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I have seizures and they affect my speech

Tue, 01/25/2005 - 16:10

Hi,

 I am 33 years old and I have been having seizures now for about 3 years. It happened shortly after a toxic reaction to topomax. I was in the hospital for a week then and every since then I have had minor seizures off and on. When I do it affects my speech and I stutter bably and lose my thoughts and words. I feel so weird when this happens. I don't know anyone else like this. I have bipolar and dissociative identity disorder (multiple personality). I heard people with these illnesses can have seizures, I just don't know what type. I hate being like this. It makes me more depressed. I am getting so frustrated. I have two young boys and they don't understand why all of a sudden I loose my words or thoughts or I sound funny as they call it. My oldest one is 7 and he does ok. He helps me with my words and he answers the phone for me when I am having trouble talking. I just don't know what to do. My therapist wants to know more information about why it affects my speech but I have nothing to offer because I have been struggling to find information myself. Does anyone have suggestions?

Kym

Comments

me too.. its frustrating...

Submitted by ruthserrano on Wed, 2018-12-12 - 06:54
me too.. its frustrating... especially when i also lose my capacity to hear... 

THE MIGRAINE BABBLE: WHY YOUR

Submitted by mcvay on Sat, 2019-01-12 - 07:21
THE MIGRAINE BABBLE: WHY YOUR WORDS GET JUMBLEDPosted by Paula Dumas | Nov 17, 2016 | 299 .  I found this article. If you can share. I have migraines and get this just before it gets really bad.  

Hello Kym I also go through

Submitted by Jaime_5c9ee22aab2b0 on Fri, 2019-03-29 - 23:39
Hello Kym I also go through this too. I have left Temporal lobe epilepsy.  I lose comprehension, spelling, speech and the ability to find correct words. I was diagnosed over a decade ago. I have found that over simulation such as being on computer on cell phone all the way to dehydration, constipation and lack of sleep really affect me with this very frustrating part of epilepsy. In general mine will last anywhere from 2-4 day's severity is a toss up! 

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