The Tucker Carlson Show - Dr. Patrick Soon-Shiong: You’re Being Lied to About Cancer, How It’s Caused, and How to Stop It
Episode Date: March 26, 2025Dr. Patrick Soon-Shiong is a surgeon who made billions inventing cancer drugs. He says that Covid, and the vaccines that didn’t stop it, are likely causing a global epidemic of terrifyingly aggressi...ve cancers. (00:00) Why Are Cancer Rates Rising in Young People? (06:16) What Is Causing This Cancer Epidemic? (14:52) Is There a Connection Between Covid and Cancer? (29:33) Why Dr. Soon-Shiong Never Got Covid (42:36) How Big Pharma Tried to Undermine Dr. Soon-Shiong (51:35) Dr. Soon-Shiong’s Analysis of RFK Jr. Paid partnerships with: ExpressVPN: Go to https://ExpressVPN.com/Tucker and find out how you can get 4 months of ExpressVPN free! MeriwetherFarms: Visit https://MeriwetherFarms.com/Tucker and use code TUCKER2025 for 10% off your first order. Learn more about your ad choices. Visit megaphone.fm/adchoices
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And when you started, it seemed like we were moving in the West
toward the elimination of cancer.
Smoking was a huge emphasis,
get rid of tobacco,
and cancer rates will drop.
Obviously, smoking does cause cancer,
and we got rid of it, basically,
but cancer rates went up,
and that is a very rarely remarked-upon mystery
that really bothers me.
Tell us, since you made billions of dollars
selling your companies,
but you're still involved in medical research,
which I admire,
where are we now with cancer?
What are you seeing in cancer rates? Well, what's really worrisome to me now is not just the rate,
but the population in which it's increasing, i.e. the younger people. So we're
clearly seeing an increase in certain types of cancer like pancreatic cancer, ovarian cancer,
and we're seeing that colon cancer, and we're seeing it in younger people.
Just to set a baseline, what's the 10-year survival rate for pancreatic cancer?
It's horrible. I think, you know, if you have pancreatic cancer today,
I don't think there is a 10-year survival rate, so to speak.
Yes.
What there is, however, if you have patients who are what we call
failed all-standard care, the survival rate is in months.
You measure it in two months.
That's certainly my understanding, having watched a lot of people die of it.
So, advanced pancreatic cancer is a death sentence.
Where are you seeing it now?
Well, I got to tell you a really concerning story.
It's not only I'm seeing it now, I'm seeing it in younger people.
And for the first time in my career, you know, when I left UCLA, I was doing all the Whipple's, which is a surgery to actually remove most of the pancreas, a very big operation.
You're a surgeon as well.
I'm a surgeon.
Yes.
And I was also doing pancreas transplants for type 2 diabetes and islet cell transplants and stem cell transplants.
So I had this diverse activity as a UCLA assistant professor.
But I never saw pancreatic cancer in children.
And the greatest surprise to me was a 13-year-old with metastatic pancreatic cancer that
the family called us to help. And to me, that was not only devastating, it emphasized the idea that we're seeing
people with higher incidence of pancreatic cancer and younger. Right now in our clinic
we have 45 year old, 50 year old. And what was sad about this young boy, by the time
he came to see us, he had exhausted all standard of
care and he came from Butler, Pennsylvania.
And all the major medical centers really had exhausted all their therapy.
By the time he came to see us, his body was ridden and he passed away. So, seeing cancers now in younger people,
and almost a rise, almost like, I don't want to call it a non-infectious pandemic,
but this is what I think is going to worry some in the world,
not just in the United States, but largely in the United States,
we're beginning to see this, and it's really worrisome.
A non-infectious pandemic of cancer,
including deadly cancers.
Correct.
Like pancreatic.
In your career, which I think is about 50 years
of working on this,
how many 13-year-old pancreatic cancer patients
have you seen?
Never.
Never.
I inquired around because it bothered me so much now
of why
this is happening
so Dr. Stephen Day
was a good friend who
was trained with me at UCLA
when I was at UCLA
he's now at the Angelus Clinic and I called him
and he said listen Patrick
I'm now seeing an 8 year old, a 10 year old
an 11 year old withold with colon cancer.
Colon cancer?
Colon cancer.
We've never seen that.
We're seeing now 30-year-old, 40-year-old ladies, young ladies with ovarian cancer.
So this is a real phenomenon of a rise of cancer in early people, in young people.
And really need to get to the bottom of that.
Do you notice a difference in the virility of the cancer,
of the speed with which it moves?
Well, I'm getting reports, they've even called it turbocharged cancer.
Yes, I've heard that phrase.
Right? I'm getting reports of that now,
that people that have been in remission before even
are now getting back to cancers and very rapidly progressing.
So if you really think about what the cause of cancer is, you know, and I did a piece with Sanjay Gupta many, many years ago on 60 Minutes.
And I said, you know, the cause of cancer is its inability,
it's not the rapidity of its growth,
but its inability to die.
And its inability to die is because it either hides
from the cells that matter,
i.e. your natural killer cells,
your T cells,
or, and this is what I'm really worried about,
your body and the cancer
has found a way to
suppress your
killer cells.
And once they do that, once
they activate what are called the suppressor
cells, and you call
yourself immunosuppressed,
then I
think you see this rapid progression
because there's nothing stopping them.
What could possibly be causing this?
Well, I think if you look back of causes, you know, ironically,
when I was doing at UCLA, I was working on pancreas transplant
where I want to immunosuppress the patients.
Yes, you have to.
Yeah, because you prevent it. And then I was working on cancer where I don't want to immunosuppress the patients. Yes, you have to. Yeah, because you prevent it.
And then I was working on cancer where I don't want to immunosuppress.
So I needed to understand the body's mechanism.
And we have a crazy, wonderful, exquisite balance in our body.
You have the yin and the yang of the killer cells, and these things called natural killer cells and T-cells.
Whose job is to kill anything that threatens the body?
Whose job is to kill, quite right, anything that threatens the body, whether the body has infection.
If you have TB, you have HIV, if you have hepatitis, you have COVID.
These cells are there to recognize these infected cells and kill it.
As you and I are sitting here today, our stem cells are growing in order to replenish parts of your body, your heart.
If you didn't have that, you wouldn't have a heart.
At the age of 14, You need those stem cells. But mathematically, there are some cells that are transformed,
and your body recognizes that through these natural killer cells and kills it.
I call that nature's first responder.
And that's your mechanism.
That's how we are all protected, and we are in this state of equilibrium or balance.
On the other hand, the moment either the tumor finds a way
to hide from these cells or your body's or the tumor causes these cells to be suppressed.
And that's why I call this the suppressor cells. And there are certain cells in your body
called Treg cells or myeloderived suppressor cells. It's all technical.
And when they get upregulated, you've lost your protection.
And so the question then is, how do we understand this balance?
How do we increase the killers and how do we decrease the suppressors?
So that's been 50 years of my challenge of, and how do we expose the tumor?
So on the one hand, you need to expose the tumor because it hides from the killers.
And then you activate the killers. And the other hand, you have to suppress the suppressors.
So we're truly playing a game of chess. And I think like astrophysicists, where you're looking for God's particle, where all these molecules are floating around talking to each other, all the cells are floating around talking to each other, and this dynamic interaction. Most fun lectures I gave, I gave a lot of lectures on this and tried to be non-technical because it's what I call basic immunology.
And the problem with cancer is it's been treated by oncologists and not immunologists.
And immunologists don't see patients because they look at basic immunology.
And then when you have infection and you have virology,
so this cross-disciplines of virology, immunology, oncology,
all these ologies don't talk to each other.
So you're saying just big picture for non-specialists, of which I'm, of course, one,
you're saying that cancer is to some extent a problem with your immune system.
It is everything about your immune system.
Okay, so you've got all kinds of defective cells that could become cancer or cancer in your body at all times.
At all times.
But your body is zapping them.
Correct.
Right, and that's the fundamental balance of the human body.
Correct.
And when that body gets out of balance, when the killer cells become suppressed or less effective,
that's when you get cancer.
Correct.
Okay.
I'm sorry to interrupt.
No, I love it because that's the perfect interpretation
that I couldn't do in a non-technical way
because I think I get too nerdy.
So I'm glad.
Well, you are a doctor
so but that's that that's I think is what's happening in our body we have these perturbations
but we're in equilibrium you know and that's a good thing the moment you knock yourself out of
equilibrium now what could knock you out of equilibrium and Now, what could knock you out of equilibrium? And that's why when
Bobby Kennedy is talking about and standing up about the toxins in our food, the toxins in PFAS,
the processed food, and viral infections. And really what knocks you out of balance, basically, is inflammation.
If you have inflammation in your body,
there's this, now I'm going to get nerdy again,
these cells called neutrophils that actually see an infection and tries to kill it,
which it does.
But if there's persistent inflammation, these neutrophils actually flip into a suppressor cell. So what people don't realize is that we have the yin-yang in our body that every cell has
a counter cell.
And that's where I was about to go there.
I said the most fun conversation I had where I was asked by astrophysicists or physicists who give a lecture is I named this concept of cancer a quantum theory,
like a physicist.
And that in our body, we have cells that can be in two states.
It can be a killer or a suppressor.
And like the Schroeder's cat, it could be alive or dead.
And it depends what you do with it.
And so I named the thing quantum oncotherapeutics just to be controversial
so that doctors could understand what I'm talking about
is that we need to understand the fact that you have a killer T cell and you have a killer suppressor cell.
We have an M1 macrophage that actually chomps things up and M2 macrophages that blocks that.
You have an NK cell that kills and NK cells that inhibits.
And we need to have that balance, otherwise you'll get into autoimmune disease.
But there's a thing called quantum entanglement that is this cat alive or is this cat dead?
If somebody interacts with that, and the person that interacts with that is the doctor. be enlightened enough to activate just the activators and suppress the suppressors
and change the dynamic towards the cure.
But it's very complex because it's now quantum
because all those changes are happening in minutes in your body.
These molecules, like God's particle,
where they're colliding with each other and cells are colliding and interacting, happens within minutes.
So you need to have a theory of how you interact at that level.
And in so doing, the first thing you need to understand is how does cancer happen?
And then how does it grow?
How do you stop it?
This idea of a vaccine, a cancer vaccine,
do you radiate that cancer?
Do you remove that cancer?
Do you remove the lymph nodes?
Do you give chemotherapy?
And crazy enough, over the last 50 years,
I figured out that everything we're doing
is not the word
wrong, because that's a bad statement, a pejorative statement.
It's not enlightened, a better way to say it, because everything we're doing is tipping
the scales towards the suppressor cells.
We're activating the suppressor cells.
We're not activating the killing cells.
And we can go into this conversation where I can explain that.
So the key system, which you just said, is cancer is all about the immune system.
So if you activate the immunosuppression system, you get more cancer.
So then the fundamental root cause is what's activating that immune system on the other
way.
Yes.
And that's inflammation. Something is suppressing people's immune systems,
including the poor 13-year-old boy who died of pancreatic cancer.
And the question is, what is that?
And maybe there are a lot of causes, but it is, you know,
we're not the first people to notice there's been an increase in scary cancers
in populations that didn't used to get them.
It's very obvious just from living here.
And a lot of people have pointed
to both COVID, the virus, and to the mRNA COVID vaccines as potential causes. Do you think that
they're related? The best way for me to answer that is to look at history. What we know about
virally induced cancers is well established. We know that if you get hepatitis, you get liver cancer.
Hepatitis is a virus infection.
We know if you get human papillomavirus, HPV, you get cervical cancer.
Yes.
Certain kinds of throat cancer are caused by viruses as well, right?
If you get HIV, you get Kaposi's sarcoma.
Yes.
So we call that oncogenic viruses in medical terms,
meaning viruses that are induced carcinogenic.
And the fundamental basis for that are threefold.
The hallmarks of an oncogenic virus is, one, it must persist.
And why?
Because it continues to create inflammation.
And why?
With inflammation, you get suppression, because your body is trying to suppress it.
It must inhibit the thing called P53 that's in your body to try and protect your body from not having cancer.
And if it persists and causes inflammation and inhibits P53, it begins to have the hallmarks of an oncogenic virus. So then the question is, does COVID, whether it come from the vaccine, which is the spike
protein vaccine, or from the infection, which is spike driven, that gets into every cell
of our body, because it goes to the-
Every cell of the body?
It goes wherever you have the
thing called the ace2 receptor which is in the blood vessels so wherever you have a blood vessel
in your body it's where it's going to go and if it has an ace2 receptor on that blood vessel that's
where it can go because that's the purpose of the spike protein to penetrate to hijack that ace2
receptor and get into their cells so that's why it gets in the pancreas. That's why you have brain fog,
because it disrupts the blood vessels of the brain
and causes mitochondrial dysfunction.
That's why in the colon, which has a high,
in the GI tract, there's a high ACE2 receptor.
That's why pancreas has a high ACE2 receptor,
where that's why you people have,
in the heart, you have dysfunction.
You've seen young people have sudden heart attacks all of a
sudden. You see young people with pancreatic cancer all of a sudden. You see young people
with colon cancer all of a sudden. So is it by coincidence that post-COVID infection,
post-COVID vaccine, we're seeing all these events where we know the spike protein goes
there. I don't think so. I think it's not a coincidence. So the question is, can we prove
is this what I call long COVID virus persisting? And the group at University of California,
San Francisco has now definitively proven that and published that in papers like Nature.
Can we also prove that once you have
that persistence of that virus,
does that COVID virus suppress the natural killer cell?
Does the natural killer cell actually
not only go to sleep,
becomes what you call energic?
That's now been published.
The natural killer cell has gone to sleep.
So by your definition,
we just solved the mystery right there.
I think so.
I think this is a conversation I had with the...
But wait, I mean, billions of people,
literally billions of people had the COVID virus.
Over a billion got the spike protein vaccine
so that's like we're talking like a huge percentage of the earth's population
unless i'm missing something now you understand what keeps you awake at night
and it's kept me awake at night for two years two and a half years. And that's why I sort of abandoned everything just to focus on how do we clear the virus?
Because the answer is to clear the virus.
From the body.
From the body.
The answer is to stop the inflammation because it's chronic inflammation.
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So can I ask a dumb question?
How long does the virus remain in the human body?
So far we've found three years, four years.
Is there any reason to believe it will naturally go away?
Not if your body's aim is suppressed.
So it's a circle.
You ask what causes cancer because your body's aim is suppressed.
You have in your body nature's compound.
And if the tumor or the infection or the inflammation suppresses it,
you have to find a way to reactivate
it and clear the virus.
It's literally as simple as that.
And that's the missing link that I think...
So it sounds like you're describing what could be like the worst human health crisis in history.
I don't know how to say that without saying it
it scares the pants off me
because I think
what we may be
I don't think it's virus versus man now
this is existential
I think
when I talk about the largest non-infectious
pandemic that we're afraid of, this is it.
Because while there was an increased rise in cancer in our country because of the idea of
the toxins and everything else, this immunosuppression that has occurred now globally,
and more importantly, the immunosuppression tied to inflammation,
chronic inflammation, which is asymptomatic in some times and sometimes it's not. There's 15
million Americans with long COVID. And they're not psychiatric when they have memory loss.
They're not psychiatric when they have instantaneous heart attacks. It's not psychiatric when you have an 8-year-old, 10-year-old with colon cancer,
a 13-year-old with pancreatic cancer.
So the idea was, is there a solution?
And this is what, thank God.
Well, I certainly hope so.
Because you spent your life around scary diseases.
Like, that's been your life.
And if you're scared, then that's not a good sign.
I'm scared but hopeful.
I think it's important for me to have this conversation with you.
That's why, okay, I'll share with you a conversation I had.
I got invited by the CEO of the Henry Jackson Foundation to come to D.C., I think October, November last year,
during the election phase,
and just to have a conversation about what I'm doing.
And there he brought the leader from Walter Reed,
the barter, the DOD, the NIH, the NID, all into that room.
It was just me.
And I said, it is time.
It is time for me to reveal to this learned group of leaders
about what I'm scared about.
And I spent, I think it was three hours, no slides,
just me speaking alone on the stage and all of them in the audience.
When I first started the conversation, the first sentence was, I think COVID is oncogenic.
One of the members of the audience said, that's nonsense.
I said, okay, let me explain to you what we've been doing in our research.
At the end of three hours, four hours, he said, you've got to publish this.
This is so important.
And I said, yes, we are processing the publication.
And what came out was this paper
that they biopsied the colon of young people temporarily
when no COVID, two COVID,
and showed the persistence of replicating viruses
in the colon tissue two years out.
Replicating COVID viruses?
Replicating COVID viruses.
Replicating.
Asymptomatic replicating in the tissue, meaning there's inflammation.
And when you have this inflammation, these neutrophils,
now getting geeky again,
plasticize, flip from a protective neutrophil to a suppressive neutrophil.
It's called an N2.
It's called a myeloderived suppressor cell.
That's an official name.
So now you have suppression in your body.
And it's no wonder that then converts into colon cancer.
But is this true, do you think for, I mean, have you had COVID?
No.
Lucky man.
Not lucky man. T cell man. I have a T cell in my body that protects me from a nuclear capsid.
Where do I get one?
That trial was held up by the FDA and by Collins and Fauci.
You never got COVID because your protector cells were so strong?
Not only our protector cells.
If I do get COVID, the virus clears.
You want to clear the virus.
Get the hell out of my body.
Get it out.
Wait,
I just want to pause here.
I know you're in the midst
of a much larger story,
but this is something
I think everyone can understand.
So,
I think I'm in good health.
I am in
very robust health.
Did you have COVID?
I did.
How many times?
One.
I never took the vaccine.
Okay.
But I got COVID.
Knocked me right on my butt.
It was a bad three days.
Fine.
But I don't understand.
You're older than I am.
How did you never get...
I just want to get very specific.
Like, how did...
I mean, everyone on the planet got COVID.
Okay, so let me give you some idea, okay?
One, because we understand the implications.
My wife, Dutchwood, also never got COVID because both of us.
So this is the story. We, by, unfortunately, I relate this, it's a painful thing to me,
because I relate it to Kobe's death.
It was during Kobe's time when he passed away.
And at the funeral.
Kobe Bryant, who you were close to.
Correct, very close to.
And at the funeral, at his funeral, all the people in the room,
and there's, I think, November, and I turned to Gavin Newsom and I said, listen, this is one virus I'm worried about because I was studying this virus.
You know, I understand HPV very well and I understand hepatitis.
I said, this is not a respiratory virus.
This is a dangerous virus. So I went back and I shut down our organization so that we could actually do nothing else but COVID. My entire team of hundreds
of scientists on Zoom and everything else around the world, I said, we must go after this virus
with a vaccine that clears the virus.
And the only way to clear the virus is to have what we call a T cell, an NK cell,
the cell that kills cancer cells.
And I wrote a paper with Carlos Godona that said,
COVID's like cancer and cancer's like COVID.
Meaning it's immune suppression that causes its spread.
And it's immune suppression by the COVID virus that allows it to persist.
So the only vaccine that's important is a T cell vaccine.
But that's what I'm telling you.
Virologists think about antibodies versus cellular therapy. It's foreign to them to have a vaccine that stimulates T cells.
So I said, I understand that internally.
It's a little weird since in 20 minutes you explained it to me,
not particularly high IQ, not a scientist.
I understand exactly what you're saying.
Why isn't it obvious to virologists?
Why isn't that like day one lesson in virology school that the T cells, the cells that protect you against all potential internal harm, they're the key.
Because every vaccine so far is antibody based.
Dogma.
Dogma.
Blind spots.
Okay.
Now we're cooking with guests.
Now I understand what you're talking about. Dogma. Blind spots. Nicely put. Okay. Now we're cooking with guests. Now I understand what you're talking about.
Dogma, blind spots, nicely put. Okay. I'm sorry. I keep stepping on your story. So
you figure out. You're not stepping because you're allowing, you're actually interpreting. It's
pleasure to me because I don't know what I'm saying. Sometimes the weather is going to be
so geeky. It gets lost. It's important for the audience for you to interpret. This is what Sanji
did for me
in the 60 Minutes.
He was brilliant.
He spent two years with me,
by the way,
doing a little 15-minute piece.
Wow.
Yeah, we'd come to LA,
we'd do this,
shoot, shoot, shoot, shoot, shoot.
Man, we just had breakfast.
That's it.
Okay, so you figure out early,
everyone's panicked about COVID,
okay?
But your position is they're panicked for the wrong reasons.
Correct.
And actually, maybe they're not quite as panicked as they should be because this virus could pave the way for cancer because it will suppress the immune system of the human body.
So you, in November, you said, when did you?
Right.
So by March 2020, we had the vaccine.
March 2020, we had the vaccine. March 2020. Because I had built a full GMP facility for cancer using the same vaccine that NCI had retested to COVID for the treatment of cancer,
to educate the T-cells to recognize a cancer cell to kill it.
That's called a cancer vaccine,
which, by the way, is the only vaccine in clinical trials today
to prevent cancer that the NCI is running using our technology.
Is there any way you can take the word vaccine out and call it something else?
I'm calling it BioShield.
Good.
Because vaccine just scares the crap out of people at this point.
Because it's not a vaccine in that general sense of an antibody-based vaccine.
It's your body's BioShield.
So we'll announce it on the show.
We're going to call this Project BioShield, which, by the way, in 2004, there was a BioShield Act for national preparedness against radiation, against a
pandemic of infectious diseases.
So we have the worst thing that could happen to you is to have one dose of radiation will
wipe out your NK cells and your T cells.
That's how you die.
Yes. That's how you get cancer. It zaps your immune system.K cells and your T cells. That's how you die. That's how you get
cancer. It zaps your immune system. It zaps your immune system. So we wanted to create a bio shield.
And the bio shield is to educate your body to have these T cells called memory T cells that go and
hide in the bone marrow and come out when they need it and kill that cell so it can never do damage.
That's the concept.
And it's not a foreign concept.
We published it with the National Cancer Institute.
So by March 2020, I took all my resources.
Thank God we had the resources.
So that's the sort of gift.
Was this your money?
All my money.
Okay, so I should just say, I alluded to it earlier, but you had a couple of companies making cancer drugs.
You owned all of them.
I mean, you owned, I think, 100% of the companies.
You sold them for $10 billion or something.
But rather than buy a vineyard, you continued in your work.
Is that a fair?
Very fair.
You know, as I said to you over breakfast, I had no idea about stocks.
So when the two companies were bought, and they were bought for the right reasons.
So one company was American Pharmaceutical Partners,
and we were making literally close to a million vials a day in the United States,
manufacturing of 150 different SKUs for every part of the hospital,
and we're safe for heparin.
So Fresenius said, we want to buy you.
We said, great.
And then I developed this molecule that was feeding the tumor
that could actually activate the immune system
to activate the macrophages called the braxane.
And Selgin said, we want to buy you.
I said, great.
And the purpose for my selling them was not for the money.
Clearly it was for the money,
but the purpose of the use of the money to pursue
this dream of this astrophysics to find God's particle in your human body to activate your
immune system. That was the purpose of this money. And that's what I've done with the money. I spent
about $3 billion of this money. I've not gotten one penny from the government. Not even one dime.
You're the only one. one penny from the government. Not even one dime.
You're the only one.
Yeah.
And maybe that's the freedom and the liberation allow me to say what I can say now.
Yes, that's right.
So, again, I keep pulling this away
because there's a lot here that's interesting,
but how did you not get COVID?
Okay.
So, I recognized that.
So Peter Marks and I had these conversations.
So he was head of CBA.
And I was in pinging him with the science because this is a biologic.
And I was saying to Peter, listen, Peter, I need to show you that we need to create a T cell vaccine.
And he said, well, we don't do T cell vaccines.
Everybody's doing the other vaccines, but great.
Let's continue.
The antibody vaccines.
Antibody vaccines.
And then he called me and he said, we're going to create warp speed.
And he's a star trekking and I'm a star trekking.
I love warp speed.
I said, okay, we're going to do this in warp speed.
Absolutely.
But the only way, Peter, you're going to do this in warp speed,
you need, we need as a country to have NIH and BARDA fund a trial
where we take macaque monkeys, we give them a vaccine
and everybody should throw their vaccine in because I don't
care if it's not mine or theirs, whoever's vaccine to clear the virus. The only way to
this experiment, you give the monkeys the vaccine, it's under your control. You have a hundred
monkeys, everybody gets a set of vaccines, and then you infect the monkeys in the BSL-3 facility with a high dose of COVID.
And then you see in their lungs and the tissue that there's no virus after seven days.
Absolutely. That was warp speed. So I was one of eight of warp speed. Then I get a call, Patrick, you dewarped.
You, I said, test my vaccine anyway.
They did a vaccine test of the NIH in Barda.
It cleared the virus, as I predicted.
There was no virus in the lungs after a big infection.
So I said, okay.
I'm dewarped.
And this was a Francis Collins scheme and Anthony Fauci scheme and Monsi Slaoui scheme.
And one day we're going to talk about the conversation I had with Monsi
Slaoui and what I've learned about Francis Collins in that event. And they were going to go after
this antibody vaccine, which is this mRNA vaccine with spike. And I said, this is too important.
I told my people, we're going to build our own vaccine with our own money. I couldn't get enough
material other than to do one batch and we're going to do a phase one trial and we're going to inject as many people that we
can do in the phase one trial i'm one of them i injected myself um and your wife and then and
we're going to measure i won't. I drew my own blood and tested,
and I have T-cells to nucleocapsid and to spike,
which means if I were to get COVID, touch wood,
the T-cells, now our memory T-cells, would clear the virus.
So we then tried, begged, begged, because not for funding even, but for the plastic
bags that were now restricted as you grow these things to Pfizer and Moderna, all the materials
that you need in a biologic facility. Got zero.
I've only got one batch.
So I said, I'm going to South Africa and inject these in patients with HIV
because that's the biggest test you could have.
You couldn't generate T-cells in the patients with HIV
and do this phase two and phase three trial in South Africa.
So we did that.
And then I called Peter
and I said, Peter. I'm sorry, what were
the results like? T-cells.
The people that
interestingly enough,
it doesn't say, just so
you know,
you have to differentiate
does it actually prevent the penetration of the virus versus the load of the virus versus the clearance of the virus?
These are three different things.
So we think it prevents the penetration, but we don't know because as soon as it does penetrate, it would clear, so you wouldn't even know.
Or the T cell vaccine.
This is anecdotal, but some of the people who got our T cell vaccine, their family members got COVID.
They didn't get it, obviously, the vaccine, and they didn't get COVID from a time while living with their family.
The issue of clearing the virus in transmission was the key.
So an antibody vaccine may reduce the viral load and therefore reduce death,
which is a good thing that President Trump did.
But the next generation of clearing the virus was what was needed.
And both should have been developed simultaneously.
It wasn't.
I'll share with you to this day.
It's a mystery to me why.
But the opportunity to clear the virus was actually known, I think, by Collins and by Fauci that it did not clear the virus.
The spike vaccines.
The spike vaccine.
The Pfizer, Moderna.
The antibody vaccine does not, and to this day, does not clear the virus.
That seems like a big deal.
Well, just what we talked about. clear the virus, and you have pieces of the virus in there, especially spike, whether
from the infection or from the vaccine, and now you get another infection.
Now the virus brings along this nucleic capsid.
Now it reconjoins and replicates again in these, what they call privileged sites, two years later.
So what we're seeing, now we're back to persistence.
That's now published just months ago.
And this is what I shared with NIH secretly four months ago.
And persistence, asymptomatic persistence but with inflammation,
and reduction of p53, and immunosuppression,
are all the hallmarks and recipes for cancer.
And coming back to your first question is,
why are we seeing an increase in young people?
I think all of the above.
The toxins, the history, the red dye, the PFAS, the COVID, all of the above.
Does both COVID and the COVID vaccine lower over time the human immune system?
The vaccine itself upregulates temporarily the antibodies.
But if the vaccine, the spike protein breaks off,
and the RNA or DNA goes into the cells,
and from infection or the vaccine, that's where the controversy is, right?
It could be both.
And the vaccine doesn't clear the virus.
That's the key.
It doesn't clear the virus. And that's why we were told, of course, you take the virus and then you can't get COVID or transmit it,
but neither one turned out to be true. Demonstrably untrue.
Well, it's not only demonstrably untrue, it was knowingly untrue. That's what's bad about it.
Would seem like that's criminal, actually. I mean, if I tell you that, you know,
this car gets 40 miles to the gallon and instead it blows up, that's a crime.
You can't sell anything under false pretenses.
That's a crime.
I don't see how this is not a crime.
Well, as you said over breakfast, it's not a conspiracy if it's true.
I believe you're writing a book with that title.
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So, and you know that they knew?
You've established for a fact that the developers of this and our public health authorities knew that the COVID vax would neither prevent infection nor transmission.
Yes. And worse, I think, you know, it's not well known that during the first President Trump election, he offered me a position.
And I turned it down because I said to him I really could help him from outside in better than and I had too much to do I really was working on this thank God working on this um potential cure for
cancer as well as clearing the virus with COVID this this what I call the missing link which we
can talk about this activator of the unnatural killer cells this bio shield and we have this
bio shield now so it was the right decision for me
not to go into the government during that time
and to stay out.
This was 16, 17?
Correct.
But worse, I've since discovered,
not by my inquiry,
but it's been revealed to me,
emails about Francis Collins
and some politicians work hard
to prevent me from even joining, becoming head of NIH. And I think that was the motivation all
the way downstream that we asked, okay, so what happened to this vaccine? So I called the FDA
and said, okay, I can't do a randomized placebo-controlled trial now
because you've got Pfizer's, Moderna vaccines all over the place,
so let me be the booster.
And Peter Marks, to his credit, was the one who said, absolutely.
Peter Marks, to his credit, was the one who says,
I'm worried about this COVID vaccine and this long COVID.
I want to study the effects of this vaccine.
Peter Marks would then say to me, Patrick, fine, go ahead.
I injected the first three patients as a booster.
I get the call from the FDA to say, you have to stop.
I said, why?
To this day, they never explained to me.
It wasn't Peter.
It was people around Peter said, you must stop.
So we stopped.
And there was nothing more we could do anyway,
because we didn't have any of the resources, the money, the supplies to complete a phase three.
So the government has a monopoly on some of the materials that you need to do this kind of testing in a bio lab. Is that, is that correct?
Correct. But now we into Biden era.
So now we in the Biden era that said, I must stop. This is 2020 now.
No, no beyond. Yeah. It was, yeah.
It was during the Biden era.
And I think there think there was this
sadly I'm not a
conspiracy theorist but now I've come to
realize it truly was a deep state
inside there that
had a motivation beyond
it's hard
to say it's the most devastating to
say beyond public health
and you know I just tweeted recently of It's sad to say, it's the most devastating to say beyond public health.
And I just tweeted recently of how few people could hurt so many.
And that's why when I tweeted about finally we have the right person in HHS with Bobby Kennedy, we'll take this on.
And that we have doctors that will be like Marty McCary,
who I don't know, but I do know he's a surgeon who can understand and touch and feel what it means
to be there on behalf of the patient.
And my support for that,
I think we have a chance now to completely turn this around
in this next i think this last election was in part about that i think the national realization
that covet was there was something very dark there it wasn't just a virus that happened upon us uh
naturally that there was there was there was a lot of evil uh bound up in it but just to back up a
second you said you have learned from watching COVID
that a few people can hurt so many.
Who are those people?
I think the main culprit really sitting there was Collins.
Francis Collins.
Francis Collins.
And he controlled, I mean,
I had shared with President Trump
that Francis Collins should not be the NIH director
he offered
me a job
Peter Thiel nominated
me
and I've since found emails
of Francis Collins
sending
an email to a politician that
alarm bells, alarm bells, Peter Thiel has nominated Patrick Soon-Shiong, we have to find a way to stop it.
Why?
To this day, power, greed, political need.
He did the same thing with Craig Vento. I remember during Clinton's time with the Human
Genome Project, where Craig Vento invented the sequencing machine for tens of millions of
dollars, and he was spending billions of dollars doing nothing but wanted the credit.
I think what happens to you when you get into Washington, the ego, greed, and power changes your mindset.
So I can't give motivation to that.
All I can tell you is when I saw that email, I was devastated
that somebody would actually go to that extent
and then send that same email to the CEO of Bio, which is all big pharma.
And that CEO of Bio said, let's go to Google search to find some dirt on him.
Dirt on you?
On me.
To stop me from being nominated to be head of NIH or whatever.
Let's Google him to stop him?
Let's Google to find some dirt, some bad stuff, negative research, whatever they want to find.
They probably couldn't find any dirt on me, but that was the interchange between them.
On email.
But the funny thing is, you made a product, and by the way, a clarification of terms.
My understanding was a vaccine was administered to a healthy
person to prevent him from
getting the disease. You're describing
a product, the one that you made,
that you can inject into an
infected person, and it cures the infection.
That sounds more like a conventional medicine than
a vaccine. It's a therapeutic. A therapeutic.
Correct. So, you know,
I use the word vaccine because that's what they understood.
You know, it's dogma in terminology.
Right.
But you're giving this to people who have COVID, who have HIV.
Well, I want to give it to people who don't have COVID so they can actually get COVID.
I am now giving to patients with HIV.
I'm giving to people with HPV.
I'm giving it to people who are getting
cancer and have cancer. And more importantly, there's one in 280 Americans, one in 280
Americans have this thing called Lynch syndrome. What Lynch syndrome is, is a genetic
predisposition of an 80% increase of colon cancer, ovarian cancer, breast cancer. It's a genetic predisposition where your cells don't repair themselves.
I lost a friend to this, yes.
We are in clinical trials for the BioShield for patients with Lynch syndrome.
We now have 100 patients enrolled already, giving them this BioShield.
That'll prevent cancer.
So it's one of the first trials of prevention of cancer,
rigor and treatment of cancer.
Then this drug, this BioShield,
I keep on not wanting to call it a vaccine,
has just gotten approved in 2024 for bladder cancer.
We now have people who have failed everything,
who would have their bladder removed.
Think about that, your bladder removed,
the 9% mortality just from the surgery alone,
where we've given them this bio-shield,
that's all they got is a subcutaneous injection,
or, sorry, into the bladder,
and they are now free of disease, still, complete remission,
nine years out.
Alive today.
We can talk to them.
Published.
We have patients with metastatic pancreatic cancer.
We just published.
We're free of disease five years out.
Senator Reid, who came to see me after having failed all other treatment with his pancreatic cancer, sprained his liver,
came to see me and he said to me,
Patrick, I'm here, but I checked with Francis Collins who said, don't go.
I said, well, Senator Reid, your choice is oncoming.
And we gave him the therapy.
And he, C-19 he went down to normal.
He lived for two years free of disease.
He actually was very active.
We had a patient with Merkel cell carcinoma, which is a terrible disease of failed everything.
He came into our clinic, complete response.
Nine years out,
he died of other causes.
The reason I met Robert Jr.,
I've not known him for about four months,
is I called Bobby Shriver.
His cousin.
His cousin.
And the reason I knew Bobby Shriver
because Bobby called me
seven years prior to that
saying,
Patrick,
I'm on the city council
of Santa Monica
and the mayor of Santa Monica
has this terrible tumor
in his head and neck.
It's ulcerating
under his chin,
ulcerating through his jaw
and UCLA
and see the sign.
I said,
he's got two weeks to live.
He's got to go to hospice.
Can you see him?
I said, absolutely, Bobby.
I think he needs our natural killer cells.
He needs our bio-shield.
So I brought him to our clinic,
which we have in Los Angeles,
in El Segundo.
The nurses broke into tears.
The nurses said, Patrick,
what are you doing?
You should say he has to go to hospice.
You should give this man.
I said, no, you don't understand.
We can dynamically activate this.
And this is all as an outpatient.
We got him into complete remission.
Complete remission.
Is he still alive?
So it healed.
And this melted the tumor.
He went home.
Because it was exposed,
a little bleed happened in the blood vessel.
His family took him to St. John's. And then they called me frantically and says,
the doctor says, do not resuscitate. I said, what? Let me speak to that doctor. He said,
well, it's bleeding and it's got this thing. I think it was in his late 70s, 80s. I said,
please clip it.
It's a complete response, and we're going to do a flap to cover that.
He did.
We did the flap.
He lived for two years, ate, was able to eat.
So when I called Bobby and I said, Bobby, you remember what we did?
He said, absolutely, Patrick.
A lot of people have asked me to introduce to Robert.
You know, Robert and I don't speak very much.
We've had an argument about his ideas.
And I said, I understand.
But I'm going to give you a number to Robert, to Bobby Kennedy, and he'll call you.
Bobby called me in 10 minutes. And I said, Bobby, I'd like to
introduce myself. He said, Patrick, can I meet with you? I said, please. And he came to meet
with me at my home. And we had this long conversation. And I realized, I've just,
I watched your show with him.'s what he is an authentic
man with a sense of purpose
conviction, courage
he says what he really believes
sometimes it may be wrong
sometimes it may be right
but he says what he believes
and I really believed
oh my god here's somebody
who would have the courage
to take on the
world and ask the questions.
And I said, I'm going to support you.
That's what happened.
That's how I got to know him.
Amazing.
He was dismissed by, no, not just dismissed, attacked and vilified by a lot of people in
the medical establishment, I would say, everybody.
Why were you willing to listen to him?
Because what he's saying is exactly what I was saying.
And I'm sort of attacked by the same people because of the dogma that's out there.
So let me give you this example.
I said, Bobby, and I shared with him the story about Hope Hicks. I said that you probably just walked out to the office and I walked in in 2016, in 2017. I said, listen, people think of
you as saying you shouldn't have a polio vaccine, that you're an anti-vaccinator.
What you really are saying,
you're worried about the excipients inside the vaccine.
About the what?
Okay, so that's the technical,
the materials that go in with the vaccine.
Yes, the mercury, etc.
The mercury, etc.
So I understand there's a polio vaccine,
there's one, two, three, four polio vaccines that have now been manufactured.
And now that all of a sudden there's a new polio vaccine that's manufactured in which we have cow's serum, calf serum, inside that vaccine.
And I know and you know, everybody knows, in the UK knows, you can get prion disease from this calf serum because you can't measure that.
So that got approved in four days with just because of safety, the way dogma is happening.
But there's other polio vaccines.
So you can take the other polio vaccines, but don't take that one.
Just like I was telling you about, maybe I was telling you about propofol story over
breakfast.
And you should explain it that way, that you want it just to be examined.
And he said, exactly.
I said, okay.
Not only did I get him, he is asking the right questions.
And people are scared to ask these questions because it's perverse incentives.
And that was what bothered me. But in science, shouldn't any question be allowed?
Exactly. So when I tweeted, I said, he knows more science than most doctors.
He's much of a... It's a good thing you're rich,
because you'd be out of a job tweeting stuff like that.
But it is, right?
And that's what's a blessing, I think.
You know, I live the American dream,
and that's why you said,
okay, I made this money.
The money is for the purpose
of me being able to do this.
And I was very concerned
about being too loud about it,
because if this deep state
would hold up the approval,
and they did, by the way, they put us into complete responsibility. I got a thousand
requests for information. My submission was close to 700,000 pages in order to get this thing
through. 700,000? It's like the US tax code. This drug has been in trials now for eight years.
2015.
How long was the Pfizer mRNA COVID vaccine in trials?
Months.
A month?
Not even.
So that's why I'm trying to say, you know, when you...
I know which one I'm taking.
When you talk about the user fees,
so we thought that the user fees was going to accelerate the approval
where the FDA gets user fees from the farmer.
It turns out that the big pharma user fees are so large,
it pays for the salary for all these reviewers.
So now the biotech companies, the young biotech companies are throttled.
So the big pharma that does this is incremental, little dots that just follow the revenue.
There's checkpoints, multi-billion dollar, Merck's, what, 20 billion, 30 billion on revenue.
Bristol-Myers follows it.
AstraZeneca follows it.
Roche follows it. AstraZeneca follows it. Roche follows it. They're all the same, but it's all about
incremental sameness and follow the dollar. But the innovation is really at these young
biotech companies that are throttled. This is what needs to be changed by the FDA today.
They need a complete revamp where people with skill sets and the skill sets of the modern science,
not the old drugs, have to be in place to understand what's at stake here.
Time for another True Life Alp story. I got a call from a friend of mine yesterday,
honestly, true story, who said his girlfriend had just broken up with him over Alp. He wouldn't
stop. And I thought to myself, that's kind of sad.
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Imagine if I'd married her.
Now I know.
I was saved.
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through a major American city, pulled over by a cop in a speed trap.
Cop takes his license registration, goes back to the patrol car, runs him,
comes back, looks in the window, and sees a tin of Alp on the dashboard.
Pauses.
Stunned.
Says to my friend, you use Alp?
Yeah, I do.
Says my friend.
So do I, says the cop.
We all do.
He looks at my friend thoughtfully and goes, drive safely, sir.
And hands back his license and registration.
No ticket.
So in two days, he's saved from a tragic marriage to a girl who doesn't like Alp and a speeding ticket.
All true.
It's more than a nicotine marriage.
In an age of 350 million, people are guessing there are about 350 million Alp stories.
Email us yours.
We want to know and read it on the air.
Email tellall at alppouch.com.
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Give us your Alpouch.com. Tell all at Alppouch.com. Give us your Alp story.
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Well, you have to take the conflicts out too.
I mean, if a reviewer is paid by the company whose drugs he's reviewing, that's like such an obvious conflict. In no other world would that be acceptable.
Not only wouldn't be acceptable, if then that reviewer has also the role to block an innovator. It gets worse.
Again, this just seems like crime to me.
Yeah. I mean, I don't know. If this were going on in another country outside the United States, and I'm an American, so I give the United States every benefit of every doubt.
It takes me forever to realize something's corrupt because it's America.
It's not corrupt.
But if this were happening, I would just name the country, China, South Africa.
You know, I'd be like, well, that's the most corrupt thing I've ever heard.
Well, that's exactly the fear I have now.
The Chinese don't have this restriction.
And their innovation is now outstripping us.
Think about that.
I've always said America's lead in healthcare and biomedical innovation is the best in the world. And if we could use biomedical innovation as foreign policy for Africa and to Asia and to India,
to bring that to the rest of the world, that's how we lead.
I now read the papers and the Chinese science is now outstripping us.
Look what happened to AstraZeneca just last week.
They just spent $2 billion investing in China now.
That's a tragedy for us.
Not for manufacturing?
For innovation.
Oh, so that's not good.
Not good.
Because the idea was we offshore all the manufacturing,
but the ideas regenerate here.
So AstraZeneca is an English company.
So what I'm saying is
the fundamental problem
I think lies at the FDA
and even the NIH.
So the change that Bobby's
bringing in with Jay now being a head
of NIH and Marty being a head of FDA
and Bobby himself having the
courage to stand up to talk
both against the food industrial complex
and the pharma complex
take on the mercs of the world
and the phisos of the world
I think we have
maybe an opportunity what I call
a period of enlightenment
and really I'm all about enlightenment
and if you can look at
the Sanjay piece we are there now
so I want to actually send out
can I stop and ask you a question though
so your position is that cancer
but not just cancer
all kinds of illnesses are caused
by weakened immune system
and inflammation
it's all about the immune system
your body functions
you live or you die
by the immune system
the senescent cells aging is the immune system.
The cells in your body that allow you to go to 100 years old, 120 years old,
is based on the activity and the function of the immune system
because the immune system is what's regulating your healthy cells.
Can we just go through, I know this is not like patentable this is not your business but it's what are some of the obvious things a person can do to strengthen his immune system so you ask
what activates the natural killer cell so this is your it's like know, when you look at the leaf and you talk about apoptosis and the leaf actually sits and goes brown and it changes, but then it goes back up.
So all of human nature, all of nature is filled with this biology of this balance.
So you have, you're a product of nature.
I mean, literally you're a product of when you were tadpole and a fish as we came out.
So this cell is evolved since the Cambrian age.
Think about that.
This cell, this natural killer cell in your body.
I published my first article in Natural Killer Cell in 1990.
This cell was only discovered in 1970s.
Think about that.
And we've ignored that cell.
This is what I call the missing link.
I'm going to announce that at the American Urology Conference in Las Vegas in the end
of this month.
We have discovered, I've not discovered the missing link, we've discovered the
awareness of this missing link and how to activate this missing link. So the idea is to activate the
natural killer cell. It has 30,000 receptors on this cell. What this natural killer cell does,
it replenishes itself with sleep. So sleep is important. It replenishes itself with sleep, so sleep is important.
It replenishes itself with light, with sunlight.
And I believe there's a certain wavelength, the red wavelength in the sunlight that it
actually requires for it to be stimulated.
This is why people get sicker in the winter.
Exactly.
That's why Seattle has the highest suicide rate.
Think about that, right? So, these things, and if you look at the places like Norway and Sweden where there's very little sun, Finland.
So, nature's all about light, sunlight.
So, that's why I think this is...
I like obvious observations.
Nature's all about sunlight, of course.
Plants don't grow without sunlight.
Right.
And at the end of the day, we're either about neutrons, photons, and electrons.
That's what we are.
We, as a human being, is nothing else but a battery and end gate.
When you think about that, right?
So we have a bunch of electrons and neutrons and charges that are floating through us that actually interact.
And that's how I think of the human body.
That's why I said I think of it as an astrophysicist.
It's crazy, but that's how my mind works.
So sleep, getting sunlight.
And having food that doesn't immunosuppress your biome.
The bacteria in your body sends out materials
that actually will immunosuppress or activate.
What are the immunosuppressive foods?
Unfortunately, I think most natural foods are fine.
It's the toxins in the food,
exactly what I said, the excipients.
So when you talk about the red dye, the processed foods,
all this unnatural processed stuff
ultimately cause inflammation.
Now, when it gets back to this plasticity of inflammation, inflammation causes immunosuppression because it causes all these cells to flip from the killer state to the suppressor state.
That's why we said we have this dichotomy of is the cat alive, is the cat dead?
You see it too in the elderly.
It's why an infection or a diabetic foot infection can lead to a systemic infection and kill the person.
Correct.
Right.
That's why, you know, when this guy discovered that H. pylori causes gastric ulcer, they said, you're nuts.
It's acid.
I remember that so well.
So well.
So now when you think about that, so that's what I'm saying.
But that's a consensus now, right? Acid does not does not cause ulcers well it's the cause and effect so h pylori causes
the the inflammation and then the acid that's measuring your stomach activates it but it's
not the core cause correct correct but it's all about dogma that's why i call this a vaccine but
it's a bio shield so so you have to fight dogma. Part of the problem is you're fighting.
So I will ask you, I wanted to ask us to do an experiment.
I'm all for it.
Where we pick up the phone, call any random oncologist, not to shame them,
primary care physician, pick up the phone and said, you do a CBC, correct?
Yes.
Can you define what a CBC is?
A complete blood count.
Just you take a blood and you look for...
Yeah, the blood screen that everyone has.
Blood screen.
Yeah.
For whether you're anemic or not anemic.
Yeah, yeah.
People understand that, right?
Red blood cells.
And you see these red blood cells.
And you give chemotherapy and radiation.
And you ask, what do you look for?
Well, we look to see if you're anemic.
So we can give you this drug that Amgen makes called Epigen.
We look to see whether your platelets have gone down.
So we can give you a platelet transfusion.
We look to see whether your neutrophils have gone down
so that you don't get an infection called neutropenic fever.
So we give you this drug, Neupogen.
Well, the problem
is, does red blood cells cure cancer? No. Does platelets cure cancer? No. Does neutrophils kill
cancer? No. What kills cancer? The natural killer cells and T-cells. So in that CBC, there's a thing
called the lymphocytes, correct? Do you look at that? No. The only cell that is important that kills cancer,
99.9% of oncologists will say,
we don't pay any attention to that.
That is surprising.
The people will determine, that does seem ass backwards.
Why, if you're not, not to attack oncologists, but if you're fighting cancer, why do you ignore the one cell that fights cancer?
That's the experiment I wanted us to do.
That's a little mysterious. Am I missing something?
That's exactly. That's the missing link. The final frontier, the E equals MC squared, the God's equation.
That is the key element in your body that we've been missing for 50 years.
For 50 years.
But it's even worse than that.
Those missing link, we've actually destroyed with chemotherapy.
We've destroyed with radiotherapy and we've destroyed with checkpoint inhibitors.
We've destroyed with steroids.
Guess what we give to patients?
Chemotherapy, radiotherapy, steroids and checkpoints.
Am I missing something?
I don't know anything about this.
You know, I was a Russian studies major.
But I have no, just because I'm 55, I know a lot of cancer patients. I have always been skeptical that the protocol is effective based on.
So what I have noticed is those therapies seem to beat back the cancer in the short term.
But then so often you watch it come roaring back.
You know, I'm in remission and then wham, you just get hit by a tidal wave of cancer and eliminated.
So if you see my writings, I have written so many times, you win the battle and you lose the war.
So this is not, I'm not imagining this phenomenon.
You're not imagining it.
You win the battle and you lose the
war the reason you win the battle is because you see this little blip of a response with chemotherapy
and then the moment you stopped or not even again you've actually now killed the cells that are
there to protect you you've upregulated these suppressor cells and you get metastasis and you
sorry you know you have to go to hospice think that. That's what we've been doing for 50 years. That's a dogma that I'm
fighting. So what, okay, so let's just say I leave here and I'm diagnosed with, you know,
a serious life-threatening form of cancer. What would you recommend I do next? So this is where you play chess and don't play
checkers. This is where you play go, where you say, okay, what is the cancer doing first?
Well, guess what? The cancer is not stupid. So he's figured out a way to hide from these killer
cells. So the first thing you have to do is you have to expose the receptors on the cancers
of the killer cells could recognize that. So even in the presence of chemotherapy,
you don't use chemotherapy to kill the tumor. You use a tiny dose of chemotherapy just to stress
the patient
the cancer
and the cancer says
oh my god something's coming at me
and it starts exposing itself
so you go from hide to expose
so you use the chemotherapy
at a low dose
called low metronomic dose
to use it as what I call
an immunomodulator
importantly
I was asking you're describing cancer
as almost like an autonomous entity
that has a goal, a will to destroy the human body.
It does.
But that's, I mean, you're describing like a...
It's a machine.
But with intent and kind of clever behavior,
it hides like what?
You're describing like some foreign entity in the body that's trying to kill the body.
It is.
It's like a virus.
But how can a tumor know to hide?
Because it has genomic sequencing in there that actually blocks the expression.
Which sounds diabolical.
It is diabolical.
That's why I spent 50 years trying to understand. It's not a human brain.
It's biology and how biology can mutate and actually, your body is a beautiful thing.
It's an exquisite thing. So it has to have this thing called epigenetics. So it has the genomic
sequencing that says, I'm not going to express this. So we can now stress that and block the block,
and it now expresses something on its surface that our T cells can recognize.
So that's the first step.
Smoke it out.
Smoke it out.
But your body has mechanisms to smoke it out.
It gets even more complicated.
Your body has a thing where you can induce what
we call damps, which is damage associated molecular patterns, but forget that. It's a way
of actually smoking it out. So now your T cells can recognize it. Okay, so now you've done step
one. That's just step one. That's one molecule. So this is why I think the FDA needs to understand
we're fighting a war where you need battlefield awareness all simultaneously, where you have to orchestrate your Marines, your Army, your Navy, your Air Force, all in the right place.
So that you can use the tumor in your body to act as a weapon, as the vaccine.
Because a tumor has molecules
that is foreign to the rest of your body.
And if you educate your T cells
to recognize as molecules
that is foreign to the rest of your body,
that T cell can remember.
Now you have a memory T cell.
So for the first time in 2024,
in our package insert,
we have a molecule called the bio shield now.
I'll call it the bio shield.
They can activate the natural killer cell,
activate the killer T-cell,
and drive memory T-cells.
We now have bladder cancer patients
who would have lost their bladder
in complete remission for nine years and still alive.
And so the protocol is you low-dose,
you administer low-dose chemo
to identify where the tumor is.
You smoke it out.
You smoke it out.
But at the same time, you need to have the natural killer cells and T cells ready.
So you give them the bio shield that upregulates and stimulates your natural killer cells and
T cells.
What about radiation?
Does that play a role?
That'll kill your natural killer cells and T cells.
So no.
Unless,
and this comes out unless,
today the radiation is what they call
70 gigabits,
huge doses.
Unless you give
a tiny little dose
just to the tumor,
no else,
to smoke it out.
So you use radiation
in a very different way
called SBRT,
a low dose.
To identify rather than destroy. To identify rather than destroy.
To expose rather than expose.
So the algorithm is expose, from hide to expose.
The next algorithm is activate and proliferate your NK cells.
And that's with the subcutaneous injection.
The next algorithm is to educate your T cells with a vaccine that you anticipate that it's going to be exposed.
So you now have educated T cells ready.
So you've got educated T cells, you've got NK cells.
And the next thing is to activate your macrophages so they become killer macrophages.
And the next step is to suppress the suppressors.
You do that all simultaneously.
How much human suffering is involved in this?
There's a lot in a conventional course of cancer therapy.
All as an outpatient.
We've done hundreds of patients now.
So someone taking this course is not going to, is he going to lose his hair?
All as an outpatient.
What's even outpatient. No.
What's even more exciting.
Because that matters for cancer patients.
I mean,
it's hard to be a cancer patient.
It's horrible.
Yeah.
But we've now seeing patients now in complete remission.
More importantly,
I want to treat patients before they need surgery.
So I can use the tumor itself in the body
as the vaccine
to educate the body and the T-cells
all about that tumor.
What's even more exciting now,
we can take blood from you,
one pint,
and extract the natural killer cell in the T-cell
and grow billions
and store it in cryopreservation,
just like you do, I don't know, from cord blood.
We now have the ability to grow these natural killer cells and give it to anybody.
So I always said for the first time we could become the American Red Cross of cancer, our country, and use these innovations as foreign policy.
So could, looking back, do you think it was unwise to require the population to get the Pfizer and Moderna vax?
It depends
on the time.
I think it's unwise
to keep on giving this nonsense.
I shouldn't say that. I should be careful
when I call it nonsense.
The idea of giving an antibody
vaccine and then create another antibody vaccine
and another antibody vaccine that chases
your tail?
I don't know what that's doing, those spike proteins.
It's not ridding your body of COVID, though.
It's not.
Is it creating even more variants in your body?
I don't know.
But is that possible?
I see the idea, and I'm such a scientist,
I need to actually go and actually pull out these variants and sequencing them.
That's what we're doing now.
Is it theoretically possible?
It's theoretically possible.
Could there be any change to a person's DNA from taking this?
Well, that's what this does.
It's what the mRNA vaccines do.
Correct. It converts into DNA, and it converts into replicating,
and that's what it does, and it replicates an RNA virus. It converts into DNA and it converts and replicating and that's what it does and it replicates
an RNA virus
and becomes
the virus.
Well, as someone
who's clearly
you've made reference to
a couple times
interested in evolution
to change
the DNA of a species
is to change
the species over time.
No, I don't think
it integrates.
My concern is that
this virus
is all about itself.
Very selfish virus.
Selfish virus.
In fact, the fact that it's now less deadly is in the virus's interest.
The virus doesn't want to kill you because you are the incubator.
Think about that.
The virus wants you alive.
You're speaking in a way that suggests intent and forethought.
It's biology. It's evolution. Everything is evolution.
It was the intent to go from a tadpole to a human being.
I don't know, but to consider the possibility you have something, or the certainty that you have something within your body that is acting against your body's interest on purpose.
Yeah, because it needs you to be the incubator. So, you know, the
the veracity
when it
was so man-made.
So, you know, viral evolution
when it would be called
affinity maturation,
it matures itself so that it can be more infective.
That's one thing it tries to do as a virus.
I mean, these viruses are living organisms.
And when I say living, they don't have brains or anything else,
but they have machinery that is very sophisticated.
They have what they call promoters and et cetera.
Why would you make something like that on purpose?
Well, there are viruses in nature.
Of course.
Which theoretically will go through what you call maturation that normally do not infect
you.
They're not species.
They're species specific.
But why would you then change that?
And that's what this, you know, gain of function study was so dangerous.
That's why it was prohibited.
It's so self-evidently evil to even play with something like that with the potential consequences which we're now seeing.
13-year-olds getting pancreatic cancer.
Like, how could anyone do that?
And why aren't those people in prison?
Well, it was banned, right?
It was banned in the United States.
Yeah.
Hence the Wuhan lab partnership.
Well, so we subverted it.
Now you talk about, you know,
why so few people could harm so many.
How they got around that
is for the investigators to find out.
But, I mean, you're someone
who's created cancer drugs,
who spent a lot of his life in a lab.
That's why you're a billionaire.
So you know a lot about this topic, obviously.
And it's clear to you that that's just too dangerous to be doing that, right?
Yes.
To take animal viruses and make them...
You can't control it.
Because you've done affinity maturation
that state would have taken tens of maybe millions of years in that fusion protein they created this
fusion protein and created and then then they created this vaccine but i think i think bonnie
graham was the part with collins and everything else that were so proud to create this RBD and make it stable.
Think about it.
The spear hit the tip of the spear that goes into your cell.
We're going to make it stable.
That's why this vaccine was produced.
This was the mRNA vaccine was produced.
So you've taken a virus that has now gone from bats to man only because I think the skin function work.
You then create a vaccine by taking the spearhead of this virus that is now being created to get into you and make the spearhead even more stable and put it on the vaccine and says, here we go.
This seems super crazy. So just from the perspective of a layman
again, if I've never had
COVID and I get
the
Pfizer vaccine,
mRNA vaccine,
if I got it three years ago, can you detect COVID
in my body now?
Possibly.
See, that's just crazy town.
Look, I know of a... I won't name her, but she was a very senior person at the FDA.
And she just got the vaccine, that's it.
And within weeks, she got brain fog, loss of memory. So, there's clear evidence that sometimes the vaccine is the cause,
and sometimes the virus is the cause.
So, that's what I'm saying.
It's not mutually exclusive.
I understand.
But it's all about the spike.
But the idea that you would be introducing the COVID virus
into a body that was not infected by the COVID virus.
It's like...
You went after the wrong protein, basically.
I've been begging them to go after the nucleocapsid protein
because the nucleocapsid protein,
which is in the core of the virus,
is not the tip of the spear.
And if you have a T cell, it lasts for 17 years.
We know that from previous COVID infections.
But they refuse to do it.
It seems like a human tragedy at an unimaginable scale.
Completely. It devastates me.
Well, that's incredibly bracing.
And I think you're one of the very few people I've ever met who has the absolute authority to speak on this.
And yet you've not been encouraged to speak about it, it sounds like.
I've not been what?
Encouraged to speak about it.
Yeah, because I'm not a political person
and I have this bigger picture that we have to find a solution,
not just for COVID, but for cancer.
And the irony is this bio-shield works for both.
And the only chance... Because they're connected, it sounds like.
Completely connected. I had no idea that the political deep state was so powerful and so vicious and so egotistical
that they would stop good science.
So now I'm out there speaking because the drug got approved.
But that's not enough just for bladder cancer.
It has the same treatment effect for pancreatic cancer,
lung cancer, triple negative breast cancer.
It is the only molecule for 50 years
that upregulates these killer cells, period, the missing link.
Well, you never got COVID.
So that's, you really never got COVID?
Never got COVID.
How many people do you know who didn't get COVID?
The President of the United States got COVID like four times.
So if you did get COVID, there's three antigens in the virus.
There's a spike, there's a nucleocapsid, and there's a thing called the M protein, M.
And if you have, when you do your blood test, you can see if you have the M protein.
If you have the M protein in your antibody or T cell or antibody to the M protein, that
means it came from the virus.
If you have no M protein, it came from somewhere else.
Could come from the vaccine. I have no M protein and I have T cells to N and I have
T cells to S.
So you could basically lick a park bench and not get sick.
No, it doesn't exactly. So now you need to differentiate and not conflate the ability
to the virus to infect. It could still infect me, But my body has the protection, the bio-shield,
to clear it immediately.
Within seven days.
Clear it. Is this a lifelong
protection? Well,
based on the science of the
what they call MERS-1, where
it was infected, 17 years
is protection. That was the original
coronavirus outbreak. Correct. 17 years
as nuclear T-cells is out there. So, I'll take coronavirus outbreak. Correct. 17 years as nuclear T cells
is out there.
So,
I'll take that.
I'll take 17 years.
Exactly.
And you can get a booster.
Now,
what we're working on
is a universal
COVID virus vaccine
for all
coronaviruses
because it's in.
So,
what we did,
oh,
that's a good
segue to that.
So,
during my genomic sequencing,
I was building the whole machine learning supercomputing network
and I ran the National Lambda Rail for the Cards particle
and I built supercomputers and AI way before AI was.
And I presented the AI model to President Obama,
believe it or not, in the one pager for healthcare.
So our supercomputer, we combined ourselves with Microsoft
so that we had the largest GPU cloud during COVID.
And we were able then to actually look at the infectivity of every species,
every variant of COVID with every human type.
There's a thing called HLA.
So that we could actually look at how the virus would change and avoid the T cells.
The only thing that it could never do was change the nuclear capsid and never could avoid the T cells.
We made that software public at ISTL public and published it,
so that anybody could test.
Based on your HLA, your HLA and my HLA type would be slightly different.
There's hundreds and thousands of HLA types.
And know whether this sequence, if you had that sequence in your body, would be protective.
Through that, we are developing what we call a universal COVID vaccine.
BioShield T-cell vaccine.
And we have it.
But how do you do it?
So one of my thoughts
was just to give it away to somebody.
I actually offered to give it away
to Regeneron and to Amgen way back,
but they were too busy.
Everybody was too busy during the COVID time.
So one of the ideas now
was for me to actually go to the Serum Institute in India
and say, here, please go build this and make this available to the world.
So, you know, just so much we could do as an organization.
We're a tiny little biotech company relative to the Merck and the Pfizer's.
But that's what my goal is.
My personal goal is when you say I'm still doing it, I don't have a vineyard.
The resources that was given to me is like God's gift, I believe, that allowed me to do this.
So, you know, we have hundreds of employees, 40 acres of land in Los Angeles. The other tragedy was I took over this facility in Dunkirk that New York State had
put $200 million in, completely empty, brand new, amazing facility for national preparedness.
And I called Chuck Schumer to help me make that available for the country.
Nothing. It's still sitting there, available for the country as a national
preparedness manufacturing site in Dunkirk, New York, for which we put $50 million in,
but there's no employees in there right now. Nothing. That's crazy. It is really ridiculous,
right? Without leadership, without skill sets in leadership, and without informed leadership, how we as a country could go down the wrong path.
And I'm so hopeful that these next four years could change that.
So this has been an amazing story.
You're obviously very famous in the medical research world and controversial, but I'm, I'm, I'm sold on what you said.
So everything that you've done is,
you know,
you'll have a great obit because of it.
Then you decided to buy the LA times in 2018 ish.
And,
you know,
owning a,
the main newspaper in the country's second biggest town makes you obviously a
media mogul,
but it makes you a political figure as well. And is so complicated like why would you do so why would
you you don't need that why would you do that well i think it really helps to know how i grew up
right so i grew up in south africa as a part eight i because south africa didn't have i did
not see a tv until the age of 21 believe it or not no tv no tv south africa didn't have, I did not see a TV until the age of 21, believe it or not.
No TV?
No TV. South Africa didn't have TV.
So not that I didn't watch TV.
Period. So it was just books and newspapers.
That was the only way I got educated, books and newspapers.
To the extent that I would go every day as a newspaper boy to the printing press in Port Elizabeth,
sit at the printing press,
get the first one off the press, read it, and then run with about two, three hundred papers throughout the city. That would be what I did and grew up. So I fell in love with the printing
press, the clicky-clack and the oil and the smell. And when the opportunity came, remember,
as I said, I had this amazing gift of the resources of selling these two companies that I never anticipated in life.
With Michael Farah saying he took over this company called, and then named it Tronc.
And he was going to shut down the Washington Bureau and move all the...
So he owned the LA Times?
He owned the Tribune, actually, the whole thing, yeah, at that point, yeah.
Chicago Tribune, the Tribune company.
The whole Tribune company, which included LA Times and San Diego Tribune.
And he knew how desperately I wanted the LA Times
because I had helped him invest to buy the rest of the Tribune.
So I was a minority shoulder then.
And he came to me and said,
Hey, Patrick, you want it?
Here's the price.
You've got 48 hours to decide.
And it's $500 million.
No due diligence.
No due diligence?
That's what I said.
Who would take that deal?
Only crazy people.
It's half a billion dollars and you can't see the books yeah nor can you go
visit the newsroom because on monday we're going to actually shut all that and move them all out
and i don't want you to talk to these people and you have until monday to decide and i was running
a conference in la um with all my scientists and the National Cancer Institute
and all the scientists were there
at this hotel
and I said oh my god
so I went upstairs
and we got a private room
and I brought all the people into the room
and I said I want to do it
and I called my wife
I said we want to do this
I think this is an opportunity
for us to have a voice for the people
especially if they're going to shut down Washington they're going to shut down LA we us to have a voice for the people,
especially if they're going to shut down Washington,
they're going to shut down LA.
We'll never have a paper here.
This is one of the most important things.
So by Monday, I signed it.
And that was it.
And you paid him $500 million?
$500 million.
How grateful was he?
Very.
Sorry.
I'm sorry to laugh.
If you hadn't made so much money, I wouldn't be laughing because it would be mean.
But that's incredible.
So Phil Anschutz saw me. I've got some stuff I'd like to sell you.
Oh, so Phil Anschutz saw me at the next Laker game.
He says, you know, Patrick, I always thought you were such a smart guy until yesterday.
But, you know, i have no regrets i think what i did then
was said okay i'm going to take everything i know in healthcare that rocket ship that i showed you
and and then create because during that time bezos would have this arc he'd had the software and he
had the washington post and his team came to see me and said, listen, we've got this ARC software that we want to run.
I said, no, I don't like this old software.
I'm going to go build a completely new software content management system that could take podcasts, video, live streaming, because I want this newspaper to be an educational moment for people.
And at the end of the day a newspaper is not just
a newspaper it's a basis of engagement i want to engage users as a tool to engage with people
because that's how i grew up so we took the risk and we built this content management system took
us five years and we launched it and which could talk to the printing press and talk to magazines it could
talk to podcasts it talked to video talk to live streaming and now it's just gone live it's called
la times studio and la times live and the next thing we're going to do is called la times next
and the la times next um and a gentleman called eric beach and I are forming so that we could create a platform that would allow
voices to be heard and free speech to be heard unencumbered by either opinion or news.
So now we have three platforms. We have a platform of news, which supposedly is facts.
We have a platform of opinion, which are now changed to voices. Meaning everybody
should have a voice. Whether you're right voice,
left voice, central voice. Do you like
Coca-Cola, Pepsi-Cola, whatever
voice. And
then a complete
platform that allows
free speech
and video,
podcast.
And now I have that platform.
And we've built the infrastructure to accommodate that platform.
And I'm excited by LA Times next because we're going to have a studio in DC.
We have a studio in LA.
We may have a studio in Nashville.
And shows like this are important.
Because I believe long forms like this is how you communicate for people who are interested.
And it could be fun.
It should be engaging.
It should be interesting.
And that's why I bought the paper.
Well, those are great reasons as far as I'm concerned.
But they come with them.
The purchase comes with it.
A lot of people who work at the paper, I've worked in newsrooms my whole life, and I know that they hate change.
They hate the owner no matter what.
Everybody hates the owner just on principle.
There are a ton of unhappy people in journalism.
I would say the overwhelming majority, for whatever reason, we could speculate.
And they're very hard to manage and
they're roughly about a hundred or maybe even more percent uh left wing everywhere including at you
know supposedly conservative places they're all lefties so how do you deal with that by being
honest and transparent head on um and i i openly shared with them, I said, listen, we cannot be echo chamber,
I won't tolerate it. It's okay if you're left wing, but you need right wing. So I offered Scott
Jennings an opportunity to write on the paper. And I said, we need all voices. And so I said,
listen, I don't know who made these rules, because I came into this newspaper, I don't know who made these rules because I came into this newspaper.
I don't know the difference between a columnist and op-ed or editorial page and news.
And now when you're merging all of these, can you imagine the layperson not really understanding the difference?
That's right.
And I want you to say news is news and you're the newsroom.
Fine.
Theoretically, everything's edited.
You've checked it. You fact-checked it.
But when it comes to an opinion, I want to change that to be voices.
And I want all voices to be heard, all American voices to be heard.
And, you know, the Kamala Harris endorsement, I took a lot of heat because the editorial board resigned by my taking a stand that we cannot be an echo chamber of opinions not based on facts. So just for those who didn't
follow it, and it was quite a story for a couple days there, it was during the campaign,
the editorial board, correct me if I'm wrong, wanted to endorse Kamala Harris. And you said no. What did they say to you?
And what did you say back to them?
Well, I can't put in.
Oh, come on.
You've gone pretty far already.
I can just say that we're not happy.
But what was their pitch?
So the pitch was, we as a board have met and we have this prepackage.
We know this is outrageous, blah, blah, blah.
This prepackage, what does that mean?
We had a prepackage endorsement.
What do you mean prepackage?
They'd already written it?
They'd already written it.
After talking to Kamala Harris?
Never having met her.
They never met Kamala Harris?
Never met her.
Isn't the editorial board supposed to interview the candidates?
By the way, the editorial board never met even. I'm on the editorial board. So I said, I'm't the editorial board supposed to interview the candidates? By the way, the editorial board never met even.
I'm on the editorial board.
So I said, I'm on the editorial board.
Kamala Harris was in LA all the time.
Correct.
In your neighborhood, actually.
Correct.
Raising money.
Raising money, keeping the traffic in trouble, raising money.
And I'd never met her.
And nor did the board ever met her.
And I said, this is unacceptable.
And they know, as you could see, because it's a left-leaning,
they wrote terrible stories about President Trump.
Had they met him?
Not met him either.
So my statement to them was, listen, you may have an opinion,
but all of us should have an opinion based on facts.
I mean, one of the statements that came, and I won't name him, came from a person that said
within this concept that Vice President Kamala Harris was the most consequential
vice president in the history of the United States. So I said...
No, I shouldn't lie. I don't mean to be dismissive. What, on what basis did the
person say that? Having never met her and one, so now exactly, you just hit it on the head. And I
said, on what basis do we say that? What are the facts? Can we actually show the record of that?
So I said, you know, it boiled down to, look, we're not going to do that. We're just not going
to do it. What did the person say when you asked?
Why are you saying she's the most consequential vice president of the United States?
Like, what are the facts that underlie that judgment?
I obviously had disagreed with that person, and there are no basis for that other than,
you know, as you said, a personal echo chamber. You know, and look, I think
I don't
know what they're trying to protect. They're trying to
protect,
if I'm trying to find, I'm trying to find the kernel
of basis.
The audience, because the audience
is left, so they need to be left. I don't
think that's right. I think, meaning
our audience, we lost a lot of viewers,
right? I mean, thousands of people, we lost a lot of viewers, right? I mean,
thousands of people unsubscribed. But I don't think it's right that we should be this canceling society. I think we should be a society that can have a civil discourse like we're having now
and disagree, it's okay, and understand each other's point of view. That's what I think is
the value of the paper when you talk about voices. So that's what I'm instigating now. And so I've taken the opportunity-
Let's go back to the Kamla thing really quick. So
were they, they were shocked that you canceled that?
They were worse than shocked. They resigned.
They resigned.
So I had three, right now, 90% of my editorial board has resigned.
So where did they go?
Because there are no editorial writing jobs left in the world.
I have no idea.
So, look, I think it's important.
Look, the fact that I had the courage to resign, some of them.
Now, Kevin Murad, I fired.
I fired Kevin before they resigned.
Why did you fire him?
One, because of leadership. Two, because of...
I've got to be careful. I don't want to disparage him.
I fired him because I didn't believe he was the right person
of taking the paper where it needs to be.
He was formerly at the Washington Post.
Washington Post, yeah.
I remember that well.
And then after that episode,
the editorial board, the rest of them resigned.
And now we're rebuilding.
Look, we have to, and what's exciting to me
is I'm rebuilding with young people.
And what's exciting to me is this opportunity
with LA Times Next and LA Times Studio and then the newsroom.
Terry Tang is doing a fantastic job.
She's working hard to take on the people and the productivity.
The productivity?
Well, increasing productivity.
Oh, you're employing journalists?
Okay, so that's the world I understand. Yes, there are some productivity issues there.
Yeah, yeah, yeah. When you write one slug a month, I think that's not going to be good.
Been there. Been there. Yeah. So, it's been an experience. But look, we're there in for the
long haul, I think. And look, it's just not us, by the way.
We've got to save these local newspapers.
I agree.
Right?
We've got to save the ability to have local discos.
Now with the LA Fires, it's even more important, right?
Look, I called out Karen Bass and Gavin Newsom.
And these politicians...
You know them both.
I know them both.
I text with them both.
And I complain to them both. And what I tell the public both. I know them both. I text with them both, and I complain to them both.
And what I tell the public is what I tell them.
So I don't say anything behind their back.
I personally say, I said, you're not doing the right thing.
Whether it be the homelessness.
The homelessness, they did a terrible job.
Yes.
Completely wasteful job.
So these are the kinds of things that I think it gave us the opportunity to have
a say in our community, you know, and that's what I'll continue to do. Now we'll position
ourselves in DC and I think the next four years will be really, I hope, monumental.
Doctor, thank you for spending all this time.
All right. No, it's been fun and a pleasure. Thank you.
Thank you. Thank you.
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