| Thread | Last Post | Replies |
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| Introduction and a question | 19 Dec 2003 22:23 GMT | 23 |
I have suffered from epilepsy for about 19 years; I was diagnosed soon after my 16th birthday. My first attack was little more than a black out while pushing a moped along the road; the 2nd attack included convulsions this was on September 9th. It was at this stage I was
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| It was nice while it lasted ... | 17 Dec 2003 02:34 GMT | 5 |
I kept an appt with my neuro a few weeks ago & seemingly with everything stable, he reduced my medication of Lamictal from 900 mg to 800 mg per day. That reduced my evening med by 1 tablet, & I know that there are people out there that
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| VNS to be activated december,5th | 16 Dec 2003 17:17 GMT | 5 |
hello group. it's been awhile since i wrote. i was implanted on november,20th with a VNS device which will be activated on the 5th of december. late today i had another
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| Son has Progressive Myoclonic Epilepsy /Drs.want us to try VNS | 16 Dec 2003 16:33 GMT | 1 |
My husband & I are having to decide whether or not to have our 16 year old son have Vagus Nerve Stimulator implanted. He has Progressive Myoclonic Epilepsy and has the mental capacity of about a 2 year old (in most areas.) He has seizures off and on throughout the day some ...
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| little girl with partial seizures | 15 Dec 2003 02:16 GMT | 24 |
When my daughter was 4 she had a seizure, she just dropped down while playing, and her eyes rolled back in her head and was unresponsive. She had a normal CT scan, but didn't have an EEG. We noticed today (she is now 5) as she stood on stage as an angel in her
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| Brain Surgery for Epilepsy | 12 Dec 2003 12:42 GMT | 3 |
I apologise if this one has been asked before; I am considering brain surgery as a treatment for my uncontrolled complex partials. Can anyone pass on their experiences or knowledge relating to the removal of some or all of the right temporal lobe ? Any information would be
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| topamax | 12 Dec 2003 05:12 GMT | 1 |
How to Make Money Fast. READING THIS COULD CHANGE YOUR LIFE! I found this on a Bulletin board and decided to try it. A little while back, I was browsing through newsgroups, just like you are now, and came across an article similar to this that said you
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| 5 year old hit by first seizure yesterday | 11 Dec 2003 01:11 GMT | 36 |
My five year old son had a 5 minute seizure at school yesterday. Arms and legs stiff, foaming mouth and eyes curled back. It's the first one he's ever had. Two days before he had an unexplained high fever and the day before he a stiff neck he could not
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| Illegal Driving | 10 Dec 2003 22:25 GMT | 66 |
We all know about the issues involving seizures and driving. Some of "know people" who have driven despite having lost their licenses because they (we) have epilepsy. I would like to get a sense of how common that might be.
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| Recommended Los Angeles neurologists? | 10 Dec 2003 02:10 GMT | 1 |
Can anyone on this board recommend a good neurologist in Los Angeles, preferably UCLA, Westwood, Santa Monica area? I am currently looking over doctors right now with my medical plan and there are just too many too choose from.
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| Muscle and/or Tendon Pain | 09 Dec 2003 16:30 GMT | 6 |
For quite some time now I've been experiencing pain in my arms - forearms & upper arms up to the shoulders, but not in the shoulders themselves. This always develops during the night while I'm sleeping with extreme pain although it gets better once I'm up & about and I
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| Drug Cocktail | 09 Dec 2003 15:45 GMT | 13 |
Here's one for the chemists; I take 400mg of Dilantin (phenytoin) daily in a bid to control my complex partial epilepsy. Yesterday the seizures seemed more severe than normal so before going to bed I took 5mg of Antenex (diazepam) which was prescribed a
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| seizure and adhd | 09 Dec 2003 13:46 GMT | 1 |
i was wondering if anyone on here has a child with adhd as well as taking antiseizure meds mine is 13 and takes 800mg of tegretol daily as well as 56 mg of concerta were having lots of probs with him and wondered if it was the meds
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| 'bout changin'meds | 09 Dec 2003 06:14 GMT | 2 |
I'd like to hear some experiences you all may have had during a med change. My AED's are really expensive and now a divorce is being thrown at me. I may have to use the public assistance insurance and they don't cover my meds. Fear just seems to keep crowding my thoughts.
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| Questions - Strange nights for this epileptic | 09 Dec 2003 05:41 GMT | 6 |
I hope somebody on this board can answer or at least understand some of the questions I have. I have been diagnosed with epilepsy for about 5 years and HAVE NOT had a full blown seizure in over a year and a half.
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