
12-27-2007, 07:09 PM
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| New Member | | Join Date: Dec 2007
Posts: 2
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I have only been on topamax for a short time and have had more seizures on it then I have had in the years since my diagnosis with epilepsy as a teenager. Granted the petit mal seizures have lapsed I have had two grand mal seizures since July and it seems like very small things trigger them, things that I never had to worry about before. I also find that I'm much easily short tempered and emotional on the medication to the point that I sometimes wonder who I am when I hear myself speak to others. My actions don't even seem like my own, especially when handling my son and the people who work under me. I feel for your son as I would not know how to handle such a medication when I didn't have the words to describe what it was doing to me, even now its hard for people to understand that my actions sometimes really are not me and are induced by a drug I am forced to take just to function. I have tried so many medications since my diagnosis 10 yrs ago I'm beginning to give up hope that I will ever live a normal life, and fear that my son has a future of this to look forward to. I don't know what drugs you have tried for your son, but I was most controlled on Depakote and Lamictal however Depakote (valproic acid) has the side effect of shutting off your ability to know when you are full. (something ym doctor never mentioned to me) I took it for 6 yrs and complained constantly that i was gaining tons of weight and was just written off that it was a side effect and atleast I was controlled. It wasn't until I met with a female doctor who explained exactly what it did to your body. So if they suggest it, it is a great drug for the seizures but monitored the snacking because he will constantly think he's hungry and want to eat even if he just had a huge meal and it can definatly get ahead of him. |