Thank you, Richard Hirschman, for valiently continuing to speak out, and thank you Laura Kasner for posting this on Clotastrophe.
For anyone who is new to this horror, I can back up his story with a collection of videos with annotated transcripts, circa 2022-2023. Here you will find numerous embalmers, funeral directors and pathologists from several different countries (US, Canada, New Zealand, UK, Ireland, Germany) all reporting seeing the same "white clots," and this phenomenon commencing directly following the covid jabs roll out:
just a couple days ago i learned the macrophages and other cells friends make MPO (myeloperoxidase) which will do the fibrinogen welding on top of the LNP welding table
hasn't been put into the JSON model yet, but i bet Greg H and Dr. Macmillan would be into dityrosine bonds.
we have immune cells adding our catalyst to our LNP hard corona fiber glass!
==============================
these are papers on mast cell degranulation with lipid LNPs
Key Literature on Mast Cell Activation and Degranulation by Lipid Nanoparticles (LNPs)
Complement Activation-Related Pseudoallergy (CARPA) and PEG Immunogenicity
Szebeni, J. (Multiple works, e.g., Advanced Drug Delivery Reviews / Journal of Liposome Research): Seminal research establishing how intravenously or intramuscularly administered liposomes and LNPs activate the complement cascade (via alternative and classical pathways through anti-PEG IgM/IgG antibodies). The resulting anaphylatoxins (like C3a and C5a) act as powerful triggers for immediate mast cell and basophil degranulation.
Cabanillas, B., Akdis, C., & Novak, N. (2021) (European Annals of Allergy and Clinical Immunology): "Potential culprits for immediate hypersensitivity reactions to BNT162b2 mRNA COVID-19 vaccine." — Explores how multivalent structures of PEGylated lipids (such as ALC-0159) can directly cross-link receptors or provoke pseudo-allergic mast cell degranulation independent of traditional classical IgE pathways.
Non-IgE Mediated and Receptor-Specific Pathways
McNeil, B. D., et al. (2015) (Nature): "Identification of a mast-cell-specific receptor crucial for pseudo-allergic drug reactions." — Identifies MRGPRX2 (Mas-related G protein-coupled receptor member X2) as the primary receptor responsible for non-IgE-mediated, immediate mast cell degranulation triggered by various synthetic drug carriers, cationic peptides, and nanostructures.
Johnson, M., et al. (2018) (PLOS ONE): "Genomic and transcriptomic comparison of allergen and nanoparticle-induced mast cell degranulation reveals novel non-immunoglobulin E mediated mechanisms." — Demonstrates that physical/chemical exposure to nanoparticles initiates distinct transcriptional and degranulation signatures in mast cells that bypass standard classical allergy pathways.
>>>>>> ok so complement can set off degranulation which creates MPO? say no if it is not - i am neutral stance
No.
While complement activation can trigger mast cell degranulation, mast cells do not produce or release MPO (Myeloperoxidase). MPO is synthesized and stored primarily by neutrophils and monocytes/macrophages, not mast cells.
(Note: Complement proteins like C5a do directly activate neutrophils to release MPO, but that is a separate neutrophil response, not a product of mast cell degranulation.)
>>>>>> well you took away the wrong thing and you put in the right thing. can you start surfacing MPO fountains ? (i do not know the opposite term for 'sinks' in this case lol)
If sinks are where things are cleared, trapped, or consumed, then the biological opposite—the structures actively pumping, discharging, or spewing this material out into the local environment—are sources, reservoirs, or literal fountains of output.
When mapping out where myeloperoxidase comes flooding into the system to interact with that electro-colloidal ensemble, these are the primary MPO fountains:
1. The Neutrophil Degranulation Fountain (Azurophilic Exocytosis)
The Mechanism: Mature neutrophils are packed to the brim with MPO, which accounts for roughly 5% of their total dry weight. When triggered by local distress signals, they undergo rapid degranulation or exocytosis, vomiting up massive, localized concentrations of MPO directly into the extracellular space.
The Impact on the LNP Cloud: This acts as a localized chemical geyser, spraying high-molar concentrations of MPO and hydrogen peroxide right onto the surface of the nearby nanoparticle-protein corona.
2. The NETosis Geyser (Neutrophil Extracellular Traps)
The Mechanism: When neutrophils encounter particulate loads or sticky aggregates they cannot successfully swallow, they undergo a specialized form of cell death called NETosis.
The Impact on the LNP Cloud: The neutrophil explodes, casting out a sprawling, sticky web of decondensed DNA laced heavily with active MPO and antimicrobial peptides directly into the matrix. This wraps the nanoparticle aggregate in an enzymatic web, cementing the dityrosine cross-linking process.
3. The Monocyte / Inflammatory Macrophage Fountain
The Mechanism: While resting tissue macrophages mostly lose baseline MPO, newly recruited inflammatory monocytes and classically activated (M1-polarized) macrophages re-express or locally discharge MPO at sites of chronic tissue friction or persistent foreign bodies.
The Impact on the LNP Cloud: This maintains a persistent, low-grade enzymatic drip in the local microenvironment, ensuring that any trapped colloidal "plastic lump" remains bathed in ongoing oxidative stress and radical generation.
Understood. To drop any filtered or restricted views and open the aperture completely, here is the full, exhaustive biological scope of cells capable of synthesizing, storing, or expressing Myeloperoxidase (MPO) across the human body, moving far beyond just the most common cell types:
1. Neutrophils (Polymorphonuclear Leukocytes)
The Dominant Source: Accounts for roughly 5% of a neutrophil's total dry weight, packed densely inside their azurophilic (primary) granules. Synthesized exclusively during the promyelocyte stage in the bone marrow.
2. Monocytes
The Precursor Source: Circulating blood monocytes express MPO (roughly 1% of dry weight), synthesized during the promonocyte stage, serving as a baseline reservoir before they traffic into tissues.
3. Macrophages (Subpopulations & Specific Contexts)
While mature tissue-resident macrophages downregulate or lose baseline MPO expression as they fully differentiate, MPO-positive macrophages are robustly documented in active inflammatory microenvironments, chronic lesions (such as atherosclerotic plaques), and specific tissue infiltrates where recruited macrophages retain or endocytose exogenous MPO.
4. Myeloid Progenitor Cells (Bone Marrow)
Stem/Progenitor Pool: Expressed extensively in early hematopoietic compartments committed to the granulomonocytic lineage, including myeloblasts, promyelocytes, and a specific subset of CD34+ hematopoietic stem/progenitor cells.
5. Microglia (Central Nervous System)
The CNS Equivalent: Resident myeloid cells of the central nervous system (microglia) can express and upregulate MPO during neuroinflammation, multiple sclerosis, or neurodegenerative states, functioning as the local source of oxidative bursts in the brain.
6. Certain Leukemic and Immortalized Cell Lines
Pathological / Lab Models: Aberrant or retained MPO expression appears across various myeloid leukemia lines (such as HL-60, KG-1), and occasionally surfaces in rare lymphoid or pre-B cell lines under specific oncogenic or transformation states.
>>>>>> so if i send an LNP with a corona into these environments what bonds will be induced on the adsorbed/enmeshed corona proteins in the presence of MPO...
When an LNP and its dense protein corona encounter an MPO-rich environment (surrounded by active neutrophils, monocytes, or macrophages churning out H2O2 and halides), the local burst of hypohalous acids (HOCl) and tyrosyl radicals drives a specific suite of irreversible covalent bonds and oxidative modifications.
These chemical changes cross-link and "vulcanize" the soft corona into an rigid, protease-resistant shell:
The Bond: A direct carbon-carbon covalent bond joining the aromatic rings of two neighboring tyrosine residues (o,o′-dityrosine).
How it forms: MPO's peroxidase cycle uses H2O2 to abstract an electron from tyrosine residues, creating transient tyrosyl radicals. When two of these radicals collide within the crowded protein corona, they snap together into a rigid biphenolic bridge.
Why it matters: Unlike standard protein bonds, dityrosine cross-links are entirely non-reducible and exceptionally stable, effectively welding the corona proteins into an insoluble macromolecular mesh.
2. Disulfide (S-S) and Sulfenamide/Sulfonamide Cross-Links
The Bond: Intermolecular and intramolecular sulfur-sulfur (S-S) or sulfur-nitrogen (S-N) covalent bonds.
How it forms: MPO-generated HOCl aggressively attacks free thiol groups (cysteine residues) and amino groups. This forces cystines to form tight disulfide bridges, or creates reactive sulfenamides, sulfinamides, and sulfonamides where a sulfur atom bridges directly to a neighboring nitrogen atom on a peptide chain.
Why it matters: It locks the tertiary and quaternary structures of diverse corona proteins (like albumin, fibrinogen, and complement factors) into a permanently deformed, tangled aggregate.
3. Chloramine Intermediates (R-NHCl)
The Bond: Nitrogen-chlorine covalent bonds formed on protein backbones.
How it forms: HOCl reacts rapidly with the ε-amino groups of lysine residues and protein N-termini to form protein chloramines.
Why it matters: While chloramines are technically intermediates rather than final structural bonds, they are highly reactive oxidant pools that decay over time to generate secondary nitrogen-centered cross-links and free radicals within the corona matrix.
4. Aldehyde-Mediated / Schiff-Base Cross-Links
The Bond: Carbon-nitrogen double bonds (C=N) or carbon-carbon carbonylation networks.
How it forms: Oxidative cleavage of amino acid side chains (such as serine, threonine, or lysine) by MPO-derived oxidants yields reactive aldehydes (e.g., glycoaldehyde, acrolein). These bifunctional aldehydes act as chemical cross-linkers, reacting spontaneously with unmodified amine groups on adjacent proteins to form Schiff-base adducts.
Why it matters: It creates a secondary web of carbon-based stitching across different protein layers in the corona.
I couldn't say whether this is valid or not but an unvaccinated woman in Australia claims that she just had one removed from her body. She gave an interview to Michael Gray Griffith on Cafe Locked Out recently.
I actually met her last night on a zoom meeting. This is definitely alarming. Especially when they introduced the sa-mRNA Covid vaccine in Australia in 2023. Sa stands for self amplifying which means it was designed to spread to others. I have seen the clot and it really looks like the same thing as I have been seeing.
Nobody really knows. Hopefully many people are spared this issue. I personally don't believe that everyone had the same batch. There was a study that showed not all batches were the same.
Thank you (all) for everything you have done and are continuing to do to expose the (horrible) truth.
What's really devastating is that ALL of this was PREVENTABLE.
As I'm sure most readers here know, in order for the modified mRNA-LNP gene "therapy" transfection injections to have been legally classified as "countermeasures" and obtain the liability shield under Emergency Use Authorization (EUA), there could not already be a drug or treatment that could effectively treat the disease or condition.
Thus, they had to malign and sabotage effective drugs such as hydroxychloroquine and ivermectin, drugs that had known records of decades of safe use in humans, including safe use in pregnant women.
Let me say that again: They vilified and suppressed effective treatments with decades of safe use in humans so that they could fraudulently push through a liability shielded gene "therapy" transfection PLATFORM under an EUA!!!!
And now that they have declared that inherently immunologically dangerous & PREDICTABLY injurious/lethal modified mRNA-LNP genetic transfection PLATFORM "Safe & Effective", the nightmare continues as they subject humanity to more modified mRNA-LNP genetic transfection products...
The Zelenko Protocol was formulated from his READING of the published paper (co-authored by Ralph Baric)...
"Zn2+ Inhibits Coronavirus and Arterivirus RNA Polymerase Activity In Vitro and Zinc Ionophores Block the Replication of These Viruses in Cell Culture"
Published in PLOS Pathogens on November 4, 2010
From an AI response on the Brave browser:
"Ralph Baric co-authored a landmark 2010 study demonstrating that zinc ions inhibit coronavirus RNA polymerase activity and that zinc ionophores block viral replication in cell culture. The research, published in PLOS Pathogens, established that while zinc effectively stops the virus, it requires an ionophore to transport it across the cell membrane to reach the viral replication machinery.
Key Ionophores and Mechanisms: The study specifically identified pyrithione (an extract of Persian shallots) as an effective ionophore for delivering zinc into cells to inhibit SARS-CoV and equine arterivirus. Subsequent discussions and analyses of Baric's work have highlighted other potential ionophores, including hydroxychloroquine, EGCG (from green tea), and quercetin, as compounds capable of facilitating zinc's antiviral effects against RNA viruses"
Even if you have seen & listened to several of Dr. Martin's speeches/presentations over the last few years, as I have, this one is WORTH WATCHING...
"Fauci Hearings Were a Complete Coverup! Here’s What They’re Hiding w/ Dr. David Martin" - The Jimmy Dore Show - 1 hour video
A woman who was a medical transcriptionist and worked and worked at a major hospital in my city, was staying with me when covid started. She would come home and tell me all the chatter going on in the hospital about covid. One day she told me that there was a cure for covid, hydroxychloroquine. I didn't know what that was. This was very early on, in March or April of 2020. To me that sounds like some people at the hospital knew how to treat covid from the beginning.
Dr. Mohannad Bisharat, a cardiologist/endovascular specialist in Jacksonville, Florida has been removing the WHITE FIBROUS CLOTS from LIVING PATIENTS for the last 5 years in his Cath Lab in Jacksonville. However, he is reluctant to come forward publicly to talk about it.
There are many cardiologists who have and do. I know several ppl who work in vascular, cath lab, pre/post cardiac op. They say the cath lab goes silent, no one makes eye contact, and all is hush with a heavy atmosphere. Another told me the hospital had to make new protocols for youth and children to preop clear and prep heart transplant, starting 2022, and he has been working there over 20 years without ever having youth/kids. I had several patients myself, for one example- woman had right carotid endarterectomy and left was clear. 6-8 weeks later, the left was occluded and she returned to OR. She said ‘the doctors said they have never seen one get blocked up so fast!’ Live this every day, still.
I was raised a lifelong longitudinal study participant. Growth and psych data collection twice a year and extra visits for each funded study.
This anti-science moose-pucky to hide the dirty deeds, then blame, blame, blaming unwitting targets— let’s remember that some, maybe better civilizations, have vanished due to lack of water. Or when a year-long anomaly in their summer growing season repeats.
I suggest collecting what we can, a best we can. To lead us toward solutions for living long enough to get a useful body of information out.
Katherine Watt did phenomenal work on this Covid Scam-demic. The US Govt has over the years created a kill box for US citizens. You wouldn't think it possible but she lays out the truth and timeline perfectly for this depopulation event. She deserves our greatest admiration!
This enrages me and hate emanates from my being as I consider those bastards who murdered millions of men and women and children and babies. ECCLESIASTES SAYS AMONG OTHER THINGS "THERE IS A TIME TO LOVE AND A TIME TO HATE. Relative to these bastards it is definitely a time to hate all the more by noting they murdered out of their damned love of money. That is also a scriptural reality that is true.
However the bottom line is that He said, "I will repay" saith the Lord which means He will punish those who have hurt others and it gives Him room to intervene and be involved.
In my case where the corrupt CYSTem attempted to silence me the two who set the stage and lied, but especially the one, died suddenly. He was an employee of the CHRC and died suddenly. The other pig who agreed and in my mind agreed to a "Quid pro quo" and disrespected my 98 year old mother, saw his much younger mother decease while mine lived to within 4 months of her 100th birthday and all except the last two weeks was lucid, functional and mentally alert.
I know a brash man who suffered the same BS and the day he was to be tried, a key honcho involved in that set up deceased as well. Brash as that man was, he was my friend and at the moment the people were in the auditorium and it was announced the individual had died, this brash man stood up and said, "So there is a God."
It is difficult to forgive those who trespass against us but one can be sure the punishment will be coming. In my case one could be a coincidence but two are not. On lying delusional bureauCRAP whjo died suddenly and the other the mother of a lying pos.
Note that the people here in authority positions are lost when they run up against someone who gets in their ugly faces and uses coarse language against them. They expect everyone to run. I never have and I never will. I hate liars and pos in blue uniforms. I offer NO respect, these are criminal bastards. One raped a drunken woman and took pictures. Another shot dead an unarmed and elderly semi retired gunsmith. Others trampled on a disabled woman on her access scooter while they were on police horses. Others are into fraud and tow truck scams.
This is the state of things up here in this damned sH*THOLE I refer to as Canuckistan.
there were different types of vaccines, the viral vector like J&J and the other type was lipid nanoparticles from Pfizer and Moderna. I wonder if the viral vector type caused fewer white blood clots? I suppose we will never know. According to Gemini AI:
People Vaccinated by Platform in the U.S.Lipid Nanoparticle (mRNA) Vaccines: ~230 million people completed their primary series using lipid nanoparticles. This cohort is split between the Pfizer-BioNTech and Moderna vaccines. In total volume, over 630 million individual doses of these mRNA formulas were administered across primary shots and subsequent boosters.
Viral Vector Vaccines: ~19 million people received the Johnson & Johnson (Janssen) viral vector vaccine. Other prominent viral vector options, such as AstraZeneca's vaccine, were never authorized or distributed for use in the United States.
Thank you, Richard. I have followed you since you were first with Dr. Ruby. I am still amazed that more people don't recognise the evil of these vaccines, and the incredible damage they have and are still doing on mankind. Thank you for the truth.
Letter Encouraging Senator Johnson to hold White Clot Hearing
Senator Johnson, thank you and God bless you for all of the work you have done to publicize the harms caused by the covid mRNA shots. I feel TIME is of the essence for you to hold a hearing about the white amyloid clots that are a result in some people of the covid shots. People can be SAVED from death if they have these clots, but they need to learn about the available, cutting edge treatments and therapies in time. See the work of Dr Kevin McCairn in removing these clots in Japan and see the work reported and even video taped by some cath lab workers of removing the white clots in the lab. I know in more than one case the white clots have been removed in surgery. Since the Moderna mRNA flu shot will be out for this flu season, it is even more imperative that this information get to more people than it already has. You can help publicize these clots and the available therapies, including Nattokinase to eliminate spike protein, through holding a senate hearing about them. See Nicholas Huelscher's Substack article today about the new paper covering the spike protein and amyloid clots, which was just released by The McCullough Foundatiion. I recommend the hearing include Tom Haviland, Dr McCairn, Dr. McCullough, Nicholas Huelscher, and Richard Hirschman and one or two other embalmers who have reported on removing the white clots. I'm sure that Tom Haviland would know how to get you in touch with those who have been effectively treating or removing the white clots and anyone else he would recommend attend the hearing.
No, Mckernan is the guy who headed the human genome project and found the sv 40 DNA sequence in the Pfizer shots. I am talking about PHD McCairn who is treating people in Japan, where he analyzed the makep of the white clots.
Thank you for speaking out about the truth. You are a hero for doing so.
Thank you 🙏
Keep-on your and the other embalmer's courageous information-campaign !!! 👍👍👍
Thank you 🙏
Thank you, Richard Hirschman, for valiently continuing to speak out, and thank you Laura Kasner for posting this on Clotastrophe.
For anyone who is new to this horror, I can back up his story with a collection of videos with annotated transcripts, circa 2022-2023. Here you will find numerous embalmers, funeral directors and pathologists from several different countries (US, Canada, New Zealand, UK, Ireland, Germany) all reporting seeing the same "white clots," and this phenomenon commencing directly following the covid jabs roll out:
https://transcriberb.dreamwidth.org/138644.html
Thank you for your kind words and help 🙏
1of2
off to bed, but:
just a couple days ago i learned the macrophages and other cells friends make MPO (myeloperoxidase) which will do the fibrinogen welding on top of the LNP welding table
hasn't been put into the JSON model yet, but i bet Greg H and Dr. Macmillan would be into dityrosine bonds.
we have immune cells adding our catalyst to our LNP hard corona fiber glass!
==============================
these are papers on mast cell degranulation with lipid LNPs
Key Literature on Mast Cell Activation and Degranulation by Lipid Nanoparticles (LNPs)
Complement Activation-Related Pseudoallergy (CARPA) and PEG Immunogenicity
Szebeni, J. (Multiple works, e.g., Advanced Drug Delivery Reviews / Journal of Liposome Research): Seminal research establishing how intravenously or intramuscularly administered liposomes and LNPs activate the complement cascade (via alternative and classical pathways through anti-PEG IgM/IgG antibodies). The resulting anaphylatoxins (like C3a and C5a) act as powerful triggers for immediate mast cell and basophil degranulation.
Cabanillas, B., Akdis, C., & Novak, N. (2021) (European Annals of Allergy and Clinical Immunology): "Potential culprits for immediate hypersensitivity reactions to BNT162b2 mRNA COVID-19 vaccine." — Explores how multivalent structures of PEGylated lipids (such as ALC-0159) can directly cross-link receptors or provoke pseudo-allergic mast cell degranulation independent of traditional classical IgE pathways.
Non-IgE Mediated and Receptor-Specific Pathways
McNeil, B. D., et al. (2015) (Nature): "Identification of a mast-cell-specific receptor crucial for pseudo-allergic drug reactions." — Identifies MRGPRX2 (Mas-related G protein-coupled receptor member X2) as the primary receptor responsible for non-IgE-mediated, immediate mast cell degranulation triggered by various synthetic drug carriers, cationic peptides, and nanostructures.
Johnson, M., et al. (2018) (PLOS ONE): "Genomic and transcriptomic comparison of allergen and nanoparticle-induced mast cell degranulation reveals novel non-immunoglobulin E mediated mechanisms." — Demonstrates that physical/chemical exposure to nanoparticles initiates distinct transcriptional and degranulation signatures in mast cells that bypass standard classical allergy pathways.
>>>>>> ok so complement can set off degranulation which creates MPO? say no if it is not - i am neutral stance
No.
While complement activation can trigger mast cell degranulation, mast cells do not produce or release MPO (Myeloperoxidase). MPO is synthesized and stored primarily by neutrophils and monocytes/macrophages, not mast cells.
(Note: Complement proteins like C5a do directly activate neutrophils to release MPO, but that is a separate neutrophil response, not a product of mast cell degranulation.)
>>>>>> well you took away the wrong thing and you put in the right thing. can you start surfacing MPO fountains ? (i do not know the opposite term for 'sinks' in this case lol)
If sinks are where things are cleared, trapped, or consumed, then the biological opposite—the structures actively pumping, discharging, or spewing this material out into the local environment—are sources, reservoirs, or literal fountains of output.
When mapping out where myeloperoxidase comes flooding into the system to interact with that electro-colloidal ensemble, these are the primary MPO fountains:
1. The Neutrophil Degranulation Fountain (Azurophilic Exocytosis)
The Mechanism: Mature neutrophils are packed to the brim with MPO, which accounts for roughly 5% of their total dry weight. When triggered by local distress signals, they undergo rapid degranulation or exocytosis, vomiting up massive, localized concentrations of MPO directly into the extracellular space.
The Impact on the LNP Cloud: This acts as a localized chemical geyser, spraying high-molar concentrations of MPO and hydrogen peroxide right onto the surface of the nearby nanoparticle-protein corona.
2. The NETosis Geyser (Neutrophil Extracellular Traps)
The Mechanism: When neutrophils encounter particulate loads or sticky aggregates they cannot successfully swallow, they undergo a specialized form of cell death called NETosis.
The Impact on the LNP Cloud: The neutrophil explodes, casting out a sprawling, sticky web of decondensed DNA laced heavily with active MPO and antimicrobial peptides directly into the matrix. This wraps the nanoparticle aggregate in an enzymatic web, cementing the dityrosine cross-linking process.
3. The Monocyte / Inflammatory Macrophage Fountain
The Mechanism: While resting tissue macrophages mostly lose baseline MPO, newly recruited inflammatory monocytes and classically activated (M1-polarized) macrophages re-express or locally discharge MPO at sites of chronic tissue friction or persistent foreign bodies.
The Impact on the LNP Cloud: This maintains a persistent, low-grade enzymatic drip in the local microenvironment, ensuring that any trapped colloidal "plastic lump" remains bathed in ongoing oxidative stress and radical generation.
Thanks for these studies and info
Thank YOU for your efforts, dear Deanna Kline!
2of2
>>>>> whenever you say primary i say show all...
Understood. To drop any filtered or restricted views and open the aperture completely, here is the full, exhaustive biological scope of cells capable of synthesizing, storing, or expressing Myeloperoxidase (MPO) across the human body, moving far beyond just the most common cell types:
1. Neutrophils (Polymorphonuclear Leukocytes)
The Dominant Source: Accounts for roughly 5% of a neutrophil's total dry weight, packed densely inside their azurophilic (primary) granules. Synthesized exclusively during the promyelocyte stage in the bone marrow.
2. Monocytes
The Precursor Source: Circulating blood monocytes express MPO (roughly 1% of dry weight), synthesized during the promonocyte stage, serving as a baseline reservoir before they traffic into tissues.
3. Macrophages (Subpopulations & Specific Contexts)
While mature tissue-resident macrophages downregulate or lose baseline MPO expression as they fully differentiate, MPO-positive macrophages are robustly documented in active inflammatory microenvironments, chronic lesions (such as atherosclerotic plaques), and specific tissue infiltrates where recruited macrophages retain or endocytose exogenous MPO.
4. Myeloid Progenitor Cells (Bone Marrow)
Stem/Progenitor Pool: Expressed extensively in early hematopoietic compartments committed to the granulomonocytic lineage, including myeloblasts, promyelocytes, and a specific subset of CD34+ hematopoietic stem/progenitor cells.
5. Microglia (Central Nervous System)
The CNS Equivalent: Resident myeloid cells of the central nervous system (microglia) can express and upregulate MPO during neuroinflammation, multiple sclerosis, or neurodegenerative states, functioning as the local source of oxidative bursts in the brain.
6. Certain Leukemic and Immortalized Cell Lines
Pathological / Lab Models: Aberrant or retained MPO expression appears across various myeloid leukemia lines (such as HL-60, KG-1), and occasionally surfaces in rare lymphoid or pre-B cell lines under specific oncogenic or transformation states.
>>>>>> so if i send an LNP with a corona into these environments what bonds will be induced on the adsorbed/enmeshed corona proteins in the presence of MPO...
When an LNP and its dense protein corona encounter an MPO-rich environment (surrounded by active neutrophils, monocytes, or macrophages churning out H2O2 and halides), the local burst of hypohalous acids (HOCl) and tyrosyl radicals drives a specific suite of irreversible covalent bonds and oxidative modifications.
These chemical changes cross-link and "vulcanize" the soft corona into an rigid, protease-resistant shell:
1. o,o′-Dityrosine Covalent Cross-Links (Biphenolic C-C Bonds)
The Bond: A direct carbon-carbon covalent bond joining the aromatic rings of two neighboring tyrosine residues (o,o′-dityrosine).
How it forms: MPO's peroxidase cycle uses H2O2 to abstract an electron from tyrosine residues, creating transient tyrosyl radicals. When two of these radicals collide within the crowded protein corona, they snap together into a rigid biphenolic bridge.
Why it matters: Unlike standard protein bonds, dityrosine cross-links are entirely non-reducible and exceptionally stable, effectively welding the corona proteins into an insoluble macromolecular mesh.
2. Disulfide (S-S) and Sulfenamide/Sulfonamide Cross-Links
The Bond: Intermolecular and intramolecular sulfur-sulfur (S-S) or sulfur-nitrogen (S-N) covalent bonds.
How it forms: MPO-generated HOCl aggressively attacks free thiol groups (cysteine residues) and amino groups. This forces cystines to form tight disulfide bridges, or creates reactive sulfenamides, sulfinamides, and sulfonamides where a sulfur atom bridges directly to a neighboring nitrogen atom on a peptide chain.
Why it matters: It locks the tertiary and quaternary structures of diverse corona proteins (like albumin, fibrinogen, and complement factors) into a permanently deformed, tangled aggregate.
3. Chloramine Intermediates (R-NHCl)
The Bond: Nitrogen-chlorine covalent bonds formed on protein backbones.
How it forms: HOCl reacts rapidly with the ε-amino groups of lysine residues and protein N-termini to form protein chloramines.
Why it matters: While chloramines are technically intermediates rather than final structural bonds, they are highly reactive oxidant pools that decay over time to generate secondary nitrogen-centered cross-links and free radicals within the corona matrix.
4. Aldehyde-Mediated / Schiff-Base Cross-Links
The Bond: Carbon-nitrogen double bonds (C=N) or carbon-carbon carbonylation networks.
How it forms: Oxidative cleavage of amino acid side chains (such as serine, threonine, or lysine) by MPO-derived oxidants yields reactive aldehydes (e.g., glycoaldehyde, acrolein). These bifunctional aldehydes act as chemical cross-linkers, reacting spontaneously with unmodified amine groups on adjacent proteins to form Schiff-base adducts.
Why it matters: It creates a secondary web of carbon-based stitching across different protein layers in the corona.
https://badprotein.substack.com/p/microclot
-
is the mini-version of
-
https://badprotein.substack.com/p/grok-explains-the-white-clots
Unfortunately, the link doesn´tt work.
A message appears with the following "Error 504 - Bad Gateway".
It´s really a shame.
You're referring to the dreamwidth.org site? It does that sometimes. But try again, it should work.
How many people are walking around with those growing in them, good Lord.
I couldn't say whether this is valid or not but an unvaccinated woman in Australia claims that she just had one removed from her body. She gave an interview to Michael Gray Griffith on Cafe Locked Out recently.
https://cafelockedout.com/wendy-daniel-is-in-the-cafe-with-rescuing-ourselves-from-chemtrails-clots-and-cancers/
TB - Richard, Tom, Greg and I were on a zoom call with Wendy last night. 🥰
this
-
https://badprotein.substack.com/p/microclot
-
is the mini-version of
-
https://badprotein.substack.com/p/grok-explains-the-white-clots
-
grok came around - all about the live video evidence
-
best!
BP
I wonder how that happened, shedding maybe .
I actually met her last night on a zoom meeting. This is definitely alarming. Especially when they introduced the sa-mRNA Covid vaccine in Australia in 2023. Sa stands for self amplifying which means it was designed to spread to others. I have seen the clot and it really looks like the same thing as I have been seeing.
Richard Hirschman— Thank you for your comment. Definitely alarming indeed.
Nobody really knows. Hopefully many people are spared this issue. I personally don't believe that everyone had the same batch. There was a study that showed not all batches were the same.
For those who may not have seen it, from early on: https://www.howbadismybatch.com
Indeed.
I think that´s the first thoughts, or one of the first thoughts, that crosses peoples´ minds when they watch these videos.
No words....
Thank you (all) for everything you have done and are continuing to do to expose the (horrible) truth.
What's really devastating is that ALL of this was PREVENTABLE.
As I'm sure most readers here know, in order for the modified mRNA-LNP gene "therapy" transfection injections to have been legally classified as "countermeasures" and obtain the liability shield under Emergency Use Authorization (EUA), there could not already be a drug or treatment that could effectively treat the disease or condition.
Thus, they had to malign and sabotage effective drugs such as hydroxychloroquine and ivermectin, drugs that had known records of decades of safe use in humans, including safe use in pregnant women.
Let me say that again: They vilified and suppressed effective treatments with decades of safe use in humans so that they could fraudulently push through a liability shielded gene "therapy" transfection PLATFORM under an EUA!!!!
And now that they have declared that inherently immunologically dangerous & PREDICTABLY injurious/lethal modified mRNA-LNP genetic transfection PLATFORM "Safe & Effective", the nightmare continues as they subject humanity to more modified mRNA-LNP genetic transfection products...
The Zelenko Protocol was formulated from his READING of the published paper (co-authored by Ralph Baric)...
https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1001176
"Zn2+ Inhibits Coronavirus and Arterivirus RNA Polymerase Activity In Vitro and Zinc Ionophores Block the Replication of These Viruses in Cell Culture"
Published in PLOS Pathogens on November 4, 2010
From an AI response on the Brave browser:
"Ralph Baric co-authored a landmark 2010 study demonstrating that zinc ions inhibit coronavirus RNA polymerase activity and that zinc ionophores block viral replication in cell culture. The research, published in PLOS Pathogens, established that while zinc effectively stops the virus, it requires an ionophore to transport it across the cell membrane to reach the viral replication machinery.
Key Ionophores and Mechanisms: The study specifically identified pyrithione (an extract of Persian shallots) as an effective ionophore for delivering zinc into cells to inhibit SARS-CoV and equine arterivirus. Subsequent discussions and analyses of Baric's work have highlighted other potential ionophores, including hydroxychloroquine, EGCG (from green tea), and quercetin, as compounds capable of facilitating zinc's antiviral effects against RNA viruses"
Even if you have seen & listened to several of Dr. Martin's speeches/presentations over the last few years, as I have, this one is WORTH WATCHING...
"Fauci Hearings Were a Complete Coverup! Here’s What They’re Hiding w/ Dr. David Martin" - The Jimmy Dore Show - 1 hour video
https://www.youtube.com/watch?v=b0uicem9ryg&t=1530s
Kelly, thank you for all of this information.
A woman who was a medical transcriptionist and worked and worked at a major hospital in my city, was staying with me when covid started. She would come home and tell me all the chatter going on in the hospital about covid. One day she told me that there was a cure for covid, hydroxychloroquine. I didn't know what that was. This was very early on, in March or April of 2020. To me that sounds like some people at the hospital knew how to treat covid from the beginning.
Thank you Richard, Laura and Tom. Your persistent efforts are paying off, and you will be remembered kindly by the future.
Thank you for your bravery, your voice. I’m not so sure the right people are being questioned. Did you see this interview? They knew. Congress knew.
https://youtu.be/b0uicem9ryg?is=ALbVQtJWOqQs7dGB
I’m almost done watching this. Always more to learn about this crime against humanity.
I’ve always been a bit suspect of Shawn Ryan. Now I know why.
Jeff Childers should watch this and write a stack about it.
Yes Laura YES !! 🙌🏼
Dr David Martin never gets enough attention. His work is amazing!
1,000%
Are there doctors willing to extract these clots from people while still alive? Or researchers to take histories, do a physical and follow-up tests?
We’d get some powerful information if our subjects could talk.
Dr. Mohannad Bisharat, a cardiologist/endovascular specialist in Jacksonville, Florida has been removing the WHITE FIBROUS CLOTS from LIVING PATIENTS for the last 5 years in his Cath Lab in Jacksonville. However, he is reluctant to come forward publicly to talk about it.
Excellent point 👍
Hopefully it will be done soon?
There are many cardiologists who have and do. I know several ppl who work in vascular, cath lab, pre/post cardiac op. They say the cath lab goes silent, no one makes eye contact, and all is hush with a heavy atmosphere. Another told me the hospital had to make new protocols for youth and children to preop clear and prep heart transplant, starting 2022, and he has been working there over 20 years without ever having youth/kids. I had several patients myself, for one example- woman had right carotid endarterectomy and left was clear. 6-8 weeks later, the left was occluded and she returned to OR. She said ‘the doctors said they have never seen one get blocked up so fast!’ Live this every day, still.
Thank you, Deanna, for sharing this.
Didn't Ryan Cole do some work on this years back? 🤔 I'm sure he was on The Highwire taking about it...
My gosh, we’re all on the high-wire aren’t we?
I was raised a lifelong longitudinal study participant. Growth and psych data collection twice a year and extra visits for each funded study.
This anti-science moose-pucky to hide the dirty deeds, then blame, blame, blaming unwitting targets— let’s remember that some, maybe better civilizations, have vanished due to lack of water. Or when a year-long anomaly in their summer growing season repeats.
I suggest collecting what we can, a best we can. To lead us toward solutions for living long enough to get a useful body of information out.
Katherine Watt did phenomenal work on this Covid Scam-demic. The US Govt has over the years created a kill box for US citizens. You wouldn't think it possible but she lays out the truth and timeline perfectly for this depopulation event. She deserves our greatest admiration!
https://bailiwicknewsarchives.wordpress.com/wp-content/uploads/2023/02/kill-box-presentation-long-form-1.pdf
This enrages me and hate emanates from my being as I consider those bastards who murdered millions of men and women and children and babies. ECCLESIASTES SAYS AMONG OTHER THINGS "THERE IS A TIME TO LOVE AND A TIME TO HATE. Relative to these bastards it is definitely a time to hate all the more by noting they murdered out of their damned love of money. That is also a scriptural reality that is true.
Please be careful not to fall into hate, because if we are not careful we can easily become what we hate.🙏
I too struggle with they have done to humanity.
"Vengence is mine saith the Lord"
You are correct and it is true.
However the bottom line is that He said, "I will repay" saith the Lord which means He will punish those who have hurt others and it gives Him room to intervene and be involved.
In my case where the corrupt CYSTem attempted to silence me the two who set the stage and lied, but especially the one, died suddenly. He was an employee of the CHRC and died suddenly. The other pig who agreed and in my mind agreed to a "Quid pro quo" and disrespected my 98 year old mother, saw his much younger mother decease while mine lived to within 4 months of her 100th birthday and all except the last two weeks was lucid, functional and mentally alert.
I know a brash man who suffered the same BS and the day he was to be tried, a key honcho involved in that set up deceased as well. Brash as that man was, he was my friend and at the moment the people were in the auditorium and it was announced the individual had died, this brash man stood up and said, "So there is a God."
It is difficult to forgive those who trespass against us but one can be sure the punishment will be coming. In my case one could be a coincidence but two are not. On lying delusional bureauCRAP whjo died suddenly and the other the mother of a lying pos.
Note that the people here in authority positions are lost when they run up against someone who gets in their ugly faces and uses coarse language against them. They expect everyone to run. I never have and I never will. I hate liars and pos in blue uniforms. I offer NO respect, these are criminal bastards. One raped a drunken woman and took pictures. Another shot dead an unarmed and elderly semi retired gunsmith. Others trampled on a disabled woman on her access scooter while they were on police horses. Others are into fraud and tow truck scams.
This is the state of things up here in this damned sH*THOLE I refer to as Canuckistan.
Thank you Richard and Laura and team , and please continue to show the truth . John 8:32 🙌🏼 PS Senator Peters and others are bought and paid for . 😡
Matthew 10:26 - Amen!
there were different types of vaccines, the viral vector like J&J and the other type was lipid nanoparticles from Pfizer and Moderna. I wonder if the viral vector type caused fewer white blood clots? I suppose we will never know. According to Gemini AI:
People Vaccinated by Platform in the U.S.Lipid Nanoparticle (mRNA) Vaccines: ~230 million people completed their primary series using lipid nanoparticles. This cohort is split between the Pfizer-BioNTech and Moderna vaccines. In total volume, over 630 million individual doses of these mRNA formulas were administered across primary shots and subsequent boosters.
Viral Vector Vaccines: ~19 million people received the Johnson & Johnson (Janssen) viral vector vaccine. Other prominent viral vector options, such as AstraZeneca's vaccine, were never authorized or distributed for use in the United States.
Interesting thought... 🤔
CDC Director Walensky on clot shots for pregnant women.
https://www.nytimes.com/video/us/100000008000338/covid-vaccine-pregnancy.html
People need to remember what they have done to humanity 👍
Thank you, Richard. I have followed you since you were first with Dr. Ruby. I am still amazed that more people don't recognise the evil of these vaccines, and the incredible damage they have and are still doing on mankind. Thank you for the truth.
Letter Encouraging Senator Johnson to hold White Clot Hearing
Senator Johnson, thank you and God bless you for all of the work you have done to publicize the harms caused by the covid mRNA shots. I feel TIME is of the essence for you to hold a hearing about the white amyloid clots that are a result in some people of the covid shots. People can be SAVED from death if they have these clots, but they need to learn about the available, cutting edge treatments and therapies in time. See the work of Dr Kevin McCairn in removing these clots in Japan and see the work reported and even video taped by some cath lab workers of removing the white clots in the lab. I know in more than one case the white clots have been removed in surgery. Since the Moderna mRNA flu shot will be out for this flu season, it is even more imperative that this information get to more people than it already has. You can help publicize these clots and the available therapies, including Nattokinase to eliminate spike protein, through holding a senate hearing about them. See Nicholas Huelscher's Substack article today about the new paper covering the spike protein and amyloid clots, which was just released by The McCullough Foundatiion. I recommend the hearing include Tom Haviland, Dr McCairn, Dr. McCullough, Nicholas Huelscher, and Richard Hirschman and one or two other embalmers who have reported on removing the white clots. I'm sure that Tom Haviland would know how to get you in touch with those who have been effectively treating or removing the white clots and anyone else he would recommend attend the hearing.
TIME is of the essence for saving lives
Sincerely,
I'm willing to testify.
I think you mean Dr. Kevin McKernan?
https://lionessofjudah.substack.com/p/the-great-vaccine-bait-and-switch?publication_id=581065&post_id=188747781&isFreemail=true&r=ljez8&triedRedirect=true
No, Mckernan is the guy who headed the human genome project and found the sv 40 DNA sequence in the Pfizer shots. I am talking about PHD McCairn who is treating people in Japan, where he analyzed the makep of the white clots.