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[announcer] Help everyone
explore new worlds
and ideas.
Support your PBS station.
[narrator] From
the moment of conception...
The clock is running.
Cells multiply.
Chemicals react.
Bone, tissue, and blood
are manufactured.
It's the final leg
of the incredible
nine-month journey
that made us.
When our eyes open
for the first time
as our sense of vision
switches on,
when our lungs prepare
for the first breath
as, in a moment,
we have to face
the outside world...
[baby crying]
...and survive on our own.
It all must come together
with exquisite precision
because one mistimed event
or faulty gene
could have
a life-changing effect.
-[horn blows]
-[crowd cheering]
[narrator]
To survive on the outside,
there's one vital part
of the body
that must be ready
for anything.
It gives your body
its shape and strength.
The skeleton.
[whistle blows]
An adult skeleton is made up
of over 200 bones...
[whistle blows]
Which gives us shape
and movement.
They protect
your vital organs.
[crowd cheering]
And muscles
attached to the ribs
enable your lungs to expand
and fill with air.
[athlete] Set! Hut!
[narrator]
And it's in the womb
that this phenomenal
architecture is built.
Without it, our bodies
have no structure at all,
making it virtually
impossible to survive.
But there's one little girl
who has defied all the odds.
Janelly is nine-years-old,
but she looks
over half her age
because when she was born,
her body lacked
the ability to make bones.
[woman speaking Spanish]
[translator] We love Janelly
with all our hearts,
and we try to give her
lots of love
because we thought
maybe tomorrow
we won't have her anymore.
[speaking in Spanish]
[narrator]
Janelly has an extremely
rare bone disorder
called hypophosphatasia.
It went undetected in
the womb,
but shortly after
she was born,
her parents started
to realize
something was wrong.
[woman speaking Spanish]
[translator]
I started noticing it
about three or four weeks
after her birth.
She wasn't growing.
She wasn't putting
on weight.
It got really, really bad.
[narrator]
Janelly's condition affects
every bone in her body,
including her skull.
When she was born,
she had to rely on
a ventilator to breathe
because she had
no ribs to protect
her lungs,
and doctors didn't know
if her brain was damaged.
We all began without bones
in our body.
As the body first
takes shape,
it begins
by growing cartilage,
the soft, flexible tissue
that forms the foundation
of what, in time,
becomes our skeleton.
Then over several months,
a magical process unfolds.
Bit by bit, this cartilage
starts to harden into bone.
By week 25, the pelvis,
our largest bone,
is forming.
Our bones are formed
by special cells
called osteoblasts.
They swarm around
the skeleton
coating the soft cartilage
with a hard,
calcium-based mineral.
[crowd cheering]
But this process
also produces
a damaging chemical
which stops our bones
from hardening.
So the body has developed
a response.
A gene is activated,
creating a crucial protein,
TNSLAP, that neutralizes
the damaging chemical,
letting bone formation
continue.
But Janelly lacked
this all-important gene
that enabled cartilage
to continue the process
of turning into strong bone.
[woman speaking Spanish]
[translator] She was on
the verge of death
many times.
[man speaking Spanish]
[translator] They told us
the best thing to do
would be to disconnect her
there and then
because she wouldn't be able
to have any quality of life
and she couldn't
go on suffering.
[Dr. Simmons]
All right, Janelly.
[narrator] Dr. Jill Simmons
has been treating Janelly
for the past seven years.
Gonna listen to you.
Yes. We are.
[woman speaking Spanish]
She couldn't move
her arms and legs.
She couldn't lift
up her head.
She couldn't even really
turn her head right to left.
[Janelly laughing]
Her lungs had nothing
to hold them open
with no ribs.
It was a really
sad situation,
um, because the truth is,
without your bones,
you, you can't breathe.
You can't eat.
You can't even move.
It, it's really...
It's, it's really not
compatible with life.
[narrator] But then
out of the blue came hope.
News of a new drug
being trialed in Australia.
[Dr. Simmons]
We had heard about the drug,
but it was very early
in the clinical trial.
There was almost
nothing known
about it at this point,
but at, at this point
in Janelly's life,
there was also
no other option.
So this was when
she was at her worst.
[narrator] Compared
to an X-ray of a normal
18-month-old child's,
Janelly's made grim viewing.
It showed
a total lack of bones.
[Janelly cooing]
Bone development takes place
not just in the womb,
but also all the way through
to our teenage years.
Janelly's doctors
didn't know whether
the drug would help her,
but they hoped that it might
allow her to form bones.
[Janelly cooing]
We offered it
to her parents,
and they took a
leap of faith
and decided to try it.
[narrator]
After an agonizing,
six-month wait,
they X-rayed her,
and what they saw
was amazing.
The drug appeared to replace
the missing protein
Janelly's body
couldn't produce.
Janelly had started
to develop real bones.
[Dr. Simmons]
I think when you
look at the X-rays,
it's one of the most
miraculous things
that I've ever seen
as a doctor.
Here we were,
seeing bones grow
from where there had been
no bones before,
and it was
an incredible experience.
High five!
Mommy.
[laughs]
[speaks Spanish]
[speaking Spanish]
[woman speaking Spanish]
[translator] The doctor
came in and told us,
"We've got wonderful
news for you."
We looked at each other,
and he said,
"Janelly is starting
to have bones."
We said, "Thank God."
[narrator] Doctors
don't know how far
Janelly's
miraculous recovery will go
or if she will walk one day.
[Dr. Simmons]
You know, to see a child
who probably
would not be alive
anymore now happy
and growing bone
and breathing on her own,
I mean,
that's why we all get into
medicine in the first place.
To really of been a part
of something that
had no hope
and really turn it
to something
that is so positive
has been incredible.
[narrator]
But everyone is hoping
she will grow stronger
all the time,
continuing to defy the odds.
[man speaking Spanish]
[translator] Our plan
for her is to go on
looking after her,
take it day by day
as she improves,
and not lose hope
that someday
she will be able to walk
and lead a normal life.
[narrator] Now 26 weeks,
and the fetus is about
one-foot long,
weighing around 24 ounces,
and every day,
it's growing in size.
Deep inside the veins,
vital changes
are taking place.
The fetus has been producing
its own blood,
which carries oxygen
to every tissue in the body,
delivering the energy
that fuels
its extraordinary growth.
But it can only do this
thanks to a special kind
of blood.
Fetal blood cells contain
a different kind
of hemoglobin
than adult cells,
with a greater affinity
for oxygen.
It allows the baby to absorb
oxygen from the
mother's blood
through the placenta.
But now in the 26th week,
the fetal blood
is slowly changing
into adult blood,
which will be able
to take its oxygen
from the air outside
the womb.
[monitor beeping]
Not all blood
ends up the same.
There are 35 different
blood groups,
and within these groups,
a blood type
is based on antigens
which can form
thousands of different
combinations.
Our blood type is defined
by the genes we inherit
as well as random mutations
that may occur in the womb.
And the one we end up with
may affect the way
we live our lives.
[crying]
[Thomas]
When I heard about my blood,
I thought, "Oh,
I really have
to be careful."
You never know
what can happen.
[narrator]
Thomas has Rhesus
null blood.
It's the rarest type
in the world.
Only 41 people
have ever been found
with the same blood as him.
Thomas is a librarian.
He walks to work
because he has
to avoid all risks.
If anything happened to him,
finding a blood donor
would be almost impossible.
[Thomas]
Consciously or not,
I've tried to find
a safe activity,
safe, uh, work.
[narrator] Thomas' blood
has to be stored in Paris
and Amsterdam.
A long way to go
should he be in any danger.
Early in pregnancy,
proteins and sugars
known as antigens
appear on the surface
of each blood cell.
And it's the presence
or absence of these antigens
that determines blood type.
Most of the time,
we aren't aware of antigens,
but our immune system
will attack blood
from someone
with incompatible antigens.
It could cause
the blood to congeal,
which can be
life-threatening.
Some antigens
are high-prevalence,
which means they're found
in the red blood cells
of most people,
so most of us have blood
that's compatible
with other blood types.
But some blood types
are incredibly rare
because random
genetic mutations
can knock out blood groups,
and when this happens,
it makes finding a donor
much harder.
In Thomas' case,
an incredible coincidence
of two genetic mutations
left his blood cells
devoid of a whole group
of antigens.
It means that his blood
is the closest thing
to universal blood
that anyone else
could receive,
but should Thomas
need a transfusion,
he would be in trouble,
as his blood attacks
almost all other types.
I know that I have to be
really careful in my life.
But, uh, there is one thing
I, I cannot resist.
[wind whistling]
I feel this kind of freedom.
I can forget everything,
and I feel well.
It might be risky,
but, uh, as long as I can,
yes, I will do it.
[narrator] Thomas
never leaves home
without his documents
showing the location
of the nearest source
of his rare blood.
Everywhere I go, I have
my blood information
with me.
This is the paper
which says which type
of blood I have
and that in case
of emergency, uh,
they can call, uh, Paris,
and they are also in contact
with Geneva.
[narrator] With only
two places in Europe
that have compatible blood,
it's essential
he avoids accidents.
I touch wood
it never happens.
[chuckles]
[narrator]
With bones hardening
and blood maturing,
the incredible march towards
being a living,
breathing baby
is well under way.
It's time to prepare
for the world
and the people we'll meet
once we're born.
[Kerstin muffled]
"Old mother Hubbard
went to the cupboard
to fetch her poor dog
a bone."
[narrator] And to do that,
we'll need our senses,
first of which to develop
is our hearing.
[Kerstin muffled]
"Once she got there,
the cupboard was bare,
and so
the poor doggy had none."
[narrator] No bigger
than a grain of rice,
this amazing, coiled,
snail-like structure,
the cochlea, is the sensory
organ for our hearing.
"She went to the baker's
to buy him some bread.
[muffled]
But when she came back,
the poor dog was dead."
[narrator]
Sound waves cause fluid
inside of the cochlea
to move,
a motion that is picked up
by 30,000 tiny hair cells.
[low rumbling]
At 28 weeks, sounds coming
from the outside world
should spark these tiny
hair cells into life,
sending signals to our brain
which we interpret as sound.
[static signals]
And it's time for Kerstin
to find out
if her baby has developed
the sense of hearing.
[man] So we can see
the internal structure of
the baby's brain.
And there's the baby's
little cheeky face
looking at us.
[Kerstin] Oh, it's amazing
how much it's grown.
[machine whirring]
[narrator]
We want to discover
if Kerstin's baby can hear,
so we've devised
a simple test.
To make sure that mom
can't subconsciously
influence
her baby's responses,
we are going to shut out
the outside world.
[squeaking]
Yeah. It's definitely
changing the pattern now.
-Baby put his hand over
his face when it started.
-[man 2] Did it?
[narrator] Changes
in the baby's heart rate
when we make sounds...
-[whistle blows]
-[doctor] And again.
-[ringing]
-[rattling]
[narrator] ...suggests
we can hear in the womb.
But do we remember
any of those sounds we hear?
-Are we capable
of forming early memories?
-[squeaking]
At the top of your body,
the most important organ
of them all
is beginning to
get organized.
Cells are developing,
connecting every
region together.
Most of the brain's growth
is now in the wiring.
Our new connections
are growing fatty sheaths
that insulate them
and create the circuits
that will form the mind.
"Old mother Hubbard
went to the cupboard
to fetch
her poor doggy a bone.
But when she got there,
the cupboard was bare,
and so the poor doggy
had none.
[muffled]
She took a clean dish
to get him some tripe.
When she came back,
he was smoking a pipe.
She went to the fishmonger's
to buy him some fish..."
[narrator] In a study,
a group of pregnant women
read a rhyme to their unborn
babies every day
for six weeks.
"When she came back,
he was dancing a jig.
She went to the cobbler's
to buy him some shoes,
and when she came back,
he was reading the news.
She went
to the seamstress..."
[narrator] They then stopped
for a couple of weeks
before starting to read
to them again...
"She went to the hatter's
to buy him a hat.
She went to the joiner's
to buy him a coffin...
When she came back,
the poor dog was laughing.
She went to the barber's
to buy him a wig."
[narrator]
And what they found was
because they were now
familiar with the rhyme,
their heart rates dropped.
[muffled voice]
They became nice and calm,
but when they were read
an unfamiliar rhyme,
there was
no response at all.
[Kerstin muffled]
"She went to the baker's
to buy him some bread,
and when she came back,
the poor dog was dead.
She went to the joiner's
to buy him a coffin.
But when she came back,
the poor dog
was laughing..."
[narrator] Suggesting
that lingering in the back
of their mind
was a memory of the stories
their mothers had read them.
[heart beating]
Even before birth,
the brain can store
memories,
but these memories
will not last.
No one is capable
of recalling
memories from the womb
because the brain areas
that store memories
long-term
won't be developed
until after
two and a half years of age.
This is also a time that
our other senses evolve.
[heart beating]
At 29 weeks in the enclosed
world of the womb,
something amazing
is happening.
We're starting to see.
[muffled plane radio]
Nestled deep
in the South Pacific
-is this tiny atoll.
-[plane engine whirring]
For your eyes,
it's a feast of beauty,
yet this place is known
as "Color-Blind Island."
At the back of our eye
on the retina,
light-sensitive cells
called rods and cones grow.
At 29 weeks,
our rods are so sensitive
that this allows us to see
a black-and-white image.
But from now on,
a momentous change begins.
The cone cells
are being wired up,
which will allow us
to see color.
Light-sensitive proteins
will convert red,
green, and blue,
the separate components
of light entering our eyes
into nerve impulses.
These are sent to
the brain and interpreted
as a color image.
[electrical charges]
But if these vital proteins
misfunction,
the world will look
like this
24-7 for your entire life.
With their cones
not working,
the affected islanders
all struggle
with the painful, burnt-out
image when the sun is up.
[man speaking
local language]
[translator]
I find it difficult
to go outside in the sun.
When it's sunny,
I cannot see to do my work.
[children laughing]
[narrator] It's not
just the sensitivity
of their eyes
that's the problem.
Being color-blind
affects all aspects of life.
[woman speaking
local language]
[translator] When it comes
to cooking food,
my daughter has a hard time.
We need to inspect the food
before she cooks it,
because she can't tell
if it's off.
[man speaking
local language]
[translator]
That's a beautiful dress.
What color is it?
[laughing]
[man speaking
local language]
[translator] None of these
bananas are ripe.
[speaking local language]
[translator] We cannot see
what colors are there.
We see the colors,
but they say it's wrong.
What do you see here?
Do you see any numbers?
Nothing.
[narrator] Most people
aren't really color-blind,
but color-deficient.
Being able to distinguish
20 of the 100 hues
most people can see.
But, intriguingly, 10%
of the population
of Pingelap
are destined to live
in a totally
black-and-white world.
[children playing]
In 1780, Pingelap was all
but wiped out by a tsunami.
A community of just
20 people survived,
one of which was their king.
He was believed
to have been color-blind.
Scientists believe
he had a fault in a gene
that allows us to see color,
and he passed this down
to his children.
[thunder rumbles]
[bell ringing]
[bell ringing]
[singing hymn]
Because of the remoteness
of the island and
its religion
that discourages
marriage to outsiders,
this genetic fault
has been passed down
through the generations.
[singing continues]
And continues to affect
the population today.
[indistinct chattering]
But as the sun goes down,
they gain
an amazing advantage.
[man speaking
local language]
[translator] I can see
the land mass
and small lagoon.
I can see also the big rock.
[narrator] You and I
have no chance of seeing
what Herrol can see,
but our super
sensitive camera
reveals, amazingly,
he really can see
in the dark.
So it could just be that
the part of Herrol's brain
that normally interprets
color is now being used
as extra processing for his
monochrome night vision.
In the middle of the night,
Herrol and his friends
are hunting flying fish.
They are attracted
to the flame
and fly towards it
as if it's moonlight.
[Herrol speaking
local language]
[translator]
This type of fishing is fun,
especially if we
catch plenty.
My family is expecting
fresh fish.
We can't just go to market
and buy food.
Even though it's hard,
it's what we do.
It's our job.
[narrator] During our time
in the womb,
we go through the most
incredible transformation
from a single cell to a baby
that's able to make sense
of its world.
A lot of what makes you
who you are,
from your height
to the color of your skin,
is decided by the genes
you inherit from
your parents,
but these are nothing
like as inflexible
as we once thought.
We're discovering
that the outside world
influences genes
in the womb,
preparing the fetus
for what is to come.
This is the new science
of epigenetics,
and it may help explain
the rise of one
of the developed world's
most serious diseases...
Diabetes.
I used to eat fish and
chips and Indian food.
Snacks over here,
coffee time.
[narrator] Freddie and Lal
have very similar lives.
-Subway...
-Potato chips...
Dunkin' Donuts...
Sweets, something salty.
[narrator] They live
in the same city.
They do the same job.
They even eat
the same type of food.
[Lal] Twenty-four hours,
everywhere is open.
Subways are running.
Even sometimes
you're not hungry,
you eat the burger.
You eat the burger.
After a while, you go
to have a cup of coffee.
You want to have some donut
or some candy.
You never give a rest
to your stomach. [laughs]
You keep eating
and keep eating.
[narrator] But Lal,
unlike Freddie,
has developed
type-2 diabetes.
His body is no longer
able to regulate
the sugar in his blood.
[Lal] When I find out
I'm diabetic
and my doctor tell me,
I was a bit, a bit shocked.
I was, really, I thought
I'm going to die soon.
He... You know,
my doctor said,
"Nothing is going
to happen like this,
but you have to take care
of yourself.
You have to take
the medicine
the rest of your life
and watch what
you're eating."
[narrator]
But some scientists
believe that the secret
as to why Lal has diabetes
and Freddie doesn't
can be traced back
to the womb.
They were both born
in India...
[cycle bell rings]
...but with
one crucial difference.
[Freddie] I was born
and brought up in Mumbai,
and, uh,
it's a very fast life,
uh, 20 million people.
[Lal]
I'm born Punjab.
My village was
a small village,
and life was very simple.
[narrator]
Like millions of Indians,
Lal's life is very different
to his mother and father's.
They lived a rural life.
[Lal]
Life was totally different
here and there,
and over there,
we was eating
all the natural food.
Rice, some dal, some rotis,
some vegetables,
and over and over,
and we was very happy.
[narrator] The theory
is that if mom's diet
was low in fat, sugar,
and calories,
then her baby adapts.
It becomes
incredibly efficient,
built to extract
as much energy as it can
from the low-calorie foods
available.
[cars honking]
The problem comes
when you end up
living in a very different
environment.
Lal's diet is very different
to his parents,
much richer in fat, sugar,
and calories,
and, unfortunately,
it's not the kind of diet
that his body was programed
in the womb to expect.
As a result, statistically,
Lal is more likely
to be obese
or develop diabetes.
He fits large
population studies
that have tracked people
who were born in villages
and moved to cities.
They are far more likely
to develop diabetes
later in life.
[bell rings]
In contrast, Freddie's mom
would have been eating
a much higher
calorific diet.
Fries with that...
Number five, fries.
[narrator] Living
in the busy city of Mumbai.
[Freddie]
Recently, I've been eating
Italian food,
pizzas and all,
Spanish food.
The other day,
I had Brazilian food.
[narrator] It seems
Freddie was built in
the womb for city life,
and this doesn't only apply
to Freddie and Lal,
but to populations
throughout the world.
They are part of
a global trend
as people move
from the country
to the city.
We're living through the
greatest migration
in history
and with it,
an increase in diabetes.
While we have identified
a trend,
the actual process
of how a mother's diet
affects her baby is unclear,
but there are clues,
and these can be found
in an extraordinary
epigenetic study
carried out
on some very special mice.
These mice have been bred
so that they're
genetically identical,
but they look
completely different.
Unbelievably,
the only difference is,
the mom of the little
brown mouse
was given food supplements
during pregnancy,
things like folic acid
and vitamin B12.
Crucial genes were switched
on and off,
a process called
methylation,
leading to a normal,
healthy, brown mouse,
but the mother of the mouse
with the ginger coat
was not fed
these supplements,
and the genes
remained unaltered.
He is not only
bigger and fatter,
but also much more
vulnerable to things like
cancer and diabetes.
In mice, at least,
if the mother's diet
is deficient
in essential nutrients,
it can have
life-changing effects
on her offspring.
And we're beginning
to suspect
that this may well be
the case in humans, too.
[Lal] I think the diabetes
is like the gift
I have from America.
You see, all my sisters
and my brothers,
they're living in India.
They're not...
None of them
have diabetes.
But still, I love America.
[laughs]
[narrator] Although
we can't say for sure
that Lal's disease
is a result of nutrition
in the womb,
the statistics in
the mice study
strongly points us
in that direction.
And all around the world,
the hunt is on
for other epigenetic forces
that could permanently
change our DNA.
[train horn blows]
Seventeen years ago,
Quebec was in the middle
of the worst ice storm
in living memory.
[cars honking]
The community
was thrown into turmoil.
[siren blaring]
[Julie]
Outside was very,
very scary.
We didn't know
what's happening,
and we don't have any radio,
so we don't have any news.
We have no phone,
no electricity,
so, uh, we were alone,
very, very, very alone.
We didn't see the light
on the end of the tunnel.
Uh, it was like a war zone,
[chuckles]
I mean, war zone.
[narrator] The ice storm
left a trail of destruction,
but the landscape wasn't
the only thing affected.
Vincent's life may have been
changed forever
because his mom Julie
was in her last months
of pregnancy at the time.
Julie was one of hundreds
of expectant mothers
trapped by the storm
living under extreme stress
who later became part
of a unique human study.
It's long been wondered
what impact stress can have
on children in the womb,
and the ice storm
gave Dr. Suzanne King
a unique chance to find out.
[Dr. King] There are
very few studies in humans
on prenatal stress.
It just would not be ethical
to submit a pregnant woman
to stress to see what,
what effects it has
on the children.
But with a natural disaster,
mother nature randomly
distributes the stress.
[Julie]
I was wondering,
"Are we going
to have enough wood?
Are we going to have
enough, uh, food?"
We had no money.
Banks were closed,
so what are we gonna do?
And we were 22 days
without electricity.
[narrator]
Julie was 35 weeks pregnant,
and living without
any power at all.
She was under severe stress
at a vital time in
the development of her baby.
The question for
Professor King
was whether this stress
had been passed on
to the unborn children
during the storm.
That's the day
Vincent was born.
He was eight pounds,
40--14 ounces.
Here, he's about
two weeks,
about two weeks.
[narrator] Professor King
had to play
an extraordinarily
patient game.
She closely monitored
the children as they grew,
testing their mental
and physical development,
as well as analyzing
their DNA
at various stages.
Here is Vincent
with a Santa Claus.
[narrator] From three
to 15 years of age.
That's at four-years-old,
and now at 17.
[laughs]
[Vincent speaking French]
[translator]
I've had two MRI's.
I've done saliva tests.
I've done memory tests.
[heart beating]
I'm happy to do this
because it's for science
to help the world develop
and find out
if it's had an effect
on my life.
[heart beating]
[narrator]
When Professor King
analyzed her data,
the results were shocking.
[heartbeat quickens]
[horn blares]
Children
in the high-stress group
had significantly impaired
language and motor skills.
[exclaiming]
At the age of two, they were
using 30% fewer words
than those
in the low-stress group,
and the health
of the high-stress group
was also worse.
They were more likely
to suffer from autism,
asthma, and obesity.
[Julie] Vincent,
he has a lot of allergy
to dairy food, nuts,
and, uh, seafood,
and Vincent has
problems with language.
He's seen a therapist about
that for about seven years.
[crowd cheering]
Why is he allergic? Why?
Nobody in the family
had food allergy.
Nobody have problems
to speak.
[narrator] But what's
even more remarkable
is that Professor King
discovered that the stress
the children
had been exposed to
had left a unique signature
in their DNA.
While we're developing
in the womb,
a complex process known
as methylation takes place.
It can switch some genes on
and others off,
which alters the way
our genes actually work.
And this process
can be affected
by the environment
we're exposed to.
[crowd cheering]
And this is what
Professor King discovered.
She found a direct
correlation
between the amount
of methylation
in the DNA of the children
in the high-stress group.
[crowd cheering]
And the number of days
that their mothers
had lived without power
during the ice storm.
[King]
So, for example, the greater
the number of days
without electricity,
the lower the IQ
of the child,
the lower their, uh,
language development.
Um, even, uh, the way
they played was different.
These affects
could be massive.
[narrator] There's still
a long way to go
before we can
completely understand
how the outside world
influences the way
we are built,
but Professor King's study
proved for the first time
that the environment
we're exposed to in the womb
can have an effect
on our genes,
and these changes
can continue to affect us
for the rest of our lives.
It's now around 36 weeks
and nearing the end
of our development.
All of the vital organs
are built and tested...
...except one.
For our entire time
in the womb,
our lungs lay dormant,
flooded with liquid,
but strangely,
we practice breathing
in anticipation of that
first air-filled breath.
[muffled inhalation]
[muffled exhalation]
[Sam] The whole aim of
the game is to be as relaxed
as possible,
so no stress, no worry,
getting into your own little
world, disappearing, really.
[muffled exhalation]
You kind of focus inward,
and you get very in tune
with what your heart rate
is doing
and what your levels
of oxygen are
and whether you need
to breathe or not.
Your mind is under
more control,
and you're not panicking,
you're not worrying.
You're just keeping
everything
slow and relaxed.
[narrator]
Sam regularly pushes
her lungs to their limit.
She is a free diver.
She can explore
the depths of this lake
on one single breath
for minutes at a time
without coming up for air.
[Sam] It's very quiet,
it's very peaceful.
It can be very beautiful.
You haven't got your phone
to think about.
You haven't got any beeps
or distractions
or people calling for you.
There's none of that
going on,
so it is quite
a private space, really.
You're in a real moment
of peace and serenity,
and, and you kind of
tune into
that nothingness
and enjoy that
instead of everyday life.
[muffled inhalation]
[narrator] Our lungs
have been growing
like branches of a tree,
and now,
just weeks from birth,
a massive flood
of growth hormone
kicks off a vigorous change.
Thousands of tiny saccules
blossom.
These are alveoli,
the secret to breathing.
It's incredible that Sam
practices the sport
of free diving.
Her lungs never got
the chance to fully develop.
[Sam] I was born six weeks
premature back in 1972,
and at that stage, six weeks
premature was quite severe.
I mean, it's still
not that great today,
but it was quite a big deal
in those days.
It was quiet scary
for my parents, apparently.
It also meant that
I was born
without everything,
perhaps, grown to how strong
it should before...
Before I was born,
especially my lungs.
[narrator] Being premature
means Sam developed
far fewer alveoli.
Her lungs have
a reduced capacity
for absorbing oxygen.
But, amazingly,
Sam has overcome
the disadvantage
she was born with
and has trained herself
to be able to dive
for up to five minutes.
[Sam] If you don't
really know how far
you can go
or how long you can stay,
and sometimes you might
overstay your welcome.
If you get too excited
or nervous,
then your heart starts
racing.
Your diaphragm
starts to contract,
and then you need
to come up,
so you've got to be
very in control of
your thought processes
and, to some extent,
of your body.
If you know that you've
got some weaknesses
and you, uh,
take care of that
with your life
with how you eat,
how you exercise,
what you do,
it doesn't
need to be obsessive.
If you are looking
after yourself,
means you can do the things
that you love doing.
It's possible.
You just got to work at it
maybe a little bit harder
than somebody, perhaps,
who wasn't born premature.
[narrator]
Sam is living proof that,
whatever the circumstances
of your first breath,
how you live your life
and the choices you make
can help you to overcome
those early obstacles.
After nine months
of development,
the body is fully built.
One single cell
has transformed
into trillions
of different cells.
In an astonishing concert
of biology,
25,000 genes have activated
at just the right time.
Floods of hormones
have signaled
the most miraculous
and life-changing
transformation.
But now the tiny human
has outgrown its resources,
and it's time to leave
the comfort of the womb.
Around 280 days
after this miraculous
journey first started...
The countdown
to birth begins.
The hormone oxytocin
triggers contractions
which increase in intensity.
[people speaking
indistinctly]
[woman 1 groaning]
[woman 2]
Well done. Well done.
[narrator]
The cervix gradually
starts to dilate
over many hours...
[breathing deeply]
Until the baby moves
into the birth canal.
The baby is preparing
for a monumental change
to take place.
The lungs must switch
from an unused
sack of liquid
to an organ filled
with air.
[man] Big push for me,
big push.
[people speaking
indistinctly]
[woman 2] Another big push.
You still got
contractions...
-[woman 2] Another big push.
-[people speaking
indistinctly]
[woman 2]
Here take a breath in.
Another big push.
[people speaking
indistinctly]
[people speaking
indistinctly]
[groans]
[ticking increases]
There we go.
[man] Oh, wow!
That was quick.
-Oh, little baby.
-[woman 2] Well done!
[narrator] And with
the first breath,
the nine-month journey
is complete.
-Oh, that's just it!
Thank you very much.
-[chuckles]
3.972, which is
eight pounds, 12.
[man] It's a boy...
Eight pounds, 12 ounces.
[narrator] Birth, of course,
is just the beginning.
From now on,
we will learn, grow, adapt.
Our life will be
immeasurably enriched
by our relationships
with other people,
but our time in the womb
will have left
an indelible mark.
It will have shaped
our futures in so many ways.
After all, these were
the nine months
that made you.
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