The Ultimate Human with Gary Brecka - 302. The Antibiotics That Reversed Alzheimer's Blood Marker - Dr. Richard Horowitz
Episode Date: September 8, 2026Mold toxins show up in 90% of Dr. Richard Horowitz's chronically ill patients, and Lyme shows up in more. After 41 years and 13,000 cases, he just published the first documented reversal of an Alzheim...er's blood marker using nine weeks of oral antibiotics. CLICK HERE TO BECOME GARYS VIP!: https://bit.ly/4ai0Xwg Get Dr. Richard Horowitz’s book, “Ending Chronic Illness“: https://bit.ly/4642G7q Connect with Dr. Richard Horowitz Website: https://bit.ly/4iKFUZB YouTube: https://bit.ly/46oRSkt Instagram: https://bit.ly/4xEbPjd Facebook: https://bit.ly/465RFlT X: https://bit.ly/4gHIZHi Thank you to our partners A-GAME: “ULTIMATE15” FOR 15% OFF: http://bit.ly/4kek1ij AION: “ULTIMATE10” FOR 10% OFF: https://bit.ly/4h6KHAD AIRES: "ULTIMATE20 " FOR 20% OFF: https://bit.ly/4a3Duze BAJA GOLD: "ULTIMATE10" FOR 10% OFF: https://bit.ly/3WSBqUa BODYHEALTH: “ULTIMATE20” FOR 20% OFF: http://bit.ly/4e5IjsV COLD LIFE: THE ULTIMATE HUMAN PLUNGE: https://bit.ly/4eULUKpCYMBIOTIKA: "BRECKACYM30" FOR 30% OFF: https://bit.ly/4tjyluP GENETIC METHYLATION TEST (UK ONLY): https://bit.ly/48QJJrk GENETIC TEST (USA ONLY): https://bit.ly/3Yg1Uk9 GOPUFF: GET YOUR FAVORITE SNACK!: https://bit.ly/4obIFDC H2TABS: “ULTIMATE10” FOR 10% OFF: https://bit.ly/4hMNdgg HEALF: 10% OFF YOUR ORDER: https://bit.ly/41HJg6S PEPTUAL: “TUH10” FOR 10% OFF: https://bit.ly/4mKxgcn SNOOZE: LET’S GET TO SLEEP!: https://bit.ly/4pt1T6V WHOOP: JOIN & GET 1 FREE MONTH!: https://bit.ly/3VQ0nzW 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 - Introduction: Alzheimer's, Lyme and inflammation 01:20 - Memory loss in a parent 06:30 - Reversing an Alzheimer's biomarker 09:00 - Mycotoxins in 90% of patients 11:00 - Why 42% over 55 face dementia 16:00 - Migratory pain and diagnosing Lyme 18:20 - Why the CDC Lyme test fails 22:28 - Why doxycycline fails for chronic Lyme 31:02 - MS and rheumatoid arthritis misdiagnosed 38:11 - Mold and heavy metal testing 43:13 - Low testosterone and Lyme 46:37 - Long COVID, adrenals and autoimmunity 50:30 - The girl on 480 milligrams of morphine 56:30 - The nine-week oral protocol 01:01:30 - Glutathione, NAC and blocking inflammation 01:15:15 - The Alzheimer's biomarkers to order 01:32:20 - What does it mean to be an Ultimate Human Disclaimer: This podcast is for informational purposes only and does not provide medical advice. It is not intended for diagnosing or treating any health condition. Always consult a licensed healthcare professional before making health or wellness decisions. Gary Brecka is the owner of Ultimate Human, LLC which operates The Ultimate Human podcast and promotes certain third-party products used by Gary Brecka in his personal health and wellness protocols and daily life and for which Ultimate Human LLC and / or Gary Brecka directly or indirectly holds an economic interest or receives compensation. Accordingly, statements made by Gary Brecka and others (including on The Ultimate Human podcast) may be considered promotional in nature. Learn more about your ad choices. Visit megaphone.fm/adchoices
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42% of people, 55 years or older, expected to become demented.
And yet, they spend $2.4 billion a year at the NIH, and no one has come up with a solution for it.
When we realize that we spend $5 trillion a year on health care, we estimate that 85% of all chronic disease is preventable.
We have to start looking at things like our chemical supply, our food supply, our water, our air, as micro-toxic environments that accumulate over time.
And ultimately, what does it come down to?
Inflammation in the brain.
All chronic disease is driven by chronic inflammation.
But where's the inflammation coming from?
Bacteria, viruses, parasites, fungi, microbiome issuans in the gut,
vitamin mineral deficiencies, sleep disorders.
We are waking up to infectious disease and toxicity
as a root cause of some of the most prevalent chronic conditions
that plague society of mankind.
And I don't know why this happened in medicine,
but they're like naming a disease and throwing trucks at it
instead of getting to the underlying causes.
For folks that are watching this, like, where do we start with testing to just get a dashboard
of what kind of villain we're after?
For those of us who want to optimize our health, I discovered that...
Hey guys, welcome back to the Ultimate Human Podcast.
I'm your host, human biologist Gary Brecker.
Today's episode is deeply personal for me.
Like a lot of people my age, I've been watching my own mother's memory decline.
I've been searching for answers, not just a diagnosis of it's aging.
My guest is Dr. Richard Horowitz, a board service.
certified internist who's treated over 13,000 patients over 41 years, he is widely considered the
closest thing that the chronic illness world has to a master diagnostician. Dr. Horowitz developed
the MS-IDS model, 16 hidden factors from Lyme disease and Bartonella to mold and
toxins that quietly drive everything from brain fog to Alzheimer's. He just published the first
study showing this same model reversing P-Tal-217, the most sensitive Alzheimer's biomarker there is.
using a nine-week protocol.
If you or someone you love is dealing with unexplained chronic illness
or watching a parent decline like mine is,
and being told there's nothing that can be done,
this conversation is going to give you real, actionable hope.
Let's get into it.
Hey, guys, welcome back to the Ultimate Human Podcast.
I'm your host, human biologist, Gary Brecker,
where we go down the road of everything,
anti-aging, biohacking, longevity, and everything in between.
And today is one of those in-between podcasts.
It's going to be a very personal.
journey for me and my family. I am so excited to have this guest on the podcast because his
core competency fills a void that I have been trying to fill for over 10 years. You know, we talk
about the body spontaneously just going wrong, Alzheimer's, dementia, early onset, cognitive
decline, neuroinflammatory disorders, autism, ADD, ADHD, OCD, all of these chronic illnesses,
autoimmune. And we just seem to have adopted the philosophy.
that for whatever reason, the body has somehow spontaneously just begun to malfunction.
Nothing could be further from the truth. I've been talking about mold, mycotoxins, parasites,
viruses, and heavy metals for the last 10 years, but it's really a paucity of expertise in the
medical community. And our next guest, Dr. Richard Horowitz, is probably the closest thing
that the chronic disease world has to a master diagnostician.
And he is a monolithic giant.
I'm excited to read his book.
And welcome to the podcast.
Thank you, it's great to be.
Dr. Horowitz.
I'm so excited for this.
And I, you know, when I was prepping for the podcast,
I thought about the framing around this
and all the different avenues that we could go down.
But, you know, I'm on a very personal journey right now.
Like a lot of people, my age, I'm 55 years old.
I know I look 20, so don't like that shock you.
I was thinking 25.
25, okay.
I'm just trapped in this gorgeous spot.
but um you know like a lot of people my age um you know we're facing that decision about our parents
you know is it time to bring them back in with us is it time to get them into some kind of assisted
care memory care um you know a skilled nursing facility and it's a really hard decision and what really
prompted this journey for me you know my parents live in tennessee and i'm in miami so i don't
I wasn't seeing them that often.
My dad was calling me sort of more and more frequently
about my mom repeating herself all the time
and sort of forgetting things.
And then the pattern tightened,
meaning like her short-term memory got worse and worse
and worse and seemed to cataclyly go off of a cliff.
So this is a very personal journey for me
around neuroinflammatory issues, Alzheimer's,
dementia, cognitive decline, because nothing's worse than losing a living loved one.
And, you know, to be able to alleviate that pain for people would be one of the greatest
gifts to humanity. And I feel like your work is heavily centered around that very problem that
I'm dealing with right now.
You know, it's interesting. When I started off as a board certified internist, I was not expecting
to be a specialist in Lyme disease or Alzheimer's disease or autism or ADHD, none of these things.
But interestingly enough, my spiritual teachers,
I did my training in Belgium for seven years in French
at the Free University of Brussels.
And I met Tibetan teachers.
I was learning meditation there at the time.
And I went to one of my spiritual teachers
at the end of medical school and I said to him,
Lamagenden, what's the most important thing you want me to know?
I'm about to go out into the world as a doctor.
And he said, Richard, the most important thing
is exchange yourself with others.
Put yourself in people's shoes and do for them
what you would want done for yourself.
He said, if you do this, everything will go well.
Well, interesting on my journey, so now it's 41 years in medicine, having seen over 13,000
people, I just turned 70, by the way.
Yeah.
And I just can't believe at this point that I've developed a model that is extremely
effective for not just chronic Lyme, but I just published the first study in the Journal of
Alzheimer's Disease Reports.
I saw that.
Where we found that all 16 of the same factors, which I call MSIDS, multiple systemic infectious
disease syndrome, the same 16 factors I've been looking at in chronic Lyme that have gotten people
better are now published for Alzheimer's disease, and I just reversed Ptow 217, the most
sensitive and specific Alzheimer's biomarker for the first time ever in the world using a nine-week
oral antibiotic protocol, very short term. So I'm really curious to hear about your mom's case and
see how I can help because these are the kind of people I've helped all the time in my practice.
Yeah, I would love it. In fact, you know, I'll document it. I'll put it transparently out on
social media. I'm doing everything that I can do.
with the knowledge that I have and the community that I have,
which I will say has been very effective.
You know, last 12 weeks has been incredible shift
in my mother's journey.
Hyperbarics, you know, red light therapy, lithium orate,
very, very, very clean diet,
getting her glycemic profile down.
She's been in that pre-diabetic range,
like so many elderly men and women,
for almost a decade,
heavily insulin resistant,
on statin medication for 20,
five years now, heavy statin medication.
I mean, just the cessation of her cholesterol medication,
I saw not an immediate, but I would say a noticeable return.
And that's been talked about in the literature that sometimes statins,
you do have to be careful with cognitive decline.
Yeah, yeah.
Because they also lower K-10 levels,
and we know that mitochondrial dysfunction is one of the things in Alzheimer's disease,
right in dementia, you have to watch for it.
Yeah.
But what I find fascinating, you know,
thankfully your work is now starting to receive
the bright light that it deserves
because HHS is very focused on Lyme.
And I think that we are waking up
to infectious disease and toxicity
as a root cause of some of the most prevalent chronic conditions
that plague society of mankind.
Mold, mycotoxins, parasites, viruses, heavy metals.
And that once these things are in the body,
You get these behavioral characteristics
that mimic all kinds of chronic disease
and we start trying to treat the chronic disease
but nobody's going into the soil and saying,
hey, what is the bug or the parasite
or the viral pathogen that lit this fire?
And why are we going after the villain?
You know, why are we only focused on amyloid plaques
and neurofibrillary tangles
and, you know, the byproduct of these conditions
and not the genesis?
You're absolutely 100% on target
In fact, it is in the 16-point model,
it is infections and toxins that is always at the top of the list.
So in this model that I describe an ending chronic illness,
which has been the model I've developed over 41 years of 13,000 people.
The infections that we've seen are not just one bacteria.
It's not just Lyme disease.
We find clemenade pneumonia.
We find mycoplasma species.
There are 18 different species of Bartonella,
which most doctors have never heard of.
Maybe.
Yes.
And on top of that, we do see viral reactivation in people.
Long COVID caused people to reactivate Epstein Barr
and herpes virus six.
But people get toxoplasmosis.
A third of the world's population has toxo.
It's been associated with neurocognitive decline.
Babesia, the parasite I see all the time,
is associated with it.
And finally, even fungal infections,
they find fungus in the brains of people with Alzheimer's,
not just in the gut.
And it's interesting, most people know about Candida syndrome,
right, if you're in the functional medicine space.
Right.
They may not realize, though,
that when you get leaky gut
and intestinal hyperpermeability,
and you've got Candida Oak growth in the grut,
it's actually affecting your brain at the same point.
They found fungus there.
You combine these infections with toxins like mold.
90% of my patients are now showing positive
for multiple mycotoxins.
90%?
I don't want to gloss over that statement.
90% of your patients are showing positive results for mycotoxins.
Okrotoxins, trichlothicines,
glyotoxins, aflotoxins.
They're showing up in all of these patients.
And we do find that when we detox the patients,
and I've created some very simple protocols.
Everything, by the way, I've tried to do over my career
is oral, generic, easy to find, you know, solutions
that anyone in the world can find this to do it.
So I've detox thousands of people from mold.
I was loaded with heavy metals myself.
I had to take the amalgams out of my mouth
because I was so mercury toxic.
And I was afraid of what it was going to do to my body
from the free radical oxidative stress.
So this is common at this point.
So as you said earlier on, as we're getting older,
Alzheimer's disease at this point, the NIH, these are figures from them, 42% of people,
55 years or older, expected to become demented.
That is mind-numbing.
That is ridiculous.
You would even remotely accept that.
And yet, they spend $2.4 billion a year at the NIH, and no one has come up with a solution
for it.
So this article that I just published where there's 16 factors now gives people hope.
It's like, hold on.
I have cognitive decline.
I have Alzheimer's, and we'll talk about the biomarkers.
I'd like to see your mom get.
But there's things now that give people hope.
Like, I don't just have to go on an anti-ameloid antibody
like lachanamab dinanamab,
which they just showed in a Cochran review
is really not making much difference.
Now, maybe if you addressed the infections like Lyme
and Bartonella and pulled out the mold
and addressed all these other inflammatory factors,
these drugs might actually be more effective.
And that's something,
and I know Secretary Kennedy is very interested, right?
In looking at these chronic diseases,
God bless them,
because we needed someone to take a look at this.
Yeah, you know, I think that, you know,
when we realize that we spend $5 trillion a year on health care,
where the sickest, fatest, most disease-riddenation in the world,
we estimate that 85% of all chronic disease is preventable.
And, you know, we have to start looking at things like our chemical supply,
our food, our food, our water, our air,
as micro-toxic environments that accumulate over time.
You know, I've sat in front of so many functional medicine doctors,
and I think they would all agree that immunofatigue,
this slow progressive overwhelming of the immune system
is one of the greatest hallmarks of aging, right?
Just exhausting the immune system
with low-grade fights going on on so many different fronts.
Absolutely.
And in fact, what I think most people don't know
is that regarding your immune system,
Lyme disease causes chronic variable immune deficiency
and 20% of my patients
and 85% have subclass deficiencies.
You then get Bartonella on top of Lyme,
you'll see again even worse immune functioning.
And what is Bartonella?
So Bartonella is another bacterial infection.
It's intracellular.
It's showing up in 80 to 90% of my chronically ill patients at this point
who say, Doc, I'm tired, I'm achy, I have joint pain, muscle pain,
I have brain fog, I have mood swings, I'm depressed, I anxious, I can't sleep.
Bartonella is showing up in a large number,
and most doctors don't even need to look for it.
But when you combine Lyme and Bartonella,
and then you get long COVID,
which exhausts your T-Cast.
cells. So now Lyme and Bart have exhausted your B cells from the bone marrow making antibodies.
Long COVID exhausted your T cells. And then you get gliotoxins on top of that from mycotoxins.
Now you've poisoned your immune system with these bacterial infections. No wonder people are
coming down with cancer. I'm coming down. Your immune system is being basically impacted by these
infections and toxins. The toxins are affecting the microbiome of your gut. You need a healthy
microbiome because most of your immune system is in the pyres patches of the gut. So all these
toxins, if you're not supporting the microbiome with prebiotics and probiotics and even postbiotics,
right, and eating a proper diet, how can you expect your immune system as you get older, right?
I'm 70 or your mid-50s. How are we going to make it to 100 to make the oxygen in good health
and strong? Yeah. It's not, it's not going to be as easy if you don't look for these infections
and toxins. I couldn't agree with you more. So to unpack all of this, because I want to try to
keep this conversation narrow because there's so many, so many places that we could go.
Let's just narrow in on lime because I think lime is the great undiscovered pandemic of the last century.
I really do because the number of patients that we have seen with chronic Lyme infections
that actually manifested first as EBV or cytomegalovirus or another form of infection.
And if you were looking myopically at it, you said, okay, I wiped out the.
the, this, you know, the EBV titers are back in normal range.
And symptoms don't improve.
In fact, symptoms get worse.
You know, progressive cognitive decline continues,
maybe even accelerates.
So, you know, for folks that are watching this,
like where do we start with testing with panels
to just get a dashboard of what kind of villain we're after?
Sure.
So the first thing, most important thing to learn about Lyme
is it's a clinical diagnosis.
Okay.
You don't make the diagnosis based on a blood test.
It's by taking a proper clinical history.
Now, interesting, you learn in med school that 90% of all diagnoses are based on pulling it out of a patient.
They say the patient will diagnose themselves if you listen long.
And it's true.
Right.
And I can tell you after doing this for 41 years and 13,000, it is true.
It is listening to the patient, but you have to know how to take a proper history.
So I have on my website CanGet Better.com, a questionnaire that we validated in 1,600 people.
we published this in 2017
in the International Journal of Medicine.
We looked at three medical practices
who did Lyme disease, healthy patients.
It turns out if you score over 63 on this questionnaire,
it's two standard deviations above the mean.
It's very high probability of Lyme.
But specifically, there is one specific factor
people need to know about Lyme
that shows up in 95%
which is migratory pain.
If you have migratory muscle pain,
migratory joint pain,
one day your knee hurts
and two days later your shoulder hurts
and three days later your ankle hurts,
that is a hallmark symptom of Lyme
as well as migratory neuropathy.
Tingling, numbness, burning, stabbing sensations,
even vibration.
If it migrates, the number one disease
that does that is Lyme.
There's no other disease that causes migratory neuropathy
and we see neuropathy in 90 to 95% of our patients.
Wow.
So if you have a chronic fatiguing,
musculoskeletal, cardiopulmonary,
neuropsychiatric illness,
meaning you're tired,
You're achy.
You have brain fog.
You can't fall asleep.
You keep waking up the middle of the night.
You're anxious and depressed,
which is also chronic fatigue syndrome,
fibromyalgia, long COVID, mold.
They all overlap the symptoms.
The way you know it's Lyme clinically,
is Lyme has good and bad days
with the symptoms come and go.
Not the case with viral infections
causing chronic fatigue or fibro
or mold that's in your body all of the time.
Sort of consistent, not transient.
Correct.
Okay.
Also, you will see in women,
especially around their menstrual cycle
when the estrogen goes down, the bugs come out.
So all of a sudden, women will tell you
right before the menstrual cycle
or during or right after,
all their Lyme symptoms get worse.
So if you have a chronic fatiguing illness
where you have good and bad days
and it's right before your menstrual cycle,
it gets worse with migratory pain.
And then you start looking at Lyme-specific bands
and also, let's say you took an antibiotic
for urinary tract infection.
And you said, gee, my joint pain
and my brain fog are better.
Or you said, gee, I'm achy all over my body.
and I can't think that's a Herksheimer reaction.
You're killing off the bacteria.
You're getting a cytokine storm.
So reactions to antibiotics when you don't know you have lime
is a clue for someone that Lyme might be there.
But there's a game I like playing called Lyme Bingo.
And in this game, you get a good lab like Hygienics Labs in California
that checks for nine different strains of Lyme.
So why don't the regular blood tests work?
Well, the two-tiered test by the CDC of an Eliza followed by a Western blood
was done on one strain of Lyme disease,
which is the B-31 laboratory strain.
That is not the strain that is in the environment
that is making most people sick.
So the tests are not going to be reliable.
So we useigenics lab.
If you get a 23 band, USP C, outer surface protein C,
31 band, outer surface protein A,
34 band, outer surface protein B, 39 band, very specific,
or in 83-93.
So you get one of these,
these bands with a chronic fatiguing
muscular-iskeleton illness coming and going,
good and bad days, migratory pain,
better or worse with antibiotics, bingo,
you have Lyme disease.
And it's literally that simple.
You score high on this questionnaire
on can get better.com over 63,
migratory pain, even one band tells you
you have been exposed.
You do not use CDC criteria.
CDC even had this on their website,
by the way, a while back.
Really?
Yeah. Okay, so somebody that has a profile
that fits the description that you just said.
On your website, does it say exactly what,
can they get this test on the website?
I assume this is Quest Laboratories.
So I call this the, well, so the test itself,
you'll get from hygienics,
but I call this the Horowitz-EmSitz questionnaire, HMQ.
The link for it is on can get better.com.
You just download it from the site.
Okay.
And the nice part about it is it's 38 questions,
questions that you'll get in many chronic fatiguing illnesses.
And it comes from my good friend Joe Boroscano.
I just adjusted it and statistically validated it.
But it's nice because when you go to your doctor,
most doctors have 15 minutes for patients, right?
If they're in an HMO model.
I was doing that kind of medicine when I first came out.
These complex chronic glial patients
are an average of 45 minutes or an hour
that we have to take with them.
But if you hand them this questionnaire,
you can just look at the questionnaire and go,
question one and 22,
fevers, day sweats, night sweats, chills, flushing,
air hunger, I can't catch my breath in a cough.
Those are symptoms of a parrot.
a site called Babesia,
which show up in 60 to 80% of my Lyme patients.
So it's like having malaria on top of Lyme.
So by just taking this questionnaire
and bringing it to your doctor
and checking migratory pain,
if you then get one of these bands back,
you've got your diagnosis.
It's not so difficult to diagnose,
but this questionnaire really helps.
Now, the treatment for Lyme, I think,
is where you have so much divergence.
Some treat it solely as a viral pathogen, ignoring,
bacterial and parasitic co-infections.
Some will just look at lime titers and say, well,
once we've done the doxycycline for 21 days and the lime tiders, you know, down,
that's all she wrote.
And then weeks, months later, patients start coming down with these types of patients.
They don't, these types of symptoms, they don't link it back to that diagnosis.
They think it's something new.
And now you're off in the wrong correction.
Yeah.
Listen, there's what I share on this podcast and then there's what I share.
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the Ultimate Human podcast. So as you said, I think people need to really know this. 14.5% of
the world's population has been exposed to Lyme according to BMG Global Health, one of seven people.
Wow. Now that's, I believe, probably, and you said it early, this is a pandemic, right? We're in a
really bad problem with this disease. So here's the problem with it. About 10.
11 years ago, John Hopkins researchers, same time it came out of the University of New Haven
with Eva Shoppies Group, Kim Lewis from Northeastern University, Stanford.
They all came out with a very important study about Lyme disease, that it wasn't a normal
bacteria.
It's what's called a biofilm persistor bacteria.
So how does that differ?
And this is, by the way, how I came up with an answer and what I believe is a cure for chronic
Lyme.
Correct.
So what are biofilm persistia bacteria is tuberculosis and leprosy?
So when I was doing HIV medicine back at Mount Sinai
in my residency, a lot of people were coming in
with mycobacteria amavium avium intracellulari.
They were coming with TB.
This was right in the middle of the HIV epidemic.
I got used to using tuberculosis drugs.
And I always wanted to use these TB drugs in line,
but I needed an excuse.
So back in 2015, when John Hopkins said,
hey, this is a biofilm persistor bacteria.
And I went, oh, you don't just mean it persists.
You mean it persists like tuberculosis and leprosy.
Now, how do they cure,
leprosy, refampin and dapsone for a year.
What did I do?
I looked at the qualities of this drug called dapsone.
So dapsone number one is anti-inflammatory.
And as we're about to discuss during this podcast,
every disease we're going to talk about today,
ADD, ADHD, autism spectrum disorder,
Alzheimer's disease, allergies and asthma,
autoimmune diseases, rheumatoid arthritis,
chronic fatigue syndrome, fibromyalgia, cancer,
cardiovascular disease,
digestive disorders, irritable bowel, inflammatory bowel, hormonal disorders, mood disorders, pain,
every one of them has all 16 inflammatory factors on the MSIDS model that I discovered in Lyme.
How do I know?
Wow.
I did a deep dive in the medical literature.
It's all an ending chronic illness.
But the point about this that's important to realize is by looking at the literature for Lyme disease
and finding these 16 factors in discovering the Dapzone is number one anti-inflammatory
because all the diseases I mentioned
have all 16 factors
and they're all driven by inflammation.
All chronic disease is driven
by chronic inflammation.
But where's the inflammation coming from?
Bacteria, viruses, parasites, fungi,
microbiomeissions in the gut.
I'm coming from leaky gut
and intestinal hyperpermeability
with mass cell activation,
vitamin mineral deficiencies,
sleep disorders.
I call these the six rivers of inflammation
driving an ocean of inflammation,
which then causes mitochondrial
dysfunction. Your hormones go off. You have potts disordernami and autonomic dysfunction. Your immune
system doesn't work. You develop liver disease with fatty liver disease driving metabolic syndrome and
liver inflammation, as well as pain syndromes and mood disorders. So in Lyme, when all these 16
factors were causing problems, when I looked at Dapsone and I said, hold on, this drug is anti-inflammatory,
gets up into the central nervous system, so I might not need IV drugs. It hits autoimmunity. Lime causes
autoimmune reactions in the body.
Many people who came to me said,
I have lupus because my antinuclear
antibodies were positive. It was Lyme
causing antinuclear antibodies.
Or, Doc, I've been diagnosed with rheumatoid
arthritis because their rheumatoid factors were positive.
Wow. But the marker for
rheumatoid, CCP, cyclic sick,
was negative. It was the Lyme
causing autoimmune reactions, causing
rheumatoid factors. Right?
So the point being,
Dapsone was anti-inflammatory,
got up into the CNS,
affected autoimmunity, and it hit
these biofilm persistor forms, white,
while lowering down inflammation.
So I decided to try it by adding in doxycycline
or minocycline.
I published my first study in 2016.
It was a home run out of the park from the beginning.
Wow.
My wife who had been sick for 25 years
with chronic Lyme is now eight years in full remission
since she did dapsone combination therapy.
Wow.
And I have many people in full remission from this protocol.
So it can't just be that one silver bullet.
No.
No, okay.
The point I'm making here is when we believed before with Lyme that was chronically persistent
because it had different forms of the bacteria, cell wall forms, amoxicillin and IV-Rocephine hits
the cell wall form, or the bug goes inside the cells, the intracellular compartment.
That's where doxycycline or xithromax or refampin or quinolones go.
Or it had what's called cystic forms, L-form cell wall deficient forms that was flageal or
plaquinole or metronidazol.
We thought the bug would kept changing forms,
but until 2015, we didn't know it had biofilm persistor forms.
And I have now published by 11th article in the medical journals, right?
Ten of them are by me, one is by Tufts University,
where they showed that giving refampin and dapsone cured lime in the animal model.
We have a model in culture showing when you add dapsone to doxy or minnow and refampin and zithro,
it lowers down these biofilm persistors.
So we now have 11 published studies, including the last one on Alzheimer's disease, showing that Lyme can be a cause.
Before it was a theory, it was hypothetical.
It was right, difference between association causation.
We've now proven it.
But the key was hitting the biofilm persistor forms of the bacteria.
So, yes, you're going to hear people do IV therapies for years.
I had a woman come in with one year of IV recephine nonstop.
She stopped the drug and within one month she relapsed.
I gave her Dapsone combination therapy.
she went years in remission with a nine-week oral generic protocol.
So now it took me almost my whole clinical career to figure this out.
This wasn't overnight.
But it was almost like right in front of your face.
It's just that, you know, when we get off on the wrong track and we think, wow, this is,
this is morphing like a virus.
You know, it's sort of COVID replicated into less infectious forms.
Right.
So when we start thinking that this replicatory cycle
where it's actually changing forms,
you lost the genesis that no, it's always been there.
It's just been, it has a biofilm that's protecting it,
not only from some of these drugs,
but also protecting it from detection.
That is exactly it.
That's the issue.
Your immune system cannot recognize these bugs
when it's under the biofilms.
That's exactly right.
And in fact, why do you go to the dentists?
So then you don't have the antibodies.
Right.
And why do you go to the dentist
and take the plaque off your teeth?
It's because,
Formonus ginger valis, which causes a cause of Alzheimer's,
is under the biofilms on your teeth.
That's why you have to have the plaque taken off.
It's why we go to the dentist several times per year to do it.
These biofilm infections, by the way,
they've been around forever.
Endocarditis of the heart.
Candida infections of the gut is a biofilm infection.
Salmonella is a biofilm infection.
Joint infections, right?
When you get a joint replacement,
these are biofilm infections that happen.
So these biofilm infections have been around for a long time,
but for Lyme, it was not known until about a
decade ago.
Wow.
And I tried putting in, by the way, for a randomized multi-center placebo trial, unfortunately,
the NIH turned it down because of politics.
And that's why I'm so happy that Senator Kennedy, you know, finally got in there.
Secretary Kennedy got in.
We need somebody at the helm who really is taking this seriously.
Yeah, and I think he is taking it seriously.
And, I mean, there are Lyme committees and subcommittees and there is a bright light
being shown on this disease right now because, again, the end destination for a lot of
these chronic infections is our other neuropathologies. And now we're down the road of these
neuropathologies and we missed the genesis of them. So can we, I want to stick with Lyme for a minute,
and then I definitely want to get into Alzheimer's and cognitive decline because, you know,
first of all, it's very vindicating for me to see that someone with your level of credentials and
experience as is giving validity to the fact that a lot of these pathogenic invaders cause or mimic
these chronic conditions.
And I have long since held the belief that autoimmune is not idiopathic.
It doesn't just spontaneously and randomly, the immune system just wakes up one day and
decides to attack you, whatever random tissue it's attacking.
There is something is calling the immune system to that location, whether it's a virus or
a parasite or mold or mycotoxin or, well, you know, Lyme.
And having the diagnostics to give us that data
so that we know who the villain is is the first step.
No, it's crucial, so I'll take two autoimmune diseases.
Let's take MS, multiple sclerosis and rheumatoid arthritis.
Okay.
All 16 MSid factors that I had published in the literature for Lyme,
and this is in my new book and the chronic illness,
apply to MS.
So I've had many patients come in with
because MS is a demiliting disease,
except the demyelination was not due to multiple sclerosis,
which has now been shown to Epstein-Barr variants,
but also, as you said, it's the immune system attacking from what?
Chlamydia pneumonia, right?
By the way, MS was not in the Faroe Islands years ago
until the British invaded the Faroe Islands.
They knew that there was an infectious cause
for MS from years ago.
Rumatoid arthritis, there's a bacteria in your mouth
called Agrabatobacter.
If you have this bacteria, it tells,
your immune system to cause autoimmune reactions in the body, as well as having the wrong
microbiome in your gut. You have the wrong previtellus species, from micudis, bifidobacterium.
You don't have the right short-chain fatty acids in your gut. That's going to drive some
of these autoimmune reactions. So in both MS and in rheumatoid arthritis, and I've had many
patients come to me with these diagnoses, we got them off their metatrexateate. We stopped their
ABC drugs for MS with Avinx, Betaserin, copaxone, steroids, because it wasn't true MS. It was
lime and Bartonella and mold driving an autoimmune demilinating disease, but we also had a look
at the microbiome. We still had to address the mitochondrial dysfunction. The hormones were thrown
off from the lime. So we still had a look at the 16 points. But once the bugs, the bacteria and
the toxins, these two major factors which were driving autoimmunity, these people got tremendously
better. Wow. So and even the people who have true autoimmune disease, you have a patient,
and it's in my book, the patient had true rheumatoid arthritis,
but methotrexate and steroids and a rava and emerald,
they weren't working. Why?
He came in with migratory pain.
Well, migratory pain is the hallmark of lime.
Rumatoid arthritis is bilateral symmetric pain.
We treated as lime and that all of a sudden
his autoimmune drugs worked.
They weren't working because he had bacteria
and parasites like Babesia that were helping
to drive this autoimmune inflammation in his body.
It's no longer enough to name a disease
and throw drugs at it.
You must unlayer every illness into these 16 points,
especially for you and I, people that are healthy, right?
I feel great, but I have to look at my own toxin levels.
I have to make sure I don't have infections.
I'm taking prebiotics and probing.
I'm doing everything I can for these 16 points
because I wanna live a long healthy life
and optimize my health, but how can you optimize
if you've got infections and toxins and issues
with your microbiome?
Yeah.
So you've gotta look at all of these factors
if you wanna stay well,
even if you're not, you know,
a sick and chronic-agre in a preventative zone.
So can we go through those 16?
Yeah, sure, let's do it.
I think this would make a lot of sense
because these are ways to shine bright lights
on areas where we're not normally looking
in a human body.
So where do we start?
Obviously, we start with the panel.
Right, so let's start, so these 16 factors,
let's start with the six rivers of inflammation
that cause an ocean of inflammation.
Okay.
As we said, all chronic disease
we're seeing a real rise in chronic diseases,
as you said.
86% of our healthcare costs, 70% of the deaths,
18% of the GDP in this country is from chronic illness,
and we don't have a model to address chronic illness.
So it turns out when I did a dive into the medical literature,
and I looked for ADD, autism, out, all 16 points.
So what are the first six?
Infections, there's four types.
A, bacterial, B, viral, C, fungal, D, parasitic.
So the bacteria that most of the time,
in my patient population will cause problems,
are intracellular.
They're inside the cells.
That could be mycoplasma pneumonia,
mycoplasma fermentans,
chlamydia pneumonia,
Borrelia beredorferi Lyme disease,
other Borrelia species,
18 species of Bartonella.
So whenever these bacteria
go into the intracellular compartment,
they cause a huge amount of inflammation
and you get chronic fatiguing,
musculoskeletal, neuropsychiatric illness, right?
So that's just one piece of the puzzle,
especially when you've got these intracellular bacteria.
But you can have strep,
also causing an autoimmune reaction with pans pandas, right?
Not just causing a huge dramatic fever or glomelian nephritis,
causing autoimmune reactions.
And Lyme does the same thing with these autoimmune reactions, right?
So that's one piece of the puzzle is bacteria.
Bacteria.
Viruses, CMV, Epstein-Barr, herpes virus six,
but also HSV-1, HSV-2, parvovirus.
Many of these viruses are associated with Alzheimer's dementia.
They're associated with autoimmune illness.
Many diabetics, if you're not yet a type 1 diabetic,
They show that early on in life, some of these viral infections will cause that autoimmune issue
to start coming out.
And most people have been exposed to these bacterian viruses.
Now we've got parasites.
Toxo is one third of the world's population.
And Babesia microte, Babesia duncanai, Babesia otocolii, these different species of parasites
are now getting in, driving inflammatory reactions in the body.
So if anyone's listening and says, I have day sweats.
I have night sweats.
I have shaking chills.
I have air hunger, I can't sleep to catch my breath or a cough.
Those are classic symptoms of babesiosis.
We see this in a large percentage
of our chronically ill population.
And then Candida, you know,
I didn't really learn about Candida,
except in immunosuppressed patients in med school.
Candida syndrome, these people, let's say that you and I are well.
But let's say you start falling asleep
at 10 o'clock in the morning after breakfast
or at 2.30 in the afternoon, you just take a dive.
That oftentimes is reactive hypoglycemia
due to metabolic syndrome and too much insulin spikes, right?
but Candida syndrome is associated
with many of these people with hypoglycemia.
So let's say people are optimizing their health.
They're doing high intensity interval training.
They're getting enough sleep.
They've got a clean diet.
They're off sugar.
But they're tired all the time.
Many of these patients I found have candida overgrowth
in their gut because they took courses of antibiotics
and the doctors never gave them probiotics
with prebiotics to get the right bacteria.
I've had Candida syndrome.
I know what it is.
My wife has had it.
It causes the same symptoms
as chronic Lyme, as long COVID,
you'll see exactly the same symptom.
Even with mold, it's fatigue, it's brain fog,
it's muscle and joint pain.
You treat with fluconazol or etrocanazol
or a nystatin, all of a sudden,
their fatigue and brain fog is better.
Wow.
So all four bacteria, viruses, parasites, fungi,
need to be looked at in this model,
especially for people like us that are healthy,
but want to stay strong and healthy as we get older.
The second is toxins.
As we've talked about, mold toxins,
they're showing up and up to 90% of my patients.
With okra toxins, glial toxins,
I'm in the mole capital of the world, right here in Miami.
Miami, yes.
And many other areas, you know,
I think people, as the weather has changed
and people have gotten flooding now from their basements,
from changes in the climate.
A lot of people are getting mold.
We had it in our house.
It was a $150,000 renovation
because they did not shut off the chimney flu
and the water was coming down.
We had black mold.
Now, my wife and I never got sick,
and I wondered, was it all these,
supplements that I'm taking all day long.
I saw your supplement.
Oh, I have something with me if you want to see.
You know, and we're going to talk about these inflammatory pathways.
Why I suggest, we'll get to this afterwards, for inflammatory pathways specifically
that need to be either stimulated or blocked to stay healthy, because these infections
and these toxins that are driving inflammation, there are certain underlying inflammatory
pathways that we can work with nutraceuticals and diet that can kind of balance us and
keep it healthy.
But so there's a test from real-time laboratory.
in Texas.
You take 2,000 milligrams of glutathione.
You get into sauna, you sweat a little bit
to mobilize the toxins.
We're finding mold in a lot.
And again, you can do serum mercury lead,
arson academy aluminum.
But a lot of times you need to do like an EDTA challenge
or a DMSA challenge to look for metals.
Is it a 2,000 migs of glutathione?
Is that oral?
So you take it.
I actually do it orally.
Okay, take it.
Go in, what, a liter of fluid while you're in there,
maybe mineral water or no, no fluids.
No, no.
So we make sure they drink an eight ounce glass
a purified water every 15 minutes to hydrate.
They take oral liposoma glutathione,
get into sauna to sweat for 15, 20 minutes.
We found the people that didn't take glutathione
that didn't sweat, you don't see the mold toxin show up as much.
So, and by the way, we're just talking about a few toxins among,
I know you know this, thousands that are getting into the body.
Right, right.
So they have now shown, the CDC is now shown between 150 and 200 toxins show up
and everybody's blood and urine on a regular basis.
The truth is it's thousands of toxins.
all carcinogenic, affecting your hormone.
Why are women having a problem getting pregnant?
Why are mems spurn count down by 66%?
Yeah.
It's from these environmental disrupting chemicals.
It's going to another 1% a year
and female fertility rates are going down.
Male sperm counts are going down.
I mean, these two are diverging.
These toxins are affecting the hormone receptors in the body,
which is why people were having problems with fertility.
Right?
So, and they're blocking your hormone.
So your hormone testing looks normal
for your thyroid and your adrenals,
but you're getting blockage
for these hormone receptor sites.
by the environmental toxins.
So infections and toxins are the first two most important.
But number three and four is the microbiome of your gut,
followed by leaky gut,
intestinal hyperpermeability, and mass cell activation.
So every disease I looked at,
from autism, ADHD, Alzheimer's, cancer,
cardiovascular disease, chronic fatigue, fibro, mood disorders,
it was an abnormal microbiome of the gut
with the gut brain axis
that was driving inflammation.
So if you've taken any courses of antibiotics
without the right probiotics,
and even if you haven't,
these environmental toxins
are destroying the microbiomes of people's gut.
So I take four different probiotics a day.
Really?
With a prebiotic from orthomolecular
called MGP fiber.
It's got soluble and insoluble fiber,
so it's taking some of those toxins
and the liver entropatic circulation.
And I'm even taking a postbiotic called PDC activate
with a type of a strain of a bacteria
that drives my immune system
to get my natural killer cells
and T cells more activated for viruses.
So the microbiome is extremely important.
If you don't have enough short chain fatty acids
in from these bacteria,
you're gonna get inflammation in your body.
And I had leaky gut.
Do you know, I had asthma and allergies early in my life
and did not know that it had mass cell activation
and histamine sensitivity.
I was allergic to over 50 to 60 foods.
Wow.
I healed my gut, got off these histamine foods.
I have no more asthma.
My allergies are much better.
So did I have to take asthma meds
for the rest of my life?
No, I needed to get to the underlying causes
of where the allergies and asthma from.
Gosh, asthma is such a pandemic.
So three and four is your microbiome, leaky gut.
Five is vitamin mineral deficiencies.
Now, most people will check B12,
but they may not know there's a marker
of B12 deficiency called methamelonic acid.
We see a lot of people with a cult B12 deficiency.
Or they check their minerals,
but they don't know that 99% of their minerals
are inside the red blood cells.
So you need magnesium for 300 detox of
enzyme in your body.
So you get all these toxins in.
If you don't have enough magnesium,
you can't get rid of them.
And then you're getting asthma,
irritable bowel, and back spasms.
What are these all have in common?
Magnesium deficiency, right?
So it's not a question of taking Roaxin
for your back spasm or asthma sprays.
You need to look for magnesium deficiency.
If you don't have copper,
you need it for superoxide dismutase to deal
with all your free radical oxidative stress.
If you don't have zinc,
you have an aldehyde problem in your body
from your phase one liver detox.
but you have to check red blood cell zinc,
red blood cell magnesium, red blood cell copy.
We find up to 20% of these chronically ill patients
are all mineral deficient.
Now are these intracellular nutrient assays?
There's not serum blood studies,
like you would get a normal lab corp that says your magnesium.
No, those are your lab core and quest.
Lab core and quest, but they're not serum blood tests,
they're intracellular.
We do serum and we do red blood cell.
Okay, but it's true standard labs.
So it's, okay.
Yeah, bio reference, Quest,
lab corps. So you could just add that diagnostic code and just do RBC, RBC hemoglobin.
Absolutely. And even R79.9 in this ICD9 code is like, you know, laboratory abnormality.
Right. We've never had patients had problems getting insurance to cover these tests.
Okay. So vitamin mirrors and the sixth is insomnia, sleep disorders. Now here's the problem with sleep.
All 16 MSSIDs factors that we're talking about underlying insomnia, but Lyme causes people to not fall asleep, keep waking up in the middle of the night.
so does Bartonella.
But you might have a young thin woman
who might say, I have sleep apnea.
It's like 10% of young thin women
even have obstructive sleep apnea.
Or men as they get older,
have benign prostatic hypertrophy.
Or mood disorders, depression, anxiety,
are keeping people up at night.
If you have insomnia,
you get an elevation in cytokines
like intralucin 6
and that throws off your whole system.
So if you don't get to sleep, right,
nothing else you're doing, right?
You're trying to pull these nails.
Nothing is going to work.
So those are the six main factors.
It's infections, toxins, microbiome issues, leaky gut with mass cell activation, vitamin
mineral deficiencies, and sleep disorders.
Wow.
Right? So those are the six main factors.
So now you've got all this inflammation coming from different sources.
It has downstream effects.
What is the downstream?
Number one is mitochondrial dysfunction.
Yeah, the genesis of everything.
I mean, you know this well because I know your work.
That's the genesis of aging.
The mitochondria is the powerhouse of the cell.
If you have mitochondrial dysfunction, your brain cells don't.
work. The heart doesn't work after heart attacks.
It causes liver dysfunction, one non-alcoholic fatty liver disease.
Same thing with Crohn. You need functioning mitochondria
for every cell and every, you know, organ in your body.
Yes.
But there's nothing surrounding the mitochondria like your DNA of histones to protect it
from the free radicals. There's nothing protecting your mitochondria.
So everyone is doing mitochondrial regeneration, which I do daily,
ATP 360 from research nutritionals, CO-Q10, acetyl-carnatine.
people will take certain probiotics
to get urolithin in A to get higher.
So I do ergothyanine from mitoprime from zymogen.
I'm doing this daily.
But if you're doing mitochondrial generation
and you still have free radicals of tracking your mitochondria,
you might say, well, why am I still tired
if I'm doing mitochondrial generation?
I'm getting to sleep and I'm exercising
because the infections and the toxins and the microbiome
had not been adequately addressed,
so your mitochondria is still under stress.
And then the hormone,
get thrown off because this inflammation
affects the hypothalamic, pituitary axis.
So men in their 20s come in with low testosterone.
And they're coming in on beta HCG shots and creams,
and I'm thinking, hold on, nobody figured out
why a 25-year-old male has low testosterone.
Lime is the number one cause of low testosterone
in my population.
And how do we get it back up?
We give them clomophane and arimidex.
I give them a drug that they use for women in pregnancy,
which stimulates lutenizing hormone in the brain,
tells the testicles to make testosterone,
no shots, no creams.
We get the pituitary to kind of jumpstart again.
And then we give them a remodex and astrosol
to stop the testosterone from aerotizing to estrogen.
I get the testosterone from 100 to 600
with a low dose of these drugs that are all generic,
right, easy to get from your doctor.
Yeah, our clinical director's done that for young males
for years.
I mean, because you know, putting these young men
on hormone replacement therapy
and starting them on testosterone injections
in their early 20s is my numbing.
I mean, that's...
It shrinks the testicles.
It shrinks the testicles, low as the sperm count.
Right, I mean, you're not gonna have children easily early.
So you have to get to the, and I don't know why this happened in medicine, but they're like naming a disease and throwing trucks at it instead of getting to the underlying causes.
And a lot of doctors and patients out there don't realize that is a very common cause, but also the adrenal cland.
This may sound surprising to you, but 99% of my patients have low adrenal function.
Wow.
Everyone on a DHA-C-Cortisol salivary test, not blood,
salivary testing, we find phase one, phase two, phase three.
Cortisol, aldosterone, like all of the-
Well, especially, aldosterone's more with the blood pressure control,
but D-H-E-A-Cortisol thrown off in most
of this population because they're under stress.
So let's say you're optimizing your health,
you're exercising, you're taking mitochondrial supplements,
you're getting to sleep.
A lot of people have never checked their adrenals
through a salivary test, and we're finding in most,
even in long COVID,
All 16 MSSID factors we're talking about today,
and it's all in end of chronic illness.
It's the last chapter of my book, VAS for viruses.
All 16 factors are affected in long COVID.
I published it two years ago in the journal Microbiorganism.
Most doctors don't know that adrenal support
is needed for these people with long COVID.
It's not just Epstein-Barrin-H-V-6 reactivation, right?
And your serotonin goes down
because the bifidobacterium, your gut was thrown off.
So now they're giving him fluvoxamine,
this drug that raises your serotonin,
but why?
Because it threw off your microbiome
from the COVID, affecting your bifido.
But they're not going backwards
to look at the biochemistry and the biology.
It's a systems biology problem.
So we've got mitochondria hormones.
Then we've got the immune system
thrown off by these toxins, as we said, in infections,
or autoimmunity.
Lyme causes ANAs, rheumatoid factors,
antithirogly.
ANAs, like just a high anti-nuclear antibody.
One of my favorite biohacks
outside of breathwork,
by far is mineral salts, Baja gold sea salt. It's got all of the trace minerals that the body
needs. You know, most of us are not just protein deficient, meaning amino acid deficient or fatty acid
deficient. We are mineral deficient. So a quarter teaspoon of this in water, first thing in the
morning will make sure that you get all of the essential minerals that you need. It tastes amazing.
In fact, I made a steak today. I actually made a grass fed steak with grass fed butter and I put
just mushrooms and a little bit of rosemary and I sprinkled Baja Gold C salt all over the top.
Try it. It'll be your new favorite for cooking, too. It's the cheapest and one of my favorite biohacks. I don't know. A $15 or $20 bag of this will probably last you five years. It's literally the world's best biohacking secret. Now let's get back to the ultimate human podcast. So antinuclear antibodies are caused by environmental toxins and Lyme disease.
Wow. Same thing with rheumatoid factors. People come in and say, I think I have Hashimoto's thyroiditis. My antithyroid globulin and antithyroid peroxidase are positive. Lyme causes that through a
process called molecular mimicry.
So your immune system is trying to go after the bug, but instead of just going after the
tail of the spirok, it goes after your thyroid. It goes after your pituitary.
Because the proteins are similar, right?
Correct. It goes after your myelin sheets. You get anti-milin antibodies. You get demilination,
which looks like MS or looks like ALS. 10% of our ALS patients who came in did not have
true ALS. Wow. They had Lyme-induced ALS. We were able to stop the process and reverse.
it. Wow. Right now, most unfortunately, our genetic with superoxide dismutase problems,
but if you're the one out of 10 that's lucky, they didn't know that the demyelination was from
infections, from toxins, from the wrong microbiome. So in other words, all these factors on the
MSIDs model are interacting with all the rest causing demyelination. And then your immune
system is suppressed by these toxins and infections with autoimmune reactions. Then we have the liver.
One third of the world's population has fatty liver. Why is that a problem? And
That's caused by PFAS, by the way.
Yeah, non-alcoholic fatty liver.
Not alcoholic.
It's called non-alcoholic fatty liver disease.
So why is that a problem?
It causes metabolic syndrome and insulin resistance.
And you get cirrhosis later on in life with liver cancer
and your doctor never knew because you had no symptoms.
These are a silent liver disease
that is affecting one third of the world's population.
Wow.
And metabolic syndrome and insulin resistance
is related to Alzheimer's disease.
It's related to,
It's related to cardiovascular disease.
It's related to cancer.
So every one of these MSIDS factors
is affecting every other disease that's there.
And this is not known,
and I didn't even know this
until I started writing end in chronic illness.
So we're dealing with the liver,
the hormones, the mitochondrial,
autoimmune immune pain syndromes.
People would come in,
I had a woman come in on 480 milligrams
of morphine sulfate for pain.
This was a young woman,
oh, you're gonna love this story.
Wow.
She's 15 years old, she comes from the south,
She's actually from the Tennessee area.
She comes in with her mom.
But no trauma, no, no post-surgical was just pain.
Just comes in.
Her mother flies her up in a wheelchair from the South.
And she says to me, I've seen eight doctors,
including seven neurologists,
no one can figure out what's wrong with my daughter.
She's tired, she's achy.
She stands up and she starts passing out.
You'll probably know what that's about to be.
Yeah.
And she's got this incredible pain,
this neuropathic pain in her body on morphine.
The pain is not controlled with 480 milligrams
of morphine. Oh my gosh. So I take it, I give her the HMQ, the Horowitz-Mpsons questionnaire, and she says,
yes, I have migratory pain all over my body. Now I'm going to show you how I made a diagnosis
without a blood test. I went, well, there's only seven diseases in medicine that cause migratory
pain. You don't have lupus, right, based on the way she was presenting with butterfly rasses.
She did have got a cochle arthritis. She didn't have inflammatory bowel disease. She didn't
have writer syndrome. So in other way, she didn't have these other diseases that caused migratory pain,
right? She then, we stood her up with her mom,
and she started, her heart weight went to 140.
She had pots dishononemia, postural, autostatic tachycardia syndrome.
What are the four major causes of pots?
Lyme disease, Bartonella, long COVID,
which at the time when I saw her COVID wasn't even around, and mold.
Those are the four major cause that usually cause postural autostatic tachycardia,
although Ella Danlo syndrome and Marfan's and other things with,
as you know, with hypermobility syndrome can be affected.
Yeah, she has it.
Yeah.
She's not by him.
Has pots.
So we knew already are,
so it's the pots
that's causing
these pseudo seizures
that she was having.
So she picks up her shirt,
I examine her,
and she's got these
stretch marks
across her body
that are purplish,
and she was never overweight.
She had the classic
Bartonella stretch marks
that were present
across her breast marks.
They looked like
somebody gained
and lost 200 pounds,
and these are very classic
for Bartonella.
So right now,
migratory pain,
I knew she had Lyme.
Right?
Potts, we knew
because we stood her up
and her heart went up, and her blood pressure drop.
We knew she had Bartonella because she had the classic rash,
like Lyme has the bullseye type rash,
which half the time, by the way, doesn't look like.
I haven't heard of the stretch marks.
So it is a classic.
If you look it up, I can show you the journals.
Yeah, no, I believe that.
They're purplish or they're whitish.
And a lot of times they're perpendicular to the skin plane,
but a lot of times they're whitish
and they look like a Christmas tree pattern
where they're perpendicular and they can be purplish.
And they change, by the way, when we treat it.
But she also said to me, yes, questions,
one in 22 on the age computer, I have drenching sweats.
Now, this girl's 15 years old.
Now, when men would come in with drenching sweats,
I used to say, I'll bet you're in manipause.
They liked the joke, by the way.
But so she had babesia.
So without ever doing a blood test,
I said to the mother, I know why you saw eight doctors
and your daughter's sick.
She has Lyme, she has bobezia,
she has bartonella and she has pots.
So she left the office, we drew the blood.
I put her on, and at the time,
we weren't doing as much with dapsone.
I put her on doxycycycycy.
I gave her salt, fluids, and licorice to raise her blood pressure.
Salt fluids are in licorice.
Just to raise her blood pressure, right?
And we started treating the Babesia with some malarone.
She flies in one month later.
This girl was in a wheelchair unable to walk on morphine.
She's off the morphine.
She's walking out of her wheelchair and she has no pain whatsoever.
After one month of treatment of her Lyme Babesia Bartonella
and treating her pots appropriately.
And now you would use something more biofilm
Now I would use Dapsone therapy with these biofilm agents.
At the time, we didn't even know this.
But the point being, that was the 90% we talked about
is how do you make a diagnosis?
You pull it out of the history out of the patient.
It was by taking a good clinical history
and examining her.
Wow.
And I've had patients in wheelchairs who couldn't walk.
We treated their parasite with Babesia.
They get out of wheelchairs and they start walking
because the parasite was affecting their immune system
and making them so weak they couldn't.
Or a woman who couldn't talk for five years.
Words would not come out of her mouth.
It was called dysarthria and aphasia.
Like if she had a stroke, she went to Mass Channel,
nobody could figure it out.
It was Bart Nella.
We treated Bart and she started saying words.
So I have seen these kind of crazy cases
where people have seen 10, 20, 30 doctors.
The key that I'm noticing for all these chronic fatiguing
musculoskeletal neurocyte is you gotta go back
to the 16 point Msids model.
It's where I'm finding the solutions
and I've done this for 41 years.
And does that panel catch all of these?
I mean, the panel that you just described
earlier in the podcast, it catches all of these,
because I've got to put a link to that in the podcast notes.
Yes. And also, you know, in my prior books,
but in the chronic illness, I discussed the panels
in the first 30 or 40 pages,
I discussed the panels for Lyman Bartonella.
What are my favorite labs?
What are the labs you're going to do from mold?
What are the labs we use for the adrenal dysfunction?
All of this is in the book
so you can take it to your doctor
and you can work with your functional medicine doctor
or train your doctor, right?
And just teach them what these tests,
but everything is laid out clearly
as a roadmap to get these paper back to health.
Wow.
And then once you have this data on the pathogenic invader,
it can't be as simple as that short course of antibiotics
and then a long course of probiotics, or is it?
So the interesting part for Lyme is for the people,
like my wife was sick for 25 years with Lyme disease.
And before I knew the dose of dapzone
that was needed to cure Lyme,
and I'll tell you, the universe is very kind to me.
So I was in prayer years ago
of please let me have solutions
for these chronically ill patients.
So what happens?
A guy comes into my office,
he's seven years sick.
I give him the Dapzone protocol,
but at the time I was using 100 milligrams a day.
He comes in month four and he says,
Doc, I'm feeling terrible.
I said, oh, what's going on?
He said, oh my God, I'm so tired.
I'm achy, I'm brain fog.
I said, oh, what are you taking?
Well, I'm taking Doxy, I'm taking refampin
and I'm taking Dapzone twice a day.
I said, oh my God, you're taking too much Dapzone.
You're taking double the dose.
I said, stop.
it, come back in a month.
He comes back in a month.
He was sick for seven years and he goes, Doc,
I feel amazing.
I went, huh?
He said, I'm off all my treatment.
My energy is fabulous.
My brain fog has gone.
The joint, I said, what?
I said, don't do anything.
I don't want you taking any more medication.
Come back in three months.
He goes back in three months, he says, I'm well.
Is he still on it?
No.
No, he's off.
Because he took double,
he took 100 milligrams of Dapsone for one month,
which I didn't know at the time
was enough to get Lyme in
remission, we thought we didn't know the dosage.
Right.
So for Bartonella, it's a little different.
But ultimately, what we found out is it's a nine-week oral protocol.
So my wife who did 50 of Dapsone for a year said, Doc, a hubby, I feel great.
She stopped it.
She was PCR positive for Lyme in her blood.
Wow.
We did a hundred of DAPSone.
Huh?
The hundred of Dapsone.
We did a hundred of Dapsone for six months.
She said, I feel great.
She stopped it.
She relapsed.
I said, you know, honey, this guy just came into my medical office.
He took a double dose of Dapsone.
Would you like being my guinea pig?
She said, absolutely, Rick.
She took 100 of Dapsone twice a day.
She's eight years in remission.
For how long?
Eight years.
No, no, no.
For how long did she take the...
One month.
30 days.
But now she had done a year of Dapsone at 50 milligrams.
Right.
Six months of Dapsone at 100.
So she did a year and a half of lower dose
and she lowered the biofilm
persistural load of the bacteria.
So she only needed one month.
But ultimately, I got this protocol
after tweaking this and playing around with.
thousands. Yeah. It's a nine-week oral protocol. So if you don't have Babesia and Bartonella or mold,
and you take this protocol for chronic Lyme, you will most likely go into remission. I publish this,
it's at least 50% of the people that go into long-term remission. Most of the people that don't,
they have active parasites like Babesia. They have other intracellular bacteria like Bart. If you have
barred, you need four two-week pulses of oral, this oral generic protocol, and it's only six days of
dapzone, right? Just six days.
and that will put a lot of these Bartonella patients
into full remission.
Wow.
So I have gotten this protocol down
to very short-term oral antibiotics
while giving you four probiotics twice a day,
500 trillion of these bacteria.
Four probiotics twice a day.
So no C-Diff, no problems with yeast overgrowth,
with nis statin.
And you can take that with the antibiotic.
Right, but I'm also giving you,
I'm blocking and stimulating
four inflammatory pathways,
so I'm blocking inflammation.
And I want to go through this
because this is really important.
I want to go through this too.
For those of us who want to optimize our health,
I discovered that not only are these 16 MSSIDs factors underlying cancer,
cardiovascular disease, chronic fatigue syndrome, autism,
every disease pretty much the major diseases,
but there are 16 inflammatory biochemical pathways underlying these 16 factors.
So you would recommend this even if somebody doesn't have a line,
just to go through this and like I do parasitic detox.
Correct.
So I'm going to talk to you about the first four pathways that when people take dapsum.
I'm doing this.
And by the way, this is what I take every day.
So I don't know if this is embarrassing at this point to show you,
but like that is my dinner time and this is my breakfast.
Now, you and I might be able to talk.
You don't even have eggs or steak or chicken or anything.
It's all in there.
You and I should talk after this podcast about how to maybe put this in a drink and get this
so people don't have to swallow what I'm doing.
But let me tell you why I'm doing what I'm doing.
Every family member in my immediate family
has died of a different form of cancer.
My mother died of lung cancer
and she had cervical cancer.
My father died of pancreatic cancer
and he had an early case of colon cancer.
My uncle Al, who delivered me
at my Monadies Hospital in Brooklyn,
he had a form of prostate.
Every aunt and uncle, they're all dead.
Wow.
They're Ashkenazi Jews.
I don't know what their BACA status was.
But I discovered when I was looking at cancer
that all 16 of these,
It's factors affected cancer,
but there were pathways driving cancer.
So when I did the DAPSone protocol,
and people said to me, I feel horrible
when you're killing the bacteria.
I knew I had a block inflammation,
as we've talked about.
Chronic inflammation is driving almost all these chronic diseases.
That's the roadmap to health, right?
To both stay healthy and to reverse it.
So what did I do?
The first pathway on this protocol
is blocking a pathway called NFCAPA B.
NF Kappa B is the number one switch inside your nucleus,
When it turns on, you get two necrosis factor alpha,
interleukin 1, IL-6, you get all these inflammatory molecules.
And necrosis factor is something that is prolonging or interrupting autophagy, right?
I mean, what?
Correct.
So you bring up a very important point.
So our cells need autophagy.
We need to clean house.
Right.
On time, yeah.
In time.
So if you have damaged mitochondria, if those mitochondria do not go through autophagy,
If you can't clean those out and get rid of them,
that's gonna lead to Alzheimer's disease.
That can lead to autism.
That'll lead to cancer.
Damaged mitochondria without autophagy
is going to lead to this problem, right?
So these inflammatory pathways
are showing up in autism and cancer,
and chronic, in all of these diseases.
So when I give people this Dapsone protocol,
I'm not just giving them antibiotics.
I'm giving them probiotics to support the gut,
but I'm giving them NAC, NACC,
N acetyl Sistine, a precursor of glutathione, right?
Right?
Which is what?
Which is what?
Which is a precursor for glutathione.
Enacetyl cystic.
Enacetyl cystin helps the body,
cystin, you need cystin glycine glutamic acid
to make glutathione.
Right.
So if you're eating a high protein diet
with lots of cysteine, right?
Way-based protein, you're getting a form
to help your body to make glutathione.
Why is glutathione so important?
It's the number one master antioxidant in the body.
Now when people died of COVID during the first wave,
we talked about this earlier.
They were dying from ARDS, acute,
respiratory distress syndrome.
They had white outs in their lungs.
Most people don't know that you have
140 times more glutathione in your lung tissue
than anywhere in the world.
They did not know that.
So if you have toxins from the environment
and you used up all your glutathione.
And now you got the virus
using up glutathione.
And you didn't have enough glutathione,
you were gonna get acute, right?
So in the protocols I use,
we block this first switch that drives inflammation
using NAC, alpha-lypoic acid, really interesting.
It regenerates glutathione intracellulally.
It's water soluble, fat soluble, gets up into the brain.
It regenerates mitochondrial function.
And it's one of the most powerful antioxidants that exists
while regenerating mitochondria and regenerating glutathione,
and then we give them glutathione.
So the first thing that I do, and this is the supplements I take.
NAC, alpha liposac acid, glutathione.
I'm blocking that number one switch, right?
NF Kappa B, which shows up in autism, Alzheimer's,
cancer, chronic fatigue, every major chronic disease,
pretty much you're gonna see.
Wow.
The second pathway I stimulate called the NRF2 pathway.
So NRF2 really important pathway.
Yeah.
This is how you stop your genetic,
so every one of my family died of cancer.
This pathway tells your genetic structure
to hit the P53 cancer gene and shut it down
and open up your detoxification pathways
to help shoveling out these environmental toxins.
All of these psychotective proteins.
Correct.
Exactly, that's it.
So how do you stimulate NRF2?
turmeric curcumin, broccoli seed extract,
sulfuricine glucosinate.
If I, oh my God, that is like one of my favorite supplements
of all time.
Because that is so important in hitting this P53 gene,
do you know that they gave sulfurphane
to autistic kids between 100 to 300 milligrams
and they started reversing autistic syndrome?
Because it hits a biochemical pathway called the mTOR pathway,
right?
The mechanistic target of rapamycin,
which you need for longevity.
Right.
Well, the mTOR pathway,
people think autism and Alzheimer's,
they're two different diseases, they're not.
They're on a different spectrum of neuro-inflammation
in the brain.
And if the mTOR pathway is hyper-stimulated
in autism and Alzheimer, how do you lower it?
Broccoli seed extract.
When they give Alzheimer's patients,
we're gonna talk about your mom later.
Okay, good.
When they gave sulforaphate glucosinilate
to people with dementia,
they noticed their cognition improved
because it stopped this overactivation of this pathway.
So broccoli seed extract with curmin,
with green tea, EGCG, right?
Very, very important.
So Cochermin, green tea, broccoli seed,
and very, very important with broccoli seed extract.
These will stimulate a pathway called NRF2.
The third pathway is called NLRP3 in phlamasomes.
Now this is important in cancer,
in Alzheimer's disease, in most chronic illnesses
that you're going to see.
How do you shut it down?
Well, it turns out these first two things we talked about,
NFCAPB, NRF2, if you take these supplements
with curmin, broccoli seed extract.
Resveratrol, by the way, is also a great NRF2 stimulator.
It hits the certhuan genes of the body for longevity,
right? It's part of my protocol.
It also affects NLRP3 in flammasomes,
but you also do it with low-dose naltrexone
and low-dose melatonin.
Wow.
So in al-D., so if you have a problem
sleeping with LDN, I take actually mine in the morning
just to make sure it's not,
but I take 4.5 milligrams of low-dose-naltrexone
compounded through infuserv in Florida.
It's my favorite compounder.
And I take it with very low dose, one milligram melatonin,
to block NLRP3 inflammatory lymphombs.
And the fourth is inflammatory prostate glandums.
Take, if you're eating healthy fish,
which difficult these days, you can, you know,
wild organic salmon.
Fish has great omega-3s, but I take a mercury-free fish oil.
I take ortho-a-o-o-megra-molecular.
But these first four pathways are among 16 inflammatory,
but when you look at all 16 pathways,
if you were to take things that block NF-CAPA B,
an acetyliscylasease, alpha, hypoic acid.
Now, I should tell you, you have to be careful
with alpha hypoic acid.
If you're hypoglycemic like I am,
if you take 1,200 milligrams,
which is pretty much, you have to be careful
with blood sugar swings.
Yeah.
Now, not one of my patients died during COVID
when I gave them this protocol.
Why?
We now know that there were microclots
that were forming with COVID,
and now some people think
these spike proteins are in the body
causing inflammation in these nutrifil
extra cellular traps.
It's driving inflammation.
Why did none of my patients
have a problem because I told them,
and it's still on my website from 2020,
because I published the first article
on glutathione for COVID,
I told him to block NFCAPA B.
I didn't realize at the time that COVID virus
needs to lower glutathione to replicate.
I didn't know that either.
When my patients now get COVID.
It needs to lower glutathione to replicate.
So influenza virus has to lower glutathione to replicate.
Wow.
So does den fever, so does HIV.
So does COVID.
So by taking, when I get COVID, I've had it twice,
I take 2,000 milligrams of glutathione three times a day
with any six times a day, three times a day.
Three times a that's the maximum dose
that you normally can take.
Okay, 6,000.
And not one of my patients who did this generally ever fell ill.
Not one person died.
I only had two people in the hospital
and they were both immune deficient by the way for COVID.
But when you stimulate NRF2 with curmin,
resveratrol, broccoli seed, green tea extract,
you take NACC, alpha lipos, glutathione.
You take LDN, Militonin and a multi-mineral
supplement, very important.
Yeah.
I take Minorex from Zymogen, which has copper and zinc and magnesium.
I take magnesium malate as well as magnesium glycinate.
Sometimes you'll threanate if I have a problem sleeping at night.
But you need a multi-mineral, as we talked about, for these detox pathways.
And I told people to do this with omega-3 fatty acids.
All of my patients did well during COVID simply by looking at the virus driving inflammation
and saying, how do we block inflammation?
How do we lower inflammation?
It was very logical, so Paxlovid is very good
to stop the virus from replicating.
People get less long COVID when they take it.
But it's still, as you know, people get relapses
and they get rebounds.
And a lot of people get Epstein-Borin-HV-6.
And this could be from the glutathione deficiency.
Correct.
So again, you've got to look at your immune system.
It's not just getting COVID.
Do you have these other infections and toxins
and microbiome issues?
All of this is now shown up with long COVID.
Wow.
So for these like 45 million Americans with long COVID
who say, I don't know what,
what to do.
The last chapter in ending chronic illness, V is for viruses,
it shows you how every one of these 16 MCIDS factors
is associated.
Look at your adrenals, look at the microbiome of your gut, right?
And you'll find if you address, by the way,
a lot of these people that had a marker of long COVID
called VEGF, vascular,
it wasn't from the virus affecting the endothelium
driving inflammation, it was Bartonella.
Was it the VEGF driving up to cause this angiogenesis?
That can also be a good thing.
Right, I mean, upregulating VEGF for tissue and wound repair.
Correct.
Like anything in the body, it's all about balance, right?
But in the patients, when I did a long hauler panel through Patterson's lab in California,
and I looked and I found that their cytokines and chemokines were up and they had VGF.
Through the roof.
Through the roof.
Okay.
It wasn't just from spike proteins that were sitting inside the endothelial driving, right, the inflammation.
Because they didn't know they had Bartonella.
Bartonella causes elevations in VEGF.
And I suspect at this point
that a lot of the long COVID patients out there
because I've seen many of them
that have gotten better,
they didn't know they had Lyme,
they didn't know they had Bartonella,
they're viruses that reactivated
and I have in the book
some solutions for EBV
that I think need to be looked at.
Epstein Barr is a horrible virus
that causes cancer,
burkitts lymphoma, right?
Not just chronic fatigue center.
And everybody's got it.
It's really widespread.
And so it undulates too.
So if you look at the antivirals
for Epstein Bar.
Yeah.
It's like all these viruses
these drugs like Artenis, they're not easy to tolerate.
It turned out when I was doing the deep dive
in the medical literature,
that spironylactone, a drug they used for women
with PCOS to lower testosterone,
and dipyrodamol, persantene,
a drug that's used to stop strokes
with transidishemic attacks,
if you combine these drugs,
which are very well tolerated
with an antiviral like famyclyver,
it shuts down the virus
at every stage in the replication.
Now, don't get me wrong.
I need a randomized multi-center trial,
Secretary Kennedy, if you're listening to this,
let's get the monies in this.
But the point I'm making is,
I did this dive in the literature
and it's like I discovered all these things
that it's like, oh my God,
so many people are going to benefit,
but yes, we do need the money
put into these studies
because association does not always equal causation.
But I do believe I found an answer
for a lot of these illnesses
that people are suffering.
This gives them hope.
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Wow.
Wow.
So I am definitely going to put this protocol in the show notes
and even the lab values in the show notes.
I want to switch gears to not necessarily my mother per se,
but cognitive decline.
Alzheimer's, dementia, because as you said, if 42% of the population over 55 years old,
which I'm about to turn that population, is expected to get one of these cognitive ailments,
that to me is mind-numbing.
It is.
And it can't be that all of a sudden, half of the world's population at that young age is going to
suffer from.
That's correct.
And ultimately, what is it?
down to inflammation in the brain, right?
So all of these diseases we're talking about,
whether it's neuroinflammation,
these microplastics that get into your arteries.
Yeah, insulin resistance in the brain.
It's the genocry strokes, heart attacks
when they get in here.
So what's interesting about inflammation,
inflammation in the brain, Alzheimer's.
Inflammation in the heart, heart attacks,
congestive heart failure.
Inflammation in the joints, rheumatoid arthritis.
Inflammation in the skin, scleroderma, psoriasis.
You name the organ, and I'll show you
where inflammation is causing disease we're talking about.
So then the problem is, well,
where's the inflammation coming from?
So unfortunately, they spent $2.4 billion a year of NIH funds,
and I had to be the first guy who told them
that there's not just an association of Lyman Alzheimer's,
but causation, and by the way, it's not the only cause.
We'll talk about this to a second.
All 16 MSSIDs factors that we're talking about today,
the six rivers of inflammation
of infections, toxins,
microbiome, leaky gut,
with mass cell activation,
vitamin mineral, sleep disorders,
10 downstream effects, mitochondrial,
hormonal dysfunction,
liver disease, pain syndrives,
immune, autoimmune,
all of these factors
are been showing up in Alzheimer's.
So in this article,
I just published,
if someone went to the neurologist
and said,
I have cognitive decline
and they did a Moka test,
right, Montreal Cognive Assessment,
and they didn't score well on it.
This is exactly what happened to my mom.
And they did Alzheimer's biomarkers.
So what are these biomarkers you need to check?
And these are not being routinely done, by the way, by physicians.
So you first want to check.
And this is, by the way, my favorite is Quest Labs, covered by insurance.
The amyloid beta 4242 ratio is the first biomarker you want to check.
Okay.
If you have a low ratio, that is bad.
You don't want low.
Normally we think, you know, a low ratio means you're taking the sticky protein amyloid beta
42 and you're depositing it in your brain.
That's not what you want happening.
So first biomarker amyloid beta 424.
Second, p-tow phosphorylated tau-181.
Third biomarker, p-tow phosphorlated tau-217.
Now, that is the most specific sensitive
and specific biomarker for Alzheimer's,
and that's the biomarker that it reversed
with the nine-weekedapsone protocol in my patient.
Now, what's great about this study that I just published
is this patient was sick with chronic Lyme for 15 years
and had not touched one antibiotic in 15 years.
All I did was give her the nine-week oral dapsone protocol
and three months later her Alzheimer's biomarker
completely reversed to normal
and I didn't realize it at the time
when I published this in the Journal of Alzheimer's Disease Reports.
No one had ever done this before
in the world medical literature.
Wow.
The anti-ameloid drugs lower these biomarkers by 23% in six years.
Oh my God.
I lowered it by 63% in nine weeks.
because the amyloid was being driven
by Lyme Borrelia burgdorferi.
Okay.
So you need Ptow 181, Ptow 217,
and the last one is neurofilament light.
Now, this is a non-specific marker of inflammation,
not specific for Alzheimer's,
but what's nice about that is if you have hypertension
or cardiovascular wrists or even other diseases,
and you have inflammation from IL6,
no matter what the cause.
Like an endothelial marker?
Yeah.
That neural filament light will show up as a marker
saying you better do a better job
in the inflammation in your body.
The fifth biomarker is if you are APOE-44,
which is the genetic marker for Alzheimer's,
which by the way, none of the patients
I checked in my practice were APOE-44.
Wow.
They still reversing biomarker.
So, well, because of the pathogen, yeah.
Yeah.
So, but the last one is called
glial fibroac acidic protein, GFAP.
Okay.
So if you are Alzheimer's APOE-44,
you want to get GFAPE,
leal fibricic acid because if that's positive,
your 10 year risk down the line is gonna be high,
you're gonna develop dementia.
You don't have to do that biomarker
if you're not APOE44.
Okay. Now I discovered in my patients
before I finished clinical practice after 41 years
of seeing 13,000 these patients,
that half of my patients were showing up
with these Alzheimer's biomarkers.
Wow.
And I asked a colleague of mine.
The predisposition genetic markers?
No, no, no.
The actual blood mark.
Okay.
Oh yeah.
Okay.
were showing up with low beta amyloid 4240 without even having a predisposition, which means
one of these pathogenic invaders. Correct. Wow. And they were never, and you're not taught in
internal medicine. Do a prostate exam. Go for a colonoscopy. Check your cholesterol. Check your blood pressure.
Check your hemoglobin. All good. But now that you know the risk of dementia is 42%. Wouldn't you
want to check your Alzheimer's biomarkers? Of course you do. Because it's silent. You want to know if you
have neuroinflammation in your brain before it happens, right?
So these are covered by Quest Laboratories by LabCorp,
but I like Quest specifically the way they do it.
So you would want your mom specifically,
if she's having issues,
to look at these biomarkers.
Now, you also want to look, however,
at the 16 MSSIDs factors we talked about.
Now, I don't know your mother's clinical history at all,
but I would want it to fill out the HMQ on my website,
can get better, and see what her score is.
We're filling it out right after this podcast.
We'll speak about it.
I want to know, does she have any migratory pain?
I want to know if she has any neuropathy with tingling numb.
I want to know what her symptoms are, right?
So I want to look at the infections, but not just Lyme.
I want to look at Bart.
I want to commit a pneumonia.
So I, and this is all in my book.
This is under A is for autism, ADHD, Alzheimer's, allergies, asthma.
So in one of the chapters in any chronic illness,
you will find all 16 MSSID factors.
All you got to do is take it to your doctor,
go to the lab and go, these are the bugs I want to check.
This is the way I'm going to check mold.
You just go through the list.
It's a checklist.
It's simple.
So that is what we need to do.
And you and I are going to be in correspondence
because I want to show you
that this is possible
and prove this to you
because I've already seen results in my patients.
By the way, the number one effect of Dapsone,
the number one of all these patients
is cognitive improvement.
Wow.
So when I published my 10- Any age.
Any age.
I've had 80-year-old people come in.
Doc, I'm tired.
I'm achy.
My brain's not working.
I'm sure I have out.
Alzheimer's like, you know, Alzheimer's, you have Lyme.
I treat them with Dapsone, and they come back months later and go, oh my God, it wasn't,
I was getting old, because I hear this all the time.
I'm getting old.
It's like, getting old doesn't mean anything.
I'm 70 years old.
I feel like I'm 25.
That has nothing to do with it.
So, but you treat the infections that were underlying, the fatigue, the pain, the cognitive
difficulties, right?
The neuropathy, the sleep disorder, the mood.
Do you know that one out of five people in the U.S. is depressed and anxious?
We have mental health.
Yes.
We have a mental health epidemic.
all 16 factors on the MSSID's model
are causing mood disorders
from depression, anxiety,
OCD, bipolar disorder, and schizophrenia.
I've had people with schizophrenia with hallucinations
reverse the hallucinations
by treating the lime and the bartonella
and getting rid of mold,
not giving them zyprexa for the rest of their life
for their psychotic break.
Medicine needs to know.
You can't just name the disease
and throw drugs at it.
You've got to unlayered to the 16 root causes.
and that is what is in chronic illness.
This is why I think ending chronic illness,
I hope will be,
it will be really kind of the manual for people,
both for patients who say,
hey, I'm well, but I don't want to get sick.
For the patients who say,
I've gone to 30 doctors,
I can't figure out why I'm ill, right?
For the providers that say,
oh my God, I'm seeing all these chronicleal patients,
I don't know what to do, right?
And for those parents that say,
and I just got this call from this patient,
this, I get calls from all over the world.
I got one just yesterday from a UK, from a mom.
My five-year-old is so sick with Lyme.
I can't find a doctor to treat.
How do I get them better?
It's heartbreaking, listening to these stories.
Everything I have published is in the open access medical literature.
You just go to the open access literature.
All of my protocols are in the literature.
You don't need to speak to me.
It's all published for you.
Everything I did is oral generic.
So it's the cheapest, fastest way to get you better
because we're in a worldwide epidemic.
So Alzheimer's, yes, you need to go through those 16 points
and you need to go through these Alzheimer's biomarkers.
That's gonna be for me the first step
to see kind of what is going on.
Do you know if your mom has actually been checked
for these things?
No, she hasn't.
I know that she hasn't.
For mold or for mold?
Yeah, I've done a vibrant wellness mold metals.
Mycotoxins, Aflatoxin A was there,
Aflatoxin B.
So she had these.
Okra toxin.
Oh yeah.
She had, as most my patients have too.
Yeah.
Yeah.
Yeah.
And the beauty is, I found that there's a protocol and I describe it.
But I want to do the rest of this testing.
Yeah.
Yeah.
Yeah.
In any case, yeah, so in that case, this testing is going to be very important.
But also, what I describe in any chronic illness, we now know that inflammation,
chronic inflammation is underlying chronic disease.
So I have a part in the book where I'm going to give you stage one, stage two, stage three testing.
Stage one testing is general inflammatory markers.
CRP, C-reactive protein,
indirect marker of interleukin 6,
erythrotite sedimentation rate,
TGF beta 1, which we see in lime, we see in mold.
C4A, we see in lime, we see in mold, right?
So MMP9, which you can see in joint inflammation,
we see in line.
So I'm gonna give you the 10 general markers of inflammation,
but then the second stage is, well,
not all these biomarkers necessarily show up.
So you can do, and I'm sure you know this,
you can go to functional medicine laboratories
and check lipid peroxides
to see how much free radical stress
is affecting the outer membranes.
You can do eight hydroxyguine
to see how much your DNA is affected
or protein carbonyls to see
how much oxidative stress affects your proteins.
So you go to a precision point diagnostics
or doctor's data, some good functional medicine lab,
and you get, so all of these biomarkers done,
this is the second level of testing
with, let's see, a T-Bars test.
To see how much free radical oxidative stress
because CRP may be normal,
said rate may be normal,
a VGF may even be normal with Bart.
Sometimes it shows up high,
with long COVID sometimes, it does it.
It changes over time.
But the third level of testing is what we're talking about
for your mom.
You wanna go ahead and get these Alzheimer's biomarkers
biomarkers done and maybe even get chemokines
done from somebody like Patterson's lab
to see whether you've got CXL3, CXL4, CXC,
look at these chemokines
that are now looking at these very specific biochemical pathways.
So you can go backwards and go, hold on,
the interferon gamma's high, is that maybe a virus?
Or is it, so you can kind of go backwards
when you get back the results of all this testing.
And so I divide it up into these three levels
of inflammatory testing, which makes sense
in seeing how you do these biomarkers.
Wow.
And these are multiple labs.
So so far you've named five labs.
Right, but although the good news is
a lot of them can be done through Quest,
LabCorp BioRef.
They can be done through local lab.
I wanna definitely get the baseline done
as many as we can through Quest.
Yeah.
I mean, I like, you know,
Doctors Data, Airon,
like when I'm doing,
doing a DHA cortisol saliva,
I like functional medicine labs.
Yeah.
If I'm doing a six-hour year at MSA challenge for metals,
I like doctors date in Chicago.
Yeah.
But that's a $60 test, right?
I mean, these are not expensive tests.
Right.
I think the saliva test is 100.
These are not expensive tests for people to do.
And yet they're so important because here you're trying
to optimize your health, you're doing mitochondrial,
you're exercising.
If your adrenals are low, you may never figure out
why I just never feel like I've got that
that bump to get through the day.
because you missed that one nail in the foot
of the 16 points that you just left it off.
That's the beauty of a checklist.
You don't have to be a rocket scientist.
Just look at the checklist
and start looking and just seeing,
what have you checked?
What haven't you checked?
It's a very logical way
of just approaching all of these different chronic illnesses.
And even for people that are like in my condition
that just want to be the best version of themselves,
they should still just prophylactically do this protocol.
So that you can, because we all have something.
Of course.
Right, I mean, the, you know, just a daily environmental exposure.
We all have something without even fear mongering.
And this is a way of at least cleaning that slate so that it doesn't accumulate and become.
Correct.
I mean, look, I'm in good health.
I'm 70 years old.
I feel great.
But my whole family died of cancer.
There's not one person left.
Wow.
So here's the thing.
I want to block NFCAB because I found out that NFCAPAB even in cancer.
It's not just affecting Alzheimer's and autism and ADHD.
That same switch is affecting cancer as well as mood disorders, right?
So it's kind of like when you block that switch or you stimulate NRF2 with resveratrol and
curmin and broccoli seed extract and green tea, you're opening up your detox pathways.
You're hitting the P53 cancer gene.
You know, you're lowering down inflammation in the body.
So if you're doing hyperbarics and you're doing saunas and you're doing, right, all of the great
things you're doing, I mean, you took me around.
I mean, God bless you.
It's fabulous what you're doing.
Thank you.
But if you've still got free radical oxidative stress
coming from infections and toxins of the microbiome,
you're-
swimming uphill, yeah.
Right, exactly.
It's like trying to detox someone from a mold infection
while they're still in a moldy home, you can't do it.
I mean, that's the cardinal rule of detoxification.
You know, is remove the toxic loads.
So I think living on the planet,
I mean, the reason I'm swallowing these supplements
is once I learned that these biochemical pathways,
that there are these 16 M-SIDS factors,
with 16 biochemical pathways underlying.
Even these first four pathways in ending chronic illness,
just with these 10 or 11, 12 supplements,
you're already covering most of these 16 biochemical pathways.
And it shows up in almost every chronic disease I looked at
from depression to anxiety.
So, you know, we've got a suicide,
750,000 people, right, who suicide, you know, worldwide.
We lose more of our military servicemen
to suicide than we do to battle.
Yeah.
You know, when you start looking at those kind of statistics,
The same with law enforcement.
I mean, these rates are so high.
And by the way, in my population,
a lot of these people had PTSD.
And the mind-body connection was so strong in these people
that if they had abuse,
if they had physical abuse, emotional abuse,
or sexual abuse.
And I always ask about this because I had
some abuse issues when I was young
and I understand what they were going through.
If we treat them,
if we treat the infections,
if we remove the toxins,
and work the microbiome,
and do the mitochondrial,
and we don't affect, and we don't work on the brain,
we don't work on the mind and the emotions
by doing vagal retraining and limbic retraining, right?
I have to get through people,
not just through EMDR, eye movement reprocessing,
or doing cognitive behavioral therapy.
I've got to do limbic retraining
with the antihopterdhydridebral retaining
or the gutta amygdala insular retraining
or primal trust.
I have to use ways of getting into your brain
with the amygdala and hypothalamus
and going, you're wired for illness.
because you had severe stress and trauma as a youngster.
A lot of these people took on like,
there must be something wrong with me.
And when you feel that,
when you've been traumatized,
your immune system won't work well.
You can't fight the infections.
You can detoxify.
So I found in some women that when I address the PTSD
through vagal and limbic retraining,
all these other things I was doing
to make them better finally work.
But if I didn't address it,
and that's also, think about it.
People optimized their health
with high intensity,
interval training and mitochondrial,
getting to sleep and proper diet.
But stress, stress kills.
You might be in a high stress job
and all the things you're doing,
your adrenals are taking a hit,
your immune system taking a hit.
The only time I get sick
and your immune system is taking a massive hit.
Is when I'm stressed out,
I don't get a good night's sleep,
the virus will show up.
If otherwise, I never get sick from things,
but I meditate on a regular basis, right?
I do stress, so people,
if they wanna optimize their health,
and by the way, I even have the meditation techniques
taught to me from my Tibetan teachers,
I have them in ending chronic illness.
Oh, wow.
They taught me very, and I have a medical.
How long do they take?
Five minutes three times a day.
Five minutes three times a day.
Anybody can do this.
Anybody can do this.
Even walking meditation outside on the street,
you can look at the empty clear nature of your mind
and pay attention to the inner environment
and the outer once you learn how to do this.
I was trained by, I've been very fortunate.
I've been trained some really some incredible Tibetan masters.
It's 45 years I've been training with them
and working with them.
So I have a medical detective substack, by the way,
that is free.
I have a five-part meditation series,
and I took their 45 years of teaching
on the nature of mind of how to awaken,
and I put it into a five-part substack on meditation.
And again, this is all free for people to get,
because I wanted to make sure this information is out there,
but even stress reduction, optimizing,
how many people actually really unload during the day?
And it's one of the most essential things
for optimizing to stay healthy
because you don't want to get short telomere,
you know what short telomeres does longevity.
You know what meditation does?
It lengthens your telomeres.
It affects your autonomic nervous system
and brings down your cortisol
and brings down your autonomic
and all that epinephrine in your body.
You need to take a little break
from a high-stress job and environment.
So true.
Just five minutes, three times per day.
And I made sure all of these kind of techniques
are in the book so people could really benefit.
Wow. Dr. Horowitz, this has been just an incredible...
I have to have you back.
I mean, there's so much to unpack here.
I am gonna allow my audience to follow this journey.
I've documented it so far with my mom
and I'll throw myself in there and document my journey.
And this has been a really profound discussion.
For my audience that wants to know how to find you,
obviously I'm gonna put a link to the book,
but how can they find you a social media or website?
So I'm at all the social media channels.
You can find me at can get better.com.
Can get better.
And then chronic illness.com.
Okay.
Facebook, Dr. Richard Horowitz.
So if you look up Dr. DR. Dr. Richard Horowitz,
I have a Facebook account.
Ali's helping me with Instagram.
So yes, it's on all the social media.
Okay, great.
So two other things.
One, we're going to go into my VIP group
because I told my VIPs that you were coming
and they've got some great questions for you.
If you're interested in becoming a VIP,
you can just go to the Ultimate Human.com forward slash VIP
and just sign up to be a VIP guest in mind.
You get private podcast, private time with me,
hours and hours of live Q&As.
You can ask me anything.
This is going to be.
be an amazing journey, Dr. Horwitz.
I'm really excited to go on it personally
and to take my mother on this journey.
I wind down all my podcasts by asking
all of my guests the same question.
What does it mean to you to be an ultimate human?
What does it mean?
What does it mean to you to be an ultimate human?
So for me, an ultimate human is to maximize the potential.
It's to maximize the physical, emotional,
mental, and even spiritual, potential
of every human being.
Wow.
So this book and the chronic illness,
it addresses the physical.
It addresses, obviously,
all the toxins and infections we talked about,
but also the emotional about talking about
I had trauma as young.
I've done my healing journey.
You did.
But I believe to be the ultimate human,
it's physical, it's emotional,
and it's spiritual.
And because I have had the blessing
of studying with these enlightened masters,
which I met them in Belgium
in my medical school.
So very left-brain, right brain of you.
Yeah.
That's exactly it.
And so what I got from them is,
they basically said that all things are possible.
All things.
But to get to that state where all things are possible,
you have to go from your dualistic perception
of me, you, good, bad, happy, sad, man, woman,
what I can do and what I can't do
because our ego is wired in this life
to limit our potential.
And I believe because of some people
have had the blessings of wonderful parenting
and some have had challenges,
but because we've all had challenges,
in our lifetime.
For me, the ultimate human beings at this point,
you wanna do your best to find out what your gift is to the world.
What is your, what is your unique gift?
You've obviously discovered yours,
which is sharing your biological insights,
right of systems biology and how you can get the word out to people.
I hope I've discovered my, this is my new gift.
I thought it was a gift for Lyme.
Then it turned out it was a gift for Alzheimer's
and chronic fatigue and all these diseases.
But how did I even get to this?
It's because my Tibetan teachers taught me
always work for the benefit of others.
always work with compassion.
People are suffering.
Try and relieve their suffering.
Have love.
When you say, I want to love you,
it's like, I want you to be happy.
Suffering, compassion.
If you combine love and compassion
in your daily journey
and doing all the things
that optimize your health
and doing high intensity interval training
and mitochondrial,
but for me it's on all levels.
It's got to be physical, emotional, mental,
and especially the spiritual level
because if you're missing for me that dimension,
then some of achieving your full potential
of what is really possible.
I believe, by the way,
that the only reason I have written this book
or done anything I've discovered in medicine
is because my teachers taught me
that when you get to the state
of the open, relaxed mind,
where you meditate and you go to the bottom of the ocean
where your true nature exists
and you can achieve this and touch this level,
all things are possible at this level.
And I believe that there is a way
of working with that spiritual component
that when you have the proper motivation
of wanting to benefit people
and do the best for them in their lives,
I believe with that particular motivation
and then integrating the physical, emotional,
mental component,
I think we can become the ultimate human.
But for me, it's also that spiritual component
and that's why I've integrated into the book
and I've done the medical detective substacks
because I think they've given me
such insights into the nature of mind
into what is possible.
I think most people don't realize
that they can go beyond the limit,
of what they normally think,
because the ego gives you limits of,
I can do this, I can do that,
but once you transcend the ego
and you go from dualistic perception
to this unlimited open state of mind
where all things are possible
in what they call the state of Dharmakaya,
it's very interesting because I didn't know in medicine,
I could maybe, maybe find a cure
and an answer for certain cases of Alzheimer's,
for certain cases.
I only wanted to go in medicine to benefit,
but the way they taught me to plant the seeds
was plant the seeds of aspiration prayers.
May I be of greatest benefit
to the greatest number of people
to relieve their suffering.
I did that every day,
45 years ago when I started doing medicine.
I must believe that I'm a spiritual human experiment
that these seeds I planted
end up being with you today and writing this.
Because I can't imagine how else,
how I meant publishing all these studies
and finding all these things.
It was through that motivation
of trying to benefit others.
I was just led to the right place,
was ultimately working through that spiritual connection of how can I benefit others? How can I be
of service? And that, for me, I think that is really, I think needs to be integrated. And especially
from the stress component, just living the lives we're living, you need little meditation
breaks during the day. Oh yeah, definitely. Dr. Horowitz, you are the ultimate human.
Thank you for coming on the podcast.
Thank you. Until next time, guys, that's just science.
