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My Brain Likes to Rock and Roll!!!

Fri, 06/09/2006 - 13:58
Shocks in my head are the biggest part of my epilepsy but they seem to be the least talked about on these posts. I missed my morning dose of Topamax the other day and all day... bam, bam, bam!!!! I thought I was under attack inside my head. The scary part was I didn't realize I had missed my does until I got home to take my evening dose so I thought my medicine had quit working. On one hand I was relieved the medicine was working on the other hand I was freaked out that missing one dose could bring it on so strong. Is it just a small subset of the E community that gets these brain shocks? tingling, sensations, pulses? zaps? knocks? rattles? rock and rolls? sensations? flutters? clicking?, thunderstorms? taps? spasms? Whatever you call them. Weigh in if you don't mind please. Thanks.

Comments

Re: Re: My Brain Likes to Rock and Roll!!!

Submitted by Ramblinman on Sun, 2006-06-11 - 15:30
Impossible?!?!?!? I once heard that in order for a city to put up a stop sign at an intersection that didn't already have one that a certain number of accidents had to occur at that intersection for the city to fianlly put one up. It sounds like before some neuros believe that something is possible they have to hear it from a certain number of patients for him/her to believe it or read about it in one of their text books. I refuse to go to a neuro that believes they can predict and control the human brain or that believe they can say what is or isn't possible for it to do when it is already short-circuting!!!! Arrogant bleeeeeeeps!!!!!!!

Re: Re: Re: My Brain Likes to Rock and Roll!!!

Submitted by gretchen1 on Sun, 2006-06-11 - 15:54
I LOVED that = "that's impossible". Well then, what's the implication? You're a liar? I used to get that crap from m first wannabe neuro clunker too. I was going through horrid AED trials. Have since found out he didn't have a clue how to do an AED trial correctly. Such as if you're having horrid side effects you go OFF that medication, you don't ratchet it up and down for 3 months. I always got the crimp with any new AED after going through some horrors on 3, so I could read any possible side effect to make sure what I was feeling was a side effect, not something else. One night very quickly everything looked purple or had a strong colored purple cast. At the sametime I had had a seizure and when I recovered my right side would barely move. Obviously my first bout with Todd's Paralysis. But it scared me. I'd never even heard of Todd's Paralysis. I called him in the evening and told him these things. I'm sorry but seeing everything look deep purple was not listed in the literature nor was paralysis and I was fairly sure I was having a stroke and was very frightened. I wasn't trusting my brain at that time for anything. He said - he didn't "recognize" the symptoms but he wasn't worried, didn't sound much to HIM and see him in the morning. First first off I wasn't worried, second why didn't a neuro recognize Todd's. I wasn't worried about HIS worry I was terrified. What about my worry? I couldn't move my right side, I couldn't see right. Then I wondered if he was saying - you're a kook. Then I started wondering maybe I AM a kook. You can not make a telephone diagnosis. I at least learned that in nursing school. I asked him should I go to the ER, he said no, I'll see you in the morning, now loosing patience like I'm a whiney 3 year old. Finally I broke down and said I'm scared, I really think I'm having a stroke. Nope, he didn't think so. My husband and I were so intimidated about all these new things. I'd already had to reschedule my neuropsych eval twice because I was too mindless on Lamictal before to be able to speak I was getting worried about these drugs. So we SNUCK off to another town's emergency room. Thesse conditions very easily diagnosed and they said you're having a medication reaction and Todd's Paralysis. I was HAPPY then I was having paralysis and everything looked purple so I could rub it in this "doctor's" face the next day. The next day when I realized my doctor and I were competing? I felt we probably had a bad relationship but in our area -he was IT. The one, the only neuro. Now that I've had E this long my personal opinion is it can make you feel, experience any old thing it wants to. My very good epileptologist see's me periodically and always asks me - what's new. Then he LISTENS, and he EXAMINES, and if he has no explanation he says so but he never acts like I didn't or don't have these things. He does tell me he keeps an inventory on his computer of all these sensations and wierd events patients tell him and it is a very LONG list. Thank you, I need that respect. I am getting worsening peripheral neuropathy from one of my AEDs is the thought in my feet thus current huming. But I've had this for well over a year- and I just started huming. And I do not like it,one bit. I was on chat last night and my head started clicking. I didn't think I lost cognition when that happened but when it let up for a few, I could see my typing was falling apart and got off. Gretchen

Re: Re: Re: Re: My Brain Likes to Rock and Roll!!!

Submitted by Spiz on Sun, 2006-06-11 - 21:39
I get shocks at the top/back of my head and also above my left ear that are very sudden, sharp and painful. I've always said my brain was short-circuiting again. Take care! -Spiz

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