Howdy!
I saw mention made of "going to university" in another thread. Instead of
burying my post there, I thought that I'd start a new thread about it.
As soon as you start you should check out 2 resources and get acquainted

Hi,
This is my first post. I hope I am not redundant to other's questions
but I have read may posts and nothing really touches specifically on
what I am feeling lately.

A relative of mine suffers from Burger desease since many years, but is now
getting worse.
I'd like to know where I can find skilled centres able to treat this
desease, mainly in Italy or close countries.

Anyone else in this group taking drugs for seizures due to low grade tumor
that has not been surgically removed?  If so what drug(s) have worked best
for you?  I'm taking 500mg Dilantin and 1000mg Keppra/day and the recently
added Keppra has made a big difference in reducing my ...

 I am supposed to have a 72 hour EEG. My "doctor" would not say what he was
looking for. He has increased my seizure medication. I heard that this is to
trace where seizures originate in the brain. What does the EEG entail? Is it
really reliable if the doctor has increased the ...

This is a small question about Depakine Chro 500 which I have been taking
for about approximately two weeks now. Right now, I do not suffer from any
side effects which is great :-)))
One of those scarry things I read on the Internet is that when one takes

I would like to try this med for a few days to see if I can deal with the side
effects. I don't have prescription insurance and my dr doesn't have any free
samples. Anyone have any extras that I could try? Greatly appreciated.

Based on advise from my neurologist, I started taking 1000mg of Depakine
Chro.
After a couple of weeks, I will have to tell her how it went and if there is
a need to increase/decrease the dose I am taking. She also stated I do not

http://neuroland.com/sz/
It's touts itself as information for physicians. There's some great article
links.

What is the difference on an EEG between a hyp and a spike.  My daughter was
diagnosed with IS; we  had an EEG and the tech said he saw spikes but not
hyps. Can anyone explain?
Thanks

BlankHowdy Dave used to post regularly here and has a site about living with Epilepsy plus his experiences with a Vagus Nerve Stimulator (that he had some problems with later).
  His Main Doorway is in Post below that was done before here (posted by Pablo).   From there, Howdy ...

Has this group been dormant?
I haven't seen any new posts since April 19. It is April 21.
Thanks.
Mark

By now it is becoming obvious: not all posts are getting through on all
servers.
This might not pertain to you, but you would never know because you would
not see the posts you don't get.

Please I could use feed back, I feel that I am alone there are no support groups
where I am living.
I am 34 now, it all started in 1987..when I was 17, I'm sure we all remember our
first one, or at least part of it.