skin as a moisturizer. 
“It wasn’t as bad as the mental barrier in my own mind,” the ex-catwalk star reminisced. “I felt a cool buzz. Intuitively, it just felt good. I drank my urine on and off for a while from there.”
Casey began drinking his own urine on a daily basis back in 2008 and hasn’t looked back. He has even completed a “seven-day urine fast,” drinking nothing but his own urine for an entire week. He also bottles his pee, lets it “ferment” and uses it in an enema. “I would cultivate my own urine and ferment it in a sealed Mason jar for two weeks before transferring it into my rectum,” he explained. “Aged urine enemas are so powerful for your health and I got my six-pack abs after doing them. It flushed out my gut and that’s when I got really ripped.”
Casey uses his urine also as a moisturizer, which he believes helps maintain his appearance. “What it did for my mood and muscle building was amazing. I put it on my skin, especially when I’m on the beach, and it’s so electrifying and strengthening,” he cooed. “It’s a big psychological leap for people to use their own urine as a moisturizer but it’s so euphoric and anti-aging. Uric acid is used in high-end skin care products.”
“I’m 55 years old and most people don’t look and feel like I do at my age. No one can deny that I’m ripped, and that’s down to the fact that I love being extremely healthy and practicing natural healing methods.”
Casey claims Big Pharma is terrified of people learning that the secret to their health lies within themselves.
“What so many pharmaceutical companies don’t want to tell you is that we as humans are the secret to health. That’s what I try to teach people in everything I do,” he stated.
“People should be scared if they’re eating s–tty food and doing pharmaceutical drugs. Why should they be scared to try their own urine?”
____________________________
Personally, I feel that Casey believes the sun might be shining out of his arse. In any case, it is hard to deny that the former Versace model is suffering from proctophasia and/or is taking the piss.
In Germany, the anti-vax movement is frighteningly strong and it constitutes one of the main reasons for the relatively immunization rate. In no small part, this is due to the many anti-vax Heilpraktiker who practice in Germany. In an attempt to put the record straight, the ‘Verband Klassischer Homöopathen Deutschlands’ (VKHD, Association of Classical Homeopaths of Germany) recently published an article entitled ‘Heilpraktiker – Homeopathy – Vaccination’ (Heilpraktiker – Homöopathie – Impfen). Here is a short excerpt (my translation):
… There is a clear conceptual similarity between homeopathy and vaccination [1]. From a historical point of view, this was already reflected in the early days of homeopathy, when its discoverer, Samuel Hahnemann, expressed himself very positively with regard to the smallpox vaccination newly introduced at that time [2]. Thus, it is historically wrong to insinuate that users of homeopathy have a fundamentally negative attitude towards vaccinations [3]. In this context, terms such as “vaccination opponents” or “vaccination refusers” are misleading and defamatory [4].
A critical (not skeptical) approach to the topic of vaccinations is basically a characteristic of people with medical expertise. Such an attitude corresponds to the critical consideration necessary in daily practice and in each individual case to advise on suitable therapy options [5]. Properly working alternative practitioners give differentiated advice accordingly [6]. A fundamentally vaccine-rejecting attitude is precisely not a characteristic of a critical assessment that has taken place. The same applies to an unreflective recommendation of vaccinations or therapy methods, without taking into account individual factors as well as scientific and social backgrounds [7].
For the VKHD, we cannot give exact figures on recovered, vaccinated, or unvaccinated members. It is not the responsibility of a professional association to demand such information from its members [8]. We assume that alternative practitioners who provide information on vaccinations do so in accordance with a responsible ethical attitude, regardless of their own vaccination status [9] …
I have taken the liberty of inserting some references into this text. They relate to my comments, which are as follows:
- A conceptual similarity between vaccination and homeopathy exists only in the minds of homeopaths. They often claim that both use highly diluted remedies. This is wrong because homeopathic remedies do not usually contain active ingredients, whereas vaccines do. This fact also explains why homeopathics do not produce immune reactions, whereas vaccines do.
- Correct! Hahnemann was in favor of vaccination. That is why he would be ashamed today if he knew how many homeopaths oppose vaccination.
- What has this got to do with ‘historical’? I assume that the ‘insinuations’ refer to the situation today. Further, I don’t think anyone is suggesting that all homeopaths are ‘fundamentally’ opposed to vaccination. However, that many of them are anti-vaxers is an indisputable fact.
- I would rather think they are accurate.
- Correct.
- How can they without any medical background?
- Is it to be implied here that real medical people do?
- Maybe not ‘demand’, but inquire or request would be possible and desirable, wouldn’t it?
- It is nice that you believe this. But belief is not evidence.
Aromatherapy, the use of essential oils for medicinal purposes, exists in several guises. One of them is inhalation aromatherapy which is a complementary therapy used in different clinical settings. But is there any sound evidence about its effectiveness?
The aim of this review was to assess the effectiveness of inhalational aromatherapy in the care of hospitalized pediatric patients.
A systematic review of clinical trials and quasi-experimental studies was conducted, based on PRISMA recommendations, searching Medline, Web of Science, Scopus, SciELO, LILACS, CINAHL, Science Direct, EBSCO, and updated databases. The Down and Black 2020, RoB 2020 CLARITY, and ROBINS-I 2020 scales were used through the Distiller SR software to verify the studies’ internal validity and risk of bias.
From 446 articles identified, 9 fulfilled the inclusion criteria. Seven were randomized controlled trials (RCTs), one pilot RCT, and one non-randomized quasi-experimental trial.
Different outcomes were analyzed, with pain being the most frequently measured variable. None of the 6 studies that evaluated pain showed significant effects with inhalation aromatherapy. Additionally, non-significant effects were found regarding nausea, vomiting, and behavioral/emotional variables.
The authors concluded that the findings are still inconclusive, and more evidence is required from future studies with high methodological quality, blinding, and adequate sample sizes.
Inconclusive?
Really?
Call me a skeptic, but I think the findings show quite clearly that there is no sound evidence to suggest that inhalation aromatherapy might be effective for kids.
This study assessed the effectiveness of Oscillococcinum in the protection from upper respiratory tract infections (URTIs) in patients with COPD who had been vaccinated against influenza infection over the 2018-2019 winter season.
A total of 106 patients were randomized into two groups:
- group V received influenza vaccination only
- group OV received influenza vaccination plus Oscillococcinum® (one oral dose per week from inclusion in the study until the end of follow-up, with a maximum of 6 months follow-up over the winter season).
The primary endpoint was the incidence rate of URTIs (number of URTIs/1000 patient-treatment exposure days) during follow-up compared between the two groups.
There was no significant difference in any of the demographic characteristics, baseline COPD, or clinical data between the two treatment groups (OV and V). The URTI incidence rate was significantly higher in group V than in group OV (2.9 versus 1.2 episodes/1000 treatment days, difference OV-V = -1.7; p=0.0312). There was a significant delay in occurrence of an URTI episode in the OV group versus the V group (mean ± standard error: 48.7 ± 3.0 versus 67.0 ± 2.8 days, respectively; p=0.0158). Limitations to this study include its small population size and the self-recording by patients of the number and duration of URTIs and exacerbations.
The authors concluded that the use of Oscillococcinum in patients with COPD led to a significant decrease in incidence and a delay in the appearance of URTI symptoms during the influenza-exposure period. The results of this study confirm the impact of this homeopathic medication on URTIs in patients with COPD.
Primary endpoint, comparison of the number of upper respiratory tract infections in the two treatment groups during follow-up
This prospective, randomized, single-center study was funded by Laboratoires Boiron, was conducted in the Pneumology Department of Charles Nicolle Hospital, Tunis, and was written up by a commercial firm specializing in writing for the pharmaceutical industry. The latter point may explain why it reads well and elegantly glosses over the many flaws of the trial.
If I did not know better, I might suspect that the study was designed to deceive us (Boiron would, of course, never do this!): The primary endpoint was the incidence rate of URTIs (number of URTIs/1000 patient-treatment exposure days) in the two groups during the follow-up period. This rate is calculated as the number of episodes of URTIs per 1000 days of follow-up/treatment exposure. The rates were then compared between the OV and V groups. The following symptoms were considered indicative of an URTI: fever, shivering, runny or blocked nose, sneezing, muscular aches/pain, sore throat, watery eyes, headaches, nausea/vomiting, diarrhoea, fatigue and loss of appetite.
This means that there was no verification whatsoever of the primary endpoint. In itself, this flaw would perhaps not be so bad. But put it together with the fact that patients were not blinded (there were no placebos!), it certainly is fatal.
In essence, the study shows that patients who perceive to receive treatment will also perceive to have fewer URTIs.
SURPRISE, SURPRISE!
The Corona Committee (Corona Ausschuss) was founded in Berlin in July 2020 by the lawyers Viviane Fischer, Antonia Fischer, Dr. Reiner Füllmich, and Dr. Justus Hoffmann. Its aim is to provide a “factual analysis” of the coronavirus events and the consequences of the measures taken against them. In live sessions lasting several hours, the committee hears experts from all COVID-affected fields.
In an interview, Dr. Fuellmich said: “The decision to set up a Corona Inquiry Committee came about in the first telephone conversation Viviane Fischer and I ever had. After I had spoken out in the USA via various videos since April 2020 about the fact that the principle ‘audiatur et altera pars’ (hear the other side as well) had been blatantly violated here on the part of the government, I had come back to Germany from the USA because I felt that this was now my place and that I had to stand up here to ensure that our democracy and our constitutional state did not go completely to the dogs. I wanted to organize a symposium on the legal issues surrounding Corona, but I didn’t know any critical lawyers in Germany. I called my old friend Dr. Wolfgang Wodarg, whom I knew from the Justice Working Group at Transparency International, and he then referred me to Viviane Fischer.”
The ‘Speerspitze‘, an “anonymous collective of contrarians, Corona deniers, Nazi witches and conspiracy heretics” considers the work of the Corona Committee to be “one of the most important pillars of the fight against the madness to which we have been subjected for the last year and a half and [has] great respect for all the activists, actors, and interviewees of the Committee who publicly denounce with their name and face what is happening.” Numerous further websites have joined in the promotion of the Corona Committee.
However, if you look at the information that the Corona Committee is disseminating, and if you are able to think critically, you are likely to come to very different conclusions:
– There is the expert who warns that the unvaccinated could soon be picked up and put into concentration camps. There is the threat of a “manhunt”, and loving parents might then have to hide their children under the boards of the floor at home to prevent them from being sprayed to death.
– There is the man who claims that Israel’s government is currently carrying out a holocaust on its own population (“You can see that by how many people are dying from the vaccinations”). A guest declares that there are “something like living octopuses” in the vaccine against Corona.
Anyone who takes a look at the many tediously long videos will quickly realize that every Corona denier, vaccination opponent, conspiracy theorist, mask opponent, and lateral thinker, no matter how paranoid, have their say here and spreads their pipe dreams under the guise of evidence-based information with the nodding approval of the lawyers present. Opposition is never raised and there is no trace of ‘audiatur et altera pars’; everyone agrees: worldwide, all governments are hell-bound at smashing everything there is to govern.
For those who are still not fed up, the website of the Corona Committee offers written answers to 31 very specific questions. Here is just one.
QUESTION: IS THE COVID-19 DISEASE SEVERE AND WIDESPREAD?
ANSWER: No, most people have no or only mild flu symptoms. Children and adolescents are extremely rarely affected. Post-mortem examinations by a Hamburg forensic pathologist on over 100 elderly people who died with a positive corona test revealed at least one other serious cause of death in all cases. Other published figures are mostly based on non-transparent attributions and assumptions without excluding other causes. Often, no attention was even paid to other pathogens or previous medication.
Factual analyses?
Afraid not!
For a long time, I have been wondering where the penetratingly vociferous opposition to COVID vaccinations in Germany might come from. After studying the dangerous nonsense that the Corona Committee has been spreading for many months, I wonder a little less.
(texts in German were translated by me)
Conversion therapy has been banned last week in Canada. These therapies – also known as sexual orientation change effort (SOCE), reparative therapy, reintegrative therapy, reorientation therapy, ex-gay therapy, and gay cure – rely on the assumption that sexual orientation can be changed, an idea long discredited by major medical associations in the US, the UK, France, and elsewhere. The new law makes “providing, promoting, or advertising conversion therapy” a criminal offense. It will also be an offense to profit from the provision of conversion therapy. In addition, the bill states a person cannot remove a “child from Canada with the intention that the child undergo conversion therapy outside Canada.” Prime Minister Justin Trudeau hailed the law’s Royal Assent: “It’s official: Our government’s legislation banning the despicable and degrading practice of conversion therapy has received Royal Assent — meaning it is now law.”
Conversion therapy is the attempt to change an individual’s sexual or gender identity by psychological, medical, or surgical interventions. Often, informed consent is insufficient or lacking. In conventional medicine, numerous treatments have been tried for this purpose, some of them dangerous and all of them ineffective. In alternative medicine, approaches that have been advocated include:
- Homeopathy (see below),
- Hypnotherapy,
- Spiritual healing,
- Prayer,
- Eye Movement Desensitization,
- Rebirthing,
- and others.
- Faith-based organizations or leaders
- Licensed healthcare professionals
- Unlicensed healthcare professionals
As previously reported, the German ‘Association of Catholic Doctors’ claimed that homeopathic remedies can cure homosexuality. Specifically, they advised that ‘…the working group ‘HOMEOPATHY’ of the Association notes homeopathic therapy options for homosexual tendencies…repertories contain special rubrics pointing to characteristic signs of homosexual behavior, including sexual peculiarities such as anal intercourse. And a homeopathic remedy called ‘Dr. Reckeweg R20 Glandular Drops for Women’ was claimed to treat “lesbian tendencies.” The product is “derived and potentised from fetal tissues.”
Several countries are now in the process of banning conversion therapy. France has already banned it and so has Germany. The UK government intends to introduce a legislative ban on the practice of conversion therapy. The consultation on how to best do this is open until 4 February 2022.
By guest blogger Ken Harvey
Loretta Marron was the catalyst. The ‘critical thinking’ bug hit her as a child, reinforced by a BSc in Physics. If something didn’t sound logical, she couldn’t let it go. She had to check. She killed many a party by disputing misinformation – with evidence. 
TV advertisements for magnetic underlays got her going, then homeopathic remedies, followed by ‘natural’ cures for cancer. To investigate outlandish claims and submit complaints, she needed to consult with experts. These included Professors John Dwyer (Medicine and Immunology) and Alastair MacLennan (Obstetrics and Gynaecology). They were always willing to help.
They also had concerns about universities teaching pseudoscience, such as ‘subluxation theory’ in chiropractic and ‘meridians’ in Traditional Chinese Medicine.
In late 2011, Professor Dwyer proposed that Loretta join forces with Professors Alastair MacLennan, Marcello Costa (neuroscientist), and Rob Morrison (science communicator) to form a new organisation promoting scientific evidence in health care. Friends of Science in Medicine (FSM) was born. John Dwyer was the inaugural President and Loretta Marron Chief Executive Officer (CEO).
The aim was to emphasise the importance of basing Australian health care on scientifically sound research and established scientific knowledge published in peer-reviewed journals of accepted standing. Valuing scientific rigour is especially important in an age where unsubstantiated health claims are rampant and scientific consensus is ‘imbalanced’ by the views of extremists.
FSM’s focus is helping consumers and health professionals to make more informed choices about medical interventions, medicines, and medical devices. We do this by submitting complaints about unethical practice, analysing policy, making submissions, encouraging regulators to act, and being a credible source of expertise for the media and others. We also encourage tertiary institutions and medicine and health sciences students to critically appraise therapeutic products and services as part of the courses offered.
Currently, FSM has more than 1,200 leading scientists, clinicians, lawyers, and consumer advocates as supporters. We also work closely with organisations such as Australian Skeptics and Choice (Australian Consumers Association).
I took over as President from John Dwyer in 2019. Loretta remains FSM CEO. The founding members continue their involvement as consultants. Ten years on, it’s worth reflecting on what has been achieved and the ongoing challenges.
An appendix lists some of the areas in which FSM has been involved and the outcomes achieved (often with the help of others).
Unethical promotion of therapeutic goods and services remain an ongoing concern. The advertising of therapeutic goods is subject to provisions in the Therapeutic Goods Advertising Code, first promulgated in 1999. Until July 2018, complaints about alleged Code violations were heard by the Therapeutic Goods Advertising Complaints Resolution Panel (CRP), thereafter by the Therapeutic Goods Administration (TGA).
FSM members submitted numerous complaints to the CRP and analysed the outcome. If a complaint was upheld, the CRP could only ‘recommend’ that it be removed. If it was not, the complaint was referred to the TGA for action. We found that certain companies consistently ignored the determinations of the CRP and, when referred to the TGA, took resulting action.
In July 2018, FSM engagement with numerous consultations and reviews eventually resulted in the TGA taking over the advertising complaint system. The TGA was given stronger investigative and compliance powers and a revised, legally enforceable advertising code. However, given the TGA’s previous track record, we continued to submit complaints, including many previously upheld by the CRP, but for which promotion continued.
An analysis of the first 12 months of the new system found that the TGA had classified most complaints as ‘low priority’. These were either ignored or closed by sending the advertiser a ‘Regulatory Obligation letter’ which stated that no further action would be taken. While the letter sometimes worked, often it did not. Stronger compliance powers were rarely used. The new complaint system was also less transparent than the one it replaced. For those low priority complaints with published outcomes, no details of the product, advertiser, or alleged Code violation were published, and no follow-up was recorded. Of 121 higher priority complaints, 79% failed to meet their key performance indicator, time to closure in 60–90 days. These included complaints about dangerous sports supplements and ineffective weight loss and hangover products.
In August 2020, an independent review of the first two years of the TGA’s compliant system was published. The study noted an unexpectedly high volume of complaints since the TGA took over the advertising complaints system, producing a large and growing backlog. A government-appointed consultant (ThinkPlace Pty Ltd) stated that providing more resources would not be in the public interest. Instead, they recommended a more cost-effective and efficient approach: amalgamating all complaints into an information database from which the TGA could consider compliance priorities.
As a result, complaints were closed by sending complainants a letter stating that their complaints will be used for ‘intelligence’ to set priorities. The TGA said risk assessment informed whether a complaint was converted into a case for investigation or stored in their information database to determine future compliance priorities. Therapeutic goods associated with COVID-19 were declared ‘priority 1’, while weight loss, hangover, and four other products groups were said to be ‘priority 2’.
A focus on COVID-19 stimulated the TGA to deal with some of these complaints more effectively. However, apart from token action on individual products, no systemic action was taken on weight loss, hangover products and many other objects of our complaints.
More recently, the TGA’s complaint database for 2018 -2020 has been removed and replaced by a new database containing only a few complaints pre-2021. In addition, the fields of many ‘products’ and ‘responsible person’, are missing. The TGA say that migration of data to the new system is continuing. Meanwhile, complainants now only receive an automated acknowledgment.
Transparency remains a problem as there is no clear indication of how many complaints the TGA receives, what they are about, how many are filed for ‘intelligence’’, how many are actioned, and what outcome eventuates.
Given this lamentable state of affairs, in association with Australian Skeptics, it is proposed to publish reports on all complaints submitted to the TGA in 2022 and their outcomes. Past experience shows that documenting problems, pointing out underlying issues and putting forward solutions can produce progress. But patience and persistence are required.
FSM has grappled with unethical advertising of pseudo-medical interventions. Controls differ for practitioners regulated by the Australian Health Practitioner Regulation Agency (AHPRA) and those regulated by State and Territory Health Complaints Commissioners. The former includes medical practitioners, pharmacists, nurses, chiropractors, osteopaths, and Traditional Chinese Medicine practitioners. The latter includes naturopaths, homeopaths, and practitioners of western herbal medicine.
FSM has held regular meetings with AHPRA senior managers. We have also met several of their national boards and attended stakeholder forums. Chiropractic was an initial focus. Many practitioners advertised that chiropractic care in pregnancy could shorten labour duration and prevent caesarean delivery – despite the absence of evidence. Pregnant women were warned that labour often resulted in the newborn babe’s spinal misalignment, which could lead to numerous problems unless put right by regular chiropractic adjustments. It was also claimed that chiropractic ‘adjustments’ could improve attention deficit hyperactivity disorder, infantile colic, and ear infection.
In 2015, FSM submitted hundreds of complaints to AHPRA, alleging that chiropractic websites were in breach of both s.133 of the Health Practitioner Regulation National Law Act 2009 and the Chiropractic Board of Australia’s Guidelines for advertising regulated health services. These provisions prohibit advertising which is false, misleading, or deceptive, creates an unreasonable expectation of beneficial treatment, or can encourage the indiscriminate or unnecessary use of health services.
Five years have passed since the Chiropractic Board first asked practitioners to ensure that their websites met legal advertising requirements. Over this time, the Board’s sole approach to this problem was educational. Although chiropractors consistently had the highest advertising complaints of all practitioners (38 per 1,000 chiropractors in 2013–14), no penalties nor disciplinary action had been applied for advertising offences.
FSM argued that repeated advertising offences required appropriate penalties. We also pointed out that some practitioners now invited patients to consult them about services they were no longer permitted to advertise. We said that limitations should be placed on chiropractic practice which lacked evidence.
AHPRA responded that, although it could act on misleading advertising, it had no power to restrict the scope of practice of chiropractors (or other registered practitioners). We said that, if lack of good evidence makes it illegal to publicly advertise a treatment, then it should be equally illegal to offer it to patients privately; after all, the real harm is caused by the treatment, not the advertising.
In 2019, following damning publicity and further representations, the Victorian Health Minister eventually instructed Safer Care Victoria (SCV) to undertake an independent review of the practice of chiropractic spinal manipulation on children under 12 years. The result was a recommendation that spinal manipulation should not be provided to children under 12 years of age, for general wellness or for the management of conditions such as hyperactivity disorders, infantile colic, or ear infections.
The Chiropractic Board has also stated that chiropractors are not trained to apply any direct treatment to an unborn child and should not deliver any treatment to the unborn child. Neither should they provide materials, information or advice that is anti-vaccination in nature. After numerous complaints from FSM members, the Chiropractic Board finally referred a prominent anti-vax chiropractor, Simon Floreani, to the Victorian Civil and Administrative Tribunal (VCAT). His registration was suspended for 6 months, and conditions placed on his re-registration.
FSM has not just been concerned about chiropractors. We have complained (with varied success) about medical practitioners promoting stem cell therapy for multiple sclerosis, Traditional Chinese Medical practitioners claiming that acupuncture can treat infertility and dubious laboratory tests used in complementary and alternative medicine.
In conclusion, the peddling of unproven and sometimes dangerous remedies has existed throughout human history.
There will always be companies (and individuals) who put the pursuit of profit before ethical behaviour. There will always be advocates for de-regulation and regulators captured by industry. To protect consumers there must be opposing forces. That is the role that FSM is proud to play, along with colleagues from the sceptical community and consumer movements.
Appendix
FSM activities and outcomes (often in association with others), 2011-2021.
- Removal of extravagant claims for acupuncture from the World Health Organization website and instigation of a WHO evidence review.
- Involvement in the 2015 Review of the Australian Government Rebate on Private Health Insurance for Natural Therapies. This led to removal of cover for therapies that lacked evidence such as homeopathy, iridology, reflexology and naturopathy (currently being reviewed again to see if additional evidence exits).
- Removal of unproven/disproven courses or modules from Australian universities.
- Removal of continuing professional development (CPD) points required annually by relevant registered practitioners for a number of AltMed courses.
- Following complaints to the TGA, removal of some illegal medicines not on the Australian Register of Therapeutic Goods (ARTG).
- De-listing some complementary medicines and medical devices (such as ‘bio-resonance’ machines) lacking evidence.
- Getting the TGA to declare two products of self-declared ‘Foods for special medical purposes’ illegal therapeutic goods and have them removed from the market-place.
- Publishing academic articles, in peer-reviewed journals, documenting regulatory problems investigated and solutions suggested.
- Publishing articles in lay media on current problems including in The Conversation, MJA Insight and Pearls and Irritations (around 200 over the last 5 years).
- Responding to consultation requests from the TGA, Medical Boards, National Medicines Policy Review, and others.
- Achieving the suspension of anti-vax chiropractor Simon Floreani’s registration.
- Stimulating the Chiropractic Board to publish standards on pregnancy and paediatric care.
- Responsible for the setting up of AHPRA’s ‘Advertising Compliance’ section, including their pilot auditing system (yet to report).
- Responding to requests for information from journalists.
- Correction of misinformation from the Victorian government’s ‘Better Health’ Channel.
- Providing a complaints avenue for people who want to remain anonymous.
The ‘Control Group Cooperative Ltd‘ is a UK Company (Registration Number: 13477806) is registered at 117 Dartford Road, Dartford, Kent DA1 3EN, UK. On its website, it provides the following statement:
The Vaccine Control Group is a Worldwide independent long-term study that is seeking to provide a baseline of data from unvaccinated individuals for comparative analysis with the vaccinated population, to evaluate the success of the Covid-19 mass vaccination programme and assist future research projects. This study is not, and will never be, associated with any pharmaceutical enterprise as its impartiality is of paramount importance.
The VaxControlGroup is a community cooperative, for the people. All monies raised will be re-invested into the project and its community.
Volunteers for this study are welcome from around the world, providing they have not yet received any of the SARS-CoV-2 vaccinations and are not planning to do so.
So, the Vaccine Control Group (VCC) aims at recruiting people who refuse COVID vaccinations. The VCC issues downloadable and printable COVID-19 Vaccine self exemption forms that you can complete (either online or by hand) supplied by: Professionals for Medical Informed Consent and Non-Discrimination (PROMIC). The form contains the following text:
COVID-19 vaccines, that have been administered to the public under emergency use authorisation, have been
associated with moderate to severe adverse events and deaths in a small proportion of recipients. There are currently insufficient available long-term safety data from Phase 3 trials and post-marketing surveillance to be able to predict which population sub-groups are likely to be most vulnerable to these reactions. However, clinical assessments have identified a range of conditions or medical histories that are associated with increased risk of serious adverse events (see Panel B). Individuals with such medical concerns, along with those who have already had COVID-19 and acquired natural immunity, have justifiable grounds to not consent to COVID-19 vaccination. Such individuals may choose to use alternate approaches to reduce their risk of developing serious COVID-19 disease and associated viral transmission. UK and international law enshrines an individual’s right to refuse any medical treatment or intervention without being subjected to penalty, restriction or limitation of protected rights or freedoms, as this would otherwise constitute coercion.
I do wonder, after reading this, what scientific value this ‘study’ might have (nowhere could I find relevant methodological details about the ‘study’). In search of an answer, I found ‘Doctors & Health Professionals supportive of this project’. The only one supportive of the VCC seems to be Prof Harald Walach who offers his support with these words:
A vaccine control group, especially for Covid-19 vaccines, is extremely useful, even necessary, for the following reasons:
- We are dealing with a vaccination technology that has never been used in humans before.
- All studies that have planned a control group long term, i.e. longer than only 6 weeks, have meanwhile been compromised, i.e. there are no real control groups around, because those originally allocated to the control group have mostly been vaccinated now. So there are no real control groups available.
- Covid-19 vaccinations are one of the biggest experiments on mankind ever conducted – without a control group. Hence those, who are either not willing to be vaccinated or have not yet been vaccinated are our only chance to understand whether the vaccines are safe or whether symptoms reported after vaccination are actually due to the vaccination or are only an incidental occurrence or random fluctuation.
Comparing unvaccinated people and those with a vaccination history regarding Covid-19 vaccines long term is important to determine long-term safety, because in many instances in the past some problems only were seen after quite some time. This can happen, if auto-immune processes are triggered, which often occur only in very few people. Hence, it is also important to have a long-term observation period and a large number of people participating.
Prof. Dr. Dr. phil. Harald Walach
This does not alleviate my doubts about the scientific value at all. Prof Walach, promoter of so-called alternative medicine (SCAM) and pseudoscientist of the year 2012, has in the past drawn our attention to his odd activities around COVID and vaccinations. Here are three recent posts on the subject:
- Prof Harald Walach is really unlucky
- Is Prof Harald Walach incompetent or dishonest?
- COVID-19 vaccinations: Prof Walach wants to “dampen the enthusiasm by sober facts”
In view of all this, I do wonder what the VCC is truly about.
It couldn’t be a front for issuing dodgy exemption certificates, could it?
Dr. Mehmet Oz is one of the most influential promoters of outright quackery. I once (many years ago) met him at a meeting where we both were lecturing. My impression was that he does not believe a single word he speaks. Oz later became a TV star and had ample occasion to confirm my suspicion.
Oz’s wife, Lisa, is a Reiki master and has spoken widely of her insights into energy and health. Mehmet Oz appeared as a health expert on The Oprah Winfrey Show. In 2009, Winfrey offered to produce a syndicated series. The Dr. Oz Show debuted in September 2009 and became the most successful promotion of charlatanery in the US. During a Senate hearing on consumer protection in 2014, Senator Claire McCaskill stated that “the scientific community is almost monolithic against you” for airing segments on weight loss products that are later cited in advertisements, concluding that Oz plays a role, intentional or not, in perpetuating these scams, and that she is “concerned that you are melding medical advice, news, and entertainment in a way that harms consumers.” This judgement was supported by a 2014 analysis published in the BMJ; here is the abstract:
Objective To determine the quality of health recommendations and claims made on popular medical talk shows.
Design Prospective observational study.
Setting Mainstream television media.
Sources Internationally syndicated medical television talk shows that air daily (The Dr Oz Show and The Doctors).
Interventions Investigators randomly selected 40 episodes of each of The Dr Oz Show and The Doctors from early 2013 and identified and evaluated all recommendations made on each program. A group of experienced evidence reviewers independently searched for, and evaluated as a team, evidence to support 80 randomly selected recommendations from each show.
Main outcomes measures Percentage of recommendations that are supported by evidence as determined by a team of experienced evidence reviewers. Secondary outcomes included topics discussed, the number of recommendations made on the shows, and the types and details of recommendations that were made.
Results We could find at least a case study or better evidence to support 54% (95% confidence interval 47% to 62%) of the 160 recommendations (80 from each show). For recommendations in The Dr Oz Show, evidence supported 46%, contradicted 15%, and was not found for 39%. For recommendations in The Doctors, evidence supported 63%, contradicted 14%, and was not found for 24%. Believable or somewhat believable evidence supported 33% of the recommendations on The Dr Oz Show and 53% on The Doctors. On average, The Dr Oz Show had 12 recommendations per episode and The Doctors 11. The most common recommendation category on The Dr Oz Show was dietary advice (39%) and on The Doctors was to consult a healthcare provider (18%). A specific benefit was described for 43% and 41% of the recommendations made on the shows respectively. The magnitude of benefit was described for 17% of the recommendations on The Dr Oz Show and 11% on The Doctors. Disclosure of potential conflicts of interest accompanied 0.4% of recommendations.
Conclusions Recommendations made on medical talk shows often lack adequate information on specific benefits or the magnitude of the effects of these benefits. Approximately half of the recommendations have either no evidence or are contradicted by the best available evidence. Potential conflicts of interest are rarely addressed. The public should be skeptical about recommendations made on medical talk shows.
During the presidential campaign in 2016, Oz supported Trump and hosted him on his TV show. In 2018, Donald Trump appointed him to the President’s Council on Sports, Fitness, and Nutrition, Oz was criticized as an example of choosing “pundits over experts”. Recently, Oz announced he intends to run for the U.S. Senate as a Republican.
In April 2020, Oz also spurred controversy because he said that children should be sent back into schools despite the fact that the novel coronavirus pandemic had only just begun and there were no vaccines or therapeutics yet available. “I tell you, schools are a very appetizing opportunity,” he said, claiming that resuming classes “may only cost us 2 to 3 percent in terms of total mortality,” according to his “reading” of medical journals. The mistake was so substantial that Oz later provided a kind of half-apology, saying that he “misspoke.”
“There is a battle raging for humanity”, claims Dr Carrie Madej, a US osteopathic doctor (in the US, osteopaths are [almost] conventional physicians). She thinks she has discovered how Big Tech collaborates with Big Pharma introduced new technologies in the coming vaccines, that will alter our DNA and turn us into hybrids. This, she submits, will end humanity as we know it, and start the process of transhumanism: HUMAN 2.0 They use vaccines to inject nanotechnology into our bodies and connect us to the Cloud and artificial intelligence. This will enable corrupt governments and tech giants to control us, without us being aware of it.
Dr. Carrie Madej is from Dearborn, Michigan, and received her medical degree from Kansas City University of Medical Biosciences in 2001. She then completed her traditional internship at The Medical Center in Columbus, Georgia, and internal medicine residency at Mercer University in Macon Georgia. Dr. Madej served as a private clinician and medical director of clinics in Georgia until 2015. Dr. Madej also served as an attending physician for the Pennsylvania College of Osteopathic Medicine. She has served as a public speaker and was featured in the documentary, “The Marketing of Madness” about the overuse of prescription psychotropic medicines. Dr. Madej now dedicates her time educating others on vaccines, nanotechnology, and human rights via multiple platforms and speaking engagements.
IN HER NEWEST SCORCHED EARTH DISCUSSION, Dr. Carrie Madej simply Can NOT stay silent about the ABSOLUTE DANGERS of the Covid-19 “vaccines” any longer! In fact, in this SCATHING PRESENTATION, she literally describes the ‘Killer Concoctions’ as ‘THE FRANKENSTEIN CODE” and HAMMERS the ‘Purveyors of the Poison Jab’ as ‘Murdering Psychopath Witch Doctors’ who are HELL BENT on the TOTAL DESTRUCTION & ANNIHILATION of the ENTIRE HUMAN RACE, as we know it today.
The ‘Kung Flu’ (as it’s been referred to by none other than POTUS Trump), is only ‘KILLING PEOPLE who are already suffering from cancer, diabetes, heart disease and a plethora of other autoimmune problems’ – so now WHY IN THE WORLD IS EVERYBODY being told to get the ‘Killer Jab’ when the risk of DIRE & GROTESQUE INJURY FAR OUTWEIGHS the risk of dying from Covid-19 or the fake Delta Variant, or Beta, or Gamma or WHATEVER ELSE THE DEMONIC FAUCI & GATES CONCOCT NEXT?! Get ready for a BEATING unlike you’ve seen in recent days, as Dr. Madej RIPS THE THROATS straight out of these Deep State Demons in this ‘DO NOT MISS’ Epic Video! Grab the popcorn, and get ready for a trip down the Rabbit Hole and a takedown of Satan’s Army!
This was published by the ‘REPUBLIC BROADCASTING NETWORK’ (RBN) who also published articles such as ‘Who are the Jews behind the coronavirus vaccines?‘
Dr. Carrie Madej is certainly no fan of COVID vaccines: Doctor Carrie Madej says she personally examined multiple vials of the vaccines that are being forced into people’s arms, and she was horrified by what she saw. She says she cried harder than she ever has before. Elsewhere she explained in detail:
“First it looked just translucent. And then as time went on, over two hours, colors appeared. I had never seen anything like this. There wasn’t a chemical reaction happening. It was a brilliant blue, and royal purple, yellow, and sometimes green,” she said.
She later shared that when she asked nanotech engineers what the emerging brilliant colors might come from, the engineers said the “only thing they knew that could do that” was a white light, over time, causing a reaction on “a super-conducting material.” In this case, Madej noted, white light came from the microscope itself.
She pointed out that an example of a super-conducting substance would be “an injectable computing system.”
Madej went on, “These fibers were appearing more and more. Some of the fibers had a little cube structure on them, I’m not sure what that was. And also metallic fragments were in there. They were not metallic fragments I’m used to seeing. They were exotic. They were very opaque.”
In time, Madej said, “all the particulates, all these colors started moving to the edge” of the cover slide. “There was self-assembling going on, things were growing. They looked synthetic.”
Madej noticed something else quite strange: “There was one particular object or organism, I’m not sure what to call it, that had tentacles coming from it. It was able to lift itself up off of the glass slide. It appeared to be self-aware, or to be able to grow or move in space.”
She found it disturbing but said she thought, “Maybe that was a fluke in a way, maybe that was just that one vial.”
Some time later, the same lab obtained more vials from a different batch of Moderna shots, as well as a J&J vial. Madej was concerned to see the same things she had observed in the first vial.
“Another one of those tentacle-like structures appeared,” she said. “This was now completely under the cover slip, so there was no movement because it wasn’t on the edge, but I just couldn’t believe I saw another one. Same thing.” Madej also saw the “same colors” appear over time, as well as the fibers.
In the J&J vial, Madej said, there was “definitely a substance that looked like graphene. They all had graphene-like structures in there. Whether or not they were, I don’t have the capability of testing them in order to know at this lab, but that’s what they appeared to be.”
The vial’s contents also had “fatty substances, a sticky glue-like substance that would be considered a hydrogel in those, both of them.”
The J&J vial “also had colors appear.” “Their colors were different, like a fluorescent pastel kind of color. Again, a lot of synthetic structures in there as well.” Madej also noticed many “spherical ring structures” in the J&J contents.
“I’ve never seen anything like this before. They’re not supposed to be in these injections. What are they going to do to somebody? What are they going to do to a child? I started crying when I saw these the second time under a microscope, because it was confirmation of everything I saw the first time,” Madej said.
Madej again appeared on the Stew Peters show on October 20 to discuss her findings from a Pfizer jab vial as well as another J&J vial. “What I’m seeing in all of these manufacturers are synthetic substances, graphene-like, also these nano-carbon tubes,” Madej said.
“In this particular J&J” vial, Madej saw “round spheres, which were not air bubbles.” She continued, “There’s many of these rings, and as time went on they would get thinner and thinner and expand out and then finally extrude out some gelatinous material — I’m not sure what it was, but different kinds of things were inside these spheres. So they’re almost like a delivery structure, that’s what they were doing.”
On one of these rings, Madej saw what “looked like a translucent organism that went around, and back and forth.” Madej first “thought it was another water parasite,” but after continuing to observe its movements, “thought perhaps it was moving in a more robotic way.”
Madej saw the “same kind of synthetic things” in the Pfizer jab, as well as “something that looks similar to teslaphoresis. That’s when these little graphite-like black, metallic particles start to coalesce into strings, like a spider web. They do that through any external force — it could be light, it could be a magnetic force, it could be an impulse, like a frequency. Anyhow, all these little particles would then coalesce and form their own neural network, or their own fibers, or wires.”
After listening to Madej’s findings and seeing the photo and video documentation she provided, Peters commented, “It’s like I’m watching a seriously bad B-movie, a horror thriller.”
Madej believes the tentacled entity she found in the Moderna jabs has a connection with the organism hydra vulgaris. “It is one of the model organisms that the transhumanists like to study and look at. They feel that this is an amazing organism for humanity,” said Madej, in part because “it’s immortal in the lab setting” and “continuously produces its own stem cells.”
“It never stops. You can chop it up into little bits, put it in a petri dish and it forms itself again and again,” she continued. “They’re thinking, wouldn’t this be great if we could put this inside of a human body’s genome, and then if your hand was chopped off by a trauma, you could grow a new hand.”
My friend Joe Schwarcz recently wrote a brilliant article about Dr. Madej. He concluded by asking: Is Dr. Madej a maddeningly malicious malfeasant, or does she just have a few loose marbles? I fear that it might be both.
