Thursday, April 29, 2010

Re: [epilepsy] Re: where is everybody

 

Julie,
Yea, mine are all due to stress, and over doing it, and everything about.
So I just give it all to God as he says to lay it at his feet. I know that is hard to do, because I do have a 21 one year old, who thinks she knows everything, and I am so glad that she doesnt live with me and I can take her back to her apartment! It just we dont get along that well, and now that I have been giving my cares to god, my weeks seem to do alot better as so do my days. Im not as stresses out, but when I work out is the best feeling ever. I havent been able to, because I have been sick and cant seem to shake this off. I havent had a sz, but today has been the first day of a true aura. So I pray that it is not one coming on.
Deb from Texas

________________________________
From: TIMOTHY BALDWIN <tbb1@prodigy.net>
To: epilepsy@yahoogroups.com
Sent: Thu, April 29, 2010 1:02:55 PM
Subject: Re: [epilepsy] Re: where is everybody

 
Julie Hope,

Part of what you mentioned is probably a problem that I've noticed too,alot of times when my time since being aware of a seizure has gotten to or just beyond the time for one to happen.I have one.Afterward I think that it was may've been due to stress or the thought that brought it on.If I wouldn't have thought of it,maybe it wouldn't have happened.

Tim Baldwin    

____________ _________ _________ __
From: Julie Hope <epilepsyhealth@ sasktel.net>
To: epilepsy@yahoogroup s.com
Sent: Thu, April 29, 2010 1:50:33 PM
Subject: Re: [epilepsy] Re: where is everybody

 
Makes you wonder doesn't it why some people have seizures and others don't. I know if I personally don't get
sick and keep my immune system up, or watch I don't get stressed out/over excited, and watch all the things
that may trigger a seizure for me I am ok. Another thing is getting past the thought of looking over my
shoulder and afraid of a seizure happening, be happy etc. I am ok. I use to think oh oh, Glen will be gone
for the day what happens if I have a seizure and nobody is here, that grows and grows in the back of your mind
and sure enough that is when I will have one. Acceptance is the key to mine. I have it, don't know when it
may come, but at the same time am not going to watch for it coming. Also working or doing whatever I have to
do at an even pace. Don't hurry me, let me be me. Slow and easy gets it done.
Julie

Julie Hope
epilepsyhealth@ sasktel.net
http://www.2betrhea lth.com
----- Original Message -----
From: "Shan" <surpriseshan2@ aol.com>
To: <epilepsy@yahoogrou p s.com>
Sent: Wednesday, April 28, 2010 3:47 PM
Subject: [epilepsy] Re: where is everybody

And what causes epilepsy?

--- In epilepsy@yahoogroup s.com, Julie Hope <epilepsyhealth@ ...> wrote:
>
> The biggest majority of times we do not know why we have seizures. Unless we have some underlying cause to
> pinpoint.
> A lot of the tests we take are to eliminate these things...like stroke, diabetis, things like that they can
> actually say is the cause. Otherwise we just plumb have Epilepsy.
> Julie
>
> Julie Hope
> epilepsyhealth@ ...
> http://www.2betrhea lth.com
> ----- Original Message -----
> From: "Deb few" <na_na_76904@ ...>
> To: <epilepsy@yahoogrou p s.com>
> Sent: Wednesday, April 28, 2010 6:21 AM
> Subject: Re: [epilepsy] Re: where is everybody
>
>
> That is true, because my seizures have never shown up on one. And I take genric brands on one of my meds for
> sz.
> I have gone to other dr's and they dont even know why I have them.
> Deb from Texas
>
>
>
>
> ____________ _________ _________ __
> From: Millie Myers <mylmy@...>
> To: epilepsy@yahoogroup s.com
> Sent: Tue, April 27, 2010 11:15:31 PM
> Subject: Re: [epilepsy] Re: where is everybody
>
>
> Jamie,
>
> Just because a sz doesn't show on the EEG doesn't mean she doesn't have EP.
>
> Quite a few of us have better luck with the brand name than generic.
>
> Millie
>
> ----- Original Message -----
> From: Jamie
> To: epilepsy@yahoogroup s.com
> Sent: Tuesday, April 27, 2010 10:16 AM
> Subject: [epilepsy] Re: where is everybody
>
> My daughter Megan (9 years old) is the reason I joined. We are still trying to get a diagnosis. First the
> neuro said looked liked epi. but they have never showed on EEG. SHe only has them at night and the look like
> simple partial. They come in clusters sometimes as often as every cople of minutes and sometimes 45 minutes
> apart. She is on generic for Kepra. Each time we would increase the dose we had a couple of weeks without
> any,
> omce we had 13 weeks with out an episode. We thought okay we got it but they came back.
> Her neuro is referring her to Stanford where they will look at sleep as well as seizures. Hopefully we can
> get
> some answers but at least she hasnt been having them night after night any more and her emotional helath and
> physical health has imporved so much since we started treating her.
> Thank you all for this site. It really helped me especially at the beginning and continues to do so.
>
> Sincerly,
> Jamie
> --- In epilepsy@yahoogroup s.com, hanan khimish <hkhimish@ .> wrote:
> >
> > Hello everybody,
> > I open my mail every day and I was surprised that I have not seen any mails on the site for two days.I
> > hope
> > there is nothing wrong.
> > Best wishes.
> > Hanan
> >
>
> [Non-text portions of this message have been removed]
>
>
>
>
>
>
>
> [Non-text portions of this message have been removed]
>
>
>
> ------------ --------- --------- ------
>
> Just a friendly reminder: Please remember to sign your post and remember to clean up messages when you reply
> to them. This is especially important if you are on digest. This not only helps out the list owner but, it
> makes messages much easier to read when they arrive in our inboxes.
>
> Yahoo! Groups Links
>

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