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Epilepsy testing
My son is going to have the epilepsy testing done on the 13th he will be in the hospital for 7 days. Can anyone tell me what to expect...they said thathe will have an MRI, EEG and then take him of his meds......I wanna have a plan an a idea ofwhat to expect when I go..
Thanks Oh and to anyone that has had brain surgery to remove the affected part of the brain can you chime in, Im having a terrible time even thinking about doing this.. Kimberley |
If it's anything like what my husband went through in May, here's the scoop.
They will hook your son up with electrodes (glued to his head). These will record his brain activity the entire time he's in the hospital. They will probably have a video of him during his stay. The doctors will slowly wean him off his meds to help bring seizures on so they can record the information. It took 5 days before my husband had seizures and they ones he had were horrific to watch. My husband has tonic clonic sz and they are bad enough to witness when he's on meds but when was weaned off, they were 100 times worse! Don't feel guilty if you cannot watch or stay by your son's side during the seizures. After 3 seizures, I decided to go home. I couldn't take the visual any more. I was a complete wreck mentally and physically. They recorded 6 seizures. Unfortunately they were unable to pinpoint where his seizures were beginnning. They concluded they were starting much deeper than what the electrodes could pick up being attached to the head. I pleaded with the nurses that 3 seizures were enough and to start him back on his meds, but the doctors wanted to capture as many as possible. It broke my heart seeing my husband going through so much. Later that night they started his meds up again. The next day was Saturday and I went to see him. I knew he was in a lot of pain and he couldn't talk. He just sat in the bed quietly sleeping. The following days he got his strength up little by little and started getting stir crazy. The doctors told us the next step if we wanted to know where his seizures were beginning, they would have to open his head and place electrodes on the brain. We haven't opted for that step yet. He started a new add on - Lyrica, to Tegretol XR and Lamictal. Good luck and don't knock yourself down if you can't handle the rough stuff during this visit. I was so grateful for the Epilepsy Unit nurses and sitters at Beth Israel here in Boston! |
thanks
thanks for all the information, Im not sure what I should bring with us, for him to do....he is 12, I was wondering if Im allowed to bring snacks for him that he likes, etc.
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Here is a link to my VEEG information. Don't let it freak you out, though. Make sure you don't bring chewing gum though, they won't let him have it (chewing messes up the readings). |
kenausril, I had this done for 3 days and the worst thing was the boredom & trying to sleep at night with a light shining on me. I had a TV so that helped but take other things to do...maybe somehow you can hook up a laptop (or there's battery), some magazines he likes, crossword puzzles, paper & pencils, does he have an I-pod?. I'm sure theres other things to take but I can't think. Also take an eye mask or something, to put over eyes if he wants.
Good luck to your son :wink: |
Hi kimberly
I'm an old woman so it sure won't be the same for your 12 year old ;) but I've had the VEEG twice in a university hospital and I've had no problems at all. Sure it's no fun but but I was happy to see the amount the doctors were learning about my seizures.
My first stay before surgery in 2006 was 4 days and my last stay, this year, was 5 days. Both times I had my "usual" complex partial seizures after reducing meds. My husband refused their offer to spend night and day (no charge) with me. I took lots of books, embroidery, cross word puzzles, stuff like that. Food was awful but I did just fine. They tried to "force" me to have seizures so there were "tests" with the 'light shows', bikes and things like that. Time went pretty fast. |
Yes, they let you bring any food you want in. David's parents and I took turns bringing in italian food for him and Dunkin Donuts coffee.
David complained how bored he was. I brought him his iPod, magazines, DVD player and books. There was a TV in the room. He loved watching the Red Sox games at night but during the day, he was just bored to tears. He used his cell phone a lot to talk to friends. |
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Hi,
When I had my e.e.g they did everything that everyone else has mentioned except how they made me drink diet soda because it caused me to have sz. and they also kept me awake for many hrs. to make me have a sz. I did word search puzzles and did a lot of writing while I had my veeg done. Other e. testing that I had done was an MRI, Ct scan, Pet scan, Spect scan and wada test. All of these tests show the area of the brain causing sz. along with what area of the brain is being used for most of a persons memory and speech. I found the wada test amazing, that's where they give a person a shot in the groin and half of the brain goes to sleep for awhile and then they have you read index cards, and look at pictures of the same person but 2 are the same and 1 is different. You have to pick out the picture that is different. It's amazing how I was able to do all of this with the right side of my brain asleep but when they put the left side to sleep. I couldn't speak even though I knew what the words were they wouldn't come out of my mouth it was like someone whose had a stroke and ends up with a speech problem. Here's wishing you and your son only the best. May God Bless You Both! Sue |
I just had one 2 months ago. Unfortunatly, I was in the noisy area, so do bring some headphones & great ear plugs. I would have left shortly had I not had them. Whining complainers I have no patients for. Had a DVD to kill time. Like it's been said, anything to keep from being bored to death.
Comfy clothes. Gowns are a joke, so pack his every day wear. As stated prior, eye patches come in handy. Aside from the crappy food, noise & that cord that kept being twisted it was not a big deal. |
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