Saturday, May 30, 2009

Re: [epilepsy] hi



Yes,I feel them come on sometimes as My eyes start to get really blurry.  and sometimes I get really confused and sometimess other people can tell because of my eyes to.  My mother was in labor for 6 days and 6 nights for me and it put a lot of presser on my head.  She carred me so low that when she sat down she was ackulle siting on my head.  My dr. said that I should not live alone but I do not thve a choose right now.

________________________________
From: uniquepnk tds.net <Uniquepnk@tds.net>
To: epilepsy@yahoogroups.com
Sent: Saturday, May 30, 2009 10:37:28 PM
Subject: Re: [epilepsy] hi

Nancy,

Yes I do get disability. I would never be able to make it without the
medical card to pay for my medicine and doctor visits. I am not married, but
I would never be able to make it without the help of my boyfriend and
family.I have been very blessed to have somebody around the times when I
have had seizures.Somebody can not be here all the time, but that is very
seldom. My boyfriend can usually tell by looking at me and the way my eyes
look whether it is safe for me to be by myself or not.As for my eyesight, my
vision is not the best in the world. I have wore glasses since I was in
elementary school, but I can see ok.I rarely have headaches since I have
been on Keppra and Neurontin for the seizures. I used to have some pretty
bad ones that I would have to sleep off.I started having seizures when I was
a baby. I am 40 now.I went down a set of stairs when I was 6 months old. I
started having them after that happened. I get a bad taste in my mouth a lot
of the time before I have the seizure. I grit my teeth and slobber a lot. I
can not remember much about them, but my boyfriend tells me that I mumble a
lot and try to do things I don't know I am doing. They last a few minutes
usually, but every now and then a little bit longer.Stress and hormones seem
to cause a lot of the seizures I have.Things I have no control over. Your
seizures sound like they are dangerous for you to be by yourself. Do you
ever feel them coming on?Sometimes I do and sometimes I don't. Well I guess
I will talk to you later, write anytime. Take care of yourself.

Tammy

On Sat, May 30, 2009 at 3:44 PM, Nancy Livesay <nlivesay1801@ yahoo.com>wrote:

>
>
> Do you get disiability? How do you live? I am single and have know way of
> supporting myself. Theese are in my eye sight and I can not see when I have
> them. Sometimes it is in just my right eyea as the dr. says the right side
> is worse. I also have very bad headacks. What are your simtons. How long
> have you had seizures?
>
> ____________ _________ _________ __
> From: uniquepnk tds.net <Uniquepnk@tds. net <Uniquepnk%40tds. net>>
> To: epilepsy@yahoogroup s.com <epilepsy%40yahoogr oups.com>
> Sent: Saturday, May 30, 2009 3:17:53 PM
> Subject: Re: [epilepsy] hi
>
> Welcome to the group. I have complex partial seizures that are the result
> of
> a head injury. There is plenty of information here. If I can help you with
> anything, write anytime. Take care.
>
> Tammy
>
> On Sat, May 30, 2009 at 10:13 AM, potter darnell <cigars1small@ yahoo.com
> >wrote:
>
> >
> >
> > Just wanted to let everyone know I have joined the group
> > cigars1small
> >
> > [Non-text portions of this message have been removed]
> >
> >
> >
>
> [Non-text portions of this message have been removed]
>
> [Non-text portions of this message have been removed]
>
>
>

[Non-text portions of this message have been removed]

[Non-text portions of this message have been removed]

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