Schizophrenia, Cancer and the Hoff

Schizophrenia and cancer: the adrenochrome balanced morphism.

Abstract

Cancer might be expected to be more common amongst schizophrenics than the general population. They frequently live in selenium deficient regions, have seriously compromised antioxidant defense systems and chain-smoke. The available literature on the cancer-schizoprenia relationship in patients from England, Wales, Ireland, Denmark, USA and Japan, however, strongly suggests that the reverse is true. One of the authors (Hoffer) has treated 4000 schizophrenics since 1952. Only four of these patients has developed cancer.

Since low cancer incidence has been recorded amongst patients treated by both conventional physicians using pharmaceuticals and by orthomolecular doctors who emphasize vitamins and minerals, it follows that this depressed cancer incidence must be related to the biochemistry of the disorder itself. Taken as a whole, therefore, the evidence seems to suggest that schizophrenics, their siblings and parents are less susceptible to cancer than the general population.

These relationships seem compatible with one or more genetic risk factors for schizophrenia that offer(s) a selective advantage against cancer. There is experimental evidence that appears to support this possibility. Matrix Pharmaceuticals Inc. has received a US patent covering the composition of IntraDose Injectable Gel. This gel contains cisplatin and epinephrine (adrenaline) and is designed to be injected directly into tumor masses. Cisplatin is a very powerful oxidant which will almost certainly rapidly convert the adrenaline to adrenochrome. While the manufacturers of IntraDose consider cisplatin to be the active cytotoxic agent in IntraDose, it seems more likely that adrenochrome and its derivatives may, in fact, be more effective.

IntraDose gel has undergone or is undergoing a series of Phase III open-label clinical studies, being injected into patients’ tumors that have been identified as the most troublesome by their physicians. The results have been impressive for breast cancer, malignant melanoma, esophageal cancer and cancer of the head, neck and liver. The evidence suggests that there are balanced morphisms in schizophrenia that result in above normal exposure to catecholamine derivatives. Since such catecholamines are both hallucinogenic and anti-carcinogenic abnormally high exposure to them simultaneously increases susceptibility to schizophrenia and reduces the probability of developing cancer.

These observations have significant implications for the treatment of both illnesses.

linkRoll_2020.03.19

I really need to meditate on why I collect webpages. Why I abuse the tab function and the associated memory use just to allow these links to then grow into an insurmountable hurdle preventing me from…Am I overthinking this too much?

It’s probably just the caffeine…8)


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What If’s-2019-03-31

What if…Something as simple as Prilosec or Nexium could aid in disrupting the lifecycle of cancer? Imagine that. An over the counter antacid used in an off-label manner leading to countless spontaneous remissions of various types of cancers.

I think I have connected those dots and I’m not the only one. Yay…

Utilization of omeprazole to augment subtherapeutic voriconazole concentrations for treatment of Aspergillus infections.

Mycosis fungoides responding to systemic itraconazole.

Repositioning of proton pump inhibitors in cancer therapy.

ASPERGILLUS TREATMENT: Black Mold-Utilization of omeprazole to augment subtherapeutic voriconazole concentrations for treatment of Aspergillus infections.

What If’s-2019-03-01

Happy March 2019-

What if…Bio-scenario_001-Life begins at conception and ends once decomposition ends.

What if…Cancer is a part of that biological process, a molecular bio-remediation tool used that has remote switching by the hosts immune system but no off switch. These cancers are proteins who’s DNA can be disrupted and modified.

The reason there is no off switch is because there is no need for one. These are the clean up crew that is activated upon chemical signaling caused by host death. Why would a Consumer, designed to do just that need an off switch? These cells that the cancer consume already had that function built in called apoptosis.

On occasion a host is resuscitated after the host death message is sent. The problem now being that the host is alive again but with cancer crew having already been activated.

These cancer cells once activated are set to consume the host and will continue to do so until disrupted and eradicated or until all host tissue has been consumed.

On their own each of these cells, even at post invasion levels can be overcome by the hosts immune system if it is functioning at a minimum of 90% capacity. If host immunity is below 80% full scale colonization can begin.

More to come…

…What triggers initial colonization of what will eventually become identified as a problematic cancer in the future. A tumor?

…Mary, Jesus, spot & blemish?

…3rd Trimester, Goal Posts and immune system autonomy between mother and child.

…how far back can we go with cleansing diets and digestive enzymes on full tilt?

Looking again…At the skin as an atmosphere for our body. The subcutaneous layer of our skin being equivalent to soil on Earth. Where do we make changes to our outermost layer of skin?

What If’s-2018/12/22

What if…Regarding cancer, rather than trying to think outside the box, maybe we should be looking at it and wondering if it was ever a box to begin with.

What if…We have been looking at what we call cancer too closely and have missed the bigger picture. Focused too acutely on individual cells, or too deeply inside of them. That cancer needs to be observed like a forest…From a distance.

open-box

What if…The majority of human disease is simply septic in nature or toxin based in origin?

Is there anyone historically that has attempted to cure cancer, not at the individual level, but at a multi-generational/genetic level? Seeking gains at the multi-generational level.

What if…There were no such thing as genetic lines of disease?

What if…Disease were simply a continual passing down of bad alimentary habits passed from one generation to the next resulting in the same malady in both parent and child?

-Michael J Loomis