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#1
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Petit-mal seizures (Speech arrest)I've had epilepsy since 1979, controlled by meds. I get a form of petit mal seizures that my Dr. calls "speech arrest". It only lasts a few seconds, I am aware of what is going on around me but I can't respond. When I try to talk, my speech is slurred (more than usual). Most people have no problem speaking but I have to concentrate to form every word. (all the time but twice as hard during a speech arrest). Everybody thinks I'm stoned all the time. Boy, I didn't realize that we take our speech for granted so much. Randy
__________________ Diagnosed with epilepsy and ulcerative colitis in 1979, Been on meds ever since. 275mg-dilantin/day 120mg-pheonobarb/day 3,000mg-Mesasol/day |
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#2
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| The sad thing is that even if you learned sign language, you might have difficulties communicating with seizure activity. I've had dreams where my body does not respond in synch with my mind (like the ubiquitous running in slow motion dreams). It's frustrating!
__________________ Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback Would you like to help support this forum? |
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#3
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| aphasia n : loss or impairment of the power to use or comprehend words Lovely word. A part of my life. Not only from the simple particals but from the Dilantin. Damned if you do or damned if you don't. Sometimes an simple partial will be so bad I cannot speak, however I am aware of what is being said to me. I had a few of those in the hospital after my knee replacement. They sure did freak out the nursing staff, but then they always think the worse if you are unable to respond. The Dilantin makes me trip all over my tongue I say things in reverse, wrong words of words that don't mean anything. At work I am on a microphone and deal with customers, one on one and when this happens, I just play into as a joke like being overworked. Most people are understanding and laugh about it. Hell, why not. I sound crazy half the time might as well enjoy it. This aphasia does carry over into posting on the internet as well. My spelling stinks because my brain is saying one thing, my eyes see another thing and my fingers are doing whater the heck they want to do. I proof read several times but still find errors later on. Life is never dull. We ARE haveing fun now, damn it!
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#4
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| Originally Posted by Birdbomb :
__________________ Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback Would you like to help support this forum? |
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#5
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| Ranman, Same thing happens to me, I call them brain cramps though. I have to say it can get very trying at times. I spent the day yesterday not being able to think or talk. Of course I had a complex partial by the end of the day, they usually go hand and hand. Donna- Dilantin makes it so that I can't get two words out of my mouth without sounding stupid. hate it, hate it, hate it!!!!
__________________ seizure since age 12, focal resection 1992, VNS 2002 removed 2003. Lamictal 400mg, Topamax 100mg daily. |
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#6
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Are we having fun yet?The last two days of the work week, last week, in the mornings, not one consonant was formed while I was speaking. There is another bitch in my work area that doesn't believe that I am sensitive to perfume. Then there seems to be an increase in the number of times my eyes roll to the top of my head. |
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#7
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| Had the same thing happen to me many times when i got absence seizures back when i was first diagnosed. Especially when i got excited and was in mid sentence it would go like this " But you can't seriously believe that ! (pause +blank stare) haaaaooooowwwww .....caaaaaaaannnnnnnn (feeling like i want to throw up) yeeeeeewu pppposssssssibbbbbllllly...... think that?" . Awed observer - "Dude are you on crack?". Doesnt happen anymore when i'm on meds. I usually get myoclonic seizures. I think the best way of describing it is when you have a bad connection on the phone and can hear yourself speak as well so you talk really slowly and try to get your words out consciously
__________________ Dr. Arvind Ramaswamy |
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#8
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How did I find this out? Over the past 28 years, there were several times when I had to disregard my dilantin for up to 2 weeks at a time due to my ulcerative colitis flare-ups (I had to double up on my UC medication which would cause the diantin to become toxic) and during this time I had no speech arrests however I did run a serious risk of a seizure. Once I went back on the dilantin, the speech arrests started again however, the frequency was dependant on the amount of stress I was under. Randy
__________________ Diagnosed with epilepsy and ulcerative colitis in 1979, Been on meds ever since. 275mg-dilantin/day 120mg-pheonobarb/day 3,000mg-Mesasol/day |
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#9
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| I'm not sure if this is relevant, but I have to ask: Yesterday I was trying to talk and my tongue felt like it was swollen, I was really having trouble getting my words round it and also couldn't talk loudly, which was fine if I was talking to the person next to me, but not to someone on the other side of the room. I had to slow down alot, it really got on my nerves, it probably lasted a couple of hours. I must admit I only started Tegretol a couple of weeks ago, but I thought most of the side effects had worn off. Anyone else get this? Munchy xx |
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#10
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no medsMine does seem to be a part of the absence seizure process. Sometimes I think I'm talking, but not. Sometimes I think I am saying a particular word, but say something else, or the root derivative of a word, sometimes I cannot pronounce any consonant, and my tongue seems swollen. Sometimes (and I wasn't aware of doing this) when I'm tired, I start screaming. |
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#11
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| Did somebody post something? I must had missed it! That's what it's like when I have an Absence.... However - when I talk funny, act like a drunk, talk gibberish, slurring words, nonsense, "totally off the wall" --- but it is NOT a Complex or Simple Partial; for the behavior is different ---> especially the key behavior is when I am repeating myself is the major sign that an Atypical Absence is about to start. This how it's like when I have an Atypical Absence, and plus my speech becomes so slurred - like one has given me far too many shots of Jack Daniels, or worse they complain that I'm mumbling ... I think Birdy can explain how I sound like when I have an Atypical Absence ... 'cause I was on the phone with her when my son slammed it down not realizing who it was I was talking to, but of course I didn't remember being on the phone until I was out of it ~ I still have not a clue what I said, but my son said I was out of it! But I did PANIC and FRET for I had NO IDEA whom it was I was talking to at that time of the night! I cannot remember if I PM'd Birdy or emailed but *whew* I got the response that she was the one who was on the phone! ![]() It just happens so quickly, so suddenly, and worse, it can go "back-to-back" and grow worse, hence, why my son sends me off to bed and I'm sound asleep in a flash. The strangest thing is - I have no memory of these events at all, or what I have stated, did, or done! I feel really like a jacka$$ at times when my son tells me the things I had said or I would feel like one heck of an embarrassed sunburnt sheep! ============== For this reason is why I begin to question if there are MORE Atypical Absence than Neurology / Neuroscience realizes? If one reads all the postings from so many who have been declared as Absence (but not Atypical Absence) - there is a slight difference between the Absence and Atypical Absence in the behavior, I've read up on it, but when I looked into the EEG patterns, it's almost really hard to detect because they are almost identical in a lot of ways, but there is one tiny thing that gives way to making it an Atypical Absence, very easy for Neurologists & Epileptologists to miss it; and I am almost positive that the computers are missing it as well. You really have to look at it! When they told me I had both Petit Mal (Absence), Non-Typical Absence (I can't find any reference on this one, so I am unsure what a Non-Typical Absence is, or it could have been an old terminology that isn't being used anymore) and Atypical Absence. Moreover, I had been informed that one can have both - Absence and Atypical Absence.
__________________ Sharon ![]() Support the Team STIGMA TERMINATORS HEADSTORMS RESOURCE CENTER " Vujà Dé - The feeling you've never been in here before! " |
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#12
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| I have similar problems after a seizure. Sometimes I feel OK but I'm told that my wording will make no sense, other times I can understand what's being said to me but I can't get my words together to respond to anyone. Occasionally I am quite fine after a seizure & have no problem at all.
__________________ It's no longer a question of staying healthy. It's a question of finding a sickness you like. -Jackie Mason |
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#13
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| I also have trouble writing during the post-ictal phase. I just had a seizure an hour ago. I went to mark the time of the seizure down in my excel program but couldn't write anything down after the numbers (like seizure, noc etc). I looked at yesterdays seizure which I marked down as noc (nocturnal) so I copied the same thing by todays seizure even though it wasn't nocturnal. It's an hour later & I'm back to being able to type & understand what I read. I also find when speaking post-ictallyI can't remember words despite being able to understand them.
__________________ It's no longer a question of staying healthy. It's a question of finding a sickness you like. -Jackie Mason Last edited by epileric; 12-09-2008 at 05:07 AM. |
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| Thread | Thread Starter | Forum | Replies | Last Post |
| What part of the brain is used for speech and memory? | RachelR | The Kitchen | 6 | 06-10-2008 12:41 AM |