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Welcome to the Coping With Epilepsy Forums

Welcome to the Coping With Epilepsy forums - a peer support community for folks dealing (directly or indirectly) with seizure disorders. You can visit the forum page to see the list of forum nodes (categories/rooms) for topics.

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Jeannie55

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I am new to the site. I got here by Goggling questions about Vimpat. From what I have read so fare I am very happy to have found it and I have a ton of questions. I look forward to talking to a lot of people. :)
 
Hi Jeannie55, welcome!

Glad you found us!

Best,
Nakamova
 
Hi Jeannie,
So what's your story? Do you have epilepsy? If so how long have you had it? Do you know what triggered them? I'd be curious to know. Hope you feel welcomed.
 
Hello and Welcome :hello: Enjoy browsing around. This site is full of great people always willing to listen and help you out.
 
Thank you eveyone for the welcome.
Cordero: Yes I have epilepsy, my symptoms started about 15-16 years ago but were never truly diagnosed until last year. I have had one doctor told me it was mental issues, had another that tell me it wasnt epilepsy but a disease in my brain ( but not epilepsy), I finally went to a doctor who sent me to a specialist in Miami, Fl. who put me on a 24/7 EEG and found the true problem, Epilepsy of the Right Temperal Lobe. That was almost a year ago.
As for triggers I dont have any, the seizures just happen when and were they want. The diffrent types have increase and they have gotten worse over the years.
The doctor who claimesd I had a disease in my brain tryed me on many of the other meds for epilepsy and I have had very bad reactions to many of them. At this time I am on Vimpat 100mg 3x a day and it seems to be working pretty good and no depression or rashes.
 
Wow, that's amazing that you went that long before they diagnosed it as seizures. It must have been frustrating at first when they diagnosed it as mental issues. Hope Vimpat continues to work. Best wishes.
 
I feel your 'pain' Jeannie55. I was first diagnosed at 15 with PTSD and put on zoloft, pretty much figured an open and shut case by mental health. I didn't start having TC's until I was 25 and they wouldn't begin to admit what had been going on all those years were simple partials until I was 28. Never needed a psychiatrist, needed a neurologist. Didn't need zoloft, needed AED's. Frustrating to say the least, and life changing as 10 years without the e diagnosis has caused complications. Glad to hear you found someone who knew what they were doing - all the best of luck in the world to you!!
 
Welcome dear friend!
Its good to here that atlast u have a doctor who can understand ur syndrome and illness. We are here to help u anytime and any of ur health related issues. I too had to change many doctors and medicines too. This is a tough path but leads to a point where u definitely come to know that u are much more strong than the world as u can suffer much more and still live. Keep smiling always!!
 
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