Thanks for forwarding that recent article. There are indeed many connections between ASU, the ASU McCain Institute (Sedona Forum), and Soros’s Open Society.
ASU is also the only university tied to Sam Altman’s Open AI, interesting considering President Trump brought Altman in front of the TV cameras very publicly soon after his inauguration earlier this year.
I’m quite certain President Trump has his eye on ASU, it’s president CIA IQT Chairman Michael Crow, and his broader network.
Stunning information. What you have gathered and put together is very well documented. The amount of work you’ve put into this is incredible. Thank you so much for sharing this. My mind is blown right now. I’m trying to wrap my head around all this. Whew! It’s a lot to unpack! I know this has been planned for years but I was focused so much on the usual cast of psychopaths involved. Now I see how it’s all intertwined. So much evil in this fallen world. Can’t wait to exit…
5/13/25. ASU Received Millions In Soros Money In Recent Years
Arizona State University (ASU) received over $3.4 million in funds from the nonprofit founded by leading Democratic dark money donor George Soros.
The online data guru Jennica Pounds, known by her username @DataRepublican, named ASU as a recurring recipient of Soros funds as part of nearly a decade of grants from the Open Society Foundations (OSF).
[I always knew McCain was a traitor.]
From 2018 to 2022, the ASU Foundation received $169,000 for the Mary Lou Fulton Teachers College; $200,000 for the Connected Learning in Crisis Consortium; $1.2 million for the McCain Institute for International Leadership; $200,000 for improving learning amid crises and conflict; $22,000 to bring together global educational leaders, and $24,000 for the New American University.
One of OSF’s largest donations to ASU was over $1.5 million for English Second Language (ESL) at the Open Society University Network (OSUN).
Other Arizona-based entities to receive Soros money were:
Arizona Wins ($3.875 million);
Living United For Change in Arizona ($3.3 million);
One Arizona ($1.8 million);
Our Voice, Our Vote Arizona ($1 million);
League of Conservation Voters ($750,000);
Inter Tribal Council of Arizona ($500,000);
Community Foundation for Southern Arizona ($500,000);
Arizona Community Foundation ($400,000);
ADRC Action ($300,000);
PODER ($100,000);
Poder in Action ($75,000);
YWCA of Southern Arizona ($60,000)
Arizona Center for Empowerment ($37,000, and another $325,000 through the Center for Popular Democracy, a partner organization)
Arizona Coalition to End Sexual and Domestic Violence ($25,000);
Start at 43:30, We now have the tools where virologists can’t make any more excuses where they can’t sequence the virus directly.
There is now a technique [2023] where they can sequence up to 2 million contiguous bases at a time. There is no limit.
So all you need to do is take these virologist and say give me some pure virus, let’s sequence it and we should get lots of continuous sequences that show us that viruses have the sequence that you’ve drawn in these cartoons.
What pure virus? They CLAIM to have pure virus, right? …
At 45:30 I’m telling you that it’s a new thing where they have tried to use pure virus made with pure CLONES and tried to INFECT CELLS and SEQUENCE the RNA.
And they did NOT get what they expected, and no one seems to realize it. This was before and after March 11, 2020. That’s the hilarious part and the reason these “no virus” people are so crazy.
46:45 You do understand that every Western government has been behind the scenes, instructed in the dangers of gain of function viruses since 2002.They have been TOLD that this is the most dangerous thing and more dangerous than nuclear weapons.
Who’s telling them?
The WHO, the U.S. government, the U.S. military, the Chinese military, the UN, everyone talks about the danger. How many people are sophisticated to know whether this is true or not? How many people are in a position to know whether that’s true or not?
They PLANNED TO DO THIS. They had a worse-case scenario planned and they were looking for an excuse to TRIGGER IT.
Once they were given the EXCUSE TO TRIGGER IT, THEY USED IT AND HAVEN’T LOOKED BACK.
What was the excuse?
[The fear of danger], the sequence and the CLAIM of a new virus. That’s all they needed.
It’s a mismanaged pandemic the moment you think it’s a pandemic.
1) Respiratory viruses exist; 2) co-infection occurs where the presence of one RNA doesn’t rule out the presence of another. Most of these people could’ve had a flu and we wouldn’t know or a respiratory virus or pathogen is relevant and we wouldn’t know.
Three years later, it was evident it was all planned. Jay thinks they were looking for an excuse.
Did the Chinese know we were looking for an excuse and gave us one? [After all weren’t the Biden’s were in bed with China?] Or did we release viral CLONE in a number of different places on earth to get signal we needed in order to have the excuse?...
They have never proved to us that the virus wasn’t there before 2020 because there’s no PCR or sequencing before 2020.
It appears to be all about human augmentation starting with the African Clawing Frog's stem cells (and/or genes). They call this Xenobots, but when they GMO humans, it's called Anthrobots.
Cyrus Parsa was found with a bullet to his head Feb 2025.
Two scientists created this technology, endangering the entire race and it’s not just a va=x; it was given to D=A=R=P=A. They used FROB stem cells and they mixed it with robotics--the first artificial life. What they want to do is program it so it can go in and say, “heal people” but what it’s done, if you recall the movie, Terminator, that T2 was going after Arnold, it was more advanced but it was human. What this frog, mixed with robotics (or machines) can develop into is hybrid animal machine systems that can do what T2 can do.
Moreover, it can also mutate and cause diseases in multiple different ways around the planet.
Cyrus: The entire world, from every directions there’s multiple risks coming after humanity. When I filed extinction codes for the majority of the human race, I just didn’t find one thing. I put in there drones, microbots, metaparticles, machines, robotics, bioengineered, cybernetics, conflicts, famines and multiple different things. It’s like the entire puzzle is almost like a plandemic to extinct the individual human race. Everything at first is pointed at China and it’s interconnection to OUR big tech companies…
It’s almost like an invasion of humanity.
More on FROGS:
On Jessica Rose’s Substack, watch the video. Wowzer at 1 minute how they transferred light activated proteins into NERVE cells and then CONTROL them using only LIGHT CELLS.
Optogenetics links gene technology with optical methods [permanently]. It may [can] influence neuro NETWORKS and even one day overcome diseases [and give disease?].
The starting signal for optogenetics came in 2002. But wait, there was another membrane protein that reacts to light in the green algae.
It permits the algae to use light for orientation.
With the molecular biological tools now available the researchers succeeded in transferring the GENE for ALGAE into FROG’s eggs. These now produce the corresponding protein [genetically modified, just like they are doing to humans thru the v=a=x].
The protein is a LIGHT RECEPTOR (the algae and a ion combined). The channel reacts to blue light. It opens up and lets positively charged ions flow into the cell.
Optogentics scientists use this mechanism by smuggling the GENE with the BUILDING INSTRUCTIONS [CODE or sequence] for the channel into the genetic material of the NERVE CELLS. So this channel can now work inside the [CELL] membrane.
If it is stimulated by light, positively charged ions flow INTO THE CELL.
This changes the tension across the [CELL] membrane and the neighboring original channels also open up.
In this way, the cell is depolarized and an ACTION POTENTIAL ARISES. But the opposite effect ALSO occurs. Halorhodopsin reacts to ORANGE light and smuggles negative ions INTO THE CELL. This then deactivates the cell. Switching CELLS ON AND OFF USING LIGHT.
WHY THESE FROGS?
These frogs are more than just frogs.
Human central nervous systems (CNS) injury is irreversible.
Xenopus laevis has a high potential to regenerate the brain and spinal cord during larval stages and have the capacity to fully regenerate after severe injury to the CNS.
They grab the frog’s stem cells (which kills the frog) during the larval stages as it loses the capability during metamorphosis.
The optic nerve can regenerate throughout the frog's lifespan.
Here, we review CNS regeneration in frogs, with a focus in X. laevis.
We start with an overview of the anatomy of the Xenopus central nervous system (CNS), including the main supraspinal tracts that emerge from the brain stem, which play a key role in motor control and are highly conserved across vertebrates
Xenopus, a classical laboratory model organism, with increasing availability of genetic tools like transgenesis and genome editing, and genomic sequences for both X. laevis and X. tropicalis.
Most importantly, Xenopus provides the possibility to perform intra-species comparative experiments between regenerative and non-regenerative stages that allow the identification of which factors are permissive for neural regeneration, and/or which are inhibitory.
The African clawed frog model organism has also been used as a tool to study cellular processes like cell movement, cell fate, cell cycle, the cytoskeleton, chromatin, ion channels, and apoptosis. The Xenopus genus has both diploid (X. tropicalis) and allotetraploid (X. laevis) species, often used in genetic research. These frogs have been widely used to discover many different genes involved in congenital heart defects, kidney disease, cancer, gastrointestinal and pancreatic disorders, neurological diseases, muscle atrophy, and human ciliopathies.3
Bravo, Kristen! An exhaustive tour-de-force that truly begs the question: Why is this not being investigated? Thanks for your extremely thorough research. Hopefully, this will reach a wide enough audience (and the relevant authorities) to actuate a proper inquiry.
Thanks for forwarding that recent article. There are indeed many connections between ASU, the ASU McCain Institute (Sedona Forum), and Soros’s Open Society.
ASU is also the only university tied to Sam Altman’s Open AI, interesting considering President Trump brought Altman in front of the TV cameras very publicly soon after his inauguration earlier this year.
I’m quite certain President Trump has his eye on ASU, it’s president CIA IQT Chairman Michael Crow, and his broader network.
Stunning information. What you have gathered and put together is very well documented. The amount of work you’ve put into this is incredible. Thank you so much for sharing this. My mind is blown right now. I’m trying to wrap my head around all this. Whew! It’s a lot to unpack! I know this has been planned for years but I was focused so much on the usual cast of psychopaths involved. Now I see how it’s all intertwined. So much evil in this fallen world. Can’t wait to exit…
Kristen, you'll have fun with this one!
5/13/25. ASU Received Millions In Soros Money In Recent Years
Arizona State University (ASU) received over $3.4 million in funds from the nonprofit founded by leading Democratic dark money donor George Soros.
The online data guru Jennica Pounds, known by her username @DataRepublican, named ASU as a recurring recipient of Soros funds as part of nearly a decade of grants from the Open Society Foundations (OSF).
[I always knew McCain was a traitor.]
From 2018 to 2022, the ASU Foundation received $169,000 for the Mary Lou Fulton Teachers College; $200,000 for the Connected Learning in Crisis Consortium; $1.2 million for the McCain Institute for International Leadership; $200,000 for improving learning amid crises and conflict; $22,000 to bring together global educational leaders, and $24,000 for the New American University.
One of OSF’s largest donations to ASU was over $1.5 million for English Second Language (ESL) at the Open Society University Network (OSUN).
Other Arizona-based entities to receive Soros money were:
Arizona Wins ($3.875 million);
Living United For Change in Arizona ($3.3 million);
One Arizona ($1.8 million);
Our Voice, Our Vote Arizona ($1 million);
League of Conservation Voters ($750,000);
Inter Tribal Council of Arizona ($500,000);
Community Foundation for Southern Arizona ($500,000);
Arizona Community Foundation ($400,000);
ADRC Action ($300,000);
PODER ($100,000);
Poder in Action ($75,000);
YWCA of Southern Arizona ($60,000)
Arizona Center for Empowerment ($37,000, and another $325,000 through the Center for Popular Democracy, a partner organization)
Arizona Coalition to End Sexual and Domestic Violence ($25,000);
Sonoran Prevention Works ($15,000)
Source: https://azfreenews.com/2025/05/asu-received-millions-in-soros-money-in-recent-years/
Biologist Jonathon Jay Couey was canned for speaking out in PA and at Children's Health Defense. His Substack: https://gigaohmbiological.substack.com/p/a-new-biology-101?utm_source=substack&utm_content=feed%3Arecommended%3Acopy_link
Most importantly, he explains his theory on just what COV was on this Odysee video. Excerpts are below:
(2023-01-20) PlanetWavesTV - Eric F Coppolino interviews Dr. Jay Couey
https://odysee.com/@Oisin.page:f/(2023-01-20)-PlanetWavesTV---Eric-F-Coppolino-interviews-Dr.-Jay-Couey:3
Start at 43:30, We now have the tools where virologists can’t make any more excuses where they can’t sequence the virus directly.
There is now a technique [2023] where they can sequence up to 2 million contiguous bases at a time. There is no limit.
So all you need to do is take these virologist and say give me some pure virus, let’s sequence it and we should get lots of continuous sequences that show us that viruses have the sequence that you’ve drawn in these cartoons.
What pure virus? They CLAIM to have pure virus, right? …
At 45:30 I’m telling you that it’s a new thing where they have tried to use pure virus made with pure CLONES and tried to INFECT CELLS and SEQUENCE the RNA.
And they did NOT get what they expected, and no one seems to realize it. This was before and after March 11, 2020. That’s the hilarious part and the reason these “no virus” people are so crazy.
46:45 You do understand that every Western government has been behind the scenes, instructed in the dangers of gain of function viruses since 2002.They have been TOLD that this is the most dangerous thing and more dangerous than nuclear weapons.
Who’s telling them?
The WHO, the U.S. government, the U.S. military, the Chinese military, the UN, everyone talks about the danger. How many people are sophisticated to know whether this is true or not? How many people are in a position to know whether that’s true or not?
They PLANNED TO DO THIS. They had a worse-case scenario planned and they were looking for an excuse to TRIGGER IT.
Once they were given the EXCUSE TO TRIGGER IT, THEY USED IT AND HAVEN’T LOOKED BACK.
What was the excuse?
[The fear of danger], the sequence and the CLAIM of a new virus. That’s all they needed.
It’s a mismanaged pandemic the moment you think it’s a pandemic.
1) Respiratory viruses exist; 2) co-infection occurs where the presence of one RNA doesn’t rule out the presence of another. Most of these people could’ve had a flu and we wouldn’t know or a respiratory virus or pathogen is relevant and we wouldn’t know.
Three years later, it was evident it was all planned. Jay thinks they were looking for an excuse.
Did the Chinese know we were looking for an excuse and gave us one? [After all weren’t the Biden’s were in bed with China?] Or did we release viral CLONE in a number of different places on earth to get signal we needed in order to have the excuse?...
They have never proved to us that the virus wasn’t there before 2020 because there’s no PCR or sequencing before 2020.
Great work, Kristen! Thanks for exposing this.
It appears to be all about human augmentation starting with the African Clawing Frog's stem cells (and/or genes). They call this Xenobots, but when they GMO humans, it's called Anthrobots.
Cyrus Parsa was found with a bullet to his head Feb 2025.
https://odysee.com/@Psinergy_vault:8/Cyrus-Parsa-Interview-With-Tore:5
At 38:30 min Cyrus reported:
Two scientists created this technology, endangering the entire race and it’s not just a va=x; it was given to D=A=R=P=A. They used FROB stem cells and they mixed it with robotics--the first artificial life. What they want to do is program it so it can go in and say, “heal people” but what it’s done, if you recall the movie, Terminator, that T2 was going after Arnold, it was more advanced but it was human. What this frog, mixed with robotics (or machines) can develop into is hybrid animal machine systems that can do what T2 can do.
Moreover, it can also mutate and cause diseases in multiple different ways around the planet.
Cyrus: The entire world, from every directions there’s multiple risks coming after humanity. When I filed extinction codes for the majority of the human race, I just didn’t find one thing. I put in there drones, microbots, metaparticles, machines, robotics, bioengineered, cybernetics, conflicts, famines and multiple different things. It’s like the entire puzzle is almost like a plandemic to extinct the individual human race. Everything at first is pointed at China and it’s interconnection to OUR big tech companies…
It’s almost like an invasion of humanity.
More on FROGS:
On Jessica Rose’s Substack, watch the video. Wowzer at 1 minute how they transferred light activated proteins into NERVE cells and then CONTROL them using only LIGHT CELLS.
Optogenetics links gene technology with optical methods [permanently]. It may [can] influence neuro NETWORKS and even one day overcome diseases [and give disease?].
The starting signal for optogenetics came in 2002. But wait, there was another membrane protein that reacts to light in the green algae.
It permits the algae to use light for orientation.
With the molecular biological tools now available the researchers succeeded in transferring the GENE for ALGAE into FROG’s eggs. These now produce the corresponding protein [genetically modified, just like they are doing to humans thru the v=a=x].
The protein is a LIGHT RECEPTOR (the algae and a ion combined). The channel reacts to blue light. It opens up and lets positively charged ions flow into the cell.
Optogentics scientists use this mechanism by smuggling the GENE with the BUILDING INSTRUCTIONS [CODE or sequence] for the channel into the genetic material of the NERVE CELLS. So this channel can now work inside the [CELL] membrane.
If it is stimulated by light, positively charged ions flow INTO THE CELL.
This changes the tension across the [CELL] membrane and the neighboring original channels also open up.
In this way, the cell is depolarized and an ACTION POTENTIAL ARISES. But the opposite effect ALSO occurs. Halorhodopsin reacts to ORANGE light and smuggles negative ions INTO THE CELL. This then deactivates the cell. Switching CELLS ON AND OFF USING LIGHT.
WHY THESE FROGS?
These frogs are more than just frogs.
Human central nervous systems (CNS) injury is irreversible.
Xenopus laevis has a high potential to regenerate the brain and spinal cord during larval stages and have the capacity to fully regenerate after severe injury to the CNS.
They grab the frog’s stem cells (which kills the frog) during the larval stages as it loses the capability during metamorphosis.
The optic nerve can regenerate throughout the frog's lifespan.
Here, we review CNS regeneration in frogs, with a focus in X. laevis.
We start with an overview of the anatomy of the Xenopus central nervous system (CNS), including the main supraspinal tracts that emerge from the brain stem, which play a key role in motor control and are highly conserved across vertebrates
Xenopus, a classical laboratory model organism, with increasing availability of genetic tools like transgenesis and genome editing, and genomic sequences for both X. laevis and X. tropicalis.
Most importantly, Xenopus provides the possibility to perform intra-species comparative experiments between regenerative and non-regenerative stages that allow the identification of which factors are permissive for neural regeneration, and/or which are inhibitory.
Source: https://us1-browse.startpage.com/av/proxy?ep=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&ek=58313953525552425131524652463966&ekdata=239e96fcd8f86656fb8342fbbd2901a6
The African clawed frog model organism has also been used as a tool to study cellular processes like cell movement, cell fate, cell cycle, the cytoskeleton, chromatin, ion channels, and apoptosis. The Xenopus genus has both diploid (X. tropicalis) and allotetraploid (X. laevis) species, often used in genetic research. These frogs have been widely used to discover many different genes involved in congenital heart defects, kidney disease, cancer, gastrointestinal and pancreatic disorders, neurological diseases, muscle atrophy, and human ciliopathies.3
Source: https://us1-browse.startpage.com/av/proxy?ep=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&ek=58313953525552425131524652463966&ekdata=4e00f51d1321fe6737b4151c5cd41f1a
Bravo, Kristen! An exhaustive tour-de-force that truly begs the question: Why is this not being investigated? Thanks for your extremely thorough research. Hopefully, this will reach a wide enough audience (and the relevant authorities) to actuate a proper inquiry.