Yesterday i watched a youtube of Prof Seyfried re cancer.
PS says that almost all cancers are due to mitochondrial damage, which causes some kinds of cells to ferment, & this fermentation is aided by sugars (that we have eaten)(& by eating carbs, ie fruit & veggies & starches), & is aided by glutamates that we have eaten (eating glutamates is unavoidable, glutamates are especially found in meats & dairy etc)(as well as in plant products).
PS says that cancer is not a DNA thing.
Amazing.
Every day i learn how ignorant i have been/am. But yesterday was a life changer.
I will have to check again, but, PS i think duznt say that fructose is bad, he says glucose is bad. So, i am not sure whether fruit is bad, fruits have mainly fructose, but, i think that all fruits have at least a little glucose, so, i would steer clear of fruits (fruits have been banned in my house for years now).
Professor Thomas Seyfried: Cancer is NOT caused by "bad luck" or your genes! It's mitochondrial!
Dr. Thomas Seyfried (Charity Channel) 12.6K subscribers Subscribe 4,401 views Premiered Dec 10, 2023
Support Dr. Seyfried! Get the summary book directly from us and donate by doing so: https://www.cancer-as-a-metabolic-dis...
Dr. Thomas Seyfried, discusses cancer as a metabolic disease. He holds a Ph.D. in Genetics and Biochemistry from the University of Illinois and has a background in neurology. Dr. Seyfried has received numerous awards and honors from various organizations, and he has over 150 peer-reviewed publications. He is also the author of the book "Cancer as a Metabolic Disease: On the Origin, Management, and Prevention of Cancer," published in 2012.
We are a group of enthusiastic medicine students who want to support Prof. Seyfried! Because he never really asks for money... but we know he needs it!
That's why we created this channel: To spread his word and give you the opportunity to give to his research in a lot of different ways! We will post all the newest videos by him in one place, make special edits, post stuff from collegues in the keto-cancer field as well and we will produce audiobooks of his work!
Yesterday diet was such an easy game to play.
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crawler
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Yesterday diet was such an easy game to play.
Last edited by crawler on Thu Apr 04, 2024 10:13 pm, edited 2 times in total.
STR is krapp -- & GTR is mostly krapp.
The present Einsteinian Dark Age of science will soon end – for the times they are a-changin'.
The aether will return – it never left.
The present Einsteinian Dark Age of science will soon end – for the times they are a-changin'.
The aether will return – it never left.
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crawler
- Posts: 872
- Joined: Sun Oct 28, 2018 5:33 pm
Re: Yesterday diet was such an easy game to play.
https://www.youtube.com/watch?v=oKblOdaE8JQ
Transcript
The role of the mitochondrial in cancer
0:00
so Thomas can you please tell me the
0:03
role that the mitochondri play in the
0:06
development of cancer they they are a
0:10
second living living organism inside a
0:13
cell um they're actually have their own
0:15
genetic material and they are the
0:18
organel that breathes the air to make
0:20
the energy so um and what warberg found
0:25
was that all normal cells uh have these
0:28
um organel that take in the oxygen um
0:32
and the cancer cells have a defect in
0:35
that in that organel so uh they take in
0:38
less oxygen and they produce uh lactic
0:41
acid which is an exam which is a waste
0:43
product of glucose fermentation they
0:46
call it lactic acid fermentation and
0:49
that proves clearly that these tumor
0:51
cells are are not getting energy through
0:53
any kind of an oxidative mechanism so as
0:57
long as they have the fuel to continue
0:59
their ferment ation they will survive so
1:03
all cancer cells and every one that
1:04
we've looked at they have damage in
1:06
their structure of that organel that
1:09
means that all cancer cells regardless
1:12
of what you want to call them are all
1:13
fermentors they're using a ancient
1:15
fermentation Pathway to survive so that
1:19
means that there's a very simple way to
1:20
kill them you just have to take away
1:22
their fermentation energy and uh feed
1:25
them things that they can't they can't
1:27
use fatty acids and Ketone bodies are
1:30
not fermentable you they're un you need
1:33
uh oxygen to get energy from Ketone
1:35
bodies and and cancer cells don't use
1:38
oxygen so it's a very clear way to kill
1:40
the majority of cancer cells and then
1:43
the amino acid is also glutamine is also
1:46
the second fermentable fuel uh uh
The importance of glutamine
1:48
glutamine is the most abundant amino
1:50
acid in our body it's everywhere um so
1:53
in order to imp and besides our immune
1:56
system needs glutamine our Ura cycle
1:59
needs glutamine
2:00
our dig gut cells all depend on
2:03
glutamine um so if you go too
2:05
aggressively on attacking glutamine you
2:08
also can cause metabolic disturbances in
2:10
the body so that's why we developed the
2:12
Press pulse theory of of of strategy we
2:16
can control glucose constantly because
2:19
glucose is a non-essential metabolite
2:21
our body does not need glucose we can
2:24
make glucose from within at very low
2:26
concentrations but the glutamine issue
2:28
you have to get get the body into a
2:31
ketotic state and then we hit the
2:33
glutamine just briefly boom weit bing so
2:36
it's pulsed it's like a pulsing and that
2:39
just oh I have a few cancer cells here
2:41
they go down okay then we let the
2:43
glutamine come back but not too many
2:44
come back just a little bit then they
2:46
hit down come back a little bit hit down
2:48
and the next thing you know gone so um
2:51
again you have to use knowledge of of
2:54
what how do we kill cancer cells without
2:56
harming the normal cells and that's the
2:58
strategy that we're developing Ving as
3:00
dosage timing and scheduling that's
3:02
where we are now we're perfecting dosage
3:05
timing and scheduling and once we have
3:07
those conditions perfected or uh
3:10
modified we'll be able to manage the
3:11
majority of cancers with with minimal
3:13
minimal effort but we're right there at
3:16
that at that point so we do everything
3:18
pre-clinically in my lab I have the best
3:21
pre-clinical models of cancer G blastoma
3:24
system systemic metastatic cancer the
3:27
very types of cancers that we see in
3:29
humans so we can practice on all this in
3:31
the preclinical system and once we see
3:34
what works really well we go right to
3:36
the clinic with it and my physician
3:38
colleagues tell me whoa I did I did what
3:41
you said we're working out different
3:42
slightly different dosages and timing
3:44
but this but the results are really
3:45
quite remarkable so that's how it works
3:48
I I develop the concepts I test the the
3:51
the pre-clinical system and then we
3:53
translate there are very few people on
3:55
the planet doing what I do it's because
3:57
I have the best models and I have the
4:00
concepts and I have uh willing uh
4:02
participants Physicians that are willing
4:04
to try this many of them realized that
4:07
what they were doing in the past is not
4:08
working they're harming their patients
How cancer cells get their energy
4:10
so all major cancers are similar in
4:14
having uh Reliance on a fermentation
4:17
metabolism to survive without energy
4:21
nothing can grow so where do these cells
4:24
get their energy from how do they get
4:25
their energy once you understand how the
4:27
cancer cell gets energy
4:30
um then you can Target that and they'll
4:33
die it's not that complicated oh can we
4:36
kill cancer cells if we take away their
4:38
fermentation yes what do they ferment
4:41
they ferment glucose and the amino acid
4:44
glutamine so if we take away glucose and
4:46
glutamine they should die and the answer
4:49
is yes they will die so um and they
4:53
can't burn fatty acids or ketones so the
4:55
solution to the cancer problem
4:58
becomes
5:01
recognized so why nobody is doing this
5:04
so and in fact when I say that one of
5:07
the
5:08
problems people think it's too simple um
5:12
people want things to be complicated so
5:14
nothing can make a simple condition more
5:17
complicated than saying that gene
5:19
mutations are responsible for this
5:21
disease because it's infinitely
5:23
complicated and people think oh yeah you
5:25
know so we're going to use all these
5:26
strategies because cancer is such a
5:28
complicated disease and when I tell them
5:30
no it's very simple you can just kill it
5:32
by taking away I can't believe it it's
5:34
too simple warberg had the same problem
5:36
they said it was too simple people don't
5:38
want Simplicity they want they want
5:41
complicated stuff when it comes to oh
5:43
you know I have to go through this and I
5:44
have to go through that so how do you
5:46
break through this I don't know
5:47
conceptually and theoretically it's not
5:50
that complicated but practically to
5:52
manage cancer uh it does require
5:56
knowledge about how you will in fact
5:58
lower those two fuels
6:00
um which then becomes responsible of the
6:03
patient it's it's you know it's funny to
6:06
me um people sometimes have this
6:08
attitude that I have this terrible
6:12
disease maybe it was caused by God or
6:15
something maybe I did some bad things so
6:18
I'm going to take chemo and radiation
6:19
and I'm going to suffer and because I
6:22
suffer it should get rid of my cancer
6:24
because suffering is kind of like the
6:26
the the the penalty you have to pay or
6:28
something along these lines but then you
6:30
come along and say well the concept is
6:32
not that complicated but when you stop
6:35
eating for a week you feel like you're
6:37
really suffering because our brains are
6:38
addicted to glucose so once you get
6:41
through the glucose addiction actually
6:43
the management of the cancer becomes so
6:44
much better so um so we have to transfer
6:48
this idea of painful suffering from
6:51
toxic poisons into a self self-directed
6:55
uh uh reduction of food intake um or
6:58
taking diets that lower glucose uh and
7:02
Elevate Ketone body so the cancer can be
7:04
better managed so what should we eat
What should we eat
7:06
more of and what should we eat less of
7:10
well I think the bet the the basic thing
7:11
is eat is eat less of of everything you
7:14
might be eating um because that that the
7:18
the best way or but when you tell people
7:20
to get rid of their cancer that you have
7:22
to stop eating for a month they think
7:23
you're crazy um oh well this guy's got
7:26
must be nuts who can stop eating for a
7:28
month many people feel that if they stop
7:29
eating for 3 days they're going to be
7:31
dead this is how little knowledge we
7:33
have of of our incredible capabilities
7:35
of living on the planet without eating
7:38
but we're trying to make water only
7:40
fasting which will kill cancer cells
7:41
quite effectively uh um more more
7:44
reasonable with a with a diet that is
7:47
palatable nutritious and um uh will
7:52
lower the blood sugar and and Elevate
7:54
the ketones so we say we developed the
7:57
glucose Ketone index count calculator to
8:00
allow people to know if they're in a
8:02
zone for killing cancer cells so they
8:04
always ask me what can I eat um and I
8:07
say well eat anything you want and then
8:11
check your GK glucose Ketone index if it
8:13
throws makes the glucose Ketone index I
8:15
don't eat that so only you'll every
8:18
person will find their balance amount
8:20
they should eat and what they should eat
8:21
to keep the ratio down and that number
8:24
will tell you that you're killing cancer
8:25
cells so how do I know if it's working
8:28
it always works when you're in the that
8:29
zone oh I can't get into that zone I've
8:32
done everything I can I can't get down
8:34
to 2.0 or below oh what do you I'm
8:36
eating this me I said well don't eat any
8:38
of that just drink water and see oh it
8:40
went right down okay now add back the
8:42
foods that will keep you in that zone
8:43
without throwing you out of so it's it's
8:45
an experiment on each individual and
8:47
they experiment what they can and cannot
8:49
eat how much they should eat and how
8:50
much they can't eat so that's all worked
8:53
out for individual people and they keep
8:55
their records they keep a log of all
8:56
this so it's like a diabetic you can't
8:58
eat that can't eat this I'm keeping my
9:00
blood sugar low so it it all it all
9:02
works from the
9:05
individual so tell me why is it that uh
Otto Warberg
9:08
the work that Otto warberg did that we
9:11
didn't continue in that path OT warberg
9:14
knew what the origin of cancer was the
9:17
problem is his quantification of lactic
9:20
acid and oxygen consumption was um uh
9:25
misunderstood uh this is an extremely
9:28
important Point uh I'm preparing a
9:32
publication to uh show how OT warberg
9:36
and the entire uh uh field of cancer at
9:40
that time uh were uh were
9:44
misinterpreting their observations so we
9:47
just have taken warberg concept polished
9:49
it all up and now can explain clearly
9:52
what the origin of cancer is once this
9:54
the cancer field comes to understand
9:56
this then they have no choice but to
9:58
Target GL glucose and glutamine
9:59
simultaneously it becomes the obvious
10:02
and clear pathway for managing all
10:05
cancers and this is another thing that
10:06
gets everybody all upset they think
10:08
breast cancer is different from colon
10:10
cancer different from brain they're all
10:11
very very similar they need those fuels
10:14
to grow they can't use oxygen that's the
10:16
similarity they're all genetically
10:18
different they look different under the
10:20
microscope but they're all similar they
10:22
need fermentation Target the
10:24
fermentation and you can manage this
10:26
disease so that's the B when you get
10:28
enough people that respond well healthy
10:31
didn't lose their hair didn't get all
10:33
this toxicity uh and their cancer very
10:36
deadly type of a cancer uh goes away
10:38
more and more people will want to do
10:40
that and that it just takes time for the
10:43
the field to to come to recognize this
10:45
if you're doing radiation for brain
10:47
cancer and you know that it's actually
10:49
contributing to the death of the patient
10:50
and someone clearly told you that and
10:52
how it's happening how do you feel
10:53
continuing to do that it becomes a moral
10:56
question is it moral to treat somebody
10:59
with a therapy that you know will kill
11:00
them before you didn't know that you
11:02
thought you were doing good now the
11:04
evidence says by doing that you're going
11:06
to kill your patient how Okay so well
11:09
I'm going to do it anyway that's immoral
11:11
so then they have to deal with the moral
11:13
question what what are the reactions
Cancer is a Dogma
11:16
when you talk about this I mean among
11:17
the oncologists well they don't want to
11:19
hear about it it's like a religion okay
11:23
you how how hard would it be to tell um
11:27
a person who who is a devout uh
11:30
practices Islam devoutly and then you
11:34
tell him Judaism is the correct religion
11:36
do you think that guy is going to change
11:37
his religion no it's it's a Dogma it's a
11:41
a system belief so the idea that cancer
11:45
as a genetic disease has become a Dogma
11:47
dogmatic view in the brain it can't be
11:50
anything other I was trained from high
11:52
school College medical school all my
11:55
professors told me cancer is a genetic
11:57
disease the National Institutes a health
11:59
says it's a genetic disease therefore I
12:01
feel Justified doing what I'm doing even
12:04
though I see this other I can't accept
12:05
it even if it's right I can't accept it
12:08
because I'm dogmatically brainwashed
12:10
into thinking I'm indoctrinated to think
12:12
this is what it is so you have to break
12:14
I find indoctrination is more powerful
12:16
than most genes I mean when your brain
12:18
is solidified into a way of thinking
12:20
Some people would rather die than change
12:22
their political belief religious belief
12:25
or their belief in in a they're going to
12:26
fight tooth and nail to keep dogmatic
12:30
view
but in cancer you're
13:56
dealing with all these people that are
13:58
dying and suffering uffing So eventually
14:01
your dogic view is going to have to
14:02
change if you want to make a difference
14:04
in this in this in this world in in
14:06
treating this particular disease so it's
14:08
a treatable disease without toxicity
14:11
quite
14:11
costeffective get over it um it's going
14:15
to happen it's only if you're doing all
14:16
that it's only just holding back the
14:18
lives of these people you're preventing
14:20
people from living a better life you're
14:22
standing in the way of progress and the
14:24
progress we're making is just simply
14:26
going back and and and and modifying
14:30
what was already known and bringing it
14:32
into a more clear perspective so the
14:34
clarity of what warberg did we've
14:35
cleared up a lot of the misinformation
14:37
and the misunderstanding his theory was
14:39
correct the output of explaining his
14:41
theory was was not correct so we've
14:43
corrected that now we know and there
14:45
should be no reason to do anything other
14:48
than focusing on this because it works
14:50
and people can live a lot longer if not
14:52
having res complete resolution what
Chemotherapy Radiation
14:55
about chemotherapy and radiation doesn't
14:57
it do any good
15:00
well obviously had some I mean we have
15:01
what we call a lot of cancer survivors
15:04
so um we have millions of cancer
15:07
survivors who have taken radiation and
15:09
chemo uh and and by that they're alive
15:13
uh longer the pro the problem is is that
15:16
when your body is subjected to chemo and
15:18
radiation the cancer may not have
15:21
survived but you've damaged
15:23
significantly many organ systems so you
15:26
suffer from cardiovascular disease and
15:29
one of the one of the neuros psychiatric
15:31
impact of being subjected to those
15:34
chemicals is hor is is quite impactful
15:36
on a lot of people hormonal uh digestive
15:39
problems in other words you are
15:41
confronted with a new series of health
15:44
issues uh the cancer may not be there
15:46
but your body has been damaged and now
15:48
you become a patient for these different
15:50
kinds of uh of of problems that came as
15:54
the result of being exposed to highly
15:56
toxic uh chemicals and a prot es so
15:59
metabolic therapy is nice because not
16:02
only do you get rid of the cancer you
16:05
you also allow the body to heal itself
16:09
and become even more uh healthy in a lot
16:12
of different ways so you avoid all the
16:14
toxic effects that you would get from
16:16
those standards so yeah I mean they work
16:19
uh for a lot of people but you pay a
16:21
significant price your body play pays a
16:23
significant price in damage from
16:26
radiation and chemo and but everybody
16:28
says I'm so happy I can deal with with
16:31
um digestive issues with neuros psych
16:33
psychosis uh uh I'm so happy I'm still
16:36
alive uh but why don't we say well we
16:38
can keep you alive better and you won't
16:39
have to have any of that everybody would
16:42
want to do that why would they want to
16:43
subject their body to any kind of a
16:45
toxin if I knew there was another way to
16:46
do it and then all of a sudden we'll
16:48
look back in a hundred years and say I
16:52
can't believe we did all that crazy
16:54
stuff to those cancer patients you look
16:56
back and you say what profound lack of
16:58
knowledge when when there was a guy
17:00
warberg who actually had it
17:02
pegged the problem is is nobody hears
17:07
about it um because they're not being
17:10
published so what I do is I'm writing
17:11
case reports on individuals and showing
17:14
all the data and look what happens to
17:16
this patient look what happens to but
17:18
they're not oh well you need a big
17:19
clinical trial before I'll believe it so
17:21
you don't believe that all these people
17:23
could be real because there's not they
17:24
weren't part of a of a of a of a trial
17:28
now the problem with clinical trials is
17:31
you have a drug and no drug okay and
17:34
then you do switch over we take and we
17:36
double switch over well you're every
17:38
person in metabolic therapy is getting a
17:41
kind of a diet it's hard to say what are
17:44
you what kind of what are you getting
17:45
what kind of and then switching back and
17:47
forth is it is it moral to take a person
17:50
who's really managed cancer and switch
17:52
them back to the to a different kind of
17:54
a drug when they're already managed you
17:56
can't do that so we have to redesign the
17:58
way way clinical trials are done for
17:59
metabolic therapy you cannot use the
18:02
standard pharmaceutical approach for
18:04
doing CL I can't believe unless we do
18:06
this clinical trial dictated by
18:07
pharmaceutical companies no no no you
18:09
got to get rid of that you have a
18:10
different we we look at survivability
18:13
how long does the patient survive
18:15
relative to what the field has shown we
18:17
have so many survival curves for all
18:19
these different Cancers and if we can
18:21
push that down double three four times
18:23
survival you're telling me that that
18:25
that's that we can't use that data
18:27
because it wasn't done by a traditional
18:29
type of clinical trial I mean this is
18:31
nonsense complete nonsense so you have
18:34
to then reestablish how we're going to
18:36
do new clinical trials for it and then
18:38
will they use it even after you do all
18:40
this and the answer is we don't know so
18:43
the origin of cancer is mitochondrial
18:45
damage how does that happen from any
18:46
number of different things in the in in
18:48
your own body or in the environment any
18:50
all leading down the same path so we put
18:53
it all together and there's I did all
18:55
this research I tracked down every one
18:57
of these risk factors and find out what
18:59
did they do they all damaged the
19:00
mitochondria not a mystery if you read
19:02
the literature and you understand the
19:04
scientific literature what I'm saying is
19:06
not mysterious it's there in the
19:08
literature just people don't they don't
19:10
know about it I I try to publish the
19:11
books I try to do everything I mean what
19:13
are you going to do grab somebody s you
19:15
I
19:17
mean so uh um they don't
19:21
recognize uh cancer as a metabolic
19:23
disease when you realize that it's a
19:25
metabolic disease and the mutations in
19:27
the cancer cell prevented from being
19:29
they're they're locked into a very tight
19:31
fermentation if you can't ferment
19:33
they're going to be dead and they don't
19:34
have the ability to adapt like the
19:35
normal cells have it all goes back to
19:37
evolutionary biology if you don't
19:40
understand evolutionary biology you do
19:41
very stupid things okay like imuno
19:44
therapy very stupid so uh um and you do
19:47
all these crazy things because you don't
19:49
understand evolutionary biology what are
19:50
you supposed to do you know and the
19:52
unfortunately the field doesn't they
19:53
look at you're like you might as well be
19:55
talking to a plug socket because they
19:57
don't even know what the hell you're
19:58
talking talking about so uh um I'm tell
20:00
it's terrible right all these guys they
20:03
talk like they know what they're doing
20:04
You Don't Know Jack if they knew what
20:05
they doing why are they doing this crazy
20:07
stuff to these poor cancer patients so
20:09
you see how it all comes together it's
20:11
all comes together because I understand
20:13
evolutionary biology and when you
20:16
understand that you know how to uh
20:17
that's so many nice ways we can kill
20:20
cancer cells without toxicity you just
20:22
exploit their weakness their metabolic
20:24
weakness and when you realize how many
20:26
ways we can kill cancer cells without
20:27
tox toity it's just so almost infinite
20:31
once you understand the system so it
Metastasis
20:33
just takes time uh that's another thing
20:35
metastasis which is the singular most
20:38
complicating factor of cancer because if
20:40
all tumors grew in place we would have
20:43
uh we would just cut your arm off or cut
20:45
whatever and it's gone but it spreads so
20:48
uh how does it spread what's going on
20:49
with the spread so what we discovered
20:52
was an interesting kind of cancer in the
20:55
mouse it came out of the brain
20:56
spontaneously but when we put it put it
20:58
in the flank it spread like wildfire
20:59
throughout the whole the whole body of
21:01
the
21:02
Mouse um and then it took us 10 years of
21:07
vigorous constant research what kind of
21:10
a cell what is that cell what kind of a
21:13
cell is this thing that spreads all over
21:15
the body uh because this is what is
21:18
responsible for the majority of cancer
21:19
deaths um so we found out that it was a
21:23
biological it was a maccrage a micral
21:25
cell which is derived from macras is in
21:28
the brain it's a localized thing so
21:31
maccrage huh wow that's macras is are
21:35
the only cell that can move in and out
21:37
of our tissues so we have resident
21:39
macrofagos in all of our cells they're
21:42
residents they're like a police
21:43
department and then we have white blood
21:45
cells circulating through our
21:46
bloodstream and that's like the the army
21:48
so when you have a stab wound white
21:51
blood cells come out of the blood and
21:53
they transform into these macrofagos and
21:55
they're there to kill bacteria clean up
21:57
the wound they're very fusogenic they
21:59
fuse together to to to work and heal the
22:02
wound in the cancer what we have is that
22:05
there's a inflammatory group of cells
22:08
like chronic inflammation hypoxia
22:10
whatever causing what looks like a wound
22:12
to the body so the the body sends in the
22:15
immune system uh if the local guys can't
22:17
handle the immune system and they now
22:20
they throw out growth factors and cyto
22:22
kindes to heal the wound and what that
22:24
does to the to a cancer cell like a stem
22:27
cell doesn't have the capacity it just
22:30
grows in place um it makes them grow
22:32
more so these immune cells fuse they
22:35
fuse together with these other kinds of
22:38
destabilized cancer cells that have M
22:41
mitochondrial abnormality and they're
22:43
growing this but they can't spread
22:45
they're not but this cell has the
22:47
genetic apparatus to already move in and
22:50
out of tissue so when that cell fuses
22:52
with this other cell now you get
22:54
destabilized mitochondria in a cell
22:57
that's programmed so it becomes a rogue
22:59
macres moving in and out of the cells
23:02
wow this is like
23:04
unbelievable so how do I know this why
23:07
would I tell you this if I didn't know
23:09
what I was talking about so we went
23:11
through every major cancer that we know
23:13
of and examined genetic readouts of
23:16
maccrage products every major human
23:19
cancer has all of these characteristics
23:22
of macrofagos so they all started from
23:25
this procedure John the late John po
23:28
University was screaming at the top of
23:29
his lungs this is a fusion hybridization
23:32
between macrofagos and St cancer stem
23:34
cells producing this metastatic cell
23:36
that can now readily spread throughout
23:38
the body so after we made this discovery
23:41
that nobody believes because they're
23:42
locked into this mindless genetic
23:45
thinking so first thing is say what do
23:49
macrofagos eat what's their fuel what do
23:52
they do they well they'll eat anything
23:54
but they gobble up stuff and they bring
23:56
it to their lome and then they can get
23:58
energy from what they do but one of
24:00
their Prime fuels is glutamine
24:02
macrofagos in the immune system are
24:03
driven by glutamine aha so then we found
24:07
they're fermenting the damn glutamine so
24:09
now we know how to kill metastatic
24:11
cancer cells you take away the glucose
24:12
and the glutamine and we've shown this
24:15
so everything comes back to knowing the
24:17
biology of the problem and what cells
24:19
are eating what they eat and what their
24:21
biology is and how do you put all that
24:23
together and you can come up with a
24:25
clear idea of what cancer is and how to
24:27
manage it
24:28
uh very
24:29
successfully what's wrong with this why
24:32
can't anybody understand this well the
24:35
money issue is something but eventually
24:37
the people want to live and and uh so I
24:40
just defined to you the strategy and
24:43
believe me it's going to happen because
24:45
we can't keep our head in the sand for
24:46
too long it's one of the great tragedies
24:48
in the history of medicine and sometimes
24:51
you have to take a little levity and you
24:53
have to realize how incredibly
24:55
disconnected we are uh from from knowing
24:58
how to do things when the when the when
25:00
the when the solution is staring you in
25:02
the face and you choose not to use it
25:04
that's tragic that's tragic so uh yeah I
25:08
mean I mean what am I going to do but
25:10
what you uh I see it and I have I have I
25:15
have a voice and that voice is in SC
25:18
peer-reviewed scientific Publications
25:20
participation on on on journals
25:22
editorial boards I have the knowledge I
25:25
do the research I can communicate the
25:27
research we have patients that are
25:29
surviving this is evidence so I'm not
25:32
some lunatic I have hard evidence that
25:35
supports everything that I'm saying let
25:37
the P let the public choose to accept it
25:39
or not so there has to be some public
25:41
outrage it's never going to come from
25:43
the hospitals it's not going to come
25:45
from the pharmaceutical companies it's
25:46
got to come from the people just like Dr
25:49
Ral was saying the people must be
25:51
educated to know that there is a viable
25:54
scientifically established alternative
25:56
to this crazy stuff that they're doing
25:58
at the top medical schools and once the
26:00
patients once the people realize that
26:02
you're going to start to seeing things
26:03
happen because nobody wants to go
26:05
through this kind of crazy stuff so when
26:07
they say we've made um big big progress
26:11
in stopping cancer they always go back
26:13
to the
26:14
1991 when when cancer was on a really
26:17
rocket rise because the smoking so now
26:20
they stop smoking cancer goes down so
26:23
today we're seeing a rise of cancer but
26:25
they say look how much better we did
26:27
well we stop smoking all the all the
26:29
major advances in cancer come from
26:31
prevention not from treatment treatment
26:34
has been an abysmal failure for the most
26:36
part so so it's it's changing in
26:38
Behavior so if you change your diet and
26:41
lifestyle and and you can certainly
26:43
manage cancer prevent it but I don't
26:46
think people want to change their diet
26:48
lifestyle until they get cancer once
26:50
they get cancer then they're they know
26:52
that they're they're going to have to do
26:53
something so then that's when it happens
26:56
but um but but yeah the smoking CA
26:58
anti-smoking campaign is largely
27:00
responsible for the perceived advances
27:04
in cancer it's all prevention very
27:06
little very very little to do with
27:07
treatments or diagnosis and all this
27:09
kind of stuff so uh um and they already
27:12
know some of these diagnostic breast
27:14
mammograms they can put people at risk
27:16
for for further uh spread biopsies and
27:19
all this kind of crazy stuff that
27:21
they're doing is why are you doing a
27:23
biopsy oh I have to know if you have
27:24
stage one or stage two or stage three
27:26
well if you had stage three you would
27:28
never want to stick it and if you have
27:30
stage one you stick it it could become a
27:31
stage two or three why are you doing
27:33
that well we do it because we were
27:34
trained to do it would you ever think
27:36
about I didn't know about that I you
27:38
read the damn literature for Christ's
27:39
sake these people don't read the
27:41
scientific literature to show what
27:42
they're doing to put these people at
27:44
risk I can't tell you how many oncolog I
27:46
did a big interview with um Peter AA he
27:50
said Tom you shouldn't be saying things
27:51
like this not science what do you mean
27:52
Peter I said for Christ sake do you read
27:54
the the literature well I didn't see
27:55
those articles well I'll share them with
27:57
you I have a whole slug of them
27:58
published in the top medical journals
28:00
biopsy spread cancer so what are you
28:02
doing that
28:03
for you know this is nuts in so many
28:08
levels it's complete nuts and it's not
28:11
getting better it's getting worse so it
28:13
be one thing to say ah C fre you know
28:15
we're Cancer's already we're doing
28:16
really well you I I think you know let's
28:18
just go let's stay the course are you
28:20
kidding me let's taking over it's
28:22
replacing heart disease as the number
28:23
one killer of people on the planet
28:25
millions and millions of people are
28:26
dying from cancer and it doesn't have to
28:29
happen
Transcript
The role of the mitochondrial in cancer
0:00
so Thomas can you please tell me the
0:03
role that the mitochondri play in the
0:06
development of cancer they they are a
0:10
second living living organism inside a
0:13
cell um they're actually have their own
0:15
genetic material and they are the
0:18
organel that breathes the air to make
0:20
the energy so um and what warberg found
0:25
was that all normal cells uh have these
0:28
um organel that take in the oxygen um
0:32
and the cancer cells have a defect in
0:35
that in that organel so uh they take in
0:38
less oxygen and they produce uh lactic
0:41
acid which is an exam which is a waste
0:43
product of glucose fermentation they
0:46
call it lactic acid fermentation and
0:49
that proves clearly that these tumor
0:51
cells are are not getting energy through
0:53
any kind of an oxidative mechanism so as
0:57
long as they have the fuel to continue
0:59
their ferment ation they will survive so
1:03
all cancer cells and every one that
1:04
we've looked at they have damage in
1:06
their structure of that organel that
1:09
means that all cancer cells regardless
1:12
of what you want to call them are all
1:13
fermentors they're using a ancient
1:15
fermentation Pathway to survive so that
1:19
means that there's a very simple way to
1:20
kill them you just have to take away
1:22
their fermentation energy and uh feed
1:25
them things that they can't they can't
1:27
use fatty acids and Ketone bodies are
1:30
not fermentable you they're un you need
1:33
uh oxygen to get energy from Ketone
1:35
bodies and and cancer cells don't use
1:38
oxygen so it's a very clear way to kill
1:40
the majority of cancer cells and then
1:43
the amino acid is also glutamine is also
1:46
the second fermentable fuel uh uh
The importance of glutamine
1:48
glutamine is the most abundant amino
1:50
acid in our body it's everywhere um so
1:53
in order to imp and besides our immune
1:56
system needs glutamine our Ura cycle
1:59
needs glutamine
2:00
our dig gut cells all depend on
2:03
glutamine um so if you go too
2:05
aggressively on attacking glutamine you
2:08
also can cause metabolic disturbances in
2:10
the body so that's why we developed the
2:12
Press pulse theory of of of strategy we
2:16
can control glucose constantly because
2:19
glucose is a non-essential metabolite
2:21
our body does not need glucose we can
2:24
make glucose from within at very low
2:26
concentrations but the glutamine issue
2:28
you have to get get the body into a
2:31
ketotic state and then we hit the
2:33
glutamine just briefly boom weit bing so
2:36
it's pulsed it's like a pulsing and that
2:39
just oh I have a few cancer cells here
2:41
they go down okay then we let the
2:43
glutamine come back but not too many
2:44
come back just a little bit then they
2:46
hit down come back a little bit hit down
2:48
and the next thing you know gone so um
2:51
again you have to use knowledge of of
2:54
what how do we kill cancer cells without
2:56
harming the normal cells and that's the
2:58
strategy that we're developing Ving as
3:00
dosage timing and scheduling that's
3:02
where we are now we're perfecting dosage
3:05
timing and scheduling and once we have
3:07
those conditions perfected or uh
3:10
modified we'll be able to manage the
3:11
majority of cancers with with minimal
3:13
minimal effort but we're right there at
3:16
that at that point so we do everything
3:18
pre-clinically in my lab I have the best
3:21
pre-clinical models of cancer G blastoma
3:24
system systemic metastatic cancer the
3:27
very types of cancers that we see in
3:29
humans so we can practice on all this in
3:31
the preclinical system and once we see
3:34
what works really well we go right to
3:36
the clinic with it and my physician
3:38
colleagues tell me whoa I did I did what
3:41
you said we're working out different
3:42
slightly different dosages and timing
3:44
but this but the results are really
3:45
quite remarkable so that's how it works
3:48
I I develop the concepts I test the the
3:51
the pre-clinical system and then we
3:53
translate there are very few people on
3:55
the planet doing what I do it's because
3:57
I have the best models and I have the
4:00
concepts and I have uh willing uh
4:02
participants Physicians that are willing
4:04
to try this many of them realized that
4:07
what they were doing in the past is not
4:08
working they're harming their patients
How cancer cells get their energy
4:10
so all major cancers are similar in
4:14
having uh Reliance on a fermentation
4:17
metabolism to survive without energy
4:21
nothing can grow so where do these cells
4:24
get their energy from how do they get
4:25
their energy once you understand how the
4:27
cancer cell gets energy
4:30
um then you can Target that and they'll
4:33
die it's not that complicated oh can we
4:36
kill cancer cells if we take away their
4:38
fermentation yes what do they ferment
4:41
they ferment glucose and the amino acid
4:44
glutamine so if we take away glucose and
4:46
glutamine they should die and the answer
4:49
is yes they will die so um and they
4:53
can't burn fatty acids or ketones so the
4:55
solution to the cancer problem
4:58
becomes
5:01
recognized so why nobody is doing this
5:04
so and in fact when I say that one of
5:07
the
5:08
problems people think it's too simple um
5:12
people want things to be complicated so
5:14
nothing can make a simple condition more
5:17
complicated than saying that gene
5:19
mutations are responsible for this
5:21
disease because it's infinitely
5:23
complicated and people think oh yeah you
5:25
know so we're going to use all these
5:26
strategies because cancer is such a
5:28
complicated disease and when I tell them
5:30
no it's very simple you can just kill it
5:32
by taking away I can't believe it it's
5:34
too simple warberg had the same problem
5:36
they said it was too simple people don't
5:38
want Simplicity they want they want
5:41
complicated stuff when it comes to oh
5:43
you know I have to go through this and I
5:44
have to go through that so how do you
5:46
break through this I don't know
5:47
conceptually and theoretically it's not
5:50
that complicated but practically to
5:52
manage cancer uh it does require
5:56
knowledge about how you will in fact
5:58
lower those two fuels
6:00
um which then becomes responsible of the
6:03
patient it's it's you know it's funny to
6:06
me um people sometimes have this
6:08
attitude that I have this terrible
6:12
disease maybe it was caused by God or
6:15
something maybe I did some bad things so
6:18
I'm going to take chemo and radiation
6:19
and I'm going to suffer and because I
6:22
suffer it should get rid of my cancer
6:24
because suffering is kind of like the
6:26
the the the penalty you have to pay or
6:28
something along these lines but then you
6:30
come along and say well the concept is
6:32
not that complicated but when you stop
6:35
eating for a week you feel like you're
6:37
really suffering because our brains are
6:38
addicted to glucose so once you get
6:41
through the glucose addiction actually
6:43
the management of the cancer becomes so
6:44
much better so um so we have to transfer
6:48
this idea of painful suffering from
6:51
toxic poisons into a self self-directed
6:55
uh uh reduction of food intake um or
6:58
taking diets that lower glucose uh and
7:02
Elevate Ketone body so the cancer can be
7:04
better managed so what should we eat
What should we eat
7:06
more of and what should we eat less of
7:10
well I think the bet the the basic thing
7:11
is eat is eat less of of everything you
7:14
might be eating um because that that the
7:18
the best way or but when you tell people
7:20
to get rid of their cancer that you have
7:22
to stop eating for a month they think
7:23
you're crazy um oh well this guy's got
7:26
must be nuts who can stop eating for a
7:28
month many people feel that if they stop
7:29
eating for 3 days they're going to be
7:31
dead this is how little knowledge we
7:33
have of of our incredible capabilities
7:35
of living on the planet without eating
7:38
but we're trying to make water only
7:40
fasting which will kill cancer cells
7:41
quite effectively uh um more more
7:44
reasonable with a with a diet that is
7:47
palatable nutritious and um uh will
7:52
lower the blood sugar and and Elevate
7:54
the ketones so we say we developed the
7:57
glucose Ketone index count calculator to
8:00
allow people to know if they're in a
8:02
zone for killing cancer cells so they
8:04
always ask me what can I eat um and I
8:07
say well eat anything you want and then
8:11
check your GK glucose Ketone index if it
8:13
throws makes the glucose Ketone index I
8:15
don't eat that so only you'll every
8:18
person will find their balance amount
8:20
they should eat and what they should eat
8:21
to keep the ratio down and that number
8:24
will tell you that you're killing cancer
8:25
cells so how do I know if it's working
8:28
it always works when you're in the that
8:29
zone oh I can't get into that zone I've
8:32
done everything I can I can't get down
8:34
to 2.0 or below oh what do you I'm
8:36
eating this me I said well don't eat any
8:38
of that just drink water and see oh it
8:40
went right down okay now add back the
8:42
foods that will keep you in that zone
8:43
without throwing you out of so it's it's
8:45
an experiment on each individual and
8:47
they experiment what they can and cannot
8:49
eat how much they should eat and how
8:50
much they can't eat so that's all worked
8:53
out for individual people and they keep
8:55
their records they keep a log of all
8:56
this so it's like a diabetic you can't
8:58
eat that can't eat this I'm keeping my
9:00
blood sugar low so it it all it all
9:02
works from the
9:05
individual so tell me why is it that uh
Otto Warberg
9:08
the work that Otto warberg did that we
9:11
didn't continue in that path OT warberg
9:14
knew what the origin of cancer was the
9:17
problem is his quantification of lactic
9:20
acid and oxygen consumption was um uh
9:25
misunderstood uh this is an extremely
9:28
important Point uh I'm preparing a
9:32
publication to uh show how OT warberg
9:36
and the entire uh uh field of cancer at
9:40
that time uh were uh were
9:44
misinterpreting their observations so we
9:47
just have taken warberg concept polished
9:49
it all up and now can explain clearly
9:52
what the origin of cancer is once this
9:54
the cancer field comes to understand
9:56
this then they have no choice but to
9:58
Target GL glucose and glutamine
9:59
simultaneously it becomes the obvious
10:02
and clear pathway for managing all
10:05
cancers and this is another thing that
10:06
gets everybody all upset they think
10:08
breast cancer is different from colon
10:10
cancer different from brain they're all
10:11
very very similar they need those fuels
10:14
to grow they can't use oxygen that's the
10:16
similarity they're all genetically
10:18
different they look different under the
10:20
microscope but they're all similar they
10:22
need fermentation Target the
10:24
fermentation and you can manage this
10:26
disease so that's the B when you get
10:28
enough people that respond well healthy
10:31
didn't lose their hair didn't get all
10:33
this toxicity uh and their cancer very
10:36
deadly type of a cancer uh goes away
10:38
more and more people will want to do
10:40
that and that it just takes time for the
10:43
the field to to come to recognize this
10:45
if you're doing radiation for brain
10:47
cancer and you know that it's actually
10:49
contributing to the death of the patient
10:50
and someone clearly told you that and
10:52
how it's happening how do you feel
10:53
continuing to do that it becomes a moral
10:56
question is it moral to treat somebody
10:59
with a therapy that you know will kill
11:00
them before you didn't know that you
11:02
thought you were doing good now the
11:04
evidence says by doing that you're going
11:06
to kill your patient how Okay so well
11:09
I'm going to do it anyway that's immoral
11:11
so then they have to deal with the moral
11:13
question what what are the reactions
Cancer is a Dogma
11:16
when you talk about this I mean among
11:17
the oncologists well they don't want to
11:19
hear about it it's like a religion okay
11:23
you how how hard would it be to tell um
11:27
a person who who is a devout uh
11:30
practices Islam devoutly and then you
11:34
tell him Judaism is the correct religion
11:36
do you think that guy is going to change
11:37
his religion no it's it's a Dogma it's a
11:41
a system belief so the idea that cancer
11:45
as a genetic disease has become a Dogma
11:47
dogmatic view in the brain it can't be
11:50
anything other I was trained from high
11:52
school College medical school all my
11:55
professors told me cancer is a genetic
11:57
disease the National Institutes a health
11:59
says it's a genetic disease therefore I
12:01
feel Justified doing what I'm doing even
12:04
though I see this other I can't accept
12:05
it even if it's right I can't accept it
12:08
because I'm dogmatically brainwashed
12:10
into thinking I'm indoctrinated to think
12:12
this is what it is so you have to break
12:14
I find indoctrination is more powerful
12:16
than most genes I mean when your brain
12:18
is solidified into a way of thinking
12:20
Some people would rather die than change
12:22
their political belief religious belief
12:25
or their belief in in a they're going to
12:26
fight tooth and nail to keep dogmatic
12:30
view
but in cancer you're
13:56
dealing with all these people that are
13:58
dying and suffering uffing So eventually
14:01
your dogic view is going to have to
14:02
change if you want to make a difference
14:04
in this in this in this world in in
14:06
treating this particular disease so it's
14:08
a treatable disease without toxicity
14:11
quite
14:11
costeffective get over it um it's going
14:15
to happen it's only if you're doing all
14:16
that it's only just holding back the
14:18
lives of these people you're preventing
14:20
people from living a better life you're
14:22
standing in the way of progress and the
14:24
progress we're making is just simply
14:26
going back and and and and modifying
14:30
what was already known and bringing it
14:32
into a more clear perspective so the
14:34
clarity of what warberg did we've
14:35
cleared up a lot of the misinformation
14:37
and the misunderstanding his theory was
14:39
correct the output of explaining his
14:41
theory was was not correct so we've
14:43
corrected that now we know and there
14:45
should be no reason to do anything other
14:48
than focusing on this because it works
14:50
and people can live a lot longer if not
14:52
having res complete resolution what
Chemotherapy Radiation
14:55
about chemotherapy and radiation doesn't
14:57
it do any good
15:00
well obviously had some I mean we have
15:01
what we call a lot of cancer survivors
15:04
so um we have millions of cancer
15:07
survivors who have taken radiation and
15:09
chemo uh and and by that they're alive
15:13
uh longer the pro the problem is is that
15:16
when your body is subjected to chemo and
15:18
radiation the cancer may not have
15:21
survived but you've damaged
15:23
significantly many organ systems so you
15:26
suffer from cardiovascular disease and
15:29
one of the one of the neuros psychiatric
15:31
impact of being subjected to those
15:34
chemicals is hor is is quite impactful
15:36
on a lot of people hormonal uh digestive
15:39
problems in other words you are
15:41
confronted with a new series of health
15:44
issues uh the cancer may not be there
15:46
but your body has been damaged and now
15:48
you become a patient for these different
15:50
kinds of uh of of problems that came as
15:54
the result of being exposed to highly
15:56
toxic uh chemicals and a prot es so
15:59
metabolic therapy is nice because not
16:02
only do you get rid of the cancer you
16:05
you also allow the body to heal itself
16:09
and become even more uh healthy in a lot
16:12
of different ways so you avoid all the
16:14
toxic effects that you would get from
16:16
those standards so yeah I mean they work
16:19
uh for a lot of people but you pay a
16:21
significant price your body play pays a
16:23
significant price in damage from
16:26
radiation and chemo and but everybody
16:28
says I'm so happy I can deal with with
16:31
um digestive issues with neuros psych
16:33
psychosis uh uh I'm so happy I'm still
16:36
alive uh but why don't we say well we
16:38
can keep you alive better and you won't
16:39
have to have any of that everybody would
16:42
want to do that why would they want to
16:43
subject their body to any kind of a
16:45
toxin if I knew there was another way to
16:46
do it and then all of a sudden we'll
16:48
look back in a hundred years and say I
16:52
can't believe we did all that crazy
16:54
stuff to those cancer patients you look
16:56
back and you say what profound lack of
16:58
knowledge when when there was a guy
17:00
warberg who actually had it
17:02
pegged the problem is is nobody hears
17:07
about it um because they're not being
17:10
published so what I do is I'm writing
17:11
case reports on individuals and showing
17:14
all the data and look what happens to
17:16
this patient look what happens to but
17:18
they're not oh well you need a big
17:19
clinical trial before I'll believe it so
17:21
you don't believe that all these people
17:23
could be real because there's not they
17:24
weren't part of a of a of a of a trial
17:28
now the problem with clinical trials is
17:31
you have a drug and no drug okay and
17:34
then you do switch over we take and we
17:36
double switch over well you're every
17:38
person in metabolic therapy is getting a
17:41
kind of a diet it's hard to say what are
17:44
you what kind of what are you getting
17:45
what kind of and then switching back and
17:47
forth is it is it moral to take a person
17:50
who's really managed cancer and switch
17:52
them back to the to a different kind of
17:54
a drug when they're already managed you
17:56
can't do that so we have to redesign the
17:58
way way clinical trials are done for
17:59
metabolic therapy you cannot use the
18:02
standard pharmaceutical approach for
18:04
doing CL I can't believe unless we do
18:06
this clinical trial dictated by
18:07
pharmaceutical companies no no no you
18:09
got to get rid of that you have a
18:10
different we we look at survivability
18:13
how long does the patient survive
18:15
relative to what the field has shown we
18:17
have so many survival curves for all
18:19
these different Cancers and if we can
18:21
push that down double three four times
18:23
survival you're telling me that that
18:25
that's that we can't use that data
18:27
because it wasn't done by a traditional
18:29
type of clinical trial I mean this is
18:31
nonsense complete nonsense so you have
18:34
to then reestablish how we're going to
18:36
do new clinical trials for it and then
18:38
will they use it even after you do all
18:40
this and the answer is we don't know so
18:43
the origin of cancer is mitochondrial
18:45
damage how does that happen from any
18:46
number of different things in the in in
18:48
your own body or in the environment any
18:50
all leading down the same path so we put
18:53
it all together and there's I did all
18:55
this research I tracked down every one
18:57
of these risk factors and find out what
18:59
did they do they all damaged the
19:00
mitochondria not a mystery if you read
19:02
the literature and you understand the
19:04
scientific literature what I'm saying is
19:06
not mysterious it's there in the
19:08
literature just people don't they don't
19:10
know about it I I try to publish the
19:11
books I try to do everything I mean what
19:13
are you going to do grab somebody s you
19:15
I
19:17
mean so uh um they don't
19:21
recognize uh cancer as a metabolic
19:23
disease when you realize that it's a
19:25
metabolic disease and the mutations in
19:27
the cancer cell prevented from being
19:29
they're they're locked into a very tight
19:31
fermentation if you can't ferment
19:33
they're going to be dead and they don't
19:34
have the ability to adapt like the
19:35
normal cells have it all goes back to
19:37
evolutionary biology if you don't
19:40
understand evolutionary biology you do
19:41
very stupid things okay like imuno
19:44
therapy very stupid so uh um and you do
19:47
all these crazy things because you don't
19:49
understand evolutionary biology what are
19:50
you supposed to do you know and the
19:52
unfortunately the field doesn't they
19:53
look at you're like you might as well be
19:55
talking to a plug socket because they
19:57
don't even know what the hell you're
19:58
talking talking about so uh um I'm tell
20:00
it's terrible right all these guys they
20:03
talk like they know what they're doing
20:04
You Don't Know Jack if they knew what
20:05
they doing why are they doing this crazy
20:07
stuff to these poor cancer patients so
20:09
you see how it all comes together it's
20:11
all comes together because I understand
20:13
evolutionary biology and when you
20:16
understand that you know how to uh
20:17
that's so many nice ways we can kill
20:20
cancer cells without toxicity you just
20:22
exploit their weakness their metabolic
20:24
weakness and when you realize how many
20:26
ways we can kill cancer cells without
20:27
tox toity it's just so almost infinite
20:31
once you understand the system so it
Metastasis
20:33
just takes time uh that's another thing
20:35
metastasis which is the singular most
20:38
complicating factor of cancer because if
20:40
all tumors grew in place we would have
20:43
uh we would just cut your arm off or cut
20:45
whatever and it's gone but it spreads so
20:48
uh how does it spread what's going on
20:49
with the spread so what we discovered
20:52
was an interesting kind of cancer in the
20:55
mouse it came out of the brain
20:56
spontaneously but when we put it put it
20:58
in the flank it spread like wildfire
20:59
throughout the whole the whole body of
21:01
the
21:02
Mouse um and then it took us 10 years of
21:07
vigorous constant research what kind of
21:10
a cell what is that cell what kind of a
21:13
cell is this thing that spreads all over
21:15
the body uh because this is what is
21:18
responsible for the majority of cancer
21:19
deaths um so we found out that it was a
21:23
biological it was a maccrage a micral
21:25
cell which is derived from macras is in
21:28
the brain it's a localized thing so
21:31
maccrage huh wow that's macras is are
21:35
the only cell that can move in and out
21:37
of our tissues so we have resident
21:39
macrofagos in all of our cells they're
21:42
residents they're like a police
21:43
department and then we have white blood
21:45
cells circulating through our
21:46
bloodstream and that's like the the army
21:48
so when you have a stab wound white
21:51
blood cells come out of the blood and
21:53
they transform into these macrofagos and
21:55
they're there to kill bacteria clean up
21:57
the wound they're very fusogenic they
21:59
fuse together to to to work and heal the
22:02
wound in the cancer what we have is that
22:05
there's a inflammatory group of cells
22:08
like chronic inflammation hypoxia
22:10
whatever causing what looks like a wound
22:12
to the body so the the body sends in the
22:15
immune system uh if the local guys can't
22:17
handle the immune system and they now
22:20
they throw out growth factors and cyto
22:22
kindes to heal the wound and what that
22:24
does to the to a cancer cell like a stem
22:27
cell doesn't have the capacity it just
22:30
grows in place um it makes them grow
22:32
more so these immune cells fuse they
22:35
fuse together with these other kinds of
22:38
destabilized cancer cells that have M
22:41
mitochondrial abnormality and they're
22:43
growing this but they can't spread
22:45
they're not but this cell has the
22:47
genetic apparatus to already move in and
22:50
out of tissue so when that cell fuses
22:52
with this other cell now you get
22:54
destabilized mitochondria in a cell
22:57
that's programmed so it becomes a rogue
22:59
macres moving in and out of the cells
23:02
wow this is like
23:04
unbelievable so how do I know this why
23:07
would I tell you this if I didn't know
23:09
what I was talking about so we went
23:11
through every major cancer that we know
23:13
of and examined genetic readouts of
23:16
maccrage products every major human
23:19
cancer has all of these characteristics
23:22
of macrofagos so they all started from
23:25
this procedure John the late John po
23:28
University was screaming at the top of
23:29
his lungs this is a fusion hybridization
23:32
between macrofagos and St cancer stem
23:34
cells producing this metastatic cell
23:36
that can now readily spread throughout
23:38
the body so after we made this discovery
23:41
that nobody believes because they're
23:42
locked into this mindless genetic
23:45
thinking so first thing is say what do
23:49
macrofagos eat what's their fuel what do
23:52
they do they well they'll eat anything
23:54
but they gobble up stuff and they bring
23:56
it to their lome and then they can get
23:58
energy from what they do but one of
24:00
their Prime fuels is glutamine
24:02
macrofagos in the immune system are
24:03
driven by glutamine aha so then we found
24:07
they're fermenting the damn glutamine so
24:09
now we know how to kill metastatic
24:11
cancer cells you take away the glucose
24:12
and the glutamine and we've shown this
24:15
so everything comes back to knowing the
24:17
biology of the problem and what cells
24:19
are eating what they eat and what their
24:21
biology is and how do you put all that
24:23
together and you can come up with a
24:25
clear idea of what cancer is and how to
24:27
manage it
24:28
uh very
24:29
successfully what's wrong with this why
24:32
can't anybody understand this well the
24:35
money issue is something but eventually
24:37
the people want to live and and uh so I
24:40
just defined to you the strategy and
24:43
believe me it's going to happen because
24:45
we can't keep our head in the sand for
24:46
too long it's one of the great tragedies
24:48
in the history of medicine and sometimes
24:51
you have to take a little levity and you
24:53
have to realize how incredibly
24:55
disconnected we are uh from from knowing
24:58
how to do things when the when the when
25:00
the when the solution is staring you in
25:02
the face and you choose not to use it
25:04
that's tragic that's tragic so uh yeah I
25:08
mean I mean what am I going to do but
25:10
what you uh I see it and I have I have I
25:15
have a voice and that voice is in SC
25:18
peer-reviewed scientific Publications
25:20
participation on on on journals
25:22
editorial boards I have the knowledge I
25:25
do the research I can communicate the
25:27
research we have patients that are
25:29
surviving this is evidence so I'm not
25:32
some lunatic I have hard evidence that
25:35
supports everything that I'm saying let
25:37
the P let the public choose to accept it
25:39
or not so there has to be some public
25:41
outrage it's never going to come from
25:43
the hospitals it's not going to come
25:45
from the pharmaceutical companies it's
25:46
got to come from the people just like Dr
25:49
Ral was saying the people must be
25:51
educated to know that there is a viable
25:54
scientifically established alternative
25:56
to this crazy stuff that they're doing
25:58
at the top medical schools and once the
26:00
patients once the people realize that
26:02
you're going to start to seeing things
26:03
happen because nobody wants to go
26:05
through this kind of crazy stuff so when
26:07
they say we've made um big big progress
26:11
in stopping cancer they always go back
26:13
to the
26:14
1991 when when cancer was on a really
26:17
rocket rise because the smoking so now
26:20
they stop smoking cancer goes down so
26:23
today we're seeing a rise of cancer but
26:25
they say look how much better we did
26:27
well we stop smoking all the all the
26:29
major advances in cancer come from
26:31
prevention not from treatment treatment
26:34
has been an abysmal failure for the most
26:36
part so so it's it's changing in
26:38
Behavior so if you change your diet and
26:41
lifestyle and and you can certainly
26:43
manage cancer prevent it but I don't
26:46
think people want to change their diet
26:48
lifestyle until they get cancer once
26:50
they get cancer then they're they know
26:52
that they're they're going to have to do
26:53
something so then that's when it happens
26:56
but um but but yeah the smoking CA
26:58
anti-smoking campaign is largely
27:00
responsible for the perceived advances
27:04
in cancer it's all prevention very
27:06
little very very little to do with
27:07
treatments or diagnosis and all this
27:09
kind of stuff so uh um and they already
27:12
know some of these diagnostic breast
27:14
mammograms they can put people at risk
27:16
for for further uh spread biopsies and
27:19
all this kind of crazy stuff that
27:21
they're doing is why are you doing a
27:23
biopsy oh I have to know if you have
27:24
stage one or stage two or stage three
27:26
well if you had stage three you would
27:28
never want to stick it and if you have
27:30
stage one you stick it it could become a
27:31
stage two or three why are you doing
27:33
that well we do it because we were
27:34
trained to do it would you ever think
27:36
about I didn't know about that I you
27:38
read the damn literature for Christ's
27:39
sake these people don't read the
27:41
scientific literature to show what
27:42
they're doing to put these people at
27:44
risk I can't tell you how many oncolog I
27:46
did a big interview with um Peter AA he
27:50
said Tom you shouldn't be saying things
27:51
like this not science what do you mean
27:52
Peter I said for Christ sake do you read
27:54
the the literature well I didn't see
27:55
those articles well I'll share them with
27:57
you I have a whole slug of them
27:58
published in the top medical journals
28:00
biopsy spread cancer so what are you
28:02
doing that
28:03
for you know this is nuts in so many
28:08
levels it's complete nuts and it's not
28:11
getting better it's getting worse so it
28:13
be one thing to say ah C fre you know
28:15
we're Cancer's already we're doing
28:16
really well you I I think you know let's
28:18
just go let's stay the course are you
28:20
kidding me let's taking over it's
28:22
replacing heart disease as the number
28:23
one killer of people on the planet
28:25
millions and millions of people are
28:26
dying from cancer and it doesn't have to
28:29
happen
STR is krapp -- & GTR is mostly krapp.
The present Einsteinian Dark Age of science will soon end – for the times they are a-changin'.
The aether will return – it never left.
The present Einsteinian Dark Age of science will soon end – for the times they are a-changin'.
The aether will return – it never left.
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