Anyone need advice or talk? Living with Grand-Mals and A ok still :)

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Many of you have replied that you suffer from t/C's and I assume take meds but it doesn't seem that anyone's seizures are under control.
My t-c seizures are under control, they have been for nearly 5 years now on Lamictal. And I would probably have an even longer seizure-free track record if I hadn't tried twice to go med-free in the 13 years since diagnosis.

But I understand your point. I think you need to keep in mind that a lot of people come to CWE when the diagnosis is new or unclear, or when things AREN'T working -- so the membership is probably disproportionately represented by folks who have just begun to look for the right treatment, or for whom the meds haven't been entirely successful.
 
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Hockeyandringettemom

Nakamova is quite correct in what he says, I was getting it very hard to cope after all these years and I was lucky enough to find C.W.E. and yes I still use it as a crutch in ways but the people here are understanding who listen but they will let me know in the end its me and they will try and help.

My t-c seizures are under control, they have been for nearly 5 years now on Lamictal. And I would probably have an even longer seizure-free track record if I hadn't tried twice to go med-free. But I understand your point -- Keep in mind that a lot of people come to CWE when there diagnosis is new, or when things AREN'T working, so the membership is probably disproportionately represented by folks for whom the meds haven't been entirely successful, or who are newly-diagnosed and are still looking for the right treatment.

There is no shame in being able to say friends help me.
 
controlled seizures

Is all relative. I have always been on one medication, with an occasional Valium added to the mix. I have been seizure free for as long as 10 years. Then, ten years ago I went status. My eegs have been mostly normal. Frequency of seizures can change as well as the types that you have. Lots of factors involved. I take nothing for granted when it comes to my brain. My denial no longer exist given the fact I almost lost my life to this disorder. I am proactive now!
 
status epilepticus is acute repeated seizures or one seizure that lasts more than 10 minutes without regaining consciousnes. a medical emergency that requires immediate attention. a tonic clonic usually lasts from 2 to 4 minutes, after that watch very close, and at the five minute mark without consciousness it's 911 time (time needs to be accounted for for them to get there as well).
 
Oh okay I knew about those time lines (made sure my family knew) but had no idea the really bad one went by that name. Thank God or fate or whatever you each believe in that Gigi is alive and well and enjoying life to the fullest!
 
yeah it's best known that way. if that's the case and you're at 5 minutes just tell 911 that it's a status seizure, (hopefully) they know their shit and that's all that needs to be said.
 
Okay my husband has a good question: So far, I convulse for about 30 seconds, then I'm still, then I'm snoring. Reports from people around me say that when they try to wake me up I tell them I'm tired or I just want to sleep and will even roll over put my head on my folded arms and sleep. I have no memory of speaking to anyone when I eventually do wake up.
So the one time he was with me at home (granted got to me just after convulsing had stopped and was already snoring), he just got a pillow for my head and sat beside me and let me sleep. I woke up on my own after about 20 mins. Was he wrong to leave me sleeping? He's wondering now if he should have tried to wake me up even if it was to just get a sleepy response?
Of course I will ask the doc but I value the advice shared here.
 
no that sounds okay (but always keep in mind on here this is people with E talking and not professionals). lol i must say tho alot of times we seem to know more as it's US dealing with it.
he wasn't wrong to leave you sleeping. if you're 'sleeping it off' and not convulsing anymore that's a good thing. he should just stay with you and watch you until you wake up and are coherent and doing things on your own again, which shows the seizing is over and conciousness is intact. that's the goal :)
 
For me personally, letting me sleep off a t/c then slowly waking me before a trip to the hospital is best. Trying to wake me immediately after a seizure has stopped is both frightening and confusing. I hope that helps :-)
 
oh yeah, sleep sleep sleep. even if it's for five minutes or five hours, whatever your body and brain are asking for. ya just go with it, and when you wake up baby yourself as best you can. pj's, movies, couch and blankets. a few days off work, comfort food, whatever makes YOU feel better and helps heal the shock both mentally and physically that you just went through.
 
I agree that unless you've seriously injured yourself during the seizure it's probably okay to be left to sleep it off. I've slept most of mine off. If there's any doubt though -- play it safe and head to the ER.
 
Do any of you have any pointers on what to do when the t/c's become frequent enough that it starts to seem as if every muscle hurts all the time, and the general fatigue never really goes away anymore?

Since August, the frequency of my t/c's has been steadily increasing. I've never been completely seizure-free, except for a period of about five years between the ages of 18 and 23 that now seems like a miracle. But the tonic-clonic seizures used to be sporadic and, as someone wrote above, manageable with appropriate doses of 'sleeping it off' and 'babying' afterwards.

Things are different now. For the month of March, 2013, I stopped counting after t/c #50, which occurred on March 26. They often seem to happen in clusters: I can go three days without having a seizure, and then have four of them on the same day -- but it's not status epilepticus, as I invariably regain consciousness for up to several hours between them.

The net result, for me, of having 50 tonic-clonic seizures over a period of four weeks, is that I feel sore and tired all the time. "A few days off work" is not really an option in that scenario, or I'd have to stop going to work at all.

Before you ask: yes, I've seen my neurologist multiple times over the past few months, and once every three months before that. In the four years since I went back on meds, we've tried eight different medications in various dosages and combinations. Medications that used to work well for me when I was younger don't seem to do anything anymore, and some of the newer ones (like Keppra) appear to actually make the seizure activity worse.

I am not a good candidate for surgery (my seizure activity can't be isolated to a specific region in my brain). And yes, there is a tumor-like abnormality on my brain scan (they're calling it a cyst, which I suppose is less alarming, even if only slightly so), which was first observed about a year ago, but according to one doctor, could just as well have been there since before I was born. It doesn't seem to be growing, or if it is, it's growing very slowly. Nobody seems positive that it has anything to do with my epilepsy, or with the increasing frequency of my seizures. And even if it did, they would be hesitant to take it out, as there would be a reportedly significant risk of permanent vision problems afterwards.

There is one hospital within my reach that does the NVS implant surgery, but I was disqualified as a participant in their program due to other neurological issues I have (I have a mild case of cerebral palsy, which is a movement disorder).

I've now been put on the Modified Atkins Diet, even though my neurologist initially advised against that, on the grounds of it being 'too complicated to stick with'. I've been at it for about a week now, and initial results seem somewhat promising, but not exactly life-altering. I had two tonic-clonics at work yesterday, and was about as useful as a sack of potatoes for most of the rest of the day.

I've essentially been told, by three different doctors, that my issues are 'known and extremely chronic', and that even though we can keep trying to fiddle with the meds until we find something that works at least a little bit, it's likely that I'm just going to have to make peace with the fact that I can have a seizure at any time.

In other words, I have to learn to live with this. But I don't know how to live with fifty seizures a month. I don't even know how to live with ten of them in a month. Like I said, I'm sore and tired all the time. I am extremely lucky in having found a workplace, and a group of colleagues, where I am not looked at askance for having epilepsy, and where nobody complains if I show up three hours late one day, and make it up whenever I can. But it still feels like a huge fight.

I made a list, recently, of 100 things I want to do before I die. It's my way of reminding myself that life is still worth living. Because sometimes, I forget why I'm still trying.

So, besides looking towards the future, what else should I be doing to make the road ahead a little smoother?
 
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Hi Saranoya, sounds like you've been dealt a tough hand. I hope the Modified Atkins starts to make a real difference. Hang in there -- it can take at least 1 to 3 months to really notice a reduction in seizure frequency.

Another thing you might look into is neurofeedback. More info here: http://www.coping-with-epilepsy.com/forums/f22/eeg-neurofeedback-501/ A good book about it is "A Symphony in the Brain".
 
Saranoya,
I hate to hear about the hard times that you have been having :( you sound like an incredibly strong person with great will.
I wish that I had some great solution or suggestion that I could recommend, but it sounds like you are doing a great job exploring your options.
The book (A Symphony in the Brain) that Nakamova recommended is suppose to be really good! I just ordered it from Amazon, but have yet to read it so I can't tell you if it was useful.
Whatever you do, don't give up! The answer is out there somewhere
:hugs:
 
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