Illegal variant info, AP Mea Culpa, Ivermectin fake news, Graphene oxide controversy, AIDS story, FDA approval fail, Jamie Dorley, Tracey Stroup, Nutritional Frontiers, CBD, Dietary supplement status, Sleep satisfaction, Emotional wellness and MORE!

September 7th, 2021 3-5PM ET

Tuesday on The Robert Scott Bell Show:

You aren’t legally allowed to know which variant gave you COVID-19 in the US, even if it’s Delta Sam Reider, a musician from San Francisco, got a call from the California Department of Public Health in June. Though fully vaccinated, Reider had recently tested positive for COVID-19 after teaching music at a summer camp. The health department asked him to take a second test at a local Kaiser Permanente. Reider assumed it was because authorities wanted to find out whether he had a Delta infection. He, too, was curious — but when he got the test results back, he was surprised to learn that doctors couldn’t give him any information about his variant. “When I got the follow-up from Kaiser, they said it’s positive, but they didn’t have any of the sequencing information,” Reider told Insider. That “felt odd to me,” he said. Several legal barriers prevented Reider and his doctors — as well as nearly all Americans who have tested positive for the coronavirus — from knowing which variant was to blame. The Centers for Medicare and Medicaid Service (CMS), which oversees the regulatory process for US labs, requires genome-sequencing tests to be federally approved before their results can be disclosed to doctors or patients. These are the tests that pick up on variants, but right now, there’s little incentive for the labs to do the work to validate those tests.

Do you have the Delta Variant? It’s illegal for you to know As my long-time readers know, I’ve spent the past year demonstrating that the SARS-CoV-2 virus doesn’t exist. Therefore, the Delta Variant is a fantasy based on a fantasy. However, I make forays into the official bubble where, of course, millions of people believe the virus and the Variant are real. I show that within the bubble, all sorts of internal contradictions and absurdities abound. Recently, I quoted official sources who stated that the current PCR test can’t differentiate between SARS-CoV-2 and the Delta Variant [1]. Only through deeper genetic sequencing of patients’ swab samples—a procedure that isn’t routinely done—can testers tell whether a person has the original SARS-CoV-2 or the Delta. In order to know whether the Delta is widespread, a predictive computer model would have to be assembled. These models are notoriously inaccurate. The bottom line? The tidal wave of propaganda asserting the Delta is everywhere, and is responsible for the escalation of COVID cases, is a sheer fabrication. The propaganda is based on a computer model. That’s where the official bubble is, or was, when a new revelation surfaced. Buckle up for this one. On the scale of fabrications, it ranks right near the top. You see, the genetic sequencing process, carried out to determine whether a patient’s swab sample reveals the original SARS-C0V-2 or the Delta…that process hasn’t obtained certification from the US government.

Mea Culpa: Associated Press Falsely Claims 70% of Mississippi Poison Control Calls Due to Ivermectin Adding to the litany of mea culpas regarding the use of ivermectin – a still unproven alternative treatment for the coronavirus – the Associated Press recently issued a correction to a report alleging that 70% of poison control cases in Mississippi were linked to the drug’s ingestion. Published in late August, the original article said that up to 70% of calls to Mississippi Poison Control were related to the use of ivermectin. Several days later, the Associated Press issued a correction putting the actual number at 2%. This story was first published on Aug. 23, 2021. It was updated on Aug. 25, 2021 to correct that the number of calls to poison control about ivermectin was about 2%. Incorrect information provided by the Mississippi Department of Health had said the number was 70%. The Associated Press did, however, make a clear distinction between ivermectin used for livestock animals and ivermectin used to treat humans. In Mississippi’s case, 70% of calls relating to ivermectin were side effects stemming from “medicine purchased at livestock supply centers used to treat humans.” At least 2% of recent calls to the Mississippi Poison Control Center are about people ingesting ivermectin, with 70% of those calls being about livestock or animal formulations of the anti-parasite medicine purchased at livestock supply centers, Mississippi Department of Health officials said.

American Scientists Confirm Toxic Graphene Oxide, and More, in Covid Injections It is a human right, and global law governed under the Nuremberg Code, that vaccine specific ingredient information is disclosed.  It is critical, required and necessary information so anyone, from any country in the world, can make an informed decision whether or not to consent to medical intervention.  Because the full list of ingredients of the Covid “vaccines” have not been made available, Dr. Robert Young and his team conducted research to identify the specific ingredients in the Pfizer, Moderna, AstraZeneca and Johnson & Johnson Covid injections.  On 20 August, they published their findings. Dr. Young is a biochemist, microbiologist, and clinical nutritionist.  He and his team of scientists have confirmed what the La Quinta Columna researchers found – toxic nanometallic content which are magneticotoxic, cytotoxic and genotoxic to plants, insects, birds, animals and humans – all life on the planet.  One of the “vaccines” even contained life-threatening parasites. Taken together, the “vaccine” components – which include graphene oxide among many others and which may be influenced by radiation sources external to us – create a toxic chemical and radiative soup inside our bodies.  Anyone who has a Covid injection is seriously putting their lives at risk. We previously covered some of La Quinta Columna’s research in two articles: Spanish Researchers Find Covid-19 Vaccines Contain TOXIC Levels of Graphene Oxide; and, The real pandemic – Covid-19 or Graphene Oxide? Poisonous Nano-Material found in Covid Vaccines and Face Masks. For additional resources visit Orwell City, a website that translates, transcribes and adds English subtitles to a good portion of La Quinta Columna’s materials.

Question of The Day!

Hello Super Don and RSB:
There is a book about The true story of AIDS
I would like to read it but there are so many books in that subject, I want to get the right one. I am sure I have heard this mentioned on your show.
Thanks, eh!

Survey: Majority of Unvaccinated Say FDA’s Approval of Vaccines Doesn’t Change Their Mind Most of the United States’ unvaccinated population are not moved by the Food and Drug Administration’s (FDA) approval of Pfizer’s vaccine for the Chinese coronavirus, a recent ABC News/Washington Post survey found. The survey found that unvaccinated Americans are overwhelmingly unfazed by the FDA’s approval of Pfizer’s vaccine — a move President Biden hoped would prompt private businesses to “step up” vaccine requirements. While the survey found the majority of Americans have gotten the jab, data suggests the remaining unvaccinated population, comprised of roughly 90 million in the U.S., are firm in their decision to refuse the shot, wholly unmoved by the FDA’s approval of Pfizer’s jab. Only 16 percent of the unvaccinated said the FDA’s approval shifts their position, making them more likely to get vaccinated. The vast majority, 82 percent, said the FDA’s approval “makes no difference.” Sixteen percent also said they would get the shot if it were required by their employer, but according to the survey, “many more say they’d quit” altogether. Additionally, the survey found unvaccinated Americans remain skeptical of the vaccines’ safety and effectiveness — seven out of ten. “Nine in 10 see vaccination as a personal choice rather than a broader responsibility and just 16 percent have been encouraged by someone close to them to get the shot,” the survey found.

Hour 2  Special Guest – Jamie Dorley and Tracey Stroup

Allen James Dorley III A.C.S.M.

CEO, Co-Founder, Owner

Jamie Dorley has been involved in the natural health field in a variety of capacities for over twenty years. Holding a Bachelor of Science degree from Slippery Rock University in community health, and certification from the American College of Sports medicine as a certified trainer, Jamie’s career includes having counseled and coached athletes, executives, and school teams, and many years serving as a sales executive and formulator for several national nutritional and sports supplement companies. As co-founder with Dr James Winer of Nutritional Frontiers, Jamie is the current CEO and  oversees the formulation and distribution of premium therapeutic quality nutritional supplements through health professionals nationwide. His expertise is highly valued by the many patients whom he has helped with a wide variety of health challenges since joining the staff of Winer Wellness Center in 2007.

Tracey Stroup has been in the health and wellness industry for over 25 years.  She has a B.S. in Exercise and Sports Science from the Pennsylvania State University with a minor in Nutrition. She has also continued her education taking courses in biochemistry, biology and food science. Tracey is a Certified Digestive Health Specialist from the Food Enzyme Institute. She once dreamed of going to medical school but turned down her acceptance to pursue a career in natural health. She completed her designation as a Naturopathic Doctor from Trinity School of Natural Health with additional courses as a Master Herbalist, Iridology and is a Certified Natural Health Professional.


Tracey’s career in Natural Health has been vast.  Her first career path was as a personal trainer and quickly advanced to Fitness Director of several gyms.  She eventually opened her own personal training studio from 2005 – 2012 where she employed three additional trainers with an average clientele of 200+ clients a week.  Upon attaining her natural health designation, Tracey became an instructor for her Alma Mater.  During that time she owned a successful natural health practice in her hometown utilizing the trilogy of health approach with each client: mind, body and spirit.  Within her practice she co-owned a juice bar and corporate wellness company. Tracey has been the Vice President of Operations for a natural health college establishing curriculum, partnerships with large supplement companies and creating natural health business management strategies for graduates of the program.  Tracey was recruited by a leading Biocommunication company as their Vice President of Operations where she designed practitioner software, educational concepts and marketing strategies to promote their software and brand.

Analytical Report – Certicate of Analysis

The FDA Defers to Pharma, Nixes CBD as Dietary Supplement On Aug 12, the FDA formally rejected two New Dietary Ingredient (NDI) applications seeking to establish CBD as a lawful dietary supplement. Apparently, the fix was in from the start. The FDA never intended to approve the applications by Charlotte’s Web, a pioneer CBD brand, and Irwin Naturals, a legacy supplement company that has jumped into the CBD space. Although millions of doses of CBD have been consumed in the United States, the FDA claims it has insufficient data to assess if there’s a dosage of CBD that’s safe for consumers. Irrespective of real or imagined safety concerns, it seems that the FDA was committed to delivering a predetermined thumbs-down verdict in keeping with the “exclusionary clause” of the 1994 Food Drug and Cosmetic Act, whereby supplements can’t contain pharmaceutical ingredients. In effect, the FDA equated the CBD in the unregulated market (isolates as well as full-spectrum hemp extracts) with the cannabidiol in Epidiolex, the FDA-approved pharmaceutical CBD (mixed with ethanol and sucralose, the artificial sweetener) that’s used to treat pediatric epilepsy. Ironically, invoking the exclusionary clause implies recognition on the FDA’s part that the CBD sold as supplements could also be therapeutically beneficial – given that the same ingredient is found in pharmaceutical CBD. Out of deference to Pharma, the FDA has refused to provide a regulatory framework for CBD supplements, which technically are not legal but remain on the shelves because of a lack of federal enforcement. So now it will be up to Congress to clarify CBD’s status and craft a better policy for producers and consumers.

CBD Use Associated With Improvements In Sleep Satisfaction Proper sleep is foundational when it comes to physical and mental health. Anyone that does not get proper sleep will likely be quick to point that out. When someone doesn’t get proper sleep they are more likely to be irritable, experience memory issues, and have a harder time concentrating and focusing. Long term physical effects can also be experienced, including high blood pressure, a weakened immune system, weight gain, and increased risk of heart disease. Popular sleep medications come with their own buffett of potential side effects, including digestive issues, dizziness, sleep walking/talking, and many other undesirable things. Fortunately for those that suffer from sleep issues, the results of a recent study indicate that a popular cannabinoid may be able to help. A team of researchers in Brazil recently conducted a study in which some participants were provided CBD and others were provided a placebo. Thirty three people participated in the study, all of which suffered from REM sleep behavior disorder (RBD). Many participants reported extreme cases of RBD involving violent leg and arm movements during REM sleep, as well as frequent nightmares. According to the results of the study, consumption of 300mgs of CBD prior to sleeping was associated with ‘temporary improvements’ in the participants’ reported sleep satisfaction level. Unfortunately, the results of the study also indicated that there was no long term reduction in the frequency of RBD.

CBD Use Associated With Improved Emotional Wellness We are living in the midst of some truly hard times. Due to the ongoing pandemic and many other factors, emotional wellness is something that many people struggle with. It was estimated that roughly one out of every seven people globally struggled with mental health as of 2017, and it’s likely a safe bet that the problem has only gotten worse. Emotional wellness is a subset of overall mental health, and is often described as a person’s ability to successfully navigate the stresses that come with life, and to be able to adapt to change during difficult times. Depression has increased during the pandemic all over the world, as have anxiety and emotional exhaustion, and people are looking for ways to reduce that depression. According to the results of a new study, CBD may be able to help. A team of researchers in Brazil recently conducted a clinical trial to explore CBD’s relationship with depression, emotional exhaustion, and anxiety. The clinical trial conducted by researchers with the University of São Paulo in Brazil involved a cohort of 120 ‘frontline health care professionals’ half of which were administered 300mgs of CBD daily and the other half having not used CBD. “This randomized clinical trial found that the efficacy and safety of daily treatment with CBD, 300 mg, for 4 weeks combined with standard care was superior to standard care alone for reducing the symptoms of emotional exhaustion, anxiety, and depression among frontline health care professionals working with patients with COVID-19,” the study’s authors stated. “Cannabidiol may act as an effective agent for the reduction of burnout symptoms among a population with important mental health needs worldwide.” the researchers concluded.

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