From James C.Belcher
James Clinton Belcher, Head of State
The United States of America
We Are The Lab Monkeys
Biden set to implement 200% tariff on Russian aluminum, which will worsen U.S. inflation
(Natural News) During his State of the Union Address on Tuesday, Joe Biden tried to claim that his economy was a success by lying about job ‘creation’ and downplaying inflation — though the latter would not even be a problem were it not for his economic policies and those of Democrats in Congress.
At the height of the COVID pandemic-induced global supply chain crisis, Democrats passed major spending bills which continue to flood a product-starved market with money; more money with less to buy equals skyrocketing prices after creating artificial demand.
Now, the Biden regime is set to explode the price of aluminum — and everything made with it — by imposing a 200 percent tariff on aluminum manufactured by Russia, according to Bloomberg:
The US is preparing to slap a 200% tariff on Russian-made aluminum as soon as this week to keep pressure on Moscow as the one-year anniversary of the invasion of Ukraine nears, according to people familiar with the situation. President Joe Biden has yet to give the official go-ahead, and there have been concerns in the administration about collateral damage on US industries, including aerospace and automobiles, said the people, who asked not to be identified discussing internal deliberations.
The move, which has been contemplated for months, is also aimed at Russia, the world’s second-largest aluminum producer, because Moscow has been dumping supplies on the US market and harming American companies. The timing of the decision could slip past this week, one of the people said.
“Russia, the world’s largest aluminum producer after China, has been a significant source of material for the US market. Most of it is value-added items, rather than in bulk product, with US buyers ranging from building and construction to automotive,” the report added, effectively admitting that prices are going to soar.
The move is only going to further the development of a Global South economy led by BRICS — Brazil, Russia, India, China, and South Africa, along with a host of other nations joining ranks eager to shed the U.S. dollar-dominated system where the American deep state makes all the rules.
In October, following a two-day summit with Saudi Arabia, South African President Cyril Ramaphosa confirmed that the oil-rich kingdom is likely to join the growing BRICS coalition consisting of core members Brazil, India, China, and South Africa.
“The Crown Prince (prime minister Mohammad bin Salman bin Abdulaziz al Saud) did express Saudi Arabia’s desire to be part of BRICS and they are not the only country,” said Ramaphosa, according to a Times Live report.
The bloc first met in 2009 and has always generally been seen as an economic alternative to the Western-dominated global economic order. Following Russia’s invasion of Ukraine, the West has pulled back engagement with and resources from Moscow, which is being seen as hastening the growth of BRICS as more countries flee the self-destructive left-wing cultural chaos of Western countries.
“We did say that Brics having a summit next year under the chairship of South Africa in SA, and the matter is going to be under consideration. A number of countries are making approaches to Brics members, and we have given them the same answer that it will be discussed by the Brics partners, and thereafter, a decision will be made,” Ramaphosa continued, according to Times Live.
In an assessment of the emerging situation, The Conservative Treehouse also noted: “A global financial and economic cleaving is underway created by the western nations chasing ideological climate change energy policy, while the rest of the world remains pragmatic toward oil, coal and natural gas as energy resources. Essentially, western governments’ following the ‘Build Back Better’ climate change agenda which stops using coal, oil, and gas to power their economic engine, while the rest of the growing economic world continues using the more efficient and traditional forms of energy to power their economies.”
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Green fail: Many of Scotland's wind turbines are being powered by diesel fuel generators that are leaking hydraulic fluid
(Natural News) The lunacy of the far left’s ‘climate change’ agenda is once again coming home to roost, this time in Scotland, where Western civilization essentially began and where it’s gone to die.
According to Breitbart News, scores of the country’s ‘green energy’ windmills are being run by diesel generators, many of which are leaking hydraulic fluid into the countryside.
“Scottish Power — led by a Spaniard, Ignacio Galan, and actually a subsidiary of Spanish firm Iberdrola — conceded that some 71 of its turbines had to be hooked up to diesel generators to keep them warm in December, according to the Sunday Mail, with a whistleblower telling the left-leaning newspaper that problems with the turbines are deep-seated,” the report said.
The whistleblower said: “During December 60 turbines at Arecleoch and 11 at Glenn App were de-energised due to a cabling fault… In order to get these turbines re-energised diesel generators were running for upwards of six hours a day.
“Turbines are regularly offline due to faults where they are taking energy from the grid rather than producing it, and also left operating on half power for long periods due to parts which haven’t been replaced,” the whistleblower continued. “Dirty hydraulic oil is also regularly being sprayed out across the Scottish countryside due to cracks in mechanisms. Safety standards have not improved since a worker was killed in 2017 at Kilgallioch wind farm.”
Another outlet reported that more than 1,000 gallons of leaking hydraulic oil were summarily “sprayed over the countryside” by the swirling wind turbines, which of course, negates the ‘environmentally friendly’ purpose behind the windmills in the first place.
“The Scottish Government wants to make our country attractive to foreign investors as 40 percent of the wind that blows across Europe blows across Scotland. However, that should not mean we put up with our waterways and nature being polluted with carbon from diesel generators and hydraulic oil,” the whistleblower continued in their interview with the Sunday Mail.
“People should be aware that, while their energy costs continue to rise, our windfarms are not operating as efficiently as they could be due to corporate greed,” the whistleblower continued, echoing left-wing talking points. But, according to Breitbart London, that could be a reference to the millions of dollars that Scottish Power’s Spanish CEO made in 2021, as ordinary Scots were paying exorbitant energy bills (which isn’t the fault of the energy company but rather liberal energy policies that prioritize inefficient power generation over fossil fuels that are cheaper).
To that point, however, Richard Tice, the Reform Party leader (formerly the Brexit Party) complained recently that around 83 percent of Great Britain’s offshore wind turbines are owned by foreign companies, with the largest being the government of European Union member Denmark.
“We British taxpayers are paying huge inflation-linked subsidies to create ever larger profits for the Danish taxpayer. What’s the advantage of that?” Tice said.
Take Back Control: Reform Party Calls for End of Foreign Ownership of Utility Firms https://t.co/vM9Hpc0pMY
— Breitbart London (@BreitbartLondon) February 2, 2023
Colin Smyth, a Member of the Scottish Parliament (MSP) for the leftist Scottish Labour Party in the region, admitted that “having to use diesel generators to de-ice faulty turbines is environmental madness” while going on to rip the Scottish government over the fact that their “rhetoric on net zero is very different from the reality” while accusing them of “dishonesty.”
The rapid and nonsensical pivot to massive windmill and solar farms to power our modern economies is pointless. Not only is the technology not sufficient to generate enough energy, but there literally is no genuine, replicable data proving that our modern lives are producing ‘enough emissions’ to ‘change the climate.’ The climate has been ‘changing” the entire history of the planet and will continue to do so no matter what humans do, short of destroying the world with nuclear weapons.
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Pass The Salt with Coach Dave: David Sumrall reveals cops provoked J6 protesters with flashbangs – Brighteon.TV
(Natural News) Citizen journalist David Sumrall has revealed that law enforcement provoked the Jan. 6 protesters to storm the Capitol by using flash grenades.
He made this revelation during his appearance on the Feb. 6 edition of the Brighteon.TV program “Pass The Salt.” Sumrall told program host Coach Dave Daubenmire that the police shot grenades into the peaceful J6 protesters, presenting footage posted on social media to back up his claim. He added that people showed up in Washington, D.C. doing the right thing and bringing no tools of violence whatsoever.
Daubenmire agreed with his guest, adding that the truth needs to get out so the American people will know what really happened on Jan. 6, 2021. The high school football coach, his wife and some friends went to the nation’s capital to peacefully assemble and petition the government for redress of grievances – which the First Amendment guarantees.
According to Daubenmire, there are some people who want Americans to forget about the Jan. 6 Capitol siege and move on from it. However, he remarked that those same people continue to spread the lies about the incident.
Sumrall, the founder of StopHate.com, noted that Americans themselves are distracted by so many things that they forgot about the deaths of Ashli Babbitt and Rosanne Boyland, alongside the attacks made against the J6 protesters. (Related: The Sentinel Report: StopHate.com founder David Sumrall says police brutality is over the top and people need to see it – Brighteon.TV.)
Daubenmire moreover debunked the claim that police officers died during the incident, pointing out that the only people who died that day were peaceful protesters killed by the actions of government authorities.
J6 protesters still languishing in DC gulag
“I’m not going to forget Jan. 6, and I’m not going to forget the real story of what happened on that day,” Daubenmire told his guest. “I’m still talking about that because there are guys still in jail.
In response to a question by the “Pass The Salt” host about those still in jail, Sumrall said it is not always the path people want to take due to being a difficult journey. But regardless of how painful being jailed for exercising one’s rights may be, Americans need to understand what they have lost and what they are set to lose.
Sumrall then challenged Americans to question themselves if they still have freedom, given what happened to the J6 protesters terrorized by their own government.
According to Daubenmire, the Washington, D.C. gulag is full of many innocent people, and government officials – including elected Republican officials – are not speaking about it.
Ultimately, Sumrall said getting the truth about the J6 incident is the biggest awareness program in the history of mankind and the biggest turning point for the American nation. Americans must wake up, understand what is happening in the country and speak out against the wrongdoings of the government.
Watch the Feb. 6 episode of “Pass The Salt” with David Sumrall below. “Pass The Salt” with Coach Dave Daubenmire airs every Sunday at 7-8 p.m. and Monday at 11 a.m.-12 p.m. on Brighteon.TV.
More related stories:
MTG calls for investigation into civil rights abuses experienced by Jan 6 defendants.
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Latest mRNA Vaccine for RSV Wins Expedited Review
Moderna just moved one step closer to bringing mRNA-1345, an RSV shot, to market
The U.S. Food and Drug Administration granted the experimental shot fast-track designation in August 2021
Now, Moderna’s mRNA RSV shot has been given Breakthrough Therapy Designation, which allows for faster development and an expedited review period
RSV is usually not serious; most people experience only mild, cold-like symptoms and recover on their own in a week or two
Moderna plans to file for FDA approval of mRNA-1345 in the first half of 2023
Along with Moderna’s mRNA RSV shot, Pfizer and GSK have also developed RSV vaccines that are awaiting regulatory approval
Get ready. A new mRNA shot is barreling down the runway and may be available as soon as fall 2023. This time, it’s not to target SARS-CoV-2 but, rather, respiratory syncytial virus (RSV), a pathogen that typically causes mild cold-like symptoms.
Pfizer and Moderna are racing to bring their RSV shots to market, and Moderna just moved one step closer with its mRNA-1345. The U.S. Food and Drug Administration (FDA) granted the experimental shot fast-track designation in August 2021. Now, Moderna’s mRNA RSV shot has been given Breakthrough Therapy Designation, which allows for faster development and an expedited review period.
You may have seen RSV making headlines more often than usual this winter — in lock-step with the mRNA shots soon to be released to save us all from it. In November 2022, the World Economic Forum (WEF) warned RSV could cause a “tripledemic” along with COVID-19 and flu.
It reported case numbers of RSV rising in the U.S. and Canada, because children weren’t exposed to this and other common infections during COVID-19 lockdowns.
The U.S. Centers for Disease Control and Prevention also warned:
“CDC surveillance has shown an increase in RSV detections and RSV-associated emergency department visits and hospitalizations in multiple U.S. regions, with some regions nearing seasonal peak levels. Clinicians and public health professionals should be aware of increases in respiratory viruses, including RSV.”
Still, RSV is usually not serious; most people recover on their own in a week or two. While it can lead to severe illness, including bronchiolitis and pneumonia, in infants younger than 1 year and older adults, almost all children have had an RSV infection by their second birthday
— and most recover from it just fine.
We saw from Operation Warp Speed how pharmaceutical companies and governments have bragged about the speed with which they can approve new shots, however. And the RSV shot is no different. At this point, the obligatory RSV propaganda seems perfectly timed to ramp up with the coming release of a new RSV jab.
The FDA granted Moderna’s mRNA-1345 Breakthrough Therapy Designation based on a Phase 3 trial involving 37,000 adults aged 60 years and older.
The mRNA RSV shot had a reported efficacy of 83.7% against RSV-associated lower respiratory tract disease. Moderna plans to file for FDA approval of mRNA-1345 in the first half of 2023.
The shot initially would be intended for adults aged 60 and over, but Moderna is also testing its mRNA RSV shot in children via an ongoing Phase 1 trial.
“With this designation, we look forward to productive conversations with the FDA in the hopes of bringing our RSV vaccine candidate for older adults to the market safely and quickly,” Moderna CEO Stéphane Bancel said.
Moderna’s RSV shot uses the same lipid nanoparticle as its COVID-19 injection. The primary difference between the two shots is the coding of the mRNA. In the RSV shot, the mRNA encodes for a prefusion F glycoprotein. Prefusion F protein is a protein that mediates the RSV virus’ entry into your cells and is known to elicit a neutralizing antibody response.
Under normal circumstances, it’s hard to imagine an RSV vaccine built on a novel mRNA platform getting fast-tracked, but we’re no longer in normal times. The rollout of mRNA COVID-19 shots has, as predicted, paved the way for any number of new mRNA-based injections going straight to human trials. RSV is just the beginning.
At the WEF’s Davos Agenda 2022, at a session titled “COVID-19: What’s Next?”
Bancel was open about Moderna’s plans to combine multiple shots, such as a COVID-19 shot, a flu shot and RSV shot, into one injection — coming in 2023 — to avoid “compliance issues.” He said:
“The other piece we’re working on is for 2023, is how do we make it possible from a societal standpoint that people want to be vaccinated?
And we’re going to do this by preparing combinations, we’re working on the flu vaccine, we’re working on an RSV vaccine, and our goal is to be able to have a single annual booster, so that we don’t have compliance issues, where people don’t want to get two to three shots a winter, but they get one dose, where they get a booster for corona, and a booster for flu and RSV, to make sure that people get their vaccine.”
When asked how soon this would occur, he continued:
“So the RSV program is now in Phase 3, the flu program is in Phase 2 and soon in Phase 3, I hope as soon as second quarter of this year. So the best case scenario would be the fall of 2023, as a best case scenario …”
At the 2023 WEF meeting in Davos, Bancel again spoke about mRNA shots, this time stating he’d “like to have mRNA capacity on every continent.”
It seems they’re well on their way.
As of January 2023, Moderna has 48 programs in development, including “36 programs in clinical trials encompassing investigational mRNA infectious disease vaccine candidates and mRNA therapeutic candidates spanning seven different modalities.”
In a news release, Bancel reported:
“Applying our experience and using our mRNA platform, we are developing vaccine candidates that we believe could one day help prevent hospitalizations and deaths from some of the most prevalent respiratory viruses.
We are also progressing several respiratory vaccine candidates, including combination vaccines against multiple respiratory viruses, and are committed to building our respiratory franchise.
By pursuing combination products to protect against a range of diseases, we believe that we can potentially help decrease morbidity and mortality from respiratory disease, lower healthcare costs and increase health security globally.”
The Pentagon’s secretive Defense Advanced Research Projects Agency (DARPA) has been working for years to develop an antibody to any virus within 60 days of collecting blood from a survivor.
Its Pandemic Prevention Platform program, known as P3, “aims specifically to develop a scalable, adaptable, rapid response platform capable of producing relevant numbers of doses against any known or previously unknown infectious threat within 60 days of identification of such a threat in order to keep the outbreak from escalating and decrease disruptions to the military and homeland.”
DARPA also lunched ADEPT:PROTECT (Autonomous Diagnostics to Enable Prevention and Therapeutics: Prophylactic Options to Environmental and Contagious Threats) to develop technologies — like mRNA — that can be rapidly deployed against emerging infectious diseases and biological weapons.
It was September 2019 when Moderna announced it had developed mRNA-1944 — the first systemic mRNA therapeutic to show production of a secreted protein in humans — courtesy of financial support from DARPA’s ADEPT:PROTECT program.
Months later, the COVID-19 pandemic would result in the development of the first experimental mRNA gene therapy, which has been distributed among the masses. The Highwire reported:
“With uncanny foresight, Moderna’s expeditious mRNA endeavor … had immediate manufacturing support from the Coalition for Epidemic Preparedness Innovations (CEPI) to ensure the pandemic’s gene-editing jabs traversed the globe. Significantly, CEPI was founded in 2017 by the WEF, the Bill & Melinda Gates Foundation, the Wellcome Trust, and the governments of Norway and India.
Aligned with the same goals as DARPA, CEPI is a global syndicate of public-private organizations whose mission is to highlight pandemic threats, continuously prepare for the next “Disease X,” and advance vaccines.
Presently, over 13 billion doses of COVID-19 vaccines have been administered worldwide. With vaccine manufacturers protected from liability, evidence increasingly indicates that mRNA injections are not just failing but, more significantly, are causing many serious adverse events, including myocarditis, increased risk of cancer and stroke, and death.”
Past attempts to develop RSV vaccines have ended in tragedy, particularly in the 1960s. In a trial on infants, two babies died after first appearing to tolerate the shot. The problem occurred during the following cold and flu season, when 80% of those vaccinated caught RSV and had to be hospitalized. Only 5% of those who received the placebo shot were hospitalized for RSV.
The issue is antibody-dependent enhancement (ADE), a problem that’s also occurred in the development of coronavirus shots. In 2020, Timothy Cardozo of NYU Langone Health and Ronald Veazey with the Tulane University School of Medicine set out to determine if enough research existed to require clinicians to disclose the specific risk that COVID-19 shots could worsen disease if the recipient is exposed to circulating virus — similar to what occurred in the RSV trial.
They reviewed preclinical and clinical evidence, which revealed that ADE is a significant concern, noting:
“COVID‐19 vaccines designed to elicit neutralizing antibodies may sensitize vaccine recipients to more severe disease than if they were not vaccinated. Vaccines for SARS, MERS and RSV have never been approved, and the data generated in the development and testing of these vaccines suggest a serious mechanistic concern:
… that vaccines designed empirically using the traditional approach (consisting of the unmodified or minimally modified coronavirus viral spike to elicit neutralizing antibodies), be they composed of protein, viral vector, DNA or RNA and irrespective of delivery method, may worsen COVID‐19 disease via antibody‐dependent enhancement (ADE).”
They concluded that, in order to meet medical ethics standards of informed consent, people who receive COVID-19 shots should be clearly warned of the “specific and significant COVID-19 risk of ADE.”
This didn’t happen, and it likely won’t for RSV shots, either.
Along with Moderna’s mRNA RSV shot, Pfizer and GSK have also developed RSV vaccines that are awaiting regulatory approval. Pfizer is even targeting its RSV shot to pregnant women, claiming it can help prevent RSV in newborns. While Moderna is also planning trials in pregnant women, GSK stopped its pregnancy trial in 2022 due to safety concerns.
But no matter which pharmaceutical company ends up being first to bring it to market, the RSV vaccine is clearly on the way. It could potentially be available by fall 2023, and the way RSV was hyped over the winter, it likely won’t be long before this shot moves beyond the older people target and expands to infants and children, becoming another requirement on the official vaccine schedule.
But considering the multitude of problems associated with the mRNA COVID-19 shots, I’m not optimistic about the development of a fast-tracked mRNA shot against RSV. The risks of these experimental, fast-tracked shots are serious, while, in most cases, RSV is not.
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Disclaimer: The entire contents of this website are based upon the opinions of Dr. Mercola, unless otherwise noted. Individual articles are based upon the opinions of the respective author, who retains copyright as marked.
The information on this website is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended as a sharing of knowledge and information from the research and experience of Dr. Mercola and his community. Dr. Mercola encourages you to make your own health care decisions based upon your research and in partnership with a qualified health care professional. The subscription fee being requested is for access to the articles and information posted on this site, and is not being paid for any individual medical advice.
If you are pregnant, nursing, taking medication, or have a medical condition, consult your health care professional before using products based on this content.
“First Do No Harm”: Doctor Fired for Helping Patients
By: Tessa Lena
The story of Dr. John Day in Texas is an illustration of just how upside-down the medical establishment is today
All throughout the “COVID pandemic,” Dr. Day was serving his patients and doing his job with soul
Not only was he doing his job with soul — being the only one at his clinic who was actually treating COVID patients — he was also helping patients on his free time and volunteering at the clinic by growing a community garden
When the vaccine mandates were announced, Dr. Day declined the injection and also spoke up against the dehumanization of the “unvaccinated”
While, based on Abbot’s executive order, the clinic administration could not proceed with the plan of firing Dr. Day for declining the injection, he was none the less fired in October 2021 for “offending” people with his views and for helping a disabled patient in a wheelchair run a difficult errand, on his “off” day
This story is about a caring and fearless family doctor in Texas, Dr. John Day, who was fired from his job for having a soul — and for not selling out to the robots. Recently, I had the joy of interviewing Dr. Day, and I was simply struck by his almost child-like purity and the warrior courage with which he stood his ground.
Dr. Day was serving his patients and actually “saving lives” all throughout the “COVID pandemic.” Early on, when appropriate, he prescribed hydroxychloroquine and ivermectin — and once he was forbidden from doing so by the clinic administration, he still found ways to help his patients using available treatments. When the vaccine mandates were announced, Dr. Day objected to the mandates and spoke against the dehumanization of the “unvaccinated.”
Being an all-around soulful, pure-hearted human being, he was also helping patients on his free time and volunteering by growing a community garden at the clinic. And it seems like, at some point, his pure-hearted, humble presence became just too uncomfortable for the functionaries and the administrators. Perhaps, his presences reminded them of the existence of the soul, something they didn’t want to look at. So they fired him.
It seems to me that they fired him so that their own cowardice would stop reflecting in the mirror of his selfless actions — so that their cowardice, in their own eyes, could pass for “just following orders.”
As I wrote on my Substack, Dr. Day has “spent most of his career working in areas of medicine that are patient-focused and light on industry glamor, including in-patient psychiatry at a public hospital in Texas.”
In late 2019, he heard reports out of China and began to follow the “pandemic” story closely, especially any information he could find on available treatments. On a side note, in case anyone has forgotten, here is a 2005 study, published on the NIH website, titled, “Chloroquine is a potent inhibitor of SARS coronavirus infection and spread.”
Anyway, in the thick of 2020, after researching Chloroquine and Hydroxychloroquine as potential treatments, Dr. Day started prescribing Hydroxychloroquine to the patients who he thought could benefit from it.
From the get-go, the situation was made difficult by the overall chaos. Many doctors were themselves scared, getting EKGs for patients (required to prescribe HCQ) was hard, COVID test results were taking forever to come back while HCQ needed to be prescribed early on (and frankly, as we know, the tests themselves were a joke — but they still needed to be used), etc.
Even so, in the midst of that chaos, Dr. Day was calmly doing what he could, and he was the only physician at the clinic actively treating COVID patients. However, soon enough, a lot of pressure was created from above to banish Hydroxychloroquine, and so was told by the clinic administrator to not prescribe it.
Then in August 2020, Dr. Day became familiar with the COVID protocol by Professor Thomas Borody, an Australian gastroenterologist who had made a name for himself for developing an antibiotic protocol to treat H. Pylori (a bacterium, famously linked to stomach ulcers by Australians Robin J. Warren and Barry J. Marshall). Here a press release, printed by NASDAQ.com, in August 2020:
“SYDNEY, Aug 19, 2020 – (ACN Newswire) – – Triple therapy specialist Professor Thomas Borody, famous for curing peptic ulcers using a triple antibiotic therapy saving millions of lives, today released the COVID-19 treatment protocol to Australian GPs, who can legally prescribe it to their COVID-19 positive patients, and can also prescribe it as a preventative medication.
Borody says this could be the fastest and safest way to end the pandemic in Australia within 6-8 weeks.”
Having learned about ivermectin’s potential healing effect on COVID patients, Dr. Day became one of the brave doctors in the U.S., actively using ivermectin to treat COVID. His patients were getting better, and he didn’t lose any.
But then, “in a Stalinesque manner,” he was forbidden by the clinic administration to prescribe not just HCQ but also ivermectin. “Dr. Day then came up with mostly over-the-counter combinations that mimicked the medicines he could no longer prescribe to the patients for political (fascist?) reasons.”
Then, “when the mandates were announced, Dr. Day declined the injection and was scheduled to be fired — but then the plot got even thicker. In August 2021, Governor Abbot issued an executive order undermining vaccines mandates in Texas. Then, Dr. Day was fired for “cause,” namely, for helping a disabled patient, on his free time, get her stolen ID renewed at the DMV — and also for “offending” people by expressing his strong views on the mandates.”
“Dr. Day was fired by the administration on his ‘off’ day as he, in his gardening clothes, was planting vegetables in the clinic garden. His small victory was that the plan to fire him in secret, on the day when he wasn’t supposed to be there, didn’t work out. He walked into the office in his gardening clothes, and all his colleagues saw what happened.”
Remarkably, even though they so it, no one stood up for him. No on objected. Today, the hero doctor is dedicating his time to blogging and remodeling his house. Before I interviewed him, he was also interviewed by another hero doctor of our times, Dr. Meryl Nass.
To find more of Tessa Lena’s work, be sure to check out her bio, Tessa Fights Robots.
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Disclaimer: The entire contents of this website are based upon the opinions of Dr. Mercola, unless otherwise noted. Individual articles are based upon the opinions of the respective author, who retains copyright as marked.
The information on this website is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended as a sharing of knowledge and information from the research and experience of Dr. Mercola and his community. Dr. Mercola encourages you to make your own health care decisions based upon your research and in partnership with a qualified health care professional. The subscription fee being requested is for access to the articles and information posted on this site, and is not being paid for any individual medical advice.
If you are pregnant, nursing, taking medication, or have a medical condition, consult your health care professional before using products based on this content.