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Does anyone else struggle with becoming disabled? I can't drive within six months to a year of a seizure, and therefore, I have to ask people to drive me around. I also can't work, and I can't cook. It's leaving me without a purpose in life, and at the moment, the most I can do is light activity, and most days, I just lay in bed, wishing things could be different. My seizures are pretty frequent. I'm left feeling like a burden since I can't do much of anything on my own. Even showers can be hard. Does anyone relate?
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Psychogenic non epileptic seizure
Seizure
Epilepsy
Irritability and Anger
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Many individuals with epilepsy have expressed similar feelings of frustration and feeling like a burden due to their inability to drive or work. They often struggle with asking others for help, especially when it comes to transportation. Some also express difficulty in accepting their condition and the limitations it imposes on their daily lives.
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