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Epilepsy & Seizures | Last Active: 8 hours ago | Replies (21)
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Replies to "Epileptic seizures are not a choice. I don't wake up and say, wow today wod be..."
I write to try and keep people from going down the road I did. It wasn't a pleasant journey. I need to tell more about my TBI journey for people to understand.
My disability is determined based on how I live with the possibility of having a seizure. A seizure is disabling, I don't let the possibility of having a seizure cause me to become totally disabled.
Seizures ended my life as a CPA, I went from being productive to being a burden. My life changed in seconds with a TBI from a car accident. It was as if I had a sudden onset of dementia, I couldn't think straight, remember where I was or what I was doing, got lost walking around the block. Someone had to be with me 24 hours a day. I no longer had a life. I became so despondent that it scares me to think of what I might have done and how close I was to doing it. I had to change my thinking.
I don't wake up thinking today's a great day for a seizure, I wake up believing today will be a great day. I try to see a seizure as an event in my day and not my total day. Yes, a seizure is humiliating, I often apologize after one. I know there are people who don't want to be in public with me because I may embarrass them with a seizure. I can't let that person control my day and I encourage everyone else not to let that happen.
There are days I just want to crawl up in a corner and vanish from the world. I can't allow myself to dwell on those days or I'm "dead" long before I die.