Chelle
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Hi! I am so excited to have found this forum. This week I was re diagnosed with Partial Seizures in the Left Temporal Lobe. My journey started out at the age of four when I had my first seizure. At that time I was diagnosed with focal seizures and took tegretol for several years. When I was about eleven my mom noticed I stop having the "fainting" or "passing out" and the doctors took me off my medicine. Through out this time I have learn that my seizures didn't go away only changed to staring spells and odd feeling in my head. I thought and was told by some that I was just a careless person, unorganized do to my memory, too emotional and moody, made careless mistakes, and a "witch" because I couldn't control my temper. Now at the age of 27 I have learned that my seizures effect my memory, mood, spelling and speech. My doctor has said that with the right medicine I will feel awesome once my epilepsy is under control. But the effects of those years when I wasnt on any treatment make me feel that people including family members and ex-employers were cruel because I truly couldn't control these symptoms.I have epilepsy but I don't have an obvious disease so people just think I am a difficult person. I am relieved to know my diagnosis but angered at the way I have been treated in the past. Does anybody share a similar experience?