Tag Archives: clots

NZ – Many of the injuries and deaths recorded are blood clots, strokes and heart attacks (Health Forum NZ)

Note: The NZ citizens’ register now has 70 confirmed NZ deaths (see below)

From The Health Forum NZ page @ Facebook

Here in New Zealand we continue to roll out the CV V at pace.
Every day of my life is currently filled with taking messages about New Zealanders who have died or suffered serious injury after their CV V.
We are creating a Citizens Database, in a similar fashion to Israel.
MANY of the injuries and deaths we record are blood clots, strokes and heart attacks.
Israel is one of the most Vd countries in the world, having signed a sole supply contract with Pfizer….in return for the release of the medical data of all Israelis, to Pfizer.
A new data summary from Professor Retsef Levi finds:
25% INCREASE IN CARDIAC ARRESTS AND HEART ATTACKS (age 16 to 29 years)
83.6% INCREASE IN HEART ATTACKS IN WOMEN (aged 20 to 29)
According to the study, this increase was correlated with Mass vaccination.
WHILE ISRAEL SHARES THIS DATA, OUR NEW ZEALAND GOVERNMENT REMAINS SILENT, BUT TO COERCE AND EVEN MANDATE THE JAB….ALL THE WHILE IGNORING THIS DATA WHICH SHOULD INSTEAD BE INFORMING OUR PROCESS.

https://drive.google.com/file/d/1QT2uUC4j9I2cVpsD1prkScBg0gUqI52x/view?fbclid=IwAR0vFrT9WWd9m4xa6QvTDCAaIxDnyiMVlyWicUan2P-3QRXf4cVBt4RWOos

BELOW: NZ DEATHS

RELATED (from the NZ Doctors nzdsos.com website):
https://nzdsos.com/2021/07/22/deaf-to-the-deaths/

British Medical Journal letter to the editor on haemorrhage, blood clots and thrombocytopenia related to the CV Jab

Posted at The Health Forum NZ Facebook page:

BRITISH MEDICAL JOURNAL LETTER TO THE EDITOR APRIL 2021
Dear Editor
The recent reports of cerebral venous sinus thrombosis (CVST) following administration of CoViD-19 viral vector vaccines (AZ/Oxford and J&J/Janssen) have a peculiar clinical presentation exhibiting haemorrhage, blood clots and thrombocytopenia.
We previously proposed a mechanism [1-2] to explain the vaccine-induced prothrombotic immune thrombocytopenia (VIPIT) and reported that the genetic CoViD-19 vaccines (both viral and non-viral vector-based) may directly infect platelets or megakaryocytes triggering mRNA translation and consequent spike protein synthesis intracellularly.
This may potentially result in an autoimmune response against platelets and megakaryocytes. The consequent thrombocytopaenia may lead to internal bleeding and spontaneous blood clots. We also proposed that the increased circulatory levels of acute-phase proteins, as observed in the pre-clinical vaccine studies in animals, may also be a contributory factor in putting the haemostatic system at an increased thrombotic potential [3].
The pharmacovigilance data confirmed the CVST incidences with all genetic vaccines (viral or non-viral vector), however, the regulatory authorities in their recent investigations reported that the CVST was unusually accompanied with thrombocytopenia in subjects injected with CoViD-19 viral vector vaccines (such as AstraZeneca and J&J/Janssen) than those injected with mRNA vaccines. We, therefore, looked at the preclinical studies of these vaccines to ascertain their biodistribution to body tissues (for instance brain) beyond the injection site for a possible explanation of the rare fatal clots formed in the brain.
Although, the modern viral vectors that are used in CoViD vaccines are silenced (replication-deficient), each dose of the vaccine contains a very high viral load (e.g., 50 billion viral particles per dose in Ox/AZ or J&J/Janssen CoViD-19 vaccines whereas 100 billion viral particles per dose in the Sputnik-V). The viral particles are unlikely to be confined to the muscles at the injection site; they are free to distribute across the body and drain through the lymphatic system; their apparent volume of distribution is likely to be very high. The biodistribution of ChaAdOx1 containing HBV in BALB/c mice (study 0841MV38.001) indicated the highest viral levels at the injection site, but low levels of virus were still detected after 24 hours of injection in all other tissues (including blood, brain, heart, inguinal lymph node, kidney, liver, lung, gonads, and spleen). The proportional tissue distribution of viral vectors in the body tissues away from the injection site was likely to increase with time, however, biodistribution beyond 24h post-dose was not studied. The biodistribution of ChAdOx1 encoding nCoV-19 following intramuscular injection in mice (study 514559) was ongoing at the time of its regulatory approval [4]. The study 514559 was aimed to examine the biodistribution of ChAdOx1 nCoV-19 in bone marrow, brain, spinal cord, sciatic nerve, and other body tissues. The data from this study is not yet available in the public domain but this might provide evidence of vaccine delivery in the brain. We, therefore, agree with your comments that all vaccine-related data and analyses in possession of the regulatory authorities must be published in full without any further delays.
However, in the absence of the results of study 514559, the biodistribution of ChaAdOx1 HBV in mice (study 0841MV38.001) CONFIRMS THE DELIVERY OF THE VACCINE INTO THE BRAIN TISSUES.
THE VACCINE MAY THEREFORE SPUR THE BRAIN CELLS TO PRODUCE COVID SPIKE PROTEINS THAT MAY LEAD TO AN IMMUNE RESPONSE AGAINST BRAIN CELLS, or it may spark a spike protein-induced thrombosis.
This may explain the peculiar incidences of the fatal CVST observed with viral vector-based CoViD-19 vaccines. There is very little information in the public domain to assess the biodistribution of all genetic vaccines, however, it is anticipated that if it is characteristic to the viral vector employed in the vaccine, then the other vaccines using similar technology may also lead to the same safety concerns. Some examples of these vaccines include AstraZeneca/Oxford (Chimp adenoviral vector), J&J/Janssen (Human adenoviral vector 26), CanSinoBio (Human adenoviral vector 5), and Sputnik V (Human adenoviral vectors 26 and 5).
For COVID-19 mRNA Vaccine (Pfizer or Moderna), THE BIODISTRIBUTION STUDIES IN ANIMALS WERE NOT CONDUCTED. The surrogate studies with luciferase and solid-lipid nanoparticles (Pfizer) CONFIRM A BIODISTRIBTUION TO THE LIVER AND OTHER BODY TISSUES beyond the administration site [5].
For Moderna, the biodistribution of mRNA-1647 (encoding CMV genes) formulated in a similar lipid nanoparticulate delivery system confirms a biodistribution beyond the injection site, in particular, the distribution to the lymph nodes, spleen and the eye was noted [6]. However, the detailed tissue-specific distribution of mRNA vaccines encoding SARS-CoV-2 spike proteins (Pfizer or Moderna) is not fully known that can offer invaluable insights into the potential safety of these vaccines in peoples with pre-existing conditions or those on certain medications.
THE DETAILED BIODISTRUBTION DATA INCLUDING PHARMACOKINETICS OF VARIOUS COVID VACCINES WERE NOT CONDUCTED BY THE MANUFACTURER because the studies demonstrating biodistribution of antigens were considered ‘not required’ by the regulatory authorities on the premise that vaccines work by an immunological response than the classic pharmacological approach.
However, such an exemption may barely justify the conventional vaccines such as those incorporating whole inactivated virus, split virion, or the sub-unit vaccines, that directly attracts an immune response post-injection.
On the contrary, modern genetic vaccines work on the premise of gene delivery, therefore, a detailed biodistribution and pharmacokinetic evaluation of the formulated product is invaluable in understanding the potential impact of vaccine encoding gene transfection to various body tissues beyond the site of injection. Vaccines are one of the great discoveries in medicine that has improved life expectancy dramatically. However, if genetic vaccines were to be sustained beyond the CoViD19 pandemic, a tissue targeted approach may be the way forward to limit the antigen (the encoding gene) distribution to the intended tissues only to improve the vaccine safety profile for a global mass public rollout. In comparison, the conventional vaccine approaches (classic non-genetic formulations) have a long history of human use across much wider age groups (infants to elderly) and have an established safety profile despite the current challenges in antigen propagation and large-scale production in a timely manner using conventional methods.

Photo by Natasha Connell on Unsplash

Jeff Rense and Erica Kahn: Un-Vaxxed showing DEADLY clots, shedding signs after simply being near the vaxxed

From seemorerocks.is

Jeff Rense and Erica Kahn discuss accumulating anecdotal evidence that the vaccinated are transmitting something to the unvaccinated as well as signs of deadly clots.

One example is of someone given chest compression 5 days after the vaccination resulting in blood coming out of every orifice. The doctor’s response: “this couldn’t have anything to do with the vaccine.”

READ MORE

https://seemorerocks.is/jeff-rense-and-erica-kahn-un-vaxxed-showing-deadly-clots-shedding-signs-after-ssmply-being-near-the-vaxxed/?fbclid=IwAR0Sz__BezMOsuJ7tC8sJiokY1GXnTF2o9U4SZlsp5tYOP5d8PFQOahgM9Y

Surgeon who operated on young Italian CV vaccine victim comments: ‘We are dealing with something that is not normal’

From freewestmedia.com

The surgeon who operated on an Italian girl, Camilla Canepa, who died at the age of 18 from the effects of the vaccine, said he has never seen anything like this. “It’s not normal,” he added.

Camilla Canepa was operated on by Gianluigi Zona, director of the neurosurgical and neuro-traumatological clinic of the San Martino hospital: “I had never seen a brain that was affected by such an extensive and severe thrombosis.”

The neurosurgeon on duty in San Martino that night was Alessandro d’Andrea, who also called the chief physician to his side at the operating table. “We decided to have a decompression craniotomy, in which the skull is opened to relieve internal pressure.”

Zona recounted the experience: “All venous sinuses were blocked with thrombi, a scenario I have never seen in my many years in this profession. Think of the venous sinus as the river in the middle of a valley where several streams converge. If a dam is built in the middle of the watercourse, the river swells and the tributaries can no longer drain at this point, so that the pressure rises upstream.

“I’m neither a virologist, nor an epidemiologist, nor a coroner, but given the image I saw in the girl’s head, it is clear that we are dealing with something that is not normal.”

The parents of the 18-year-old who died, told the media: “She had no disease.”

READ MORE

https://freewestmedia.com/2021/06/27/surgeon-who-operated-on-young-italian-vaccine-victim-you-have-never-seen-anything-like-this/?fbclid=IwAR2bwa8tW-QKTx2rRFNN8bKNivYOCy4XeusFMFOuQagtRtlI2GVtbUM2e2g

Photo: freewestmedia.com

Dr. Tess Lawrie: COVID vaccines unsafe for human use

The following is the text of the open letter written by Dr. Tess Lawrie to Dr. June Raine, chief executive of the UK’s Medicines and Health Care Regulatory Agency (MHRA) demanding the halt of the mass rollout of COVID vaccines after discovering a “high number of COVID-19 vaccine-attributed deaths and ADRs [adverse drug reactions] that have been reported via the Yellow Card system”. The Yellow Card review includes reports from January 4, 2021 to May 26, 2021.

Dr. Lawrie goes on to summarize the findings of their rapid report on ADRs. Here are some of them:

  • “sudden death” of 438 people following vaccination;
  • 152 fatalities from brain bleeds and clots;
  • 103 fatalities from pulmonary embolism;
  • and 81 due to cardiac categories;
  • 13,766 bleeding, clotting and ischaemic ADRs were identified;
  • 54, 870 ADRs and 171 fatalities due to immune system disorders
  • Some people who experienced “infection” ADRs were cases of re-activated latent viruses, including Herpes Zoster or shingles (1,827 ADRs), Herpes Simplex (943 ADRs, 1 fatal), and Rabies (1 fatal ADR).
  • 157,579 people experienced pain after vaccination
  • 185,474 or 21% of all ADRs were categorized as nervous system disorders. A variety of neurological disorders were noted, including paralysis, palsy, Guillain-Barre, multiple sclerosis, neurodegeneration, seizure, among others.
  • 4,771 people experienced visual impairments including blindness

Dr. Lawrie says that their preliminary review suggests that the ADRs they found was not limited to any one vaccine (all vaccines were causing ADRs).

The open letter goes on to say: “The nature and variety of ADRs reported to the Yellow Card System are consistent with the potential pathologies described in this paper and supported by other recent scientific papers on vaccine-induced harms, which are mediated through the vaccine spike protein product. It is now apparent that these products in the blood stream are toxic to humans. An immediate halt to the vaccination programme is required whilst a full and independent safety analysis is undertaken to investigate the full extent of the harms.”

Editor’s Note: Governments have been said that their implementation of lockdowns, masks, physical distancing, and now, universal vaccination, are precautionary measures to prevent the devastation of societies. It then follows that if governments were truly protecting societies, then they know that the most prudent approach is to suspend all vaccination campaigns.

Governments and their regulatory agencies knew from the beginning that all these vaccines were experimental products. As such, careful collection of data is a must. Now that the data for millions of vaccine recipients is here, and hundreds of thousands of vaccine injuries are appearing, it is time for governments to accept that these vaccines are dangerous and must be stopped [see New study: Vaccines are the likely cause of adverse effects and deaths following vaccination].

DOWNLOAD THE PDF
http://medisolve.org/yellowcard_urgentprelimreport.pdf

SOURCE: https://covidcalltohumanity.org/2021/06/14/dr-tess-lawrie-covid-vaccines-unsafe-for-human-use/

Canadian Doctor: 62% of His Patients Vaccinated for COVID Have Permanent Heart Damage, “Microscopic Blood Clots”

From globalresearch.ca

We have previously covered the story of Dr. Charles Hoffe, the brave doctor who has been practicing medicine for 28 years in the small, rural town of Lytton in British Columbia, Canada.

After he had administered about 900 doses of the Moderna experimental mRNA COVID-19 injections, he sounded the alarm over the severe reactions he was observing in his patients who chose to get the shot (he chose NOT to get it himself), which included death.

The result of him sounding the alarm was a gag order issued against him by the medical authorities in his community. He defied this gag order and was interviewed by Laura-Lynn Tyler Thompson on her show where he sounded the alarm. See: Canadian Doctor Defies Gag Order and Tells the Public How the Moderna COVID Injections Killed and Permanently Disabled Indigenous People in His Community

His punishment for going public to warn others on the dangers of these experimental shots was that he was relieved from hospital duty and lost half of his income: Canadian Doctor Removed from Hospital Duty after Speaking out about COVID “Vaccine” Side Effects

Last week, Dr. Hoffe was interviewed again by Laura-Lynn Tyler Thompson, and he continues to share his findings with the public regarding the experimental COVID-19 shots.

Dr. Hoffe is truly a hero today, risking not only his reputation, but probably his very life to bring important information regarding the COVID-19 shots that the Globalists who control the corporate media and social media are trying very hard to censor.

In this latest interview, Dr. Hoffe states that the blood clots that are being reported in the corporate media as being “rare” are anything but rare, based on his own testing of his own patients who had recently received one of the shots.

The blood clots we hear about which the media claim are very rare are the big blood clots which are the ones that cause strokes and show up on CT scans, MRI, etc. The clots I’m talking about are microscopic and too small to find on any scan. They can thus only be detected using the D-dimer test.

Using this test with his own patients, Dr. Hoffe claims that he has found evidence of small blood clots in 62% of his patients who have been injected with an mRNA shot.

READ MORE

https://www.globalresearch.ca/canadian-doctor-62-patients-vaccinated-covid-have-permanent-heart-damage/5750198?fbclid=IwAR1OQZmMac6bkLRmGVv_0xZ9Vi_QS-zjU6tkqJFoWG3Htr8hksGCJptOz3o

Inventor of mRNA Interviewed About Injection Dangers: he has grave concerns about the lack of transparency of side effects, censoring of discussion and the lack of informed consent

Story at-a-glance

  • Dr. Robert Malone invented the mRNA and DNA vaccine core platform technology. He has grave concerns about the lack of transparency of side effects, censoring of discussion and the lack of informed consent that these bring
  • Free SARS-CoV-2 spike protein is biologically active — contrary to initial assumptions — and causes severe problems. It is responsible for the most severe effects seen in COVID-19, such as bleeding disorders, blood clots throughout the body and heart problems. These are the same problems we now see in a staggering number of people who have received the COVID-19 “vaccine”
  • The spike protein also has reproductive toxicity, and Pfizer’s biodistribution data show it accumulates in women’s ovaries. Data suggests the miscarriage rate among women who get the COVID “vaccine” within the first 20 weeks of pregnancy is 82%
  • Israeli data show boys and men between the ages of 16 and 24 who have been vaccinated have 25 times the rate of myocarditis (heart inflammation) than normal
  • The COVID-19 injections have emergency use authorization only, which can only be granted if there are no safe and effective remedies available. Such remedies do exist, but have been actively censored and suppressed

READ AT THE LINK:

https://articles.mercola.com/sites/articles/archive/2021/06/21/mrna-inventor-interviewed-about-injection-dangers.aspx?ui=a0c4f64f8c29c8eee11503979a030c301541928856f6f673f655dbcc6044b4e9&sd=19000101&cid_source=dnl&cid_medium=email&cid_content=art1HL&cid=20210621_HL2&mid=DM916194&rid=1189175467&p4=20210203&p5=

Photo: pixabay.com

With not one long term study in sight to prove its safety, the NZ Govt still plans to vaccinate your child with the CV VX

From The Health Forum NZ fb page

In the coming months, New Zealand will start vaccinating children aged 12 and above.

Below, the thoughts of an American Doctor (and a member of The Health Forum NZ fb group) Ray Sahelian, regarding the potential risks and benefits of vaccinating this age demographic


Quote…

Vaccinating 12 to 15 year-olds?
FDA has allowed the use of Pfizer’s Covid-19 vaccine in this age group. We do not even have one long-term study from an independent academic center to determine the full extent of harm or death from getting the shots compared to harm and death from being exposed to the Covid virus itself. I could understand this rationale if the vaccines provided near 100 % protection for a lifetime and prevented viral transmission from one person to another (they may do so initially, but progressively less as time passes). These vaccines are moderately protective for a limited period, not even considering the constantly mutating variants. After injection with an mRNA vaccine, spike proteins (made primarily in the liver and deltoid muscle) travel to the central and peripheral nervous system, heart, skin, lungs, lodge in cells lining blood vessels, and may lodge practically everywhere in the body, triggering an inflammatory response. We could, and will, have cases of nerve dysfunction, paralysis, seizures, myocarditis, heart rhythm disturbances, skin rashes, hives, lung tissue damage, clots, and bleeding… not even including immediate and potentially fatal allergic and anaphylactic reactions. Recently a 17-year-old 6’9” tall Utah high school basketball player was vaccinated, started having headaches, and was taken to the hospital and found to have blood clots in his brain. There is a link towards the end of the comments section from a local news station. If I had a child I certainly would not comply to him or her getting such an injection before we meticulously determine the full long-term effects in adults, including potential future susceptibility to autoimmune diseases. And we have yet to do so. I know some people will counter with the argument that Covid is such a serious disease and therefore we need to protect our children. Of course a Covid infection can be serious and fatal. But such risk in the young is minimal compared to the elderly or those with chronic health issues. I would like anyone who challenges my narrative to provide definitive proof that the benefits of vaccination in this age group outweigh the risks from vaccine harm (considering also that repeated booster shots will be necessary). Death from Covid is 8,000 times more common in those over the age of 85 than in the below 17 age group (see the first comment for a link to the CDC statistics). I am all for vaccines that have had a decades-long track record.
Please visit raysahelian com (there is a link from my FB home page) for my regularly updated article (which was deleted by FB) on spike proteins and how the vaccines work — I’ve had new insights — and an ever-growing comprehensive list of side effects, and why they happen. I keep being asked about “shedding” so I have included a paragraph on this topic.
When you watch the mainstream news you are repeatedly presented with the benefits of vaccines in an enthusiastic manner, but hardly warned about the complications that occur. Not being aware of other perspectives I can understand how your viewpoint would be formed.

Recently a 17-year-old boy was hospitalized with myocarditis after Pfizer and initiated a GoFundMe page. An 18-year-old girl from Nevada had seizures and is in a coma after J and J, while a 12-year-old girl was paralyzed during the Moderna vaccine trial (anyone see these mentioned on national TV?). The public deserves full, honest disclosure. We want to trust our national health authorities that they are openly sharing with us what they know, even if these occurrences are infrequent. Check out the CDC-maintained VAERS website and read for yourself the countless case reports submitted by nurses and ER doctors who are encountering patients coming in with horrific reactions to the vaccines (the second and third comments). I feel sorry for these already-stressed health care providers who are trying as best they can to help patients with a myriad serious reactions, and no one has forewarned them how to treat such complex vaccine-induced injuries. And I challenge anyone who claims vaccination is our primary path to herd immunity in the USA. The annual flu vaccine has not accomplished this goal. Prove to me that the current imperfect first-generation Covid-19 vaccines will… especially against an ever-morphing virus. Some of the highest vaccinated countries in the world are having high case numbers again. Eight members of the New York Yankees baseball team were infected after being fully vaccinated (see articles in comments). I have thoroughly studied the benefits and risks of these vaccines and have determined they are not suitable for my particular situation at this time… and an offer of a free donut will not entice me. Many of us plan to wait. In the meantime we do not appreciate being bullied and blamed by the media, or by people who have a different understanding of this complicated issue. Those who truly believe vaccination provides them with excellent protection should not be overly concerned being around others who are not. There is already enough division in this country, and within some families; it is not helpful to add more.

FYI from The Health Forum page

Image by florentiabuckingham from Pixabay

6 deaths from 16 to 75 YOs … all documented at the covid blog

Kamrynn Thomas: 16-year-old Wisconsin girl develops blood clots, dead 11 days after experimental Pfizer mRNA shot

Alan Sporn: 75-year-old Chicago cancer survivor dies of COVID-19 nearly two months after second Pfizer shot

Anne VanGeest: 35-year-old Michigan woman dead 11 days after experimental Johnson & Johnson shot

John Medved: 58-year-old Minnesota man develops blood clots, dead 21 days after Johnson & Johnson shot

Griselda Flores: 61-year-old California woman dead two days after second experimental Moderna mRNA shot

Francine Boyer: 54-year-old Canadian woman develops blood clots, dead 14 days after experimental AstraZeneca shot

Photo: pixabay.com