Hi Rebecca,
Boy can I feel for you! I went 20 years not driving! My life was affected beyond words by not driving. That isn't even touching upon my seizures themselves! That's not even touching upon how medication side effects affected my life. We all know those different feelings.
One thing I always thought about driving was that I wasn't jealous, I wasn't saying why me ect... I always put myself down as a person! Feeling I was a failure. It took me so many years to accept who I am, the situation I'm in and go from there. I never ever wanted to be a parent because I never felt I would be able to be a good parent because of all it takes. That is just my feelings about my situation in life. Yea, I know where you are coming from Rebecca! Life isn't easy for people who's seizures aren't under control. I'm not saying there is an easy way to deal with it, that I'm not saying. I really don't know what I am trying to say here now(smile)! But hey, 25% of people can't drive who have epilepsy. That is about 750,000 of people with epilepsy in the United States. Its tuff I know since I couldn't drive for 20 years! And never know what day or hour my driving will have to stop by a seizure coming on for an unknown reason! That, is on my mind allot!
Steve
--- In epilepsy@yahoogroups.com, "Rebecca" <par_thomas@...> wrote:
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> Whenever I hear about people driving with seizures I think Jealous. I know I am. I am a mother of 2 children that should be in preschool and I cannot drive them. I have to depend on people to purchase regular daily groceries, and household items. If we are out than too bad. My son will tell me he is bored and wants to go somewhere and I cannot take him. Doctors appointments, I am sure you can imagine, are hell. I do not understand why some people with epilepsy and reoccurring seizures get to drive and others get their license taken. I have been without driving privileges for 2 years now and I would give anything to get to the store and buy my own milk.
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> Rebecca
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