The Ultimate Human with Gary Brecka - 270. Dr. Tania Dempsey: Mast Cells, Chronic Fatigue, & Hidden Inflammation
Episode Date: May 19, 2026Up to 1 in 5 people may have this condition and never know it and the diagnoses they've been handed instead, from PCOS to IBS to chronic fatigue, may all be pointing at the same hidden cause. In this ...episode, I sit down with Dr. Tania Dempsey, Johns Hopkins-trained internist and one of the leading researchers on Mast Cell Activation Syndrome, who tells me that 100% of her PCOS patients test positive for MCAS, and walks me through why mast cells may be the most overlooked driver of chronic illness in modern medicine. If you've been told your symptoms are idiopathic, or that nothing's wrong even though everything feels wrong, this is the conversation that finally connects the dots. CLICK HERE TO BECOME GARY’S VIP!: https://bit.ly/4ai0Xwg Get Dr. Tania Dempsey’s audio book, “Mast Cell Matters”: https://bit.ly/4drrnOf Listen to Dr. Tania Dempsey on all your favorite platforms! YouTube: https://bit.ly/4dcVlqs Spotify: https://bit.ly/4dsS9G2 Apple Podcasts: https://bit.ly/3PjGhy6 Connect with Tania Dempsey Website: https://bit.ly/4dKXgTe YouTube: https://bit.ly/4dcVlqs Instagram: https://bit.ly/4f7kHrd Facebook: https://bit.ly/3R6sOdz LinkedIn: https://bit.ly/4ddPilv 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/4eULUKp CYMBIOTIKA: "ULTIMATE10" FOR 10% 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 H2TAB: “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 Intro of Show 03:52 - The biology of mast cells 05:34 - Inflammation, allergies, and dystrophisms 09:00 - Connective tissue, POTS, and Ehlers-Danlos 09:40 - Gary's daughter and the toxic load 13:24 - Symptoms from head to toe 18:20 - GLP-1 receptors on mast cells 23:47 - Identifying the upstream triggers 27:38 - Treating viral and bacterial loads 31:35 - The herpes virus family and reactivation 35:47 - SOT therapy and targeted mRNA 38:17 - The immunofatigue theory of aging 45:03 - Therapeutic plasma exchange and detox 58:09 - Gut dysbiosis and the microbiome 1:00:58 - Cryptosporidium and parasite testing 1:06:30 - Hope and the path forward 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. Learn more about your ad choices. Visit megaphone.fm/adchoices
Transcript
Discussion (0)
Right now, in my practice, 100% of patients with PCOS have Massel activation syndrome.
Up to 17 to 20% of the population may have Mass Cell Syndrome and not know it.
It mimics dozens of other conditions, allergies, IBS, anxiety, chronic fatigue, skin issues.
Massile activation syndrome, it's a chronic inflammatory, multi-system condition.
Everyone has mass cells.
Mass cells are your front line of your immune system.
They're helping us, but they can also damage us.
They're chemical messengers and when their system is faulty, they can chronically secrete these without an invasion as if one was occurring.
Let's look at the root and understand, you know, that the mast cells are affecting the motility.
They're causing inflammation in the gut.
They're making it more difficult to tolerate certain foods.
This is such a fascinating underserved area of medicine where we start really looking at root causes and how symptoms don't necessarily link back to the pathology that people are diagnosed.
with, it may be something even deeper.
But also, I want to give hope because I think there's so much that we can do.
And that's why I do the work that I do, because I help people every day.
For someone that's watching this, what would be some of the category of potential symptoms or
ailments, right, that they would be suffering from, where you would say, this might be at the root
of that.
I always think about it as three themes that we see very commonly in people who have this.
One is in...
Hey, guys, welcome back to the Ultimate Human Podcast.
I'm your host, human biologist, Gary Breka, where we go down the road.
of everything, anti-aging, biohacking, longevity, and everything in between.
Today's podcast is going to be one of those in-betweens.
I'm so excited about this guest.
I was actually first turned on to her because of my VIP community, my most loyal followers
that are part of my subscription program.
It's an amazing community.
And I let them know who comes on the podcast before I bring them on the podcast.
And I also ask them for suggestions on guests that they'd like to see on the podcast.
They find some of the most innovative people in all of modern medicine.
A lot of the guests that have been on here, MDs, PhDs, researchers,
the people that are really moving the needle for humanity,
but don't yet have a voice,
have landed here because of my VIP community.
So I just want to give a shout out to you guys.
Thank you so much for finding Dr. Tanya Dempsey.
I am so excited for this podcast.
I'm excited to be here.
Because I believe that your expertise
and you're board certified in internal medicine from Johns Hopkins,
but you're also an integrated medicine specialist,
which I find that it's like being an artist and an engineer.
Like they usually don't exist in the same, you know, person.
It's very, I think it's the ultimate use of the left brain and the right brain,
you know, because medicine for so many decades has been so algorithmic, right?
Like, if this, then that, if this, then that, you know,
get to a diagnosis just slot it into one of the 38,000 categories.
that exist for us to define pathology and disease.
And very often, you have to zoom out and look at the whole person.
And, you know, as I did the preparation for this podcast,
I pulled Malia aside my podcast manager and I was like,
this is going to be one of the best guests we've ever had on.
Oh, gosh.
So I'm really, I'm super, super excited about this.
I'm honored to be here.
Yeah.
And I'm honored to have you.
You know, you have a core competency in something called
mass cell syndrome. And I'd love for you to give my audience a, you know, a little definition
of what that is. But what's fascinating about it is it's underlying so many of these other
conditions that people are suffering from, but just can't put a finger on. Yeah. So what is
mass cell syndrome? Yeah, mass cell activation syndrome. It's a, it's a chronic, inflammatory,
multi-system
condition.
It's a syndrome,
right,
not a disease.
We have to be clear,
but there's a,
it's a huge spectrum.
The way I think about it
is I like to start
at the biology level.
Let's talk about the mast cells
because everyone has mass cells.
Mass cells are your front line
of your immune system.
So anybody faced with an infection,
strep, flu,
whatever,
their mass cells will fight,
will help fight.
They get into gear
and they call in the rest of the soldiers
to help them fight off the infection.
So everyone has them.
They help us deal with the environment.
They help us deal with our external environment,
our internal environment.
And they're pretty much everywhere.
They're in every organ of our body.
They're in our skin, in our brain,
in our stomach, our lungs, our respiratory tract,
just basically everywhere.
Kind of waiting to protect us.
They're our front line.
They're part of that primitive immune system.
that just fights.
And the way they fight is they manufacture these various chemicals, we call them mediators,
and they will explode and release these chemicals in attempt to fight what they see as far and as bad, as danger.
And when they release these chemicals, they not only affect what they're trying to kill,
but they actually affect the tissues that they're releasing these chemicals in.
Okay, so there's the good side of the Masso and then the bad thing.
side of the mass cells. So they're helping us, but they can also damage us. So in mass
activation syndrome, what happens is the, so again, everyone has these, but in the syndrome,
these mass cells are already dysfunctional. They're not just waiting for the next attack. They're
actually constantly sensing that something is wrong. So at baseline, they're leaking these chemicals
out, causing a baseline of inflammation. And that inflammation could be anywhere in the body
in multiple places in the body,
but most people will know
that they always have, let's say, gut issues
or they always have joint issues or muscle issues
or, you know, they usually know
that there's a specific area
where their inflammation is,
but sometimes it's very subtle.
And then what happens with mastole activation syndrome
is those mass cells that are already primed,
they then, when they see a foreign attack on them,
they explode even more.
And then they basically go into this,
state of continuous activation,
constantly releasing these chemicals,
causing more and more inflammation.
So everyone was talking about the cytokine storm
during COVID, that's partially due to the mass.
So these are cytokines, histamines,
other inflammatory factors?
Over 1,200 different chemicals actually
have been identified that mass cells can make.
Everyone talks about histamine,
because histamine's an easy one to talk about.
Yeah, but histamine is sort of a category, right?
There's a number of histamines.
Cytokines are kind of a category too.
is not just acetylachine.
Correct.
So these have, they're chemical messengers,
and when their system is faulty,
they can hypersecrete or chronically secrete these
without an invasion as if one was occurring.
But then, but then there are invasions.
There are triggers in the environment.
It could be mold on the outside.
It could be other chemicals, toxins.
On the inside, it could be hormones.
Basically, the way I think about mass cells
is that they're really, they're monitoring change,
changing the environment on the outside,
changing the environment and the inside again.
And again, they're supposed to help us.
But in mass-electivation syndrome,
they become dysfunctional, they overreact,
and then they start to react to things
that they really shouldn't even react to.
Normal people who don't, well,
people who don't have mass-electivation syndrome
would not even notice a particular scent,
a particular chemical that, or toxin that,
yes, all toxins are,
are potentially dangerous, but this is a level beyond what others would feel.
And unfortunately, then it leads to this sort of multisystem inflammatory state where they are,
you know, again, constantly in this inflamed position.
Some of them have allergic type symptoms or allergies.
You don't have to have.
You can have asthma highs.
IBS, those kinds of things.
Correct.
But you don't have to have allergic type phenomena to have.
to have mass activation syndrome.
I always think about it as three themes
that we see very commonly in people who have this.
One is inflammation for sure.
And then we say plus minus allergic phenomena.
So some people have those obvious signs of allergy.
And some people have, they feel like they have allergies
to pollen or food or whatever,
and they get allergy tested.
Very often, it's all negative.
And the allergist doesn't even know what to tell them.
Like, what's the reason that they're reacting, right?
The reason is because these mass cells are dysfunctional.
And they are involved in allergy
in some patients.
But in this case, it's an allergic phenomenon very often.
And then the third thing that we see quite often, which is a theme,
is what we call dystrophisms or abnormal growth and development of cells.
So we see things like tumors.
We see things like cysts.
We see things that affect the connective tissue,
things that are affecting any growth or repair.
So even things like sarcomas and...
Potentially.
Really?
Potentially.
What is the...
What is the condition with the fatty deposits under the skin?
Well, there's lipidema.
Lipidema.
Yeah, which is actually pretty clear that it is a mass cell-driven phenomenon.
Right.
Yeah.
So, you know, my daughter was diagnosed with pot.
Now, this positional orthostatic tachocardia syndrome when she was younger.
She's 27 now.
But when she was in her early 20s, she would have issues.
And, you know, it's positional orthostatic, but you know,
she didn't have to change positions to feel this like hypotensive episodes, right?
I mean, she would just feel faint sitting in a chair like we are right now.
Sometimes it would happen when she changed positions, you know,
and eventually we went down the rabbit hole.
She was later diagnosed with Ellers Danlos.
So she was, you know, hyper-mobile.
And so this connective tissue issue led to all kinds of consequences
because when you have hyperlaxity in your joints,
you also have another connective tissue.
So, you know, mouths are hyperlux, joints are hyperlux.
So this causes gut disruption.
That's right.
And, you know, I didn't really ever subscribe to the fact that she had this pots
because even though she had some of the symptoms,
I refused to believe that it was just idiopathic positional orthostectarkey.
Right, I agree.
Cardia syndrome.
So we just embarked on a massive journey to clean the tank.
Right? You know, when a fish get sick, we clean the tank.
When humans get sick, we don't do anything to the tank.
We mess with the human.
We worry. We worry about the fish. Right. Yeah.
And so there was heavy metals.
She had a mold mycotoxin infection. She's been very public about this.
We've talked about it on some of my detox challenges.
And she had the MTHFR gene mutation.
So we began supplementation, methylated multivitamins for that, red light therapy.
But after we cleared the mold and the mold,
and the mycotoxin infections,
fungal infections,
and reduced her heavy metal toxicity,
it all went away.
Now, she still has hypermobile joints.
God issues have cleared up,
recurrent sore throats have cleared up,
skin inflammation, you know, has cleared up.
And I wonder if what we inadvertently did
was fix a mass cell activation syndrome.
It may have very well been what was going on with her.
Yeah, what you did was you taught
the mass cells, that there isn't anything to fight anymore.
The mycotoxins are gone, the heavy metals are gone.
All those things are making the mass cells more reactive.
So now they're quieter.
Mass cell activation syndrome probably doesn't go away.
Right.
I think that's like the unfortunate thing that people don't want to hear sometimes.
It may still be there.
She may still be susceptible.
But they're quiet.
Yeah.
And she can live a full life.
Yeah.
Boom.
I mean, you know, red eyes coming back from L.A.
Or, you know, when she doesn't,
doesn't get, you know, sleep or she's in a high-stress state for a period of time,
like when she's going through nursing school, we would see these conditions coming more frequently.
They pop up because you know they're there, but there's so much you can do.
And this is what I love about the work that I do, is to give people hope, right?
Yes, there are these unfortunate things that can happen to the body,
but there's so much you can do when you recognize what you need to do to keep your body healthy
and how to keep your muscles safe.
It takes time for a lot of people.
It's not as quick a journey because they don't know the stuff that you know.
Thankfully, you're in the business.
You sort of understand.
But a lot of people don't know, right?
And they're suffering and they're reacting and they can't leave their house.
But no one has been through it with them to understand, you know, maybe the house that they're in, that they're sick and that they can't get out of is actually full of mold.
Maybe that is, you know, maybe if they left or they were able to remediate, then they're massive.
would settle down and they would, you know, recover and some of the things.
What would be some symptoms that somebody could be suffering from right now that's watching
this podcast? As a lot of people watch this podcast for answers to questions they haven't been
able to get. And by the grace of God, you know, some of the guests I've had on here have really
changed a lot of lives. And so for someone that's watching this, what would be some of the
category of potential symptoms or ailments, right, that they would be suffering from,
where you would say, this might be at the root of that.
Yeah.
So really starting from like the top of the head and all the way down, headaches, migraines,
underappreciated basically due to mass cell activation syndrome most of the time,
at least in my practice.
You can see a number of different symptoms related to the respiratory tract.
You know, people who have chronic post-nasal drips, people who have chronic respiratory issues,
sleep apnea even.
I would maybe even put in that same category.
gut issues for sure, you know, this term irritable bowel syndrome is a ridiculous term.
It really is. Just a category. It just takes all of the symptoms and gives them one name.
Yeah.
Instead of giving it's not even a thing. It's not even a thing.
It's just gas bloating, diarrhea, constipation, irritability and cramping.
Yeah. And here's an antidepressant to help you. This is sort of like what's provided, right?
But let's look at the root and understand, you know, that the mast cells are affecting the motility.
They're affecting, they're causing inflammation in the gut.
they're making it more difficult to tolerate certain foods.
So, like, you know, that's a condition IBS that I think that we need to just stop calling it
IBS and think about it as a mass cell-driven phenomena.
And again, I can go all the way down, hormonal issues for women.
You know, we often see women have more symptoms around puberty.
That's a sign of, there may be some of an MCAS-related issues.
PCOS, polycystic ovarian syndrome as a mass-cell-related.
Oh, wow. That's a huge one right now.
Huge.
Yeah.
You know, when I started my practice or when I started practicing,
medicine 30 years ago, I was really interested in women's health. And so I saw a lot of women
with PCOS. So I was really passionate about it. When I figured out MCAS, I realized that they're
actually the same thing. And I would say, and as a doctor, you always have to be careful about saying
anything is 100%. But right now, in my practice, 100% of patients with PCOS have mass
el activation syndrome. Wow. So it is actually the same thing. Wow. That is phenomenal. So is there a definitive
test for MCAS for Massel activation?
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It is challenging to test, okay?
I'm lucky because I've set up a lab in our office where we can do the testing that's necessary.
What we're looking for to diagnose it is we're looking for those chemicals that they're releasing.
And now they release 1,200 chemicals.
We don't have tests for all 1,200.
We have a couple handfuls of mediators that we can measure, and we can measure it in the urine.
We can measure some in the blood.
But the samples have to be so carefully taken care of.
They have to be refrigerated at all times.
The lab has to process them properly.
So what we find is that in the community, a lot of people are trying to get a diagnosis and they're told we can't find anything.
There's nothing there.
We have a little bit better luck because of the equipment that we've invested in in our office to be able to do the testing.
But, you know, in a sense, it's a clinical diagnosis, and I always tell patients this, you know, if you have these, you know, a set of symptoms and we know that you have an inflammatory multisystem condition and we don't have any other explanation, most likely it's this.
It would be great to test.
We actually published a paper called The Consensus 2 Criteria for...
I saw that.
You've actually published a number of papers, not just that one.
You've been a busy woman.
Very busy woman.
I really think, because the work that I do, while I'm in the integrative functional medicine world,
I also come from that, you know, conventional world.
And I understand what publishing really does.
Like, it really gives me credibility in the work that I do, right?
I'm not just, you know, pushing supplements for no reason.
I'm not just doing the things.
I'm doing it because I'm studying it.
I love that.
Now, you're talking about the publication 2026,
diagnosis and management of patients with mass cell syndromes.
It was 2020.
Oh, yeah, I've got another one here in 2020.
It's a consensus.
This is a very accomplished young moment, by the way.
Yeah, 2025.
She did the utility of GOP1 receptor agnes in Massel activation syndrome,
which is an area.
We should definitely talk about that.
I'm also very, very interested because, you know,
these GLP ones now, especially,
read a true tide are being kind of implicated in their ability to reduce a lot of these
inflammatory disorders and neuroinflammatory disorders and hormone balance and cognitive function.
You know, I'm reading a lot of, they're not well, I think the conclusions are well authored,
meaning there is certainly an impact.
They always say you just need further research.
But they seem to be consistently pointing towards support.
supporting a lower inflammatory state.
I don't have the expertise to know what the causal link is between those.
Maybe you do.
Well, I can tell you why I think it's helping mass el activation syndrome.
What we did for the study is we looked at 47 patients.
It was a case series, essentially.
And which GLP did you use?
Actually, we included both semaglutide and terseptit for that study.
Okay.
So Red at True Tide, we don't have the research yet.
We don't have enough patients on that.
And of course, it's not, you know, fully FDA approved yet.
But I can tell you my anecdotal, you know, experience with it.
But in that study, we just pulled in patients who were both on semaglutide or terseptide.
And we looked at, you know, before and after, basically, whether symptoms were before,
whether symptoms were after.
We included only patients who met this consensus to criteria for mass electivation syndrome.
So they had to have a formal diagnosis.
They had mediators that we found.
So we knew that they had mass activation syndrome.
And what we found was this incredible improvement across so many different, you know, parts of the body.
And what we understand is that the mast cells, this is what's so fascinating about the mass cell,
the reason they are, you know, basically monitoring the environment is because they have receptors on their surface.
So not only they make these mediators inside, but on the surface, they have these receptors that are like,
I think of them as like satellites.
They're basically scanning the environment.
and things can bind to these receptors and send a signal.
Well, mass cells have GLP1 receptors on their surface.
They have GIP receptors on their surface.
So these drugs are literally binding to the mast cell.
Wow.
And sending a signal, you know, basically all is well.
Nothing to do, calm down.
Right.
So it's basically stabilizing the mass cell.
Now the mass cell is not releasing all these cytokines and chemicals and inflammatory mediators.
and now the body can start to heal.
And that's what we're seeing.
So it's a direct effect on the mass cell,
which is really fascinating.
That is super fascinating.
You know,
and I think so many of these chronic low-grade
underlying infections,
lime, mold, mycotoxin, fungus,
you know, there's a whole class
of allopathic physicians
that think that mold is completely nonsense.
And, you know, I've been smirched for that too,
that everybody has mold, mold exists in our body.
It's been around for centuries.
mold's not the issue.
I would take the polar opposite side of that coin.
Miami happens to be the mold capital of the world.
So congratulations, Miami.
I have a lot of patients from Miami who come up to see me
and they don't know why they're sick.
Your clinics in New York, right?
Yeah, we're in New York, yeah.
In...
We're in Westchester County.
Westchester County, yeah.
Okay.
So, and you have this lab in there,
and you do blood, urine, saliva?
Just blood and urine.
and look for these mediators.
We do all this, you know, we do these other kits
that are saliva kids.
We know, we do a lot of different things.
But the mass cell stuff is blood in urine.
But a really good, reliable test
is something you should probably do in office.
Yeah.
Right.
So that you get the proper treatment of these things.
I like to make a diagnosis
because it opens up treatment options, right?
But sometimes you just can't.
And, you know, I think like you have to treat the patient,
not the lab work, right?
And that's the problem that, with medicine in general, right?
Everyone looks at labs and they say,
oh, yeah, your thyroid looks normal.
it's in the normal range and this is in the normal range, right?
And we have to be careful, the same thing with mass cell activation syndrome.
If I'm measuring 10 mediators and they're negative in this patient,
but there are 1,200 mediators that their mass cells could make,
but I can't measure all of them,
but they have all those signs and symptoms of it.
I have to treat the patient.
Yeah.
So what's your frontline defense?
Like, where do you start on a course of treatment?
So do you then, once you decide that they have mass cell activation,
syndrome, do you then start looking for the villain? Like, now are you going on a dive for metals,
for mold, for mycotoxin? Maybe an underlying Lyme virus is just probably the most mismanaged
virus in all of modern medicine. It's probably the most pissed on, misunderstood, yeah, the bacteria,
the parasitic co-infections. And how tricky the virus is itself, dorsal recanglion, you know,
hiding in the dorsal reganglion, it's capacity to undulate, you know, go asymptomatic for periods of
times and then be symptomatic. I think it doesn't behave like a normal viral infection.
Well, Lyme is a bacteria, but you mean viruses in general? The virus is in general.
Yeah, yeah, yeah, yeah, yeah. So when, so when, so now that you have somebody with
Massel activation syndrome, what's the next course of action? Exactly what you said. We have to
identify triggers. I always say step one is you need to know why they're reacting this way.
Now, there are definitely going to be people
who had triggers years ago
and their mass cells just never stopped.
And so I can't find any current triggers.
That's a small number.
Generally speaking, we find, you know, chronic...
They might say, oh, I had Lyme 20 years ago, I was treated.
I don't think that's the problem now,
and then I test them, and they have chronic Lyme,
chronic Bartonella, chronic Babesia, chronic Epstein Bar,
you know, et cetera, et cetera, right?
Epstein Bar is another one that, for,
I don't know for what reason, maybe it's...
long COVID, maybe it's related to the, you know,
everybody emerging from the pandemic and having weakened immune states.
But these, even the level of titers in dormant,
what we were considered dormant EBV are off the chart.
Yeah, I've never seen so many positive PCR tests for Epstein-Barr.
Neither have I.
Pre-COVID, we would, you know, make some assumptions
if they had something called an early antigen antibody,
we would say, maybe it's reactivated, you know, it looks like, you know, but now we have PCR that's
showing that the virus is actually replicating in the blood and one after another after another,
I've never seen so many. Yeah. And that's proof. And recurrent, and dormant and dormant and
I mean, and these cycles go on for years. Exactly. And they just wreak havoc on their daily life.
I mean, they're exhausted. They've got brain fog. It interrupts their sleep patterns. It disrupts their
hormones. It gives them non-viral symptoms that seem to be like mood and mental disorder kind of
related symptoms, exhaustion, vertigo. I mean, the number of symptoms that I've seen come out
of these patients that have these reactivations of Epstein virus is probably just as broad as mass cell.
But it's the virus, the symptoms are really, I think, through the mast cell. Because all
All those symptoms- just the virus triggering the mass cell,
the mass cell triggering the vertigo, the fatigue,
and all these others,
because all those symptoms are actually caused by the mass cell.
Right.
So I think it's the infections that are constantly spurring them on,
spurring the mass cells on, you know, just like,
please, you know, just keep going, keep going, keep fighting.
And so these people in this, you know, inflammatory, you know,
soup constantly, yeah.
Yeah.
And do you see this on their like CBC?
Do you see it on their white blood cell count?
And where do you find this chronic loagate in?
inflammation?
It's a good question, right.
So, again, like these mass cell tests that we do, you know, we can identify, you know,
we'll look for histamine, we'll look for metabolize of histamine in the urine called
methyl histamine.
You know, so there, those are inflammatory mediators.
But sometimes you have to look elsewhere.
You have to look at other, you know, inflammatory markers.
Interestingly, a lot of mass cell patients don't have elevated, let's say high sensitivity,
C-reactive protein, for instance, right?
Sometimes it will be elevated,
but I'm surprised at the level of inflammation some people have
and they have normal CRPs.
Sometimes you'll see a little bit of like the sedrate, ESR,
you know, maybe that will bump up a little bit.
But still, the level of inflammation that they feel and have,
it's not always so detectable in the blood.
You know, there are other markers.
Sometimes I'll look at a VEGF.
That's an interesting marker that can sometimes tell us a little bit about
mass cells actually release VEGF.
Some people believe Bartonella also makes the body release VEGF.
Wow.
So we can kind of use some markers as a gateway to understand, like, what are the things we have to look at?
That's kind of how I, how I...
So what would be the typical villains that you would start to test for as soon as you saw,
as soon as you confirm the MCAS diagnosis?
So what I usually do, you know, when I see a patient, I'm not only thinking about MCAS,
I'm also always thinking about the triggers and the other things that could be in that soup in them, right?
So, you know, I take a history, and if there's any history that suggests exposure to animals,
exposure to cats, exposure to fleas, or ticks, or lice, or, you know, there's all these questions
that I ask, I make an assumption that they could have a vector-borne infection.
And so I'm sort of testing almost simultaneously.
I'm saying, you know what?
I think you have mass activation syndrome.
Let's prove that.
But you have risk factors for vector-borne infections.
So let's test, you know, Lyme, Babi-Bi or Bartonella, maybe some other infections.
you have fatigue, you have some of these other things.
Maybe they have a history of a feeling worse after COVID.
Then I'll do all the viruses.
Epstein Barr and CMV and H.HV6, many of them are reactivated.
And so I'm kind of like casting a pretty wide net
because I know that these patients are not going to,
it's not going to be a simple process of like identifying MCAS and treating it.
I know that there's all this other work that I have to do.
I'm also going to concentrate and help put them on things to calm those mass cells.
down, but I know that I won't achieve that until I get rid of this other stuff, right?
The toxin load.
The mycotoxins are always, I get that history of, you know, were you ever exposed to mold?
Do you have water damage?
Do you have any, you know, evidence to believe that you might be exposed?
A lot of people will say no.
Mm-hmm.
And you have to, you have to dig.
Sometimes you have to show them the test to prove that they have something for them to go the next,
you know, the next step.
But it's, you know, because people don't want to believe.
Yeah.
And also, mold doesn't always show up.
It's not like...
It's not always that pungent smell of mold.
No, sometimes it's no smell.
Because that's usually bad, bad.
Right, by that it's bad.
But it could be in the HVAC system, you know, blowing in.
You don't even know it.
That's the most commonplace, right?
So you have a beautiful house, brand new, no water damage,
but it's in the HVAC system because it hasn't been cleaned properly.
And it's literally blowing throughout the house.
And now, making you sick.
And again, people don't recognize that because they don't know what to look for.
So what do you do when you, I'm always curious about how you address EBV.
These are current EBV infections.
Yeah.
Because I'd love to talk about EBV and Lyme specifically.
So in, you know, an Epstein bar is not really a virus that you caught.
It's sort of one you've had for a long time.
And it can be mono being, you know, showing up as Epstein Barr later in life.
So what makes it reactivate and is that a weakened immune state?
is it, you know, it doesn't necessarily need to be a full-blown autoimmune deficiency,
but just a weakened immune state that doesn't allow the, you know, the virus to stay dormant.
I mean, there's a lot of replicatory cycles.
I mean, and I think, you know, a few people realize this is actually wound into your DNA in us, right?
I mean, the virus is in there.
And every time it's zipping and unzipping, it has a chance to raise its ugly head.
And so it...
It potentially cause cancer and other things, too, which people don't appreciate.
I think so too. I mean, there's a whole thread of evidence now of, you know, viral links to cancer.
Because all cancer, regardless of its form or its origin, was at one time a healthy cell. So something caused the metabolic shift, right? It could cause the metabolism of that cell to break down, and now you have a cancer cell.
So the question is, what broke the machinery, the metabolic machinery of the cell? But when you see these recurrent EBV infections, you know, I've used,
a lot of these homeopathic remedies,
eight week EBV remedies with some level of success.
How are you addressing those chronic viral reactivations?
Yeah.
So, you know, so just to give a little background, right?
So most people, by the time they're an adult,
have had mono, auto nucleosis, right?
Some people remember it.
Yeah, everybody's out of EVV.
Right, but some people don't remember it, right?
And so they say, how the cat can this be?
I don't remember ever having mono.
Right.
It could be a very mild, respiratory infection, you think is a cold, right?
Some people have it more severe.
Some people have it more mild.
So you have it.
And then these types of viruses, Epstein Barr is part of a family called the herpes virus family.
These herpes viruses reactivate.
You know, people who have, let's say, herpesy virus, you know, herpes simplex one or two.
You know, they get cold sores or whatever, right?
They reactivate.
They go quiet and they come out.
Epstein Bar is the same way.
So they're supposed to just sort of sit around and, and, and, and, you know, and, and, you know,
sit in the cell and not do anything, right?
But as the body gets stressed,
as the immune system gets dysfunctional,
if the immune system is trying to fight something else,
it's trying to fight Lyme,
or it's exposed to mold,
or you have a really, you know,
really traumatic event or stress in your life,
or you're not sleeping, right?
There are all these different factors
that then allow the Epstein bar
to start replicating and leave the cell.
And once it leaves the cell,
it activates mass cells
and it activates other parts of the immune system.
So actually the immune system
becomes more dysfunctional, right?
This is the problem.
It becomes a vicious cycle of immune dysfunction
becoming worse and worse
with more and more of these infections
kind of taking hold.
And so I always think about Epstein Bar and Lyme
and all these other infections as really the weight to get to it.
We could talk a lot about protocols
and things that I use,
but the reality is what I say to patients
is that you're never going to kill
all the Epstein Bar.
You're never going to kill all the Lyme.
You're never going to kill.
you're all your Bartonella and all the stuff in your body.
It's there where we carry it all through our lives,
even strep, by the way, which is interesting.
You never really get rid of it.
It can live in your gut.
But the key is to build your immune system up
so that it can handle the infections.
So how do we do that?
So we think about, I think about,
because, you know, my lens is the mast cell,
so I'm a little bit obsessed about the mast cell.
So I'm, no, I love this.
I mean, it just explains so much.
Oh, I'm glad.
Yeah, I mean, it really, it really does.
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It tastes amazing.
In fact, I made a steak today.
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So, you know, I think about it as if I can stabilize the mass cell,
then I'm going to also help the immune system handle the infections better.
But I also have to lower the load of the infection so that the mast cells and the rest of the immune system
can recover. So I think of it as a dance. You know, so we have to do a little bit here and lower the load.
We're not going to kill all of it, but we've got to get them back into hiding. But we also have to
work on that immune system so that it recognizes that it just can keep it at bay, right, so that the body can recover and heal.
Right? So that's really like my approach to all infectious diseases at this point.
Sometimes we have to lower the load and we have to go at it with, let's say, antivirals.
Yeah, we can use medication antivirals if we're talking about Epstein-Barr.
we have herbal antivirals.
We can do homeopathic things.
We can do a variety of different types of IV therapies that we use
that have antimicrobial properties.
Ozone, you know, IV ozone.
We use a couple of different ways that we do it.
That is, it's a, it's a, you know, disinfectants, essentially,
so it kills.
We, you know, we can use other things to help, again,
the immune system recover by lowering the load.
and that's, you know, that's what we do.
Now, the other, one of the, one of the treatments that I'm really excited about that I think is,
really has a more holistic kind of way of approaching this, but also a really molecular,
scientific way is to use a technique called supportive oligonucleotide technique or SOT therapy.
It's also now called Q Restrain.
And it's basically a lab that's able to create an RNA to match the DNA.
of the virus or the bacteria or the parasite
or whatever you're trying to focus on.
Wow.
And you actually can directly bind to that infection
and cause it to stop multiplying and actually they die.
That's my favorite treatment actually.
So it's like a trained MRNA.
Yeah, essentially.
Wow. And they make this synthetic MRNA.
To match specifically the infection that you have.
Where do they do that?
Well, I do it.
You do it.
Come to New York, yeah.
Yeah, you're like the Elon Musk of viruses over here.
Well, I have a lab that I work with, you know, I'm not the only one.
But this is like, to me, really exciting because it's super exciting.
It allows me to avoid a lot of anti, you know, microbials, a lot of medication,
especially in my patient population that they're very sensitive.
Yeah.
Even to herbs.
And a lot of, there's very little in the way of targeted immunotherapy out there in the world right now.
I mean, there are a lot of blanket immunotherapies.
Right.
but nothing that is targeted like this.
And do you ever use things like peptides like Thimason Alpha
to build the immune system?
Love. Love. That's my favorite one.
I'm a big one too.
I'm a huge peptide.
By the way, I'm working to get the FDA to allow that back on the bulk list.
Yeah, awesome.
Marty, if you're listening.
But, you know, it needs to be accessible
because peptides are a game changer for so many patients.
So you put some people on thymus and alpha,
you know, there are different ways to dose it sometimes, you know, twice a week.
but it just, it really does allow, you know, their T cells to come online,
for the body to start working.
And sometimes I even see people feel their fatigue get better just with thymus and alpha,
which is not specifically supposed to help fatigue directly.
No.
But the immune system is recovering.
It's indirectly good.
You know, it's interesting.
I got to ask a really introspective question on a stage talk a few months ago.
Somebody asked me, they said, if you were to put the top 50 experts in the world,
top MDs, PhDs, researchers in longevity and aging in a room,
and ask them to agree on one theory of aging.
What do you think that theory would be?
It's like, wow, that's a really good question.
I think we would all agree on the theory of immunophatee.
You know, this, I'm not saying it's the only theory in aging,
but a slow progressive overwhelming of the immune system,
you know, back to the fish in a tank analogy,
little algae grows in the tank,
fish is a little tired, fish is doing just fine.
You know, you had two drops of chlorine, he's fine,
and then you had four drops of chlorine,
and then you had a little bit of bromide,
and then you clog the filter.
And, you know, eventually this micro-toxicity
overwhelms the immune system,
and the tank, the environment, is too dirty
for the immune system to properly function.
And now...
I love that analogy.
You may use that freely, if you'd like.
Yeah, no, I've heard you use the fish tank before.
I love that.
It's just to get people to start thinking about their environment
and toxicity and like, you know,
I'm a big fan of a lot of these new blood filtration technologies
in use for resists.
Therapy Plasma Exchange, we're doing it in my office.
Are you?
You just do everything.
I know, that's why my kids.
My kids are always, like, oh no, what's she gonna come back with?
I go to another.
Her kids are off camera, but she always been the mad scientist.
Like, I can see you guys growing up
and like mom's in there with like the chemistry set, you know.
Pretty much.
And they were.
Back to the future movie.
Yeah, and they were my subject.
They've tried a lot of things.
They look pretty good though.
They're pretty healthy.
Yeah, they're healthy.
I mean, he's got a little bit of a foot coming out on the side of the head there, but I'm sure, okay.
No, but I think that, you know, finally the frontier of medicine is opening up.
And we're actually starting to believe more in what God gave us than less than what man makes us.
Meaning like the best defense we have to live a long, healthy, happy life is our God-given immune system.
And when it gets run down and disabled,
or disabled, it not only can't protect us, it can't police us, right?
I mean, because it does a lot of functions internally to regulate cellular autophagy and
cellulosin essence.
And so this really is like, you know, as a single source, healthy immune system is
really our best defense against all cause.
Yeah.
Mortality and infection to disease.
So you have a patient that's positive for MassHealth syndrome.
you begin to start looking for the villain.
You find Epstein Bar, maybe underlying lime.
A lot of people had Lyme years ago.
They did the doxycycline for whatever, 21 days.
They felt better.
And they're like, okay, I don't have Lyme anymore.
Exactly.
Right?
Just like when I get influenza and I'm down for a week and then I'm back up,
I'm like, okay, I don't have the cold anymore.
Not realizing that you may still have it and be asymptomatic.
And it may just be waiting for its opportunistic moment
for the immune system to get run down again.
we can again rear its ugly head.
So these therapies of walking somebody out of these syndromes,
I want to read some of the links to this mass cell syndrome
because up to 17 to 20% of the population may have mass cell syndrome
and not know it.
It mimics dozens of other conditions.
Allergies, IBS, anxiety, chronic fatigue, fibromyalgia,
potts, skin issues.
And this is why patients kind of,
ping-ponging around to different specialists because medicine is hyper categorized.
You know, you're going to a neurologist for this.
You go to internal medicine for this.
You've got infectious disease for this.
And nobody's actually looking at the whole picture.
And so for these people that find themselves in this myriad, where do they start?
What other conventional therapies are you using?
You're using things like sauna, gut binders.
Do you look at diet, gut microbiome?
Is this all apart?
Yes, yes, yes.
Okay, great.
This is all a part of.
It's all a part of it, yeah.
But I think it also has, what I love about, you know,
my center is called AIM Center for personalized medicine.
So it's all personalized, right?
So not everyone is going to be able to tolerate a sauna.
You know, mass cells can be very heat sensitive.
Right.
So I have a subset of patients, interestingly, that do really well in sauna,
but I have a lot of patients who don't do well in sauna, right?
So maybe some of them just need to work up, you know, to it.
So we have to start slower.
Sometimes we'll never going to be able to get them into a sauna.
So we have to find other ways to detox.
And so we're always looking at ways to, again, approach the toxicity load that we have to deal with, right?
Because the reality is we're all constantly dealing with this.
No question.
Yeah, I mean, this is the life we live.
And so a lot of people will say, well, why do you need all these technologies?
Like, why do you need to do all this stuff?
And it's because even if we're as healthy as we think we can be, even if we eat perfectly,
even if we sleep perfectly, even if we do all those things, right, we still have to fight against what we're working.
to fight against what we're constantly breathing in and being exposed to, right?
So I think like people should know that even healthy people still have to have to keep up
with, you know, our bodies.
But for people who are sicker, obviously it's a little bit more advanced, a little bit more
complicated.
So yeah, so I do all those things.
What I love is we do a red light therapy.
We have a red light bed.
I saw that you have a red light bed as well, right?
So for a lot of mass cell patients, that has actually been really, really helpful in reducing
inflammation, helping my end up.
Interestingly, that was, not to cut you off of it,
that was one of the biggest things
that we implemented for my daughter
when she had pots.
And which, the more you're,
the more I'm talking to you,
the more I think it was Massile activation syndrome
by far, and we just inadvertently
calm them down by getting
toxicity out of everybody.
And, and then, you know,
I pointed to the mold and the metals
and, but really those were just the triggers,
not the actual issue.
Not the root.
Not the root.
so I didn't go deep enough into the soil.
But red light therapy was amazing for her.
Yeah, yeah, and it is for a lot of patients.
So that's why I bring in all these different modalities
because I have to figure out what's going to be the easiest way, right,
to get to the root, to all the roots.
I love therapeutic plasma exchange as a detox.
I know it's a little bit aggressive.
It is aggressive, but I'm...
Have you tried it?
I've done it twice.
And I've also done inus phreasis where they return the plasma.
So they filtered the plasma.
was fascinating to me.
So my wife and I did it for our anniversary.
I mean, talk about nerd.
That's definitely something I would do too.
Hey, babe, I got you something great for your interview.
You're going to love this.
We're going to over to this clinic and we're going to get these dual canylus put in
and we're going to, but we have side-by-side beds and they'll play nice music.
But we did it in Dubai and, you know, unfortunately you can't get the innes phrasis here.
Not yet.
It's coming.
Yeah, I hope so.
No, no.
They're working on it actually.
Oh, really?
I really hope so.
because this whole idea of subtractive medicine to me is very fascinating, right?
Not adding anything to the body removing.
Removing.
Removing what it's dealing with.
You know, that's why, you know, sweat, stool, urine, detoxification, binders,
you know, therapeutic plasm exchange, anisphoresis, EBO2 ozone with filtration.
And I'm always fascinated by how much stuff comes out of that collection tank.
And you know what we did was we sent it to the lab as urine.
Okay.
Oh, right, right.
So we collected in there.
And because they actually wouldn't run the sample.
They won't run it.
Yeah, they won't run it.
So hopefully the labs aren't watching this.
But so I sent it as urine.
It shows you're in kidney failure.
So you have to ignore that part because it's not actually urine.
But the list of toxicity that comes out of those ebu treatments that ends up in that collection
tank tank and causes all that bone and everything.
Sometimes the top comes right off and it's foaming out of there.
That has got to be good for you to take it out.
And the same with the plasma.
We're still trying to find.
I have a lab that I think is going to help us test the plasma that we're getting out of
people.
But you could see sometimes.
That's really good too because right now they don't do it.
Like Switzerland does it.
Yeah, we don't do it.
But I have somebody who may be interested in doing a study with me.
Wow.
But you could see the color of the plasma.
And the more you do, the treatment of the TPE,
you'll see the plasma starts to get clearer and not as cloudy.
But we're doing blood and urine analysis on patients pre and post.
And actually, so we may not be able to directly test the plasma yet,
but we will, but we can test the body and we can see the level of toxins go down.
You know, BPA comes down, PFS, forever chemicals.
We're doing a study right now on forever chemicals.
And it looks like, you know, it is removing it.
Yeah, yeah, yeah, yeah, it looks like it's removing it.
That's so good.
That's what's amazing.
Yeah, it's exciting now too
because you can actually test the levels
of microplastics too.
Yes, that's what we're doing.
I've been reading a lot about
the presence of microplastics
in these fibrinogen bonds
that are in these atherosclerotic plaques
that are causing hardening,
narrowing, soft blacking in the arteries.
And biofilm for people who have long COVID
and some of these other infections
and I can't get rid of it,
everything is sort of like clumping together
in the blood.
And what do you do for those kinds of things
out of kinase.
Balaki, lumber kinase.
So all the kinases, you know, great.
And, you know, therapeutic Plasma Exchange
actually does pull out some of the biofilm,
which is really, I think, exciting too.
Because some of them are just really resistant.
So I love the supplements.
I love being able to break them down,
but they don't, sometimes doesn't work.
Sometimes we have to use anticoagulants, actually.
Like a heparin?
Like heparin or eloquist.
There are a bunch of different ones that you can use.
Sometimes you have to just really kind of thin,
the blood out as much as possible
to get the bugs out of these biofilms.
You know, I think of biofilms is like a spider web.
It's just, you know, holding on to everything.
And until we can get them out,
all the treatment in the world, all the ozone
and all the, you know, anti-microbials,
even this SOT therapy, like nothing is going to work
if everything is in this, you know,
kind of fibridogen, you know, platelet.
It's just a soup.
Yeah, yeah.
And a lot of these,
a lot of these pathogens are attracted to heparin.
You know, they, you know, I mean,
heparum binding sites, you know,
there are filtration technologies, one called Xterra,
which I've also done,
and they use heparin binding sites
to draw out certain pathogens,
fungi, mold and mycotoxins,
certain viral pathogens,
even CTCs circulating tumor cells
that are,
that like to bind to these heparin binding sites.
It doesn't put the heparin back into the body,
but they do clon,
around these heparum binding sites.
Isn't that interesting because mass cells make heparin?
Okay.
It's the one cell in the body that actually releases and manufactures heparin.
Really?
Yeah, that's one of the mediators that we can actually test for.
So then it makes me wonder, yeah.
Yeah, yeah, it does make me wonder too.
So you see elevated levels of heparin in the blood.
Yeah.
Because these mass cells are.
Yeah, that's how we identify.
Which makes a lot of sense because you don't want,
you don't want clumping and clotting if you have pathogen, right?
You don't want to wall it off or seal it in.
You want to actually...
Presumably.
Yeah, I mean, you wonder like why the mass cells make all these things, right?
So maybe that's part of it.
But what I think, where I think it manifests very often,
not to get too off topic,
but I think about women who have really like heavy menstrual periods.
High estrogen, you said, can activate as well.
Yeah, and can activate, exactly.
So I think with the mass cells, what's happening at the level of the uterus is they're releasing heparin.
And so these women are like hemorrhaging.
They're having these really, really heavy periods because of mass cells, which are being, yes, are being triggered by changes in estrogen levels or other hormone levels that are releasing hebrin.
Now that blood is thinner and it's coming out faster, yeah.
So they have these menorrhate.
Menorrhagia.
It's such a hard word to say.
Yeah, yeah.
Aminorrhea, amenorrhagia, whatever it is.
But lots of bleeding for, you know, during their menstrual sites.
Again, so fascinating.
I mean, especially given the percentages of the population
that may have muscle syndrome.
Yeah, like 20% is tremendous, right?
Think about that.
It's like one in five.
And that's probably more.
I think there's more than 20,
but, you know, that's the study was like 17%.
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Now let's get back to the Ultimate Human podcast.
So for folks that have this things like thymusin alpha, binders, saunas, obviously cleaning up the diet, testing for metals, mold, microtoxins, viruses and parasites, these panels that it will actually look for things that could be hyper-exciting the immune system.
and therefore these mass cell syndromes,
that's kind of the place to start hiking.
Yeah, that's a good starting place.
So we do a lot of stool analysis,
we do microbiome analysis, we do parasite testing
in the blood and in the stool.
And yeah, parasites are actually quite pervasive.
They're pervasive and they're very real.
In fact, you know, I was reading a study
on multiple sclerosis on this parasitic theory,
they call it the clean hands theory,
where the over-revasive
sanitation and reducing the healthy parasitic colonies.
Right.
Maybe causing the immune system to hyperactivate to some of these cestodemotodes and these
helmuth parasites in MS patients.
And at least this one study that I looked at, which was post-mortem autopsies, they found
similar or identical deficiencies.
And I want to misquote the study.
I'll actually put a link to it in the show notes
in case I misquoted it.
They found similar or are identical colonies
that were vastly missing from these patients
with MS.
And they hypothesized that
this overstandization, you know,
where you actually don't have the healthy parasitic colonies
were actually causing the immune system
to have this autoimmune reaction to myelin.
And they found corkscrew parasites
in some of the locations.
where the immune system was attacking.
Because if you think about it, you know, why the immune system can dissolve myelin
or attack myelin, why isn't it sort of uniformly attacking it everywhere?
Why does it seem to be taking rifle shots?
Oh, that's interesting.
Seemingly randomly around the body or maybe concentrated in areas of the brain.
I mean, there's myelin covering all of our nerves.
So why is it not affecting or evenly dissolving this?
And I thought it was very, you know, very interesting that there could be a bug thing.
theory behind it. Yeah. Yeah, I'm one of those people, I think there's a bug theory behind almost
all the chronic diseases we see. I disagree with you at all. I just, I just every single patient,
every single patient I test for who has Parkinson's or Parkinson's-like infections, or I mean
conditions, Alzheimer's, you know, I can look at different manifestations of mental illness,
OCD, anxiety, depression. You almost always have gut issues.
Yeah, all of them.
Almost all test positive for vector-borne infections.
I find parasites in them, and I find Bartonella almost across the board.
Yeah, our clinic director had a Dr. Carey Sarda.
She had a patient she was treating that came down to see her for Parkinson's.
Been six years diagnosed with Parkinson's, completely unresponsive to traditional therapies.
Neurologist, couldn't figure out what was going on.
The mood collapse, the dystonias, the dysthytico-cannesias, the whole sequence of events.
and when she did the viral testing,
it was one of the highest, not Lyme titers,
West Nile titers, that the lab had ever seen.
Oh, wow.
And ironically, he had an office in South Beach
and was commonly visiting South Beach
when the largest Zika mosquito outbreak in South Beach.
It's coming back 12, 13 years, 11, 12 years.
There was a period where even,
Even customs was not allowing pregnant women, you know, that were coming through to go to Miami Beach because the Zika mosquito was so prevalent.
They got it under control.
But that's what carries the...
But it also carries West Nile.
And it was one of the highest titers that they'd ever seen.
It was active.
Never tested for it.
And so she went after the, you know, the virus.
And I won't say all of the symptoms went into remission, but I would say it's...
75, 80% improvement in his symptoms because he didn't have Parkinson's.
He had Parkinsonisms from the viral infection.
And a lot of these viruses seem to have very similar etiologies or at least presentations
to things like Parkinson's, which are very often diagnosed by observation.
Well, it's an inflammatory response.
It's just I think that there's a vulnerability.
I always think of it, like people will say, well, why did I get this condition,
Parkinson's light condition and somebody else got, you know,
different, you know, got Crohn's or colitis or got, you know. So I think there's a vulnerability
that people carry. Maybe it's genetic. Maybe it's hard to find. But then there are these, you know,
infections or triggers or toxins or whatever that then triggers that genetic vulnerability to come out.
Right. And it's presenting in this way. And so you have to, you know, alleviate or remove the
triggers. You might still have some symptoms left because some of that is maybe even genetic to some
extended. It got already turned on. You mean like methylation pathway issues or poor waste
elimination or things like that? Yeah. Like some things you're just never going to be able,
let's say the damage is done. I'd like to think that I can reverse all, you know,
all damage in everybody, but it's impossible, right? Right. So some damage is already done. But if you
remove, let's say that infection, maybe you can heal a lot of the damage. Right. That's the,
yeah, calm them down, boost the immune system. Because immunodisregulation,
you know, the consequences of that encompass all of the things that we've talked about so far.
And it mimics so many other pathologies.
These poor people are just literally running around the country or running around the world sometimes
trying to figure out what could be causing this.
And I would disagree with you at all that I think, you know, the bugs are related to a lot of these issues.
Let's go into the gut for a minute, if you don't mind.
how important is gut dysbiosis, the gut microbiome, you know, that single-cell layer of protection that we have on the luminal wall of our gut, sort of separating our inside environment from our outside environment.
What can we do to care for it?
And how often do you think that there is a gut-related anomaly in Massel syndrome?
I mean, again, I don't like...
You're probably going to say 100%.
Like, yeah, I was, right, I was going to say like 99, 98 or whatever.
You know, there's a, and it's interesting because I do have patients who swear they have no gut problems at all.
And the gut is not their problem.
They have all these other neurologic and other other systems involved, right?
And I go, really?
You have like, no, nothing?
Like, I almost never see it, right?
So then I'll have them do a test, you know, I'll do some stool testing, right?
And I'm like, well, you actually have it.
I don't know why you don't feel it, but there's definitely something going on there.
and that's where the bulk of your immune system is, right?
70%, yeah.
So it's hard to imagine.
There's so many mast cells that line the entire GI tract.
Oh, yeah.
So, you know, you have to think like if they have a mass cell condition,
the mass cells in the gut are involved on some level.
Maybe some people are more sensitive to feeling it and some aren't, right?
But I think it looks, and in the toxic world we live in,
it's very, very difficult to maintain, you know, a proper digestive system.
I would agree with that.
Right?
the food that you eat, you know, the pesticides on the food, the toxins, the glyphosates,
things like you could be so careful and still get exposed to things that are going to eventually
like break down that but layer.
Early antibiotic use, you know, as children, right, frequent strep infections very, very commonly
will cause a dysbiosis, right?
So people may not notice anything until it's sort of like the straw that breaks the camel's
back, right?
So they're living with some dysbiosis, they're not, you know, they're not, you know, they don't have a lot of symptoms yet.
But there's usually then something that then brings it out fully.
They get into the course of antibiotics or they get, again, they have a stressor in their life.
They get, you know, they get COVID.
They get something.
And then all hell breaks loose.
And then now they have major gut, gut issues.
And so, you know, it's about, you know, feeding the good microbiome there, right?
So a lot of them, a lot of the good stuff is gone.
There's a lot of bad stuff, right?
So it's actually finding that balance between killing some of the bad and getting more of the good, right?
And so there are a lot of tools.
What does something like that look like?
What does a typical protocol look like?
I know it's not a one-size-fits-all.
I mean, and in terms of gut testing, are you doing GI maps?
Are you doing like a Viome stool test?
I'll do like gut sumer from Vibrant wellness.
I like that one a lot.
Sometimes the GI map, I don't want to say anything bad about it.
I've just found some inconsistencies with their testing.
You've got to be really careful with the testing,
and they're actually, I know several people
who are trying to do comparison studies
between the different labs to see, you know,
why some labs are picking up parasites
and some labs are not picking up parasites
and the same samples, right?
Wow.
So we're just trying to, we're trying to...
So the testing is actually in some ways
a little bit rudimentary, but I've, I've been, you know, pleased with some of the GI tests that
we've, we've tried.
Yeah, I'd use vibrant a lot.
Yeah, but they have, they have a lot of good panels.
They have a lot of good panels.
They have a detox challenges and things.
Yeah, and the, and we use their urine test for the total talks.
Yeah.
Before we do the therapeutic plasma exchange, you know, and after, right, so we like a lot of
their stuff.
So, so customer could be a good, a good place to start.
I love doing parasite-specific parasite testing.
I don't rely on, you know,
anyone lab to pick up the parasites,
because parasites are really hard to find.
They are, yeah.
I think of it, I use this analogy with patients, right?
I think of parasites like they're like Spider-Man.
They have, like, suction cups on their hands.
They don't have fun.
But, you know, like, imagery.
So they're, like, sticking to the wall of the intestine.
And so when you have a bowel movement,
they may fall into that stool.
They may not.
Right.
And so you may not find it until you test and test and test.
So I have a lab that I really like
that has been really good.
at finding a lot of these parasites.
Wow.
And I am really shocked at what we're finding.
And not to go too off topic, but you know what's really interesting to me as a,
when I was doing my residency at NYU in the city, we saw a lot of HIV patients,
patients with that type of immunodeficiency, immunocompromised states.
And they used to have this, we used to find this parasite in them all the time called
Cryptosporidium.
And I was taught that Cryptosporidium is a, is a parasite.
that only infects people with really suppressed immune systems,
cancer patients, HIV.
I see it probably in 75% of my patients.
Wow.
But they're not HIV or cancer patients, right?
So that tells me that part of this mass activation syndrome
and all the other things that I'm seeing
is suppressing the immune system so much
that we're seeing parasites that should not be in relatively healthy people.
Wow.
And are you doing regular frontline things,
is ivermectin, van benazole, menendazole.
Okay.
Elinia.
Alinea and all the, yeah.
I usually do a sequential type of protocol with them.
I find, listen, I love herbs and I love natural stuff, but for parasites.
Yeah, I've heard the same thing.
You need the drugs.
You got to bring the big, you got to bring the guns.
So again, so when I'm approaching a patient, if they have the parasites, I'm going to do a parasite protocol.
If they don't have parasites, you know, maybe I'm going to start with some other stuff, right?
I'm working on the diet.
A lot of the patients have low short-chain fatty acids, you know, so I may use a buturate.
Sourcrowd, even fermented vegetables.
Sometimes, but some of my Massel patients can tolerate it because it's high in histamine.
So, you know, so it's, again, very personalized.
That's a good point, yeah.
We're a little challenged because we like things that we think are good, may backfire.
So, so, but we have to, you know, kind of inch towards that.
I have a patient right now who is able to, had really bad massel stuff, but like started
to be able to introduce sourcrow and stuff.
So that's amazing, right?
Like, wow.
For the free fatty acids.
Yeah, yeah.
But we can use buterate.
We can use some other things.
We can, you know, again, it's about balancing the gut.
We can use immunoglobulins like, you know, like an IGG type of product that has, you know,
it's basically bovine serum immunoglobulins.
You can use colostrum if people can tolerate dairy.
All these things, I mean, again, there's like, there's no perfect way to do it.
It's just defining it the right way for the patient.
Yep.
So it's about balance and it's about.
killing sometimes and then it's about quieting those mass cells down in the gut directly
so that the immune system is not constantly in this kind of cycle.
Hyperinflamatory state. Yeah. Dr. Dempsey, this has been absolutely fascinating.
I really hope you'll come back on the Holt of Human Podcast because I want to follow this.
All right. My VIPs are so excited for you in the VIP room. They've got a whole litany of questions
for you. And I appreciate you too, also agreeing to stay today.
to speak to them in a live format.
This is such a fascinating, I think,
underserved area of medicine
where we start looking at,
really looking at root causes
and how symptoms don't necessarily link back
to the pathology that people are diagnosed with.
It may be something even deeper
that has caused this immune system,
mass cell activation,
but caused the immune.
system be so run down that it's, you know, essentially can't protect itself anymore.
Exactly.
And it's more pervasive than we can imagine, right?
This is the thing.
I think the more people, the more toxic our world gets.
Yeah.
The more COVID and all these other things that people get.
Or the more like, you know, weird infections, like this winter was kind of crazy with a lot
of, oh my gosh, monkey pot.
I mean, you name it.
Yeah.
So the more that immune system just gets revved up and revved up, you know, unfortunately,
I think this is like really a pandemic in a way of mass electrivation.
syndrome. And so, like, I think everyone really needs to know this, right? Because the thing is,
like, people listen and say, well, this doesn't apply to me, you know. I do all these things
and I'm healthy, but it may apply to somebody that's close to you. Yes. And it may apply to you
eventually, hopefully not. Right. But also I want to give hope because I think there's so much
that we can do. And that's why I do the work that I do, because I help people every day.
Yeah. This is so fascinating. For my audience who wants to know more about you or can,
where they can find you. Where can they find you? Okay. So my center, AIM Center for
personalized medicine. My website, DR. Tanya Dempsey.com,
Instagram, DR. Tanya Dempc, MD, Facebook, D.R. Tanya, you know, like all that stuff. I have
YouTube. I put all that in the show. That's for you. Yeah, I'm trying to think what I'm missing. And then,
and then my podcast, Mass Cell Matters. I saw you have to, you had a podcast Mass Cell Matters.
I love that. I'm going to have you on that. I would love to be on there. Yeah.
We see eye to eye on a lot of things for sure. Yeah. Yeah. So absolutely fascinating.
guys, please, I'll put all of that in the show notes below.
I'll put the study that I referred to earlier in the podcast.
And until next time, that's just science.
