Dr McCullough Covid vax protocol

[Towzerone]

Gaert Van derbussche said the other day the protocol of Natto Bromelaine etc that McCullough sells does NOTHING against the spike
ZERO ...its basically snake oil

[pamojja]

Ironic, that spike protein itself has analogies to snake venom.

But seriously, covid was simply a weak cold - as was already seen at the very beginning in the lab of the Diamond Princess - so that almost any home remedy, common sense in lifestyles, and not being near to life-expectancy was protective. Doing nothing until the face turns blue, and then becoming ventilated only, was clearly the worse possible apprach.

On the Diamond Princess, under worst crowded condition of about 3700 persons, 712 became infected with the virus, 331 remained symptom-free, none died from the younger crew (the median age of the passengers was 69), but still on board 7 passengers died only (at about 78 median age), which is about 1% of infected in a most vulnerable population. Some less propagandized flu-seasons have much higher mortality rates, definitely in that age-group.

The jab is of course a different animal, instructing to produce spike protein endogenously. But even here most recover, some wounded of course need more ammunition. But that was also mentioned in McCullogh's paper: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10663976/

Bromelain, a proteolytic enzyme sourced from the stem of pineapples [49], has been traditionally hailed for its healing and anti-inflammatory capabilities, particularly in cases of arthritis and injury. Of significance is bromelain's anticoagulant activity. It downregulates PGE-2 and thromboxane A2, promoting a relative prostacyclin abundance in platelets. Furthermore, it aids in fibrinolysis by promoting plasminogen conversion to plasmin and inhibiting platelet aggregation [50]. Kritis et al. demonstrated that bromelain can obstruct SARS-CoV-2's entry into cells by cleaving its spike protein and reducing ACE2 and TMPRSS2 expression [51]. This enzyme can also hydrolyze glycosidic linkages, which comprise spike protein's glycosidic shield that helps protect it from immune responses [52]. To attenuate inflammation, bromelain, in part, downregulates the pro-inflammatory prostaglandin E?2 (PGE-2) through inhibition of NF-kB and cyclooxygenase 2 and inhibits inflammatory mediators [51]. Thus, bromelain exerts multiple mechanisms of action against spike protein�s toxic effects and persistence. Bromelain has been used as a daily dosage of 200-2,000 mg; thus, 500 mg is a suggested initial dose [53]. Bromelain is mainly safe with low toxicity, but it can amplify bleeding risk and affect the absorption rate of several medications, potentially leading to drug interactions [54].

Curcumin, a polyphenol extracted from turmeric, is renowned for its anti-inflammatory properties and its ability to modulate inflammation during viral infections. Curcumin also supports fibrinolysis and the process of anticoagulation [51]. Beyond its traditionally recognized benefits, curcumin has shown promising antiviral actions against a wide range of viruses, including influenza, hepatitis, and notably, SARS-CoV-2 [55]. It achieves this by obstructing the spike protein's binding sites (ACE2 receptors and TMPRSS-2). Curcumin's anti-inflammatory effects are realized through inhibiting NF-?B signaling [56]. An in-silico study found that curcumin can inhibit the spike protein of the Omicron variant through interaction with its amino acids [57]. Randomized trials have consistently indicated decreases in high-sensitivity C-reactive protein (hs-CRP) and other markers of inflammation in situations involving spike protein-induced infections or injuries [58,59]. Curcumin is non-toxic at doses up to 8,000 mg a day [60]. Large doses, particularly with ill-absorbed formulations, can lead to gastric complications [61]. Enhanced absorption of curcumin is achieved in combination with piperine, or with nano or liposomal formulations, which are available as over-the-counter oral supplements. Doses vary widely depending on the formulation, but 500 mg twice a day has been shown to be a common and safe dosage regardless of curcumin type [61].

Hydroxychloroquine, a well-known FDA-approved antimalarial and anti-inflammatory, adds additional support for immunocompromised patients by inhibiting the binding of spike protein to human cells [62]. A real-time meta-analysis of 413 published peer-reviewed studies for hydroxychloroquine as a treatment for COVID-19, including a total of 529,687 patients, shows a statistically significant lower risk for mortality and hospitalization, along with accelerated viral clearance [63]. This effect was the strongest when patients were treated early, indicating the importance of early treatment. Since hydroxychloroquine accelerates viral clearance, it subsequently assists in spike protein removal, and it may be a great addition to base spike detoxification. This compound has been found to be well-tolerated, safe, and not associated with a risk of ventricular arrhythmia at a dose of 200 mg twice a day provided that the expected prolongation of QTc is managed along with other drugs with serial ECGs. Gastrointestinal symptoms may occur [64].

Colchicine, an FDA-approved alkaloid found in the plants Colchicum autumnale and Gloriosa superba, has been traditionally used in therapeutics for its anti-inflammatory properties [65]. This compound can reduce the risk of myocardial infarction and stroke [66]. Moreover, colchicine may reduce myocardial injury in the presence of spike protein [67]. Pleurodynia has been diagnosed post-COVID-19 vaccination and may be indicative of cardiac inflammation [68]. The COLCORONA trial demonstrated that colchicine was safe and had a favorable impact on COVID-19 and its immediate post-acute sequelae. In patients with PCR-confirmed COVID-19, colchicine lowered the rate of hospitalization and death compared to placebo [69]. A meta-analysis of five randomized trials, including a total of 16,048 patients, found that colchicine decreased COVID-19 severity and decreased C-reactive protein (CRP), indicating its potent anti-inflammatory effect in the presence of spike protein [70]. Thus, the addition of colchicine is indicated when a patient presents with pleurodynia post-COVID-19 vaccination or post-infection. Moreover, 0.5 mg twice daily has been shown to be a safe and effective dosage for the treatment of COVID-19 [65,69,70].

Additional compounds that may assist in spike protein detoxification and degradation include the following:

N-Acetylcysteine (NAC): It dissolves spike protein through the destruction of disulfide bonds and prevents binding at ACE2 [52,71,72].

Glutathione: It disrupts spike protein disulfide bonds [72].

Ivermectin: It binds and inhibits spike protein [73].

Quercetin: It binds and inhibits spike protein [74].

Apigenin: It binds and inhibits spike protein [74].

Nicotine: It disrupts glycosylation on spike protein and blocks possible spike protein-nicotinic cholinergic receptor interaction [75,76].

Emodin: It blocks the spike protein-ACE2 interaction [77].

Fisetin: It binds and inhibits spike protein [78].

Rutin: It binds and inhibits spike protein [79].

Silymarin: It binds and inhibits spike protein [80].

Words from a non-practitioner are cheap. Practitioners try everything what possibly could help.

[Towzerone]

yeh I got a hold of 200 ivermectin tabs from India Mart for less than $150
still have them they worked great

[pamojja]

I'm glad I didn't need any. Until today, never had covid. Though I would have all co-morbidities, I also supplement comprehensively and changed my life-style due to that long ago.

Last month on vacation I did however get some just in case for my old father (postal medicine imports are illegal here otherwise):

Ivermectin 12 mg x 10 tablets, strip for 150,- IRs.
HCQ 200 mg x 15 tablets, strip for 106,68 IRs.

Exchange rate was 91,- IRs per Euro

[Saw]

Gaert Van derbussche said the other day the protocol of Natto Bromelaine etc that McCullough sells does NOTHING against the spike
ZERO ...its basically snake oil

Was listening to an interview with a former CDC biologist and he thought it laughable that someone could take an enzyme and it
would only attack the spike and leave all other proteins alone. But then who really knows what these white clots are?
It should be an easy enough experiment for anyone in possession of these white clots to test nattokinase or other enzymes
in vitro.

[Blargus]

I would hope there would be a public correspondence between Dr. Geert and McCullough on this. There are many positive reviews on twc website and supposedly positive clinical effect of the spike support and base spike detox so says McCullough.

https://www.twc.health/collections/covi ... ul-formula

Seems reasonable to me that anti-inflammatory anticoagulant and circulation booster would have some positive effect even if it didn't get rid of spike protein so to say it's nothing seems an exaggeration. McCullough seems pretty careful and reasonable in his approach to me also pretty straightforward in citing papers as posted.

If you boost the levels of enzymes in your blood like nattokinase and bromelain through supplementation, wouldn't that possibly have an effect on the supposed spike proteins in the bloodstream since it does in vitro?

[Towzerone]

yeh not sure but saw something that said that Vit C asnd even EDTA dissolves clots
Clots seem to be causing a ton of issues in the heart and brain