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Conspiracy of (HeLa) Cells
- Thread starter Regina
- Start date
P
Peatress
Guest
Henrietta Lack.
A BBC propaganda documentary about her
View: https://rumble.com/v32555w-1997-documentary-henrietta-lacks-the-way-of-the-flesh-bbc-adam-curtis-hela-.html
A BBC propaganda documentary about her
View: https://rumble.com/v32555w-1997-documentary-henrietta-lacks-the-way-of-the-flesh-bbc-adam-curtis-hela-.html
Last edited by a moderator:
I was just about to post it. Thx
I'd love to have haidut's take. Because the mad scientists are still obsessed with them for population control.
Peatful
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- Dec 8, 2016
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Yes, to all. Cancer cells are basically stem cells, which are maintained almost entirely by glycolysis and are in a reductive state (a requirement for proliferation). Recent studies proved that all that it takes for "normal" cells to acquire the "cancer" phenotype is for OXPHOS to fall at the expense of glycolysis and for the cell to shift towards reduction. That raises intracelluler pH, which prevent apoptosis. Conversely, acidifying the cell by lowering lactate production and raising CO2 production (which happens only through OXPHOS) either makes a cell undergo apoptosis (if it determines it is too damaged to continue operating) or differentiate back into a specific organ/tissue cell. The excessive glycolysis and lactate overproduction is driven by excessive supply and oxidation of fat by the cell, which blocks glucose oxidation via the Randle Cycle (i.e. lowers NAD/NADH ratio and thus entry of pyruvate into the Krebs Cycle). Thus, lowering supply of fat (from diet or lypolysis) and/or directly inhibiting the oxidation of said fat has been shown to be curative for many tumors.
Restoring oxidative metabolism has curative effects on cancer (leukemia)
A great study, which directly demonstrates not only the OXPHOS deficiency characteristic of all "cancer" cells, but also proving that restoration of OXPHOS is highly therapeutic (and likely curative) for leukemia. Just as importantly, the study demonstrates that cancer cells have, in fact...
Acidosis (Warburg Effect) Drives Cancer Through Increased Fat Oxidation (Randle Cycle)
The evidence continues to pile on that naming the (in)famous observation made by Otto Warburg in regards to cancer an "effect" is one of the most profound falsehoods the medical profession has ever concocted. Almost a century after the Warburg "Effect" term was coined, the evidence rapidly...
Cancer Cells Addicted To Fat And Use Fat Oxidation For Survival
Ray has written several times that while cancer cells use glucose for their normal activities they use fat to evade apoptosis and increase metastasis. Thus, according to Ray, using substances that block fat oxidation can be therapeutic. Niacinamide and aspirin are some of the most beneficial...
Niacinamide Can Cure Liver (and Maybe Pancreatic) Cancer
This study shows that depletion of NAD is a direct cause of the so-called hepatocellular carcinoma (HCC), which is the most common type of liver cancer. People with HCC often develop metastases in the pancreas and in advanced stages, the condition is indistinguishable from pancreatic cancer...
Oh thank you very much for your lengthy explanation and all the links.Yes, to all. Cancer cells are basically stem cells, which are maintained almost entirely by glycolysis and are in a reductive state (a requirement for proliferation). Recent studies proved that all that it takes for "normal" cells to acquire the "cancer" phenotype is for OXPHOS to fall at the expense of glycolysis and for the cell to shift towards reduction. That raises intracelluler pH, which prevent apoptosis. Conversely, acidifying the cell by lowering lactate production and raising CO2 production (which happens only through OXPHOS) either makes a cell undergo apoptosis (if it determines it is too damaged to continue operating) or differentiate back into a specific organ/tissue cell. The excessive glycolysis and lactate overproduction is driven by excessive supply and oxidation of fat by the cell, which blocks glucose oxidation via the Randle Cycle (i.e. lowers NAD/NADH ratio and thus entry of pyruvate into the Krebs Cycle). Thus, lowering supply of fat (from diet or lypolysis) and/or directly inhibiting the oxidation of said fat has been shown to be curative for many tumors.
Restoring oxidative metabolism has curative effects on cancer (leukemia)
A great study, which directly demonstrates not only the OXPHOS deficiency characteristic of all "cancer" cells, but also proving that restoration of OXPHOS is highly therapeutic (and likely curative) for leukemia. Just as importantly, the study demonstrates that cancer cells have, in fact...raypeatforum.com
Acidosis (Warburg Effect) Drives Cancer Through Increased Fat Oxidation (Randle Cycle)
The evidence continues to pile on that naming the (in)famous observation made by Otto Warburg in regards to cancer an "effect" is one of the most profound falsehoods the medical profession has ever concocted. Almost a century after the Warburg "Effect" term was coined, the evidence rapidly...Cancer Cells Addicted To Fat And Use Fat Oxidation For Survival
Ray has written several times that while cancer cells use glucose for their normal activities they use fat to evade apoptosis and increase metastasis. Thus, according to Ray, using substances that block fat oxidation can be therapeutic. Niacinamide and aspirin are some of the most beneficial...Niacinamide Can Cure Liver (and Maybe Pancreatic) Cancer
This study shows that depletion of NAD is a direct cause of the so-called hepatocellular carcinoma (HCC), which is the most common type of liver cancer. People with HCC often develop metastases in the pancreas and in advanced stages, the condition is indistinguishable from pancreatic cancer...
The "brilliant" doctors and scientists that study these cells (to kill us) not only get the warburg effect assbackwards, they think of these cells as ways to spike the population with cancer. As well, that the proliferation is caused by a virus.
I think of them as cells living in a bad neighborhood/environment. Why bother individuating/differentiating oneself when there is seemingly nothing to become? There is nothing to support that. Just join a resentful lazy pack/blob for a low level survival.
Thank you again. I still probably can't describe "reductive" state. I can parrot that a shift away from reduction and towards respiration can trigger apoptosis or differentiation. I can parrot that NAD/NADH, as well as GSSG/GSH; pyruvate/lactate create an environment for OXPHOS where there is the energy and drive to differentiate.
I wouldn't be able to defend and describe the process to a normal geneticist scientist. I'm not there yet.
It seems to me that the obsession with HeLa cells continued thinking is similar to the black and white germ "vs" terrain theory.
It reminds me of David Bohm's insights that there are no separate things.
I don't know where to begin to open the discussion with George here.
So what if they spike the vaccines with HeLa cells. The general public is not in OXPHOS. So, I guess if the mad scientists can wrap the Hela goo up in mRNA and persistent irritants and garbage, then the unhealthy receiver would not have enough energy (NAD, etc) to kill or revert/individuate those cells. Is that what is happening with the fast cancers? The cancerous/diabetic state is already there and the injected Hela-Stein reverse transcriptase makes the environment much worse due to the chronic activation of inflammatory systems and estrogen? And this "virulence" is wrongly attributed to a "virus." It's more a vigorously primiitivizing and incoherentizing of the (dis)organism. ??
And the cancer vaccine mad scientists want to find the gene that shuts that down--rather than change and revive the NAD, etc state of the organism.
And could a Hela-Stein mRNA persistent nano-garbage cancerize a person with healthy OXPHOS?
It reminds me of David Bohm's insights that there are no separate things.
I don't know where to begin to open the discussion with George here.
So what if they spike the vaccines with HeLa cells. The general public is not in OXPHOS. So, I guess if the mad scientists can wrap the Hela goo up in mRNA and persistent irritants and garbage, then the unhealthy receiver would not have enough energy (NAD, etc) to kill or revert/individuate those cells. Is that what is happening with the fast cancers? The cancerous/diabetic state is already there and the injected Hela-Stein reverse transcriptase makes the environment much worse due to the chronic activation of inflammatory systems and estrogen? And this "virulence" is wrongly attributed to a "virus." It's more a vigorously primiitivizing and incoherentizing of the (dis)organism. ??
And the cancer vaccine mad scientists want to find the gene that shuts that down--rather than change and revive the NAD, etc state of the organism.
And could a Hela-Stein mRNA persistent nano-garbage cancerize a person with healthy OXPHOS?
P
Peatress
Guest
George Webb suggests Henrietta Lack may have been inseminated with the tumour. Start @30mins approx.
View: https://rumble.com/v32rk34-hela-high-water.html
View: https://rumble.com/v32rk34-hela-high-water.html
I think many people effectively equate cancer with kombucha/scoby. To keep the fermentation going, you add more sugar. Therefore, sugar causes the scoby to stay alive and keep growing. To stop fermentation, you can pasteurize, or use high heat or very cold temps.
How do I help a kombucha brewer understand cancerization and its reversal?
Is it that the scoby is so primitive?
How do I help a kombucha brewer understand cancerization and its reversal?
Is it that the scoby is so primitive?
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