You have heard
the term "internal energy" more times than you can count, and if you
are the kind of practitioner I am writing for, you have learned to be careful
with it. You have watched it used to explain everything and prove nothing,
demonstrated on compliant students, hedged with talk of years of cultivation
and the right state of mind. Your caution is correct. I share it.
So let me make a
claim you can hold me to, and then test on your own body inside the first ten
minutes of training — not after a decade.
There is a way of
moving in which the muscles do far less than you are used to, sometimes almost
nothing, and the movement comes out stronger, faster, and more effortless
than the muscular version — all three at once, and not as a feeling. Stronger
as muscle force delivered, faster as force arriving before a muscle could even
switch on, effortless because the body, not the will, is doing the work. These
are not three separate gifts. They are one mechanism seen from three sides.
This is what Internal Energy produces, and I mean Internal Energy in a strictly
biomechanical sense — pressure, tendon, gravity, geometry — not a mystical one.
It can be explained. It can be shown. And it can be tested and felt in minutes,
which is the one thing the mystical version can never offer you. If it could
not survive that test, I would not be writing to you about it.
Everything else I have to say hangs from that claim. Let me unfold it — and let me be careful, from the start, to separate what a thing is from what it does.
What
Natural Movement is — and what it only does
Here is the
definition, and I want to give it to you exactly, because most of the confusion
in this whole subject comes from stating a movement's qualities and
calling that a definition.
Natural Movement
is movement closest to the inborn, performed under existing conditions in order
to accomplish a set motor task.
That is the whole
of it. Notice what it does not say. It does not say
"comfortable," or "beautiful," or "relaxed," or
"primitive." It does not say "stronger" or
"faster" or "effortless." Those are things Natural Movement
turns out to do — its characteristics, its results — not what it is.
What it is is simply this: of all the ways you could move to solve the
task in front of you, the one nearest to the movement you were born with.
"The
inborn" is doing the real work in that sentence, so let me be precise
about it too. The newborn already moves — it kicks, reaches, pushes, grips —
using nothing it has learned. Those movements, seemingly chaotic, are ordered;
they are the expression of an inborn movement pattern the body arrives with.
Not everything inborn counts: the sucking, grasping, blinking, and breathing
reflexes are not Natural Movement, because they share neither the root nor the
goal of locomotion — the crawling, walking, running, striking, throwing,
lifting from which every motor task is ultimately solved. Natural Movement is
the movement that stays closest to that inborn locomotor source while
meeting the real conditions of the moment.
And a movement
kept clean of all cultural influence — stripped of the habits a style and a
society lay over us from birth through our powerful gift of mimicry — is what I
call Pure Natural Movement. Absolutely natural surroundings are what
that requires; but let me be careful again — the natural surroundings are a necessary
condition, not the definition. The definition is freedom from cultural
distortion.
How
it is powered: Internal Energy
Now to the
mechanism — how a movement that stays close to the inborn comes out stronger,
faster, and more effortless than the trained muscular version.
Muscle is strong,
but it is metabolically costly and slow to recruit. When you meet a load the
ordinary way, you meet it with muscle at every joint, and you pay for it — in
fatigue, in the delay before force even begins, in the wind-up that telegraphs
your intention. This is the movement most of us were trained into, shaped by a
style and a school, and I call it, without insult, cultural movement:
the inborn pattern overlaid and distorted by learned technique.
Internal Energy
is not muscular energy at all. It is the non-muscular energy stored in the
compressed spinal discs and the loaded tendons — energy put in by gravity,
weight, inertia, and the muscles that load them (the legs, the diaphragm, and
the rest) — and then released. It is what the body delivers when it stops
driving with muscle and drives instead with its own pressurized and elastic
structures. The trunk is not a solid post; it is a set of pistons — the
pressurized abdominal cavity between the diaphragms, the loaded intervertebral
discs — that store and redirect force. The tendons and the sheet-like
aponeuroses are springs that return almost all of the energy put into them, and
return it faster than a muscle can shorten. Gravity is a free and constant
supply, if you let the body fall into its work instead of holding itself up
against it. Internal Energy is the coordinated output of these — pistons,
tendons, and gravity — while the muscles do the one thing they are fast enough
to do well: hold a state, set the timing, and get out of the way. (The body's
own proportions belong to a later part of the story: they do not supply the
energy, they govern how it is spent.)
That held state
has a name — Maximum Dynamic Relaxation, MDR: not going limp, but
holding the least tension the movement requires and no more, so the springs
stay loaded and the pistons stay charged, ready to release. Most practitioners
cannot do it at first, not because it is subtle, but because we are trained to brace
— to answer load with muscle — and the whole skill is unlearning that answer.
This is why the method takes time to master even though its results can be
shown at once. The claim is testable in minutes; the mastery is the years.
So one of the
plainest characteristics of Natural Movement is that it draws on Internal
Energy to the maximum in every single action — asking of muscle only what
muscle uniquely must provide. That is a thing it does, and it is why it
is stronger, faster, and more effortless. It is not what Natural Movement is.
Hold that line and the whole subject stays clear.
There is an old
name for this. The ancient Chinese called it wu wei — effortless action,
action that does not force. I do not borrow the term as poetry; in ISAI it has
a mechanical meaning. The movement is performed with little or no muscular
effort because the muscles are largely not the ones doing the work — the springs,
the pistons, and gravity are. Let me be exact about "little or no,"
because I will not overstate it: some muscle is always spent — the legs, the
diaphragm, the holding of MDR — and gravity and the loaded tissues supply the
rest. Wu wei is not zero energy. It is the near-disappearance of muscular
effort: the body run on its weight and its springs instead of its contractions.
From that, three
things follow, and let me put numbers to them, because the numbers are honest
and they are enough. Any movement costs two times added together: the latency
before force even begins, and the action itself. A muscle pays on both.
Its latency — the electromechanical delay before it produces any force — is
thirty to a hundred thousandths of a second; then its action is slowed again by
the time it needs to build force and by the fact that under load it shortens
well below its top speed, another hundred to two hundred thousandths. A
pre-loaded tendon, or the pressurised discs of the spine, pay almost nothing on
either count: the latency is near zero, because nothing has to switch on, and
the release itself runs in perhaps thirty to a hundred thousandths, faster than
the muscle could shorten. Set the two side by side and a whole movement that
costs the muscular body something like a hundred and thirty to three hundred
thousandths of a second can cost the elastic body as little as thirty to a hundred.
Typically that is several times faster; at the extreme — the fastest natural
release against the slowest muscular one, thirty against three hundred — it is
up to ten times faster. That is the faster.
It is also more
powerful, because a spring releases in a fraction of the time the muscle
took to load it, and power is energy divided by time. Nature shows this at its
limit in the small catapults — the mantis shrimp's strike, the chameleon's
tongue — which exceed what their own muscles could ever deliver by many times
over; in the large muscles of a human the margin is more modest, and I will not
pretend otherwise, but the principle is identical, and it is why a released
strike lands heavier than a pushed one. And it is more accurate,
because a self-terminating movement — a whip that ends itself — has nothing to
brake and little to correct, and it does not telegraph its direction before it
goes.
And there is a
further gain that appears only once you see the whole sequence rather than the
single act. Because it is all one pattern, a chain of movements is not a
series of separate techniques, each of which must be started and then stopped
and then the next one started again. It is one continuous pattern deforming
from shape to shape, and the joins between movements simply disappear. Nothing
stops; nothing has to be re-launched. This spares the body the repeated cost of
starting and braking — but more than that, it removes the re-initiation delay between
movements, so a sequence flows at a speed a stop-and-start body can never
reach. It is also, for the same reason, unreadable: nothing resolves or resets
to announce what is coming, because the movement never comes to rest to choose.
And it can turn anywhere at any instant without effort, because redirecting a
movement already in flight is only another deformation of a surface that is
already moving — not a new movement to begin.
The
one pattern, and why it is not a shape
Here is where
ISAI parts company with everything you have trained.
The inborn
movement pattern is one. It expresses itself as Natural Movement — and a
pattern is never the same thing as its expression, any more than a language is
the same thing as a sentence. There are not many inborn patterns, one per
reflex or per technique; there is one, and it expresses itself through movement
so diverse that an untrained observer sees an infinity of different movements
where there is, underneath, a single source.
That single
pattern expresses itself through trajectories — paths the body's parts
travel, carrying their velocities and accelerations — and those trajectories
are what I call Fish Play. A relaxed arm released as the torso turns
traces a single closed lobe in space, rising up one side, curving over,
descending down the other — the same kind of path a fish makes turning in
water. The name is drawn from that path, the fish's turn, not from any swimming
wave: it names the shape of the trajectory.
The word
"pattern" will mislead you if you picture a fixed figure, a set shape
the body traces. It is nothing of the kind. Fish Play is one family of
trajectories precisely because it is not rigid. Think of a rubbery surface: it
stays one continuous surface, yet you can push it dynamically in any direction
and it deforms to meet the push. Fish Play is like that — its trajectory
parameters change continuously, in direction, amplitude, timing, curvature, so
the single pattern flows into a strike, a step, a throw, a turn without ever
becoming a different pattern. One deformable thing meeting each situation by
changing its shape, not a catalogue of many techniques filed one per case.
And because it
deforms so freely, the movement in most cases does not look like the
canonical shape of Fish Play to an untrained eye. There is no obvious
undulation on the surface, no visible wave — the canonical form has been
deformed, folded, and spent into something that reads, to the naïve observer,
as an ordinary punch or step. The pattern is in the cause, not the appearance.
Seeing it is itself a trained capacity — which is exactly why the same movement
that looks unremarkable to a spectator is unmistakable to a hand placed on it.
This is why, in
ISAI, the kinematics come first — the trajectory and the way the body
moves along it. The internal mechanism is not directly visible; the trajectory
is. You read the pistons and tendons off the movement, the way an engineer
reads internal forces from observed motion. Learn to see the trajectory, and
the mechanism becomes legible.
The
ground under the claim — and where it ends
I am not asking
you to take the biology on faith either, so let me be as careful about the
evidence as I am asking you to be about the claim.
That the body is
built to move first and do everything else second is not my idea; it is
mainstream vertebrate biology. The backbone is older than lungs — it began as
the organ of the fish's swimming wave. The zoologist David Carrier showed that
in a running lizard the very bending that drives the stride squeezes the lungs,
so the animal cannot breathe well while it runs: the architecture serves
movement, and breathing negotiates around it. And the machinery of coordinated
movement sits below the brain — the Central Pattern Generator, a spinal circuit
that produces full locomotion on its own, without the brain and without
feedback, first demonstrated in the cat and the lamprey and traced back to that
same axial swimming wave. We carry the human fingerprints of it: the newborn
who steps before it has learned anything, the righting reflexes that orient the
whole body without instruction, the old reflexes that vanish under mature
control and re-emerge when that control is damaged — the ancient layer, still there
beneath the new.
That is real
ground, and it is the ground your skepticism can stand on. But I will show you
the seam, because a researcher owes you that. The biology establishes that an
inborn, axial-rooted movement machinery exists. It does not establish my
further claims: that there is exactly one inborn pattern, and that it
expresses itself through the trajectories I call Fish Play. Those are my
hypotheses. I have built my practice and my students' practice on them for
decades, and we can demonstrate what they do — but I have found no publication
that proves them, and I will not pretend otherwise. What is testable in minutes
is the Internal Energy — the stronger, faster, more effortless movement with
less muscle. The single-pattern claim is the theory I offer around it, marked
as theory, for you to weigh against your own experience.
Why
this is unlike anything you have trained
Every system you
know, however deep, is built the same way underneath: a body of techniques,
learned and layered, refined over years — and, in the internal schools, an internal
energy treated as a separate, higher attainment you cultivate on top of the
movement and hope one day to marry to it.
ISAI is not built
that way, and this is the whole difference. There is no separate department.
Natural Movement exists by means of Internal Energy — the movement is what the
energy makes possible, and the energy is renewed by the movement, each feeding
the other in a loop, topped up by gravity. There is no higher teaching to
graduate to, nothing bolted on above the movement. And it does not ask for your
faith for a decade before it shows you anything. It asks for ten minutes.
That is the
claim, and the invitation. Not that my internal energy is more powerful than
another school's — that is an argument no one can win. But that mine is testable,
on your own body, at the first meeting, in the currency you actually trust,
which is force felt and force delivered. Bring your skepticism. It is the right
tool. Then put your hand on the movement and see whether it does what I have
told you it does.
If it does — and
I would not stake the work on it if it did not — then the whole logic of your
training turns over. You are no longer adding technique to build a better
movement. You are removing the cultural interference laid over the one inborn
pattern you were already born with, until it can express itself again through
the body it was always meant to use.
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