“We do not believe any group of men adequate enough or wise enough to operate without scrutiny or without criticism. We know that the only way to avoid error is to detect it, that the only way to detect it is to be free to inquire. We know that in secrecy error undetected will flourish and subvert.” –J. Robert Oppenheimer
This is a great selfie video, done by a young lady with a glorious Southern accent, chronicling her week of COVID-19 and recovery, treated with ivermectin.
It’s short – just under 7 minutes – but it captures a lot of information about symptoms and relief by the drug.
I can’t embed the video here due to the very obnoxious auto-play – you have to watch it on Gab TV.
I will, instead, provide a brief synopsis here for those who don’t want to put in the time to watch right now.
Ivermectin Day 1
The young lady starts the video laying in bed, having just taken ivermectin on DAY 3 of COVID, but DAY 1 of Ivermectin.
She will mention symptoms during the remainder of the video as she remembers them.
Later on Day 1
She is now sitting up in bed.
One important thing she notices is that her headache from the last two days (COVID days 2 and 3) is now subsiding. This tells me that ivermectin may be acting directly (and immediately) against cerebrovascular actions of the spike protein. She also notes that she is not as weak.
Ivermectin Day 2
She has just taken her second dose, but notes that she is describing changes due to the FIRST dose (Ivermectin Day 1).
She states that she feels completely different – “so much better”. No body aches, fever is down, reduced congestion, “feel like a different person”.
“This stuff is amazing – it’s really working good for me.”
She then logs back on and does a medical disclaimer that she’s not giving any advice – just telling her experience. LOL!
Later on Day 2
Obviously she’s gotten up and changed clothes.
The young lady describes herself as “almost 100%”, and that she feels like she could do a workout. Energy back, no headache, very little congestion, cough infrequent. She does mention that her nose was “running all night, pouring like crazy” on the night of Day 1, but that now it’s OK.
Likewise, her throat was still sore on Day 1, “like I was swallowing needles”, now it’s much better. “I feel 1000% different.”
Still Later on Day 2
At this point, she recognizes what has been called “brain fog”, and that her thinking was clouded on the previous days (she uses more descriptive terms – worth a listen). Ivermectin Day 2 was better – she talks about all the things she did – but the prior days, she was unable to do simple tasks which she describes.
[WOLF – Clearly this effect of the spike is (IMO) one of the things that plagues long-haulers. Why on EARTH we would give people mRNA to make this stuff inside and possibly even dump the instructions to DNA – I have no clue. Ridiculous!]
She also notes that she was still suffering anosmia on Day 2, and she describes that effect in detail. She notes that she lost BOTH her taste and smell on COVID Day 2.
Ivermectin Day 3
She actually goes out for a run!
She considers herself “completely back to normal” after the first two doses, since she doesn’t believe that the third has “kicked in” yet. She engaged in many activities, worked out, energy levels back to normal, but still a little bit of congestion and cough.
She does a GREAT retrospective of how sick she was on the first three days (COVID Days 1-3 / Ivermectin Day 1) – how exhausted she was.
Ivermectin Day 4
Obviously she has put on makeup and is “feeling so good today”.
She describes a little bit of congestion and “loose stuff”.
“I feel so good. I feel so good.”
Ivermectin Day 5
This is her last day of ivermectin. Day 5 of ivermectin, Day 7 of COVID.
She notes that she started ivermectin based on TESTING – that she got a positive test on her THIRD TEST, which was either late on the second day of COVID, or on her third day of COVID. This is important, because it means she was already experiencing systemic symptoms on Day 2, including anosmia, loss of taste, exhaustion and mental clouding, and yet it was only shortly after THAT, that she tested positive.
She “feels like a million bucks”, however she notes that she has STILL lost her senses of taste and smell, although she thinks that she might have actually begun to taste biscuits and bacon just a bit.
She notes that she no longer has any chest congestion or cough [meaning lower respiratory symptoms]. She also notes that she never had any oxygen issues (“PTL!”)
The End / Thank You
She states that she’s “over all this COVID crap” and that she’s done.
She thanks everybody who sent her well-wishes and comments, and notes all the people who thanked her, and who believe they have or will benefit from her videos which she posted.
“I am so happy that I’m able to help all of you with this, and some of your loved ones. It makes me so happy!”
There you have it. I loved this video, and wanted to spread it.
Everybody underestimates Spain. The last letter in “PIGS” is far less of an insult than an error.
Years ago, when I was at a conference, and Japanese industrial spies were getting me drunk (it was a great red wine), I decided that I had to give them SOMETHING for their time and effort, if only to keep them distracted, so instead of giving them any of our actual concerns, I gave them my personal assessment of “somebody else’s industry in Spain”. It was great information, and it was true – and as I always say, the TRUTH is the best cover of all. The Japanese were as surprised as I had been, when I realized how far and how fast Spain had come after it emerged from Franco – at that time almost as backwards as Cuba.
Whether I was ratting out Spain or bragging up Spain, DO NOT underestimate Spain. When Spain is FREE and prosperous, the WORLD prospers.
So when it came to my attention recently that “Spanish medical deplorables” had found the key to ending America’s COVID communism problem, I “trusted the science” immediately.
Reading the paper convinced me even more.
I don’t remember WHO on this site posted the first link to the “Spanish nursing home antihistamine paper“, or on what site that link was found (H/T to whoever!) [LATER – RAC found it – it was Deplorable Patriot, HERE], but the results described therein were every bit as impressive as the story of the American nursing home that saved all its residents by immediate administration of prophylactic hydroxychloroquine.
To briefly describe what happened, Spanish nursing homes were horribly impacted by the COVID pandemic, but TWO of them stood out by having almost no deaths at all.
The story there is a beautiful example of SCIENCE IN ACTION. It was a simple empirical observation, but the best science happens that way. And I quote…..
“We included antihistamines for the treatment of all patients after observing that when added to the initial treatment, our patients had a notable improvement in 24–48 h.”
After they did this – NOBODY DIED.
The Spanish crisis was between March and May of 2020. From May to August 2020, applying the therapy, there were no new cases or deaths. The results were researched and submitted for publication (received) on September 16, 2020. The paper was published online 4 months later, on January 16, 2021, and appeared in the April, 2021 issue of the journal.
aServicio de Salud de Castilla-La Mancha (SESCAM), Toledo, Spain
bCentro de Salud de Yepes, Av. Santa Reliquia, 26, 45313, Yepes, Toledo, Spain
cDepartment of Advanced and Integrated Interstitial Lung Diseases Research, School of Medicine, Toho University, Ota-ku, Tokyo, 143-8540, Japan
dAsia International Institute of Infectious Disease Control, and Department of Health Protection, Graduate School of Medicine, Teikyo University, Itabashi-ku, Tokyo, 173-8605, Japan
eMassachusetts Institute of Technology Lincoln Laboratory, Lexington, MA, USA
fDelegación Provincial de la Consejería de Sanidad. Servicio de Salud Pública, C/ Río Guadalmena, 2, 45007, Toledo, Spain
Received 16 September 2020, Revised 29 December 2020, Accepted 11 January 2021, Available online 16 January 2021.
Abstract
Background
Between March and April 2020, 84 elderly patients with suspected COVID-19 living in two nursing homes of Yepes, Toledo (Spain) were treated early with antihistamines (dexchlorpheniramine, cetirizine or loratadine), adding azithromycin in the 25 symptomatic cases. The outcomes are retrospectively reported. The primary endpoint is the fatality rate of COVID-19. The secondary endpoints are the hospital and ICU admission rates. Endpoints were compared with the official Spanish rates for the elderly. The mean age of our population was 85 and 48% were over 80 years old. No hospital admissions, deaths, nor adverse drug effects were reported in our patient population. By the end of June, 100% of the residents had positive serology for COVID-19. Although clinical trials are needed to determine the efficacy of both drugs in the treatment of COVID-19, this analysis suggests that primary care diagnosis and treatment with antihistamines, plus azithromycin in selected cases, may treat COVID-19 and prevent progression to severe disease in elderly patients.
… in a not-so-tiny nation called Spain, a nursing home had a nasty virus get into it.
It was March of 2020. The nasty virus was called Covid-19. And this nursing home, like so many others all over the world, was full of elderly, morbid people. The mean age of residents was 85 and 48% were over 80 years old. It was a killing field, like so many others…..
Within three months 100% of the residents had caught the virus. Not presumed to have — proved to have.
How do we know this? Because almost every one of them seroconverted. All but three out of 84 of them, to be precise.
Think about that last sentence for a second.
Almost every one of them seroconverted.
How’s that possible? Many of them died, right? You can’t seroconvert if you’re dead.
You would have thought this would have been all over the news. In point of fact not one mention of it was made. Further, not one write-up was made in medical journals either until January of 2021, which I missed. My bad — out of the several hundred medical journal pieces, I missed this one. It was brought to my attention on my forum and my jaw immediately hit the floor.
The jab train must continue, you see. So must the ventilator train. So must the money train, the mask train and the rest of the BS we have endured for the last 18+ months.
So must the slaughter for money, the fear, and the lies.
MORE (and it’s really worth reading the rest of Karl’s thoughts).
The answer isn’t vaccines. It isn’t remdesivir. It isn’t even blowdarts.
The answer was simply “use more OTC antihistamines”, plus Z-Pack, if you want to be extra certain, this flu season.
But you see, there would have been no crisis that way.
Seriously, I think that one of the most FAILSAFE WAYS to deal with likely or confirmed COVID (antigen tests are basically $13) is to treat with antihistamines immediately, and ask the doctor for Z-Pack (azithromycin).
If you HAVE hydroxychloroquine or ivermectin, great – but if not, then antihistamines are the stuff.
The HORRIBLE CDC, FDA, NIH, and BIG PHARMA cannot – at this moment – restrict you from getting antihistamines. And I know for a FACT that these drugs last a LONG time. They remain effective LONG after their expiration dates.
So buy some now, and by the time you need more, you will be immune, and JOE BIDEN and KAMALA HARRIS will be LONG GONE.
Well, they can lock us out of The Q Tree, but they can’t stop the truth from getting out.
Enjoy a post first over on The U Tree and now HERE.
Here is a quickie in my WAR ON REMDESIVIR.
Fellow Treeper barkerjim dropped an interesting document today, from back in July, which showed the NIH mentioning black sheep IVERMECTIN on the same page as REMDESIVIR.
Such a beautiful misdirection. These guys are MAGICIANS.
This is a perfect example of my postulate that fighting FOR ivermectin will not yield results for restoring real science as fast as fighting AGAINST remdesivir.
In fact, I would go so far as to say that the enemy realized that getting us to fight FOR the saving drug would keep us from expending our energy fighting AGAINST the murdering drug that kills us off and gives them money for doing it.
You may recall my previous posts about remdesivir.
My next piece was going to be an expansion on Karl Denninger’s recent post which places remdesivir/ivermectin and remdesivir/hydroxychloroquine in the context of Anthony Fauci and the disturbingly similar case when he was “all about AIDS” – namely, AZT/bactrim.
YES. As Cthulhu has said before, “This is not Fauci’s first rodeo.”
Before there were hydroxychloroquine and ivermectin as innocent victims – good Samaritans accused falsely before the world – there was BACTRIM.
And there was FAUCI on all of them. AZT played the murderous part of remdesivir long before we forgot that “miracle drug”.
However, this new information from barkerjim’s drop right here needs to get out right away. The Q Tree site was brought down YET AGAIN as I started working on this, and again when I resumed, so I know it’s critical stuff. The ChiComs have a huge investment – both financial and military 4GW – in the American-killing drug remdesivir. They WILL protect it.
We know from doctors and scientists quoted in my first two articles, that remdesivir has a horrible track record – shocking, really – of renal toxicity. Studies of the drug against Ebola were TERMINATED because it was killing people in the hospital.
How déjà vu.
But here it comes again.
I read the same study results that the above celebratory announcement was made over. Those results were nothing to cheer about, with shot kidneys just the horrifying icing on the death cake. In my opinion, the results were far WORSE than any prior results for hydroxychloroquine. The results – to me – made HCQ look EXCELLENT in comparison.
Yes – by controlling what is acceptable science and what is not, Fauci was able to force the world to field a BAD, DANGEROUS DRUG that made money for Gilead, over a safe, mildly (but critically) effective drug, that made money only for the generics industry, and a French company.
And to top it off, Fauci USED Trump, who could do absolutely nothing about it, to take a KILLER drug into market as the ONLY way to treat his little pandemic.
So let’s take a look at that page dropped by barkerjim. I have captured it as SIX IMAGES.
As you can see by our comments on The U Tree, most people will look at this table and think they are seeing positive and reasonable behavior by NIH. Adverse events are being discussed, and it appears that things are “even-handed” between different drugs.
And that is EXACTLY the style in which EVIL ABOUNDS IN WASHINGTON, DC (or Atlanta). Good and evil are forced into compromises where GOOD LOSES and EVIL WINS – but the result is called “meeting in the middle”.
CLOSER INSPECTION of the table gives you this, under Adverse Events for remdesivir.
Nausea
ALT and AST elevations
Hypersensitivity
Increases in prothrombin time
Drug vehicle is SBECD, which has been associated with renal and liver toxicity. SBECD accumulation may occur in patients with moderate or severe renal impairment.
Each 100 mg vial of RDV lyophilized powder contains 3 g of SBECD, and each 100 mg/20 mL vial of RDV solution contains 6 g of SBECD.
Clinicians may consider preferentially using the lyophilized powder formulation (which contains less SBECD) in patients with renal impairment.
This is some of the most remarkable “medical misinformation” I’ve ever seen. It’s truly a work of art.
NIH has HIDDEN – completely hidden – the pronounced renal toxicity of remdesivir. They have hidden it COMPLETELY. It’s GONE. What you are seeing there – the talk about renal and liver toxicity – is a BLAME-SHIFT to a substance that is used WIDELY in intravenous formulations, called sulfobutylether-β-cyclodextrin, or SBECD for short.
This substance is an EXCIPIENT.
An excipient is a substance that is used to MIX with a drug, and take that drug into a form where it can be ADMINISTERED easily. Thus, an excipient may DISSOLVE the drug, or help to dissolve it, into a liquid form. It may help POWDER the drug, so that it can be pressed into tablets or filled into capsules.
Excipients are often considered “inactive ingredients”, even though – YES – they very much can change the effective amount of a drug that the patient gets.
If I had to describe SBECD as something, it would be as a DETERGENT FOR DRUGS. It’s a kind of SOAP made from a cyclodextrin, instead of from some kind of fat or lipid.
Cyclodextrins are rings of sugar molecules that falls somewhere in between being a smaller chain sugar (like sucrose) and a starch. Cyclodextrins have lots of uses, because they form tubes that act like waffle cones for other molecules. Febreze uses cyclodextrins to trap molecules which have unpleasant odors, at the same time that they release more pleasant ones. A genius application, quite frankly.
Thus, if you make a SOAP that has a little waffle cone for drugs, you can EASILY get drugs to dissolve into a concentrated liquid form by using that soap.
See those sidechains hanging off the cyclodextrin ring? Those are the “SBE” part of SBECD. They are typical of DETERGENTS.
This SBECD stuff and things like it are VERY useful for delivery of drugs. AND they’re relatively safe, too. They are rapidly excreted through the kidneys. Yeah, you don’t want a SOAP piling up in your blood if your kidneys are not working, and THAT is the fact that is being TWISTED by NIH when they say:
Drug vehicle is SBECD, which has been associated with renal and liver toxicity. SBECD accumulation may occur in patients with moderate or severe renal impairment.
Did you catch that sleight of hand? I’m gonna show it to you.
What exactly is causing the renal problems in the FIRST PLACE that you MAY have to be careful about, so that you don’t build up the excipient FOR IT, which MAY constitute a FURTHER risk?
REMDESIVIR.
It’s a crafty little lie. If you have good kidneys, you don’t have anything to worry about with this SBECD crap. But if you have bad kidneys, the LEAST of your problems is SBECD buildup. It’s the remdesivir IN the SBECD that’s gonna kill you.
Weakened kidneys do NOT need to be hit with remdesivir.
Which doesn’t even work ANYWAY. Except to keep people LONGER in the hospital.
Now what you SHOULD be getting, when they administer remdesivir, at the point where the VIRUS is basically gone, and you’re dealing with spike protein damage, cytokine storm, and all that nasty crap, are antiinflammatory, antithrombotic, and immunomodulatory drugs. Even HCQ (a known antirheumatic) at reasonable doses had some antiinflammatory effect in late-stage hospitalized COVID cases, although steroids and other things work better.
When the virus is basically gone, and a bunch of its CRAP is left behind, there is no point administering a toxic antiviral like remdesivir, other than to send money to Gilead Pharmaceuticals and their Deep State friends.
Now, let me stop here and validate this stuff.
HERE is a link that explains how SBECD can be filtered out of blood ANYWAY if a patient has renal impairment.
Do you see what that means? SBECD is a nothingburger. It’s a DEFLECTION.
The renal problems of remdesivir are never mentioned, by quickly bringing up the risks of the excipient due to the unmentioned damage BY remdesivir.
What NIH did here was to quickly point their finger at THE OTHER GUY and said “HE DID IT!”
This is pure politicized science, where the politics is to defend the drugs and vaccines that enable the shared profits of both the Deep State and the companies that NIH, CDC, and NIAID are in bed with.
Let’s go back to that link I just gave you. THIS part of the conclusions comports very nicely with the reality of SBECD as a widely used excipient.
The finding that SBECD can be effectively removed by CVVH is clinically important, because some cyclodextrins have been associated with hepatotoxicity or nephrotoxicity due to vacuolation [3]. Although our study was small, no evidence to suggest SBECD as a cause of hepatotoxicity or nephrotoxicity was demonstrated in our study patients. This finding is consistent with other SBECD safety studies in humans [3,18]. Additionally, animal studies have only been able to demonstrate cyclodextrin toxicities when dosages more than 50-fold greater (3,000 mg/kg) than those used in humans were administered [3,19,20]. Unlike other cyclodextrins used in these animal studies, SBECD undergoes only minimal tubular reabsorption and limits concentrations within the intracellular tissues of the kidney, potentially reducing the risk of nephrotoxicity. Nevertheless, the FDA labeling for voriconazole recommends that IV therapy be avoided, if possible, in patients with a CrCl <50 ml/min [5]. Our data suggest that IV voriconazole can be safely administered in this population if the patient is concurrently undergoing CVVH.
Delafloxacin, a fluoroquinolone, has activity against Gram-positive organisms including methicillin-resistant S aureus and fluoroquinolone-susceptible and -resistant Gram-negative organisms. The intravenous formulation of delafloxacin contains the excipient sulfobutylether-β-cyclodextrin (SBECD), which is eliminated by renal filtration. This study examined the pharmacokinetics and safety of SBECD after single intravenous (IV) infusions in subjects with renal impairment. The study was an open-label, parallel-group, crossover study in subjects with normal renal function or mild, moderate, or severe renal impairment, and those with end-stage renal disease undergoing hemodialysis. Subjects received 300 mg delafloxacin IV or placebo IV, containing 2400 mg SBECD, in 2 periods separated by ≥14-day washouts. SBECD total clearance decreased with decreasing renal function, with a corresponding increase in area under the concentration-time curve (AUC0-∞ ). After IV delafloxacin 300 mg administration, SBECD mean total clearance was 6.28 and 1.24 L/h, mean AUC0-∞ was 387 and 2130 h·μg/mL, and mean renal clearance was 5.36 and 1.14 L/h in normal and severe renal subjects, respectively. Similar values were obtained after IV placebo administration. In subjects with end-stage renal disease, delafloxacin 300 mg IV produced mean SBECD AUC0-48 values of 2715 and 7861 h·μg/mL when dosed before and after hemodialysis, respectively. Total SBECD clearance exhibited linear relationships to estimated glomerular filtration rate and creatinine clearance. Single doses of IV delafloxacin 300 mg and IV placebo were well tolerated in all groups. In conclusion, decreasing renal function causes reduced SBECD clearance and increased exposures, but SBECD continues to exhibit a good safety and tolerability profile in IV formulations.
“In conclusion, decreasing renal function causes reduced SBECD clearance and increased exposures, but SBECD continues to exhibit a good safety and tolerability profile in IV formulations.“
Now, the above is not the only “New York Times” style trick that NIH plays here.
Let me list, without going into long-winded explanations, my additional favorites.
The table authors note that clinical drug-drug interaction studies have not been done, but nonetheless, they say “CQ or HCQ may decrease the antiviral activity of RDV; coadministration of these drugs is not recommended.1” – with a hanging reference.
For three OTHER potential drug interactions, communications from Gilead are cited as sufficiently exonerating. One is a non-competing generic steroid (dexamethasone) and the other two are patented big pharma antivirals from corporate “frenemy” Genentech. The interaction and “C-level mind-melding” between these two companies is very interesting. Look who just went from one to the other. Interesting times.
Some crafty shade is thrown at ivermectin by citing a possible adverse event risk and then retracting it, lawyer-style: “Neurological AEs have been reported when IVM has been used to treat parasitic diseases, but it is not clear whether these AEs were caused by IVM or the underlying conditions.” Meanwhile, the DEMONSTRATED risks of remdesivir are not even mentioned.
Bottom line – NIH is protecting Gilead on the toxicity of remdesivir, and they used FAKE NEWS tricks to do it. I keep telling people – science journalism is bad, and science governance is WORSE. It’s been CHINATIZED and OBAMATIZED.
“So, I think the real question in this crisis is what is there on our view of man and our world, and on the way in which we look on life, that makes us experience a lack of sensemaking. In my opinion, I think we must conclude it is something in our materialistic, mechanistic view of man and the world that leads up to radical destruction of the real social structures and social bonds and the feeling that life makes sense. If you believe that human beings are biological machines, then this implies, by definition, that life is senseless.”
Professor Mattias Desmet
Welcome back to Wolf’s Pub!
The Arizona audit report drops today. Let the fireworks begin. It feels like we’ve been trudging through a mucky swamp trying to get somewhere and we can see the shore but can’t quite get there.
It’s about Good and Evil. It’s been enormously painful to see the depth of corruption in our nation’s institutions. Very, very painful.
IT’S A SPIRITUAL PROBLEM
One question that has dogged me since the whole Great Reset was kicked off with the CCP Virus, is how can so many people be so fooled for so long when the truth is being trumpeted across the width and depth of independent media?
Well, I ran across an interview that Reiner Fullmich conducted with Belgian psychologist and professor, Mattias Desmet: The Psychology of Covid-19 (Mass Formation and Totalitarian Thinking):
This is an utterly fascinating discussion regarding how large groups of people fall willingly into totalitarianism.
Light bulbs were going off in my head as I listened to this interview. Professor Desmet says four things must be present in order to facilitate the conditions for a people to go down the road of societal madness:
These four conditions existed prior to Covid. Larry Turner writes about Professor Desmet’s interview here. He explains:
“If these four factors are present in enough members of any given society, Desmet says the society in question is at risk for the ‘crystallizing’ action of “mass formation” where large numbers of discontented, anxious, confused, and isolated people simultaneously and suddenly seize upon some single apparent threat and give it their entire attention and energy. The basic reason for this attention and energy seizure, according to Desmet, is that putting focus on a single apparent threat provides immediate and palpable relief from a constellation of the longstanding chronic pressures of social isolation, lack of sensemaking, and free-floating anxiety and discontent. This mobilization of individual attention and energy against some single perceived threat unfortunately, according to Desmet’s explanation of the phenomena, segues easily into increasingly totalitarian government behavior.
Desmet believes that this is exactly what has happened and is happening to greater or lesser degrees all over the globe in response to the COVID19 virus pandemic. He posits that – judging from measures of high and increasing drug use, increased job burnout and economic dissatisfaction, and increasing social isolation – that prior to the arrival of COVID19 a significant number of humans were extremely uncomfortable with their lives. With the arrival of the virus, however, they were able to unload their longstanding unfocused anxiety and discontent onto the ‘COVID19 crisis’, thereby obtaining a welcome and immediate release from their chronic discomforts and tensions. Desmet refers to the immediate feeling of relief felt by those previously heavily burdened with isolation, lack of sensemaking, and free-floating anxiety and discontent as a “mental intoxication”.
Larry Turner
Turner writes more about this phenomenon and Dr. Desmet’s explanation of it here.
What about those who don’t get caught up in the lies and mass formation? Desmet says:
“Usually it is only about 30% [of a population that gets] grasped in a mass phenomenon or hypnosis. An additional 35-45% usually does not want to raise a dissonant voice in the public space because they are scared of the consequences. So, usually about 70% who shut up – 30% because they are convinced by the mainstream narrative and 40% because they don’t dare to speak out. And then there is an additional 20-25-30% who does not go along with the narrative and says it in certain situations.”
Professor Mattias Desmet
Those who are immune tend to be independent thinkers. Take a bow, guys.
Very worth your time to listen in. I definitely feel smarter after listening to the interview and reading about it. 😊
HOUSE RULES
Well, since we’re a pretty durned sense-making and cohesive group here at the Qtree, it only requires a reminder of the rules of this place. Go here to review.
If you don’t feel like fitting in for the moment here, the Utree is a welcome and present aid to run to blow off some steam. It’s also our place to reconvene during various attacks on this site, the server, and the hosting company. Prayers all around to keep us all up and running.
SACROSANCT BEER?
Since today’s opener features Professor Desmet, a Belgian, I thought it appropriate to offer a nice selection of Belgian beers today. Here’s a nice article that explains the seriousness with which the Belgians feel about their beer.
According to the author, Tom Green,
“In Belgium, beer is sacrosanct. Committed to tradition, Belgian brewers make some of the world’s greatest and most timeless beer. In the thousands of local pubs spread across the small country, beer is a unifying source of pride for the Belgian people.”
Tom Green
I watched the video embedded within the article that talks about the fact that there are over 1,500 different Belgian beers, which is amazing considering the small size of Belgium. These people are serious about beer. I mean, beer-making and beer-drinking is pretty much the national past-time.
When all this Great Reset has been beaten to death, I want to go bar-hopping in Belgium.
Meanwhile, I present the iconic (in America) version of Belgian beer: Blue Moon Belgian White
I’ve always found it very palatable. Read here how Blue Moon came to be. And for astronomy buffs, the next Blue Moon will appear in our skies on Friday, August 30, 2023.
BACK TO THE AUDIT
This picture of the Canary Islands, where that volcano has been erupting is some firework, eh? Intense video images here.
It has been said, repeatedly and truly, that if the 2020 election is not fixed, then 2022 and 2024 don’t matter. The audits in all 50 states will reveal that our votes have been stolen, are being stolen, and will be stolen if election reform is not enacted.
I have here an absolutely fascinating video (end of article) from Gab TV that fits right into everything I know about COVID-19 and the spike protein vaccines, like the last piece of a puzzle.
The video is just under 1/2 hour in length, but it is FILLED with little AHA moments.
An extremely articulate, healthy, successful, C-level professional woman got the jab voluntarily, for the best of reasons, and caught a nasty case of something which is very similar to “LONG-HAUL COVID”, describes exactly what happened to her. She clearly has “brain fog”, but under excellent questioning by an interviewer who has talked to her before, she is continuously prompted to get the whole story out.
And her story is a DOOZY.
Her case is – in the days after injection – almost identical to the NURSING HOME PATIENTS who were also injected with Pfizer, but who DIED several days later, correlating to injection, and whose deaths were blamed FALSELY on a “super-spreader”, to cover for the vaccines – except this lady was too healthy to die, so she’s just DISABLED.
Here is the comparison video about the nursing home victims.
One of the things to listen for in the new video is the MAYO CLINIC. All your suspicions about the compromise of the Mayo Clinic will be confirmed here in spades.
Another is LYMPH NODE INFLAMMATION, which I see as a metric of vaccine migration, localization, and persistence. Based on what happened to this lady, viewed in light of what was learned from the Sorrento vaccine, which primarily concentrates in and immunizes from the lymph nodes, we can see exactly what is wrong with the mRNA approach in the Pfizer vaccine. This lady was clearly cranking out tons of spike protein into her system for 3 MONTHS.
It’s very helpful to compare this DIRECTLY with information from a doctor named Bruce Patterson, who is likely the world’s expert on long-haul COVID.
This lady’s symptoms are EXACTLY what is described for long-haul COVID in patients who can no longer engage in strenuous physical activity.
Start at around 5:00 minutes if you are pressed for time – the answers come in the next 3 minutes after that.
What you will learn is that the spike protein hangs around long after it was created, and can in fact be carried in the bloodstream by monocytes for 15 MONTHS.
Is everything starting to make sense now?
GOOD.
Stay the HELL away from boosters.
mRNA vaccines were NOT designed in the patients’ best interests. They were designed to get approval for gene therapy.
Thank you, Suzanne Newell. Your testimony of TRUTH will SET US FREE.
As we have been repeatedly warned – even by the VERY ENEMIES who are attacking us (i.e., KlauSS “Hog-Jowls” SSchwab and the WEFFEN SS), there was going to be a “cyber war” this summer – obviously timed to deal with the “fall” of the FAKE ELECTION and the CHINA VIRUS.
Thus, between the CHINAZIS and the EUNAZIS, plus the BIDENAZIS and assorted American PROGZIS, to say nothing of the GLOBONAZIS, we have a bunch of people ready to attack us.
While I try not to give away too much potentially useful (to THEM) strategic information about what is going on, it has become obvious that various forces want to make life rough for the commenters on this site.
The attack on our site include attacks on our server (and service) directly, on the people who are commenting on or viewing the site, AND on the hosting company itself.
The attack on the hosting company has been particularly insidious.
If our hosting company (who I refer to as “COUGH-COUGH.com”) can be brought down, several patriot sites will fall, including one of the most important players of all, GAB.
There has been much back-and-forth in this war. Both I and our hosts have been forced to take a variety of evasive actions over the summer.
I have never, in the entire history of this site, had to be so restrictive in terms of registrations (which must now be done MANUALLY) and user features (which had to be turned off for the non-registered users), as I have in the last few months.
And yet, despite all those measures, we just experienced one of our most serious attacks yet, locking many people out of the site, and attempting some really NASTY “get the users to turn off security” attacks, so that ANY of our registered users (and especially our authors) might get spoofed.
They are desperate, and they are persistent.
Now – with ALL of that stuff going on in MY world (remember 60,000 “Russian” phony registrations?), there is now a sustained and multifaceted attack on our hosting company, trying to distract them from the coming AUDIT ATTACKS (in my opinion).
This attack on the hosting company is a threat to ALL sites hosted by them, but most of all it is a threat to the honorable name and reputation of that company. That’s how the other side works. They are DESTROYING what they cannot legislate out of existence.
Our hosts are grateful for the support and prayers of their customers, as they, even in their time of trial, are praying for us. Thus, I ask all of you, to say a quick prayer for our hosting company.
We continue to use The U Tree as a backup, and it is functioning well in that regard. Please feel free to assemble there and to CARRY ON.
Simply carrying on is perhaps the greatest thing you can do to defeat the ChiNazi menace and the WEFFEN SS. Make their attacks pointless in the end. If you attack them TWICE AS HARD for sending you to The U Tree, then you have just invalidated all their work to get you there.
Be of good cheer, live your best life, and fight your best fight. Fear not an enemy without God.
We not only have something they don’t – we wish our treasure to be theirs as well.
And until there IS justice, we will drag the CRIMES of Anthony Fauci and Gilead “Pharmaceuticals” and their SLEAZY ASSOCIATES thorough the headlines, over and over, until people SPIT IN THEIR PATH as they walk down the streets.
So where do we begin?
Let’s take a brief look at ZYKLON D.
This is the molecule of remdesivir, a.k.a. Zyklon D (as in DEMOCRAT). This is the drug that is killing Americans – primarily “Deplorables”, in the hospital.
The shading of parts of the molecule is significant, and I’ll get to that in a future article. The shading is more significant in a NEW way, than it was in the original way.
If you remember NOTHING ELSE from this article, remember this.
Hydroxychloroquine, chloroquine, and ivermectin TOGETHER over their entire histories have not killed as many people as remdesivir kills in a SINGLE DAY.
In fact, I’m sure it’s significantly less, but I leave the exact numbers as an exercise.
What’s really nasty there, is that OUR tax dollars are being used to PAY HOSPITALS to murder us with remdesivir. As long as hospitals use this WRONG drug at the WRONG TIME (which I will explain) to kill OLD TRUMP VOTERS, they get money from the federal government.
But if hospitals use the RIGHT drug at the RIGHT time, they don’t get the cash.
So what do HOSPITAL ADMINISTRATORS – who more and more are NOT DOCTORS – do? They do what you EXPECT them to do. They do NOT do the right thing for patients.
(H/T Gudthots and GAB)
This has been a part of the general phenomenon of the “lawyering of science”. Has it made science better?
I don’t think so.
It’s beyond evil, but hey – when you have a mafiosa in charge of not only the purse strings, but the “quiver”, these sorts of things happen.
Impeachahontas Now Wearing Two Diapers Nobody expected Chris Wray to play Mafia Nan’s queen of diapers face-up on January 6, but that is exactly what appears to have happened. The only question now is WHY. To quote a friend from a former life, “AYE-YI-YI!” OK – let me back up a bit. First, I want …
And then there’s the “medical mafia”.
Do you see Trump with his hands tied over there? He had to let that jackass on the left declare that a terrible drug recruited to MURDER old Republicans was “the new gold standard of care”, because the murderer is a member of “SES”, and can’t be fired. The medical mafioso can tell whatever lie he wants, and nobody can do anything about it.
Of course, maybe it IS the “GOLD STANDARD” for DEMOCRATS and HOSPITALS.
Yes, the EVIL in charge of this nation is fairly impressive. Moscow has NOTHING on Washington.
But back to the new “secret euthanasia drug”, remdesivir.
“When you go to a hospital, even if you don’t have COVID-19, you’d be construed that way,” says Renz during his program “Lawfare with Tom Renz” on Brighteon.TV. “They get hundreds of thousands of dollars for putting you on remdesivir, putting you on ventilator and letting you die. And if you don’t follow, they’ll just intimidate you and coerce you.”
His guest on the program, Nancy Ross, has experienced that firsthand. Ross has been given the power of attorney to act on behalf of Veronica Wolski, a known patriot from Chicago who recently died from COVID-19 at AMITA Health Resurrection Medical Center.
Ross says the hospital wanted to intubate Wolski and put her on ventilator, and the doctors kept telling that every time they see the patient. “They kept reminding her of that instead of talking about other possible treatment,” says Ross, referring to the ventilator. “I just couldn’t get it.” (Related: Overreliance on ventilators led to coronavirus deaths, study shows.)
According to Ross, Wolski had been asking the hospital to give her ivermectin but her requests had been repeatedly denied.
For the uninitiated, the only treatment for the disease approved by the Food and Drug Administration (FDA) involves remdesivir. It is approved for use in adults and children at least 12 years old who weigh at least 88 pounds (40 kilograms).
Remdesivir is an antiviral medication that targets a range of viruses. It was originally developed over a decade ago to treat hepatitis C and a cold-like virus called respiratory syncytial virus (RSV). Remdesivir is not an effective treatment for either disease, but it has shown promise against other viruses.
It works by interrupting the production of the virus. Coronaviruses have genomes made up of ribonucleic acid (RNA). Remdesivir interferes with one of the key enzymes the virus needs to replicate RNA, preventing the virus from multiplying.
However, up to 31 percent of patients who received remdesivir have developed multiple organ failure and/or acute kidney failure. “Remdesivir was pulled from clinical trials because it’s too dangerous. It’s just a disastrous drug,” says Renz.
Doctor admits 99 percent of intubated patients die
Renz also shares a message he has just received about a recording from a doctor admitting that 99 percent of the patients they intubate have ended up dying. “These are just bad treatments. They just kill people,” he says.
Many hospitals are also giving COVID-19 patients with midazolam, which is questionable at best as it depresses a person’s ability to breathe. It is most frequently used before surgeries or procedures to decrease anxiety, cause drowsiness, and help with anesthesia in patients who need tubes or machines to help them breathe.
Midazolam has an FDA black box warning, which notes that the medication has been associated with respiratory depression and arrest because it can slow or stop breathing.
Ross says they also requested to give Wolski the budesonide treatment, but the hospital instead gave the patient a generic brand, which is not the best thing to have under that circumstance.
Wife dodges ventilator, survives COVID-19 with budesonide treatment
A husband from Georgia has had a better success in forcing a hospital to give his wife the budesonide treatment.
The husband named Mick tells Clay Clark during “Thrive Time Show” on Brighteon.TV that his wife has made it out of the intensive care unit two days after getting the budesonide treatment and has been able to go home in a week.
Mick says his wife is in really bad shape after a week of battling symptoms of COVID-19.
“She’s 57, has a partially collapsed lung and has preexisting conditions. Her blood oxygen was 50 and her blood pressure was 100/50,” said Mick. The normal blood oxygen level is between 94 to 99 percent. Anything below 90 is considered to be low blood oxygen.
“I went on battle mode immediately. I thought ‘this is it,’” said Mick, fearing that his wife would be put on a ventilator in which very few patients had survived.
After talking with Bartlett, Mick sends the hospital a fax message asking to put his wife under the budesonide protocol – which is 1 milligram of budesonide every eight hours. He also sends a copy to the doctor treating his wife, as well as a lawyer.
Mick cites several studies and a magazine article about the budesonide protocol, but he thinks that what catches the hospital and the doctor’s attention is his threat of escalating the matter to the ethics committee if they don’t grant his request.
Budesonide reduces COVID-19 hospitalization
Researchers at the University of Oxford has found that early treatment of inhaled budesonide reduced the need for urgent care and hospitalization in people with COVID-19 by as much as 90 percent. The study has also found that inhaled budesonide given to patients with COVID-19 within seven days of symptoms reduces recovery time.
Participants allocated the budesonide inhaler has had a quicker resolution of fever, symptoms and fewer persistent symptoms after 28 days. The study has also demonstrated that there’s a reduction in persistent symptoms in those who received budesonide.
Doctors have prescribed budesonide for more than 20 years as preventive medicine for asthmatics. Bartlett has written a paper with case reports describing favorable outcomes for two of his patients with the regimen. A lab study in the U.S. has also shown that budesonide inhibited the ability of a coronavirus to replicate and inflame the airways.
[Back to Wolf]
If, after reading all that, you’re STILL not suspicious that maybe remdesivir is problematic, then please read my previous article.
I have been a poor and rotten servant of the Lord during my too long and too miserable life. I have made innocent women cry. I have led others astray. I have turned away from those in need in their time of need, and I have lied to myself and to God about why I …
In the prior article, there is a VIDEO that explains how remdesivir WORSENS pneumonia by shutting down the kidneys. The people who killed Veronica with remdesivir are NOT telling you that. They are HIDING the fact that Veronica Wolski was KILLED BY REMDESIVIR, but the effects of kidney-failure-induced pulmonary edema LOOKS like bacterial pneumonia.
It LOOKS like the disease did it, but it’s really the DRUG. Fauci gets away with what he CAN get away with.
He’s not a doctor. He’s an administrator. As his CLASSMATES have said many times.
But let’s say that Veronica Wolski actually DID have real pneumonia – AGGRAVATED by remdesivir kidney shutdown. THAT is exactly why Didier Raoult used AZT along with hydroxychloroquine – as a rapid attack on ANY bacterial pneumonia that might develop. So AGAIN – had Veronica gotten the RIGHT DRUGS right away, she would not have died.
In fact, AZT plus even OTC antihistamines (which prevent pulmonary inflammation) will prevent death by COVID-19, as long as the patients DON’T get remdesivir.
In that previous article I did a very fast proof that hydroxychloroquine (HCQ) works, demonstrated at a national and international statistical level (the “Lancetgate effect”), but I just glossed over Prof. Didier Raoult’s first communication on the efficacy of a combination of hydroxychloroquine and azithromycin (HCQ + AZT) to prevent DEATH by COVID-19.
Here is Raoult’s comment on the uncovering of the Lancetgate fraud. Note that Raoult’s work was never attacked directly (which would have been scientifically suicidal), other than to say that his sample size was “too small” (not in my opinion) when he first communicated his findings.
Hydroxychloroquine is NOT a standard antiviral like acyclovir, remdesivir, and most of the other “vir” drugs, which are all based on what can best be described as “ringer” nucleotides, nucleosides, and nucleic acid bases.
Here is acyclovir, which as a “fake nucleoside” is very easy to understand. You can see where the name comes from – it’s an “acyclic” version of guanosine, where part of the ribose ring has been REMOVED.
Now the part they say about “without affecting the normal cellular processes” is NOT actually true. There are plenty of papers on the side effects of acyclovir. Those side effects are not USUALLY all that bad, but they are VERY REAL because acyclovir DOES impact normal cellular processes.
There are VERY FEW drugs which impact ONLY the processes of viruses, cancers, bacteria, fungi, protozoa, trypanosomes, flukes, helminths, ticks, fleas, lice, and other parasites, and do NOT at all impact host (that means US) cellular processes.
In fact, it’s not easy to say WHICH processes are purely HOST processes, and which OTHER processes are parasite processes. Host processes turn into viral processes by their ABUSE, and one of the BEST ways to stop viruses, is to simply stop the HOST processes that help the virus, until IMMUNE PROCESSES have time to identify, target, and DEFEAT the virus.
Under these tactics, the larger organism can WIN by not giving the virus what it needs.
VIRAL DENIAL IS A VALID TACTIC.
I hope that’s clear. Targeting ANY host process which helps the virus, and doesn’t hurt the host too badly when sabotaged, is a VALID way to stop a virus and beat a disease.
Most antivirals work by disrupting viral GENETIC processes, by serving as bogus pieces in RNA or DNA construction. They are like styrofoam or rubber links that create weaknesses in steel chain.
It doesn’t really matter exactly WHEN and exactly WHERE the “vir” type antivirals cause things to fail. They are simply SABOTAGE LINKS in the nucleic acid chains that viral construction depends upon.
Here is remdesivir’s sabotage molecule:
ATP is adenosine triphosphate – a critical molecule for both genetic construction AND energy transfer.
Remdesivir leads to the construction of a FAKE version of ATP (called RDV-TP above) which has two points of sabotage. One is an added cyano group – the other is an altered ring structure that cannot hydrogen bond properly, because one nitrogen has been removed, and another has been relocated.
It’s too bad that remdesivir is so toxic, but that’s the sad reality of drug discovery. MOST potential drugs have a lot of side effects, and are not all that safe.
Hydroxychloroquine and ivermectin are not all that good as antivirals, in my opinion, BUT they have the GLORIOUS property of being VERY safe. That is part of why they’re considered essential medicines for their normal uses against LARGER parasites (trypanosomes, flukes, helminths, and mites).
BOTH of those drugs have good postulated NON-STANDARD mechanisms of antiviral action – meaning these drug molecules are not bogus genetic building blocks – they disrupt something else. There is some debate on exactly how these drugs work, but it doesn’t really matter, as long as they work.
There are reasonable explanations of how they may work, there is empirical evidence that they DO work, and they are known to be safe at effective doses.
These drugs are SAFE TO USE.
Now – this is where TIME comes into play.
The main problem with remdesivir is that it is used TOO LATE in the viral process. It SHOULD be administered early in the process, on an outpatient basis, like hydroxychloroquine or ivermectin. The reason is fairly obvious. If you attack a virus after it has already multiplied, you can’t stop the damage it ALREADY DID.
REMDESIVIR BOMBS A VILLAGE OF SURVIVORS AFTER THE TALIBAN CAME AND LEFT.
Hydroxychloroquine and ivermectin, administered early, are like sending in a platoon of commandos right after the Taliban shows up.
Which strategy is going to give the most survivors?
This is a no-brainer. You don’t need a Ph.D. to see this. And yet, literally, THOUSANDS of American Ph.D.s cannot SAY this because they’re afraid of losing their jobs, their reputations, or their potential for advancement.
Thankfully, I’m retired, so I can speak the truth.
Now, as a scientist who GETS relative importances, I can see how to FIX remdesivir. I TOLD them how to fix remdesivir in spring of 2020. Let me explain this YET AGAIN.
I take note especially of the horrible record of side effects (especially total kidney failure requiring dialysis and transplant) of remdesivir in hospitalized patients – who get high doses of remdesivir because they have high levels of virus (or low POST-INFECTIVE levels, but again – the people behind remdesivir are not being logical if we take them at face value).
The fact of the matter is that remdesivir has to be given I.V. – it cannot be given orally. That is the EXCUSE for giving it so late.
But IF it was given earlier, remdesivir could be given in lower doses that would probably work just as well as HCQ or ivermectin.
That is all that is needed. Protect people from death. Less drug because less virus. Less side effects because less drug. And it’s not like a doctor’s office can’t administer a lower, safer, yet STILL intravenous dose of remdesivir on an outpatient basis. EARLY.
They never did this.
Why not?
Now, I believe it’s because curing people with remdesivir was NEVER the intent of the primary conspirators.
Profit, obviously, for many participants, is the “legitimate” motivation. But there is more.
Secret euthanasia of “useless eaters” with remdesivir WAS their intent. And that “authority” to inject people (either literally or practically) against their will requires a hospital setting. The hospital setting creates the EXPECTATION OF DEATH – and that is how they get away with it.
The people who COULD have changed things to administer remdesivir when it would have been safer did NOT, because they were either cowardly, brainwashed, politically impeded, monetarily motivated, or part of the actual conspiracy.
SO – bottom line – if you feel that you have to go to a hospital, DO NOT go unless you are assured that your doctor can treat you with drugs that YOUR DOCTOR wants to treat you with, including ivermectin, hydroxychloroquine, budesonide, and antibody cocktails.
These are the things that ACTUALLY WORK. And are ACTUALLY SAFE.
Friday is here and Wolf’s Pub is open! We’re doing a great business in the back of the pub with all the dangerous drugs around nowadays…HCQ, NAC, and Ivermectin. People are dying for ‘em.
Just some dark humor.
Chartreuse
ALCHEMY AND FAUCI
At the front of the pub, is our drink special for today, which comes from a centuries’ old manuscript dedicated to giving long life. I’d say there’s some alchemy going on there (see below). Considering that the plague continued to find victims centuries after the Black Death, it is no wonder that mankind was casting about for health treatments and elixirs of life.
I found this fascinating article about a popular tract that details how to treat for the plague. Honestly, Dr. Fauci would be most comfortable with dispensing their advice today, I think:
“This treatise tells you everything you need to know to avoid getting sick during the next pandemic. It opens by telling readers how to avoid catching the plague:
If an outbreak of the plague has happened again, you can take the following steps to protect yourself. Don’t take baths and don’t sweat; both will open the pores of your body and let the venomous air get in. Avoid lechery too because that also opens the pores and lets the illness in. Don’t eat much fruit unless it is sour or new. Don’t eat garlic or onions or leaks or anything that is going to get you in a heat. Drink lots of fluids: cold water is best with vinegar of barley water.”
The treatise then informs readers how the sickness enters and impacts the body:
It explains that every person has three principal parts: the heart, the liver, and the brains. Each part has a place in the body where it expels waste: the heart under the arms, the liver between the thighs, and the brain under the throat. The sickness comes into the body through the air, makes its way to the blood and attacks the heart, then the liver, then the brains. Each part of the body will attempt to expel venoms through the cleansing part, but if it can’t, those places will break out in plague boils.”
But first, let’s recap what the medical/pharma people have been up to, in memes of course:
From Kanekoa the Great
Now I ask you, who is more learned: an 18th century group of monks making an herbal elixir for long life, or Dr. Anthony Fauci, that lying fink who tells medical lies as easily as he breathes? On to the elixir, which probably has more medical expertise in every bottle than Fauci has had in four decades.
CHARTREUSE, ELIXIR OF LONG LIFE
Today’s special is Chartreuse, yet another monk-inspired liquor. The history of this famous liquor reads like a medieval mystery. It is made by Carthusian monks from a closely-guarded secret manuscript that details a very complex, almost alchemical recipe of 130 herbs. According to the official website:
“The Order of Chartreuse was more than 500 years old when, in 1605, at a Chartreuse monastery in Vauvert, a small suburb of Paris, the monks received a gift from Duc Francois Hannibal d’ Estrées, Marshal of King’s Henri IV artillery : an already ancient manuscript from an “Elixir” soon to be nicknamed “Elixir of Long Life”. This manuscript was probably the work of a 16th century alchemist with a great knowledge of herbs and with the skill to blend, infuse, macerate the 130 of them to form a perfect balanced tonic. In the early 17th century, only a few monks and even fewer apothecaries understood the use of herbs and plants in the treatment of illness. The manuscript’s recipe was so complex that only bits and pieces of it were understood and used at Vauvert.”
The classic Chartreuse gets its unique green color from the chlorophyll in the herbs. The video below has the history as told by two representatives involved with sales of Chartreuse.
Here’s another shorter video review of Chartreuse, which because of its alcohol content soon became more than a medicinal. The original Chartreuse was 69% ABV. Today it is 55% ABV.
There’s a plethora of cocktails that include Chartreuse, but if you enjoy the pungent complexity of herbs, with honey tones, you will enjoy this special liquor straight up or on ice. I hadn’t tasted Chartreuse in decades, so I indulged in purchasing some the other day. Wow, I’ve been missing out.
Today, there are only two monks at a time who know how to create Chartreuse. They must travel in separate cars when they go to work.
THEY ARE TRYING TO KILL US
The Conservative Treehouse details in two articles, here and here, how the federal government has overtaken dispensing life-saving monoclonal antibodies in ways that punish states with lower vaccination rates.
Florida Gov. Ron DeSantis is having none of it.
“Florida Governor Ron DeSantis responded directly to the White House effort to kill Florida residents by withholding previously agreed shipments of Monoclonal Antibodies.
During a press conference earlier today, Governor DeSantis outlined the issues Florida is facing after the Biden administration instructed the federal offices of HHS to punish the successful therapy and recovery efforts of the sunshine state healthcare system. DeSantis outlines the purchase agreement that Biden intentionally violated and also the issues created by the federal government now blocking direct purchasing of treatment from the manufacturer.”
HOUSE RULES
There’s so much evidence of medical malpractice and outright murder of patients that it is destroying the medical establishment for a generation. The ideological rot has destroyed any conscience they might have had. The LOVE OF MONEY is the root of ALL evil.
I bet they won’t be enjoying their filthy bonuses much in the future.
But here at the Qtree, we are a community of individuals who think life is precious and worth saving, and I have to tell you, I am so proud to be among y’all. I just love all of you. You’ve made these “interesting times” bearable.
If you’re new here, a review of the House Rules will give you an idea of why we stick together through thick and thin, through squabbles and disagreements. Wolfmoon has provided the Utree for us in case someone needs to duke it out, but mostly it’s a great place to reconvene if/when needed. It’s proven indispensable.
OUR ENEMY, BIG GOV CORPORATE MEDIA
NPR got caught with their pants down telling more lies about hospital bed availability in southern states. It’s beyond ridiculous at this point.
“Though the Washington Post quoted a hospital spokesperson as saying such situations were an “ongoing problem” in Alabama hospitals, not one person from the hospital confirmed the daughter’s story about the supposed capacity issues at the 43 ICUs. It wasn’t confirmed for the NPR report nor the WaPo report.
At the very least here, NPR deceived readers by making them believe two things, the first one being that DeMonia was never admitted to the Cullman hospital (false) and the second one being that the hospital couldn’t admit him due to being overwhelmed with COVID patients (also false). The Washington Post earns no brownie points for their story, either, which wasn’t much better.
And to this day, no one in any official capacity will confirm the 43 ICUs claim.”
ODDS AND ENDS
I really don’t know what to think about the Sussman indictment. I’ve gotten so cynical that I’m gonna let some time go by and events unfold before I get all giddy. Articles about it here and here and here.
Corey’s Digs with COVID RESOURCES. Excellent. Pass around to everyone.
I have been a poor and rotten servant of the Lord during my too long and too miserable life. I have made innocent women cry. I have led others astray. I have turned away from those in need in their time of need, and I have lied to myself and to God about why I did it.
But if I can save ONE person from pharmaceutical genocide, then I pray that person or a family member will put in a good word for me, and perhaps this sorry carcass of a believer can be given one more chance.
With that said, I begin doing the only thing I have ever been ABSOLUTELY CERTAIN was of some value to my fellow humans.
I will use REMDESIVIR to knock out the artillery that is pounding the only drugs saving people from the China Virus – IVERMECTIN and HYDROXYCHLOROQUINE.
It’s THAT much of a no-brainer.
It’s just hidden behind the media’s and the Biden administration’s smoke and mirrors.
The early success from hydroxychloroquine + azithromycin (HCQ + AZT) was dead easy to see in Didier Raoult’s initial communication. I could not “unsee” that success. This is how I knew that Fauci was either incompetent or a liar. I’ve explained it many times, but not today. I’m going to save your brain cells for the KILLER SHOT.
We can skip all that crap, and just let me show you TWO GRAPHS that prove hydroxychloroquine actually works.
See that jump in deaths? The one that falls back to the baseline of the graph? That is where a FAKE PAPER known as “the Lancetgate paper”, attacking hydroxychloroquine with phony data, was published to stop the use of HCQ in several countries, including Switzerland. The problem is that the Swiss are not stupid, and when they saw that withholding HCQ increased deaths, they simply reversed course.
It shows up in the data like a sore thumb. I call it “the Lancetgate effect”.
If you’re more of a graph-reader, then you may get something out of the next one.
France is the top graph. There are a LOT more deaths. This is because a communist bureaucrat married to some top politician sneakily BANNED hydroxychloroquine right before the pandemic hit
Here you can see how the data in Switzerland immediately jumped up to French levels with the Lancetgate effect. The general decline in France you see in the middle was due to the work of Didier Raoult, whose work with HCQ+AZT was gaining prominence, slowly, from the South of France, in Marseilles, but whose efforts suffered a momentary but delayed setback from Lancetgate, visible late in the Swiss increase.
Isn’t it wonderful how graphs can reflect what’s actually happening in science? Even in POLITICIZED science. This is why keeping commie mitts off the data is so important.
This was just the beginning. More and more data showed that HCQ worked, not perfectly, by any means, but pretty well, especially if given early.
Even more importantly, when the data didn’t support HCQ, community examination of the work invariably showed that there was NASTY, TRICKY, BIASED SCIENCE by those running the studies.
That was the big shocker for me. Some of the things they did to undercut hydroxychloroquine were downright VICIOUS. Almost MURDER. Not even human. Just KILLING PEOPLE to stop the drug. They literally overdosed people on their last legs with HCQ (which is actually hard to do), to try to undermine the drug.
And THAT will prepare you for what you are about to see.
What you are about to see is almost unbelievable.
I want to thank fellow QTreeper jamcooker and her dear daughter for bringing this video about the HORRORS of remdesivir to my attention.
I was not aware that many people were either as knowledgeable or more knowledgeable than I was, about how HORRIBLE a drug remdesivir really is.
The trouble is, I was lazy. I kept TELLING people remdesivir was bad, but I never went so far as to make speeches, or put together a video, or do ANY of the things that a REAL hero would do.
Nope. I was a lazy piece of shit.
I didn’t even do a dedicated blog post – when I KNEW it was killing people. Sure, I mentioned it a few times, but I never really committed.
But hey – I can do a blog post now. It’s not that hard.
So let’s just take a look at this video, and then I’ll fill you in with even more.
All the stuff I should have told you earlier.
Here is the LINK, so that you can send the video to other people.
All his talk about the kidney damage from remdesivir?
THAT is stuff that I knew. Let me explain that.
Remember THIS moment?
This was AFTER Fauci and the media went after HCQ, and after Trump for any mention of HCQ.
So when Fauci said remdesivir was the “gold standard of care”, I went and looked at the data.
The COMMENTS from other scientists said EXACTLY what I was seeing.
It was CRAP. There is NO WAY remdesivir was anywhere NEAR as good as HCQ. And HCQ wasn’t all THAT great. HCQ saved people from hospitalization and death, but it’s not like it cured the disease overnight.
I repeat. Remdesivir was CRAP. It was EMBARRASSING that Trump had to shill this stuff, just to keep our hopes up, because FAUCI was standing up for the INDUSTRY and NOT THE PEOPLE.
Some of why remdesivir wasn’t working, was because the drug was being administered too late, when there is very little virus to kill, and all the damage has been done. It’s like shooting a vary expensive GUN at the sound of a burglar’s car going over the horizon. It’s WORTHLESS.
But the data I saw was far worse than simply not working. As one commenter said, the only thing remdesivir seemed to be really good at, was making people need kidney transplants.
Trust me. HCQ at normal doses NEVER hurts people’s kidneys. Doesn’t even HURT ’em, much less destroy them.
Think about that.
THIS? The KIDNEY KILLER? Is the “GOLD STANDARD OF CARE”?
GIVE ME A BREAK.
No, it’s the OPPOSITE.
It was CLEAR to me at the time, that Fauci was a freaking LIAR.
Trump, Fauci Cheer Gilead’s Drug Results in Coronavirus Fight
Dr. Anthony Fauci makes remarks as President Donald Trump and Louisiana Gov. John Bel Edwards looks on in the Oval Office on Wednesday. (Doug Mills/Getty Images)
By Newsmax Wires | Wednesday, 29 April 2020 12:53 PM
President Donald Trump hailed good news that a Gilead Sciences Inc. experimental antiviral drug might help fight the coronavirus, and infectious disease official Anthony Fauci said data shows it appears to help patients hospitalized with COVID-19.
Fauci said the early results of a closely watched clinical trial offered “quite good news” regarding a potential therapy made by the biotechnology company Gilead Sciences Inc.
“The data shows that remdesivir has a clear-cut, significant, positive effect in diminishing the time to recovery,” Fauci said.
An experimental drug for the coronavirus has a proven benefit, according to Dr. Anthony Fauci, the head of the National Institutes of Allergy and Infectious Diseases.
“The data shows that remdesivir has a clear-cut, significant, positive effect in diminishing the time to recovery,” Fauci said.
Just listen to the conclusions of these researchers. Remdesivir is USELESS – except to make MONEY by keeping people in the hospital LONGER. I mean, getting a new kidney might take a little bit of time. Ya know?
Conclusions and Relevance
In this cohort study of US veterans hospitalized with COVID-19, remdesivir treatment was not associated with improved survival but was associated with longer hospital stays. Routine use of remdesivir may be associated with increased use of hospital beds while not being associated with improvements in survival.
In any SANE world, they would not be administering this crap remdesivir ANY MORE to ANYONE.
It’s ESPECIALLY important to note that Fauci’s LIE about remdesivir diminishing time to recovery is DIRECTLY CONTRADICTED by the MAIN CONCLUSION of this study.
A study on veterans who did not DESERVE to be treated as they were by Tony Fauci.
Now – let’s end this on a PERSONAL note.
Remember that “overpass patriot lady” who they REFUSED to give ivermectin?
They KILLED HER with remdesivir.
And the only way that they can KILL old Trump supporters LEGALLY – while making MONEY on our dead bodies – is this way. Part of that is making sure we can’t get the alternatives.
Ivermectin LITERALLY SAVED INDIA and Fauci says there is no proof it works. When India was having a massive Delta outbreak, the Media LOVED to talk about India, India, India.
But now that Ivermectin has WIPED OUT COVID in India, the Media doesn’t want to talk about India.
Bill’s not wrong about that. There is a GREAT article on Gateway Pundit, about what happened in India with ivermectin. Their keystone province of Uttar Pradesh has been LIBERATED by ivermectin.
Look at the data in the article. The title on GP is a bit misleading – the disease isn’t GONE like smallpox, but DAMN – the numbers are IMPRESSIVE.
Now it’s time to be very realistic. They do NOT give up.
They BEAT hydroxychloroquine into the GROUND with the media.
They did it to hydroxychloroquine before – they’re doing it to ivermectin right now.
Here is an EXCELLENT summary of how Fauci KNEW that hydroxychloroquine worked, and all the while he pushed the murderous moneymaker remdesivir. Do click the link below. This has a GREAT summary of Lancetgate, and links to many relevant reviews of what happened.
In MY opinion, we cannot stop these horrible monsters by simply defending the good but imperfect treatments.
In MY opinion, we need to SLICE OPEN REMDESIVIR and SPILL BLOOD INTO THE WATER to bring in the DEMOCRAT TRIAL ATTORNEYS.
And the SOONER we do this, and the SOONER we THREATEN HOSPITALS into giving the TRULY SAFER DRUGS – not because they want to, but to keep from hemorrhaging their profits, then the SOONER we end this madness.
The BEST DEFENSE is a REAL OFFENSE.
Make them PAY for KILLING SENIORS with REMDESIVIR.
We knew it was a snake when we let it in. Now, we all have to kick it out.
In which I argue that WE are the new cell culture for an uncontrolled gain of function experiment, that only WE can end.
It took me a while to figure out WHY they insisted on using the FULL SPIKE PROTEIN for these damn vaccines. This question has bugged me from the very beginning, and it got worse and worse as more and more spike protein side effects piled up.
Thankfully, sleeping late on the morning of 9/12/ 21, I had a DREAM which finally helped me see the answer.
It wasn’t exactly Kekulé’s dream, but it served the same purpose – to accept what I had not yet been able to fully see and accept.
Now, normally I would not mention that ANY of this came from a dream. There is no faster way to lose credibility, than to say “it came from a dream” – other than saying the answer came from the voice of God. But the truth of the matter is that I often find that UNRESOLVED QUESTIONS form what might be called “motifs” in my dreams, and sometimes I actually get some kind of resolution FROM the dreams.
If I tried to explain the dream itself, it would be almost meaningless to you. Things shift and change in dreams. Stone becomes brick becomes concrete and then vanishes. Stairs appear and disappear. People are there and people are gone, to be replaced by different people. One location changes smoothly into another location.
All of THAT is a jumble. This dream was a real doozy, too. Crazy! But in the dream I kept trying to resolve something – actually TWO things – which were composed of collections of ideas. These two things were like little, linear, diagrammatic collections of jewelry boxes, and it was impossible for me to SAY anything useful about the two collections, and how they related to each other, without actually interacting with them and looking into the jewelry boxes in some fashion or another, and in doing so, the collections were no longer separated and isolated from what might be called “everything else”.
It was IMPOSSIBLE for me, in the dream, to separate these things from “everything else”, if I wanted to know anything about their reality.
When I woke up, I realized the point of the dream.
The point of the dream was that the two things – IN REALITY – were both connected not only to each other, but to everything else. The point of the dream was that I needed to look at how the two things EACH interacted with everything else, to see how they were TRULY related to each other.
Not how they were SUPPOSED to be related to each other, but how they are ACTUALLY related to each other.
And THEN – in the “generality” of that moment – I realized that this “model”, if you will, applied to the COVID-19 VIRUSES (one collection) and the mRNA VACCINES (the second collection). And in THAT moment, I stopped looking at them as ANTAGONISTIC things, just because a LIAR named Fauci says they are antagonistic, but instead as SIMILAR and COMPLEMENTARY things.
As genetic material.
THAT is when “IT” hit me.
I woke up fully, and realized the following.
The VIRUSES and the VACCINES are DESIGNED to interact with each other in the realm of “everything else”, that being us humans. They are NOT designed to interact in the way we are being told. They are designed to interact in the way that they ACTUALLY DO interact.
Let me give you a simple representation of this relationship.
Consider a square. Color the top side GREEN – that represents “everything else”, not as it “should” be, but as it REALLY IS. Every point on that line segment is part of the world, relating to other points in the ways that they REALLY DO, in a “green” way. It’s ALL GREEN.
Now make the bottom two CORNER POINTS the two collections. Connect those points to the top of the square by green lines – the left and right sides of the square. Again, this is how they REALLY connect.
We are being TOLD that the bottom side of the square is RED.
Why should we believe that? What if it’s NOT red? What if it’s GREEN? What if there is a simpler GREEN ANSWER?
And IMMEDIATELY I knew what the GREEN ANSWER WAS.
The mRNA “vaccines” encoding a spike protein are designed to do in HUMANS containing the virus exactly the same thing that similarly added spike protein mRNA does in CELL CULTURES containing the virus. They are designed to CHANGE THE VIRUS – to make it GAIN FUNCTION. ALL that is needed to create the new virus is an otherwise identical injection with a NEW CODE that GAINS FUNCTION.
In other words, genetic vaccines offer an opportunity to smoothly regulate the rate and direction of evolution of the virus, without humanity knowing it. And they do it IN THE ANIMAL HOST INTENDED.
This solved many mysteries, which I will explain shortly.
This told me that there is ZERO need to go off and create a new variant in a lab. All one has to do is to change the code of the vaccine mRNA, and PRESTO – a new variant is introduced “in the wild”, with almost no chance of getting caught.
At this point, many of you are doing a WTF, so let me back up and explain this again.
What science does to “create a new virus” in the laboratory, from RNA or DNA, is to “somehow” (COUGH, COUGH, COUGH) get the RNA or DNA that they want to get into the NEW VIRUS, into laboratory cell cultures that are making OLD VIRUS. They need to get it into the cells, pretty much like they get the vaccine mRNA into our cells, using nanotech or virus vectors. THEN, the “old virus process” slips the “new genetic instructions” into the old protein shell, but as the virus spreads and multiplies, IF there is any “gain of function”, then the NEW INSTRUCTIONS in the NEW protein shell will WIN, and the result will be THE NEW VIRUS with GAIN OF FUNCTION.
Nobody really wants to spell out all the details of gain of function techniques in public, just like they don’t want to give the directions of how to make high explosives to terrorists. But THAT KNOWLEDGE IS OUT THERE, and we know roughly HOW THEY DO IT.
Honestly, it’s a bit like plant grafting, only instead of being largely in the Z DIRECTION (up), it’s in the T DIRECTION (time). You GRAFT new instructions into an old virus, until the new virus TAKES.
What they have done here is to create a PLATFORM for genetic change. Eventually it will be used to change US, but for the moment, they are clearly using it to CHANGE THE VIRUS (which is used to help change us, albeit somewhat indirectly).
Now – I said that this solved many mysteries. I’m going to list them here.
Why the full spike protein in the vaccines, despite its toxicity, and the greater likely safety of vaccines based on smaller subunits like the RBD?
Because the full spike is the main part of the virus that they’ve been changing, and which “gains function”. To get a new virus with a new spike, you have to change the instructions for the spike that get encoded in the virus. Also because you want to include the genetic instructions for ONE OR MORE FULL PIECES of the virus, if not the entire virus. That depends on exactly how the virus builds. We know (the Jaenisch paper) that the virus uploads fragments of its own RNA into the genomic DNA of the host, which come back out and are transcribed to RNA, so it will presumably do the same to pieces of the vaccine when both are present. Viruses that build from the vaccine spike variants will tend to WIN if they have gained function.
Why mRNA vaccines, despite the obvious safety advantages of protein vaccines?
Because protein is GENETICALLY SAFE – and that is NOT what they want. If the human population is now the experimental platform for virus gain-of-function experimentation, then only by being able to inject us with mRNA or DNA will viruses be able to be swiftly and decisively modified IN VIVO.
Short answer – they are not trying to change OUR genes yet – but they ARE trying to change viruses IN US. In vivo. And not in a way for our own good.
Why did they fight so hard against short-protein subunit vaccines like those from Winfried Stöcker and Sorrento?
Because if those vaccines are clearly superior to genetic vaccines due to safety or efficacy, then the conspirators will LOSE THEIR PLATFORM for genetic modification of viruses IN VIVO in the human population. Thus, these likely safer subunit and PROTEIN vaccines encountered delay after delay, and roadblock after roadblock, and in the case of the Stöcker vaccine, threats of arrest and legal trouble.
Why is Ralph Baric now doing work on chimeric mRNA vaccines that include LONGER mRNA encoding MULTIPLE proteins from SARS-CoV-2?
Because this approach toward longer and more mRNA leads closer to what they need to do – to inject us with the complete instructions for modified viruses – basically as what are called “virus-like particles” (VLPs), or by using viral vectors. These are “Fauci-compliant” in that they are “all about more and more antibodies”, and thus follow Fauci’s “antibody hypnosis” act, but clearly they will have more and more side effects, possibly including ADE.
As you can see, the vaccines are “less and less about natural immunity”, less and less about individual health, and more and more about experimentation and sociobiological engineering.
What does this have to do with Judy Mikovits?
Judy is one of the few people who have honestly explained the GAMES that the Faucists are playing with gain of function.
https://www.youtube.com/watch?v=0B17QQTr6xY
She explained that what these people have done – in complete violation of the CONTROLS that were placed on genetic engineering back in the 1970s – is to FORCE VIRUSES to “take” in human cells, allegedly in order to “see if they can or cannot take in human cells”. They are basically saying “we have to try hard to change the liquid to make the liquid catch fire, to see if it’s flammable”. This is a special kind of dishonesty.
There are MANY ways to make a virus “gain function”, but one of the FIRST and SIMPLEST is to just use tricks to make it change enough on its own, to eventually “take” in human cell culture.
It’s a lot like Nancy Pelosi and Obamacare – “you have to pass it to see what’s in it”. That is a special kind of cynical dishonesty, IMO.
But NOW they have actually HIDDEN gain of function research in PLAIN SIGHT. In us. Thanks to genetic vaccines.
Why did Adam Schiff go after Natural News and get them deplatformed?
Because the greatest danger to their plan is that humans will reject the future of human genetic modification IN VIVO. Natural News and their movement are a focal point of organized opposition. The Democrats KNEW this was coming, and they wanted the opposition out of the way.
This is also why so much work goes into discrediting these people.
But if the vaccine is for the SAME spike protein as in the virus, then how is THAT gain of function?
It’s NOT. It is ONLY if the vaccine contains DIFFERENT genetic material, DIFFERENT instructions, that any possibility for CHANGING the virus ensues.
Now tell me how you are going to go into EVERY vaccine that is given ANYWHERE in the world, and make sure that the mRNA doesn’t encode a new variant?
You can’t. That’s the evil genius of this plot.
If I want to introduce a variant ANYWHERE, all I have to do is give out a vaccine at the target location, where my vaccine looks just like the official stuff – or maybe even IS official stuff – but mine contains whatever genetic data is needed for a new virus, inside the same old nanotechnology.
You see – WE. HUMANS. OURSELVES. ARE. NOW. THE. GAIN-OF-FUNCTION. PLATFORM.
Pretty slick, if you ask me.
Could this platform be used for ADE as an intended effect?
Yes – because the variant that challenges prior antibodies is controlled by whoever launches the variant – and if that person or group is the same one controlling the vaccines, then TOUGH LUCK. And the ADE could be pinpointed in space and time, pretty much like Stalin’s Holmodor against the middle class in Ukraine. This platform of viral control can be used to control people at the individual, family, local, regional, state, national, continental, and global levels.
If we stop using these vaccines, will the variants stop?
They might stop. It will become much harder for the variants to appear, whether they are natural, and arise from vaccine evolutionary pressure, or are man-made, and require the vaccines for delivery.
Some of the best early opinions, IMO, thought that the initial genetic drift of SARS-CoV-2 was sufficiently small, that a single vaccination would cover all likely variants. While I’m not highly confident in that thought any more, I think it indicates that drift would be small, were it not for the vaccine.
So which is the plot – the virus or the vaccine?
AND logic – it’s BOTH OF THEM – the message of the dream. And it’s BOTH OF THEM in the SAME context that it would be in HUMAN CELLS. We are just “human cells on the hoof”.
The virus is out – and now they can change it “in the wild” thanks to GENETIC VACCINES – the greatest cover for genetic experimentation on viruses and humans that was ever conceived.
So how do we stop this plot?
Easy. We utterly reject genetic vaccines as a RISKY PLATFORM FOR TREATING VIRAL DISEASE, because they can be used to manipulate the disease and the diseased. The risks are not just individual – they are SOCIETAL as well. So we make them highly illegal. To get there, we use CIVIL DISOBEDIENCE FIRST. We REFUSE genetic vaccines.
For those who want vaccines, we go to old-school, time-tested, PLOT-SCUTTLING, protein vaccines. And all VOLUNTARY.
We don’t call this a RELIGIOUS objection. We are honest and call it a MORAL OBJECTION. If, however, your CHURCH OR SYNAGOGUE takes up the sword of abolition, and adheres to the morality of rejecting genetic vaccines, e.g., as considering them a form of “tempting the devil”, then you CAN validly call it a religious objection, too.
However, as an ETHICAL objection, like the objection to SLAVERY, all humans can take part.
Make no mistake – we are now in a literal HUMAN GAIN OF FUNCTION EXPERIMENT, using the whole human population as test subjects, and genetic vaccines as the obvious GOF vector.
The only way to STOP THE EXPERIMENT COLD, is to STOP USING GENETIC VACCINES.
Simple. Don’t let the snake in. Or if you HAVE let it in, kick it out!!!
