Wednesday, February 14, 2024

Cottonseed oil vs butter study dug up by @drawandstrike from 1918 showed how rats thrived on butter and withered away on cottonseed oil.

Ah, yes.  from Cambridge

Americans have eaten significant amounts of cottonseed oil since the late nineteenth century. Yet for generations, few Americans have known how often they eat foods made from the cotton plant. Crisco paved the way for this kind of consumer ignorance. Launched by the Procter & Gamble company in 1911, Crisco was a wholly new product: a solid fat made entirely from liquid cottonseed oil, the result of the novel technology of hydrogenation. Responding to tenacious prejudice against cottonseed, Crisco's marketers made consumer ignorance acceptable by promoting the idea that industrial processing was akin to purification and encouraging consumers to put trust in brands rather than to focus on ingredients. The Progressive Era is supposed to be a period when food processing became increasingly transparent, and in some ways it was. But in the wake of the Pure Food legislation of 1906 and in conjunction with an exploding food advertising industry that highlighted factory processing as a unique virtue, American consumers increasingly trusted both government oversight and industrial food production. Cottonseed oil's history is ultimately a story of consumers’ growing confidence in highly processed food and their growing comfort with ignorance about the ingredients that went into it.
 

From Health-Giving Animal Fats to Health-Destroying Seed Oils, the Old Food Switch-a-roo

20,000 people die of cancer every day this translates to 8 million people a year, half a million of which are Americans. 

At the beginning of last century, 1900, 1/20 person would get cancer; in the 1940s, it was one out of every 16 people; in the 1970s, it was one out of 10. Today, one person out of three gets cancer in the course of their lifetime.  

I liked this video when I first saw it, but reviewing it here this morning the fear-mongering is absolutely atrocious.  I like to tell people to pause, to stop and think, as does Chris Beat Cancer's, Chris Wark.  No wonder patients freak out and are shocked into an anxious state for which the doctor provides the only solution: chemotherapy. 

Over 1 million Americans are diagnosed with a new cancer every year.  All these people suddenly plunge into a dark tunnel that will radically change their life in the years to come.  

"They find themselves at the complete mercy of the disease," which is a trillion dollar industry.

While in that tunnel, each patient feeds an immense medical apparatus that employees hundreds of thousands of people and generates millions and millions of dollars for the medical and pharmaceutical industry from research laboratories to medical school prevention clinics to worldwide drug sales.  sales.  Today, the cancer medical apparatus is so large and expensive that it needs its patients in order to survive just as much as the patience need the apparatus to survive.  

01:48. Peter Barry Chowka,

The typical cancer patient spends $50,000 to treat his disease with 1 million new American cancer patients every year.  That translates to 50 billion dollars annually spent on cancer treatments in the United States . . . 

But you've got to love this gem of a follow-up comment,

but to modern oncology, cancer still remains a mystery.  

03:09. The official Theory maintains the cancer originates in the cell.  

 

Tuesday, February 13, 2024

REPOST: Reminder that when they pull out their hockey stick, you just point to the airport strip

"everything that is illegal for normal pharmaceuticals is now legal as long as Prep Act window remains open for them."

Completely different category of product which the federal government created called EUA, Emergency Use Authorization, and this category only exists under Public Health Emergency or Prep Act declaration by Health and Human Services Secretary.  So under this particular category they are regulated by a completely separate section of Food, Drugs, & Cosmetics Act, FDA, which says that "everything that is illegal for normal pharmaceuticals is now legal as long as Prep Act window remains open for them."  And as we know for COVID, the PREP Act window is open until December of 2024.  And now we also have a window open for Ebola, Marburg, and other things until the end of 2028.  And I assure you the federal government fully intends to keep these Prep Act declarations going in perpetuity because there is no way on this planet these products can comply with normal regulatory requirements.  They tried for 20 years and they failed every time.  So they decided to go on the market anyway by creating this new regulatory status for themselves.  

So under this regulatory status, there is no IRB (Institutional Review Boards) requirement. 

There is no informed consent requirement.

There is no requirement for any compliance with good manufacturing practices; rather, it says you can do it as a manufacturer voluntarily but there is no enforcement and clinical trial data is completely irrelevant.  

Also, these things can coexist with what's fully approved versions except, of course, these products have never been approved normally under investigational status and, therefore, there is no fully approved version.  There is only an EUA.  And only EUAs have always been shipped in the US with drug inserts arriving blank.  And they never complied with any rules or requirements.