Health & Fitness

07/18/22

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How Pfizer Profited From the Pandemic

According to Kaiser Health News (KHN),¹ the COVID-19 pandemic has been a real boon to Pfizer. Not only has it yielded “outsize benefits” in terms of profits, but it has also “given the drugmaker unusual weight in determining U.S. health policy.”

“Based on internal research, the company’s executives have frequently announced the next stage in the fight against the pandemic before government officials have had time to study the issue, annoying many experts in the medical field and leaving some patients unsure whom to trust,” KHN reporter Arthur Allen writes, adding:²

“When last year Bourla suggested that a booster shot would soon be needed, U.S. public health officials later followed, giving the impression that Pfizer was calling the tune.

Some public health experts and scientists worry these decisions were hasty, noting, for example, that although boosters with the mRNA shots produced by Moderna and Pfizer-BioNTech improve antibody protection initially, it generally doesn’t last.

Since January, Bourla has been saying that U.S. adults will probably all need annual booster shots, and senior FDA officials have indicated since April that they agree ... The company’s power worries some vaccinologists, who see its growing influence in a realm of medical decision-making traditionally led by independent experts ...

When President Biden in September 2021 offered boosters to Americans — not long after [Pfizer CEO Albert] Bourla had recommended them — Dr. Paul Offit, director of the Vaccine Education Center at Children’s Hospital of Philadelphia ... wondered, ‘Where’s the evidence you are at risk of serious disease when confronted with COVID if you are vaccinated and under 50?’

Policies on booster recommendations for different groups are complex and shifting, Offit said, but the CDC, rather than Bourla and Pfizer, should be making them. ‘We’re being pushed along,’ he said. ‘The pharmaceutical companies are acting like public health agencies.’”

The fact that a vaccine-pusher like Offit — infamous for claiming a baby can safely tolerate 10,000 vaccines at once³ — is questioning and pushing back against Pfizer’s influence over health policy reveals just how brazen, unethical and potentially dangerous that is.

Massive Profits Made From Useless Products

According to Allen, Pfizer’s revenue in 2021 was $81.3 billion⁴ — approximately double that of 2020 — and the COVID shot accounted for $36.78 billion⁵ of that. For comparison, Lipitor, Pfizer’s previous top selling statin, generates roughly $2 billion a year,⁶ while their strep vaccine, Prevnar 13 rakes in $6 billion a year.⁷

Its mRNA gene transfer injection against COVID now dominates 70% of the U.S. and European markets, and Paxlovid, Pfizer’s COVID drug, has become a standard treatment choice in hospitals. This, despite researchers finding Paxlovid (molnupiravir) causes severe rebound and supercharges mutations.

In a rational scenario, that finding would have put a stop to its use, but no. In an official health advisory⁸ to the public, issued May 24, 2022, the U.S. Centers for Disease Control and Prevention first warns that Paxlovid is associated with “recurrence of COVID-19 or ‘COVID-19 rebound,’” and then in the very next sentence stresses in bold print a narrative supporting its use and enriching Pfizer with instructions saying:

“Paxlovid continues to be recommended for early- stage treatment of mild to moderate COVID-19 among persons at high risk for progression to severe disease.”

Allen also notes that, during an investor call, a Pfizer official highlighted reports of Paxlovid’s failure, but spun it into “good news” for investors, as patients may require multiple courses!⁹ Obviously the objective has long ago shifted from helping humans to raping them for as much profit as possible.

Similarly, while Pfizer’s COVID jab clearly doesn’t prevent infection or spread, and Americans are rejecting the shots in growing numbers — 82.2 million doses had expired and were chucked in the trash as of mid-May 2022¹⁰ — the U.S. government still went ahead and ordered another 105 million doses at the end of June 2022.

These are intended for a fall booster campaign, at a cost to taxpayers of $3.2 billion.¹¹ The U.S. is actually paying about 50% more for each of these new jab boosters this time around — $30.47 per dose compared to $19.50 per dose paid for the first 100 million doses.

The U.S. government has also promised to purchase another 20 million courses of Paxlovid, at an eye-watering cost of $530 per five-day course. Basically, Pfizer is being financially rewarded for producing products that are useless at best and dangerous at worst, and we’re all paying for it. In case you’re curious, that is another $10.6 billion transferred from U.S. taxpayers to Pfizer.

Future Boosters Won’t Undergo Human Clinical Trials

After you likely thought it couldn’t ever get any worse, KHN also touches on, but doesn’t delve into, the fact that Pfizer suggested they skip human trials as they move forward with jabs that are reformulated for newer variants. If this strikes you as crazy, you’d be right. It’s sheer madness, but the U.S. Food and Drug Administration — a clearly captured agency — has already surreptitiously agreed to this egregious miscarriage of science.

How this wicked scheme, known as the “Future Framework,”¹² was adopted by the FDA without formal vote is explained by Toby Rogers, Ph.D. — a political economist whose research focus is on regulatory capture and Big Pharma corruption¹³ — in the video above. He also explained it in a June 29, 2022, Substack article:¹⁴

“Yesterday [June 28], the FDA’s Vaccines and Related Biological Products Advisory Committee approved a bivalent COVID-19 shot with the Wuhan strain and the Omicron variant ... Wait, hold up, I thought the FDA was voting on the Future Framework yesterday?

The policy question was whether reformulated COVID-19 shots would be treated as new molecular entities (which they are) in which case they should be subject to formal review or whether reformulated shots would be treated as ‘biologically similar’ to existing Covid-19 shots and be allowed to skip clinical trials altogether.

Apparently the FDA did not have the votes to just pass this as a policy question. If you ask anyone whether reformulated mRNA represents a new molecular entity, well of course it is, so that would require formal regulatory review.

What the FDA did instead was to smuggle the policy question in disguised as a vote about reformulated ‘boosters’ for the fall.

In essence, the FDA just started doing the Future Framework (picking variants willy nilly, skipping clinical trials) and essentially dared the committee members to turn down a booster dose — knowing that all of the VRBPAC members are hand-picked because they’ve never met a vaccine they did not like.

So of course only two people on the committee had the courage to turn down a booster dose — even though it was based on this preposterous process (that was never formally adopted) where there was literally no data at all ... By stealth, the FDA replaced a system based on evidence with a system based entirely on belief.”

Countries Held to Ransom

In 2021, secret details of Pfizer’s contracts came to light, showing they are essentially holding countries hostage to nonnegotiable demands for payment in full AND freedom from liability.¹⁵

In late February 2021, The Bureau of Investigative Journalism reported¹⁶ that Pfizer was demanding countries put up sovereign assets as collateral for expected vaccine injury lawsuits resulting from its COVID-19 jab.

Several countries, including Brazil, Chile, Colombia, the Dominican Republic and Peru, agreed to this demand, putting up bank reserves, military bases and embassy buildings as collateral. In short, theses governments are guaranteeing Pfizer will be compensated for any expenses resulting from injury lawsuits against it, so the company won’t lose a dime if its COVID shot injures people.

Shockingly, these terms are binding even if those injuries are the result of negligent company practices, fraud or malice!

In October that same year, Public Citizen published the secret contracts^17,18 between Pfizer and Albania, Brazil, Colombia, Chile, Dominican Republic, the European Commission, Peru, the U.S. and the U.K., further revealing the extent to which these countries handed power over to Pfizer. In almost all scenarios, Pfizer’s interests come first.

For example, government purchasers must acknowledge that the effectiveness and safety of the shots are completely unknown, all while indemnifying Pfizer against any and all financial liability. This is the ultimate corporate maleficence, using their leverage to force the kill shot down these countries’ throats and avoiding any personal responsibility for damages.

Even if Pfizer eventually is convicted of fraud in the U.S. and loses all its liability protection from the COVID jabs because of it, that judgment would not impact these foreign contracts. These countries sold their souls to Pfizer and have absolutely no recourse but to pay even if the shots kill everyone.

The contracts for at least four countries also secure Pfizer’s intellectual property rights even if the company is found to have stolen intellectual property rights of others. In such case, the government purchaser becomes the liable party. As explained by Public Citizen:¹⁹

“For example, if another vaccine maker sued Pfizer for patent infringement in Colombia, the contract requires the Colombian government to foot the bill. Pfizer also explicitly says that it does not guarantee that its product does not violate third-party IP, or that it needs additional licenses.

Pfizer takes no responsibility in these contracts for its potential infringement of intellectual property. In a sense, Pfizer has secured an IP waiver for itself. But internationally, Pfizer is fighting similar efforts to waive IP barriers for all manufacturers.”

Equally shocking is that countries are forced to follow through on their vaccine orders even if other drugs or treatments emerge that can prevent, treat or cure COVID-19.²⁰ Is it any wonder, then, that governments around the world have suppressed the use of safe and effective outpatient drugs like hydroxychloroquine and ivermectin?

If these drugs were allowed to be used and could be proven to work, the COVID injections would be completely unnecessary and their emergency use authorization would disappear, yet governments are on the hook for hundreds of millions of doses.

Pfizer Has ‘Habitual Offender’ Track Record

The fact that Pfizer has behaved like a criminal who works out a cover story for a planned murder before committing it is not surprising, considering its history. Pfizer, has been sued in multiple venues over unethical behavior, including unethical drug testing and illegal marketing practices.²¹

In his 2010 paper,²² “Tough on Crime? Pfizer and the CIHR,” Robert G. Evans, Ph.D., Emeritus Professor at Vancouver School of Economics, described Pfizer as “a ‘habitual offender,’ persistently engaging in illegal and corrupt marketing practices, bribing physicians and suppressing adverse trial results.”

Between 2002 and 2010 alone, Pfizer and its subsidiaries were fined $3 billion in criminal convictions, civil penalties and jury awards. They are recurrent criminal felons. None of these convictions has deterred their nefarious behavior.

In 2011, Pfizer agreed to pay another $14.5 million to settle federal charges of illegal marketing,²³ and in 2014 they settled federal charges relating to improper marketing of the kidney transplant drug Rapamune to the tune of $35 million,²⁴ as well as $75 million to settle charges relating to its testing of a new broad spectrum antibiotic on critically ill Nigerian children.

As reported by the Independent²⁵ at the time, Pfizer sent a team of doctors into Nigeria in the midst of a meningitis epidemic. For two weeks, the team set up right next to a medical station run by Doctors Without Borders and began dispensing the experimental drug, Trovan. Of the 200 children picked, half got the experimental drug and the other half the already licensed antibiotic Rocephin.

Eleven of the children treated by the Pfizer team died, and many others suffered side effects such as brain damage and organ failure. Pfizer denied wrongdoing. According to the company, only five of the children given Trovan died, compared to six who received Rocephin, so their drug was not to blame.

The problem was they never told the parents that their children were being given an experimental drug. What’s more, while Pfizer produced a permission letter from a Nigerian ethics committee, the letter turned out to have been backdated. The ethics committee itself wasn’t set up until a year after the trial had already taken place. Pfizer’s rap sheet also includes bribery, environmental violations, labor and worker safety violations and more.²⁶

Wolves in Sheep’s Clothing

Now, despite Pfizer being one of the least ethical drug companies, we’re told to trust them with our very lives, and the lives of our precious children. They’re going to put out booster shots this fall that have undergone absolutely no testing whatsoever, and we’re to simply throw caution to the wind because Pfizer — which has no liability whatsoever — says so.

In 2014, Pfizer faced a surge of lawsuits that accused it of hiding known side effects of its anticholesterol drug Lipitor.²⁷ They got off scot-free that time, as a federal judge dismissed thousands of cases alleging the drug caused Type 2 diabetes.^28,29 But at least they had liability and could be sued.

When it comes to the COVID jabs, injured patients and family members of those killed by it won’t even have the ability to sue for damages, as governments around the world have indemnified them completely, and it looks as though they might not even be liable even if they’re found guilty of fraud. But we will have to see what the courts rule on that one. Still, that any nation would agree to a contract like that is just mindboggling.

Meanwhile, mounting evidence shows the COVID shots destroy immune function over time, and Pfizer’s own trial data reveal deaths and serious adverse events numbering in the tens of thousands.

It’s hard to tell who’s more deserving of punishment — Pfizer or the equally captured federal agencies, the FDA and the CDC, that go along with them and do nothing to protect the lives of the youngest members of our society. Clearly, it’s up to us to protect ourselves and our loved ones, because wolves in sheep’s clothing are ruling the roost — they’re making all the decisions, and captured agencies are simply doing their bidding.

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Eight Signs You Might Be B12 Deficient

This article was previously published March 25, 2019, and has been updated with new information.

When you experience symptoms like fatigue, numbness, faint nausea, foggy vision or an increased tendency toward forgetfulness, you might entertain many different scenarios. Some of them might be scary, but a possibility you may not consider is that of a vitamin B12 (aka cobalamin) deficiency.

Nearly half of the American population has less-than-stellar blood levels of vitamin B12, but the symptomology is so varied that it's hard to pin down just how many people suffer from it, according to Harvard Health, which describes the "sneaky" symptomology behind a 62-year-old man's seemingly unrelated symptoms, developed over two months. According to his case report, published in The New England Journal of Medicine,¹ he had:

"Numbness and a 'pins and needles' sensation in his hands, had trouble walking, experienced severe joint pain, began turning yellow, and became progressively short of breath … It could have been worse — a severe vitamin B12 deficiency can lead to deep depression, paranoia and delusions, memory loss, incontinence, loss of taste and smell, and more."²

It's problematic that symptoms like the above may cause people to focus on treating them instead of investigating the source of the problem. Sooner or later, though, unless it's met head-on, a shortage of vitamin B12 in your system can be so devastating that serious disorders, such as Alzheimer's disease, Crohn's disease and irreversible brain damage could take their toll.

Low Vitamin B12 Symptoms Not so Unrelated After All

The list of symptoms that could be placed on a B12 deficiency's proverbial doorstep is a long one, but many symptoms are associated with your central nervous system. Too little B12 in your system might also resonate if you've experienced poor vision, weakness, tingling in your hands or feet and incidences of "clumsiness." Eight common signs that indicate low B12 levels are:

Fatigue	Anemia
Nausea	Digestive issues
Weakness	Skin infections
Mental confusion	Nerve problems

But it's also important to understand that several areas of the body can be adversely affected with a vitamin B12 deficiency, and that while many of the symptoms may seem unrelated, as the saying goes, one thing often leads to another.

Low B12 Can Cause Anemia, Which Has Its Own Set of Symptoms

As is true for every human, vitamin B12 is necessary to keep your nervous system healthy, as well as to make DNA, which is the genetic material in all cells.³ B12 is also needed to produce red blood cells, which transport oxygen throughout your body.

But with a shortage of B12, many of your red blood cells are abnormally formed and/or too large, so they can't carry oxygen; the process is disrupted. Too few red blood cells or an abnormally low amount of hemoglobin in individual red blood cells causes anemia, one of the most common and noticeable signs that a shortage is becoming a problem.⁴

Anemia can cause some of the previously listed symptoms, such as weakness, fatigue, dizziness, cold hands and feet, pale skin and chest pain, which occur because your heart has to work harder to move oxygen-rich blood through your body, The National Heart, Lung, and Blood Institute (NHLBI) reports.⁵ In turn, this can lead to irregular heartbeat or arrhythmia, enlarged heart and even heart failure.⁶

Recognizing B12 deficiency sooner rather than later is crucial, as left unchecked it can lead to permanent damage in your body.⁷ According to the Linus Pauling Institute,⁸ a B12 deficiency may also be culpable in several other serious diseases and conditions, including:

Breast cancer⁹	Chronic stomach inflammation¹⁰
Depression¹¹	Neural tube defects¹²
Osteoporosis¹³	Gastric cancer¹⁴
Thyroid dysfunction¹⁵	DNA damage¹⁶

How Does Low B12 Cause Jaundiced Skin and Dementia?

Because B12 — and a lack thereof — is closely associated with your nervous system, the sign known as "pins and needles" is one that indicates a nerve issue that should be addressed as soon as possible, and shows how interconnected your body's functions are.

Because vitamin B12 is important for the maintenance of your central nervous system, including the conduction of nerve impulses and producing the myelin sheath, it protects and "insulates" your nerves. Without this protective insulation, your nerves can be damaged, leading to symptoms like "pins and needles" in your hands and feet, as well as central and peripheral nervous system damage.¹⁷

If you've noticed that your skin has a pale or jaundiced cast, it's a warning sign that your body is unable to produce an adequate number of red blood cells. You may not have thought about it, but it's the red blood cells circulating under your skin that give it its healthy color.

Vitamin B12 deficiency can cause megaloblastic anemia, which can weaken your blood cells, after which other symptoms begin appearing. When your liver breaks down red blood cells, it releases bilirubin, a brownish substance that lends your skin a jaundiced appearance, often seen in infants.¹⁸

As if these problems weren't enough, people with low levels of B12 may also suffer problems with clear thinking, which later turns into the condition doctors call cognitive impairment or dementia.¹⁹

The symptoms often become evident when someone has reasoning difficulties and memory loss, but often, that is what is treated rather than exploring the possibility of a B12 deficiency, which could alleviate the symptoms if addressed.

An all-encompassing review in Australia in 2012 revealed associations between low vitamin B12 levels and neurodegenerative disease. A total of 43 studies revealed that "subclinical low-normal ranges are associated with Alzheimer's disease, vascular dementia and Parkinson's disease."²⁰ Another study notes:

"Vitamin B12 deficiency should always be looked for when a patient presents with memory loss, since it is generally reversible with treatment. Many neuropsychiatric symptoms have been observed, and many in patients who do not have a megaloblastic anemia.

These include memory loss, psychosis including hallucinations and delusions, fatigue, irritability, depression and personality changes."²¹

A B12 Deficiency Often Shows Up in Your Mouth

One symptom of anemia that often shows up are mouth ulcers, sometimes known as canker sores or aphthous ulcers, small yellow or white ulcers that can appear on your gums or just inside your lip. While they usually clear up in a week or two, they're often quite painful.

But a B12 deficiency can cause other symptoms in your mouth as well, including on your tongue. One study relates the experience of a middle-aged female patient — a common demographic for her symptoms — with a persistent burning sensation on her tongue for several months.

Diagnosed with glossitis, which causes a noticeably swollen, smooth, red tongue, she was given a single injection of vitamin B12, which "resulted in complete resolution of her symptoms and the normal clinical appearance of her tongue after three days."²²

Low B12 Carries Increased Risk for Serious Infections

People with deficiency in vitamin B12 are at a higher risk of infections caused by two potentially deadly pathogens. Findings of a study published in the journal PLOS Genetics²³ involved 1 millimeter-long (pencil tip-sized) nematodes or worms called Caenorhabditis elegans (C. elegans), one of the world's most basic organisms.

Vital to the study was that nematodes share an interesting characteristic with humans: They can't produce their own vitamin B12, either. As reported by MedIndia, the study involved two worm populations: one with and one without a diet sufficient in B12, showing that a B12-deficient diet harms the worm's health at a cellular level by reducing its ability to metabolize branched-chain amino acids (BCAA):

"The research showed that the reduced ability to break down BCAAs led to a toxic buildup of partially metabolized BCAA byproducts that damaged mitochondrial health … 'We used C. elegans to study the effect of diet on a host and found that one kind of food was able to dramatically increase resistance to multiple stressors — like heat and free radicals — as well as to pathogens,' said [researcher Natasha Kirienko]."²⁴

Many labs around the world use C. elegans to study the effects of disease. By feeding the worms E. coli, a common and sometimes harmful gut bacteria, and switching between E. coli strain OP50 and strain HT115, the worms' stress tolerance was "dramatically altered," Kirienko said. "We found that switching between E. coli strain OP50 and strain HT115 dramatically altered the worm's stress tolerance." Co-author Alexey Revtovich noted:

"The key difference between the two diets is the ability of HT115 and OP50 to acquire B12 from the environment … We showed that HT115 is far more efficient at this, making about eight times as much of the protein that it needs to harvest B12 as compared to OP50."²⁵

Significantly, the team also found that C. elegans on an HT115 diet had the ability to resist infection by another deadly human pathogen, Enterococcus faecalis, a leading cause of hospital-acquired infections and recognized by the World Health Organization and U.S. Centers for Disease Control and Prevention (CDC) as a superbug.²⁶

Kirienko noted that the B12 finding surprised the research team. They noticed the effect when they studied "the mechanisms of pathogenesis of Pseudomonas aeruginosa (P. aeruginosa), a potentially deadly disease in both worms and humans that infects some 51,000 U.S. hospital patients each year,"²⁷ according to the CDC.²⁸

How to Optimize Your Vitamin B12 Levels

Some people have a greater risk than others for vitamin or mineral deficiencies, but in this case vegans and vegetarians are at particular risk because B12 is derived from animal products. Additionally, older adults and people with gastrointestinal and malabsorption issues are also at risk.

Studies have also shown that those on metformin (for diabetes) and prolonged use of proton pump inhibitors (for stomach acid) are also at an increased risk for vitamin B12 deficiency, leading researchers to suggest "it seems prudent to monitor vitamin B12 levels periodically in patients taking metformin."²⁹

Because it's not manufactured by your body, vitamin B12 must come from another source — namely food and supplements. That said, good sources for cobalamin or vitamin B12 include:

Grass fed organic beef and beef liver	Lamb
Venison	Scallops
Organic, pastured chicken and eggs	Raw organic, grass fed milk
Nutritional yeast

As for supplementation, according to the National Institutes of Health (NIH),³⁰ the average person age 14 and older should get 2.4 micrograms (mcg — one-millionth of a gram³¹) of vitamin B12 per day; pregnant women should get 2.6 mcg; and breastfeeding women should get 2.8 mcg. Newborns and children up to age 13 require between 0.4 and 1.8 mcg.

The type of a vitamin B12 supplement you should take is also something to consider. Between cyanocobalamin, the synthetic form,³² and methylcobalamin, which is the naturally occurring form found in food, methylcobalamin is the better choice, one reason being that your body retains it in greater amounts.³³

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