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blackcat521
New Member


Date Joined Jan 2005
Total Posts : 13
   Posted 6/2/2005 8:20 AM (GMT -7)   
Okay, maybe I am completely crazy, I hope I am!!!!  I have noticed I have a harder time getting my thoughts in order and end up repeating myself or the same words several times and it ends up coming out like I am stuttering.  Did/has anyone else had a problem with their language or speech after being diagnosed with epilepsy or a change in medication?
 
Any input would be REALLY appreciated!
 
Christie
Sleep Apnea
Hypothyroidism
Insulin Resistance
Adult Growth Hormone Deficiency
Anemia
Epilepsy
 


kayakmom
Veteran Member


Date Joined Jul 2003
Total Posts : 585
   Posted 6/2/2005 9:55 AM (GMT -7)   
Some meds can make word finding harder. Depending on where your seizures start that can also be an issue. My son cannot talk right after a seizure. He can understand some, but cannot speak or will just be able to mumble other times.

I have word finging issues from my frequent migraine. Sometimes are worse than others...

I would talk this over with the neuro. He should be able to help figure it out whether it is meds, seizures or what.....


Hang in there. frusrating I am sure...

Graffixx_sk
Regular Member


Date Joined Sep 2004
Total Posts : 38
   Posted 6/2/2005 10:11 AM (GMT -7)   
Christie
I hope this helps you in some way find solace within your situation somehow, you see I have been diagnosed as epileptic for 24 years now and within the last year I have began expieriencing some very difficult traits such as short/long term memory loss, my speech on occassion presents itself as slurred, repetitive, annunciation can on occassion sound awkward/confusing, and of course I am having more seizures than normal and the really harsh part is that people that I have dealt with for years and strangers as well give out these very strange looks and I feel like some creature from another planet (lets show some compassion people). It seems at times that getting the words out and making my point is feudal and then somedays I am fine. My neuro does not appear to be rattled by this so I went for a secomd opinion and I was told the same thing that my neuro said, "this is a normal side effect from medication and many years of seizures". We are working on a fix through medication and I hope this presents some better results but unfortunately time will tell which appears to be the "rub". I slow down my annunciation and it seems to help to a degree but when I am in a meeting with marketing/advertising executives they dont usually have to much tolerance for someone that does not supply responses at the normal fast speed that is expected. I just do the best I can and remember this you are the same person you were last year and simply put people are gonna have to learn to live with it.
Steve

goodwitch46
Regular Member


Date Joined Feb 2005
Total Posts : 241
   Posted 6/3/2005 9:48 AM (GMT -7)   

Wow, I always thought I was just a nitwit or something. But, I've always had problems with word-finding.  People always seem to get frustrated with me because it takes a long time for me to say things sometimes.  It's even worse when a person finishes a sentence for me. (I just hate that!) 

After my last med change with Zonegran- now my tongue doesn't seem to work right.  That, combined with the word-finding,... now aren't we having fun. 

Another interesting thing that I have is that whenever I would have a seizure, I would start saying the same thing in my head over and over again.  Like maybe ten times.  I mean, as a NORMAL thing- I usually say things in my head many times anyway (does anybody else do that too?).  But right before a seizure occurrs, I will say the same sentence over and over.  And then  the seizure is happening.  You would think I would recognize this sign- I mean it's only happened a thousand and one times!!   

Glenda :-)


complex partial seizures since 22
lamictal 200mg 2x/d
zonegran 150mg 3/d


Graffixx_sk
Regular Member


Date Joined Sep 2004
Total Posts : 38
   Posted 6/3/2005 11:10 AM (GMT -7)   
You know Glenda I can certainly empathize with you on this one, when you said,"It's even worse when a person finishes a sentence for me." That just makes me so frustrated because I really try not to go "off line" as me and my friends have come to refer to it during conversations (I have such wonderful friends because this is a really big deal for me)! or how about this...you are in the middle of delivering a thought/rebutle and you forget like half of what you were going to say leaving everyone just hanging, and this has become worse over the last couple of years for me I wonder if this has any significance in regards to this last year of seizure activitie that I have been expieriencing?
By the way Glenda I was blown away by your post from 5/31 on family,friends,husband...very very nice!
Steve
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