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Raised PSAs x9 of the person’s baseline in young men for at least 30 days after the vaccine. Interesting thing they mention towards the end. Patient had PSA 0.4 initially, went up after CV vaccine, then 6 weeks later the level started to come down. What they fail to make a big deal of is the new low number is x3-4 more than initial low reading.
Enlarged prostates can cause infertility. The most common one that does it is asymptomatic- meaning the man feels no pain/problems.
Types of prostatitis that may cause infertility are mentioned below:
Chronic Prostatitis Caused by Bacteria: This is whereby the prostate gland is infected by a bacteria, and this takes place over a long period of time. It does not respond well to treatment with antibiotics although it is caused by bacteria.
Inflammatory Prostatitis that is Asymptomatic: This is whereby the condition does not present with any symptoms. It is a major cause of infertility. It is usually diagnosed when the seminal fluid is taken for a fertility test, and it shows the presence of white blood cells.
Straight from Pfizer’s document. To receive the vaccine/placebo, women had to be either incapable of pregnancy- sterilized, post menopausal- or WOCBA ( women of child bearing age) who were not pregnant, and agreed not to conceive during the study or within 30 days after. Men were given same caveat to avoid conception. Sperm donation was also banned.
It is evident from this document that while never tested on pregnant/lactating women, Pfizer was keen to get data on what happened to those pregnancies even if from “environmental exposure” which they write is from “inhalation or skin contact.” Notice that is a pregnant woman is exposed, her data does NOT go into the study itself, but is kept separate.
The only documentation I’ve read about pregnancy testing was giving the vaccine to rats and necropsying them prior to full term gestation. Here they claimed no tetragenic changes. Rats weren’t full term- seems impossible to tell. How would we know anything about neurological development or future fertility since they were never born?
A PHASE 1/2/3, PLACEBO-CONTROLLED, RANDOMIZED, OBSERVER-BLIND, DOSE-FINDING STUDY TO EVALUATE THE SAFETY, TOLERABILITY, IMMUNOGENICITY, AND EFFICACY OF SARS-COV-2 RNA VACCINE CANDIDATES AGAINST COVID-19 IN HEALTHY INDIVIDUALS
8.3.5. Exposure During Pregnancy or Breastfeeding, and Occupational Exposure Exposure to the study intervention under study during pregnancy or breastfeeding and occupational exposure are reportable to Pfizer Safety within 24 hours of investigator awareness.
126.96.36.199. Exposure During Pregnancy An EDP occurs if: • A female participant is found to be pregnant while receiving or after discontinuing study intervention.
• A male participant who is receiving or has discontinued study intervention exposes a female partner prior to or around the time of conception.
• A female is found to be pregnant while being exposed or having been exposed to study intervention due to environmental exposure. Below are examples of environmental exposure during pregnancy:
• A female family member or healthcare provider reports that she is pregnant after having been exposed to the study intervention by inhalation or skin contact.
PF-07302048 (BNT162 RNA-Based COVID-19 Vaccines) Protocol C4591001 Page 68
• A male family member or healthcare provider who has been exposed to the study intervention by inhalation or skin contact then exposes his female partner prior to or around the time of conception. The investigator must report EDP to Pfizer Safety within 24 hours of the investigator’s awareness, irrespective of whether an SAE has occurred. The initial information submitted should include the anticipated date of delivery (see below for information related to termination of pregnancy).
• If EDP occurs in a participant or a participant’s partner, the investigator must report this information to Pfizer Safety on the Vaccine SAE Report Form and an EDP Supplemental Form, regardless of whether an SAE has occurred. Details of the pregnancy will be collected after the start of study intervention and until 6 months after the last dose of study intervention.
• If EDP occurs in the setting of environmental exposure, the investigator must report information to Pfizer Safety using the Vaccine SAE Report Form and EDP Supplemental Form. Since the exposure information does not pertain to the participant enrolled in the study, the information is not recorded on a CRF; however, a copy of the completed Vaccine SAE Report Form is maintained in the investigator site file. Follow-up is conducted to obtain general information on the pregnancy and its outcome for all EDP reports with an unknown outcome. The investigator will follow the pregnancy until completion (or until pregnancy termination) and notify Pfizer Safety of the outcome as a follow-up to the initial EDP Supplemental Form.
In the case of a live birth, the structural integrity of the neonate can be assessed at the time of birth. In the event of a termination, the reason(s) for termination should be specified and, if clinically possible, the structural integrity of the terminated fetus should be assessed by gross visual inspection (unless preprocedure test findings are conclusive for a congenital anomaly and the findings are reported). Abnormal pregnancy outcomes are considered SAEs. If the outcome of the pregnancy meets the criteria for an SAE (ie, ectopic pregnancy, spontaneous abortion, intrauterine fetal demise, neonatal death, or congenital anomaly), the investigator should follow the procedures for reporting SAEs.
Additional information about pregnancy outcomes that are reported to Pfizer Safety as SAEs follows:
• Spontaneous abortion including miscarriage and missed abortion;
• Neonatal deaths that occur within 1 month of birth should be reported, without regard to causality, as SAEs. In addition, infant deaths after 1 month should be reported as SAEs when the investigator assesses the infant death as related or possibly related to exposure to the study intervention.
PF-07302048 (BNT162 RNA-Based COVID-19 Vaccines) Protocol C4591001 Page 69
Additional information regarding the EDP may be requested by the sponsor. Further follow-up of birth outcomes will be handled on a case-by-case basis (eg, follow-up on preterm infants to identify developmental delays). In the case of paternal exposure, the investigator will provide the participant with the Pregnant Partner Release of Information Form to deliver to his partner. The investigator must document in the source documents that the participant was given the Pregnant Partner Release of Information Form to provide to his partner.
188.8.131.52. Exposure During Breastfeeding An exposure during breastfeeding occurs if:
• A female participant is found to be breastfeeding while receiving or after discontinuing study intervention.
• A female is found to be breastfeeding while being exposed or having been exposed to study intervention (ie, environmental exposure). An example of environmental exposure during breastfeeding is a female family member or healthcare provider who reports that she is breastfeeding after having been exposed to the study intervention by inhalation or skin contact.
The investigator must report exposure during breastfeeding to Pfizer Safety within 24 hours of the investigator’s awareness, irrespective of whether an SAE has occurred. The information must be reported using the Vaccine SAE Report Form. When exposure during breastfeeding occurs in the setting of environmental exposure, the exposure information does not pertain to the participant enrolled in the study, so the information is not recorded on a CRF…
Seems like Pfizer is all over the female reproduction concerns, but just uses humans versus animals to test it.
No shot. I have had a prolonged reaction to another type of Pharma assault via an IV fluoroquinolone. The commonalities between them are that they alter DNA and affect GABA receptors. Low GABA explains the panicky feeling and brain fog. I suspect the “vaccine” also causes an overload of glutamate (excitatory neurochemical) as it crosses blood brain barrier. High glutamate explains the akathisia some have filmed. Glutamate may also contribute to the Bell’s palsy, etc.
Glutamate can cause psychological issues like brain fog, memory loss, chronic insomnia and depersonalization/derealization. DP/DR are some of the horrors for anyone coming off of benzodiazepines, sleep aids, or any anti-depressants. The supportive treatment there needs to be long term as it takes time to rebuild receptors and balance the neuro chemicals. I would apply the same logic to injected folks.
The common pseudo amino acid Taurine greatly reduces glutamate. If you buy it in bulk powder, dirt cheap. The things I write about are all proven via scientific studies so just go to PubMed.com and query a topic. I’m not doing all your homework.
It was given to mice who later had induced strokes, and they recovered with virtually no residuals. It has been used very successfully to inhibit seizures. Taurine greatly reduces akathisia in sufficient doses. *There is no known overdose amount, but it can lower blood sugar due to affect on Isle of Langerhans cells in pancreas so take with food. Taurine is protective to the brain and spinal cord, heart muscle, and can even reverse diabetic retinopathy.
Something else to watch for is high histamine levels. This is very common in those tapering above meds or for someone with an adverse reaction to drugs. Remember that sudden anaphylaxis is a “side effect” of the injections. ADE hyper-reaction to CV19 exposure is partially histamine dependent. Vitamin C in large doses is the greatest natural anti-histamine. Quercitin and vitamin A are also very helpful.
*Not medical advice- you’re adults, you can choose. Based on my experiences with low mitcochondrial activity/ and other neuro effects from the fluoroquinolone, I highly recommend taurine with large doses of Liposomal vitamin C should you get the injections just to hedge your bets.
If you’ve had no reactions after taking it, good for you, but others may not be so fortunate. Plus as with Fluoroquinolone damage, the effects may not be evident until 6-12months later due to DNA changes. With FQ, people can get unexplained Achilles tendon ruptures/ joint injuries from collagen breakdown as their first symptom.
“Fluoroquinolones, which perform their bactericidal effect by inhibiting DNA gyrase (a type II topoisomerase), are known to interfere with certain immune functions. Ciprofloxacin and other quinolones at >20 µg/ml inhibit peripheral blood lymphocyte (PBL) cell growth by 30 to 35%, causing impaired cell cycle progression through the S phase. Cell cycle analysis thus indicates DNA synthesis to be inhibited by fluoroquinolones at these concentrations.”
When this first emerged, my position was that the C had released a virus so that they could hold the concession on vaccines. Seemingly that has generally been true as they bought up all PPE initially world-wide and sold it for a premium. They previously held the position of either #1 or 2 in world-wide vaccine production and have been working on ethnically specific gene therapies for years. They are dedicated to the proposition that the Middle Kingdom is destined to rule the world as they are the longest continuous existing civilization. Others are non-humans to be eliminated.
What does this have to do with Fauci? Pushing the GR agenda with masks and lockdowns-pays well. Dear Doc’s wife supposedly now owns 3 homes outside USA. All purchased ’21. With a book deal and maintaining his life line with Gates, I’m sure he’ll be well compensated for his thuggery.
Remember that when Biden was about to be elected, the C released video of HB in pretty awful circumstances like sex with kids into public domain. Why? A reminder that we’re in control and that at any moment we can sacrifice you.
What do the C want? The USA is a fat juicy sheep with natural resources and space. They already own millions of acres of farmland and land adjacent to TX air base. Think it’s coincidental? Bankrupt the USA and you can move in- just like with Belt and Road. We give the C billions in loan interest while collecting NOTHING on their debts to us. Their Belt and Road program is like the Biden immigration policies- it’s an invasion to displace native inhabitants while repossessing hard assets with unpayable loans.
Western governments are rife with C backed/financed politicians and officials to do their bidding. Would point to H. Biden or the MSM ties, but why bother. Please read the book Hidden Hand:Exposing How the CCP is Reshaping the World
Interesting article on DM.
Never think they are incapable of any atrocity or deception. They are masters of bribery and blackmail.
Timeline of key studies:
2005- Bats are natural reservoirs of SARS-like coronaviruses- One of the co-authors; Dr. Shi Zhengli
2014- Effects of human anti-spike protein receptor binding domain antibodies on severe acute respiratory syndrome coronavirus neutralization escape and fitness
Jianhua Sui 1, Meagan Deming 2, Barry Rockx 2, Robert C Liddington 3, Quan Karen Zhu 1, Ralph S Baric 4, Wayne A Marasco
CV 19 creation???
2015- A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence
Vineet D Menachery 1, Boyd L Yount Jr 1, Kari Debbink 1 2, Sudhakar Agnihothram 3, Lisa E Gralinski 1, Jessica A Plante 1, Rachel L Graham 1, Trevor Scobey 1, Xing-Yi Ge 4, Eric F Donaldson 1, Scott H Randell 5 6, Antonio Lanzavecchia 7, Wayne A Marasco 8 9, Zhengli-Li Shi 4, Ralph S Baric 1 2 ( a correction of data was done 2020)
The emergence of severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome (MERS)-CoV underscores the threat of cross-species transmission events leading to outbreaks in humans. Here we examine the disease potential of a SARS-like virus, SHC014-CoV, which is currently circulating in Chinese horseshoe bat populations. Using the SARS-CoV reverse genetics system, we generated and characterized a chimeric virus expressing the spike of bat coronavirus SHC014 in a mouse-adapted SARS-CoV backbone. The results indicate that group 2b viruses encoding the SHC014 spike in a wild-type backbone can efficiently use multiple orthologs of the SARS receptor human angiotensin converting enzyme II (ACE2), replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV. Additionally, in vivo experiments demonstrate replication of the chimeric virus in mouse lung with notable pathogenesis. Evaluation of available SARS-based immune-therapeutic and prophylactic modalities revealed poor efficacy; both monoclonal antibody and vaccine approaches failed to neutralize and protect from infection with CoVs using the novel spike protein. On the basis of these findings, we synthetically re-derived an infectious full-length SHC014 recombinant virus and demonstrate robust viral replication both in vitro and in vivo. Our work suggests a potential risk of SARS-CoV re-emergence from viruses currently circulating in bat populations.
This was done at UNC Chapel Hill, a college campus with no special security. Dr. Ralph Baric still works there. The two Chinese researchers went to Wuhan. Was this virus designed to glean the herd??
Baric and Zhengli’s 2015 project, “Generating Infectious Clones of Bat SARS-Like CoVs,” involved altering a SARS-CoV virus so it could latch onto the ACE2 receptor, a protein that provides the entry point for the coronavirus to hook into and infect a wide range of human cells. (Some evidence suggests that ACE2 receptors may be more numerous in patients with hypertension, diabetes and coronary heart disease, one reason these comorbidities may contribute to susceptibility to COVID-19).
Objections to this gain of function test rippled through the scientific community for fear of escape and pandemic.
Researchers from the University of North Carolina at Chapel Hill have discovered a new bat SARS-like virus that can jump directly from its bat hosts to humans without mutation. However, researchers point out that if the SARS-like virus did jump, it is still unclear whether it could spread from human to human…
Baric and his team demonstrated that the newly-identified SARS-like virus, labeled SHC014-CoV and found in the Chinese horseshoe bats, can jump between bats and humans by showing that the virus can latch onto and use the same human and bat receptor for entry. The virus also replicates as well as SARS-CoV in primary human lung cells, the preferred target for infection.
“This virus is highly pathogenic and treatments developed against the original SARS virus in 2002 and the ZMapp drugs used to fight Ebola fail to neutralize and control this particular virus,” said Baric. “So building resources, rather than limiting them, to both examine animal populations for new threats and develop therapeutics is key for limiting future outbreaks.”
Information on Baric.
2012- Immunization with SARS coronavirus vaccines leads to pulmonary immunopathology on challenge with the SARS virus
Chien-Te Tseng 1, Elena Sbrana, Naoko Iwata-Yoshikawa, Patrick C Newman, Tania Garron, Robert L Atmar, Clarence J Peters, Robert B Couch…
Results: All vaccines induced serum neutralizing antibody with increasing dosages and/or alum significantly increasing responses. Significant reductions of SARS-CoV two days after challenge was seen for all vaccines and prior live SARS-CoV. All mice exhibited histopathologic changes in lungs two days after challenge including all animals vaccinated (Balb/C and C57BL/6) or given live virus, influenza vaccine, or PBS suggesting infection occurred in all. Histopathology seen in animals given one of the SARS-CoV vaccines was uniformly a Th2-type immunopathology with prominent eosinophil infiltration, confirmed with special eosinophil stains. The pathologic changes seen in all control groups lacked the eosinophil prominence.
Conclusions: These SARS-CoV vaccines all induced antibody and protection against infection with SARS-CoV. However, challenge of mice given any of the vaccines led to occurrence of Th2-type immunopathology suggesting hypersensitivity to SARS-CoV components was induced. Caution in proceeding to application of a SARS-CoV vaccine in humans is indicated.
NAC has long been given as the only known antidote to acetaminophen poisoning. If given in time, it prevents an accumulation of the liver toxic breakdown of the drug.
There is a brand name called Mucomyst. It is used in nebulizers for extreme respiratory infections.
NAC is given IV with vitamin C to prevent adverse reactions to radiographic contrast medium. This means the medical community understands its usefulness to clear toxins.
The boney fingers of the FDA are trying to eliminate all avenues of escape.
It is unfortunate that we now have to have validation from MIT that anti-maskers/ anti-vaxxers might be better informed than the submissive members of the public. The USA was once a symbol of ingenuity and cleverness, but has now been reduced to something out of Ideocracy.
Worked in medical community many years. Like teaching, there’s always some new technique or treatment that will revolutionize the industry. 9/10 times a group of investors got behind a guy with a gizmo/drug and pushed it purely for money. Not until there are tons of complications do we admit bad idea. Classics were the uterine mesh and thalidomide. First one used to help (?) women with post childbirth incontinence. Instead the mesh ate through the perineum causing complications and horrible pain. We all know the horrors of the thalidomide story. Even after the first flipper babies arrived, the company distributed the drug to poor nations, knowing the complications.
The science is a foregone conclusion based on who is paying. This is how medical research has always worked. When the grant is about to expire, researchers scrambling to keep their jobs fiddle. Test subjects/bad outcomes get tossed out so the data is tortured until it confesses what your overlords want. Saw it in a cancer research lab for two years. Now that AMA has come out in favor of CRT, not sure how triage will work in an ER…transgender people of color first for an infected hang nail while the white guy with heart attack waits?
Please recall that the spike protein who-do was performed on UNC Chapel Hill campus by a man who despite working with the Chinese bat woman from Wuhan is still employed there. How’s that possible? Because he brought in millions to the college. Lots of scientists opposed this gain of function experiment on the basis it might create an untreatable illness and potential pandemic and that it could easily escape from an unsecured lab onto a college campus. No one in government cared. Fauci paid.
Does this kind of nonsense get accepted by mainstream? YES. Was this drug company allowed to do this by the powers that be? YES. Why? BIG PROFITS. If you want to watch evidence, view the YT video about a start up drug that was a “long lasting opioid for intractable pain in terminal patients.” https://www.youtube.com/watch?v=WvCld2vKug8
They badgered insurance companies to approve it using false studies. They told doctors/NPs prescribing the upward treatment regimens they would give them big bonuses. This dose was so high, everyone became hopelessly addicted. Many died.
The sales manager was a classic psycopath who only cared about profit and hired other psychopaths- strippers, tradesmen, etc- with no formal educations or medical knowledge to push the drug. He openly admits it on film. One disgruntled prescriber at an avowed pill-mill did their bidding, but was unhappy enough to be filmed. Her major complaint was that they had paid her too low a rate, not that she had ruined lives. She stated that the people were going to walk out the door with a script anyway, she might as well get paid for it since she had a bunch of kids to support. Nice.
Not until there were a huge number of issues did the good ole FDA investigate. Finally the owner and others saw jail.
Medical care is an ego and profit driven animal with all kinds of input from those not directly treating patients. There are some good people, but they usually get worn down. The true new idea which actually helps people often gets trampled. The truth is the first casualty.
Masks are driven by people fearfully grasping at straws against an invisible boogey man. This becomes a way to act out their frustration and fears. Like Rachel Maddow stated,”when everyone wore masks it was easy to identify the ‘good people’. What do we do now?” Maybe act civilly toward one another?
SARS-CoV-2 mass vaccination: Urgent questions on vaccine safety that demand answers from international health agencies, regulatory authorities, governments and vaccine developers
Since the start of the COVID-19 outbreak, the race for testing new platforms designed to confer immunity against SARS-CoV-2, has been rampant and unprecedented, leading to emergency authorization of various vaccines. Despite progress on early multidrug therapy for COVID-19 patients, the current mandate is to immunize the world population as quickly as possible. The lack of thorough testing in animals prior to clinical trials, and authorization based on safety data generated during trials that lasted less than 3.5 months, raise questions regarding the safety of these vaccines. The recently identified role of SARS-CoV-2 glycoprotein Spike for inducing endothelial damage characteristic of COVID-19, even in absence of infection, is extremely relevant given that most of the authorized vaccines induce the production of Spike glycoprotein in the recipients. Given the high rate of occurrence of adverse effects, and the wide range of types of adverse effects that have been reported to date, as well as the potential for vaccine-driven disease enhancement, Th2-immunopathology, autoimmunity, and immune evasion, there is a need for a better understanding of the benefits and risks of mass vaccination, particularly in the groups that were excluded in the clinical trials. Despite calls for caution, the risks of SARS-CoV-2 vaccination have been minimized or ignored by health organizations and government authorities. We appeal to the need for a pluralistic dialogue in the context of health policies, emphasizing critical questions that require urgent answers if we wish to avoid a global erosion of public confidence in science and public health.
Here’s a news report on the conversations and memos among Pfizer execs how they’re going to raise the price since the vaccine was never intended to stop the pandemic.
Throwing in my two cents on the spirited debate going on:
Think about this for a moment…what happens if all the medical people go away? They are the group most likely “fully vaccinated”. What if instead of preventing serious illness, it sensitizes them to worse outcomes and cytokine storm? ( That’s what happened in three animal and one children’s study of similar diseases vaccine attempts.) What will happen then? I remember when Venezuela was first falling apart, a TV crew interviewed an organ transplant person who could no longer get her meds. She was beginning rejection. No doctors; no medicine. Same for dialysis patients and diabetics… it was heart breaking.
This is not outlandish thinking. If you have ever read any of the UN documents like the Wilderness Project for the USA or the UN 2030 goals, none of the most seemingly outrageous scenarios are fiction. Read the 2010 Rockefeller Foundations possible future scenarios- One was about a flu pandemic where masks, quarantine, and limited travel were forced on the public. Paraphrasing: “Once govt. leaders implement this strict control, it will not be relinquished.”
If even a small portion of the corporations and self-appointed oligarchs have their way, you and I will exist as semi-serfs working assigned jobs, transported to and from work by rail, living in govt. supplied housing, eating govt supplied worm protein. We will own nothing.
What about money? There’s the UBI (Universal Basic Income ) AOC and others keep floating. I have heard it bantered by govt. officials that to be eligible for UBI you’d have to be fully vaccinated and give up your possessions/ bank. Right now over 30% of the citizens are on the dole. E drone is losing their jobs, no small businesses…where will it end? In order to meet their Green Agenda to save the planet, we have to be in green jobs and not polluting, whatever that looks like. Such great ideas as the worm based protein is being pushed by grants. Lab grown meat is already in your local fast food places.
Farmland is being bought up by thousands of acres by a Gates organization and foreigners like the Chinese. If the Joe/Ho capital gains law passes, then farmers won’t be able to pass the land to their kids as no one can afford the inheritance taxes. No production except what they control.
Medical care? According to Dr Ezekiel Emmanuel’s Whole Lives System, only those between 14-40 yo will get it. Any problems in childhood prior? No interventions; just rely on survival of the fittest. After 40yo your work life begins to slip and problems set in. That drains the system. Not making this up; query it yourself.
The return to wilderness maps show several zones: People in cities; transitional areas with only minimal human contact, and vast swaths of animal only areas. They are trying to create their own Eden.
These are actual documents and commentary by people in power. Having a few locals you can count on with some back bone, critical thinking, and ability to pull together is a pretty smart move just in case.
Download the Fact Sheet for your area’s manufacturer from either FDA.gov or CDC.gov. For instance, query Pfizer Fact Sheet, etc. There are two versions: patient and professional. Recommend you read both as while the patient one is generic and vague where the professional makes statements like,”We do not have any data on this in pregnancy or lactation.” This exists while doctors are telling pregnant women to be injected. Guess they don’t read their own documents.
I despise the condescension and smug attitudes, especially while they are espousing lies like,”Oh it’s FDA approved” or “There’s no more risk than the flu shot.” Just sent info to one who is sure the thing is FDA approved although all the Fact Sheets by the manufacturers’ repeatedly read, “There is NO FDA approved vaccine for CV 19.” Supposedly these test rats got this and read it pre-shot. At least they signed a consent form attesting that they read it.
If they want to do this, I don’t recommend it, but up to them. Some idiots have T-shirts that read,” Vaccinated because I’m not stupid.” Well, I would retaliate, but it’s too wordy for a shirt to write,” I reject being a forced test subject for an unvetted gene therapy to profit B Gates/Pharma/ politicians.”