The Ultimate Human with Gary Brecka - 232. Gary Brecka Live at the Biohacking 360 Conference 2025 in Romania
Episode Date: January 1, 2026Gary Brecka takes the stage at the Biohacking 360 Summit in Romania to challenge modern medical dogmas and reveal how the body can heal itself when given the right raw materials. Drawing from 22 years... of mortality research, Brecka explains that the vast majority of human ailments, from ADHD and depression to hypertension, stem from nutrient deficiencies and a lack of oxygen, not genetically inherited diseases. CLICK HERE TO BECOME GARYS VIP!: https://bit.ly/4ai0Xwg Thank you to our partners H2TABS: “ULTIMATE10” FOR 10% OFF: https://bit.ly/4hMNdgg BODYHEALTH: “ULTIMATE20” FOR 20% OFF: http://bit.ly/4e5IjsV BAJA GOLD: "ULTIMATE10" FOR 10% OFF: https://bit.ly/3WSBqUa COLD LIFE: THE ULTIMATE HUMAN PLUNGE: https://bit.ly/4eULUKp WHOOP: JOIN AND GET 1 FREE MONTH!: https://bit.ly/3VQ0nzW AION: “ULTIMATE10” FOR 10% OFF: https://bit.ly/4h6KHAD A-GAME: “ULTIMATE15” FOR 15% OFF: http://bit.ly/4kek1ij PEPTUAL: “TUH10” FOR 10% OFF: https://bit.ly/4mKxgcn CARAWAY: “ULTIMATE” FOR 10% OFF: https://bit.ly/3Q1VmkC HEALF: 10% OFF YOUR ORDER: https://bit.ly/41HJg6S RHO NUTRITION: “ULTIMATE15” FOR 15% OFF: https://bit.ly/44fFza0 GOPUFF: GET YOUR FAVORITE SNACK!: https://bit.ly/4obIFDC GENETIC METHYLATION TEST (UK ONLY): https://bit.ly/48QJJrk GENETIC TEST (USA ONLY): https://bit.ly/3Yg1Uk9 Watch the “Ultimate Human Podcast” every Tuesday & Thursday at 9AM EST: YouTube: https://bit.ly/3RPQYX8 Podcasts: https://bit.ly/3RQftU0 Connect with Gary Brecka Instagram: https://bit.ly/3RPpnFs TikTok: https://bit.ly/4coJ8fo X: https://bit.ly/3Opc8tf Facebook: https://bit.ly/464VA1H LinkedIn: https://bit.ly/4hH7Ri2 Website: https://bit.ly/4eLDbdU Merch: https://bit.ly/4aBpOM1 Newsletter: https://bit.ly/47ejrws Ask Gary: https://bit.ly/3PEAJuG Timestamps 00:00 Intro 4:12 - Gary Brecka's Background as a Mortality Researcher 6:32 - The Predictive Power of Mortality Data 6:57 - The Importance of Oxygen in Disease Prevention 7:16 - The Decision to Help People Live Longer 7:42 - Debunking Genetic Myths in Modern Medicine 10:46 - Cellular Regeneration: A New Body Every 84 Days 14:16 - Understanding ADD/ADHD as Attention Overload 19:02 - The Serotonin Hypothesis and Root Causes of Depression 24:12 - The Dangers of Synthetic Folic Acid and MTHFR Gene Mutation 27:55 - OCD, Dopamine Deficiency, and the Roots of Addiction 31:33 - Solving the Dopamine Gap to Treat Dependency 34:33 - Case Study: Reversing Dana White’s Hypertension 39:56 - The Role of Homocysteine and Vascular Constriction 46:07 - Collaboration with Cardiologists on Nutrient Deficiencies 47:51 - The Process of Methylation: Refining Raw Materials 49:56 - The Secret to Longevity: Empowering the Immune System 52:17 - Hypothyroid Truths: Liver Conversion and Selenium 58:39 - Autoimmune Disease: Pathogens vs. Immune System Crime 1:05:59 - The "Caregiver Syndrome" and Self-Care Importance The Ultimate Human with Gary Brecka Podcast is for general informational purposes only and does not constitute the practice of medicine, nursing or other professional health care services, including the giving of medical advice, and no doctor/patient relationship is formed. The use of information on this podcast or materials linked from this podcast is at the user’s own risk. The Content of this podcast is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Users should not disregard or delay in obtaining medical advice for any medical condition they may have and should seek the assistance of their health care professionals for any such conditions. Learn more about your ad choices. Visit megaphone.fm/adchoices
Transcript
Discussion (0)
You want to talk about a pandemic in this world.
We have a pandemic of medicating organs in the human body that have committed no crime.
I really don't like the fact that in modern medicine we have this excuse.
It's called idiopathic.
Idiopathic means of unknown origin.
If the origin is unknown, we should not stop until we find it.
We shouldn't stop there and treat for a condition when we do not know the root calls.
There are tens of millions of people walking the face of this Earth right now that are on immunosuppressants, on anti-inflammatories, on corticosteroids, on things to manage this immune system that just went haywire.
Unlocking our immune system is the secret to longevity.
This is where true life expectancy is extended is by empowering the God-given immune system to do its job.
There is no smarter resource on the planet than your immune system.
We have adopted so many fallacies in modern medicine.
The biggest one is...
Oh, amazing.
What a beautiful country.
What beautiful people.
What amazing fun facts about your country.
You know, I was actually doing some research on Romania.
You have the heaviest building in the world.
I mean, that's so random.
It sinks one millimeter every single year.
And you're the home of Dracula.
That is pretty cool.
Transylvania is like a real thing here.
You have lots of bears.
I mean, there's so many fun facts I've learned about Romania.
Just absolutely beautiful.
Thank you so much for having me.
My name is Gary Breka.
I'm a human biologist, a researcher, biohacker.
You know, for the better part of 22 years, I was a mortality researcher for large life insurance.
And what this means was, if I got,
10 years of medical records on you and 10 years of demographic data, we could tell the
insurance company how long you had to live to the month. And I get a lot of flack for that
because people say, well, if you could predict death to the month, you would have won a Nobel
prize when I never won a Nobel Prize. But I promise you, it is some of the most accurate
research in the world. You see, the database that I used to have access to had 371
million lives. And they knew the day, the date, the time, the location, and the cause of death
for 371 million lives. And what we would do is we would pull that information back into the
record. And we would look at what are the patterns? What are the things that were causing people
to leave this earth too early? And if I was to summarize my entire career into just one sentence,
it would be that the reason why the vast majority of people
are not living longer, healthier, happier, more fulfilling lives
are for what we called modifiable risk factors.
These were relatively simple dietary and lifestyle changes
that if they would have implemented them
would have added, on average, seven years to their lifespan
and to their health span.
And this database, unfortunately, will never see the light of day.
Because if it did, it would be catastrophic.
It would benefit humanity in a way that would be so impactful
that it would upend modern medicine in a way that would be catastrophic.
So that database, unfortunately, would never see the light of day.
And during my career as a mortality researcher,
I was not allowed to have any contact with the patient.
or any contact with their treating physician.
So even if I was looking at a record
and I saw life-threatening drug interactions,
I couldn't pick up the phone and warn the patient.
At one time in my career,
I was threatened with criminal prosecution
because I wanted to contact a woman
and warn her about a life-threatening drug interaction
in a cardiac medication she was about to take.
And so on that day,
I walked into my Human Resources Director's office,
I turned in my resignation, and I decided that I didn't want to spend the rest of my life predicting death.
I wanted to spend the rest of my life teaching people to live healthier, happier, longer, more fulfilling lives.
And so that's why I'm standing in front of you today.
So thank you.
So we are going to have a lot of fun today.
We're going to talk about a lot of things we're not supposed to talk about, politics, religion, and science.
So we're going to cover it all because, and then what I'm going to do at the end of my
presentation, and I cannot emphasize this enough, and this is my favorite part of every talk
that I do, is we're going to open the floor to questions, and I'm going to take any ailment
that you or a loved one suffers from, any ailment, ADD, ADHD, OCD, manic depression,
depression, bipolar, autoimmune, cancer, migraine headaches, any ailment.
And I am going to tell you right here from this stage in front of this crowd,
what raw material is missing from that person's body that is causing that condition to exist?
You see, we have lost faith in humanity and mankind and the body's ability to heal itself.
We have gravitated more towards what man makes us and less us.
of what God gave us. And I believe so much more in what God gave us than what I do and what man
makes us that the reason why I do this is to prove to you that the body can heal itself. This is
such a magnificent machine. And we're going to go deep into that research today. So I start
every presentation by saying the same thing. Again, in my career, 22 years as a mortality
researcher, this may be the most important sentence that you read for the balance of your
lifetime in terms of how many more years do you have left on earth? What does your brain fog look
like? Your weight gain, your water retention, what does your hormone balance look like? Because in 22 years
of mortality research, we did not find a single disease ideological pathway that did not have its
roots in the absence of oxygen or was not exacerbated by the absence of oxygen.
And I'm going to give you some more details on that later.
Also, when I take the stage, I make two bold promises every time.
If you listen to what I'm going to ask you to do today and you follow it, it will add
seven years to the health span and the lifespan of every person in this room.
And the second promise that I make is the promise to take any ailment.
that you or a loved one suffers from
and tell you what's truly going on in their biology.
You see, we have adopted so many fallacies in modern medicine.
The biggest one is that what goes into my body and her body and his body and her body
and everybody else's body in this room is treated exactly the same way.
Nothing could be further from the truth.
The second is that disease is genetically inherited.
that we inherit a lot of disease and pathology from our ancestors.
If you have high blood pressure, hypertension, for example,
how many of you either have or know somebody who has high blood pressure?
Put your hands up nice and high.
Okay, that's about 50% of the room.
You know what happens in the vast majority of cases
where you're told you have high blood pressure?
They do a cardiac exam and you have a normal EKG,
and you have a normal EEG,
and you have normal heart sounds,
and you have normal lung sounds, and you have a normal die contrast study,
and a normal chest x-ray, and a normal cardiac catheterization,
and they can't find anything wrong with the heart.
So what do they do?
Medicate the heart anyway.
For a crime, we cannot prove it's committing.
And if we don't have an explanation for why you have a certain condition,
they're going to look at your family history.
And they're going to say, well, look at that.
Your mom's sister or your father's brother had high blood.
blood pressure, you have familial hypertension. You have what we called genetically inherited hypertension.
I'm here to tell you that if you look that physician in the eye and you say, what gene did I
inherit from my ancestor that caused this condition to exist? Their face will go blank. Because in the vast
majority of cases, that gene does not exist, which means that those conditions do not exist.
So we do not pass disease from generation to generation. What we pass from generation to generation
is the inability for the body to refine a raw material, a vitamin, a mineral, an amino acid,
a nutrient. This causes a deficiency which leads to that disease.
And that deficiency can be fixed.
And we're going to talk about that today, going back into human physiology,
restoring the faith in mankind and humanity and the body's ability to heal itself.
And so the human genome is specifically designed to not pass on disease.
No one in this room would be sitting here if our genes did not specifically eradicate disease.
in fact we are designed specifically to not carry pathology and disease from generation to generation
and so it's very exciting for me when we go back into human physiology and back into the human genome
and we give people the faith and the hope to heal from whatever ailment they are suffering from
you know what's amazing you have about 32 trillion cells in your body
every day that you are alive 300 billion cells that were with you
yesterday will not be with you today. And tomorrow, 300 billion cells that were with you today
will not be with you tomorrow. So every 84 days, your body is a completely new cellular human being.
If I met you today and met you 84 days from today, you would be an entirely different human
being down to the last living cell. And so why is it that we don't believe that we can heal
from whatever is facing us if every 84 days we turn over all of the live cellular structures in the body
and so the question becomes what energy are we giving those cells what frequency are we sending those cells
what nutrition are we giving those cells what environment are those cells in and if we can change
those things then we can change the outcomes you know there's so many diseases
and pathologies and stories that I'm credited with,
and they call these miracle cures.
Like I have some secret potion, right?
Gary Breka has this secret way of curing and healing
all of these conditions.
None of that is true.
I have a secret way of going back into your human biology
and just restoring the body's ability to heal itself.
And it's been a magnificent journey.
And so we're going to start here.
I want you guys to memorize this.
this, please? There's going to be a quiz on that later. So just take a few minutes, take it all in.
Once you memorize it, thank you for coming. My stage talk is over. So the reason why I show you
this slide, this is a slide. Look at you guys taking pictures. Some of you are like, I've got to memorize
that. You're great students. Thank you. I have memorized that, by the way, just so you know that
I'm smart. This is a chart of what is going on inside of every single cell, inside of every single
body sitting in this room. 300 billion times a day these transactions are going on. The reason why
I show you this slide is because if I was to continue to blow this slide up, every person in this
room would recognize the vast majority of what is on that slide. You know what's making your cellular
biology work, vitamins, minerals, amino acids, nutrients and oxygen. This is the foundation of
cellular biology. When you go into this chart and you start to pull things out of this chart,
you start to delete a certain amino acid, you deprive the body of certain minerals, you pull
certain nutrients out of this chart, you get the expression of disease. And so we're here today to go back
into our human physiology and talk about what really is the foundation of longevity,
of anti-aging, of true wellness. How do we at any age function at 100%? And how do we find
the missing raw material and then put it back into our body so it can function at its best?
And so I always start by taking some of the larger categories of things that we suffer from
as humanity. How many of you, for example, suffer from or know somebody who suffers from
ADD or ADHD? Put them up nice and high. That's great. How many of you know somebody or have
suffered from depression? Put them up. Amazing. How many of you are not going to raise your hand no matter
what I say? Okay. There's one poor lady over here that's raised her hand every time. You need to see me
after, because we need to get to work right away. So let's just pick a couple of these things.
Let's talk about attention deficit disorder. And then we're going to talk a little bit about
depression just for a moment. So attention deficit disorder, which I was diagnosed with as a very
young child, it turns out between the sixth grade and the eighth grade when I was a very small
child, my teachers thought that I was an idiot savant or that I was autistic.
It turns out I have a hyper-developed area of my brain, and I'm clinically photographic.
So I have an extraordinary capacity to record information that I see visually.
My wife will tell you, it's only visual, it's not auditory.
I don't remember anything that you tell me, but if I see it, I will record it.
I can't read for pleasure.
I rarely look at menus and restaurants.
I never read magazines for pleasure because I have this overdeveloped center of my brain.
But I was put into a program for, at the time, you know, attention deficit disorder and learning disabled children.
And essentially what this program was, they had a bunch of trampolines, and they would have these hyperactive kids like me run around in circles, and then they would sit us at a desk, and they would teach us for about 15 minutes, and then we would run around again.
And as it turns out, I didn't have attention deficit disorder at all.
I had a hyperdeveloped area of my brain, but I was nutrient deficient.
And so I know so many people that have suffered from ADD and ADHD,
and the truth about this is attention deficit disorder is not an attention deficit at all.
It is actually an attention overload disorder.
It is too many windows open at the same time.
So in the human mind, we don't just create thought.
We also break thought down.
We actually dismantle thought.
And if you create thought at a faster rate than you break thought down, then the mind gets very clouded.
So the question is not how do we take the central nervous system and put an amphetamine into the central nervous system,
Vivans, Ritalin, and Adderall, to race the central nervous system to match the pace of the mind.
That's what modern medicine says.
It says, if the mind is racing, then let's take the central nervous system.
Let's speed it up to match the pace of the mind.
And so we created amphetamines to do this.
So let's take the system that's not broken, the central nervous system.
Let's break it to match the system that is.
So the next time you have a flat tire, I want you to get out of your car and slash your other three tires.
Create equilibrium.
And then call your husband and tell them what you did.
See how that works out.
So in attention deficit disorder, the mind is opening windows faster than it's closing them.
So the focus should be on how do we quiet the mind, not how do we race the central nervous
system.
And I'm going to talk about how exactly we quiet the mind.
Because in people that have ADD or ADHD, you could be thinking about a job you're working on.
And your friend walks up.
So now you're thinking about a job.
you start talking to your friend.
And while you're talking to your friend,
you notice a logo on their jacket.
And that reminds you of a vacation you want to take.
So now you're thinking about a job,
talking to your friend, looking at the logo,
thinking about a vacation you want to take,
all at the same time.
And then your friend goes,
you know what, my grandmother passed away on Sunday.
And you go, that's a great idea, right?
And so, and we call this an attention deficit,
but it's truly an attention overload.
And so we're going to talk about how do we solve,
things like that, because there is nothing wrong with you. The body has an impaired ability to
break down the neurotransmitters of thought. The exact same thing happens in depression.
And so let's go into the slide for a second. Let's just blow up an area here, and let's talk
about depression for a second. Again, so many of you, about half this audience raised your
hand when I said how many of you have suffered from or know someone who suffers from depression?
Do you know that the, you don't have to raise your hand again, you're an overachiever right there.
Yeah, you got straight A's in, in college.
Yeah, we know.
These are the, I want you to work for me.
Yeah.
She's like, depression.
So, we have developed a theory of depression called the serotonin hypothesis of depression.
What this theory says is that if you are.
are low on serotonin, the neurotransmitter serotonin, you are by definition depressed.
So then you would think if the definition of depression is low serotonin, that the treatment
should be to raise serotonin. Makes sense, right? But that's not what we do. We take people that
are low on serotonin, and we put them on something called an SSRI, a selective serotonin reuptake
inhibitor. So what these drugs do is they ration what little serotonin you have. So by definition,
they never raise serotonin. So by definition, they never end depression. I can't tell you how many
clients of mine. I don't have patients. I'm not a physician, so I have to watch saying that
word. I can't tell you how many clients of mine I've sat across from that have suffered from
depression, and I will say, how long have you been on an antidepressant? Oh, 15.
or 18 years. I go, great. When did you think it was going to kick in? Should we just run this for
another two years and see how that goes? Right? Because by definition, we are not ending depression
this way. So serotonin, does anyone know where serotonin is made in the body? Where's the factory for
serotonin? In the gut, right here. 90% of the neurotransmitter serotonin is right here. And if you don't have it
here, you can't have it here. Depression can begin in our outside environment. It always ends
in our inside environment. Serotonin is the main driver of mood. It is the main driver of emotional
state. When the absence of serotonin, you cannot build the emotions of joy, elation, arousal,
happiness, passion, elation. So these are the drivers of our emotional state. And so,
If I went into the gut and I said, well, take a step further, how do we make serotonin?
Well, we take an amino acid.
It's called triptophan.
It's inside everybody's body right now.
And triptophan, this amino acid, gets methylated into the neurotransmitter serotonin.
So if you have a deficiency in triptophan, which the vast majority of depressive patients have,
or you have a deficiency in the raw material it takes to turn that into a neurotransmit,
called serotonin, you have a deficiency in serotonin.
And you have what we would call clinical depression.
And so what does it take to take tryptophan and convert it into the neurotransmitter,
serotonin?
It takes that exact consequence of B vitamins, riboflavin, thiamin, niacin,
niacin, panothenic acid.
It takes a very specific form of folate called methylfolate.
And it takes a very specific form of B12 called methylcobalamin.
B12 is one of the most necessary light metals in the human body.
Yes, B12 is a vitamin, but it is a metal.
And this metal, this light metal, is critical to converting tryptophan to serotonin.
If you have a deficiency in any of those raw materials, you have impaired conversion
of triptophan into serotonin, and by definition, you are depressed.
And so can we go back into the factory that makes serotonin and turn that factory back
on? Yes, I have done it more than 200,000 times in our functional medicine clinic in the United
States, and I would be more than happy to share this data with you. So we go back into the gut,
we put the raw materials back in that caused the body to methylate triptophan into serotonin.
As that neurotransmitter rises, you see these symptoms begin to eviscerate. We do the same thing
with attention deficit disorders. We put the raw material into the body.
to begin to quiet the mind.
So people can actually begin to break down,
they can begin to break down these neurotransmitters
and their mind quiets.
One of the foundations of this
is removing the ability
or removing the inability of the body
to take folic acid
and turn it into this nutrient called methylfolate.
You know what is astounding?
In the United States, in 1990,
Monsanto. I'm not a big fan of Monsanto. They probably have a hit on me somewhere.
But Monsanto convinced the U.S. federal government that we needed to spray our entire grain
supply with something called folic acid. How many of you heard of folic acid? Okay. Do you know
that folic acid is an entirely man-made chemical? Do you know that folic acid does not occur
naturally in nature? Do you know that you cannot find folic acid anywhere on the surface of the
earth, we make it in a laboratory. And folic acid is now the most prevalent nutrient in the
human diet. It is an entirely synthetic chemical. Yet we have convinced tens of millions of
pregnant women that folic acid is absolutely necessary to have a healthy pregnancy. That is patently
false. What folic acid becomes in the human body, methyl folate, is essential to a pregnancy.
Folic acid does not prevent neural tube defects.
It does nothing of the sort until it is converted into form the body can use.
So what happened when we started spraying all of our grains, all flour, rice, pasta, cereals with the chemical folic acid?
You saw skyrocketing rates of ADD, ADHD, OCD, manic depression, bipolar, behavioral disorders, impulse control,
and skyrocketing rates of postpartum depression.
In fact, there are no clinical studies.
If you're an OBGYN, I'm happy to have this debate with you.
There are no clinical studies.
You're an OBGYN, linking directly a causal relationship
between hormones of pregnancy and postpartum depression.
Yes, lots goes on in a woman's body when they get pregnant.
Their estrogen goes from in the 400s to in the 4,000s.
There are massive shifts so that the body can retain water,
pad the uterus and protect the fetus. But there are no clinical studies. But yet, we still blame
postpartum depression on the pregnancy. The truth is, postpartum depression, which usually begins
during pregnancy, postpartum depression, the onset of coincides almost universally with the woman
taking high doses of folic acid. You see, 46% of the people in this room and 46% of the people in this
world have a gene mutation called M-T-H-F-R. Have you ever heard of M-T-H-F-R? Yes. I won't tell you what the
nickname is for that gene, but you can figure it out. So this gene mutation does not allow
or impairs the body's ability to take folate and folic acid from our diet and convert it into
the usable form called methylfolate. So when this conversion is impaired, first of all, all the
acid in the world will do nothing for you. When this conversion is impaired, the body has a deficiency
in something called methyl folate, and this deficiency expresses itself as depression. Because it
occurs during the pregnancy, we call it postpartum depression, and it usually onsets during
pregnancy. What eventually happens is the pregnancy ends, the woman stops taking the prenatal
vitamin, and the symptoms go away. So we blame it on the pregnancy and not on the vitamin.
You know, the U.S. federal government, the FDA, the Food and Drug Administration,
11 days ago, just approved the first prescription strength methylfolate called folinic acid
for neurodevelopmental disorders, the treatment of postpartum depression and attention deficit disorder.
Exactly what I am going to tell you today about the missing raw material in that body.
And this leads to all kinds of consequences.
that we call mood disorders or mental illnesses.
I truly do not believe that we have a pandemic
of mental illness in this world.
I believe we have a pandemic of a lack of mental fitness.
And so we're gonna talk about how do we become mentally fit?
What do we put into our bodies so our brains are mentally fit?
The same thing happens with OCD.
How many of you have OCD?
Go ahead.
My wife better be raising her hand.
Yes, right there.
Okay, yes.
Yes. We have OCD in our marriage. I do a lot of apologizing for things I haven't done.
I mean, God forbid that I do the laundry and then dry the laundry and then fold the laundry,
but I don't put it back where it belongs. That's a character flaw of mine, and I'm deeply sorry for that.
So in OCDs, the same thing happens.
When we have disorganization in the mind, when our mind is very, very active and it runs all the time,
we crave organization in our outside environment.
Since we cannot organize our inside environment, we have to hyper-organize our outside environment.
So people with this condition, if you have a project that you're working on or something
you need to study for and pay attention and you're sitting at a desk with your computer,
the desk has to be clean. But then the room the desk is in has to be clean. And there is a sock
next to the baseboard on the floor because the sock needs to move before I can focus on what's in
front of me. Yeah, I see a lot of people going, yeah, that's me. And so how do we actually
quiet the mind? And we're going to talk exactly about that. There's another very interesting
pathway where we convert an amino acid called tyrosine into the amino acid called, I mean into
the neurotransmitter called dopamine. In the mortality space when I was doing this 22 years of
research, we had a saying in our office that the absence of dopamine is the presence of addiction.
The absence of dopamine is the presence of addiction. If I was able to stick a magic syringe in the
shoulder of anybody in this room and just suck the dopamine out of your body. You would
immediately begin to engage in dopamine-seeking behavior. What is that? Drugs, alcohol,
nicotine, permiscuity, gambling, thrill-seeking, work-a-holic, work-out-aholic. These conditions
that if you've ever known a true addict, or you've been a true addict, have a tendency to shift.
Addiction rarely, if ever, goes away. It just shifts. We might exchange one unhealthy addiction
for a healthy addiction, but it rarely goes away. And the reason for that is we do not
treat the root cause, which is the deficiency in dopamine. If you do not replace the driver
of behavior, you will have a constant drive to seek dopamine. If you show me a child that can
play video games 12 or 14 hours a day, I will show you a future addict. We need to supplement that
child as soon as possible to turn that dopamine back on. They are not playing the video game
because they like the video game. They are playing the video game because it makes them feel
normal. Nearly every form of addiction known to mankind did not begin with a search for getting
really banged up. No addict just woke up one day and said, I want to get really banged up.
Do you guys say banged up?
What do you?
In the UK, they say pissed.
What do you say here in Romania?
What?
Bat?
Bat.
Like a bat?
Okay.
That means you want to get banged up?
Okay, bat.
Okay, good.
I learned something new today.
Thank you.
So no addict woke up one day and said, I want to get that.
Okay, that's a good one.
What they did was they woke up.
and they said, I want to feel normal.
And it was the search for normalcy
where they developed an addiction.
And now, they're not running towards the high, the bat.
Right?
They are running from a low.
And so this is why I give so much of my time
to drug and alcohol and addiction treatment programs
because we have to go in and solve the dopamine deficiency,
not the clinical dependency.
Clinical dependencies are easy to solve.
Modern medicine solves them by shift.
you from one drug to another drug. Suboxone, naltrexone, all kinds of things that we use to get over
the physical addiction. And now you don't have a physical addiction anymore. You still have a dopamine
deficiency. So now the next cycle of addiction begins. If we fix the dopamine deficiency, we put this
permanently into remission. And how do we make dopamine? Well, we take the amino acid tyrosine
and we convert it into the neurotransmitter dopamine. And this is the driver of behavior. And I have
seen this thousands and thousands and thousands of times. And we could just keep going through
condition after condition after condition. And every person in this room has some raw material
that is missing from your body that is holding you back from being absolutely optimal.
And I'm going to tell you exactly how to find that raw material and then how to put it back
into the human body. I mean, wouldn't you like to know if something as simple as a mineral
deficiency, an amino acid deficiency, a vitamin or a nutrient deficiency was keeping you from being
in the best possible state that you could be? Of course we would, right? The human body is such a
fascinating machine. I might divide the audience in half by saying this next sentence. But the more
I study human physiology, the more I believe in God. I do not believe that this was created by
accident. You are never going to convince me that a billion years ago, two bacteria made love in a mud
puddle, and then a lizard crawled out, and then eventually we had a banana, and then a couple of
rabbits, and then we had apes, and then boom, there's a human. We're missing entire sections of
the fossil record to prove that. It is a fascinating machine, and you look at the engineering
behind this magnificent body, and you see that it just needs nutrients to survive. And so there's a really
fascinating case that I was made somewhat famous for.
How many of you know Dana White from the UFC or of Dana White?
Okay, so he's the bald, very outspoken CEO of the UFC,
and I met Dana White about two and a half years ago.
When I met Dana White, he was suffering from something called brittle hypertension.
So his blood pressure was so high that they kept throwing medication at it
to try to lower his blood pressure.
At the time, he was on a beta blocker,
a calcium channel blocker, an ACE inhibitor,
and a diuretic, all trying to lower his blood pressure.
Because they couldn't bring his blood pressure down,
what they did was they said,
we're gonna do the next phase,
we're gonna do a heart ablation.
We're actually gonna go in through the rib cage
and we are going to burn what's called
the atro ventricular node of the heart.
We're going to permanently disable the heart
to try to lower your blood pressure.
By the grace of God, that surgery was scheduled
11 days after I met him.
And so I met Dana, and he was on all these medications,
and I did a blood test on him.
And one of the things that I found was he had a gene mutation
called M-T-H-F-R.
And he had a second gene mutation called Comte,
and he had one called M-T-R.
So we had these gene mutations,
and what these gene mutations did to him,
was it impaired his ability for his body to take an amino acid called homocysteine
that is inside the blood of every single person in this room.
And he couldn't take homocysteine and convert it into something called methionine.
Now, that doesn't sound like a big deal until you realize.
Can I go to this whiteboard for a second?
Are there markers that I can use?
Oh, there they are. They're hiding in the back.
So they say don't talk about science and don't get, can I talk about science for a second?
So can you guys all see this?
Okay.
Depending on what you paid, you know, you get to see the whole view.
So, first of all, how many of you know what percentage of the blood in our body does the heart circulate?
How much of our blood is circulated by our heart?
100%, 70%, 70%?
It should be 100%.
You're right.
No, the heart circulates 30% of the blood in your body.
You have 63,000 miles of blood vessel in your body.
63,000 miles.
The vast majority of your circulation, if I was to draw this out,
the vast majority of your circulation is not done by the heart.
It is done by an activity called vasomotor.
70% of our circulation is not done by the heart.
70% of the circulation in your body,
there's no pressure in those blood vessels.
70% of this circulation is done by this activity called vaso motor.
Think of a snake swallowing a mouse, right?
When a snake swallows a mouse,
we don't put a garden hose in the snake's mouth
and push the mouse along.
It is a muscular contraction.
So 70% of the blood in 63,000 miles of arteries and venules called microvasculature is circulated by this activity called vasimotor.
Yet what we do is we test the 30% that is done by the heart.
This is what all of our cardiac exams look at.
EKGs, EEGs, die contrast studies, cardiac catheterizations, chest x-rays, heart sounds, lung sounds.
All these are looking at is the 30% that's done by the heart.
Yet this entire 70% is done by this activity called vasomotor.
So what happens if you have a gene mutation that causes this amino acid homocysteine to rise?
Well, as homocysteine rises and it's cruising by the inside lining of your arteries, it irritates your artery.
And when you irritate an artery, it clamps down.
And if you make the pipes smaller in a fixed system, this is a closed system, the pressure goes up.
And the pressure is rising, not because your heart is not functioning or overcontracting,
the pressure is rising because your vascular system has constricted.
And so as that pressure rises, because your homocysteine is elevated, which, by the way, is genetically inherited,
you get told you have familial hypertension.
Because that condition runs in families, you are told that you have a genetically inherited hypertension.
85% of all hypertensive diagnoses are idiopathic. They are of unknown origin.
85% of all hypothyroid is idiopathic of unknown origin.
88% of all autoimmune disease is idiopathic of unethystiac of unknowed origin.
unknown origin, and yet we medicate the organs for crimes they are not committing.
You want to talk about a pandemic in this world.
We have a pandemic of medicating organs in the human body that have committed no crime.
And so what I had to do for Dana to believe this was I had to pull 10 years of medical
records on him and physically go into his office and lay it out.
And I said, Dana, here are 10 years of medical records on you.
You have never had an abnormal EKG, not once.
You've never had an abnormal EEG.
You have had every stress test has been normal.
All your advanced cardiac workup has normal.
I don't believe that you have hypertension.
I believe that you have high homocysteine.
So we checked his homocysteine.
It was the highest I'd ever seen in my clinical career.
His homocysteine, if you know anything about this marker,
was in the low 30s.
It should be in the single digits.
It should be below nine to be in a great range.
And so this amino acid was so high, his vascular system had constricted.
What happens when the vascular system constricts?
Well, this is why the vast majority of people begin to wear readers in their 40s and 50s.
By the way, these are not readers.
They're blue-light glasses.
I do not wear glasses.
I'm 55.
I have perfect vision.
So why does our eyesight start to suffer in our 40s and our 50s?
Nothing's wrong with the rods, the cones, the macula, the retina.
Nothing's wrong with your eyes.
Nothing's wrong with your cornea.
Your intraocular pressure is normal.
All of your eye exams are normal.
Why does your eyesight begin to degrade?
Because the vasomotor circulation to the back of the eye is compromised.
And this vasomotor is connected to so many conditions in the body.
Renaud syndrome, cold fingers and toes.
That is a circulatory issue.
The vast majority of neuropathology, things like peripheral neuropathy,
are related to circulation, not your nerves.
In fact, if I wanted to give anybody in this audience peripheral neuropathy right now,
I would just put a tourniquet on your forearm.
What would happen if I put a tourniquet on your forearm?
Well, in about 10 minutes, you'd have tingling and numbness.
You'd have what we call paristhesias.
In about 25 minutes, this entire limb would go numb.
In an hour, I could pinch the top of your hand as hard as I could,
you wouldn't feel it.
Nothing wrong with the nerves in that limb.
What would happen if I took the tourniquet off?
All that sensation would return.
Right?
So I explained this to Dana, and I said,
I'm going to put you on an amino acid.
It's called TMG.
It's called trimethylgline.
T-M-G.
Because you have a gene mutation
that impairs this conversion of homocysteine.
I'm going to give you an amino acid that skips that gene mutation and allows your body to begin to metabolize homocysteine.
So over the next 21 weeks, as he began to take this amino acid, his homocysteine level began to fall.
As his homocysteine level fell, his vascular system for the first time in 25 years began to relax.
As the vascular system relaxed, his blood pressure began to return to normal.
I'll never forget the day that he called me and he said, Gary, something's really wrong.
And I said, what's up? And he said, you know, for the last few days, when I walk into the gym,
as soon as I step on the treadmill or I pick up a weight, I immediately get lightheaded. Like,
I feel woozy and dizzy. I go, that's a great sign. He's like, what the hell are you talking about?
And I said, well, when your blood pressure is high, your medication will make it normal.
When your blood pressure is normal, your medication will make you hyposystolic.
It will actually push your blood pressure too low.
This is the first sign that we can start to titrate you off of your medication.
So I brought in a physician, because I am not licensed to practice medicine,
I brought in a physician to monitor this, and we began to titrate him off of his medication.
21 weeks later, he was completely off of blood pressure medication.
To this day, two and a half years now since I met Dana White,
He has perfectly normal blood pressure, and he is no longer on medication.
And so Dana called the cardiac office in Los Angeles,
and it happened to be the head of cardiothoracic surgery.
He was seeing one of the top cardiologists in the world,
and he canceled the heart ablation surgery.
The cardiologist immediately called him back and said,
hey, listen, brother, this is not like getting a nose job or, you know, a tummy tuck.
This is not voluntary surgery.
It's not cosmetic.
You can't cancel this procedure.
This is life-saving.
And he said, well, my blood pressure is normal.
And so his surgeon said, well, the medication is finally working.
He says, no, no, no, I'm off all my medication.
And he said, I met this human biologist named Gary Brecker.
How do you think that conversation went?
And true story.
So Sage and I were sitting at dinner one night and had my phone on the table.
And there was this call that kept coming in from Los Angeles.
It was a Los Angeles number.
I was like, bz, bz, bz, and then it would go away.
Then 30 seconds later, bz, bz, and it went away.
And 30 seconds later, I was like, I better answer this.
So I answered the phone and the voice on the other side said, Gary Breka.
I said, yes.
He said, this is Dr. Ram Dan Delaya, head of cardiothoracic surgery, Cedar Sinai in Los Angeles.
I was like, oh boy, is this going to be a good one?
And he said, listen, I don't know who you are.
I don't know what you're doing.
but I don't believe in a thing that you're doing.
I believe that you're playing with people's lives.
I have insisted that Mr. White fly out to our cardiac unit
and complete his entire cardiothoracic workup again.
He said, Mr. Breka, so help me God,
if this is not perfect, this will not be the last call you get from me.
And he hung up the phone.
And my wife goes, wow, he was pleasant.
So exactly that happened.
Dana White went out to Cedar Sinai.
He spent three days in the cardiac unit.
They did an entire cardiothoracic workup.
And to Dr. Dandelaya's credit, he called me three weeks later.
And when I answer the phone, he said, Gary, I said, yes.
He said, this is Dr. Ram Dandalea, head of cardiothoracic surgery, Cedar Sinai and I in Los Angeles.
I go, you're really proud of your credentials.
Do we have to go through this every time?
You know, Gary Breka, human biologist, biohacker, researcher, mortality expert.
Thank you.
So he said, you know what, Mr. Brekka, I owe you an apology.
He said, I have to tell you in 27 years of cardiothoracic practice,
I have never seen a brittle hypertensive patient ever come off of the qualification list for heart ablation.
And I have never seen a brittle hypertensive come off of the cardiac medication.
And he said, would you humor me?
Would you mind walking me through what you did?
So we spent three hours on the phone.
We talked about homocysteine metabolism.
vascular laxity. We talked about the endothelial damage. We talked about the inflammatory cascade
that comes from calling the immune system to the wall of the arteries. We talked throughout peripheral
vaso-constriction. I was mortified when I found out that he also thought the heart circulated all
the blood in the body. He remembered from medical school that that wasn't true, so we brought him back
to that. And to this day, I now sit on a complicated case committee with Dr. Dandelaya and some other
physicians from cedar cyanide solving really complicated cases that make no medical sense that don't
fit the medical um dogma but to his credit again he was just exacerbated by the fact that we could
fix this with a nutrient deficiency so what causes us to have impaired homocysteine metabolism there's a
gene mutation and so when i look at the human genome i don't look at all of your genes i look at 12 specific
genes. I don't care about your hair color, your eye color, your ancestry, your skin tone,
whether or not you have detached ear loaves or the right length between your first and your
third digits. What I care about is what can your body take that it brings into the body
and what can it convert into the usable form and what can it not? You see, there is not a single
compound known to mankind, not one, that we put into the human body.
there is no vitamin, no mineral, no amino acid, no protein, no carbohydrate, no fat,
no nutrient of any kind that enters the human body and is used in the form that we put it in.
Without exception, everything gets converted into the usable form.
So think about how we pull crude oil out of the ground.
You cannot put crude oil into your car as gas tank, right?
Because the car doesn't understand this fuel source.
Crude oil has to be refined into gasoline.
now the car can run.
Human beings are no different.
This process of converting crude oil, the raw material, into gasoline the form the body can use,
this process is called methylation.
And if your methylation is broken, you have a deficiency.
And that deficiency can be fixed.
And if it is broken in one cell, it is broken in all 32 trillion cells in the human body.
and so fixing that affects every single cell in the human body.
This happens with detoxification pathways called glutathione and transulferation.
It happens with so many things.
In fact, a few weeks ago, I was on a panel and I got asked a question.
I thought it was one of the most difficult questions I've been asked in a long time.
And the moderator said, if you were to put all of the top anti-aging experts, longevity experts, wellness experts,
the top PhDs, MDs, researchers, and you put them all in one room, the top 50, and you said,
agree on one theory of aging. Just one theory of aging. What would that theory be? And I had to
really think about that. And I said, I know that we would all agree on the theory of immunofatig
a slow, progressive, overwhelming of the immune system. See, what causes us to age is when our
immune system is so distracted trying to protect us that it no longer has the time to police
us. When you're an infant, 65% of your immune system's activity is policing you, is monitoring
what's going on inside the castle walls. By the time you are in your 40s, it is spending 65%
of its time protecting you, parasites, mold, mycotoxins, heavy metals, and all kinds of
of micro toxins that we put into the body, and then all of a sudden, a circulating tumor cells
slips by, or a senescent cell stays for too long, what we call zombie cells, or your cellular
rate of death and regeneration called autophagy gets off. The immune system, unlocking our immune
system, is the secret to longevity. What if we could reverse that, and in later ages of life,
we could restore the immune system to spending 65 or 70% of its time policing us.
This is where true life expectancy is extended.
This is where true anti-aging occurs is by empowering the God-given immune system to do its job.
There is no smarter resource on the planet than your immune system.
We're going to talk about that for a minute.
So after 21 weeks, no more hypertension.
And he had been told, just like the vast majority of you have been told, that he had familial hypertension.
He had genetically inherited hypertension, even though no one could tell him what gene he inherited that was causing that condition to exist.
So, essentially, what I'm trying to do is restore the faith back into humanity and mankind about our body's ability to heal itself.
Let's do a couple more, maybe hypothyroid.
any of you have or know somebody who has hypothyroid? Oh, gosh, this poor lady has raised her hand
for every single thing. Yeah, you definitely need to see me after the car. No, so let's talk about
hypothyroid for a second. You know, when we diagnose hypothyroid, because the thyroid makes two
hormones, right? These are called T4 and T3. Does anyone know what percentage of the thyroid hormone
T3 the thyroid makes? How much? Is that because you follow me on Instagram? Okay, well, that's
cheating. You just cheated in front of the whole, should be ashamed of yourself. Um, no, uh, yeah,
what percentage? 20. So, wait a second, I'm diagnosed with hypothyroid or my loved one is
diagnosed with hypothyroid and the thyroid only makes 20% of the hormone that we're
using to blame the thyroid for not doing its job. So this means that there's an 80% chance
at something else, right? How many of you said you have hypothyroid? Okay, you're going to love this.
Let's just use this beautiful lady here in the front for an example. By the way, aside from
being a scientist, I'm also a great artist. It's, I mean, it's basically a photograph.
I mean, if your family saw that, they'd be like, that's her.
So the thyroid is right here in the throat, right?
And it makes these two fascinating hormones.
It makes something called T4, and it makes something called T3.
That's a terrible three.
It makes something called T3.
The vast, if not all, of hypothyroid diagnoses
are low T3, but yet the thyroid only makes 20% of that hormone.
Does anyone that doesn't follow me on Instagram and hasn't cheated by watching my videos,
does anyone know where the rest of that thyroid hormone T3 is made?
And the liver.
The liver.
It's liver.
No.
Yes.
And the liver.
The vast majority of is made the liver, some in the gut and some in the periphery.
But what happens is thyroid hormone T4 is converted into thyroid hormone T3 outside of the thyroid.
This happens in the liver.
It is called deiodinization, and it's where we take T4 and we convert it into T3.
We make some other byproducts to Iotothyrinine, and we actually make something called reverse T3, which calms the thyroid down.
But for the purposes of this discussion, we make this in the liver.
We make this by converting T4 into T3.
Now, in order to make this conversion, you need a few nutrients.
You need selenium, you need thiamine, you need iodine.
A pandemic deficiency right now, second only to vitamin D3,
which is the most common clinical deficiency in the world.
Second to a deficiency in D3 is a deficiency in something called selenium.
When we put selenium in the body, our genes turn selenium into something called selenomythionine.
It becomes something called selenocysteine, and that compound goes into the liver, and it converts thyroid hormone T4 into thyroid hormone T3.
So if you have a gene mutation, then impairs your ability to use selenium, or you have a deficiency in this nutrient, your body is missing the raw material.
it needs to make this conversion and your T3 drops.
Well, when your T3 drops and it shows up low in your blood,
you're told you have hypothyroid.
There's only a 20% chance that you have hypothyroid.
There's an 80% chance you have poor conversion of T4 into T3.
I cannot tell you the thousands and thousands of clients
that we have fixed this conversion with nutrients
and restored normal levels of T3.
and hypothyroid goes into remission.
So very often we just stop when we see an anomaly in the human body.
We say, wow, thyroid hormone T3 is low.
What makes T3?
Well, probably the thyroid.
Let's medicate the thyroid.
Levo-thyroxine, synthroid, armor thyroid, natural dissected thyroid.
Again, accusing the thyroid of a crime that it is not committing.
Instead of going back into human physiology,
and asking the first question,
does this body have the raw material it needs to do its job?
And if not, let's put that raw material back
and see how it performs.
You know what is astounding?
We believe this in plant physiology.
If you had a leaf rotting in a palm tree
and you called a true arborist, a true botanist out
to look at that leaf, they wouldn't even touch the leaf.
They would courtest the soil.
And they would say, you know what?
There's no nitrogen in the soil.
They would add nitrogen to the soil and the leaf would heal.
Human beings are no different.
When you add the right raw material to the soil, the leaf heals.
And I'm not saying in every single condition,
but in the vast majority of these conditions.
You know, I really don't like the fact that in modern medicine,
we have this out, this excuse.
It's called idiopathic.
Idiopathic means of unknown origin.
If the origin is unknown, we should not stop until we find it.
We shouldn't stop there and treat for a condition when we do not know the root cause.
This happens the vast majority of time in autoimmune.
We're going to talk about this too.
So just to throw a couple big ones out there, how many of you either know someone
or have suffered from any of these Crohn's disease?
Hashimoto's.
chagrins, multiple sclerosis. These are all autoimmune diseases. And what are you told when you get
diagnosed with an autoimmune disease? Well, if you have Crohn's disease, you're told that you
woke up one day and your immune system, for no reason, just began to attack the colon. And because
it's attacking the colon, you have an autoimmune disease called Crohn's. If it's attacking the
lacrimal gland of the eye, you're going to be told that you have chagrins. If it's burning
random holes in the myelin sheath of your nerves, you're going to be told that you have
multiple sclerosis. If it's attacking the thyroid gland, you're going to be told that you have
Hashimoto's. And then you ask your doctor, what is causing this condition to exist? It's
idiopathic. Ah, well, look at that. Your uncle and your aunt and your grandfather had it. You have
familial Hashimoto's. You genetically inherited this autoimmune disease. You genetically inherited
Crohn's. You genetically inherited your propensity for multiple sclerosis, lupus, chagrins,
any number of other conditions. Yet 88% of the time we do not know the origin, and in 100% of
the time, we hold the immune system responsible for a crime it is not committing. There are
tens of millions of people walking the face of this earth right now that are on immunosuppressants,
on anti-inflammatories, on corticosteroids, on things to manage this immune system that just went haywire.
Well, guess what happens in a human body?
If you have a pathogen, let's say, don't go anywhere, let's say that this is a mold spore,
or it's a mycotoxin, or it's a parasite, or it's a virus, or even worse,
let's say this is a heavy metal, and this is a healthy cell.
Let's say it's a thyroid cell.
Let's say that this is one of the cells in your thyroid,
and this is a heavy metal called mercury.
This metal is not going to hide like this.
It's going to hide like this.
That is an important distinction.
So much so I'm going to show it to you again.
This metal, this molds bore, this mycotoxin,
this parasite, this virus does not hide like this.
It hides like this.
Why is that so important?
because the immune system is hyper-vigilant.
It is after that.
But when it reaches the wall of a cell,
it doesn't have permission to come inside.
So if somebody robbed a bank down the street from here,
and that bank robber ran into this room
and barricaded himself in the room,
what would happen?
The police would kick down that door
to get to the perpetrator.
Were they trying to destroy the door?
Or are they trying to get to the villain?
They were trying to get to the villain.
immune system is no different. If it wants to get to this, it has to go through this. And very
often in the human body, in order to gain permission to enter a cell, it has to kick down the
door. How does it kick down the door? It manufactures an antibody to that cell. Not to
kill the cell, to kill the pathogen. In the vast majority of Hashimoto's, which I call
Hashi nonsense. In the vast majority of Hashimoto's, we have heavy metals embedded in the thyroid.
The thyroid is like a magnet for heavy metals. Mercury, arsenic, palladium, cadium, lead,
heavy metals are gravitating to the thyroid. That's what calls the immune system. You see,
the police don't just show up for no reason and start kicking in your door, right? They show up
because there is a pathogen there.
There is a villain there, and they need to get to that villain.
And to do so, they will destroy the structure to get in and capture that villain.
The immune system is no different.
It will go right through the wall of a cell,
so much so that it will manufacture antibodies to the coating on the phospholipid bilayer of that cell
in order to gain permission to come in.
Not to get to you, to get to that.
That is such an important distinction.
This is the reason why 88% of all autoimmune conditions,
are idiopathic, right? You know, a fascinating study was published by a pathologist a few
years ago. I'm happy to link this study or let you read it for yourself. And he asked the
question, he said, you know, I see so many patients that are coming through my pathology lab
with multiple sclerosis. Now, multiple sclerosis is a condition where the immune system
again, woke up one day and for no reason it began to attack the nerves. Specifically, it began
to attack something called the myelin sheath. So inside the human body, I want you to think
of a nerve as a copper wire inside of a rubber sheath. If I were to take a knife and just
nick this rubber wire, I mean, nick the rubber down to the copper wire, the signal would arc
where that damage has occurred.
Multiple scleroses are multiple sores, scabs,
on the myelin sheath.
When they actually get down to the nerve,
the nerve arcs.
And this is where you get the symptomology
from this condition.
And he said, it's very strange to me
that if the immune system is attacking the myelin sheath,
if it can dissolve this coating,
this rubber coating on the nerves,
why isn't it uniformly dissolving the myelin?
And secondly, why isn't attacking the myelin everywhere?
It seems to be very specific.
It burns a very specific hole, like a rifle shot or an arrow,
and it burns one here, and then it burns one there,
and it burns one there.
It seems to be very sight-specific.
So he did post-mortem autopsies on multiple sclerosis patients.
In 100% of those cases,
he found the same helminth parasite, the same sestoed nematode.
It's a corkscrew parasite that burrows into the myelin sheath.
And he hypothesized that if in 100% of these post-mortemopopsies,
they had the same corkscrew parasite,
that the immune system was not trying to kill you,
it was trying to save you,
it was actually trying to preserve as much tissue as possible
by not attacking all of the myelin,
by attacking the site where these exist,
and actually the step was to suppress the immune system
and hold the immune system responsible for this condition
rather than saying, could it be a pathogen calling the immune system to that site?
You see, in the human body, the immune system, like a police officer,
does not show up for no reason and just kick in your door.
The immune system is called to that location.
There is a perpetrator here, please come get it.
And we could go through condition after condition after condition.
And again, I'm not saying 100% of the time, but the vast majority of the time.
So any time we have an idiopathic diagnosis, we should stop and say, I will not accept that this is idiopathic.
I won't need to find the origin and start asking the question.
Instead of immediately saying, I'm going to go this direction and assume that the immune system has committed a crime that I cannot prove
it's committed. And for the rest of this person's life, they are on immunosuppressants or
anti-flammatories or corticosteroids because their immune system just went haywire for no reason
at all. And so this is my deep belief in what God gave us and not what man makes us.
Chemicals, synthetics, and pharmaceuticals are rarely the answer to nutrient deficiencies.
In that chart that I showed you earlier, there was not one chemical, not one synthetic, and not one
pharmaceutical. I'm not saying they do not have a role. And if you're a physician, I am not
attacking your profession, nor am I attacking Big Pharma. I don't believe that there's a conspiracy
theory going on at the top of Big Pharma or by the Medical Association to keep people sick.
I just believe this is the way that we have developed because we assume that the body has made
a mistake. When we should assume God did not make a mistake, we just have to figure out why it's here.
okay i feel like i'm throwing a lot at you guys right now my wife says that oh awesome
thank you i never know if i'm losing you like when i see people leaning back in their seat
like this and their eyes starting to roll back i'm like okay let me take my foot off the gas here
for a second because my wife is like you just eat people's face you have to give them a break
we actually got on a plane a few months ago we were flying from Miami to Dallas and we get on
the plane and I'm in an aisle seat and my family is in the three seats behind me my wife my
outspoken wife and I sit down next to this poor soul and I you know I just break into a conversation
with them I'm like oh you know what do you do he goes I'm a family medicine practitioner I'm a sleep
apnea specialist. I go, oh, are you? And then my wife, she slams her face between the seats,
and she goes, he's going to eat your face. Be careful. And I did. I put the trade table down so
he couldn't get out, and I had a three-ring binder under the seat. I put it up there. I said,
let's talk about sleep apnea. And then I just killed this poor guy for three hours.
It's really amazing. Thank you. I think they are mesmerized. Yes? Yes.
Yeah. Thank you. I'm not watching the clock, so I apologize.
Thank you very much. Ladies and gentlemen, how do you guys so much.
Yuri Breka!
