Who, Cdc, Un, Wef, Dr.brix, Gates, Dr.fauci, Pfizer, Trudeau, Schwab, Harari-patents=bioweapons???

WHO is the real enemy ???


Russell James@oneBasedBrother
Apr 6··Edited
Who's responsible for the rise in anti-White sentiment the world-over?


READ THE COMMENTS
Russell James on Gab: 'Who's responsible for the rise in anti-White senti…'
https://gab.com/oneBasedBrother/posts/110153844986057026

 

Emily Morris
·
I was tired of hearing how Trump called the virus a hoax and “did nothing” until March.... So I did research. Here’s the real timeline of what happened (all of this BEFORE we had even one death in the US) :
1/6 CDC issues travel advisory for Wuhan.
1/11 CDC tweets about corona related “pneumonia outbreak in China”
1/14 WHO tweets that there is no evidence of human to human transmission.
1/17 CDC started doing health screenings at 3 airports of travelers from China.
1/21 first case in US for someone who traveled directly from Wuhan.
1/23 WHO again says no human to human transmission outside of China.
1/27 WHO raises alert level but is still saying China has it contained.
1/28 CDC states “ While CDC considers covid a serious situation and is taking preparedness measures, the immediate risk in the US is considered low.”
1/29 White House announces Coronavirus Task Force created. Note - this is despite the WHO downplaying the threat!
1/31 Trump bans travel from China.
Media and multiple Democrats slam his decision calling it racist/xenophobic.
2/5 Trump acquitted (impeachment).
2/5 Chuck Schumer in a tweet continues to call Trumps’ travel ban from China “premature.”
2/7 White House’s Coronavirus Task Force gives press briefing.
2/9 White House Coronavirus Task Force meets with all governors regarding virus.
2/12 CDC waiting for approval from Chinese for CDC team to travel to China.
2/18 HHS announces partnership to develop vaccine.
2/21 Italy identifies its very first case in their country.
2/21 CDC tweets that it is working with States for preparedness.
2/24 Trump sent letter to Congress asking for $25B for virus effort.
2/24 Nancy Pelosi made a stop in Chinatown and encouraged people to “please come and visit and enjoy Chinatown.”
2/25 there is still no reported community spread in the US!!! (Per CDC tweet.)
2/27 first community transmission in US.
2/27 Trump appoints Pence to coordinate efforts.
2/29 FIRST reported Covid19 death in US.
It is helpful to look at the actual timeline. All of this happened BEFORE the 1st death in US.
I got most of this info from CDC tweets so anyone can look it up to check for accuracy. There were many more actions in between, I just took some highlights.

 

@AllTheDocs

 

"The sicker the patient, the better I function." -Dr. Fauci
...Wow, that's pretty sick...



Pandemic Prevention, Preparedness and Response: International Agreement, 17 Apr 2023
video


View: https://youtu.be/eh30cThhVm0

 

Read this journalist


Contentious COVID-19 Drugs

Are All Antimalarial:

May Not Be a Coincidence

Contentious COVID-19 Drugs Are All Antimalarial: May Not Be a Coincidence (theepochtimes.com)
https://www.theepochtimes.com/health/contentious-covid-19-drugs-are-all-antimalarial-may-not-be-a-coincidence_5164443.html

FEATURED
COVID TREATMENTS & REMEDIES

Marina Zhang
Apr 14 2023
biggersmaller

(Memories Over Mocha/Shutterstock)

0:0010:16



1


The COVID-19 recommendations hydroxychloroquine, ivermectin, and now artemisinin all have one thing in common: They are antimalarial drugs or have such properties.
Yet studies suggest that this may not be a mere coincidence; malaria and COVID-19 may be more similar than people may realize.

Malaria Versus COVID-19

From the outset, malaria and COVID-19 are very distinct diseases.
Malaria is a parasitic disease. An infection starts when an individual is bitten
by a mosquito carrying a parasite from the Plasmodium genus.

Upon infection, the parasite first goes to the liver and multiplies in liver cells.

Then it migrates to the bloodstream, invades and proliferates in red blood cells, and causes these cells to expand and burst.

Common malaria symptoms such as fever, chills, and sweating occur during the blood-stage infection.

Complications include anemia, and on rare occasions, cerebral malaria, liver failure, fluid buildup in the lungs,
and acute respiratory distress syndrome.

COVID-19, on the other hand, is a viral disease.

Infection occurs primarily through the inhalation of contaminated droplets.

The virus invades the body through the nasal cavities, entering the upper and then lower respiratory tracts.
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Inflammation of the lungs ensues as the body’s immune cells fight off the infection.

The person’s oxygen levels start dropping as inflammation worsens in the advent of a cytokine storm,
and the lungs become damaged. Some of the virus can also go into the bloodstream and invade other organs,
causing systemic inflammation and damage.
Several Commonalities

While one mainly affects blood cells and the other primarily affects the lungs,
both diseases are characterized by a strong inflammatory response early in the infection,
according to a 2022 paper in Frontiers in Immunology.

Symptoms-wise, both infections from malaria and COVID-19 can lead to fever, fatigue, shortness of breath,
diarrhea, and muscle pain.

If inflammation is prolonged, the body will experience a significant increase in cytokines,
and individuals can become severely injured or even die.

The two diseases are also similar in that they both sequester iron, use the same receptors
in their pathogenesis, and even share similar structures in their proteins.
Iron Storage

Both the Plasmodium parasite and the SARS-CoV-2 virus require iron to proliferate.

Therefore, both the parasite and the virus need to store iron inside the ferritin protein
within infected cells.

High or increased levels of ferritin are therefore an indication of severe disease and inflammation.

Drugs that are capable of targeting iron storage or preventing proliferation may therefore be successful
in treating both malaria and COVID-19.

Similar Receptors

The angiotensin-converting enzyme 2 (ACE-2) receptor is involved in both malaria and COVID-19 infections.
In COVID-19, the virus binds to ACE-2 to invade cells. ACE-2 is ubiquitous within the human body,
present within at the very least:

• Lungs
• Blood vessels
• Muscles
• The gut
• Nerves
• Stomach
• Heart
• Kidneys
• Pancreas
• Testes
• Uterus

Organs that have a high number of ACE-2 receptors are therefore at a higher risk of COVID-19 infection.
The significance of ACE-2 in malaria is uncertain. However, one study, as well as the one published
in Frontiers in Immunology, showed that people who have their ACE-2 receptors reduced due to
genetic predispositions are more resistant to malaria.

According to the Frontiers in Immunology study, malaria parasites use the CD147 receptors
on red blood cells to gain entry into the cell.

The COVID-19 virus also uses CD147 in the absence of ACE-2 receptors.

CD147 has also been linked to the formation of blood clots in COVID-19 infections.

Therapeutics that can target CD147 and ACE-2 may be successful in treating both malaria and COVID-19.

Similar Protein Structures

Additionally, both pathogens share a degree of overlap in their protein structures.

The COVID-19 surface N protein has at least 40 percent structural similarity
with important malarial proteins in charge of transport, attachment, and invasion.

This means that drugs that can target malarial proteins may also be able to target SARS-CoV-2 viral proteins.
Antimalarial Drugs Used in COVID-19

Early in the pandemic, many studies recommended antimalarial and anti-parasitic drugs
such as hydroxychloroquine, chloroquine, ivermectin, and artemisinin as potential treatment options for COVID-19.

These recommendations, however, soon received backlash, with one reason being that malaria
and COVID-19 seem to be very different diseases.

But many doctors and studies found these therapeutics helpful in treating acute COVID-19.

Professor Jose Luis Abreu, whose specialty is in plant science at The State University of Nuevo León,
used the proposition of “parallelism between malaria and COVID-19” as an explanation
for why antimalarial drugs such as ivermectin, artemisinin, and hydroxychloroquine
may be applied to COVID-19 in his protocol.
Have Potent Anti-Inflammatory Properties

Hydroxychloroquine, chloroquine, ivermectin, and artemisinin are all very potent anti-inflammatory drugs.

According to a study published in The Journal of Antibiotics, ivermectin is an immunomodulator
in COVID-19, meaning that it does not suppress the immune system,
but regulates it so that it does not become hyperinflammatory and damaging.

Hydroxychloroquine and artemisinin have similarly been shown to have immunomodulating effects.

Hydroxychloroquine is also approved to treat autoimmune diseases such as rheumatoid arthritis and lupus (pdf).

Studies like the one in The Journal of Antibiotics have shown that ivermectin, hydroxychloroquine,
and artemisinin may be able to prevent cytokine storms and scarring of the lungs.

Abreu has pointed out that artemisinin, due to its reaction with iron molecules,
can also produce oxygen as an end product, helping to alleviate hypoxic conditions.

As aforementioned, COVID-19 infections have also been associated with iron sequestration for viral proliferation.

Abreu argued that artemisinin, whose primary role in malaria is to target iron storage
by releasing free radicals, would also do the same in COVID-19-infected areas and kill infected cells and viruses.

Block COVID-19 Receptors and Proteins

In simulation studies, ivermectin, hydroxychloroquine, and artemisinin can bind to SARS-CoV-2 N proteins,
which have structural similarities with malaria proteins. In treating malaria, hydroxychloroquine
and artemisinin have been shown to block malarial proteins from replicating and proliferating.

All three drugs can also bind to CD147 and ACE-2 receptors, as previously reported by The Epoch Times.

These drugs can also bind to COVID-19 spike proteins directly to prevent viral attachment to cell receptors
and also prevent viral proliferation by blocking proteins that take part in viral replication.

Meplazumab, an antibody that has been approved for use in malarial treatment for its anti-CD147 activity,
has also been beneficial in treating COVID-19 pneumonia.
Antimalarial Drugs Are Also Anti-Cancer?

Ivermectin, artemisinin, and hydroxychloroquine have also been found to have anti-cancer properties.
It is interesting to note that some studies have also postulated that cancer acts like a parasite.

Like external parasites, cancer depends on its host—the human body—for food, but operates independently
and often to the detriment of the host.

Abreu said that a common feature among malaria, cancer, and COVID-19 is that all of them
require iron for proliferation, and therefore, artemisinin has been used with success
in preventing malaria, cancer, and COVID-19.

Abreu wonders if there is a link between parasites, viruses, and cancer, saying that further studies
should be done on these matters.

Ivermectin has been found to prevent cancer cell proliferation and metastasis,
and also encourage cancer cell deaths in several types of cancers.

It can also prevent the formation of blood vessels, which cancer cells need for deriving oxygen and nutrients.

Hydroxychloroquine and chloroquine can also prevent blood vessel formation and autophagy.

Autophagy is a process that removes waste from the body, then reuses and recycles cell content.

The process is a double-edged sword, and in some cases can improve the survivability of cancer cells
, hence why autophagy inhibitors can also prevent further cancer development.


RELATED TOPICS

• covid-19 drugs
• malaria drug
• Ivermectin

Marina Zhang

Marina Zhang is a health writer for The Epoch Times, based in New York.
She mainly covers stories on COVID-19 and the healthcare system a
nd has a bachelors in biomedicine from The University of Melbourne.

Contact her at marina.zhang@epochtimes.com.

Contentious COVID-19 Drugs Are All Antimalarial: May Not Be a Coincidence (theepochtimes.com)
https://www.theepochtimes.com/health/contentious-covid-19-drugs-are-all-antimalarial-may-not-be-a-coincidence_5164443.html

 

REAL AMERICANS ARE NOT PUPPETS.
WE NOW KNOW WHAT CHINA DID
TO FORM A MEDICAL COUP
(3 MINS)
video
https://www.bitchute.com/video/A49rtxmjNWAl/

 

NOT ONLY DO THEY WANT US DEAD!
THEY'RE PLAYING US LIKE F**KING FIDDLES....
video

https://www.bitchute.com/video/Br0qhtJXficm/

 

What’s in the Pfizer Documents? | Naomi Wolf

For those who don’t want to watch the video…​

​

video​

What’s in the Pfizer Documents? | Naomi Wolf​

View: https://youtu.be/T9Y_W_30hsM
​

​

Her appeal for help netted 2,500 experts willing to volunteer their time​

in reading the Pfizer documents and produce reports.​

​

The team included: physicians, RNs, bio-statisticians, medical fraud investigators, l​

ab clinicians, research scientists, cardiologists, pathologists, anesthesiologists.​

​

Wolf was barely able to manage the incoming reports,​

however what she and her staff uncovered she describes as “evidence​

of the greatest crime against humanity in the history of our species”.​

​

Here are a few of the details from the 58 reports she shared during her recent speech​

at Hillsdale College: •​

​

Pfizer knew one month after roll out the vaccines didn’t stop COVID​

despite paying for massive celebrity campaigns.​

​

They also knew they had “vaccine failure” and “failure of efficacy”;​

documents identified the third most common side effect of the vaccine is “COVID”.​

​

• Pfizer was receiving so many adverse event reports they needed​

to hire 2,400 staffers to simply process the paperwork.​

​

• Pfizer knew in May of 2021 the vaccines had caused heart damage​

in 35 minors within a week after the injection.​

​

The FDA knew since the documents all say “FDA confidential”​

at the bottom.​

​

Parents were not told of this risk until August of 2021.​

​

During those four months parents and youth alike were propagandized by celebrities and advertisements funded by the CARES act and the Bill and Melinda Gates Foundation​

to “be strong” and “do it for grandma”, despite knowing of the life threatening side effects.​

​

• Looking at the bio-chemical interaction the CDC and Pfizer,​

when asked how long do the petroleum based lipid nano-particle​

and spike protein contained in the vaccines stay in the body,​

lied and said they are metabolized.​

​

The truth is the vaccines were designed to “bio-distribute” to major organs.​

​

Meaning they cross every membrane in the human body.​

​

In women they accumulate in the ovaries​

and there is yet to be a mechanism for safely removing them.​

What’s in the Pfizer Documents? | Naomi Wolf