Who made up the “safe and effective” lie?
(media.omegacanada.win)
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I advised my mother to take it in August 2021. Mostly because she is venerable and has Bronchiolitis Obliterans Organizing Pneumonia (unknown origin). Neither her nor I expect her to be around in 10 years AND she has such extensive lower lung scarring that anything could push her over the edge. The calculus on her is extremely different and she's the exact demographic that an experimental treatment exists for. In fact pushing a non-sterilizing vaccine on everyone creates a selection pressure that will see COVID-19 either end (not a chance) or give rise to a strain that removes that advantage people like my mother stand to gain.
I, myself, am not vaccinated and was willing to endure job loss over it. My organization went with a "don't ask don't tell" policy and banned vaccination status as a topic of discussion in the workplace. Had it come to it, I'd have left my career over this.
DO NOT DO THIS. THE SPECIFIC STRESS ON THE BODY COULD CAUSE GREAT HARM IF YOU HAVE PRE-EXISTING CONDITIONS AND IS EXTRAORDINARILY HARD ON THOSE WHO DON'T. I might have taken the AstraZeneca (CoviShield?) vaccine as a cop out but I would have practiced prophylactic treatment against it. Interestingly, ivermectin is extremely strong here. My protocol would have been Ivermectin + Lysine (10+grams) + Wet Fasting. For 3 days prior to injection and for 4 days after. I'd likely have dosed vitamin C and D also but these wouldn't have a direct effect. In essence a protease inhibitor that has an additional mechanism of action on chimpanzee adenovirus. Then fasting + a very high dose of lysine to reach a level of mild arginine inhibition (coin toss here as we're creating a situation of high vascular constriction but greatly interfering with replication of the spike protein) - I would do this if I were forced to take an mRNA vaccine. You are primarily fasting to prevent yourself from consuming an amino acid profile that will offset arginine inhibition. If you have access to an arginine inhibitor there's no point in doing this. The fasting has a side benefit of reducing insulin (increasing human growth hormone) and inducing autophagy (self-eating). Vitamin C and D just generally help with viral infection. D to signal your body against turning off for winter. C for mild acidification though I don't know if it'd help here.
I believe strongly enough against taking the vaccine at my age and overall health that I'm not only willing to experience job loss over it. I'm also willing to practice a theoretical protocol if I were forced to take it. Like if it was the only way I'd be allowed to visit my dying wife. Something of that magnitude.
I still contend that the main issue with mRNA vaccines is in the delivery mechanism. The delivery materials, in my opinion, are going to play the role of the 1000 carcinogens in cigarettes and the industry used to say that part out loud as little as 5 years ago. It's going to be the asbestos of the millennial and late Z generations. There are specific issues with the spike protein too, but the lipid nanoparticles (LNP) are going to be the thing that proliferates to other vaccines and protein (mRNA) therapies. In some cases this may be fine. Where a LNP is delivery mRNA that just synthesizes a biologic medication. In cases where a LNP is an inflammatory, as with vaccine adjuvants, it's going to add to potential autoimmune injury of tissues the adjuvant is more trophic to. So like cigarettes. A life ending problem for many. Indefinitely fine for a few. Mileage varying by how much smoking is undertaken. But unlike smoking, the autoimmunity isn't just going to resolve when you stop.
Autoimmunity Issues:
My theory is that we are going to start seeing symptoms of autoimmunity in the eyes, ovaries, and adrenal glands. We are going to pretend not to understand it and treat the symptoms. Like we are going to see soaring rates of depression and ennui and blame it on pandemic trauma and long covid but this is actually going to be adrenal fatigue brought about by lipid nanoparticles being more trophic (wanting to glob on at higher concentrations per gram of tissue) to adrenal glands than say spleen tissue or liver tissue.
Same goes for cornea transplant rejection being reported. The eyes of vaccinees have adjuvants pooling in them that provoke the immune system locally which is something you do not want at a transplant site. People will just attribute the vision loss to stress and too much screen time on account of the pandemic.
The ovarian symptoms are showing up in menstrual disruption and that's harder to apologize away. Worse with this is that the menstrual disruptions are "on average" meaning there are women with extremely minor disruption watering down the disruption of women with major or catastrophic damage to their cycles and/or fertility.
Now the spike is it's own thing. Cardiovascular issues. And while the spike is produced by the virus and the vaccine, only the vaccine can potentially vector it to places where it'd normally not be in the concentrations that the vaccine allows for. Like if your medical professional asserts that "aspiration is not indicated!" because they think that it's magic, you might be in for what I'm going to describe. Aspiration was not indicated initially because supplies were limited and it was being rolled out to elderly and immunocompromised people anyway. Aspiration coming up red requires throwing out the dose so that you have a clear syringe with which to aspirate again.
So we're not aspirating. Meaning we can hit blood vessels. And people are just jabbing people every 5-15 minutes. It's tiring. In some cases they're firemen doing it.
When you hit a blood vessel, it's no longer intramuscular. The LNPs enter circulation. Their size is small enough that they should be able to pass through the blood-brain barrier. To say nothing of vascular tissue.
With COVID-19 or adenovirus vaccines, they're not going to be small enough to get through to the brain, except in the kinds of exceptional circumstances that deserve single patient case studies. Like when a common cold gets into the brain and kills or catastrophically injures the patient. It's rare but it happens.
Spike proteins reaching the brain will be incidental in a COVID-19 infection. In a vaccination that misses the intramuscular site, it becomes a strong possibility.
There's just so much about the mRNA vaccines that I'm uncomfortable with that I can't abide them. These aren't even unknowns. They're just the kinds of things that a general practitioner isn't generally going to be aware of unless they're inclined to dig deep. Same goes for a lot of academics. Most of them aren't eccentric Einstein types or as smart as the geek-blackface Big Bang Theory people portrayed on TV. And some of the brilliant ones are too smart to tie their own shoes or mile deep inch wide types parroting people with impeccable credentials who are parroting people without them.
Agree with all. u/itlivesinthewind
Except the premise that the mRNA might be beneficial for the elderly who already have comorbidities and weakened immune systems.
If anything, the frail and elderly should avoid hepatotoxic nephrotoxic drugs like Paxlovid, Remdesevir. mRNA vaccines are proven to cause transient T cell suppression. There is no value to the injections, the vast majority (>95%) of Ontario Covid ICU and Covid hospitalizations are in the elderly triple and quadruple vaccinated.
And like you said, the delivery mechanism is the toxin. There is no way to detox the LNP’s that cross the blood brain barrier.
We are seeing post menopausal women who are having abnormal uterine bleeding after their second, third and fourth doses. Referrals to gyno for this age group with this issue has skyrocketed. Same with infertility in healthy young men, the demand for spermogram is through the roof.
Arginine makes sense.
The correct treatment for severe Covid related sepsis is non-invasive ventilation, steroids, and antioxidant infusions. Most of the drugs repurposed for Covid that show any benefit whatsoever in rescuing critically-ill Covid patients are antioxidants. N-acetylcysteine, melatonin, fluvoxamine, budesonide, famotidine, cimetidine, and ranitidine are all antioxidants. Indomethacin prevents iron- driven oxidation of arachidonic acid to isoprostanes. There are powerful antioxidants such as apocynin that have not even been tested on COVID-19 patients yet which could defang neutrophils, prevent lipid peroxidation, restore endothelial health, and restore oxygenation to the tissues.
Scientists who know anything about pulmonary neutrophilia, ARDS, and redox biology have known or surmised much of this.
Swiss scientists confirmed that COVID-19 lab engineered bio weapon was a vascular endotheliitis. They also know that sepsis can be effectively treated with antioxidants. None of this information is particularly new, and yet, for the most part, it has not been acted upon.
Hospital protocols continue to use damaging intubation techniques with high PEEP settings despite high lung compliance and poor oxygenation, KILLING an untold number of critically ill patients with medical malpractice.
Because of the way they are constructed, Randomized Control Trials will never show any benefit for any antiviral against Covid.
Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this is simple; for the patients that they have recruited for these studies, such as Oxford’s ludicrous RECOVERY study, the intervention is waay too late to have any positive effect.
The clinical course of oxidation and Covid is such that by the time most people seek medical attention for hypoxia, their viral load has already tapered off to almost nothing. If someone is about 10 days post-exposure and has already been symptomatic for five days, there is hardly any virus left in their bodies, only cellular damage and derangement that has initiated a hyperinflammatory response. It is from this group that the fraudulent clinical trials for antivirals have recruited, pretty much exclusively.
In these fraudulent trials, they give antivirals to severely ill patients who have no virus in their bodies, only a delayed hyperinflammatory response, and then absurdly claim that antivirals have no utility in treating or preventing Covid. These clinical trials do not recruit people who are pre-symptomatic, they do not test the efficacy of EARLY TREATMENT. They do not test pre-exposure or post-exposure prophylaxis.
The Oxford ludicrous study is like using a defibrillator to shock only flatlines, and then absurdly claiming that defibrillators have no medical utility whatsoever when the patients refuse to rise from the dead. The intervention is too late. The Ivermectin and other anti viral trials show systematic, egregious selection bias. They are providing a treatment that is futile to the specific cohort they are enrolling.
India went against the instructions of the WHO and mandated the prophylactic usage of Ivermectin. And they were incredibly successful in preventing severe illness.
( u/tuchodi Covid Nazi won’t have a clue what I just said. ) Go get your 5th mRNA government mandated injection like a retarded monkey! Recharge your immune system with mRNA every 90 days and keep following your google science Covid Nazi!
TL:DR
Folks, you have no reason to believe anything V&C1 says. Just another anonymous Internet troll spouting off.
I was replying to Itliveswiththewind. Not replying to you Covid Nazi. I know you don’t have the ability to understand a word.
I want you to stay stupid. I want you to keep relying on google for your misinformation. Because I want you boosted and injected with as much mRNA as possible.
Recharge as often and as soon as possible Covid Nazi.
V&C1. The copy pasta queen.