myself out of seizures. Now I can't do it anymore. I know when I am going to
have a seizure now, but barely have enough time to sit down. Used to, if
somebody would just talk to me, the seizure would go away.The seizures I
have now are not bad, if anything they are better, but when I have one, they
just have to take their course.
Tammy
On Thu, Aug 26, 2010 at 6:54 PM, <jennieshadow@yahoo.com> wrote:
>
>
> How do you talk out of a seizure? This would sincerely help me!
> Sent from my Verizon Wireless BlackBerry
>
> -----Original Message-----
> From: Julie Hope <epilepsyhealth@sasktel.net<epilepsyhealth%40sasktel.net>>
>
> Sender: epilepsy@yahoogroups.com <epilepsy%40yahoogroups.com>
> Date: Thu, 26 Aug 2010 15:15:53
> To: <epilepsy@yahoogroups.com <epilepsy%40yahoogroups.com>>
> Reply-To: epilepsy@yahoogroups.com <epilepsy%40yahoogroups.com>
> Subject: Re: [epilepsy] Psychogenic seizures.
>
> Good for you though Trish ... seizure free for a year. Keep it up girl. I
> know as some of mine I can talk
> out of too should I catch it in time.
> Julie
>
> Julie Hope
> epilepsyhealth@sasktel.net <epilepsyhealth%40sasktel.net>
> http://www.2betrhealth.com
> ----- Original Message -----
> From: "trish schobert" <jiminycricketblue@yahoo.com<jiminycricketblue%40yahoo.com>>
>
> To: <epilepsy@yahoogroups.com <epilepsy%40yahoogroups.com>>
> Sent: Thursday, August 26, 2010 12:26 PM
> Subject: Re: [epilepsy] Psychogenic seizures.
>
>
>
> Julie,
> Yes I have the real ones too.that is why my doc. still has me on carbatrol.
>
> Mine started when I was 2yrs old.
>
> Trish (jiminycricketblue)
>
>
>
>
> ________________________________
> From: Julie Hope <epilepsyhealth@sasktel.net<epilepsyhealth%40sasktel.net>>
>
> To: epilepsy@yahoogroups.com <epilepsy%40yahoogroups.com>
> Sent: Thu, August 26, 2010 10:59:31 AM
> Subject: Re: [epilepsy] Psychogenic seizures.
>
>
> Hi Trish
>
> Have you ever in your life had the real kind though? Most people that have
> the
> non-epilepsy ones have the
>
> real ones too. Know I do. I have the real ones for sure, but there are
> times
> when am sure they are the
>
> non-epilepsy ones.
> Our daughter had bouts of the non-epilepsy ones and they looked like the
> real
> ones. Seeing she was already on
>
> the real meds the Dr. taking the VEEG put her on a placebo type med. for
> starters.
> Good for you though ... am so happy for you.
> Julie
> Julie Hope
> epilepsyhealth@sasktel.net <epilepsyhealth%40sasktel.net>
> http://www.2betrhealth.com
> ----- Original Message -----
> From: "trish schobert" <jiminycricketblue@yahoo.com<jiminycricketblue%40yahoo.com>>
>
> To: <epilepsy@yahoogroups.com <epilepsy%40yahoogroups.com>>
> Sent: Wednesday, August 25, 2010 9:52 PM
> Subject: Re: [epilepsy] Psychogenic seizures.
>
> Hi Tim,
> I found out that i have them.At first i couldn't understand why i had those
>
> but after working with my epi. psychologist i am now able to talk myself
> out of
> them.I was also showed how my epileptic ones were different so now I have
> been
> seizure free for almost a yr, My doc even took me off 2 of my meds i still
> take
> carbatrol though.She says I may get a drivers license now if i want to.
> Trish (jiminycricketblue)
>
> ________________________________
> From: TIMOTHY <tbb1@prodigy.net <tbb1%40prodigy.net>>
> To: epilepsy@yahoogroups.com <epilepsy%40yahoogroups.com>
> Sent: Wed, August 25, 2010 8:52:27 PM
> Subject: [epilepsy] Psychogenic seizures.
>
> Has anyone with uncontrollable epilepsy found they have PNES(Psychogenic
> Non-Epileptic Seizures).These seizures do not respond to anti epilepsy
> drugs(AED).Epilepsy seizures come on because of electrical activity.If you
> have
> a non-epileptic seizure during a video EEG and it's not on the EEG but
> looked
> like a seizure to nurses.It was probably PNES.A few people with real
> epilepsy
> also have some PNES.
> Tim Baldwin
>
> [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
>
>
>
>
>
>
>
> [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
>
>
>
>
>
>
> [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
<*> To visit your group on the web, go to:
http://groups.yahoo.com/group/epilepsy/
<*> Your email settings:
Individual Email | Traditional
<*> To change settings online go to:
http://groups.yahoo.com/group/epilepsy/join
(Yahoo! ID required)
<*> To change settings via email:
epilepsy-digest@yahoogroups.com
epilepsy-fullfeatured@yahoogroups.com
<*> To unsubscribe from this group, send an email to:
epilepsy-unsubscribe@yahoogroups.com
<*> Your use of Yahoo! Groups is subject to:
http://docs.yahoo.com/info/terms/
No comments:
Post a Comment