I am new to the group. I had my first tonic clonic sz in Nov. of 2002. As a rule my seizures occur several months apart. There are usually multiple sz in each episode. I have been taken to an ER each time I have sz.
My neurologists have asked me questions about aura preceeding the sz. I know that each sz has been preeceded by a "feeling" in my head that has been present for various lengths of time from several hours to about 20 minutes. I find it very difficult to dscribe the feeling, i.e. it is not a pain, it is not a preasure or numbness but those are the closest descriptive words. I have "feelings" in my head almost every day. These feelings can be similar to the aura but are not always. Because several months can pass between sz I have a difficult time distinguishing between the aura like feelings and the true aura. Has anyone experienced auras similar to mine and how are the auras described? And, Do any of you experience false auras.
Parksboss
I take lamictal 600 mg and topamax 100 mg
I have also been given adavan to take if I thought I was about to have a sz. Adavan given by IV has been succesfully used in the emergency room after the last two sz to prevent me from having additional sz during the episodes. This is why it is important for me to distinguish between a real aura and the false auras.
25 years old
I am 25, I started taking auras when I was 18. Mine feel sort of tingeliy and enjoylble, or so I thought. I had my first Clonic Tonic sz when I was 21. Anytime I have ever had a Fit ' i got a warning' I dont know if it is a blessing or a curse.
Hi Parksboss-
I can identify with what you mean when you say a "feeling" in your head. It's really hard for me to explain to people what goes on inside my head when I begin to feel the onset of a seizure. I can't stop it from happening and even though the "feeling" can't easily be described, I know exactly what it feels like to me. I think of it like a big weight. But it isn't on the outside of my head, it actually is on the inside of my head pushing out. At the same time, I get a feeling in my arms and under my chin like I'm holding a really big ball that is getting bigger and bigger. I feel panicky when the feeling gets intense, partially due to the feeling of claustrophobia and being crushed from all over. The feeling is all over in a matter of about a minute or so.
Although I learned after awhile what the character of these seizures where like, it didn't seem to make them any less intense when I was having them. What did seem to help the most was what I did AFTER it happened. I was always drained of energy afterwards and it really helped me to sit down and do some relaxation breathing.
I've read that a large percentage of people with seizures have non-epileptic seizures as well. It makes me wonder how many I've had! I'd still do the same no matter what the origin. I still have to take my meds. And the relaxation exercises help me anyways!
Glenda
complex partial seizures since 22
Diagnosed with epilepsy and ulcerative colitis in 1979,
Had My Brain surgery, and I was so scared, but the doctors made me feel good and and I did. They kidded with me before the surgery and before I knew it I was in recovery Thanks for helping me. Mine is on the left temporal lobe. They say it is deep it my brain.