Duration: 08:59 minutes Upload Time: 07-02-27 21:38:31 User: Ca8Amy8 :::: Favorites :::: Top Videos of Day |
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Description: Talking about my epilepsy and seizures and how I hate how the world views it, like it's something light-hearted and not serious. I also don't appreciate when the 'famous' people of youtube have to make fun of other peoples illnesses to be termed funny. It wouldn't be very damn funny if I was making fun of cancer now would it? I didn't think so Here's a link to the kind of seizures I have http://www.healthline.com/adamcontent/partial-focal-seizure I hope this has opened some peoples eyes on this subject. Feel free to comment or even video reply to me. |
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elindsabeth ::: Favorites So look up ketogenic diet, lobectomy, and vegus nerve stimulator. 07-09-18 23:37:33 __________________________________________________ | |
Ca8Amy8 ::: Favorites pennsylvania 07-09-15 22:26:10 __________________________________________________ | |
MonkeysLover12 ::: Favorites i feel so bad for you. my father has epilepsy (though he's only had 2 seizures in his life;he's on meds). do your parents like not give you meds or something? 07-09-14 01:30:53 __________________________________________________ | |
gunit4lyfenigga ::: Favorites where do u live 07-09-09 14:22:05 __________________________________________________ | |
shulkgreenpower ::: Favorites I have tonic clonics. I envy people who have auras. If I had just 5 seconds of notice.. I wouldn't have my injuries. I have broken my front teeth. When biking, I took off a strip of my face 1 inch wide by 2 inches and almost to the bone. I had one near a radiator that had the cover off.. its tines impaled my back and I woke up pulling my body off of the blades. I was so worried that my kidneys got injured. If I had some warning.. I think I'd run and hide. 07-09-07 05:50:55 __________________________________________________ | |
jessicalane24 ::: Favorites I've had these kinds of seizures for 2 years now. I feel exactly like you do at the beginning...a sense of dread, a sinking feeling, like your world is folding in on you. Strange, I know, and difficult to explain. Mine, however, don't affect my vision. Instead, I have a very strong metallic taste and smell and my mouth waters. It affects me for about a week after--I feel out of sorts for that long. Sucks! Medication helps immensely! (I only have them when I forget to take it--duh) 07-09-03 17:50:22 __________________________________________________ | |
andrewtom3d ::: Favorites i got seziers for playing too much video games, and now im on medication, and for all the people whos making fun of seziers u might get it someday, and u wouldn't like it trust me there is alot of things u cant do when u have seziers, like video games, swimming, riding ur bike, and all these other stuff u cant do. and the first time i've have a sezeries i didnt know what just happen, its like u blank out and i didnt even know it, and then few min later i woke up in a streghter in an ambulance 07-08-31 17:48:09 __________________________________________________ | |
Jeter1992 ::: Favorites I'm sorry 07-08-29 00:31:43 __________________________________________________ | |
MySeizures ::: Favorites Ask your Senator, Just like Alcoholics Anonymous, why isn't the Epilepsy Foundation available any where in USA, except designate areas? Who finances the EFA? Besides dispensing redudant self-serving brochures, how, what, where and when did the EFA helped any victim of Epilepsy since it ever came to happen around? I wonder, if the EFA have any idea that victims of seizures are losing every thing they have ever earned for persistent seizures? WHERE'S THE HELP? 07-08-23 19:48:04 __________________________________________________ | |
Twomonths ::: Favorites Do medications decrease the number of seizures, or not? I mean over long-term, not "per incident". Truly, 07-08-21 10:57:07 __________________________________________________ |
Thursday, September 20, 2007
Talking about seizures
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