New paper LIVE today that proves that the production process of modRNA was highly flawed in addition to HOW and WHY the DNA is in the vials and was not detected/reported
Exactly. The satanic cabal didn’t blunder into this, 🎯 they executed it.
The great poisoning and lockdowns were carried out deliberately, riding on the back of a fictitious pathogen, 🦠❌ toxic shots 💉☠️ packed with real L ife-N eutralizing P articles, fictitious mRNA, 📜👻 and make-believe cellular machinery, 🏭✨ allegedly coding for the production of a spike protein from a virus never proven to exist.
This wasn’t science, 🎭 it was theater-noir.
An epoch-making fraud pulled off through a tightly coordinated psyop, 📡🧠 relentless coercion, 🔒😱 and narrative enforcement dressed up as “public health.” Evidence was replaced by repetition, fear was marketed as virtue, and obedience was sold as care. 🤝🔨
And the real masterstroke?
Gaining the buy-in of large swathes of the health freedom movement, getting them to help promulgate the fear narrative and launder the fraud through trusted voices, 🚩🤦♂️ while dissent from the BS was framed as divisive.
No accidents here. 👁️
Just coordination, compliance, and control. 🕸️
A Control Grid masterclass, hiding in plain sight.
Yeah, really interesting. Dr. Yeadon correctly notes that there was no novel virus circulating that would warrant the injection of toxic shots—and that viroLIEgists have yet to provide evidence for any 'virus' using anything resembling the scientific method. I’m 'sure' Jessica’s readers are already well aware of this.
A crime , THE CRIME was committed. THEY knew EXACTLY what they did , no mistakes were made . Not one person has answered to this. 🤬Thank you Charles , Jessica and Kevin. 🩷🩷🩷
They could not care less. That's the beauty of immunity from liability. The vaccines are contaminated with trash from the manufacturing line including glass, rubber, plastic, cloth fiber, dust, etc. What's a little RNA:DNA Hybrid among all that other trash?
>>>>Tell me more about: visualizing how particle size shifts lymphatic vs systemic delivery
Copilot:
Short answer: Particle size is one of the strongest determinants of whether LNPs stay local and drain into lymphatics (favoring immune‑priming) or rapidly enter blood and distribute systemically (favoring liver and endothelium). Smaller particles tend to access lymph nodes efficiently; mid‑range particles balance lymphatic drainage and local retention; very large particles remain at the injection site or are taken up by local phagocytes
Mechanism overview
Lymphatic uptake depends on interstitial flow and the ability of particles to enter initial lymphatic capillaries through gaps and valves; systemic uptake depends on access to blood capillaries and opsonization that drives hepatic/splenic clearance. Size interacts with surface chemistry and charge to determine whether a particle is carried by lymph (slow, immune‑focused route) or swept into circulation (fast, liver‑biased route)
Size regimes and expected fate
Size bin Typical fate Practical implication
<10 nm Rapidly diffuses into blood; renal filtration; minimal lymph node targeting Systemic exposure; short circulation time
10–50 nm Efficient lymphatic entry and transport to draining nodes Good for vaccine antigen delivery to APCs
50–150 nm Mixed behavior: partial lymphatic drainage; some systemic uptake Balance between local retention and node delivery
>200 nm Mostly retained at injection site; taken up by local phagocytes Strong local depot effect; less systemic exposure
How to visualize it
Think of interstitial pores as size filters: particles below a threshold slip into lymphatic openings; larger particles are trapped in the matrix and encounter resident macrophages
Imagine two highways: the lymphatic highway is slow and leads to nodes (immune control centers); the blood highway is fast and leads to liver and spleen (clearance hubs)
Overlay surface chemistry: PEGylation and charge shift the effective size and “stickiness,” so two particles with the same diameter can behave differently in vivo
Design tradeoffs (Pfizer/Moderna context)
Smaller, less PEGylated LNPs favor lymph node delivery and stronger local immune priming; larger or more opsonized LNPs favor hepatic uptake and systemic exposure. Both Comirnaty and Spikevax tune size and PEG chemistry to bias toward lymphatic/IM behavior while minimizing systemic spread
Practical takeaway
For vaccines, 10–100 nm is the sweet spot for getting antigen into draining lymph nodes while limiting systemic exposure; shifting size by tens of nanometers meaningfully changes organ targeting and immune outcome
>>>>>>>>would LNPs merge after time in solution to make bigger particles - i wonder if a 'fresh from the freezer' shot would act differently if it sat on the counter for long enough to sit at room temperature for an hour.
Short answer
Yes — lipid nanoparticles can change over time at room temperature: they can aggregate, fuse, or shed surface PEG, and the encapsulated mRNA can degrade. A single hour at room temperature is unlikely to cause catastrophic fusion for a properly handled, recently thawed vaccine, but longer warm exposure, repeated freeze–thaw, dilution, or vigorous agitation increases the chance of larger particles and reduced potency.
What physically happens to LNPs out of cold storage
Aggregation and fusion — lipid shells can stick together or merge, producing larger particles; this is driven by Brownian collisions, reduced colloidal stability, and loss of steric repulsion.
PEG‑lipid desorption — the PEG layer that stabilizes particles can come off over time, making particles “stickier” and more prone to aggregation and opsonization.
Chemical degradation — ionizable lipids and ester linkages slowly hydrolyze at higher temperatures, changing membrane properties and reducing endosomal escape efficiency.
mRNA degradation — higher temperature and any RNase contamination accelerate mRNA breakage, lowering the amount of intact template available for translation.
How those changes alter biological behavior
Bigger particles drain less well to lymph nodes and are more likely to be retained at the injection site or taken up by local phagocytes rather than delivered to APCs in nodes.
Increased opsonization and hepatic/splenic clearance — aggregated or PEG‑shed particles are cleared faster by macrophages, shifting biodistribution toward liver and spleen and reducing effective antigen expression.
Lower endosomal escape and translation — chemical changes to the ionizable lipid and mRNA loss reduce how much spike protein is produced per dose.
Potentially altered reactogenicity — more uptake by phagocytes and faster clearance can change the inflammatory profile (often more local inflammation), though effects are complex and formulation‑dependent.
Is an hour at room temperature a big deal?
Usually not if you follow manufacturer handling: vaccines are formulated to tolerate the brief handling needed for thawing and preparation. A properly thawed vial left at room temperature for an hour before injection is unlikely to have major particle fusion or complete loss of activity.
But risk rises with: repeated freeze–thaw cycles, leaving vials at warm temperatures for many hours, diluting and then sitting, or vigorous shaking — any of these increase aggregation and mRNA degradation.
Practical implications (what changes in practice would matter)
Fresh‑from‑freezer then thawed and used promptly → minimal change in particle size/function.
Thawed and left at room temp for many hours or repeatedly warmed/cooled → measurable aggregation, reduced lymphatic targeting, lower protein expression, and altered biodistribution.
Dilution and agitation (e.g., vigorous shaking) accelerate instability and should be avoided.
Bottom line
LNPs are engineered for a balance of stability and function. Short, manufacturer‑recommended handling at room temperature is generally safe; extended warm exposure, repeated freeze–thaw, dilution followed by delay, or rough handling increases aggregation, PEG loss, and mRNA degradation — all of which reduce effective delivery and change where and how much spike protein is produced. If you want, I can outline a simple sensitivity table showing how particle size increases (e.g., 50 → 150 nm → 300 nm) shift lymphatic vs systemic delivery and expected functional consequences.
At what point does it become impossible to hide the truth any longer? Governments must have some awareness that these shots are not safe and effective but instead a catastrophe. They are so inept they’re still promoting the shots because they believe in pharma? None of this makes sense. I believe if pharma knew what they were doing their get out of jail free card gets rescinded.
The yet to be realized issue is the damage done to the DNA and RNA of those that were injected . Their potential offspring and long term prognosis for cancer and other ailments not yet noted . This then begs the question of , IS , there any difference between intentional and intentional neglect of duty . not of as single instance but over a protracted time and continued use of a drug which was absolutely known to cause death and have limited to NO effect on the intended medical application which it was intended to be promoted by both pharmaceuticals and governments , for the purposes of monetary , social ingratiating purposes or political motivations while having knowledge of the damages being done from the vaccines . While being opposed by the peoples of their country and others on the basis of those deaths and injuries the general population had noted . This becomes a complete misuse of power to knowingly create harm and then continue more harm as an attempt to cover up the harm already done and NOT admit to their mistakes . I can see a clear cut case for capital punishment under the Nuremberg Code . Failing to do so forsakes any and all credibility of any sitting government or politician who as in NZ signed pledges to not address the crowds of protested even as they gave proof of the deaths and harm to the citizens of the country , no one in power at that time is immune from liability as they are complicit to that crime . We are not awaiting the results of the SAME government's official Royal Commission's report that has no other duty than to cover up the illegal acts of the government in power at that time . It is specifically bypassing the other major party National whose representative Chris Bishop was PROMOTING the vax and mandates at the same level as those in the Majority Labour party , and yet he side stepped in that investigation . One wrong does not make one right , it makes the justification for two wrongs that become endless in replication and magnitude on the path to absolute tyranny .
This looks like the foundation of the largest class action ever against Pfizer and Moderna based on your and Kevin's cited paper above. I won't be surprised if your phones don't ring off the hook, engaging both of you as expert witnesses.
This is research that leaves no question about the residual contamination.. with the RNA /DAN sticking together and using the wrong enzyme to break it down then it's delivered into the cells via the lipid nano particles!!! Yikes .. this is a dam disaster... and one vial was found to have over 5000 more than it should have !!Thankyou for this most imprortant work Jessica and Kevin and the other gentleman that i believe is suffering from vaccine damage but lives in Japan and helps with the blood transfusion technique.. bless you all and let's hope goodness prevails or at least Science
🧬🧪 Scientists Confirm DNA–RNA “Hybrids” — despite the only evidence for either being goo produced by aggressively abusing biological material with a heady cocktail of acids, heat, centrifuges, stains, and sheer wishful thinking. 🥼👉🟤
Rumors now swirl that fake mRNA even enlisted imaginary cell organelles to “translate” a spike protein from a virus that itself has never been proven to exist. 🤡🔬🦠 The science marches on… straight through the sludge 💥🧫😂
Great work! I have some questions: (1) did you do Qbit using RNaseA+DNaseXT? You'd expect the signal to go to zero. Are you sure DNaseXT does not digest dsModRNA? (2) Why is there such a huge difference between Ori+DNaseI and Ori+DNaseXT? Is Ori DNA also in a RNA hybrid, and if so, where does this RNA come from? Or is it secondary structure? (3) Does Nanopore also sequence DNA/modRNA hybrids?
in the article, i mentioned that DNase-XT works real well on Ori. No, Ori doesn't make hybrids as far as we know. ONT does treated DNA that's 'cleaned up' so no hybrids, i would suspect. qbit = yes. no digestion of dsmodRNA by DNase-XT, as far as i know. RNase-H -> yes.
Dear Jessica, did you happen to tell Maarten how “scientists” actually isolate DNA? It’s the same ballpark bollocks they use to “isolate” viruses — poison biological material, wreck it with chemicals, and then point at the resulting artefacts as proof of concept. Science™ at its finest. LOL 🤡🧪
That's cause most people are primitive in their thinking. They have outsourced their thinking their entire lives, they have no original thoughts. Like sheep 🐑 to slaughter 👹☠️😭. They can't get out of their own way.
It is shocking and gives support to Mike Yeadon's arguments that 'mistakes were not made'
Mistakes were not made , it was on purpose…..🤬
Exactly. The satanic cabal didn’t blunder into this, 🎯 they executed it.
The great poisoning and lockdowns were carried out deliberately, riding on the back of a fictitious pathogen, 🦠❌ toxic shots 💉☠️ packed with real L ife-N eutralizing P articles, fictitious mRNA, 📜👻 and make-believe cellular machinery, 🏭✨ allegedly coding for the production of a spike protein from a virus never proven to exist.
This wasn’t science, 🎭 it was theater-noir.
An epoch-making fraud pulled off through a tightly coordinated psyop, 📡🧠 relentless coercion, 🔒😱 and narrative enforcement dressed up as “public health.” Evidence was replaced by repetition, fear was marketed as virtue, and obedience was sold as care. 🤝🔨
And the real masterstroke?
Gaining the buy-in of large swathes of the health freedom movement, getting them to help promulgate the fear narrative and launder the fraud through trusted voices, 🚩🤦♂️ while dissent from the BS was framed as divisive.
No accidents here. 👁️
Just coordination, compliance, and control. 🕸️
A Control Grid masterclass, hiding in plain sight.
Yeah, really interesting. Dr. Yeadon correctly notes that there was no novel virus circulating that would warrant the injection of toxic shots—and that viroLIEgists have yet to provide evidence for any 'virus' using anything resembling the scientific method. I’m 'sure' Jessica’s readers are already well aware of this.
I agree. But I do not see Mr. Yeadon's statements as an argument, but rather, a testimony.
A crime , THE CRIME was committed. THEY knew EXACTLY what they did , no mistakes were made . Not one person has answered to this. 🤬Thank you Charles , Jessica and Kevin. 🩷🩷🩷
"process of modRNA was highly flawed"
They could not care less. That's the beauty of immunity from liability. The vaccines are contaminated with trash from the manufacturing line including glass, rubber, plastic, cloth fiber, dust, etc. What's a little RNA:DNA Hybrid among all that other trash?
Immunity from liability is only if all legitimate information was give at the time of the signing of the contract and was accurate .
>>>>Tell me more about: visualizing how particle size shifts lymphatic vs systemic delivery
Copilot:
Short answer: Particle size is one of the strongest determinants of whether LNPs stay local and drain into lymphatics (favoring immune‑priming) or rapidly enter blood and distribute systemically (favoring liver and endothelium). Smaller particles tend to access lymph nodes efficiently; mid‑range particles balance lymphatic drainage and local retention; very large particles remain at the injection site or are taken up by local phagocytes
Mechanism overview
Lymphatic uptake depends on interstitial flow and the ability of particles to enter initial lymphatic capillaries through gaps and valves; systemic uptake depends on access to blood capillaries and opsonization that drives hepatic/splenic clearance. Size interacts with surface chemistry and charge to determine whether a particle is carried by lymph (slow, immune‑focused route) or swept into circulation (fast, liver‑biased route)
Size regimes and expected fate
Size bin Typical fate Practical implication
<10 nm Rapidly diffuses into blood; renal filtration; minimal lymph node targeting Systemic exposure; short circulation time
10–50 nm Efficient lymphatic entry and transport to draining nodes Good for vaccine antigen delivery to APCs
50–150 nm Mixed behavior: partial lymphatic drainage; some systemic uptake Balance between local retention and node delivery
>200 nm Mostly retained at injection site; taken up by local phagocytes Strong local depot effect; less systemic exposure
How to visualize it
Think of interstitial pores as size filters: particles below a threshold slip into lymphatic openings; larger particles are trapped in the matrix and encounter resident macrophages
Imagine two highways: the lymphatic highway is slow and leads to nodes (immune control centers); the blood highway is fast and leads to liver and spleen (clearance hubs)
Overlay surface chemistry: PEGylation and charge shift the effective size and “stickiness,” so two particles with the same diameter can behave differently in vivo
Design tradeoffs (Pfizer/Moderna context)
Smaller, less PEGylated LNPs favor lymph node delivery and stronger local immune priming; larger or more opsonized LNPs favor hepatic uptake and systemic exposure. Both Comirnaty and Spikevax tune size and PEG chemistry to bias toward lymphatic/IM behavior while minimizing systemic spread
Practical takeaway
For vaccines, 10–100 nm is the sweet spot for getting antigen into draining lymph nodes while limiting systemic exposure; shifting size by tens of nanometers meaningfully changes organ targeting and immune outcome
>>>>>>>>would LNPs merge after time in solution to make bigger particles - i wonder if a 'fresh from the freezer' shot would act differently if it sat on the counter for long enough to sit at room temperature for an hour.
Short answer
Yes — lipid nanoparticles can change over time at room temperature: they can aggregate, fuse, or shed surface PEG, and the encapsulated mRNA can degrade. A single hour at room temperature is unlikely to cause catastrophic fusion for a properly handled, recently thawed vaccine, but longer warm exposure, repeated freeze–thaw, dilution, or vigorous agitation increases the chance of larger particles and reduced potency.
What physically happens to LNPs out of cold storage
Aggregation and fusion — lipid shells can stick together or merge, producing larger particles; this is driven by Brownian collisions, reduced colloidal stability, and loss of steric repulsion.
PEG‑lipid desorption — the PEG layer that stabilizes particles can come off over time, making particles “stickier” and more prone to aggregation and opsonization.
Chemical degradation — ionizable lipids and ester linkages slowly hydrolyze at higher temperatures, changing membrane properties and reducing endosomal escape efficiency.
mRNA degradation — higher temperature and any RNase contamination accelerate mRNA breakage, lowering the amount of intact template available for translation.
How those changes alter biological behavior
Bigger particles drain less well to lymph nodes and are more likely to be retained at the injection site or taken up by local phagocytes rather than delivered to APCs in nodes.
Increased opsonization and hepatic/splenic clearance — aggregated or PEG‑shed particles are cleared faster by macrophages, shifting biodistribution toward liver and spleen and reducing effective antigen expression.
Lower endosomal escape and translation — chemical changes to the ionizable lipid and mRNA loss reduce how much spike protein is produced per dose.
Potentially altered reactogenicity — more uptake by phagocytes and faster clearance can change the inflammatory profile (often more local inflammation), though effects are complex and formulation‑dependent.
Is an hour at room temperature a big deal?
Usually not if you follow manufacturer handling: vaccines are formulated to tolerate the brief handling needed for thawing and preparation. A properly thawed vial left at room temperature for an hour before injection is unlikely to have major particle fusion or complete loss of activity.
But risk rises with: repeated freeze–thaw cycles, leaving vials at warm temperatures for many hours, diluting and then sitting, or vigorous shaking — any of these increase aggregation and mRNA degradation.
Practical implications (what changes in practice would matter)
Fresh‑from‑freezer then thawed and used promptly → minimal change in particle size/function.
Thawed and left at room temp for many hours or repeatedly warmed/cooled → measurable aggregation, reduced lymphatic targeting, lower protein expression, and altered biodistribution.
Dilution and agitation (e.g., vigorous shaking) accelerate instability and should be avoided.
Bottom line
LNPs are engineered for a balance of stability and function. Short, manufacturer‑recommended handling at room temperature is generally safe; extended warm exposure, repeated freeze–thaw, dilution followed by delay, or rough handling increases aggregation, PEG loss, and mRNA degradation — all of which reduce effective delivery and change where and how much spike protein is produced. If you want, I can outline a simple sensitivity table showing how particle size increases (e.g., 50 → 150 nm → 300 nm) shift lymphatic vs systemic delivery and expected functional consequences.
Debilitating through fatal, but who's gonna check our claim? 😈
The usual people....No one.
'cept our heroes Kevin, Jess & Charles 🥂🥂🥂
Of course.
At what point does it become impossible to hide the truth any longer? Governments must have some awareness that these shots are not safe and effective but instead a catastrophe. They are so inept they’re still promoting the shots because they believe in pharma? None of this makes sense. I believe if pharma knew what they were doing their get out of jail free card gets rescinded.
I do not believe they are inept. They know what they're doing. They are killing people on purpose.
Agreed. If we know how deadly these shots are, the government knew when they released them.
! 💜 !
The yet to be realized issue is the damage done to the DNA and RNA of those that were injected . Their potential offspring and long term prognosis for cancer and other ailments not yet noted . This then begs the question of , IS , there any difference between intentional and intentional neglect of duty . not of as single instance but over a protracted time and continued use of a drug which was absolutely known to cause death and have limited to NO effect on the intended medical application which it was intended to be promoted by both pharmaceuticals and governments , for the purposes of monetary , social ingratiating purposes or political motivations while having knowledge of the damages being done from the vaccines . While being opposed by the peoples of their country and others on the basis of those deaths and injuries the general population had noted . This becomes a complete misuse of power to knowingly create harm and then continue more harm as an attempt to cover up the harm already done and NOT admit to their mistakes . I can see a clear cut case for capital punishment under the Nuremberg Code . Failing to do so forsakes any and all credibility of any sitting government or politician who as in NZ signed pledges to not address the crowds of protested even as they gave proof of the deaths and harm to the citizens of the country , no one in power at that time is immune from liability as they are complicit to that crime . We are not awaiting the results of the SAME government's official Royal Commission's report that has no other duty than to cover up the illegal acts of the government in power at that time . It is specifically bypassing the other major party National whose representative Chris Bishop was PROMOTING the vax and mandates at the same level as those in the Majority Labour party , and yet he side stepped in that investigation . One wrong does not make one right , it makes the justification for two wrongs that become endless in replication and magnitude on the path to absolute tyranny .
Bring on the firing squads. I will volunteer my services for as long as it takes.
There are reasons why I can't comment on that ,, but its historically accurate in many cases ,,
This looks like the foundation of the largest class action ever against Pfizer and Moderna based on your and Kevin's cited paper above. I won't be surprised if your phones don't ring off the hook, engaging both of you as expert witnesses.
🙏🙏🙏🙏🙏
Red alert: risk of global TRANSGENERATIONAL genetic integration and cancers, from covid mRNA vaccines.
This post has 50+ scientific papers on this matter: https://tranhiep.substack.com/p/red-alert-the-risk-of-transgenerational
Please share it. The alarm must be sounded.
This is research that leaves no question about the residual contamination.. with the RNA /DAN sticking together and using the wrong enzyme to break it down then it's delivered into the cells via the lipid nano particles!!! Yikes .. this is a dam disaster... and one vial was found to have over 5000 more than it should have !!Thankyou for this most imprortant work Jessica and Kevin and the other gentleman that i believe is suffering from vaccine damage but lives in Japan and helps with the blood transfusion technique.. bless you all and let's hope goodness prevails or at least Science
🚨 BREAKING NEWS 🚨
🧬🧪 Scientists Confirm DNA–RNA “Hybrids” — despite the only evidence for either being goo produced by aggressively abusing biological material with a heady cocktail of acids, heat, centrifuges, stains, and sheer wishful thinking. 🥼👉🟤
Rumors now swirl that fake mRNA even enlisted imaginary cell organelles to “translate” a spike protein from a virus that itself has never been proven to exist. 🤡🔬🦠 The science marches on… straight through the sludge 💥🧫😂
Thank You Warrior-Sister. I'll include this in my next blog post.
Great work! I have some questions: (1) did you do Qbit using RNaseA+DNaseXT? You'd expect the signal to go to zero. Are you sure DNaseXT does not digest dsModRNA? (2) Why is there such a huge difference between Ori+DNaseI and Ori+DNaseXT? Is Ori DNA also in a RNA hybrid, and if so, where does this RNA come from? Or is it secondary structure? (3) Does Nanopore also sequence DNA/modRNA hybrids?
in the article, i mentioned that DNase-XT works real well on Ori. No, Ori doesn't make hybrids as far as we know. ONT does treated DNA that's 'cleaned up' so no hybrids, i would suspect. qbit = yes. no digestion of dsmodRNA by DNase-XT, as far as i know. RNase-H -> yes.
Dear Jessica, did you happen to tell Maarten how “scientists” actually isolate DNA? It’s the same ballpark bollocks they use to “isolate” viruses — poison biological material, wreck it with chemicals, and then point at the resulting artefacts as proof of concept. Science™ at its finest. LOL 🤡🧪
huh?
got it!
Please read the Pfizer SOP, it's even worse than the Moderna one:
Wear impervious disposable protective clothing when handling this compound. Full body
protection is recommended (scale dependent). Wear impervious protective clothing when
handling this compound. (Protective clothing must meet the standards in accordance with
EN13982, ANSI 103 or international equivalent.).
Under normal conditions of use, if the applicable Biotherapeutic Occupational Exposure
Band (B-OEB) is exceeded, wear an appropriate respirator with a protection factor sufficient
to control exposures to below the B-OEB (e.g. particulate respirator with a full mask, P3
filter). (Respirators must meet the standards in accordance with EN136, EN143, ASTM
F2704-10 or international equivalent.).
Pfizer Occupational Exposure B-OEB 5 (control exposure to <10 µg/day)
Engineering controls should be used as the primary means to control exposures. Use
process containment, local exhaust ventilation, biosafety cabinet, or other engineering
controls to maintain airborne levels within the B-OEB range. It is recommended that all
large scale operations should be fully enclosed. Air recirculation is not recommended.
My articles are in German, you'll need google translate.
https://drbine.substack.com/p/das-corminaty-sicherheitsdatenblatt
https://drbine.substack.com/p/woher-wusste-man-in-italien-bereits
https://drbine.substack.com/p/sollte-es-wahrend-der-handhabung
The Data sheets are linked in the articles.
Wow!,,,, biggest reveal yet imo. Too bad most people wouldn't believe me if I told them.
That's cause most people are primitive in their thinking. They have outsourced their thinking their entire lives, they have no original thoughts. Like sheep 🐑 to slaughter 👹☠️😭. They can't get out of their own way.
CHD is involved… Kennedy cannot look the other way . 🙏