John Pattersons's decided to make his point when nobody was listening to realities in fact.
When people talk about the Tank Man one often is catapulted back to China Tienanmen Square and the student rebellion.
But this is a story of an Australian communications technician who wanted to send a message to the world that mobile radiation levels were in his measurements far exceeding the safety limits and so he wanted to tell the world.
So shat did he do ...stole his ex bosses vintage tank / armoured personnel carrier and tore into mobile phone towers around Sydney in protest at the lack of care his bosses took when he told them of the issue and they did bot only nothing but sacked him and other workers at the time. Remember that was 2007.
Note in the video at no time is the person asked or questioned afterwards why he did the action. No public information an mobile EMF radiation was even spoken about. So unless the reader watcher delved into Johne Pattersons motives the truth would remain shrouded and the impression that he was a "nut case " would prevail.
This is the way the media who is mostly owned by the investment funds corporate world spins the truth. Mobile companies are also owned by these bohemoths of mass misinformation.
this is how mind control works. Journalists don't have to lie to no tell the truth but they just have to omit everything relevant.
This is a comment from a youtube viewer in video 1 of the incident at the time.
‘In 1997 I took a legitimate measurement. I submitted an OH&S report
that [the measurement] was a “dangerous occurrence”. This is the
highest rated danger on the OH&S scale and meant that by law the
installation should be shut down immediately.’
The result,
however, was something quite different. John was sacked on the spot.
Moreover, other staff members who found out about the measurement were
also sacked without warning.
John then proceeded down the
legislative channels that were available to him. He contacted in turn
Standards Australia, the Australian Communications Authority, the
Australian Radiation Protection and Nuclear Safety Agency, the Local
government Association, Federal Parliament and finally the military.
None of these agencies provided any support, though some authorities
confirmed that John’s measurements and his conclusion were both correct.
Finally a parliamentary committee concluded that John should deal with
the problem in his local area.
Pharma
Astra Zenica admits blood clots caused by spike protein bonding with
Platelet Factor 4 which induces coagulation and a thromboid event or
blood clot.
It also says the vaccine creates a negative charge in the body thus making it magnetic to a positive charge.
My name is Robert Malone, and I am speaking to you as a parent, grandparent, physician and
scientist. I don’t usually read from a prepared speech, but this is so important that I wanted to
make sure that I get every single word and scientific fact correct.
I stand by this statement with a career dedicated to vaccine research and development. I’m
vaccinated for COVID and I'm generally pro-vaccination. I have devoted my entire career to
developing safe and effective ways to prevent and treat infectious diseases.
After this, I will be posting the text of this statement so you can share it with your friends and
family.
Before you inject your child - a decision that is irreversible - I wanted to let you know the
scientific facts about this genetic vaccine, which is based on the mRNA vaccine technology I
created:
There are three issues parents need to understand:
The first is that a viral gene will be injected into your children's cells. This gene forces
your child’s body to make toxic spike proteins. These proteins often cause permanent
damage in children’s critical organs, including
Their brain and nervous system
Their heart and blood vessels, including blood clots
Their reproductive system, and
This vaccine can trigger fundamental changes to their immune system
The most alarming point about this is that once these damages have occurred, they are
irreparable
You can’t fix the lesions within their brain
You can’t repair heart tissue scarring
You can’t repair a genetically reset immune system, and
This vaccine can cause reproductive damage that could affect future generations of your family
The second thing you need to know about is the fact that this novel technology has
not been adequately tested.
We need at least 5 years of testing/research before we can really understand the
risks
Harms and risks from new medicines often become revealed many years later
Ask yourself if you want your own child to be part of the most radical medical
experiment in human history
One final point: the reason they’re giving you to vaccinate your child is a lie.
Your children represent no danger to their parents or grandparents
It’s actually the opposite. Their immunity, after getting COVID, is critical to save
your family if not the world from this disease
In summary: there is no benefit for your children or your family to be vaccinating your children
against the small risks of the virus, given the known health risks of the vaccine that as a parent,
you and your children may have to live with for the rest of their lives.
The risk/benefit analysis isn’t even close.
As a parent and grandparent, my recommendation to you is to resist and fight to protect your
children.
This one-pager summarizes the therapy adopted by Dr Shankara Chetty, from South Africa, to help prevent COVID-19 from progressing towards severe disease. The document focuses on the 8th day onwards of COVID-19, i.e. the inflammatory phase. It does not cover the initial viral phase, for which early treatment protocols already exist and can be prescribed before. The document is for information only, not for therapeutic advice. If you catch COVID-19, please seek immediate medical help.
The 8th Day Therapy aims at mitigating a possible hypersensitivity reaction, that can trigger an inappropriate immune response, including a possible subsequent cytokine storm. This transition from the initial viral phase typically occurs on Day 8 after the first symptoms. It’s essential for the treating physician to establish as precisely as possible the first day of symptoms, to alert the patient of the date when a possible sudden aggravation of symptoms may occur. Shortness of breath is typically associated with this aggravation.
The 8th Day Therapy encompasses 4 distinct interventions. They sometimes follow a previously prescribed early treatment protocol. Possible drug interactions need to be carefully assessed. Intervention #1: Corticosteroids Goal: To stop the hypersensitivity reaction, to stop the release of mediators and to prevent an inappropriate immune response, including a possible subsequent cytokine storm. Medication: Prednisone 80mg dly x 1 week. Note: Increase dose rapidly to get symptomatic relief quickly. CRP and IL6 values must show quick decline. Dose will vary according to variants and severity of reaction. Can go as high as 100mg tds for first few days. Wean off cautiously when CRP and IL6 are normal or patient is well for a few days. Those with prolonged reactions are difficult to wean, so consider adding Azathioprine 50mg dly to decrease steroid requirements. Intervention #2: Anti-histamines Goal: To clear the histamines that have been released.
Medications: H1: Promethazine 25mg tds x 5 days or Levocetirizine 5mg bd x 1 month to follow Promethazine H2: Cimetidine 400mg x 1 month or another H2 blocker Other anti-histamine drugs can be suitable. Intervention #3: Anti-leukotrienes Goal: To clear the leukotrienes that have been released. Medication: Montelukast 10mg bd x 5 days then dly x 1 month Intervention #4: Blood Thinners Goal: to clear platelet activating factors
Medications: Aspirin 325 mg dly x 1 month. Add Xarelto 15 mg bd if D.Dimer is raised; decrease to 15 mg dly x 1 month once D.Dimer is normal
Optional Interventions -Add appropriate antibiotics for those with fever, bacterial co-infection or raised Procalcitonin levels -Add Venteze syrup PRN for those suffering from asthma -Add Ivermectin 12 mg dly x 5 days in those with cough, dyspnea or decreased oxygen saturation - Fluvoxamine may be a suitable drug, yet Dr Chetty has so far no experience with it. By Dr Shankara Chetty, MD, with the editorial assistance of JP Kiekens / covexit.com
Strictly for Information Only, Not for Medical advice. Version of May 12 2021.
In
the video below Dr Chetty has seen a rise in the IGE immunoglobulin
level related to the immune response in vaccinated patients who then get
covid.
Day 8
The high IGE is a indicator of the auto immune response in the body to the spike protein injected, he deducts. Therefore
patients are reacting to the spike protein that the covid virus
catalyses rather than to the virus. The virus is by then dormant and
not effecting the patient.
What is IGE test ?
An immunoglobulin E (IgE) test measures the blood level of IgE, one
of the five subclasses of antibodies. Antibodies are proteins made by
the immune system that attack antigens, such as bacteria, viruses, and
allergens.
IgE antibodies are found in the lungs, skin, and mucous membranes.
They are associated mainly with allergic reactions (when the immune
system overreacts to environmental antigens such as pollen or pet
dander) and parasitic infections.
Why It’s Done
The IgE test is often performed as part of an initial screen for
allergies. Symptoms of allergies may include hives, itchy eyes or nose,
sneezing, nasal congestion, tight throat, and trouble breathing.
Symptoms may be seasonal (as with allergies due to pollen or molds) or
year-round (as with food allergies). They can range from mild to severe,
depending on the child and the allergy.
H1+ H2 blockers
H2 blockers are sometimes called H2 receptor antagonists, or H2RAs. They
reduce the amount of acid that the stomach produces. This can help
treat many common health issues, including gastroesophageal reflux
disease (GERD), gastric ulcers, and occasional heartburn.
“There are two known histamine receptors, designated H1 and H2.
H1 receptor antagonists are typically utilized to suppress the body’s
histamine-mediated effects in anaphylactoid or anaphylactic reactions.
H2 antagonists are competitive antagonists at the parietal cell H2
receptor and are typically used to suppress gastric acid secretion. H2 blockers begin working within an hour and last for up to 12 hours.
H2 Antagonists i.e. H2 Blockers, competitively
inhibit the action of histamine at H2 receptors on gastric parietal
cells, thereby inhibiting gastric acid secretion.
