Please watch yet another powerful video of another severely ill, hospitalized patient who recovered after he was allowed ivermectin. Ivermectin works at every stage of the illness but it’s best when used early on. Unfortunately, despite these stories and the now 90 studies from 963 scientists in 27 countries showing statistically significant improvement in mortality, ventilation, ICU, hospitalization, recovery, cases, and viral clearance, the drug is still banned for COVID in hospitals and for COVID in general.
Florida doctor claims he’s treated 3,000 COVID-19 patients with human version of ivermectin
This news video may get censored, so view it quickly. The article can be found here.
In short, a Florida doctor has a target on his back and has already been suspended from one hospital and fined $500 for prescribing ivermectin for COVID. However, patients are speaking out and stating that within hours of taking it, their symptoms started to disappear.
An elderly man was suffering from non-Hodgkin’s lymphoma and just finished chemo and was one of the first patients to get the COVID shot. He got COVID months after the jab. His daughter advocated for him to receive ivermectin due to the fact she herself was successfully treated with it and that after only ONE dose she “felt so much better.” (This was my experience as well)
Not until day 6 and the patient’s transfer to the ICU did a doctor agree to try ivermectin. His daughter states he was “going downhill every day” until he was given ivermectin and there was improvement.
A retired nurse got COVID and decided against the COVID shots for personal reasons. When her oxygen became low she called the Florida doctor and he prescribed ivermectin. She states “Within two hours I was starting to breathe better.”
Congressman Neil Dunn, former Chief of Staff at the Gulf Coast Hospital wrote an Op-Ed noting several global studies that found ivermectin works for COVID. He states that those saying there’s no evidence for ivermectin are willfully ignorant of the true literature. He also states that the federal government refuses to follow the scientific evidence and take a comprehensive approach to fighting COVID.
Mainstream media and the spin-doctors do not want you to know the end of the story. The elderly Sun Ng made a full recovery after a court ordered the hospital to give him ivermectin. A measly 5 days of treatment saved his life.
Sun Ng
This occurred after he had already spent 22 days on a ventilator. Imagine what would have happened if he was treated early.
Despite the court’s decision, the hospital refused to let the doctor into the hospital on the grounds that he was not “vaccinated” against COVID-19.
Following this, “An Emergency Report” was filed with the court first thing on Monday morning, Nov. 8, after brief argument from both parties, Judge Fullerton admonished Edward Hospital’s representatives and restated that he ordered them to let Dr. Bain in to the hospital on Friday to administer the life-saving drug.
12,700 doctors and scientists have signed the Rome Declaration and have endorsed ivermectin as a COVID treatment.
A Chicago-area judge saved a grandfather’s life with the single question that exposes hospitals blocking doctors from using a safe, FDA-approved drug: Why?
Sun Ng, a retired contractor from Hong Kong, traveled to Illinois to celebrate his only granddaughter’s first birthday. He got covid and was near death in a Chicago-area hospital. All other options were exhausted, but the hospital refused to give Mr. Ng a generic, FDA-approved drug with an extraordinary safety record that a doctor believed could safe his life.
Finally, a judge asked the right question about ivermectin.
“What’s the downside?”
Put another way: If a man is dying of covid in an ICU and all else has been tried, why not order a hospital to give a safe, last-ditch drug?
Edward Hospital, located near Chicago, offered three arguments as to why Sun Ng, seventy-one, should not be given ivermectin:
There could be side effects.
Ordering ivermectin would violate its policies.
Forcing the issue would be “extraordinary” judicial overreach.
On each argument, DuPage County Circuit Court Judge Paul Fullerton firmly disagreed. (See link for article)
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Summary:
An internist ultimately administered a five-day course of 24 milligrams of ivermectin, from November 8 through November 12. The doctor stated: “Every day after ivermectin, there was accelerated and stable improvement,” said Dr. Bain, who administered the drug in two previous court cases after hospitals refused. “Three times we’ve shown something,” he told me. “There’s a signal of benefit for ventilator patients.”
Meanwhile Edward-Elmhurst Health, the hospital’s managing system has thwarted ivermectin, and even after Ng’s treatment benefitted him, the hospital system filed notice that it would appeal the order it had already carried out. (You call this CYA or “cover your a _ _ )
A nurse had the audacity to suggest the patient stop all care and die naturally. Wow.
With only a 10-20% chance of survival, the judge listed ivermectin’s possible side-effects from a government website: dizziness, pruitus, nausea/diarrhea, and stated that effects were so minimal that the patient’s condition outweighs risks by 100-fold.
A Kool-aid drinking doctor had the audacity to state that the risk of ivermectin gives no benefits.
This patient’s cases is the costliest with three decisions, four court appearances, and now an appeal that is certainly moot. The attorney battled another case in the same health system that involved Nurije Fype, age sixty-eight. Her case inspired Dr. Ng to file suit. Fype, who is probably only alive today due to judicious treatment with ivermectin, is now four and a half months downstream and doing great.
While Ng isn’t out of the woods, ivermectin has made a clear difference, even in his late stage of illness – Similarly to Lyme/MSIDS, imagine what would have happened if he was treated early…..
Top ICU Doctor Suspended After Suing Hospital for Banning Life-Saving COVID Treatments
In an exclusive interview with The Defender, Dr. Paul Marik said patients are dying “unnecessarily and unlawfully” because the hospital where he is director of the ICU prioritizes expensive drugs like Remdesivir while banning more effective and less costly treatments.
A top critical care physician who filed a lawsuit against Sentara Norfolk General Hospital over its ban on administering life-saving drugs to treat COVID patients, has had his hospital privileges suspended.
Dr. Paul Marik, chief of pulmonary and critical care medicine at Eastern Virginia Medical School and director of the ICU at Sentara Norfolk General Hospital, learned about the 14-day suspension when he arrived to work on Saturday and found a letter on his desk.
The letter was dated Nov. 18 — the same day Marik appeared before a judge in Norfolk Circuit Court requesting a temporary injunction to lift the ban, Marik’s attorney said.
Judge David Lannetti did not grant the temporary injunction, but did determine Marik had standing to bring his lawsuit, allowing the case to move forward which will give Marik the opportunity to “establish his right to administer life-saving treatments that patients have been prohibited access to by Sentara,” the Front Line COVID-19 Critical Care Alliance (FLCCC) said in a statement.
Sentara’s attorneys didn’t tell Marik about the suspension during Thursday’s hearing, nor did they mention it to the judge, said Marik’s attorney, Fred Taylor, a partner at the Virginia law firm Bush & Taylor.
In a Nov. 22 letter to the judge, Marik’s attorney accused Sentara of making a material misrepresentation during the hearing by failing to disclose the letter and telling the court the hospital would not retaliate against Marik for filing the lawsuit.
“Evidently Sentara chose, for reasons of its own, not to disclose this suspension either to the court or the plaintiff during the hearing,” Marik’s attorney told the judge.
In his letter, Taylor told the judge:
“The letter [from Sentara to Marik] gives no explanation whatsoever for the ‘coincidence’ of Sentara’s choosing to suspend Dr. Marik at this particular moment, leaving only one realistic conclusion. Sentara has engaged in a blatant act of retaliation against Dr. Marik for filing this suit and for exposing to the public Sentara’s unlawful unjustified denial of safe, potentially life-saving medicines to its COVID patients in violation of Virginia statutory law and public policy.”
In Sentara’s letter to Marik, hospital officials summoned Marik to a proceeding scheduled for Dec. 2 during which, the hospital said, “no lawyer representing Dr. Marik will be permitted and no recording/video or transcript … will be made.”
Sentara said its suspension of Marik was based in part on an allegation that he informed COVID patients that his “hands were tied” and there was nothing more he could do for them.
Taylor’s letter to the judge stated:
“At the just-concluded hearing on November 18, 2021, Sentara expressly represented to this Court that it would not discipline Dr. Marik in any way for informing his COVID patients that Sentara was preventing him from giving them alternative treatments that are, in his medical judgment (and based on unrefuted evidence) safe, and potentially life-saving and medically appropriate for them.
“Yet, Sentara has now done exactly that. Indeed it had apparently already done exactly that when it was representing to the Court that it would not do so. International or not, this was a materially false representation made to the court, and Plaintiff respectfully requests that Sentara be held to account for it.”
During the Nov. 18 hearing, Sentara’s attorney, Jason Davis, raised the issue of whether Marik has standing in the case. To have standing in a lawsuit, Marik needed to show he had a stake in its outcome or suffered an injury.
Sentara said Marik did not have standing to bring his case because he hadn’t been harmed.
“Obviously, patients who are dying in the ICU can’t come to court,” Marik told The Defender. “Sentara hospital lied continuously and incessantly but at this type of hearing, I was not in a position where I could challenge the falsities.”
Taylor accused Sentara of attempting to deprive Marik of standing through a “retaliatory, pretextual suspension that Sentara kept secret from the Court, perhaps hoping Dr. Marik would respond to Sentara by offering to drop his suit if Sentara would withdraw its suspension.”
In his letter to the judge, Marik’s legal team called for a supplemental hearing to redress the new facts previously hidden from the court by Sentara.
Sentara ban on certain COVID therapies violates U.S., Virginia medical laws, lawsuit alleges
Marik filed his lawsuit against Sentara Healthcare on Nov. 9, arguing the organization is endangering the lives of its COVID patients by preventing him from using his treatment protocol, which he says has reduced mortality rates in the ICU from approximately between 40% and 60% to less than 20%.
The lawsuit alleges Sentara’s ban on the use of certain therapies against COVID violates U.S. and Virginia medical laws and the concept of informed consent — whereby “patients have the right to receive information and ask questions about recommended treatments so that they can make well-considered decisions about care.”
Marik called Sentera’s ban on administering certain medicines for COVID patients “unprecedented” and “cruel” during his Nov. 18 testimony requesting a preliminary injunction to lift the ban.
In his motion, Marik said patients are dying “unnecessarily and unlawfully” because Sentara Healthcare is “preventing terminally ill COVID patients from exercising their right to choose and to receive safe, potentially life-saving treatment determined to be appropriate for them by their attending physician.”
In an interview with The Defender, Marik said the hospital is prohibiting the use of a COVID protocol called “Math +.” The protocol includes treating COVID patients with many drugs approved by the U.S. Food and Drug Administration (FDA) which has determined the drugs are safe and effective.
Instead, according to the lawsuit, Sentara recommends doctors use “toxic drugs” like Remdesivir — an expensive medication associated with severe side effects — because the hospital receives a bonus each time doctors prescribe it.
“This case is about doctors having the ability to honor their Hippocratic Oath, to follow evidence-based medicine, and to treat our patients the best we know how. Corporations and faceless bureaucrats should not be allowed to interfere with doctor-patient decisions, especially when it can result in harm or death.”
“Our COVID-19 protocol is based on the best scientific data available, yet Sentara claimed the medications I used were toxic and harmful, which is an absolute lie,” Marik told The Defender. “It is so outrageous.”
Marik explained:
“What happened was I was using MATH+ and I was using these medications, which I think are effective. All drugs we use are FDA- approved and very safe and they’ve been proven to be very effective for COVID, but I was banned from using them because they were dangerous, toxic and there was supposedly no data to support their use. It’s a big lie.
“What they [the hospital] want me to use is Remdesivir. We know Remdesivir increases death by 3%, increases the risk of hospital stay and increases the risk of kidney and liver failure. It does not improve patient outcomes. It is toxic. But the hospital gets a bonus if Remdesivir is prescribed. They profit from the expensive drug but not the cheap drug that people can afford.”
Marik, a highly published physician with 35 years of experience, said Sentara also tried to criticize his character, even though they appointed him as the director of ICU.
Marik said he could no longer stand by while patients died unnecessarily without proper treatment, so he had no choice but to file a lawsuit allowing him and his colleagues to administer a combination of FDA-approved drugs and other therapies that have saved thousands of critically ill COVID patients in the last 18 months.
Until September, doctors had been allowed to use ivermectin and the other medicines — ascorbic acid (Vitamin C) IV, bicalutamide, dutasteride, finasteride and fluvoxamine — to treat COVID patients.
But after the FDA, Centers for Disease Control and Prevention (CDC) and National Institutes of Health (NIH) warned against using ivermectin and other medicines for COVID patients, Sentara officials created new guidelines ordering doctors not to use the drugs.
Marik argued Sentara’s COVID Comprehensive Treatment Guidelines are “preventing terminally ill COVID patients from exercising their right to choose and receive safe, potentially life-saving treatment.”
Math+ protocol used around the world to safely treat COVID
According to an FLCCC press release, the MATH+ protocol, used by Marik and physicians around the world to treat COVID, is saving lives. However, since the prohibition went into place, there has seen a sharp rise in inpatient mortality.
Marik said he and his colleagues started using the Math+ to treat COVID in March 2020, because the national and international bodies provided no guidance. “So we put together guidelines and started using the protocol on March 24, and it has evolved over time as science has evolved,” he said.
The MATH+ protocol, designed for hospitalized patients, counters the body’s overwhelming inflammatory response to the SARS-CoV-2 virus.
The protocol is based on numerous medical journal publications and decades of research — and is founded upon the belief that hyper-inflammation, not the virus itself, damages the lungs and other organs and leads to death.
The MATH+ protocol is well-tolerated with no reports of adverse medical events, FLCCC said in a press release.
According to Dr. Joseph Varon, a renowned critical care specialist recently recognized by the United Nations for his life-saving work, the MATH+ COVID treatment protocol has achieved at least a 50% reduction in deaths from the virus in the hospitals where he serves as chief of staff.
“We take an oath as doctors to do no harm,” said Dr. Pierre Kory, president and chief medical officer of FLCCC. “I can’t think of a way of doing more harm to a patient than to not administer a treatment that you know can help them. No doctor should be forced to watch their patient die knowing that more could have been done to save them, and that is exactly what Sentara is doing.”
Medications are safe and FDA-approved, but hospital wants to use ‘toxic’ drugs
Marik said until Oct. 5, he was able to use most of the medications on the MATH+ protocol except for ivermectin, which was banned in May or June.
“They’re turning this into an ivermectin thing and it’s a very safe drug — more people have died from aspirin or Tylenol,” Marik said. “It is one of the safest drugs on the planet and the data is irrefutable, but somehow with COVID it has become a toxic medication.”
Marik explained:
“What do you have to lose when a patient is dying? When a patient is dying we do everything we can to save their lives and this system and many others are prohibiting them from getting every possible medication they can. That’s how we practice medicine, we do what we can to save the person.”
Marik said it is important for people to understand that 40% of drugs in the ICU are used off-label. “That’s the standard of care,” Marik said. “Pre-COVID, the FDA encouraged use of off-label drugs and you didn’t need informed consent to use them.”
Marik said 30% of drugs prescribed in the hospital settings are used off-label and 90% of people are discharged with prescriptions for drugs being used off-label.
For example, Marik said aspirin is recommended for atrial fibrillation — an irregular heartbeat — but that’s an off-label use. With MATH+, Marik said he can talk to families to see if they want to do it, but he can’t prescribe it. Their only option is to take a toxic therapy or transfer to another hospital potentially hundreds of miles away to utilize an alternative protocol.
Marik said:
“I try to emphasize these patients are dying. That’s why they’re there. It’s an absurd proposition to propose that I get consent from the family — or tell the families they have alternatives, but I can’t use them here, and then I have to transfer them to another hospital, which is very time-dependent.
“The longer I wait, the worse the outcome and it’s a major undertaking. To transfer an ICU patient hundreds of miles away to another hospital is impracticable.”
Marik said the hospital thinks they can do whatever they want because they control the media and they control the press, and he was put in a position where we had no option but to bring the suit.
Sentara pressured scientific journal to retract paper on COVID treatments co-authored by Marik
According to MedPage Today, the same day Marik filed his lawsuit, the Journal of Intensive Care Medicine (JICM) retracted an article, co-authored by Marik, on the MATH+ protocol, which includes the use of ivermectin.
Marik said the hospital pressured the journal to retract the article because it supported the use of alternative protocols, and showed a reduction in ICU mortality.
The retraction notice cited a communication it received from Sentara Norfolk General Hospital, “raising concerns about the accuracy of COVID-19 hospital mortality data reported in the article pertaining to Sentara.”
“Sentara Healthcare felt obligated to reach out to JICM with our concerns about Sentara Norfolk General Hospital data that the authors used to make conclusions, and provide accurate data to the journal. After a thorough review by JICM’s editorial board, the article was retracted. The journal followed their retraction guidelines and procedures.”
Taylor told MedPage Today in an email, the lawsuit is not about a journal article.
“This case is about whether a hospital administration can legally prohibit critically ill COVID patients from receiving information — and treatment, if they so decide it is medically appropriate for them — about safe, FDA-approved, and potentially life-saving medicines as determined by their attending physician,” Taylor said.
A Sentara spokesperson said in a statement to MedPage Today:
“Sentara generates treatment guidelines by engaging multi-disciplinary groups of clinicians to review literature, care standards and provide expert advice. In most situations, physicians are able to deviate from guidelines to individualize care for patients. However, in some scenarios, treatments that may potentially harm patients or that are widely considered to be outside the standard of care may be limited.”
The spokesperson said the CDC, NIH and FDA “currently do not recommend the use of ivermectin as a treatment for COVID-19 due to a lack of evidence regarding its safety and efficacy.”
Marik said when he and his colleagues published their paper on MATH+, they published statistics from Sentara.
“The hospital has their own protocol and they weren’t happy the director of the ICU was using his protocol and not their protocol,” Marik said. “It was a review paper and in it we quoted mortality statistics from Sentara. The chief of the hospital gave me the data on the mortality statistics, and we had approval from the Institutional Review Board to collect data and publish it.”
After it was published, Marik said they accused them of providing false and misleading data.
“The data is accurate but obviously, with time there are some additional patients that are going to die, and that’s inevitable with any paper,” Marik said. “On follow-up, mortality went from 6.6% to 10%. They complained to the medical school, and the medical school agreed with me.”
Marik said he updated the journal article to include a note, but Sentara pressured the journal to retract the article, claiming the data was false, and then used the fact the journal article was retracted against him.
Marik said he did not bring this lawsuit because he has something to gain, it’s because he has a responsibility to his patients and physicians across the country and the world.
“I think what they need to know is that the hospital is interfering with the physician and patient relationship. The physician decides what is in the best interests of the patient, and what they’re doing is unprecedented,” Marik said. “The hospital is telling me how to treat my patients, and it goes against basic Hippocraticic principles.”
Marik said he refuses to watch another patient die from COVID knowing he was not allowed to give them proven treatments that could have saved their life.
“This case is a test case that will have implications for physicians and patients across the country,” he said.
This nifty FLCCC graphic clearly shows that African countries with community directed ivermectin treatment programs had much lower morbidity and mortality and were the strongest predictor of improved survival and recovery rates of COVID. Ivermectin distribution programs should be considered in any region with rising case counts and fatalities from COVID.
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According to another doosie on Medpage, the authors are scratching their heads in perplexity over why those in Sub-Saharan Africa aren’t struggling with COVID.
Gee, could it be that everyone is taking ivermectin for river blindness, that “horse-dewormer” that supposedly doesn’t work for COVID?
More than 99% of those infected with river blindness live in 31 countries in sub-Saharan Africa: Angola, Benin, Burkina Faso, Burundi, Cameroon, Central African Republic, Chad, Republic of Congo, Côte d’Ivoire, Democratic Republic of the Congo, Equatorial Guinea, Ethiopia, Gabon, Ghana, Guinea, Guinea-Bissau, Kenya, Liberia, Malawi, Mali, Mozambique, Niger, Nigeria, Rwanda, Senegal, Sierra Leone, South Sudan, Sudan, Togo, Uganda, United Republic of Tanzania.
How have they dealt with the problem?
Between 1974 and 2002, disease caused by onchocerciasis was brought under control in West Africa by spraying of insecticides against blackfly larvae and by large-scale distribution of ivermectin since 1989.
BINGO!
But, mainstream medicine, media, and all the Pharma-shills can not see the forest through the trees because ivermectin is, as the German’s say, “Verboten!”
“Fewer than 6% of people in Africa are vaccinated. For months, the WHO has described Africa as ‘one of the least affected regions in the world’ in its weekly pandemic reports.”
Gibraltar, the most vaccinated region, at 140%, is canceling Christmas.
This is no surprise nor a mystery to scientists who have been paying attention,” writes James Lyons-Weiler.
Weiler also states that In April, 2020, he reported that immune deficiency due to autoimmunity against immune proteins was likely due to #PathogenicPriming from similarity between SARS-CoV-2 viral proteins and human immune proteins. Go here to watch a passionate plea from Weiler, where he explains that not a single vaccine manufacturer removed these unsafe epitopes after he notified them.
But this too is an inconvenient truth that will never be reported in the news or believed by card-carrying COVIDians.
An abstract by Dr. Steven Gundry shows the COVID jabs increase endothelial inflammatory markers & acute coronary risk as measured by the PULS cardiac test which persists for at least 2.5 months post 2nd dose. This means the jabbed’s immune system is busy fighting the spike protein for at least 2.5 months.
Efficacy is below 50% for every shot now and no one is addressing what happens when the “vaxxed” become infected with a mutating SARS-CoV-2 virus, when their immune systems are busy fighting an out of control spike protein in their bodies.
Revisiting Incarnation Children’s Center – AIDS Drug Trials
February 23, 2014
(LIAM SCHEFF) – In 2004, I broke open the NIH Clinical Trial Scandal, the internationally-covered story of hundreds of New York City orphans used by government agencies and pharmaceutical companies in deadly AIDS drug trials.
In reporting this issue, I entered the orphanage where children were being used as guinea pigs, and over a period of several years, took interviews with mothers, children and childcare workers at the Incarnation Children’s Center. I also interviewed the medical director, and investigated the FDA documentation and published medical literature on the tests and drugs used, drugs which were often force-fed through nasal and gastric tubes to the children. I reported several deaths in children, and although the mainstream denied that any deaths were due to drug toxicity, they admit that over 200 children died.
(See link for article)
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**Comment**
Your tax dollars at work, directed by Dr. Fauci, head of the National Institute of Allergy and Infectious Diseases (NIAID) since 1984 – and current Hollywood star for COVID propaganda. Please take the time to listen to 10 full minutes of COVID contradictory propagandafrom our leaders, including Fauci.
Summary:
NYC hired Vera Institute to create a final report on this inhumane experiment but weren’t given access to the children’s medical records. The VERA investigator refused to take data from Scheff that listed the trials, drugs used, and recorded ‘black box’ warnings.
The report stated that out of 532 children in the study, 25 died directly during the study, another 55 died later in foster care, and the Director at VERA as of 2009 stated that 29% of the remaining 417 had died. In a follow-up interview, the head of VERA admitted that many more children had died.
According to this: one staff member, Jacklyn Hoerger, spoke out about the deceitful protocol:
“We were told that if they were vomiting, if they lost their ability to walk, if they were having diarrhea, if they were dying, then all of this was because of their HIV infection. I just faithfully gave it as I was told by doctors.” Fauci and the NIAID claimed the drugs and vaccines were the only chance for survive. (Sound familiar?)
Hoerger put that theory to the test and adopted two half-sisters. She removed the children from the experiments and watched them recover.The girls began eating properly for the first time in their lives and improved “almost instantaneously.” Hoerger concluded that the drugs were causing the children’s bodies to shut down. When the doctors and administrators found out she was ostracized as a “negligent parent.” The girls were taken from her and she wasn’t allowed to see them again.
Fauci wanted adherence at all costs – even the children’s well being. No matter what happened, doctors could blame HIV; however, NIAID and their partners presumed all the children had HIV. They never used any laboratory confirmation. (I will add that PCR testing for HIV is just as abysmal as it is for COVID and should never be trusted by itself for diagnosis)
What isn’t discussed is the fact that when parents withdrew consent, their child was removed and placed in a foster home that would comply.
Watch the documentary “Guinea Pig Kids”, and read Celia Farber and the late Liam Scheff’s expose’ on these crimes against humanity, which also a WBAI New York news-report
Both Wikipedia and the NY Times covered up the sordid details and heralded it as one of the great successes of AIDS treatment. They erroneously state that doctors obtained permission for using the foster kids, but admits that the “permissions” for many of these children are “missing,” (or were never there). They also didn’t review the children’s medical files – but still conclude it was a medical success.
Fauci got away with crime, and appears to be getting away with the current crimes against humanity regarding COVID. He’s known by many as “the Teflon man” as nothing sticks to him.
What will it take to develop new drugs for Lyme disease?
Dr. Raphael Stricker, a San Francisco internist and hematologist, is an internationally recognized leader in tick-borne disease diagnosis and treatment.
He is also a board member of LymeDisease.org.
Dr. Stricker recently delivered a recorded overview of tick-borne diseases to the European Society of Medicine Congress 2021. The title of his talk was “Lyme Disease: The New Pharma Frontier.”
As he notes in his introduction,
“Over the past year, there have been at least four novel antiviral drugs for Covid-19 that have been developed. It’s disappointing that we haven’t seen the same kind of drug development for Lyme disease over the years. [In this presentation], I’d like to focus on that type of drug development.”
Click below to view his talk.
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To answer the question: we, the sick, must do it ourselves.
https://madisonarealymesupportgroup.com/2019/10/15/disulfiram-psychosis-update/ While not fun, I’m glad I used it and went through this so I can serve as a warning to others – particularly single patients. I would not recommend this drug unless you have family/friends around you. When you go nuts, you don’t know it. The psychosis is very real. Since disulfiram has such a long half-life, it stays in your body for a long time. The anti-psychotics to reverse the effects are riddled with side-effects. I spent $20K in the UW hospital with the most severe toxic reaction to disulfiram they have ever seen. “Mad as a hatter” doesn’t even describe it. I’ve spoken with local Lyme literate doctors whom have all had patients go South on it, so it wasn’t just me.
Madison Area Lyme Support Group 
