I am Amazed! I am a new member and have been researching since my new diagnosis of Left TLE. The way you all have described your auras, symptoms before and after, and the "unexplainables" just gives me chills knowing that I am not alone. I would be rethreading several of these messages if I posted all of my symptoms. I have been on Keppra 1000mg twice daily since October 2010. I'm feeling like some small symptoms are reoccuring too frequently even if I don't have "full seizure" activity. Does anyone know how soon is too soon to increase the Keppra. I don't want to wait until a "full seizure" occurs, but I don't want to look stupid at my dr's office either. Any help is appreciated.
Write down in a notebook or diary all the things that youre experiencing. My dr was trying to wean me off of Keppra 3000mgs to Lamictal 200mgs daily. During that time period, I had a allergic reaction to the Lamictal, so I had to quit that, and was put on 2500mgs of Keppra. What I was down to at the time I had the allergic reaction. So my dr felt like it was a high enough dose, and left me on that. I went for 3 weeks experiencing numbness in my left hand and foot. No seizures, just the symptoms of the aura I would get before a seizure. When I went to my follow up appointment, I brought this up to the PA. Now this PA didnt know what the heck she was talking about. When I told her about the numbness or tingling feeling I was getting, she told me it wasnt even associated with seizures!? :roflmao:

onder: but then after i asked if I was going to be kept on Keppra, if I could go back to the Keppra XR due to the frequent headaches I was experiencing being on the 500mg tablets of Keppra, she said sure. So due to Keppra XR being only available in 750mg tablets, they put me back to 3000mgs a day. Now within 5 days of being back on this amount, the tingling and numbness I was experiencing on the 2500mgs of Keppra, had gone away! In the meantime, I had to still go see the psych dr and take papers to back up all the progress I had made over the past few months since my neuro dr tried to say I was having non epileptic seizures. After my appointment with her, she saw where I was coming from and agreed with me on these seizures being epileptic and the Keppra treating them. If they were not epileptic seizures, the Keppra wouldnt be treating them and I would be having them. Its crazy how much information we as patients can find, and then we have the struggle of presenting it to the drs to let them see where were coming from.
But in the meantime, I would be writing down everything "New" youre experiencing. Call your drs office, tell them of these things, and if you dont have a appointment set up, I would set one up, or else ask a nurse if you can get your dose of medication increased to see if these things improve.
Ive been on Keppra since the age of 18, and Im now 30. Ive had no problems with the Keppra, and anything new I have, I make sure to write down and let the drs know.
If you have any questions, please feel free to Message me.
