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employment
Wed, 10/14/2009 - 15:05Hi all:
Lost my job this past May due to mostly my brain. I worked for an attorney, and I was not cut out for the requirements such as multi-tasking, attention to detail, and a fast paced environment; not to mention my inability to concentrate and that my short term memory has packed up and left. Fast forward to August, I went through the hiring process with Fed ex, and when I got the physical I had to disclose my seizure disorder. I do not fit the criteria for the D.O.T.. A person has to be seizure free for ten years, and not on medication. My seizures are when I am sleeping and I have not had one in over six years. Dilantin is still my drug of choice. Back to the drawing board. Have been having trouble with depression, a bonus when having a seizure disorder. I am 52 years old, my only working experience is in an office and that is not an option. I am ready to declare a disability, but not sure I am ready for the red tape that goes with. I need the income, and am in good shape and health otherwise. It seems the job competition is tough and I am trying to figure out where to go next. Anyone familiar with the process of getting hired with a disability? God I hate the label.
Re: employment
Submitted by Capable1 on Wed, 2013-07-03 - 22:49
Gwen, Are you still monitoring this site?
My situation is very similar to yours and I wondered how it turned out since your post was from 2009.
I'm 54 and still employed and getting by on a temporary medical restriction to allow time to regain my skills from my last seizure 5 months ago. My previous seizure was 6 years before this. I too have trouble with multi-tasking, attention to detail, working in a fast paced environment, concentration, short term memory...my manager is ruthless in how he treats all employees but his behavior is especially focused on me and has impacted my overall health and caused more stress and auras/seizures.
If I can't perform at the levels I was previously and the group can't/won't accommodate a permanent restriction then I will be unemployed. Like you I wondered about disability, am in good shape and health so most people wouldn't know I have epilepsy. That said, I'm not sure if I would even come close to qualifying even though I am having trouble performing my occupation as a consultant and trainer.
I too liked Dilantin but upon recommendation of my Dr. because he didn't like the long term side effects of Dilantin. I was doing well on Dilantin and now on Lamictal and I don't care for the side effects.
So how did things turn out for you. I hope in looking back you are at a good place now. We both know the whole 'disability' thing is hard to grasp and harder to describe to friends when they can't know the changes we have to deal with in handling our responsibilities. Recently after forgetting details of our plans a close friend lovingly called me 'Dodo'...ouch. Sucks. Pauline
Gwen, Are you still monitoring this site?
My situation is very similar to yours and I wondered how it turned out since your post was from 2009.
I'm 54 and still employed and getting by on a temporary medical restriction to allow time to regain my skills from my last seizure 5 months ago. My previous seizure was 6 years before this. I too have trouble with multi-tasking, attention to detail, working in a fast paced environment, concentration, short term memory...my manager is ruthless in how he treats all employees but his behavior is especially focused on me and has impacted my overall health and caused more stress and auras/seizures.
If I can't perform at the levels I was previously and the group can't/won't accommodate a permanent restriction then I will be unemployed. Like you I wondered about disability, am in good shape and health so most people wouldn't know I have epilepsy. That said, I'm not sure if I would even come close to qualifying even though I am having trouble performing my occupation as a consultant and trainer.
I too liked Dilantin but upon recommendation of my Dr. because he didn't like the long term side effects of Dilantin. I was doing well on Dilantin and now on Lamictal and I don't care for the side effects.
So how did things turn out for you. I hope in looking back you are at a good place now. We both know the whole 'disability' thing is hard to grasp and harder to describe to friends when they can't know the changes we have to deal with in handling our responsibilities. Recently after forgetting details of our plans a close friend lovingly called me 'Dodo'...ouch. Sucks. Pauline