How on earth could an innocuous micro-organism discovered under a tree on a Japanese golf course possibly morph into a modern-day miracle drug that is so unbelievably multi-faceted in its applications that it almost defies our imaginations?
It is mind-boggling even to begin to get our heads around the fact that this one very mildly synthesised product could well be headed toward becoming the most incredible lifesaver in the history of humanity. Fortunately, “if it seems too good to be true, then it usually is”, thankfully, doesn’t seem to apply to this particular drug.
Of course, the fact that its single dose cost of manufacture is down to single-digit US cent levels due to it being off-patent is an enormous threat to the Big-pharma collectives’ balance sheets. Indeed when push came to shove, this product had the potential to wreak havoc on the entire industry.
Until the Covid war came along, there was no great panic and IVM’s multi-talents sat there in the shadows. There was no monetary incentive for any of its newfound purposes to be promoted when it was so cheaply produced anyway, let alone the fact that it could be manufactured reliably in ridiculously low-cost input countries like India.
That was until Mr Global foisted Covid, AKA WW3, on humanity, and the cat jumped clean out of the bag. It turned out that IVM was used in about 31 African countries on millions of people to treat onchocerciasis. This use of IVM became a monumental accidental field trial that threw up a massive control group of some 22 countries. No fancy arsed costly industry-funded trials were required. [1] quote:
“In conclusion, in the countries where Ivermectin is distributed to and used by the entire areas, it suggests to lead a reduction in mortality, to accelerate patient recovery, and to avoid death. And this analytical study will suggest that early treatment with Ivermectin may accelerate recovery and prevent worsening of symptoms in patients with mild disease. These findings can be efficiently translated into therapies for SARS-CoV-2 (COVID-19).”
No double-blinded placebo-controlled ‘peer reviewed’ blah, blah, blah, trials needed either…often, of course, these had a predestined bullshite result anyway. So instead, humanity was provided with a monumental field trial on a plate
Look no further than some of the crap and pseudoscience the vax companies claim as proof of a product for evidence of how completely unreliable these industry-underwritten ‘trials’ can be. Then add in a big dollop of criminal global regulatory capture by the Big-pharma cabal. So too the fact that what were once world-renowned medical journals such as The Lancet is now embarrassingly exposed [2] as being blatant Big-pharma shills. Add up all these factors, and all we are left with is a lethal hybrid cross between a gambling casino, a wild west show, and a Frankenstein monster that is running amuck globally.
The ever-growing list of IVM applications and [some approximate timelines
#1 Internal and external parasite control in mammals discovered 1973 sent to Merck laboratories 1974. Avermectins were found and named in 1975. A safer derivative, Ivermectin, was commercialised and released into agricultural markets in 1981.
#2 Registered in 1987 for use in human health and soon gained recognition for its huge future role as a wonder drug for the world’s poor. A drug donation program soon after, and since then, billions of doses have been administered. Many of the programs were so successful that the goalposts were changed from controlling some diseases to complete global elimination. Just in 2016 alone, around 325 million doses were used. [3]…quote: “During 1995–2010, it was estimated that the disability-adjusted life years averted via the impact on these non-target diseases added a further 500,000 disability-adjusted life years to the African Programme for Onchocerciasis Control’s 19.1 million saved due to Onchocerciasis interventions.
#3 Subsequent discovery that IVM kills the most dangerous malaria-causing parasites.
#4 Controls Myasis/Trichinosis/Leishmaniasis/sleeping Sickness/Schistosomiasis/Bedbugs/Rosacea/
#5 Asthma: quote [3] “A 2011 study investigated the impact of Ivermectin on allergic asthma symptoms in mice and found that Ivermectin (at 2 mg kg−1) significantly curtailed recruitment of immune cells, production of cytokines in the bronchoalveolar lavage fluids and secretion of ovalbumin-specific IgE and IgG1 in the serum. Ivermectin also suppressed mucus hypersecretion by goblet cells, establishing that Ivermectin can effectively curb inflammation, such that it may be useful in treating allergic asthma and other inflammatory airway diseases.’
#6 Nodding Syndrome [NS] a form of epilepsy found in Africa
#7 Many neurological diseases, including
- Alcohol use disorders
- Motor meurone disease
- Amyotrophic lateral sclerosis
#8 Discovery of IVM being a potent anti-inflammatory
#9 2012 they found that IVM had antibacterial activity, including…
Preventing infection by ChlamydiaMycobacterial Tuberculosis
#10 Discovery that it is a prophylactic antiviral agent for acute patients
- Covid19
- HIV
- Dengue
- Encephalitis
#11 Continuously accumulating evidence that IVM has a significant role to play in prevention and treatment in a variety of cancers… [5a,b,d,e,f,g]
Ehrlich carcinomaMelanomaLymphoid LeukemiaGlioblastomaBreast / Prostate/ Pancreatic/ Colon/ Gastric/ Lung/ Cervical /Thyroid/ Hepatoma/ Glioma/Melanoma/Multiple Myeloma/ Neurofibromatosis tumours
#12 Helping cancer patients with advanced acute cases and who have developed resistance to chemotherapy drugs: quote [3] “Cancer stem cells are a key factor in cancer cells developing resistance to chemotherapies and these results indicate that a combination of chemotherapy agents plus ivermectin could potentially target and kill cancer stem cells, a paramount goal in overcoming cancer.” [4c]
#13 Anecdotally so far but consistent reports from people suffering from major depression that they enjoy a significant lift in positivity within 12 hours of their first dose [same dose rate as for viral prophylactic] only personal anecdotes at this stage with no links to help either…
#14 What on earth next?
NB with points #4-#13, any research is likely to be minimal since the Big-pharma collective works research funds will not be forthcoming without revamping the entire industry. In fact, given its current almost complete obsession with profit and shareholder return, there will be far more funds available for dodgy entities to nobble and discredit IVM using designed to discredit ‘trials’ than there ever would be to reassure humanity as to the breathtaking scope of this drug.
Repurposing drugs, to be used as treatments of conditions that the developer never had the foggiest notion would ever happen, is not in the least unusual and in some Western countries [e.g. Australia] comprise ~ 40% of prescriptions. Of course, a classic example of repurposing is the aspirin product: The original developers probably never guessed that this drug would eventually become a routine go-to medication that could massively reduce damage from coronary heart attacks and strokes, primarily when used as early as possible after the event.
Then there is the story of another fascinating repurposed product developed in the Sandwich laboratories of Pfizer Ltd, the UK, in 1989. This one was trialled extensively around the world, including in NZ, to treat several cardiovascular diseases but was subsequently unsuccessful.
The puzzling thing was, though, that when many of the people that were involved in the field trial heard that Pfizer was ending their work, they were clearly peeved enough that many of them contacted the company to try to find out if it was in any way possible to continue to source the drug. Some of those people were right here in Northland, NZ. The word is that the phones were ringing so much that Pfizer decided to dig. Never before had a trial product that had failed been so universally popular with both male [and female] participants, albeit for a completely unexpected reason.
It turns out this was yet another spectacular example of a repurposed product cropping up that became hugely clinically and commercially successful for treating a seemingly unrelated ailment. That product was subsequently marketed as Viagra and, by all accounts, became a widely used drug for treating erectile dysfunction.
So why am I illustrating the animal form of the IVM product when Stromectol, the Medsafe human-approved tablet form of the drug, is readily available? Well, for starters, mainly because it is NOT available for many conditions... indeed, the MO’H’ has made it almost impossible to obtain it as a Covid prophylactic/acute treatment. As a result, many of us, including multiple members of my own family, have resorted to taking the animal form of the drug in desperation.
For a while, we could buy the illustrated mildly synthesised Boehringer product. But unfortunately, IVM’s exclusive patent held by Merck ran out some time ago. So then Big-pharma’s shills arranged for the door to be slammed on this option too. Although this product is only listed as an injection, many people had already begun using it as an oral treatment, taken in a large glass of water to help mask the bitter taste.
Meanwhile, farmers had used this method for their working dogs for forty-odd years. NB, we never used this on Border Collie-type heading dogs as they can lack the gene that allows their blood-brain barrier to stop the drug from concentrating in the brain and sometimes killing the animal. The other species I know of where this danger applies is in tortoises.
The Human form of IVM…approved in NZ in 2005
https://www.medsafe.govt.nz/Profs/Datasheet/s/Stromectoltab.pdf
How utterly absurd too that Kiwis are reduced to telling bare-faced lies to obtain Stromectal/IVM on prescription. I know, as I tried with a local GP to get it to protect myself from the earlier Covid variants on a proposed trip to Australia for myself and my partner.
Take-1 of my attempts to get a prescription for IVM
The local GP, who will remain nameless, had always appeared to be very open to alternative treatment protocols and, as such, looked a pretty safe bet to me. Far be it, though, when it came down to the truly dreadful bogey drug IVM… I naively mentioned the word ‘Covid’ in my email request, and it immediately became evident that there was not so much as a snowball’s chance in hell that she was ever going to consider prescribing it for me. The excuse was that it was off-label for Covid, and as such, she would be placing her career at huge risk by prescribing it to me. Her reply:
Take-2 of my attempts to get presciption for IVM
(this time, for goodness sake, try not to mention the war [the Covid war]).
Aha, brainwave: What if I use this cunning plan? I don’t mention Covid and approach another hapless local GP. How about with a great whopper of a story that I am off on a trip to deepest darkest Africa where I could potentially be encountering dangerous tropical pathogens and nasties? More perhaps than I could even shake a stick at. I would need the powerful prophylactic IVM to protect myself from the likes of Blind River Fever, Elephantitis, Scabies, et al. What do you know: She immediately wrote out the prescription, and I was merrily on my way, just not to Africa!
I mean, for crying out loud, what on earth has this country’s medical ‘system’ come to? We are seemingly reduced to lying through our teeth to obtain a safe, affordable, highly proven, lifesaving, and multi-purpose product: One with 3-4 billion doses used globally to date with not a single documented causally associated mortality.
So there we have it: A farcical situation where we cannot for love nor money get GPs to prescribe what is arguably the safest synthesised drug in the history of modern medicine, yet we can rock down to the local jab station and ask an inoculator, who may incidentally have only ever had 15 minutes of formal training in his entire life, yet in which our ‘system’ allows him to administer one of the most toxic medical product ever used on the human species. This vaccination programme is nothing more than the equivalent of a global lab-rat experiment. Furthermore, these Pied Piper collaborators do so without even bothering to take so much as a cursory glance at our medical history.
All mRNA Covid treatments are now scientifically proven lethal products. The Pfizer product has never passed any trials apart, of course, from those in which the manufacturer deliberately and fraudulently hid and misrepresented the results in collusion with the US FDA.
The profound tragedy for NZ is that strong signals were emerging early in 2020 that IVM was a potential game-changer for Covid-19, and yet here we are 24 months later, still ignoring this now scientifically proven fact. As a farmer highly intrigued by the subject, I discovered this vast potential early in February 2020. I informed my vets about it: All, except one, looked at me as though I was quite a few sandwiches short of a picnic and offered soothing advice on not to believe everything I read on the internet. Gosh, I needed to hear that jewel!
Chris Martenson [Peak Prosperity] https://www.youtube.com/user/ChrisMartensondotcom was the first high-profile person in the world to have enough guts to mention this topic that in doing so could even potentially get you killed. From memory, this was around March 2020. The long knives came out for him immediately. The fact of the matter is if we had deployed IVM way back then, we could well have:
- Reduce our Covid death toll to very close zero
- Improved our community health in a multitude of other ways
- Eliminated the added financial stress
- Carried on with our tourist industry fully intact: Actually, probably increased it if anything
- Avoid virtually all the business closures
- Avoided all the resultant social and mental damage
- Avoided what looks like generational derangement to a large section of our gene pool
- Emerged as a textbook example to the world of how to keep Mr Global in his place
- Avoided our country becoming a global laughing stock helplessly at the mercy of a group of homicidal tyrannical control freaks
Please don’t go looking for any sound or humanitarian justification for our Jackbooted Junta in restricting our access to IVM: You simply won’t find any. And please don’t try to work out how these rabid psychopathic shills and weasel’s minds work. That would be an exercise in complete and utter frustration and futility. At the risk of being repetitively boring, I will finish off by repeating the observation made at the conclusion of my essay from last week on this same blog:
“The fact that our Govt and institutions go along with this psychopathic debacle can only be explained by one simple, tragic hypothesis: they are invested in Mr Global’s program of corporate-funded genocide and treason.”
References
[1] https://www.medrxiv.org/content/10.1101/2021.03.26.21254377v1.full.pdf
[3] https://www.nature.com/articles/ja201711
[5a] Frontiers | Computational Drug Repositioning and Experimental Validation of Ivermectin in TreatmIvermectin, a potential anticancer drug derived from an antiparasitic drug – ScienceDirectent of Gastric Cancer | Pharmacology
[5b] Ivermectin as an inhibitor of cancer stem‑like cells
[5c] Ivermectin reverses the drug resistance in cancer cells through EGFR/ERK/Akt/NF-κB pathway | Journal of Experimental & Clinical Cancer Research | Full Text
[5d] Parasite killer Ivermectin stops cancer drug resistance | CANCERactive
[5f] Ivermectin as an inhibitor of cancer stem‑like cells
[5g] Ivermectin, a potential anticancer drug derived from an antiparasitic drug – ScienceDirect
