I Have Epilepsy............ Posted: 08-07-03 01:01am
I have epilepsy and it really bites I am
18 years old and cant do anything I have
already worked but I had a seizure at
work, I cant drive becasue the dmv wont
let me drive, I cant watch flashy lights
and thats like all the movies nowa days or
go to parties or anything. I feel like
there is nothing else for me to do im only
18 and I dont know how to go on disablity
if I can.
I hear that students that have a disorder
with their brain like epilepsy have to be
in a class that is their pase I cant think
like all the other kids can im not as fast
thats why my grades were like c's and d's
then I finally dropped out and graduted at
an adult school.
People with epilepsy dont remember alot of
the stuff that they were taught so how can
we study for a test and then take one if
we cant remember it.
I just dont know what to do anymore
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asmita
New User, Becoming EHEALTHy
Joined: 16 Aug 2003 Posts: 3
Posted: 08-16-03 08:39am
Hey randie,
I am an epiliptic......And the first
thing I wud say is "get those thoughts off
ur mind"...... There is sumthn great
about the human mind.......We have the
power to do what we want how we want and
wen we want......I don't know if u are
aware of it or not or wether u will
believe me or not but we have sumthn
called as a subconcious mind.....The more
u tell urself that u can't do it never
will u be able to do it!!!! The battle of
life is all in the head....I personally
know ppl who have cured their own brain
tumors with their will power
itself.....And u say that ppl wid epilepsy
can only be in a classroom....Welll life
is not aall about driving or moovies there
is much more to it.......So wat if ur
grades have fallen make an effort the more
u think that u cant do it u wont be able
to do it even if u have the capcity to do
it!!! Make sure u tell urself that u will
do it and watch the difference......And
remember epilepsy can be won by will
power....Trust me on this there are things
out there u can jes win so reach out
cause noone can do it for u unless u wanna
so it urself!!!!!
Take care :d
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drdorrin
New User, Becoming EHEALTHy
Joined: 18 Aug 2003 Posts: 2 Location: Vallejo, Ca
There Is Hope For Epilepsy Posted: 08-19-03 15:54pm
Hey randi-
there is hope, believe me! I've had
epilepsy for 13 years now, and I
absolutely refused to let it destroy my
life. (i'm 40 and was in an accident.)
you just have to find other ways to do
things. I can't drive either, so i've
learned to depend on buses and other
people. You ask if you have to be in a
special class? No, I don't believe so; I
was never in one (and I had seizures when
I went to chiropractic school). You just
have to tell the teacher that you have
them and what he/she should do. And i'd
advise you to make friends with someone in
the class and tell him/her what to do.
Then you're covered. You say your
thinking is slowed down--believe me,
you're not the only one with that problem.
It helps if you find someone to study
with; to pound the stuff into your head.
That helps more than you would believe.
It upset me that my grades weren't as good
as they'd been when I went to college, but
hey, I lived. Just remember, other people
have much worse problems than you do...
I have epilepsy and have so since I was 7
yrs old. Now 40, I guess I have learned
to deal with all different facets of life.
I think at this age I have sort of
learned to be so greatful and look at life
different then those who dont have to deal
with a disease. I am a financial mgr of
2 large auto stores ... Happily
married....And have raised my two
wonderful sons now 16 and 18. So now I
face epilepsy with menopause I guess.
Yea its back to the neurologist for me
this tues. I am scared ....I guess some
days go by where I believe I have this
thing beat.....
so here I go again .....But I will not let
this defeat me......I have come too far in
life ....
You whom all face this illness......Are in
my prayers
i still consider myself blessed
|
feelgood
Experienced User , Rather EHEALTHy
Joined: 09 Sep 2003 Posts: 56 Location: Calabasas
Thanks: 2
Thanked:0
Posted: 09-28-03 15:25pm
Hi randi, your medication and the right
dosage is verry important...So, keep in
touch with your doc and maybe he needs to
change either your med or the dosage, that
makes a big difference..My doctor says
that if your on the right med and dosage
you should not have any seizures, but
remember all meds have side effects, so
you just have to find one that works for
you...Now i've been on all meds and my doc
says "do you want to have your life back?"
then have the
surgery.....................Take care,
susan
I can understand how you feel,but you
can't let this stop you from anything in
the world.Ok,no matter what anone tells
ya,ok.You take your medicine,and just do
right,ok.The light bothers me,but I wear
sunglasses all the time,you learn to deal
with these kind of things,it's really easy
too.I had a hard time in school,but I
didn't go to no speical class though.As a
adult now.I still go out,cause i'm
single,but I don't drink,if you think you
have to drink to feel like you fit in,your
in the wrong crowd,your friends should
respect you,and you health ( life )
instead,good luck..Cyn
wow I just went to
the neuro doc and after 30yrs of living
with this disease it amazes me in how
little they have learned. So now he
wants to change my meds to zonegran
.....Instead of tegretol ....Has anyone
had good results or negative with this
med?
I am also being sent for an eeg and mri
with contrast .....Gosh I am so damn
depressed. I hate this disease. You
know just when you think you got it
covered .....Then this. I understand my
doctors reasoning and it has been over 15
yrs since I had an eeg .....But tell
me.....What new can they see? I know I
have experienced some recent changes since
I am 40 and pre menopausal
gosh I am hurting this morning
at work with a lump in my throat this
morning
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amavone
New User, Becoming EHEALTHy
Joined: 09 Nov 2003 Posts: 1 Location: Mozambique
Posted: 11-09-03 21:10pm
Hey!
I am 39 years old and I have been
epileptic for the past 19 years. My
friend there are restriction of course for
what we can do as epileptics. But that is
not to mean that we should take a
misreable life because of it. For all
this time I have learned that in most
cases we suffer more with the social
environment than because of the disease
itself. I mean that we normally suffer
because of the way people treat us.
Therefore what you should learn is how to
deal with this people. You should prepare
yourself not to suffer with the way people
will treat you. Of course people will try
by all means to treat you differntly but
you should be strong enough to igonre it
and show them that you can make it. :p
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jamal
Experienced User , Rather EHEALTHy
Joined: 05 Nov 2003 Posts: 60 Location: oroville,Ca
Ahng In There Posted: 11-15-03 23:16pm
Randi,
im 44 and found out at 38 that im a epy
to. Ive been thru caca to!!!!!!! Cant
drive anymore lost my job 0ver 2 years ago
because they could'nt control them with
all the different meds they put me on.
The 4 docs that I went to told me would I
go for brain surgery? I thought they were
all f-------ing crazy. Well here I am
today. I had brain surgery june of 2002
at u.C. Davis. Im not a 100% better, but
im back at my old job 2 days a weeek 5 hrs
aday taking the short bus that picks me up
at my front door for 1.25 one way. No
more car ins, car payment, gas money, aaa
card. I have my wonderful boyfriend thats
been her for almost from the beginning of
all of this. The funny thing is it all
started when I left that guy I was married
to for 19 years. So I had to go on
welfare because my job did'nt pay well
enough as a manager and clothing buyer for
a the store I worked at for 7 years, no
bennys. And that guy ihad 2 boys with
did'nt end up helping me with our boys
over the last 6 years. Now they are 18
and 20 at the end of this month. So what
saved me is medical paid for my surgery.
Do they know what causes your seizures?
I could go on and on. I tell you more
about it. When you write back let me know
were I left off. You have to make light
of it or you never get through the day
sweetie. Please write back jamie oroville
ca. By the way I can't spell worth a
caca!!!!!!!!!
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sami_1982
Experienced User , Rather EHEALTHy
Joined: 13 Dec 2003 Posts: 200 Location: Australia
Its Not the End of the World Posted: 12-14-03 06:49am
Matey...Keep that chin up I know you feel
sick and tired right now but hey maybe you
could go to a group or something and meet
fellow epileptics. I know I feel safer
when I am with someone whom knows how I
feel and what they have to do. People I
can rely in and trust. I am 21 and I was
diagnosed 2 months ago I have lost my
managers job at a supermarket and I have
had my licence taken away for 2 yrs. Im
not letting it get me down I hjave met ppl
from the net that have epilepsy that live
in sydney and we have met up and shared
our stories. Ill tell ya it helps. I am
photosensitive too I have to ware dark
glasses always and if I watch tv I have to
hold one hand over one eye for about a
minute then I can take it away and I am
ok. But I still get headaches from
watching to much tv. And too much
computer. But I dont stop going out with
my mates poker machines make me have
episodes so look on the bright side we
wont be alcaholics or gamblers.
From sam
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KiKi2004
New User, Becoming EHEALTHy
Joined: 12 Jan 2004 Posts: 2
Posted: 01-15-04 18:18pm
Hi! I am 25 years old with a 4 year old
daughter and I just found out 2 weeks I am
epileptic. I have 2 seizures now and my
life has completly changed right in front
of my eyes my activities are limited along
with my job performance and they cant get
my medicine up to the actual level it is
suppose to be at and I am scared to be
alone. If anyone wants to talk to me
please do I would really like to know more
about this and here other people
situations.
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