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Battling
Your Childs
Epilepsy
Written By
Stacey
Chillemi
Epilepsy
affects
millions of
people
worldwide,
with more
than two
million
people in
the United
States
suffering
from the
disorder. In
the United
States
alone, about
400,000
children
have
epilepsy.
Watching a
child have a
seizure can
be a scary
experience,
especially
for someone
who has
never seen a
seizure
before.
Seizures
are broken
down into
two major
categories
(generalized
seizures and
partial
seizures)
with a large
number of
subtypes.
There are
many
different
types of
seizures.
There are
seizures
that affect
the entire
brain. The
seizures I
listed below
are seizures
that are
common in
children:
Absense
seizures:
Another name
for these
seizures is
petit
mal seizures.
A child
might
suddenly
stop what he
or she is
doing and
stare off
into space
in these
brief
seizures.
The child
might pick
at their
clothes or
slap their
lips. They
will not
have any
awareness of
they are
doing. The
seizure
usually
lasts
several
seconds, and
the child
will go back
to their
normal
behavior
right after
the seizure.
Atonic
seizures
(known as
drop
attacks):
These
seizures
cause a
child to
lose muscle
control and
fall to the
ground. The
seizure
usually
lasts a few
seconds to a
minute.
Clonic
seizures:
These
seizures
cause a
jerking of
muscles on
both sides
of the body.
Myoclonic
seizures:
These
seizures
usually
cause sudden
and dramatic
muscle
spasms, and
may cause a
child to
lose balance
or fall.
Tonic-clonic
seizures
or grand
mal
seizures:
A child
might cry
out and
their
muscles
tighten and
go stiff.
Then, as
their
muscles
begin to
tense and
relax, his
body will
jerk and
spasm. Your
child’s
breathing
may become
shallow, or
even stop
for a
moment, and
their skin
may turn
bluish.
Usually, the
seizure will
last a
minute or
two.
Emergency
medical help
is not
necessary
unless the
seizure
lasts more
than five
minutes, or
unless one
seizure
immediately
follows
another
seizure.
After the
seizure is
over, the
child will
be exhausted
and may
sleep for
hours. You
should call
your doctor
afterwards
to report
the seizure
to them.
They may
want you to
come in for
tests or
they may
want to
adjust their
medication.
Partial
seizures
only occur
in one part
of the
brain. Only
the mental
or physical
ability
controlled
by that part
of the brain
is affected.
Subtypes of
partial
seizures
include:
Simple
partial
seizures:
These
seizures
cause
different
reactions
depending on
the part of
the brain
the seizure
is occurring
in. A person
might make
erratic
movements,
or have
sudden,
intense
emotions --
like anger
or fear. A
person may
also have
strange
perceptual
problems,
such as
distorted
vision or
hearing.
Other
symptoms can
include pain
or nausea.
People with
simple
partial
seizures
would not
lose
consciousness,
but they may
be confused
or unable to
speak until
the seizure
is over.
Complex
partial
seizures:
These
partial
seizures
affect a
larger part
of the
brain. They
are more
powerful
than simple
partial
seizures. A
person
during one
of these
seizures may
seem
conscious,
and may even
speak or
move around,
the child is
not really
aware of
what is
going on.
They may
seem to be
in a trance,
speaking
without
making any
sense.
Usually, the
seizure will
end within a
few minutes,
although the
person may
be confused
afterwards.
During the
seizure, try
to keep your
child away
from
anything
that can
hurt them,
such as a
desk, a
table will a
vase,
anything
that can
hurt them.
You may want
to get a
pillow and
put it
underneath
their head.
Do not try
to restrain
your child
physically.
Watching
your child
have a
seizure for
the first
time was
probably one
of the most
frightening
moments of
your life.
My parents
told me that
is most
terrifying
experiences
of their
life. Their
bedroom was
next to
mine. One
night they
heard some
funny noise
coming from
my room.
They both
went into my
room to find
me with my
eyes rolled
back
twitching,
lips blue,
mouth
chattering
and body
shaking.
Finding
out that
your child
has epilepsy
is a painful
experience.
When you
have a
child, you
only want
the best for
your
child.
When your
child gets a
cold or a
fever your
stomach
drops and
you feel
their pain.
Can you
imagine if
you find out
you child
has
epilepsy?
There may be
overwhelming
feelings of
sadness or
depression,
as parents
grieve for
what they
perceive as
the loss of
their
healthy
child. They
grieve for
the life
changes that
will their
child will
experience
having
epilepsy and
they worry
that their
child will
not be able
to
accomplish
their dreams
that lies in
their
child’s
future
destiny.
Feelings of
grief are
typical.
Many parents
as ask
themselves
"Why did my
child
develop
epilepsy?"
Some parents
blame
themselves
and feel
that it is
somehow
their fault
or wonder if
they could
have done
something
differently
to prevent
the seizures
their child
is currently
experiencing.
Let me tell
you now that
you cannot
blame
yourself.
Your child
developing
epilepsy is
not your
fault.
There are so
many causes
for
developing
epilepsy
that it is
impossible
to pin
point.
Parents may
feel
resentful
about the
new
challenges
and demands
they will be
facing, and
then
experience
guilt for
feeling this
way.
Those
feeling are
completely
normal and
all parents
go through
these
emotions
Anxiety is
the most
common
feeling
because
parents will
have a
number of
overwhelming
worries.
Some of them
are:
·
Will my
child die?
·
Will he be
brain
damaged?
·
Will my
child
experience
problems
with
developmental
skills?
·
Can I let
children
play by
themselves?
Do I have to
supervise
them all the
time?
·
Can I send
my child to
after school
activities?
·
How do I
explain to
my child
that they
have
epilepsy?
What do I
say to him
or her?
Along with
these
worries,
parents also
struggle
with the
fact they do
not know
when their
child’s next
seizure will
occur. You
will
probably
feel angry,
scared, and
resentful
that you
have no
control over
what will
happen. You
may worry
about
whether your
child is
safe while
away from
home, that
teachers or
other adults
will
mishandle
seizures, or
make the
situation
worse by
overacting.
Parents will
also worry
about the
potential
side effects
of their
child's
medications
or the
impact of
missing
school due
to seizures
and medical
appointments.
The
future may
suddenly
seem
terrifying
and
uncertain
for both
your child
and your
whole
family.
Your child
having
epilepsy is
not as bad
as it
sounds.
Medical
research has
found that
most
children who
have a
seizure do
not have
another
one.
The
medical
community
has also
found out
that a
majority of
children who
have
epilepsy
(which means
that they
have had
more than
one seizure)
will outgrow
their
seizure
disorder.
Mostly all
children
with
epilepsy are
perfectly
healthy and
normal.
Their
intelligence
level is not
affected.
They can
participate
in after
school
activities
and any
other
activities
that your
child may
enjoy.
Right
now, medical
research
tells us
that 70 to
80 percent
of children
can control
their
seizures
with
medication.
There is
no a cure
for
epilepsy.
Many doctors
feel
medication
is the
answer for
children.
Many doctors
say all
children
need is
medication
because
their
seizures not
as severe as
adults are
and with
medication,
the seizures
may go away
on their
own.
Once your
child
experiences
seizures or
epilepsy, it
will
probably
change your
family for
life. A
parent who
has a child
with
epilepsy
will have to
obtain new
responsibilities.
You will
need to make
sure that
your child
is getting
good medical
care. You
need to make
sure that
your child
is seeing a
doctor who
knows a lot
about
epilepsy and
is up to
date with
all the
recent
medical
research and
medications.
The best
doctors to
see are
epileptologist.
These
doctors
focus only
on the study
of
epilepsy.
You can find
a good
epileptologist
in your area
by
contacting
an epilepsy
clinic or
your states
epilepsy
foundation.
The main
epilepsy
foundation
is in
Maryland.
They could
probably
direct you
to the
people you
need to
speak with.
You will
have to make
sure that
your child
takes their
medication.
Skipping a
dose can
cause a
seizure.
You can buy
weekly
medication
organizers,
so your
child does
not miss a
dosage.
You should
do your own
research and
find out as
much as you
can about
epilepsy.
Do not rely
just on the
doctors.
Doctors are
human. They
can make
mistakes
too. You
need to find
out as much
as you can
about
epilepsy and
make sure
you, your
family and
your doctors
are doing
everything
possible to
help your
child.
You may
also have to
become an
advocate for
your child,
explaining
epilepsy to
family,
friends, and
teachers
(you will
have to
inform the
school.
Incase your
child has a
seizure in
school).
It is not
going to be
easy in the
beginning.
You will
probably
feel
overwhelmed,
stressed and
extremely
upset.
While it may
be tough
being the
parent of a
child with
epilepsy
sometimes,
just
remember
that
treatment
works.
Epilepsy is
not nearly
as scary as
it sounds.
Using the
medical
treatment
for epilepsy
will help
your child,
so they can
live a
healthy,
productive
life with
few
limitations.
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Stacey
Chillemi
is a
mother,
married
with
three
children.
She is
a
H.O.P.E.
Mentor
for
the
Epilepsy
Foundation.
Stacey
has
spoken
at
different
events
for
schools,
organizations,
political
events,
in
front
of
Congress
in
Washington,
and
anywhere
she
can
help
educate
people
about
epilepsy.
Along
with
speaking
Stacey
is
also a
writer
and
has
written
three
wonderful
books
to
help
cope,
inspire,
and
live
healthy
and
productive
lives.
Her
book "Epilepsy
You're
Not
Alone"
shares
encouraging
stories
and
gives
readers
a
workable
program
for
coping
with
their
disorder.
Stacey's
second
book "My
Mommy
Has
Epilepsy"
helps
educate
children
and
teaches
them
what
they
can do
if a
friend
or
love
one is
having
a
seizure.
Her
third
book,
"Epilepsy
and
Pregnancy:
What
every
Women
Should
Know",
co-authored
by Dr.
Blanca
Vasques
shows
women
that
it is
not
impossible
to
become
and
mother
and
life
does
not
end
with
epilepsy.
If you
are
interested
in
learning
more
about
Stacey,
please
visit
her
website
at:
www.authorsden.com/staceydchillemi
No
part
of
this
article
may be
copied
or
reproduced
in any
form
without
the
express
permission
of
More4Kids
Inc
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