What is Epilepsy Seizures
Epilepsy (often referred to as a seizure disorder) is a chronic neurological condition characterized by recurrent unprovoked seizures. The condition is named from the Greek epileps...
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Epilepsy (often referred to as a seizure disorder) is a chronic neurological condition characterized by recurrent unprovoked seizures. The condition is named from the Greek epileps...

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Scared & confused
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Hi I am new to this. I have quite a few other diseases/conditions & now it looks like I may have seizures/epilepsy. For about the last 12 months I have been having "blank outs" where I just stop what I am doing & stare vacantly. I get a jolt/shake feeling through my body & then confused about where I am or what I am doing. I have told Dr's & they have not seemed concerned & don't investigate it.
I also do things like I just typed up this with details, didn't click submit & then must have clicked x to close without saving. Hubby said I looked like I had fallen asleep. Anyway I was ignoring these blank outs as Dr's didn't seem concerned & too much else going on health wise ESP with ms. Wednesday I was at work & had the worst one ever. I had felt a bit out of it before lunch but after I ate felt fine. I remember about 2pm thinking I am going to take a break soon & get a drink etc. Next thing was a colleague came up to me & started talking, I could hear the voice, see she was talking but not understand anything. I suddenly jerked a lot & asked what she wanted. She said I had been staring at computer then her. She takes over from me when I finish as I am part time & she works the days I don't so we usually tell each other what we are up to workload, I looked at the work on my desk & some was face up, some face down & out of order, on the screen some had been completed & some hadn't. I was totally confused, didn't know what I had done & hadn't. I almost cried. It was 3pm which is my finish time & I don't know where that time went or what I did, It was a very scary feeling. When I went to stand up I felt like I was out of my body or out of control of it. I struggled to walk as my legs would not move when I told them to. I thought that was ms but I still couldn't put two thoughts together or make sense when I spoke. That night I could not stay awake & kept dozing off all the time. I was totally exhausted. The next day I got up & it took me forever to get organised to go to physio, I got there & was ok, it is a group for people with ms. We have coffee after in the coffee shop & I was talking to a couple of them about the previous day & they said it sounds like epilepsy. My foot/leg/arm/hands also jerk, numb etc which I thought was ms. One of them has epilepsy & said it is the same as what happens to her. Later as I was chatting to one of the others I (apparently stared blank, ) at her, then I shook myself & went to continue our conversation form a few minutes before. She stopped me & told me what had happened, exchanged a look with the girl opposite me who then said I had just had another seizure & told me what I had done. This is getting very scary as I don't know its happening & get very confused & it is happening more often. I spoke to Dr who was not concerned. I am seeing my neurologist on 22nd so will ask him about them. I know you aren't Dr's but does this sound like epilepsy to any of you & what should I do when I go to the neurologist, like ask etc. Any & all help or advice would be appreciated. Thanks, Sue Posted on 10/10/09, 07:10 am |
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Thanks for your reply & all the care, support & encouragement on here. I am still having the small blank outs, more often.
Had the eeg & struggled with the lights for sure & could barely open my eyes at the end of the test. Dont know if that means anything or not. I get the results thurs week so will be glad to know if it shows anything. Thanks again everyone.
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Good Morning AusSue,
I am new to DS, but, an old 'pro' w/ EP. :) What you have described sounds like 'absence seizures'. Here is a link that describes the various types of szs. http://www.faqs.org/faqs/medicine/... Questions for DR: http://www.nomoreseizures.com/ Please educate yourself about Epilepsy & all it's aspects, including treatments & alternative treatments. ie: medications, neurofeedback & diets. There are lots of links posted at WebMD support Group, if you need more. :) It's good that you do keep a Journal/diary. It is usually the first thing I tell anyone w/ suspected seizure activity. Foods, activities, seizure activity (time of, length of, recovery period) even your mthly., need to be included. About your EEG. Are you aware that seizure activity MUST be present to show on these tests? If yours comes back 'normal' (from what you said I doubt it will) insist on a 24-48hr portable EEG. Keep us posted. Know I care. HUGS! Love Candi
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Thanks you so much for your responses & esp to dancer for the links too. They were certainly very informative & I appreciate them as did hubby who read them too & said the absent ones would explain a lot of what has been happening. I had one or 2 of these last night too.
Thanks also about the info on eeg, I didnt know they ger ones if nothing shows. One benefit I have is that he did one a few years ago & it showed nothing so this should show changes (I hope in a way as I want to know what is causing it & how to treat it). It is scarier not knowing. I do have trust & faith in my neuro as he is thorough & listens. Will keep you updated . I cant thank you all enough for your help.
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Have been back to neuro & he said I do not have epilepsy, said something showed but thinks it could be to do with ms.
Thanks for all your support. I am relieved that it isnt ms but knowing what is wrong.
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Hello AusSue,
Please consider getting a second or third or more opinions if your symptoms persist. Insist on a portable 24-48 hr EEG. If those tests come back 'normal' & you STILL have symptoms then seek an epileptologist (seizure specialist), Usually found in the larger hospitals or 'teaching' hospitals. Honey, I trust my neuro, also. But, ALL my EEG's have been normal, except the last one. Which was the portable. Love Candi
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Thanks for your response Dancer. I did ask about the portable tests & he looked at me puzzled & said they don't do that. I am not due to see him again till march so will see what happens between times.
He did say that It could be from varying sugar levels - hypoglycemia/diabetes. I get regular tests for diabetes as it is in my family. It is not easy to get another opinion as then they want all the records tfr'd etc. Guess its going to be like the ms, long track/wait for any dx. Just going to try not to stress & keep an eye on it. Thanks again
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For the past ten years I worked in a nursing home, in which provided me to educate myself. During this time, my husband's behavior I noticed was changing. After seeing 3 different physicians and they themselves were unable to put together the signs. While taking my PSW certification we were studying epilepsy. When the next visit came I mentioned to the specialist that I felt my husband perhaps may have epilepsy and asked me what I would like done. I replied I would like an EEG and a catscan done.
They found he had left temporal lobe epilepsy. His seizures are exactly what you are explaining. They are called Petit Mal Seizures or Blankouts. He was diagnosed 3 years ago. The doctors have been messing with his meds and he just recently suffered a Grand Mal and I had to call 911. Don't let this go untreated push your doctors, to run the tests so they can fully diagnose you as being epileptic. Good Luck hope this helps.
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Thanks for your reply saphire. I am mostly keeping a record of what is happening though sometimes I forget. My gp is still concerned about it & has said that she will keep an eye on it & not convinced that it is not epilepsy or otherwise tia's which dont sound quite write even to her.
I guess I am going to have to wait & see or have something happen when I am at the Dr's. It is just one more thing going on & as usual I am never dx straight away. I really appreciate the support here esp as I dont seem to be getting straight answers.
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