Especially here at GAW (the tip of the spear IMO), we're always posting about the graphene, granted...its terrible and dangerous. Of course.
But we haven't really been discussing the FUCKING PARASITES Dr. Robert Young found (amongst other doctors, scientists etc.) in the veils of phizer and moderna.
In any case I wanna share with you a little eureka moment I had just now.
I posted a meme about Ivermectin and Deworming and how we're finding out now the vaccines actually have parasites in them...so maybe thats why Ivermectin is helping people. (Granted...I think it was working with regular Covid before the vaccines...but....was it? I'm actually not sure on the dates...)
Anyways..
I was using this picture from Dr. Robert Youngs blog for the meme > https://static.wixstatic.com/media/fbbf2b_afefe13d4e5f4c77bfe0d056275a5cc6~mv2.png/v1/fill/w_740,h_424,al_c,q_95/fbbf2b_afefe13d4e5f4c77bfe0d056275a5cc6~mv2.webp
The parasite was from a phizer vaccine veil and the **parasite is called "Trypanosoma cruzi" parasite. **
Now Dr. Judy Mikovitz has been saying that Suramin helps detox from the vaccine. She even said in that one video "Suramin is the antidote...these people wouldn't make a weapon without a antidote..." which makes sense.
Then she goes on to say that Suramin is an FDA approved 100 year old drug that treats African Sleeping sickness...
Okay cool. Well...thats neat...African Sleeping Sickness...well what the fuck is that? How is that in any way similar to the vaccine?
Well frens....
African Sleeping Sickness is caused by non other than Trypanosome Parasites.
Boom.
Hey man, nothings too out there now. We ain't in Kansas anymore.
Thanks. I read it and saved.
Nothing is out of the question for consideration.
Can you tell me how do you save a post?
Because so many articles are getting scrubbed from the internet, I have begun copying and saving items that I want to be able to find and refer to again. I label and save each in a specific folder on my computer that allows me to access and read or share it again in the future.
My 'Wuhan Virus' folder that I began in December 2019 has at the moment 2,275 items in it that include published medical studies, links to videos, interviews, articles, treatment protocols, death counts, VAERS data, Eudra Data, Yellow Card scheme data, related and pertinent community comments and related imagery and memes. I have info related to the G*tes Foundation, Dr. F**ci, RFK Jr., the NIH, the NIAID, photos of vax injuries, community vax injury websites and links, interviews with parents of vax damaged children, etc.
You want something relating to the Wuhan virus and the vax? I probably have it.
There are likely better ways than mine, but here's how I save them for myself:
I open a new Word document on my desktop, copy the URL of the article and put it at the top of the document. Then I just copy and paste the entire document including title header, author, date, pictures, and links into the Word document.
When there is a video included, I do a screen shot photo of the video, and copy the URL of the video and the title of the video and include the link so I can click the link from my word document. If there are some good comments posted on the article, I often include them, too.
When doing the copy and paste, I will go back and remove any advertisements, adjust margins, font and anything else I want and save the article as a nice, clean, readable document with just the author's intent and nothing else.
Maybe someone else here on the boards has a better way.
Hope this helps.
I don't have a better way, but believe in redundancy. I keep the files on my computer, but also put them on a flash drive. Because I really don't trust having my computer accessible by a-holes snooping due to online connection. I've also noted the connection between parasites (after reading a few articles, with pictures), and ivermectin, and now believe it would fix most of what ails humans. Hence the desperation to keep ivermectin from us.
So this makes me wonder about the discussion this site had on frequency of taking ivermectin and possible kidney damage.
I use Mendeley. This way the info can be stored in folders as well.
Not necessarily a better way but quick and easy:
I select "Reader View" (Firefox) to eliminate the adverts and crap, then Print -> Save to PDF. Then file in appropriate folder.
That’s a great method - thanks fren and Merry Christmas.
Thanks for sharing, it looks useful, I'll give it a look.
you can simply save the web page also....chrome go to the more "tools -> save page as"
Then you save a local copy of the page
also
https://webtopdf.com/
Hey, thanks!
At the bottom of all comments of posts there’s choices of things to do…like reply. There’s also a save option. It will bring up a pop up with choices in where you want to save it. To go look at things you save up at the top by your user ID. There’s a gear looking icon and an option for saved posts.
I think recently updated to
archive.md
Press save listed under the post you are reading
just bookmark it with your browser
Pages yes. I [save page as] a webpage complete, in a specific folder.
But I thought the question was how to save a post.
Cool ... dina know that
There is so much truth that we have been denied.
Why do you think the ancients called the devil a serpent
Hey! I’m on day 5 of my first 7 day fast and these guys say it helps cleanse parasites. Good to hear.
I stopped eating meat a couple months ago because I believe it poisons us spiritually and physically. I was really craving meat yesterday. But I’m also usually craving jerking off and I know that’s not good for me.
Thanks for the wiki links, never heard of that site.
I’m all in on the notion that everything we’ve been taught is a lie. History, different human creatures including giants, advanced tech using aether only a couple hundred years ago, spiritual and physical vampires, other continents past the I’ve wall, maybe lower planes accessed through a portal at the North Pole…
I still want to get a neuralink implant though!
Also here's that video where she says Suramin is the antidote (not pine needle tea, but Suramin) https://www.bitchute.com/video/1go8f8AagqpN/
https://pubmed.ncbi.nlm.nih.gov/23135008/
“Interpretation & conclusions: Our report indicates that using the 300 μg/ml/kg dose of ivermectin increases the mean survival period from 5 to 12 days. This suggests that ivermectin could be possibly used in the treatment of trypanosomiasis. Further studies will be required to show whether proper treatment may entail a single dose, as used in this study; an increased number of doses, or combinations with other drugs.”
https://pubmed.ncbi.nlm.nih.gov/18456544/
“Mice treated with tea exhibited significantly (P<0.01) reduced parasite-induced hypoalbuminemia as compared to the untreated. Since albumin is a negative acute phase protein, it shows a decrease during inflammatory conditions and therefore its elevation in the mice given tea in this study clearly demonstrated that tea ameliorated inflammation induced by T. b. brucei. Although green and white teas were superior in most of these characteristics, black tea, which is the principle tea product from Kenya, displayed remarkable properties some even comparable to those of green tea. Interestingly, tea was more efficacious than dexamethasone an established anti-inflammatory drug, demonstrating its therapeutic potential.”
https://moscow.sci-hub.se/4839/14c5245d0cffc0975ff805aaadea0aff/efferth1998.pdf
[Section 5.]
For good measure:
https://www.nature.com/articles/ja201711
[ivermectin cures everything, basically]
“The following are an indication of the divergent disease-fighting potential that has been identified for ivermectin thus far:
Myiasis Myiasis is an infestation of fly larvae that grow inside the host. Surgical removal of parasites is often the only remedy but unavailable to many of the needful people who live in poor, rural tropical communities where myiatic flies thrive. Oral myiasis has been successfully treated with ivermectin,51 which has also been used effectively as a non-invasive treatment for orbital myiasis, a rare and preventable ocular morbidity.52
Trichinosis Globally, approximately 11 million individuals are infected with Trichinella roundworms. Ivermectin kills Trichinella spiralis, the species responsible for most of these infections.53
Disease vector control Ivermectin is highly effective in killing a broad range of insects. Comprehensive testing against 84 species of insects showed that avermectins were toxic to almost all the insects tested, including the vectors of malaria and critical neglected tropical diseases such as leishmaniasis and trypanosomiasis (see below). At sub-lethal doses, ivermectin inhibits feeding and disrupts mating behavior, oviposition, egg hatching and development.54, 55
Malaria Mosquitoes (Anopheles gambiae) that transmit Plasmodium falciparum, the most dangerous malaria-causing parasite, can be killed by the ivermectin present in the human bloodstream after a standard oral dose.56, 57, 58, 59 Meanwhile, it has been demonstrated that even at sub-micromolar levels, ivermectin inhibits the nuclear import of polypeptides of the signal recognition particle of P. falciparum (PfSRP), thereby killing the parasites. Consequently, in combination with other anti-malarial agents, ivermectin could become a useful, novel malaria transmission control tool.60, 61 The use of ivermectin as an additional malaria control weapon is now receiving increased attention, driven by the growing importance of outdoor/residual malaria transmission and the threat of insecticide resistance. One outcome has been the creation of the ‘Ivermectin Research for Malaria Elimination Network’.62
Leishmaniasis Ivermectin has been proposed as a possible rodent-bait feed-through insecticide to help control the Phlebotomine sandfly vectors that transmit Leishmania parasites.63, 64 Experiments to test the impact of ivermectin on one blood-feeding sandfly vector, Phlebotomus papatasi, demonstrated that they die if the blood feed is 1–2 days post treatment. Although Leishmania major promastigotes have been shown to die or lose their infectivity after exposure to ivermectin, it does not have a major impact against L. major. Nevertheless, ivermectin is more effective in killing promastigotes than rifampicin, nystatin and erythromycin.65, 66 For cutaneous leishmaniasis, ivermectin is more effective than other drugs (including pentostam, rifampicin, amphotericin B, berenil, metronidazole and nystatin) in killing Leishmania tropica parasites in vitro and by subcutaneous inoculation, with accelerated skin ulcer healing.60 When combined with proper surgical wound dressing, ivermectin shows significant promise for curing cutaneous leishmaniasis.67
African trypanosomiasis (sleeping sickness) Tsetse flies (Glossina palpalis) fed on ivermectin-treated animals die within 5 days, demonstrating that ivermectin has promise to help control these African trypanosomiasis vectors.68, 69 Effective in killing tsetse flies, experiments in mice infected with Trypanosoma brucei brucei parasites have also shown that ivermectin treatment doubled their survival time, suggesting that there is scope for investigating the use of ivermectin in the treatment of African trypanosomiasis from several aspects.70
American trypanosomiasis (Chagas disease) When dogs infected with Trypanosoma cruzi parasites suffered a tick infestation, ivermectin treatment eliminated the ticks but had no impact on either the dogs or their infection. Triatomine bug vectors of T. cruzi feeding on the dogs relatively soon after treatment displayed high mortality, which declined rapidly as the interval between ivermectin treatment and blood feed increased.71
Schistosomiasis Schistosoma species are the causative agent of schistosomiasis, a disease afflicting more than 200 million people worldwide. Praziquantel is the sole drug available for controlling schistosomiasis, with schistosome-resistant parasites now becoming an increasingly worrying problem.72, 73 Ivermectin is a potent agonist of glutamate-gated chloride channels and as glutamate signaling has been recorded in schistosomes,74, 75 there may be an ivermectin target in the tegument. Workers in Egypt evaluating the effect of ivermectin on mice infected with Schistosoma mansoni, concluded that ivermectin has promising anti-schistosomal effects. It has potential due to its schistosomicidal activity on adult worms, especially females, and its ovicidal effect, in addition to its impact in improving hepatic lesions.76, 77 It has also been reported that ivermectin can kill Biomphalaria glabrata, intermediate host snails involved in the schistosomiasis re-infection cycle, reinforcing the prospect of using ivermectin to help control one of the world’s major neglected tropical diseases.78, 79
Bedbugs Bedbugs are parasitic insects of the Cimicidae family that feed exclusively on blood. Cimex lectularius, the common bedbug, feeds on human blood, with infestations increasing significantly in poor households across North America and Europe. Ivermectin is highly effective against bedbugs, capable of eradicating or preventing bedbug infestations.80
Rosacea Although the broad-spectrum anti-parasitic effects of ivermectin are well documented, its anti-inflammatory capacity has only relatively recently been identified. Ivermectin is used ‘off-label’ to treat diseases associated with Demodex mites, such as blepharitis and demodicosis, oral ivermectin, in combination with topical permethrin, being a safe and effective treatment for severe demodicosis.81 Demodex mites have also been linked to rosacea, a chronic skin condition that manifests as recurrent inflammatory lesions. Long-term treatment is required to control symptoms and disease progression, with topical medicaments being the first-line choice. Ivermectin 1% cream is a new once-daily topical treatment for rosacea lesions, more effective and safer than all current options,82 which has recently received approval from American and European authorities for the treatment of adults with rosacea lesions.
Asthma 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.83
Epilepsy Nodding syndrome (NS) is a mysterious and problematic form of epilepsy that occurs in parts of South Sudan and northern Uganda. It is also endemic in a locus in Tanzania but, there, the prevalence is low and stable.84, 85 The condition has serious socioeconomic implications and, like other forms of epilepsy, generates profound social stigma.86 The obvious outward feature of NS, which afflicts children and adolescents, is a paroxysmal bout of forward and downward head movement, the nodding episodes representing epilepsy seizures.87 Children with NS display varying levels of mental retardation, often alongside notable stunted growth and failure to develop secondary sexual characteristics (hyposexual dwarfism). Affected children are outwardly healthy until the nodding episodes begin, with several dying due to uncontrolled seizures.84 The cause of NS remains unknown but there appears to be an unexplained link with Onchocerciasis infection.88, 89, 90 The African Programme for Onchocerciasis Control, which operated in the three afflicted countries, adopted mass drug administration of ivermectin in 1997. However, it was not always possible to operate in conflict-affected regions. After the civil war in northern Uganda ceased, biannual ivermectin distribution in districts affected by both Onchocerciasis and NS since 2012 has coincided with a substantial drop in the number of new NS cases. No new cases were reported in 2013, although there is no conclusive evidence to prove any connection.91
Neurological disease Many neurological disorders, such as motor neurone disease, arise due to cell death initiated by excessive levels of excitation in central nervous system neurons. A proposed novel therapy for these disorders involves silencing excessive neuronal activity using ivermectin. Because of its action on P2X4 receptors, ivermectin has potential with respect to preventing alcohol use disorders92 as well as for motor neurone disease.93 Indeed, in 2007, Belgian scientists applied for a patent, ‘Use of ivermectin and derivates thereof for the treatment of amyotrophic lateral sclerosis’ (Publication No.: WO/2008/034202A3), to cover ‘the use of ivermectin and analogs, to prevent, retard and ameliorate a motor neuron disease such as amyotrophic lateral sclerosis and the associated motor neuron degeneration’.
Recent work has elucidated how ivermectin binds to target receptors and helped explain its selectivity for invertebrate Cys-loop receptors. Combined with emerging genomic information, species sensitivity to ivermectin can now be predicted and the molecular basis of ivermectin resistance has become clearer. In humans, Cys-loop neurotransmitter receptors, particularly those activated by GABA, mediate rapid synaptic transmission throughout the nervous system and are crucial for intercellular communication. They are key factors in fundamental physiological processes, such as learning and memory, and in several neurological disorders, making them attractive drug targets.94 Improved understanding of the stereochemistry of ivermectin binding will facilitate the development of new lead compounds, as anthelmintics as well as treatments for a wide variety of human neurological disorders.95, 96”
[Continued]
“Antiviral (e.g. HIV, dengue, encephalitis) Recent research has confounded the belief, held for most of the past 40 years, that ivermectin was devoid of any antiviral characteristics. Ivermectin has been found to potently inhibit replication of the yellow fever virus, with EC50 values in the sub-nanomolar range. It also inhibits replication in several other flaviviruses, including dengue, Japanese encephalitis and tick-borne encephalitis, probably by targeting non-structural 3 helicase activity.97 Ivermectin inhibits dengue viruses and interrupts virus replication, bestowing protection against infection with all distinct virus serotypes, and has unexplored potential as a dengue antiviral.98
Ivermectin has also been demonstrated to be a potent broad-spectrum specific inhibitor of importin α/β-mediated nuclear transport and demonstrates antiviral activity against several RNA viruses by blocking the nuclear trafficking of viral proteins. It has been shown to have potent antiviral action against HIV-1 and dengue viruses, both of which are dependent on the importin protein superfamily for several key cellular processes. Ivermectin may be of import in disrupting HIV-1 integrase in HIV-1 as well as NS-5 (non-structural protein 5) polymerase in dengue viruses.99, 100
Antibacterial (tuberculosis and Buruli ulcer) Up until recently, avermectins were also believed to lack antibacterial activity. However, in 2012, reports emerged that ivermectin was capable of preventing infection of epithelial cells by the bacterial pathogen Chlamydia trachomatis, and to do so at doses that could be used to counter sexually transmitted or ocular infections.101 In 2013, researchers confirmed that ivermectin was bactericidal against a range of mycobacterial organisms, including multidrug resistant and extensively drug-resistant strains of Mycobacterium tuberculosis, the authors suggesting that ivermectin could be re-purposed for tuberculosis treatment. Although other researchers found that ivermectin does not possess anti-tuberculosis activity, the results were later shown to be non-comparable due to differences in testing methods, with the original findings being confirmed by further work in Japan.102, 103, 104 Unfortunately, the potential use of ivermectin for tuberculosis treatment is doubtful due to possible neurotoxicity at high dosage levels. Ivermectin was also reported to be bactericidal against M. ulcerans,105 although other researchers found no significant activity against this bacterium.106
Anti-cancer There is a continuously accumulating body of evidence that ivermectin may have substantial value in the treatment of a variety of cancers. The avermectins are known to possess pronounced antitumor activity,107 as well as the ability to potentiate the antitumor action of vincristine on Ehrlich carcinoma, melanoma B16 and P388 lymphoid leukemia, including the vincristine-resistant strain P388.108
Over the past few years, there have been steadily increasing reports that ivermectin may have varying uses as an anti-cancer agent, as it has been shown to exhibit both anti-cancer and anti-cancer stem cell properties. An in silico chemical genomics approach designed to predict whether any existing drugs might be useful in tackling glioblastoma, lung and breast cancer, indicated that ivermectin may be a useful compound in this respect.109
In human ovarian cancer and NF2 tumor cell lines, high-dose ivermectin inactivates protein kinase PAK1 and blocks PAK1-dependent growth. PAK proteins are essential for cytoskeletal reorganization and nuclear signaling, PAK1 being implicated in tumor genesis while inhibiting PAK1 signals induces tumor cell apoptosis (cell death).
PAK1 is essential for the growth of more than 70% of all human cancers, including breast, prostate, pancreatic, colon, gastric, lung, cervical and thyroid cancers, as well as hepatoma, glioma, melanoma, multiple myeloma and for neurofibromatosis tumors.110
Globally, breast cancer is the most common cancer among women but treatment options are few. Ivermectin suppresses breast cancer by activating cytostatic autophagy, disrupting cellular signaling in the process, probably by reducing PAK1 expression. Ivermectin-induced cytostatic autophagy also leads to suppression of tumor growth in breast cancer xenografts, causing researchers to believe there is scope for using ivermectin to inhibit breast cancer cell proliferation and that the drug is a potential treatment for breast cancer.111 Triple-negative breast cancers, which lack estrogen, progesterone and HER2 receptors, account for 10–20% of breast cancers and are associated with poor prognosis. Tests using a peptide corresponding to the SIN3 interaction domain (SID) of MAD, found that the SID peptide selectively blocks binding of SID-containing proteins to the paired α-helix domain of SIN3, resulting in epigenetic and transcriptional modulation of genes associated with epithelial–mesenchymal transition. An in silico screen identified ivermectin as a promising candidate as a paired α-helix domain-binding small molecular weight compound to inhibit SID peptide, ivermectin phenocopying the effects of SID peptide to block SIN3-paired α-helix interaction with MAD, inducing expression of CDH1 and ESR1, and restoring tamoxifen sensitivity in mass drug administration-MB-231 human and MMTV-Myc mouse triple-negative breast cancers cells in vitro. Ivermectin addition led to transcriptional modulation of genes associated with epithelial–mesenchymal transition and maintenance of a cancer stem cell phenotype in triple-negative breast cancers cells, resulting in impairment of clonogenic self-renewal in vitro and inhibition of tumor growth and metastasis in vivo.112
It has been reported that ivermectin induces chloride-dependent membrane hyperpolarization and cell death in leukemia cells and it has also been suggested that ivermectin synergizes with the chemotherapy agents cytarabine and daunorubicin to induce cell death in leukemia cells, with researchers claiming that ivermectin could be rapidly advanced into clinical trials.113 This potential has been supported by reports that ivermectin displays bioactivity against chronic lymphocytic leukemia cells and against ME-180 cervical cancer cells.114 Additionally, ivermectin has been shown to potentiate doxorubicin-induced apoptosis of drug-resistant leukemia cells in mice.115 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.
Ivermectin inhibits proliferation and increases apoptosis of various human cancers. Over-expression of P2X7 receptors correlates with tumor growth and metastasis. However, ATP release is linked to immunogenic cancer cell death, in addition to inflammatory responses caused by necrotic cell death. Exploiting ivermectin as a prototype agent to allosterically modulate P2X4 receptors, it should be possible to disrupt the balance between the pro-survival and cytotoxic functions of purinergic signaling in cancer cells. Ivermectin induces autophagy and release of ATP and HMGB1, key mediators of inflammation. Potentiated P2X4/P2X7 signaling can be further linked to ATP-rich tumor environments, providing an explanation of the tumor selectivity of purinergic receptor modulation, confirming ivermectin’s potential to be used for cancer immunotherapy.116 Activation of WNT-TCF signaling is implicated in multiple diseases, including cancers of the lungs and intestine, but no WNT-TCF antagonists are in clinical use. A new screening system has found that ivermectin inhibits the expression of WNT-TCF targets. It represses the levels of C-terminal β-catenin phosphoforms and of cyclin D1 in an okadaic acid-sensitive manner, indicating its action involves protein phosphatases. In vivo, ivermectin selectively inhibits TCF-dependent, but not TCF-independent, xenograft growth without side effects. Because ivermectin has an exemplary safety record, it could swiftly become a useful tool as a WNT-TCF pathway response blocker to treat WNT-TCF-dependent diseases, encompassing multiple cancers.117
Researchers have recently reported a direct interaction between ivermectin and nematode and human tubulin, even at micromolar concentrations. When added to human HeLa cells, ivermectin stabilizes tubulin against depolymerizing effects and prevents replication of the cells in vitro, although the inhibition is reversible. This suggests that ivermectin binds to and stabilizes mammalian microtubules. Ivermectin thus affects tubulin polymerization and depolymerization dynamics, which can cause cell death. Again, given that ivermectin is already approved for use in humans, its rapid development as an anti-mitotic agent offers significant promise.118”
Hey man, excellent post. I was hearing rumblings of ivermectin use as anticancer. I wonder if this is what Trump was talking about when he said there is a cure for cancer. I was forced to take the genetic weapon shots and will be taking ivermectin every 5 days for the foreseeable future. You know something weird. I had the rona really really bad back in march of 2020 and I have had a cough ever since. It is gone now after taking ivermectin. I was taking coughing fits all the time and never went anywhere without cough drops. I thought I had lung cancer at one point and it was in my left lung when I would cough that it used to hurt. The doctor sent me for chest xrays, just some minor scaring he said not to worry about it. It is gone now. I wonder if it was the ivermectin.
Thank you and thanks for sharing about your experience. Please share this info as you see fit. Bless you, my friend.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505114/
“Ivermectin has powerful antitumor effects, including the inhibition of proliferation, metastasis, and angiogenic activity, in a variety of cancer cells. This may be related to the regulation of multiple signaling pathways by ivermectin through PAK1 kinase. On the other hand, ivermectin promotes programmed cancer cell death, including apoptosis, autophagy and pyroptosis. Ivermectin induces apoptosis and autophagy is mutually regulated. Interestingly, ivermectin can also inhibit tumor stem cells and reverse multidrug resistance and exerts the optimal effect when used in combination with other chemotherapy drugs.”
“IVM not only has strong effects on parasites but also has potential antiviral effects. IVM can inhibit the replication of flavivirus by targeting the NS3 helicase [17]; it also blocks the nuclear transport of viral proteins by acting on α/β-mediated nuclear transport and exerts antiviral activity against the HIV-1 and dengue viruses [18]. Recent studies have also pointed out that it has a promising inhibitory effect on the SARS-CoV-2 virus, which has caused a global outbreak in 2020 [19]. In addition, IVM shows potential for clinical application in asthma [20] and neurological diseases [21]. Recently scientists have discovered that IVM has a strong anticancer effect.”
The canadian government will pull the medical licence from any physician that would dare to write a script for ivermectin. In calgary my brother was telling me about his hospital doctor telling him that his friend in private practice who was busted by the government. The doc had a patient that was very sick and he wrote them a script for a few ivermectin pills. The patient went to get the script filled and the pharmacy seized the script, and reported it to the government. The next day the police along with the medical association arrived at the doctors office and shut him down with a search warrant and seized all his medical files. They pulled his medical licence immediately and told him he will never get it back.
I was trying to order ivermectin through the mail and there was no option to ship to canada. I asked the supplier why and they wrote me back saying that canada has gone insane trying to catch every ivermectin package as possible. He said that the government is acting like it is heroin or something. So they stoped trying to ship into canada.
I have loaded up on Horse Paste.....Neiiiiigh
Aye, 🐴
Thanks for the great post.
🙏
Mosquitoes are the only animal I go out of my way to kill. Flies and gnats I leave alone and corral outside.
Flies can be super annoying, but I swear some have better manners than others. I’ve had some very positive interactions with flies.
I think some may have more conscious awareness than others.
But since mosquitoes go out of their way to stab and infect, I won’t put up with that. It’s an inappropriate boundary being crossed.
If you don’t fuck with me, I won’t fuck with you.
Unfortunately, suramin needs to be injected into a vein. It's showed some promise alleviating symptoms of autism.
Showed some big promise with Autism.
Where is testing being done with suramin against autism?
Dr. Robert Naviaux, at UCSD.
https://health.ucsd.edu/news/topics/Suramin-Autism/Pages/default.aspx
Dramatic but transient improvement of ASD, showing ASD may really be a metabolic disorder.
Which explains why HBOT can help and diagnosis rates exploded after Bill Clinton allowed GMOs to be produced and sold in the US.
Any way to get this in pill or liquid form?
https://greatawakening.win/p/13zMeC7uFd/pfizer-vax-contains-a-parasite-k/c/
A post I made 3 months ago!
This link doesn't tell me where I can get some, tho.
My b. Commented on the wrong parent
I did find this tho.
https://www.caymanchem.com/product/11126/suramin-(sodium-salt)
Formulation- A solid Solubility- Water: >10 mg/ml
None that I've seen so far. There was some confusion a few months ago, when Dr.Judy Mikovits misspoke or was misquoted about pine needles being a source of suramin. She has since cleared up the confusion. However, some holistic sellers renamed pine needle extract as suramin that can be taken orally.
If anyone is feeling particularly daring, this is the injectable stuff:
https://holisticgear.com/product/suramin/
Only $1775 per gram, what a deal! 😵
You can’t get it in the US, unless you ask the CDC for it because you can’t use pentamidine for early stage sleeping sickness treatment.
Another case of the CDC screwing people over, it seems.
Great dig OP. :)
But, unfortunately:
(As of 2017) Suramin is not approved by the Food and Drug Administration (FDA) and is not commercially available.
So, how do we get it except through pine needles?
Anyone?
I haven't seen this mentioned but I have relatives in the north, very cold country, who put resin under their tongue in winter. I also don't understand this pine needles are not suramin thing. Pine needles DO contain suramin. It's where it was originally extracted from, and I'd prefer natural surmain to a lab synthesized and injected one. Back to the resin, it's not just pine either. They will gather pine, spruce, and fir sap.
You want to see some shit. Dr. John B on Twitter he is a well known Doctor of science and in Microscopy. He pulled samples from all 3 Vaccines. Mind Blowing! The outcomes and photos of patients alive and deceased from the vaccine are just as shocking.
Click on any of his pics to enlarge
https://twitter.com/drjohnb2/status/1444639912880443396
D
......
I found that Suramin is not approved by the FDA as of May 2017. I find this highly suspect, more evidence of the plan?
Suramin can be found in pine needle tea, and in survival situations it’s recommended to drink it for cases of River Blindness
This was how sailors treated scurvy as well!
Now that we are on tje topic of Lord of the Rings. I'd thunk we should introduce the Hobbits traditions into our own culture. The concept of a 2nd breakfast does have practical merit. It's worth discussing. It's like a bonus meal for people whonwork long hours in the day.
I know you're joking around but an adult dictates his own meals. There are benefits from the warrior diet of one large meal a day, there are merits to intermittent fasting, there are merits to slamming your metabolism up about 20 notches with carb cycling and high protein and fats.
Just remember to figure out how much you can eat without gaining at your current musculature and size and use that information to get a rough estimate of calories burned at rest. Then you can have your second breakfast and not become fat.
The conversation of a 2nd breakfast, leads to more focus on the event. Like yourself, there is always room for a lighter linch.
It also treats river blindness..... just like Ivermectin.
Imagine that.
Also caused by tsetse fly bites
which give people the parasites, I forgot to add that in.
Nice connection, thanks.
And suramin is also an anti cancer drug huh? Also used for autism?
Fascinating.
Very interesting....
yeah that sounds extremely familiar
But what is causing the clotting and respiratory attacks? I looked at the same article (Af Sleep sick) and I didn't see anything attributable to this.
White pine tea? Go find a Christmas tree!
Amazing article, not sure if much of it's true but it sounds amazing! https://www.wildedible.com/pine-needle-tea-natural-vitamin-c
Is pine needle tea the answer to covid vaccine shedding / transmission? Learn about suramin, shikimic acid and how to make your own extracts https://www.naturalnews.com/2021-05-09-is-pine-needle-tea-the-answer-to-covid-vaccine-shedding-suramin-shikimic-acid.html
I made some of that tea and within 3 days of taking some I found I was exceptionally drowsy and slept all day and all night.
Has anyone found the same thing happening to them?
On my runs I've been picking white pine needles (I live in toronto, theyre everywhere here) from the trees and making tea with it.
Now...Dr Judy is now out saying she never said PINE NEEDLE TEA contains suramin...and people have to stop that rumour.
But...suramin is a durivative from a durative from pine needles....soo.....I'm sure maybe shes just saying that cause theres not actual study on it and she has to be evidence based.....but im sure its there.
You're herxing from a worm die off. Look up Herxheimer reaction. Don't stop; kill all the worms.
Not possible I am sorry to say, if I sleep all day and night I will die of starvation. I have looked up this reaction, it's nothing to do with feeling fatigued all the time, it doesn't mention it at all.
I have been taking black seed oil for ten years and invermecin for two, as well as others such as vit D3 and zinc, I shouldn't think there are any worms left.
Youve been continuously taking ivermectin for two years?
Nearly two.
I don't think you're supposed to do that. If you want a good parasite cleanse get a good herbal one.
I took your advice. My tea has green strings in it and tastes like plastic and shame.
Isn’t Dr Robert Young better known as Marcus Welby MD?
https://youtu.be/iWWF5nN7fUA
Reminder to read 'parasite pill'
www.prestophoto.com/akilyoung
The simpsons prediction say just this as well.
I went out and got some all natural turpentine. Everyonve in a while i will ingest a VERY small amount of it.
Afterwards my thinking is crystal clear.
We've been talking about parasites here for a while. I fully belief this is all a parasite. Really thoug what is a virus, other than another name for a parasite.
Just like fosil fuels arent dinosaurs. It is a naturally occuring mineral deposit that will never run out.
I read it somewhere that the parasites they found in the genetic weapons have an affinity for heart muscle. Is that the reason for the heart attacks and heart pains? All I know is I took ivermectin and have not had heart problems after the death shots. (yea I took it, my choice was to lose everything and move the family to the river in the suv or take a poison. No I didnt have a choice)
My brother had a heart attack after the first one (he wouldnt take the ivermectin)
Trypanosoma cruzi: “... the most common cause of infectious myocarditis in the world.” https://www.sciencedirect.com/topics/immunology-and-microbiology/trypanosoma-cruzi
There’s a reason they don’t want us to have ivermectin.
Suramin also shows promise as a treatment/cure for autism: click here
So where can I buy suramin? It looks like it’s all pine needles extract for purchase.
Robert O. Young (he's NOT a doctor) he's a quack that never graduated. He briefly attended the University of Utah where he on a tennis scholarship, studying biology and business, NOT medicine.
Why do I say he's a quack? He promotes BS like "cellular nutrition" and "discovered the biological transformation of red blood cells into bacteria." Cellular nutrition is not something you can affect directly. Eat right Ave the body takes care of the optimal delivery for you.
Did I mention Quackwatch describes his claims as "fanciful?"
When someone says something like "SARS-CoV-2 virus now called the SARS-CoV-19," RUN THE OTHER WAY. This is bullshit. SARS-CoV-2 is the scientific designation for the virus that causes COVID-19. THERE IS NO "NOW CALLED.". This quack can't even get that simple concept correct.
Red blood cells DO NOT now, never have, and never will transform into bacteria. It is not biologically possible. RBC do not have anywhere near the internal structure or mechanisms to remotely allow such a transformation to take place. MOREOVER, this has been DISPROVEN since the 1850s and Louis Pasteur with germ theory (surmised as early as the 1500s).
Don't get me started on his bupkis "alkaline approach." It's is nothing more than repackaging EXISTING KNOWLEDGE about the bodies natural pH. Hint, blood pH is ~7.4, or sightly alkaline. Hmmm, amazing.
On top of all that, he's a CONVICTED FELON MULTIPLE TIMES OVER and a KILLER.
In 1995, he TESTIFIED at his trial that he had never claimed to be a medical doctor. Yet, here you are believing just that.
In 2001, he treated a terminal cancer patient using that bullshit alkaline approach WITH BLOODY BAKING SODA. Post-trial he had to announce AGAIN, he's not a doctor of medicine and not a microbiologist.
2014 he was arrested on 18 felonies. In 2018, a San Diego jury awarded $105M to cancer patient he told to stop receiving chemo and use his treatment. Because of him she had less than 4 years of life left.
He has no degrees from any accredited schools, he is not a microbiologist, hematologist, medical doctor, naturopathic doctor. FFS he's not even a trained scientist.
He's a fucking con-artist.
Now compare him to most of the medical community that is promoting the official narrative. They are criminals. He stands in good company despite his lack of license.
What you (presumably) derisively call "official narrative" has reputable science & decades old technology backing it up. The other is a charlatan seeking snake oil to fools.
I could explain it all to you but, with you referring to the medical community as criminals, I doubt you'd be able to follow along given you're demonstrated lack of understanding complex subjects such as law.
Understood, even so, I only used his findings, not his approaches to medicine, of which several other individuals have found in the vaccines.
Holy shitballs! This has to be the most UNCRITICAL thinking I've ever seen displayed.
WTAF!?!
How EXACTLY do you manage this level of cognitive dissonance and remain functional in society? I mean seriously how the absolute fuck does "I only used his findings, not his approaches to medicine" make sense to you?
It's inherently contradictory.
Normal, rationale, logical people DO NOT say such things. They don't accept it use findings that are necessarily a result of a flawed approach. If others are "finding similar results" and you have been handed how a flawed approach gives you those same results, critical thinking should kick in to tell you "Wait a minute. Something just might not be right with those other results."
:smdh: It's these kinds of demonstrations of failure to think that had me worried for America's future.