McCairn & Rixey Biowarfare Livestream, my thoughts & treatment info; Mycoplasma pneumoniae; Gulf War Syndrome; Terrain dysfunction - multifactorial conditions.

"Hindsight is 20/23." haha, I'm not sure who said that, someone on the Twxtter Space rather than Kevin. He laughed. / Too long for email.

Kevin McCairn’s and Charles Rixey BIGGEST POINT —> We are now hearing about a “new” outbreak of respiratory illness in children in China…. What’s up? —> Lies, and more lies probably. Mycoplasma pneumoniae is not new, more later in the section on Gulf War Syndrome, though doctors aren’t being educated on mycoplasmas per Garth Nicolson, an MD and researcher on Gulf War Syndrome and the history of mycoplasma research in a prison in the 1970s.

Mycoplasma pneumoniae, Photo by CDC on Unsplash

A point being made by Charles Rixey is that there is a long history of Gain of Function research leading up to the creation of SARS-CoV-2. And it is an incapacitating pathogen - not instantly deadly which would be too obvious - no plausible deniability. AKA - “Climate change causes myocarditis!”

• Three hour Rumble/Twxtter Space/Kevin McCairn livestream with Charles Rixey and later a few other voices from the Twxtter Space. (Rumble) {Listening to this a few times - they don’t focus on treatment because it is an open internet and not their focus. Treatment guidance is my focus and the internet is not as open as it could be. More voices on effective treatment are needed because chimeric spike is so bad and standard of care is largely kill/cull protocols - or maybe leaving people incapacitated and in need of 24-7 caregivers is the goal. You incapacitate several people that way, not just the patient.}

• Via a Substacker and also a Twxtter friend Misha:

Charles Rixey/George Webb Big News Day Today!

The point about there being a long history of GOF research culminating in the chimeric spike is old - David Martin showed us the long patent trail. The chimeric spike is a ~ computer generated sequence of previously patented work - mostly out of the US.

»so that is a BIG YES - Yes, There is a long history of Biowarfare research in the US that was combined in the ridiculously over-engineered chimeric spike and then stuck onto a coronavirus or in modified form in the CoV injections. The modified form is even worse. It seems to be more of a cholinergic blocker of the nAChR receptors -like snake venom toxin or Conatoxin (from deadly marine snails).

Charles shares seven traits of Biowarfare style gain of function work and says SARS-COV-2 modifications and the suppression of helpful treatments that occurred includes all seven. Later, a video of Garth Nicolson discusses earlier Biowarfare gain of function strategies in regards to Gulf War Syndrome and Mycoplasmas.

What are attributes of Gain of Function work?

• “The ability to manipulate the medical systems… in such a way to maximize the impact” - Kevin McCairn (of the GOF pathogen…) Use of antibiotics dropped during the CoV scamdemic - which would have left comorbid bacterial infections untreated during CoV care - like pneumonia.

• ~ “Increasing resistance to clinically useful prophyalctics, or evade detection methodologies. … Mycoplasmas would evade detection.” - Charles Rixey

The government lists seven things we are not supposed to do to a virus during gain of function research - Charles Rixey.

1. Anything that enhances the harmful consequences of the agent or toxin.

2. Disrupts immunity or the effectiveness of an immunization against the agent or toxin without clinical or agricultural justification.

3. Confers to the agent of toxin resistance to therapeutic intervention.

4. Increases the stability, transmissibility or ability to disseminate the agent or toxin.

5. Alters the host range or tropism of the agent or toxin. (*GP120 HIV insert and other pathogenic changes do the first five things.)

6. Enhances the susceptibility of a host population to the agent or toxin. (*both SARS-CoV2 virus and the mRNA injections have been shown to do this).

7. Generates or reconstitutes and eradicated agent or toxin. (*any bivalent boosters with the wildtype spike)

The (*comments) are from Charles →

The SARS2 virus and injections check off all seven ‘Don’t Do’s - re SARS-CoV2 and the seven traits of biowarfare gain of function gene sequencing work:

• SARS-COV-2 has been found to be more heat stable than typical coronavirus.

• It has many extra genes for entering receptors.

• And it has many toxic gene sequences including SEB, a bacterial endotoxin that is rated as a bioweapon.

• Also suppressing effective treatments while spreading an incapacitating bioweapon.

What helpful research has been suppressed - what does that trail show us? Mycoplasmas and intracellular infections. Suppression of iodine and magnesium research. Suppression of research into the harms of glyphosate/Roundup.

The other way to look at the long history of Gain of Function research and what it focused on (like mycoplasma species) is to also look at the long history of what topics and whose research has been suppressed in the US rather than replicated, awarded, advanced into patient care.

Lida Mattman’s work on intracellular pathogens including mycoplasma and she found a causal pathogen for Rheumatoid arthritis….had you heard that great news! Did Lida win a Nobel Prize for her work? No. Are Rh. arthritis patients treated for an intracellular pathogen yet? No.

How about Dr. Brownstein’s work on iodine and halides? Still suppressed.

How about Mildred Seelig’s work (and Andrea Rosenoff (sp?)) showing magnesium deficiency is being labeled many other things and being given many other medications that treat symptoms instead of correcting magnesium deficiency? Suppressed still. ScienceDirect summary pages frequently do not mention magnesium at all, on topics that are significantly related to magnesium metabolism.

Gosh golly, and what about pomegranate peel, a natural fusion inhibitor and antidote for SARS-COV-2? Still not mentioned by most people, including our supposed CoV health activists.

THERE IS ALSO A LONG HISTORY OF EFFECTIVE AND INEXPENSIVE HEALTH STRATEGIES BEING SUPPRESSED. Not just a long history of Biowarfare research. And that is one of the seven traits of Gain of Function biowarfare work - suggesting that for a long time citizens have been suffering from biowarfare from their own government that has a goal of promoting incapacitation. Low iodine causes apathy, reduced cognitive skill/IQ, and causes weight gain frequently along with depression, constipation and feeling cold too easily.

Other work on ‘seven’ issues of gain of function research:

“Concerns about risky research prompted the National Academy of Sciences (NAS) to issue a report in 2004 titled “Biotechnology Research in an Age of Terrorism,” listing seven “experiments of concern,” recognized as the “seven deadly sins,” that should not be pursued if they could create pathogens that are not already present in nature.

These experiments include:

1. Demonstrating how to make a vaccine ineffective

2. Developing a pathogen’s resistance to antibiotics or antiviral agents

3. Enhancing a pathogen’s virulence (i.e., lethality) or making a non-lethal microbe lethal

4. Increasing the transmissibility of a pathogen (e.g., making a non-airborne pathogen airborne)

5. Altering the host range of a pathogen by increasing the number of species it can infect

6. Enabling a pathogen to evade diagnostic testing

7. Enabling a biological agent or toxin to be weaponized.” - Laura Kahn, The Seven Deadly Sins of Biomedical Research, March 3, 2023, (gjia.georgetown.edu)

Background on Mycoplasma species:

Mycoplasma pneumoniae causes direct damage to lung cells by depleting nutrients, invading cells and causing toxin and cytokine induced damage. (Hu, et al., 2022) Treatment then, would need nutrient supplementation and use of phytonutrients like pomegranate peel that reduce inflammatory cytokines. Extra vitamin A, C, D and E and thiamine and other B vitamins are likely needed in addition to magnesium and potassium. (Vit C and thiamine: Marek Protocol)

“Mycoplasmas are the smallest free-living, wall-less and self-replicating prokaryotes having an extremely small genome size of 580–2200 kb [1, 2]. More than 200 species of mycoplasma have been identified in humans, animals, plants and arthropods, but only a few of them have been proven to cause human diseases. The main pathogenic mycoplasmas include Mycoplasma pneumoniae, M. genitalium, M. fermentation, M. hominis, M. penetrans, M. pirum and Ureaplasma urealyticum, which are identified to be responsible for humans and animal diseases in the respiratory tract and urogenital system.”

“Hereby, we comprehensively summarized and reviewed the intrapulmonary and extrapulmonary pathogenesis of M. pneumoniae infection. The pathogenesis of related respiratory symptoms caused by M. pneumoniae is mainly adhesion damage, direct damage including nutrient predation, invasion and toxin, cytokine induced inflammation damage and immune evasion effect. The pathogenesis of extrapulmonary manifestations includes direct damage mediated by invasion and inflammatory factors, indirect damage caused by host immune response, and vascular occlusion.” (Hu, et al., 2022)

Repairing our ‘Terrain’

Treating intracellular infections basically means, based on what I have learned, restoring the ‘terrain’ of the body. Intracellular infections may be normal flora that becomes too numerous, out of balance, due to other health issues like stress or toxin overload. It takes months to years to slowly rebuild health. Anything inflammatory needs to be reduced and modulating plant phytonutrients can help the gut balance and help restore healthy cytoplasm/intra and extracellular fluid. It needs to be able to be structured water for optimal mitochondrial and human health.

Pomegranate peel helps the T-cell imbalance of chronic illness and reduces the Th17 cells (Lu, et al., 2020) which are associated with autoimmune disease. (Zambrano-Zaragoza, et al., 2014)

Deficiency of vitamin A, D and E is associated with severe Mycoplasma pneumoniae pneumonia (MPP) in children and deficiency of vitamin A was also associated with non-severe MPP in children. (Xing, et al., 2020)

Pomegranate inner pith is mild enough to eat in small amounts. A therapeutic dose I use is about 1/4 teaspoon dried or a half teaspoon raw inner pith. See the small piece in the top right of the image - I minced that size piece and sprinkled it on the salad (white bits that are smaller than the seeds) The outer rind is so high in tannins I just use it in tea or extract.

Fresh inner pith and seeds is good in Cole slaw or an apple Waldorf salad. Anything crunchy would go pretty good with the seeds. I use dried powdered inner pith in baked goods or jams or soup. It thickens the broth and turns it brownish from the hydrolyzable tannins which are like humic acid then or fulvic acid - very large molecules that clump things together - like a thickened creamy soup broth. Liposome rich too probably.

See page G13. Effectivecare.info or archives here for ‘pomegranate peel prep tips’ (This post) or this pdf https://www.dropbox.com/scl/fi/qyr81immk5excqf97byfa/Pomegranate-Benefits-and-Preparation-2.pdf?rlkey=a2vr9rfs2fwr4fmd5jng3qbtv&dl=0

Anti-phospholipid syndrome may be involved in risk for autoimmune disease.

Anti-phopholipid syndrome is seen as a comorbidity with ME/CFS. It has been seen in LongCovid patients and patients with Gulf War Syndrome. The Lipid Nanoparticles used in mRNA injections contain phospholipid and it may be leading to autoimmune reactions against our own phospholipids.

Antibodies against phospholipids could cause membrane breakdown and reduce endocannabinoid availability. Medical use of marijuana products might be needed or at least a supplement of phosphatidylserine and/or phosphatidylcholine.

“Thanks to hemostasis researcher Dave McGlasson for sending this article that indicates lupus anticoagulant as an autoimmunity mechanism associated with Gulf War Syndrome. James LM, Johnson RA, Lewis SM, et al. Lupus anticoagulant in Gulf War Illness and autoimmune disorders: a common pathway toward autoimmunity. J Immunological Sci. 2021; 5: 14–18. Dave had published a similar article in a 1999 issue of Clinical Hemostasis Review: The presence of antiphospholipid antibodies in Gulf War veterans evaluated at Wilford Hall Medical Center.” - George Fritsma, Antiphospholipid antibodies in Gulf War Syndrome. (fritsmafactor.com)

The SEB endotoxin may be causing antiphospholipid syndrome after CoV injections per Geoff Pain, PhD:

Antiphospholipid Syndrome caused by Endotoxin in Covid19 Jabs

Drug/pharma induced antiphospholipid syndrome is not unknown, in fact it could almost be called common:

“From 01/11/2000 to 25/07/2021, 790 reports of suspected drug-induced APS were found in VigiBase. After excluding drugs reported by a single country and drugs with protopathic bias, fourteen drugs (n = 359 reports) were associated with APS with an IC_{0 25} > 0.

• These drugs were hormones: ethinylestradiol-etonogestrel and drospirenone-ethynilestradiol;

• platelet growth factors: eltrombopag, romiplostim;

• vaccines: Human Papillomavirus vaccine, hepatitis A and B vaccines and typhoid vaccine;

• antibiotics: minocycline;

• nonstreroidal anti-inflammatory: rofecoxib;

• biotherapy: interferon beta-1-a, etanercept;

• anti-hypertensive drug: hydralazine; bisphosphonates: alendronic acid

• and antipsychotic: olanzapine.” (Gérardin, et al., 2022) © 2022 Elsevier B.V. All rights reserved. [Bullet points added by me for ease of reading.]

Gee, I had a bad reaction to olanzapine.

Gulf War Syndrome and research by Garth Nicolson (also suppressed work and he had to leave his job due to differences of opinion).

McCairn and Rixey get into Gulf War Syndrome and mycoplasma research which turned out to be transmissible to family members. . . so it must be biological in nature to be transmissible. Maybe, but having worked in the area of prenatal health, I heard some personal information - to be blunt - the sperm of military men can be physically harmful/irritating within their spouse. Condom time. Yes, they may have transmitted something biological, but a direct load of shared toxins might also cause autoimmune conditions in a wife. Children have been affected by the Lipid Nanoparticle injections their parents received.

Glyphosate is a shared burden from the US diet that may decrease vitamin D and increase risk for autoimmune conditions or intracellular infections like mycoplasma. The soldiers and their families likely have that in common.

Mycoplasma research in the 1970s likely took place on prisoners and it made prison guards and their family members sick too. Testing showed the mycoplasma that was present had proteins from HIV. But there was no HIV present at that time (in the 70s). These mycoplasma were also found in Gulf War soldiers (including the daughter of a researcher working in this topic). Researcher - Garth Nicolson - video Nicolson: Weaponized Mycoplasmas (Non-Lethal Biological Warfare), (Youtube).

“Dr. Garth Nicolson - Weaponized Mycoplasmas
Mycoplasmas playing a big role in ALS, Parkinson's, ASD, CFS, MS, asthma, RA, IBS, AIDS...
'When they check for contaminants in vaccines, one of the common ones found is mycoplasma.'
Cancer, AIDS, Weaponized Mycoplasmas & Gulf War Illness. Prof. Garth Nicolson's hypothesis is straightforward: "The emergence of new illnesses and an increase in the incidence rate of previously described signs & symptoms are due to our toxic environment & the purposeful development & testing of Weapons of Mass Destruction." Dr. Nicolson heads the Institute for Molecular Medicine.” - Park Major, (LinkedIn) (Direct link to the video on Youtube of Garth Nicolson re Gulf War Syndrome and mycoplasma species, which Kevin and Charles discussed at length.)

ME/CFS was mentioned as a common problem that seems to have no treatment . . . unless you listen to me, who got better by greatly limiting vitamin A and carotenoids. ME/CFS seems to involve a chronic overactivation of A and carotenoids to the active retinoic acid which then causes flu like symptoms because it is intended to fight an active infection rather than being turned on chronically.

Why would vitamin A be over activated? In order to promote the original pathogens’s survival. That pathogen might not longer be present though (Epstein-Barr virus or SARS-COV-2 may cause a gene change in the liver in order to promote epithelial or endothelial cell differentiation by active Retinoic acid). Overactivation of vitamin A and carotenoids also leaves you with a deficiency of inactive vitamin A which has negative impact on night vision and on immune resistance to infection. If we are constantly trying to fight an infection, then our body is constanly inflammed and using up excess nutrients, leading to other deficiencies too.

ME/CFS patients are frequently passed off to rheumatologist per Kevin McCairn, and have little hope for improvement. Those are likely the same rheumatologists who aren't treating the intracellular pathogen cause of Rheumatoid arthritis that were identified by Lida Mattman. (Cell Wall Deficient Forms: Stealth Pathogens, 3rd Ed. 2001, a book).

Mycoplasma are found frequently in patients with ME/CFS and other chronic conditions like Lyme’s disease. Almost all patients with ALS are found to have mycoplasma.

Last section - a series of links about Rheumatoid arthritis -

Primarily to show that we aren’t told the full truth about many things and we aren’t offered treatment that is likely to help an intracellular infection in a patient that probably is in bad overall health - EMF overload, gut dysbiosis, nutrient deficiencies, toxin burden, and likely emotional stress. Intracellular infection roughly means bad terrain - the person needs to restore function in many areas of health.

https://www.niams.nih.gov/health-topics/rheumatoid-arthritis#:~:text=Researchers%20continue%20to%20study%20how,in%20the%20development%20of%20RA.

https://rheumatology.org/patients/minocycline-minocin

https://www.medicalnewstoday.com/articles/325710#:~:text=Minocycline%20is%20an%20antibiotic%20that,the%20tetracycline%20family%20of%20antibiotics.

https://www.arthritis.org/drug-guide/medication-topics/understanding-methotrexate

https://www.arthritis-health.com/types/rheumatoid/5-types-medication-treat-rheumatoid-arthritis-ra

Antibiotic use can worsen gut microbiome health which may lead to a flair-up of Rheumatoid arthritis symptoms.

https://www.news-medical.net/health/Can-Antibiotics-Increase-the-Risk-of-Arthritis.aspx#:~:text=Infections%2C%20hormonal%20alterations%2C%20and%20stress,microbiota%20changes%2C%20and%20RA%20flares.

Changes in shape and function of the thumb can occur early in arthritis progression. Photo by Towfiqu barbhuiya on Unsplash

Disclaimer: This information is being provided for educational purposes within the guidelines of Fair Use and is not intended to provide individual health care guidance.

Reference List

(Gérardin, et al., 2022) Gérardin, C., Bihan, K., Salem, J.E., Khachatryan, H., Gerotziafas, G. Fain, O., Mekinian, A., Drug-induced antiphospholipid syndrome: Analysis of the WHO international database, Autoimmunity Reviews, 21(5), 2022, 103060, ISSN 1568-9972, https://doi.org/10.1016/j.autrev.2022.103060. https://www.sciencedirect.com/science/article/pii/S1568997222000301

(Hu, et al., 2022) Hu J, Ye Y, Chen X, Xiong L, Xie W, Liu P. Insight into the Pathogenic Mechanism of Mycoplasma pneumoniae. Curr Microbiol. 2022 Dec 2;80(1):14. doi: 10.1007/s00284-022-03103-0. PMID: 36459213; PMCID: PMC9716528.

(Lu, et al., 2020) Lu XY, Han B, Deng X, Deng SY, Zhang YY, Shen PX, Hui T, Chen RH, Li X, Zhang Y. Pomegranate peel extract ameliorates the severity of experimental autoimmune encephalomyelitis via modulation of gut microbiota. Gut Microbes. 2020 Nov 9;12(1):1857515. doi: 10.1080/19490976.2020.1857515. PMID: 33382357; PMCID: PMC7751635.

(Xing, et al., 2020) Xing Y, Sheng K, Xiao X, Li J, Wei H, Liu L, Zhou W, Tong X. Vitamin A deficiency is associated with severe Mycoplasma pneumoniae pneumonia in children. Ann Transl Med. 2020 Feb;8(4):120. doi: 10.21037/atm.2020.02.33. PMID: 32175413; PMCID: PMC7049042. https://atm.amegroups.org/article/view/36821/html

(Zambrano-Zaragoza, et al., 2014) Zambrano-Zaragoza JF, Romo-Martínez EJ, Durán-Avelar Mde J, García-Magallanes N, Vibanco-Pérez N. Th17 cells in autoimmune and infectious diseases. Int J Inflam. 2014;2014:651503. doi: 10.1155/2014/651503. Epub 2014 Aug 3. PMID: 25152827; PMCID: PMC4137509. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137509/