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New To MyEpilepsy.Com
Wed, 11/08/2006 - 16:24Comments
Re: New To MyEpilepsy.Com
Submitted by hlatchjr on Wed, 2009-12-16 - 21:36
Hey Kathryn: Don't feel bad about nothing showing up in your EEG's. This has been the story of my lifes since I was in my 20's. I'm now 62, turning 63 on Dec. 21. Everytime I go in for any testing, nothing ever shows up. I've been asked to go see a Psychologist/Psychiatrist claiming that my "episodes" are the result of stress. I was treated with medication, Keppra and Lyrica for almost two years. During that time, I experienced more "seizures", or "episodes". I too had a 5 day EEG being monitored via audio and video cameras for 24/7. My "episodes" showed up on the EEG, but the doctor shrugged them of as "stress". Like I said earlier, most of my life whenever the doctor couldn't find what's wrong, the doctors said it's all in my head and I should get professional help. After taking the doctors advise, I did go to a Psychiatrist/Psychologist. After only a few visits, they would ask me why I was there. I explained what the doctor said. The told me that Psychologly speaking, nothing is wrong with me. What is wrong is of a medical nature and they have to find out what is going on. Usually after 3-4 years, either I still have the symptoms or they disappear, but by then they have either come up with a name for my symptoms or can treat me better due to a betterment in the medical field. MY POINT, DON'T EVER GIVE UP. THERE IS ALWAYS HOPE. SO DON'T DISPAIR. Just hang in there. I'm always here to offer my 2 cents if someone is willing to listen. You can also reach me at my main email address: dmndmstr@gmail.com. Keep in touch, I look forward to hearing from you again. Henry
Hey Kathryn: Don't feel bad about nothing showing up in your EEG's. This has been the story of my lifes since I was in my 20's. I'm now 62, turning 63 on Dec. 21. Everytime I go in for any testing, nothing ever shows up. I've been asked to go see a Psychologist/Psychiatrist claiming that my "episodes" are the result of stress. I was treated with medication, Keppra and Lyrica for almost two years. During that time, I experienced more "seizures", or "episodes". I too had a 5 day EEG being monitored via audio and video cameras for 24/7. My "episodes" showed up on the EEG, but the doctor shrugged them of as "stress". Like I said earlier, most of my life whenever the doctor couldn't find what's wrong, the doctors said it's all in my head and I should get professional help. After taking the doctors advise, I did go to a Psychiatrist/Psychologist. After only a few visits, they would ask me why I was there. I explained what the doctor said. The told me that Psychologly speaking, nothing is wrong with me. What is wrong is of a medical nature and they have to find out what is going on. Usually after 3-4 years, either I still have the symptoms or they disappear, but by then they have either come up with a name for my symptoms or can treat me better due to a betterment in the medical field. MY POINT, DON'T EVER GIVE UP. THERE IS ALWAYS HOPE. SO DON'T DISPAIR. Just hang in there. I'm always here to offer my 2 cents if someone is willing to listen. You can also reach me at my main email address: dmndmstr@gmail.com. Keep in touch, I look forward to hearing from you again. Henry
hi I'm new to epilespy.com
Submitted by keppra2012 on Sun, 2012-06-24 - 22:15
Hi my name is diane in May 2011 I had surgery to remove a pituitary tumor only have was removed. In february 2012 I suffered a stroke as a result if the stroke i started have seizures. was put 500mg of keppra. I later went on to have more seizures was hospitalied again in march for break through seizures. keppra up to 750mg twice aday. Had more seizures keppra up to 1000mg twice a day. Had more seizures keppra up to 1500mg twice a day. was told i had secondary epilespy as a result of the stroke surgery radiation treatment anybody else experienced anything like this. keppra makes me sleep all the time how can you work or do anything like this