Dr. Lutchmedial received his third injection, aka “booster,” on October 24. He attempted a play on words to celebrate his third shot, calling it “Vax Shot 3: Electric Flu-Galoo.” It is an apparent reference to the 1984 film “Breakin’ 2: Electric Boogaloo.” However, there is no third Breakin’ movie. Dr. Lutchmedial said he expected to feel sick after the shot because “my immune system is ramped up!”
His last Facebook post was published on November 7 at 3:10 p.m. local time. It was about visiting friends and family (his kids) at the University of Guelph in Ontario. Dr. Lutchmedial “died in his sleep” on November 8, according to CBC News.
Mr. Kazmarek passed away on October 2. His widow, Cecelia, who was also his weightlifting partner, is having a difficult time dealing with the situation. The couple just celebrated their third wedding anniversary on August 18.
Mr. Kazmarek is also survived by his mother, father and two siblings.
Mr. Kazmarek spent a lot of time in gyms. In fact he and his wife shared that passion.
Granted it is a small sample size. But we also covered the story of Mr. Michael Mitchell. He was a bodybuilder and died six days after his Pfizer mRNA “booster” shot. We’re not going to speculate as to these men’s workout routines and diets, if you will. However, you’d think being in good physical shape with a lot of lean muscle mass would be good for overall health and fighting off negative effects from artificial spike proteins. That was not the case with Mr. Kazmarek and Mr. Mitchell.
Sadly this is yet another case of surrendering to the enemy. Mr. Kazmarek knew there was some sort of sinister agenda happening with these shots. But he took the shots anyway because someone or something convinced him that injections equal freedom. Physically strong does not equal mentally tough. And sadly we’re seeing that play out in 2021 as so many big, physically strong men (see NFL players, NHL players, NBA players, etc.) are succumbing to this psy-op.
Let me start by saying, everybody acts from faith. Faith in something, no matter what it is.
A billion Catholics are not the Vatican.
The Vatican, through the Pope, has made its position clear: take the COVID vaccines.
But then there are the consciences of a billion of the faithful.
In prior articles in this series (archive here), I’ve made it clear that COVID vaccines have, in fact, relied on a fetal-tissue cell line, HEK 293, for testing, and the cell line was originally obtained via an abortion.
Moreover, the evidence points to an abortion in which the infant was delivered from her mother’s womb, alive, and then was killed by a doctor removing her kidneys for fetal tissue. Infanticide. Murder.
Does it matter whether the abortion and the murder were committed yesterday, or in a room in a hospital in the Netherlands, in 1972? Are a billion Catholics willing to say, “It was so long ago, it doesn’t have meaning anymore”?
Is that a reasonable position of Faith?
My understanding is this: Catholics believe Jesus commanded the founding of His Church, which is their Church. Does that count now? Is it wrong to contemplate what He would advise? As opposed, for example, to what Anthony Fauci would advise?
PERTH — A 37-year-old police officer and small business owner is trying to live her life as normal despite accepting the fact that she could drop dead any day, any time.
Ms. Chantal Uren is a police officer for the Western Australian Police Force (WAPOL). She said that the police force mandated vaccines for all personnel in August. Though Ms. Uren made clear that she “is not an anti-vaxxer,” she was against receiving these particular injections due to lack of sufficient information on them. There is no data about long-term effects, she said. Ms. Uren was also concerned about how the shots were rushed to the market. But she felt there was “no choice” but to receive the injections if she wanted to keep her “privileged role” with WAPOL.
Despite her reluctance, Ms. Uren received her first Pfizer mRNA injection sometime in late August. She knew immediately that the decision changed her life, and not for the better. Vertigo, nausea and hives all appeared within 15 minutes.
Ms. Uren was discharged after medical personnel “got the rash under control.” But the relief was temporary. The next day, she had a 103 degree (39.7 Celsius) fever, more hives, and more nausea. For the next four weeks, Ms. Uren suffered persistent hives, fevers, vomiting, diarrhea, and a debilitating cough. Unfortunately the worst was yet to come.
Bell’s Palsy, ruptured aneurysm and stroke
Ms. Uren was apparently still going to work through all this. But that all changed sometime in mid-September. Mrs. Uren said her eyes “felt weird” one Tuesday morning. So she took an antihistamine before driving to work. When she arrived at work, a co-worker told her that her face was “drooping sideways.”
Chantal Uren before Bell’s Palsy.Chantal Uren after Bell’s Palsy
Tomljenovic L, Shaw CA.
Author information
Neural Dynamics Research Group, Department of Ophthalmology and Visual Sciences, University of British Columbia, Vancouver, BC, V5Z 1L8, Canada. lucijat77@gmail.com
Abstract
Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. Despite almost 90 years of widespread use of aluminum adjuvants, medical science’s understanding about their mechanisms of action is still remarkably poor. There is also a concerning scarcity of data on toxicology and pharmacokinetics of these compounds. In spite of this, the notion that aluminum in vaccines is safe appears to be widely accepted. Experimental research, however, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences. In our opinion, the possibility that vaccine benefits may have been overrated and the risk of potential adverse effects underestimated, has not been rigorously evaluated in the medical and scientific community. We hope that the present paper will provide a framework for a much needed and long overdue assessment of this highly contentious medical issue.
A study published in the Journal Cell Biology and Toxicology by Kinki University in Osaka, Japan determined that in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausibility for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.
US National Library of Medicine
National Institutes of Health – Apr 2010
Minami T, Miyata E, Sakamoto Y, Yamazaki H, Ichida S.
Author information
Department of Life Sciences, Kinki University, Higashi-osaka, Osaka, Japan. minamita@life.kindai.ac.jp
Abstract
Thimerosal, an ethyl mercury compound, is used worldwide as a vaccine preservative. We previously observed that the mercury concentration in mouse brains did not increase with the clinical dose of thimerosal injection, but the concentration increased in the brain after the injection of thimerosal with lipopolysaccharide, even if a low dose of thimerosal was administered. Thimerosal may penetrate the brain, but is undetectable when a clinical dose of thimerosal is injected; therefore, the induction of metallothionein (MT) messenger RNA (mRNA) and protein was observed in the cerebellum and cerebrum of mice after thimerosal injection, as MT is an inducible protein. MT-1 mRNA was expressed at 6 and 9 h in both the cerebrum and cerebellum, but MT-1 mRNA expression in the cerebellum was three times higher than that in the cerebrum after the injection of 12 microg/kg thimerosal. MT-2 mRNA was not expressed until 24 h in both organs. MT-3 mRNA was expressed in the cerebellum from 6 to 15 h after the injection, but not in the cerebrum until 24 h. MT-1 and MT-3 mRNAs were expressed in the cerebellum in a dose-dependent manner. Furthermore, MT-1 protein was detected from 6 to 72 h in the cerebellum after 12 microg/kg of thimerosal was injected and peaked at 10 h. MT-2 was detected in the cerebellum only at 10 h. In the cerebrum, little MT-1 protein was detected at 10 and 24 h, and there were no peaks of MT-2 protein in the cerebrum. In conclusion, MT-1 and MT-3 mRNAs but not MT-2 mRNA are easily expressed in the cerebellum rather than in the cerebrum by the injection of low-dose thimerosal. It is thought that the cerebellum is a sensitive organ against thimerosal. As a result of the present findings, in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausibility for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.
A study published in the Journal Neurochemical Research determined that since excessive accumulation of extracellular glutamate is linked with excitotoxicity, data implies that neonatal exposure to thimerosal-containing vaccines might induce excitotoxic brain injuries, leading to neurodevelopmental disorders.
US National Library of Medicine
National Institutes of Health – Feb 2012
Author information
Michalina Duszczyk-Budhathoki – 1
Mieszko Olczak – 1,3
Malgorzata Lehner – 2
and
Maria Dorota Majewskacorresponding author – 1,4
1 – Marie Curie Chairs Program at the Department of Pharmacology and Physiology of the Nervous System, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland
2 – Department of Neurochemistry, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland
3 – Department of Forensic Medicine, Medical University of Warsaw, Oczki 1 str., 02-007 Warsaw, Poland
4 – Department of Biology and Environmental Science, University of Cardinal Stefan Wyszynski, Wóycickiego Str. 1/3, 01-815 Warsaw, Poland Maria Dorota Majewska, Phone: +48-22-45-82-624, Fax: +48-22-45-82-842, Email: moc.liamg@akswejamdm
Abstract
Thimerosal, a mercury-containing vaccine preservative, is a suspected factor in the etiology of neurodevelopmental disorders. We previously showed that its administration to infant rats causes behavioral, neurochemical and neuropathological abnormalities similar to those present in autism. Here we examined, using microdialysis, the effect of thimerosal on extracellular levels of neuroactive amino acids in the rat prefrontal cortex (PFC). Thimerosal administration (4 injections, i.m., 240 μg Hg/kg on postnatal days 7, 9, 11, 15) induced lasting changes in amino acid overflow: an increase of glutamate and aspartate accompanied by a decrease of glycine and alanine; measured 10–14 weeks after the injections. Four injections of thimerosal at a dose of 12.5 μg Hg/kg did not alter glutamate and aspartate concentrations at microdialysis time (but based on thimerosal pharmacokinetics, could have been effective soon after its injection). Application of thimerosal to the PFC in perfusion fluid evoked a rapid increase of glutamate overflow. Coadministration of the neurosteroid, dehydroepiandrosterone sulfate (DHEAS; 80 mg/kg; i.p.) prevented the thimerosal effect on glutamate and aspartate; the steroid alone had no influence on these amino acids. Coapplication of DHEAS with thimerosal in perfusion fluid also blocked the acute action of thimerosal on glutamate. In contrast, DHEAS alone reduced overflow of glycine and alanine, somewhat potentiating the thimerosal effect on these amino acids. Since excessive accumulation of extracellular glutamate is linked with excitotoxicity, our data imply that neonatal exposure to thimerosal-containing vaccines might induce excitotoxic brain injuries, leading to neurodevelopmental disorders. DHEAS may partially protect against mercurials-induced neurotoxicity.
VAXXED TV – Vaccines gave my son seizures
I am vaccine injured and so is my son
My baby is healthy and happy all the time
I’m a dad fighting the system
4 month vaccine injured my baby
James Neuenschwander M.D
He had a lump on his leg for a year A mother shares her observations of her son’s reactions to the vaccines given to him.
Interview recorded on May 5th, 2017 in The United Kingdom
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
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