Nan - another one! Yes, this sounds so much like what I also go through.
The symptoms of temporal lobe epilepsy are so hard to identify as
epilepsy, and often the seizures don't show up in EKGs... that we get
wrongly diagnosed or not diagnosed at all. I'm glad you are on meds that
help you and I hope you can find financial help for meds. Will you keep
in touch with me? I seriously have never met anyone who also had TLE. I
have done tons of research and I understand it, but I still am alone in
my weird little world.
Cynthia
Nancy Livesay wrote:
>
>
> Yes, I have tempole lobe and complex seizures. It effects my eye's as
> when I have one I can not see at all or my vision is blurry. I have
> really bad headacks. My dr. has me on carbitral, lamental, and
> topamax. When I was young I was to be on dilintan and phinabarbatal.
> A lot of times I do not know what I am talking about when I have one.
> I get a weird feeling like I am seeing things really far way and I can
> not see anything up close. Things up close even seem far away.
> Sometimes the after affects last all day. It is an aufle feeling.
> Buythe way, does anyone have a problem with getting there meds, you
> know money. paying for
> them.
> Nan
>
>
> ,_._,___
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