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How To Handle Your Seizures at NeuroTalk
Hi Folks,
For those of you who are willing to share any info of the do's and don't when you have a seizure please post so others can learn. It would be a big help if you would be willing to tell what type of seizure you have and the things you want people to do and the things you don't want people to do. Thanks for sharing all your info. it can be helpful to others. May God Bless You! Sue |
Hi Folks,
I have absence (petit mal), complex partial, and simple partial sz. Once in a great while a myoclonic sz. Here are the things I would want a person to do: Stay calm Let me just go about what I'm doing If I'm having a myoclonic sz. just make sure I'm laying down or sitting down so I don't fall or injure myself. What not to Do: Don't call an ambulance Try not to be afraid Never let a Dr. give me neurontin, tegretol, trileptal, or lamictal or I become very sick. Don't send me home from work. I hope the rest of you are willing to share your thoughts and May God Bless You! Sue |
Interesting Topic
Interesting thread Sue!
:) I suffer from birth defects (making it brief) which causes me to sustain neurological issues including Epilepsy - in turn I have multiple types of seizures, all of them which may or may not generalize, which may or may not go into status epilepticus (aka SE), which may or may not result back-to-back seizures whether of same type or differing type. Loss of conscious is common as well as loss of memory. I suffer from: Tonic Clonic / Tonic / Clonic-tonic-clonic Absence Complex Partial Electrographic Simple Partial Reflex - aka Gelastic: Laughing; Startle; Musicogenic Non-Typical Absence and there's more. While the usual mode for Epileptic Seizures is 5 minutes, but in my case if it lasts more than 10 minutes, call the ambulance and do not let me sleep and keep me awake; virtually the opposite of what is the usual standards for a person with Epilepsy after a seizure, there's too much danger involved on my end, and while it's natural for one to go to sleep after a seizure; the hardest part is keeping me awake. I have a tendency of being very slurred in my speech, being incoherent, disorientated, non-responsive, wandering, and I need to be kept seated and awake until the Paramedics or Ambulance Techs arrives and they will handle me from that standpoint - I'm already on the database and they know what to do as well at the Hospital. I'm classified as level 4 - critical. ==================== However the good news is after all these decades, even after two different HMO's twice in the past turned down brain surgery decades ago - I may be able to have brain surgery coming up. ::: crossing fingers :::: And if the surgery is ever done, it won't repair or restore the brain / nerve damages that have already been done; but it may slow or possibility cause healing of that which are about to become damaged / destroyed. The surgery may reduce the seizures I have (which have been on the increase), but they are unsure if it would eliminate it entirely; there's a very high chance I will most likely will always be on AEDs for the rest of my life as always, however, there's a possibility they might be able to LOWER the dosages where I won't have to take such a high dosages; and what would be nice if I didn't have to take so many either. (Sorry for the long post) |
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