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SegFish's avatar

We don't even need to hypothesize what the Spike can do; the entire United States housing stock is LOADED with PVC. To make dioxin (i.e. the most toxic part of Agent Orange), all you need to do is light that house on fire. EVERY SINGLE MODERN HOME is a deadlly toxin bomb just waiting to be activated.

I'm building a house now and while I have tried to avoid using PVC everywhere possible, it's literally impossible to avoid completely with what the industry makes available and with how the building codes are written and enforced.

I need more people elevating this concern to the highest levels of government (RFK jr); chlorinated plastics need to be banned with almost no exceptions. PVC + fire is more dangerous than DDT, asbestos, lead, mercury combined. There is NO chemical more toxic than dioxin/ TCDD.

Spike proteins can be broken down (with effort); I've been having to do this for the past few years now (due to my extreme sensitivity to the shedding) and I'm getting better at it every month using natural plant medicines. Dioxins have no antidote; it's nearly impossible to clear these things from our bodies. There's just no contest.

Swabbie Robbie's avatar

With the prices of copper rising it is hard to afford on new buildings. I am not in love with vinyl siding either. Our last home was built in 1912. - small farm house. I am sure for a long span it had a hand pump well. and an outhouse. Framing was all red and white oak. original siding was board and the original roof was cedar shake. When we bought it in 1974 it was all plumbed copper and steel pipes. Still had an outhouse in back which cam in handy when the indoor bathroom was occupied. Well was now submersible and still located right off the kitchen. We rebuilt and expanded the place bit by bit over the years. In 2020 the new owner tore it down even though it was appraised at $175K, the Barn was 30 X 60 two story with carsiding walls walls because we had converted it into our studio. Appraised at $120K New owner tore that down as well. She was from Chicago and built a McMansion which raised the property taxes from $3,200 to $11, 000. I can't imagine the costs of taking down and disposing of the scrap of two perfectly good large buildings and two sheds.

Karen Kovaz's avatar

Please forward this to Robert F. Kennedy Jr. (HHS Secretary), Dr. Makary (Head of FDA) and Dr. Robert Malone ("expert" on mRNA, member of vaccine advisory committee). Perhaps if you highlight/emphasize that the experimental mRNA injections cause this amyloidogenesis , they will finally remove all mRNA injections from the market immediately (as should have been done on day one of RFK Jr. appointed and confirmed as HHS Secretary. I believe that Malone is actually in favor of developing the dangerous mRNA platform for vaccines and will not recommend pulling them off the market (I believe it is due to his ego (as he was involved in initial development of the mRNA technology), he cannot admit that it has been a complete failure and used in the COVID injections , caused a massive number of serious long-term injuries (including heart issues, blood clotting issues, cancers, aneurysms, strokes, dementia, other autoimmune disorders, miscarriages, stillbirths, post-partum hemorrhages) and potentially hundreds of thousands of deaths around the world. There may be many cases of long-COVID health issues that extend for many months but I believe that compared to the degree of serious adverse effects and deaths caused by the mRNA COVID in jections, your focus and emphasis should be on the inherent health risks caused by the mRNA injections! The reason so many physicians continue to deny that patients have been injured (or died) from the COVID mRNA injections is because they have been told that since the beginning of the administration of the mRNA injections, that any patients presenting with adverse effects and illnesses after receiving the mRNA injections are experiencing Long COVID!!!!! This is why patients are being denied an accurate diagnosis and receiving the necessary treatment and physicians continue to recommend that these patients (especially the elderly) continue to receive the COVID mRNA boosters on a regular basis!!!! Each COVID mRNA booster increases the patient's chances of developing more serious health issues and even death! So if you continue to present your clinical observations and analyses with reporting the adverse effects as Spike Protein due to Long COVID rather than the emphasis on the mRNA injections being far more likely to directly cause these adverse health effects (see Steve Kirsch's work, and Nicolas Hulscher and Dr. Peter McCullough's work that include numerous studies that prove that the mRNA injections have caused far more serious adverse effects and deaths than in the cases of Long COVID. We need to have your knowledge and expertise in this area participate in the clarion call to remove the mRNA injections from the market completely (they are not safe or effective for anyone in any age group or even immune-compromised, etc) and send your substack articles (hopefully with emphasis on the toxicity of the mRNA injections) to the Federal officials at HHS.

Swabbie Robbie's avatar

Kevin McKernan on his Anandamide substack on 1/11/2026 talks about the DNA Contamination in mRNA Vaccines and how the plan all along was to switch to process 2 after the clinical trials.

LM Ramsay's avatar

It's hard to keep up with the increasing amounts of evidence.

Amyloidogenesis of SARS-CoV-2 delta plus and omicron variants receptor-binding domain (RBD): impact of SUMO fusion tag https://link.springer.com/article/10.1007/s10529-024-03525-9 and A case of metastatic breast carcinoma to the skin expressing SARS-CoV-2 spike protein possibly derived from mRNA vaccine https://www.jdsjournal.com/article/S0923-1811(25)00180-X/abstract

Swabbie Robbie's avatar

This stuff keeps on killing and maiming 50 years later. Now look at Round Up - glyphosate. Will we be talking about similar illnesses and death from that 50 years from now as well? The herbicide industry (Bayer Monsanto) is trying to have immunity from liability the same as the pharmaceutical industry has for its "safe and effective" vaccines.

I feel for what Mr. Szymanski has been going through. I am a lifelong bicyclist who is also 74 years old. Though not a racer, I was a long distance tourer in my young years and still have my 1973 Holdsworth Record set up as a road bike. I still ride it a bit, but I mostly ride an ebike now.

KuhnKat's avatar

Since you are still pointing to Agent Orange I have to comment.

The largest exposure to TCDD is from the open burning of plastic. The military standard was to use open burn pits in non-permanent locations. Even in semi-permanent they did not use filtration of the burn products to prevent contamination. Yes, Agent Orange had tiny amounts of TCDD. Unlikey that it harmed anyone not exposed to large amounts of it such as aerosols from the actual tanks.

Leanne Lundberg's avatar

Very interesting observation. Thank you

BadProtein's avatar

Regarding Amlyoid Flavoured Bacon and Sausage??

# Countries where Sequivity is currently licensed for use in food-producing swine:

# - United States (USDA-licensed swine RNA particle vaccines)

# - Canada (Merck Animal Health Canada publishes Sequivity materials)

# Is Sequivity used in pigs raised for pork and bacon?

Yes — Sequivity® is specifically a swine vaccine platform, and it is used in pigs that

ultimately enter the food chain for pork, bacon, ham, and other pork products.

Merck Animal Health describes Sequivity as:

- “A revolutionary swine vaccine platform” designed to combat swine diseases such as

influenza A, PCV, and rotavirus.

- Intended for use in growing pigs, including those raised for pork.

Do vaccinated pigs enter the food supply?

Yes. Merck states that vaccines developed with this RNA technology:

- “do not pose any risks to the food supply when animals are vaccinated”.

This confirms that:

- Sequivity-vaccinated pigs are part of the pork and bacon supply chain.

- Regulatory authorities consider the technology safe for food-producing animals.

Why is Sequivity used in pork production?

Producers use Sequivity because it:

- Can be customized quickly to match local strains of swine pathogens.

- Helps control diseases that reduce growth, increase mortality, or cause economic loss.

- Is safe for pigs as young as 3 days old (per Merck’s swine vaccine materials).

Summary:

- Sequivity is a swine-specific RNA particle vaccine platform.

- It is used in pigs that become pork, bacon, ham, and other pork products.

- Manufacturer and regulatory statements confirm it is safe for the food supply.

# Deep Dive: The Cellular Mechanics of Sequivity® RNA Particles

Sequivity is not a classical mRNA vaccine and not a viral vector. It uses a proprietary

RNA Particle (RP) platform that delivers non‑replicating RNA encoding a pathogen‑specific

antigen. This RNA is then translated inside the animal’s cells to produce the antigen

that triggers immunity.

The mechanism can be broken into five major stages.

------------------------------------------------------------

1. ENTRY: HOW THE RNA PARTICLE GETS INTO THE CELL

------------------------------------------------------------

Sequivity particles are RNA Particles (RP) designed to deliver genetic information but

not replicate and not shed.

Key properties:

- They contain only a gene sequence from the pathogen, not the pathogen itself.

- They are engineered to be taken up by host cells, likely via endocytosis.

- Once inside, the particle releases its RNA into the cytoplasm.

------------------------------------------------------------

2. RELEASE: RNA LIBERATION INTO THE CYTOPLASM

------------------------------------------------------------

After uptake, the RNA must escape the endosomal compartment.

Important points:

- The RNA does not enter the nucleus.

- It remains in the cytoplasm.

- It serves only as a template for antigen production and does not replicate.

------------------------------------------------------------

3. TRANSLATION: RIBOSOMES BUILD THE ANTIGEN PROTEIN

------------------------------------------------------------

Inside the cytoplasm:

1. Ribosomes bind the RNA.

2. The RNA is translated into a single antigenic protein.

3. The antigen is processed and displayed on the cell surface.

This is identical to how the cell makes its own proteins—Sequivity simply provides a

new set of instructions.

------------------------------------------------------------

4. ANTIGEN PROCESSING: HOW THE CELL PRESENTS THE PROTEIN

------------------------------------------------------------

Once the antigen is produced:

- Some is processed into peptides and loaded onto MHC class I molecules.

- Some may be secreted or displayed on the surface and taken up by antigen‑presenting cells.

This leads to:

- Cytotoxic T‑cell activation (via MHC I)

- Helper T‑cell activation (via MHC II)

- B‑cell activation and antibody production

------------------------------------------------------------

5. CLEARANCE: RNA DEGRADATION AND NO REPLICATION

------------------------------------------------------------

Key facts:

- Sequivity RNA does not replicate.

- It cannot cause disease or shed from the animal.

- The RNA is naturally degraded by cellular RNases.

- Antigen production is temporary and self‑limiting.

------------------------------------------------------------

WHAT MAKES SEQUIVITY MECHANISTICALLY UNIQUE?

------------------------------------------------------------

Feature | Sequivity RP | mRNA Vaccines | Viral Vectors

-------------------------|-------------------|-------------------|----------------

Replication | No | No | Sometimes

Genetic material | RNA | mRNA | DNA

Enters nucleus | No | No | Yes

Uses viral capsid | No | No | Yes

Antigen source | Custom sequence | mRNA | Viral genome

Customization speed | Weeks | Months | Long

------------------------------------------------------------

SUMMARY: THE MECHANISTIC FLOW

------------------------------------------------------------

1. RNA Particle enters cell

2. RNA released into cytoplasm

3. Ribosomes translate RNA into antigen

4. Antigen presented on MHC molecules

5. Immune system forms memory

6. RNA degrades naturally; no replication

# Sequivity Dose Information (RNA Particle Count)

Publicly available technical documents from Merck Animal Health do NOT disclose the

numerical dose of Sequivity® RNA Particle vaccines. No particle count, RNA mass (µg),

copy number, or concentration per mL is published in any accessible materials.

What IS known from manufacturer statements:

- Sequivity vaccines contain RNA Particles (RP) that deliver a gene sequence.

- The RNA particles do not replicate and cannot shed.

- The platform is designed to express a single antigen inside host cells.

- The exact number of RNA particles per dose is proprietary and not listed in Merck’s

white papers, brochures, or public regulatory filings.

What is NOT publicly disclosed:

- RNA particle count per dose

- Micrograms of RNA per dose

- Number of RNA copies

- Dose-response curves

- Concentration of RP per mL

Summary:

- Sequivity’s mechanism is described in detail, but the actual dose in particles is not

publicly released. Merck treats the formulation specifics as proprietary.

Who is looking for misfolded proteins in the meat? How long till they prove that one beyond a shadow of a doubt?

Swabbie Robbie's avatar

I have a question (off topic) for the brain trust here. My wife 83(today), started taking Methylene Blue 12mg (per day) capsules for only 3 days, then got shingles in the left upper chest dermatome - I believe it is T4. It may have been coincidence, but she has never had shingles before. Did have severe T2 nerve pain without a rash 7-8 years ago that began suddenly and ended just as suddenly after 3 weeks. She had chicken pox when she was 5+ years old. Has anyone heard of this happening from Methylene Blue? But more importantly she would like to know of treatments to lessen the pain and shorten the span of the shingles. (note: she has not had any vaccine since Yellow Fever shot in 1976 when we went to Papua New Guinea and never had a shingles vaccine).

Original reason for taking Methylene Blue was stiffness in her legs/trouble walking. Even though it has been 3 days since the last Methylene Blue (urine is no longer blue/it cleared after 48 hours), Her legs are stronger and she is no longer using a cane indoors.

There were no symptoms of shingles aside from tenderness/itching in rash area before it became red. After 5-6 days, no viral symptoms aside from rash. Rash has blistered.

SegFish's avatar

I would definitely stop taking the MB and start loading up on green tea extract. I recommend Vitacost brand. You can get decaf, which I recommend over the regular. Green Tea extract has a powerful antiviral effect on the herpes family of viruses. It also works topically, but the product I used to use was mysteriously wiped after achieving too much success so you'll have to figure out how to make your own topical salve.

I also recommend avoiding caffeine or any neurological stimulant (with the exception of green tea) and taking soothing chamomile and passionflower (as teas or capsules or however) or other nervines which will help to calm the outbreak as well. Freaking out will literally make the outbreak worse due to the strong mind-body relationship with the herpes family of viruses.

MB may not be the best match for her leg stiffness, though I now see you DID say that it seemed to help. It could be she ramped up with this strong medicine too quickly, or that the formulation of the capsules is not correct (many MB products are contaminated with heavy metals). I recommend Compass Labs tincture MB if it turns out that contamination could have been the trigger. No matter what MB she uses, ramping up the quantity SLOWLY is very important to avoid triggering 'healing reactions.'

SegFish's avatar

Turmeric/curcumin is sort of a general support as well and is worth trying just to help with the discomfort. It's a powerful antiinflammatory. Turmeric is not concentrated so you're talking about taking 4 capsules vs 1 with curcumin (roughly, depends upon products). It's also great medicine to have around just for dealing with the shedding in general and will help to protect her brain from the damaging effects of the spike proteins being widely shed.

Swabbie Robbie's avatar

We both use Turmeric/curcumin when feeling like we are catching something. We have capsules and tea. Both had covid in March April 2020 shook it off in about a week plus a couple days. Did the early Zelenko protocol. Never had it again, though I am sure everyone has been exposed to it multiple times.

SegFish's avatar

R.I.P. Zelenko. What a courageous and generous man who helped so many to the very end of his days.

BadProtein's avatar

Okay, the user is asking about the "multiplication factor" for pepper and turmeric. I think this might be about how black pepper (specifically piperine) increases the bioavailability of curcumin in turmeric. I’ve seen numbers like a 20x increase in absorption, which is a huge boost. It’s possible the user is referring to this, but I’ll need to check for more details to be sure. Let’s look up more info on this!

Piperine (the active alkaloid in black pepper) increases curcumin bioavailability through multiple mechanisms: it inhibits hepatic and intestinal glucuronidation, slows metabolic clearance, and can enhance intestinal absorption by altering membrane dynamics and transporter activity.

Reported multipliers range from modest (a few‑fold) to very large. A widely cited figure is ~2000% (about 20×) higher plasma curcumin when given with piperine versus curcumin alone; other studies report smaller or larger effects depending on formulation, dose, and whether curcumin is given as raw extract, nanoparticle, or with other enhancers.

Piperine is a broad bioenhancer and can increase systemic exposure of many drugs by inhibiting drug‑metabolizing enzymes and transporters. That raises the risk of drug interactions and altered drug clearance; caution is warranted for people on prescription medications.

SegFish's avatar

if it's really painful ( I hear shingles is incredibly painful), she might want to also avoid the same 'trigger' foods as for regular oral/genital herpes, the biggest ones being peanuts, pea familly of beans (i.e. hummous, split pea soup etc), chocolate, wine, etc. And absolutely NO sugar as sugar temporarily disables the body's defenses and allows all viruses free reign to multiply and will massively slow down the recovery period.

Swabbie Robbie's avatar

My wife is a big coffee drinker but not big on peanuts, split pea soup, wine, and is more moderate on sugar than I am (I am working on that). Chocolate she loves but we don't have any here at pressent. She likes teas and I think she will happily cut coffee for the time being.