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#1
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Epilepsy the word |
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#2
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| You could tell people that you have a seizure disorder. Or even a variant of a migraine disorder. But really I think the best policy is to be frank -- explain what epilepsy is and then move on. I understand your reluctance because the word epilepsy is still quite stigmatized. On the other hand this is a great opportunity to educate the people around you. Just make it clear that it isn't your whole identity. (If it's easier, think of it as being like having asthma, telling someone that you are asthmatic, that you have to be careful to avoid an asthma attack). |
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#3
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| I totally agree with Nakamova, just consider yourself as a "Person with a seizure condition" to stop all the stupid questions b/c the term "Epilepsy" carries a stigma and most of the general public are uneducated in that area and still think that you have a "MENTAL" desease. Randy
__________________ Diagnosed with epilepsy and ulcerative colitis in 1979, Been on meds ever since. 275mg-dilantin/day 120mg-pheonobarb/day 3,000mg-Mesasol/day |
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#4
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| The hardest part is dealing with stupid people people are so mean and cruel look on the news people being bullied because of being different I don't get it why people are like that |
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#5
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| It's funny how far I have come with this. I read the original post from last April and I can actually remember feeling how I did, the embarrassment and the struggle to come to terms with this condition. It hasn't been all roses and easy, but I'm ok with being me as far as epilepsy goes. I have other issues and the drugs are really hard some days, but I believe I have accepted being epileptic and I no longer feel embarrassed by it. I can explain it to people better, sometimes it's hard to explain I have just had a siezure, but I think that has more to do with the fact I have no idea what my actions were it how long I was out of it. I can finally say it is part of who I am, but by no means does it define who I am. Now to move on to the rest of my life as well as figure out how to accept the drugs. Those are still effecting me and how I act and feel. |
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difenbaker (11-07-2011) | ||
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#6
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| I have a seizure alert dog with me 24x7, so it's pretty hard to be discrete about it. But, I never tell anyone I have epilepsy. I tell them I have seizures. Epilepsy is a label, whereas seizures are something I do. The word "epilepsy" implies different things to different people, and most of those things don't apply to me. I'm a guy who does lots of things - seizures are just one of them. Similarly, I play the violin, but I wouldn't call myself a "musician". I sail, but don't call myself a "sailor". I cook, but I'm not a "chef". All of those labels pretend to say things about me that aren't accurate. Those are all things I do, not who I am. But, here's something else I've figured out: I've found that when people find out I have seizures the first time they see me have a seizure, it makes them perpetually uncomfortable from then on. However, I like tell people up-front, "Hey, I could have a seizure. If I do, it's no big deal, all you need to know is ..." If I tell them that up-front and they see that this is something I deal with all the time, and it's no big deal, then that's just out of the way. They see that I'm not worried about it, so they don't worry about it, and it's immediately forgotten and we can move on. If I leave people to wonder, they imagine the worst and it makes everyone uncomfortable. Last edited by Brent; 11-08-2011 at 12:29 AM. |
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#7
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I also do lots of things, and seizures are an imposition brought on by epilepsy, but I've learned to deal with it over the years.
__________________ "The Golden Rule is that there are no golden rules." ~George Bernard Shaw |
| The Following User Says Thank You to Cint For This Useful Post: | ||
CQ:) (11-08-2011) | ||
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#8
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| I understand. Completely. The word epilepsy scared me. I said it again. And again. I looked in the mirror as I said it. I slowed and elongated the syllables. then i stopped using my voice and just mouthed the word. No voice, just saying the word slowly to the mirror. Whoa!!! Epilepseee started looking like M&Ms. Really! Em In Emzzzz. epilepseee epiepseee em in emzzz em n emzzz epilepseee M & Mzzz. Its just a word. A word that looks rather sweet on the lips. I smile at that. |
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Janus (09-19-2012) | ||
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#9
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| Hi, did you see the vagina monologues ???? I have an understanding of the difficulty accepting that term. I have circumvented the stigma by being all me. Already eccentric. I just tell people now, now that I have accepted that I am not likely to ever see romance in my life again. Hey, I still make art. My ex wife can not stand what I've become, she much prefers the man i was before. At my age (43) and in 'early retirement' but not well-to-do means I am not eligible, so I finally stopped begging for mercy. Hey I am all, epileptic me! and enjoying life. And the patriarchal oligarchy, i say; Sir, god bless the state! by whoever its made, I didn't see nothin' sir, I was just getting LAID." Thank you leonard Cohen. |
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