Looking for feedback to help understand symptoms...

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Rag

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In this thread, I'm going to list some of the symptoms I've experienced over the years. I'd really appreciate it if people reading could take a look at what I'm going to list and compare and contrast symptoms with what they or others they know have experienced, and say what diagnoses they've had. I'm also particularly interested in reading about the subjective experiences of people with temporal lobe epilepsy or who get a lot of nocturnal seizures, and seeing how they compare to my own. In some respects the medical descriptions, based as they are on objective observation of patients rather than personal experience, are not very helpful to me. They have often left me feeling very unclear about whether the thing that is being described in the literature is the same as what I'm experiencing, and I do have a lot of questions I would like to find an anwser for.

Right, on with the symptoms (warning, this may be rather a long and self-indulgent list!). ;)

Many symptoms I get only occur when I'm asleep already.

When I'm awake, the most notable and frequently occuring symptom is a sort of fuzzy, warm, light-headed, amost dreamlike "floaty" feeling that is quite difficult to describe (so I'm hoping that some people here are going to be familiar with the thing I'm talking about, or I could go on for paragraphs and not really communicate anything!). Often it causes me to have some difficulty concentrating on anything for very long *though it doesn't really seem to affect clarity of thought, it simply makes the process of thinking for very long about anything in particular that much more difficult, and trying to do so often exacerbates the feeling*. This feeling is usually in association with later or earlier sleep- related symptoms, though sometimes I don't get anything further, and sometimes I get symptoms when asleep without having this feeling first. Sometimes I get a "butterflies" feeling of impending excitement in my stomach, or what can best be described as a numbness of the roof of my mouth; more rarely a slightly unreal taste, which seems slightly metallic (I can get a sense of it, but it doesn't seem like an actual taste, more like the memory of one, if that makes sense?).

Often the feeling described above causes me to feel lethargic and tired, though I do think I tend to get it more when feeling relaxed already, or close to what passes for my "normal" sleep time (haha, normal sleep? I'm not sure I know what that is!). Sometimes, though this is fortunately fairly uncommon, it's developed further into an overwhelming sense of exhaustion and a kind of heaviness and coldness in my limbs, and I've felt the need to lie down, often when I shouldn't *according to normal considerations of whether I've rested enough* feel tired. If it gets to this stage, I nearly always have some kind of sleep symptoms, as I'll go on to describe. If this happens, far from the need for a long sleep which I apparently had, I will typically revive shortly after symptoms have diminished *they may occur more than once when this happens, over a period of time* and feel much better and more alert, though slightly jittery, and will probably have problems sleeping normally later.

When I'm asleep (or close to sleep, it can be difficult to determine sometimes at what point it triggers) I get a further set of symptoms:

Physical: the most common occurence (happening virtually every time) is a rapid increase in heart rate and a rise in temperature which often wakes me up, especially if I have it in the absence of other symptoms. I've looked at my hands after this happens (when I've woken up, with heart palpitations and rise in temperature continuing) and often noticed a kind of fine tremor in my hands which persists for quite a while. I can often be woken up multiple times during the night by this, or be (sometimes rather dimly) aware of it occuring, while I remain asleep. It can happen multiple times then.

It's not uncommon for me to get some kind of arm movement; I think this is the most common physical symptom other than the raised heart rate and temperature, as just described. It seems most often to affect just one arm, the left more than the right, and usually involves some degree of rigidity, and either a "fluttering" movement or clenching and unclenching of the hand for a while. I have often had at least some awareness of this happening, and had it confirmed by others that it is (when there was someone else there to observe; I'm currently single!). I don't know whether or how much it happens without me being aware, obviously. The longest I've known it to (when there was someone else to observe, obviously I'm not in the best position to judge myself when it's happening) is between 30 seconds and a minute; sometimes it may continue for just a few seconds. I'm not aware of having had any violent arm movement when sleeping, though I have sometimes had odd jerking arm movements which don't seem to be under conscious control just at the point of waking up; never when I was fully conscious and alert that I recall.

I've also at times had upper body jerking (mostly the area of the torso, it seems) and head movement, either head bobbing from side to side, or opening and shutting of the jaw. I'm not aware of ever getting lower body movment at all. The torso jerking, though I think less frequent than the other things, is something I tend to be aware of, and can feel quite scary compared to the others.

Usually if I'm woken up by any of this, I do so with a kind of involuntary groan (though sometimes I feel like it might be a groan of frustration at this happening again ;) ). Occasionaly other vocalisations can happen, usually immediately before waking. On a couple of memorable occasions something was apparently very humorous, and I woke up with uncontrollable laughter at absolutely nothing. Once the strange surge of weirdness (it felt like a numb, flooding feeling in my head) that had provoked it had passed, I didn't feel so amused any more. ;)

Psychological/subjective symptoms
This is where it gets really interesting, and I'm particularly in need of feedback from others on what their experiences have been, the official literature being not so good at describing these things. I don't think I get any of these symptoms when wide awake, so it was difficult for a long time (and occasionally still is) to distinguish them from something more like unusually vivid and peculiar dreams, though the sheer strangeness of the experiences has tended to be pretty telling in itself.

Usually, concurrent with the raise in heartrate and temperature, I get strange feelings. Sometimes it's something which seems more physical in nature, a kind of white-hot, burning, elemental surge which is centred in my chest *or sometimes head* and radiates outwards through the rest of my body. It's a feeling, but doesn't have specific emotional content. It varies in intensity, from just a kind of strange, spreading warmth which is often enough to trigger other physical symptoms, to something that feels like it's taking over my whole body. Sometimes I'm not very aware of it happening, but just wake up with the aforementioned palpitations and raised temperature, feeling strange, though most commonly I will experience it to some extent.

At other times, I will be aware of this more "basic" feeling to some extent, but will also be hit by strange, overwhelming emotions. These can be fear, which can be very scary indeed (especially in conjunction with the physical symptoms, it has felt at times like my body was going to disintegrate utterly and I was actually going to die there and then). It can also be something altogether strange and indefinable (which I don't want to think about too much right now in case it triggers something!) or at least partially pleasurable. A few times it's been overwhelmingly pleasant, and seems similar (as far as I can make out) to what I've seen described as "ecstatic" seizures, but even on these occasions it can be scary beyond the subjective pleasantness of the sensations themselves due to their strange, overwhelming nature, and the feeling that my body might not be able to take it.

The first few experiences I had were all of this "ecstatic" kind or something close to it, and to begin with occured rather infrequently, maybe once every few months. After the very first time I experienced it, I knew something strange was up: "Because that, whatever it was, just doesn't happen!" but due to the fact that it was actually pleasant, and I'd managed to convince myself that maybe I'd imagined it somehow or could come up with alternative explanations, it took me a long time to look into the matter further.

Overwhelming and strange feelings are often associated with the more serious experiences; if it happens it will often happen repeatedly over the course of a night or session of sleep and leave me feeling exhausted and lethargic when I do wake up and try to do things.

As well as these feelings, I've also had strange, vivid dreams. Dreams that are not associated with other symptoms such as the palpitations or weird emotional sensations I tend to disregard as just dreams, however peculiar they are; but it's rather common for them to occur together. Oddly, when I get the feelings, they frequently have no connection with the actual content of the dreams, which though vivid may have no connection at all with the emotion they seem to be associated with. It seems to me more like they are simply occuring concurrently due to similar triggers, than that I'm getting a weird dream which is causing feelings (ie a nightmare).

Often I've had a strange feeling of detachment while this is going on (these are often lucid experiences) - I see a disjointed series of bright, colourful images, often of people doing things which make no sense, and seem surrounded by an oppressive, almost "heavy" weight of sound *buzzing, incoherent voices, or snatches of unheard music* then get hit by, say, a flood of fear, which does not relate to these in any kind of way and causes the familiar unpleasant palpitations and bodily movments... and my conscious mind is observing the whole bewildering process with a sense of ennui and thinking "here we go again, this gets boring...". I'm hoping that at least someone else will have had experiences of this kind, or I fear I may not be making much sense here!

I've also had, perhaps more frequently, extremely vivid dreamlike experiences, associated with other symptoms such as the palpitations, which have been more coherent. Often it seems like I'm experiencing the physical presence or sight, or interact with, strange beings which I can only describe as demonic *even though I don't believe in such things!* or had strange religious experiences or epiphanies (which I won't go into here), floated out of my own body, or had something happen like bugs crawling over me which I was struggling to throw off. Physical sensations (especially) and imagery seem very vivid and believable during these experiences, and I rather often have some kind of bodily movment such as tremors or jerking associated with them, I think, as well as the familiar palpitations and flood of heat. The experience as a whole can be very incongruous; I've experienced before now the sense that bugs were climbing on me during my sleep, thought I'd woken up to throw them off when actually I'm still sound asleep *with someone there awake, watching me making odd twitching movements and wondering what on earth I'm doing* and actually felt somewhat pleasant sensations while this is taking place.

On the whole, I get very irregular sleep patterns, and have great difficulty in in establishing a healthy rythym, which tends to cause me to be more tired and lacking in energy in the daytime than I'd ideally like, even when otherwise free of problems. Sometimes this is due to being woken up by the seizures (if that's indeed what they are!) sometimes by being exhausted by them and needing more sleep, sometimes it's just not possible to sleep soundly or go to sleep in the first place; it can be hard to tell whether I'm getting sleep issues because of the symptoms themselves, or because they've got me into such erratic sleeping habits. I used to be scared and apprehensive about going to sleep at all for fear of what might happen, which probably didn't help. These days, I know from experience that I'm probably not going to die of whatever it is (maybe have ceased to worry so much if that should happen one day too?), can laugh at the weirdness and craziness of all this when it's not happening (sometimes I even do at the time!) but this doesn't help to actually stop it.


Any of this sound familiar to people? Do you have any suggestions or advice? If so, I'd appreciate hearing what you have to say!
 
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i just wanted to reply that i did take time to read your post.We dont have alot in common-however-Ive had terrible sleep habits-up 2 or 3 times a night wide awake-then spacey next day-my vivid thoughts and hallucinations are when Im wide awake and I dont dream.ive often felt bugs moving on me and i had that doom feeling,but mine is not like fear of something its more like Ive accepted disaster will happen and am becoming at peace with it if that makes sense.i frequently have too much nasty tasting saliva but i choose to swallow constantly instead of spitting tring to identify i guess.Instead of labeling lack of concentration,mine is like the urge to do the next thing then the next and on and on-cant provide any one thing with appropriate time or attention to complete. The first year after my diagnosis i was scared to sleep I just knew I would die from this-now it doesnt scare me so bad but it has taken alot from me.If I can help...
 
Hi, Rag,

What you are experiencing sounds horrible. I'm so sorry.

Most of it I haven't experienced, but a couple of things I've had a variation of. I've woken up to my left leg and arm jerking. Actually, it's a little more smooth than jerking, but you get the idea. No vocalizations, just jerking.

I've had the sense of overwhelming terror - I was like a deer in headlights. But no physical symptoms with it - just fear. I actually get those quite often.

I've also felt a sense of detachment from what's around me. I sometimes wonder if that's related to the constant pain that I'm in from the elevated CSF pressure in my head (IIH). I've read that epilepsy can cause it, too.

I've been afraid of going to sleep. I think it was because of the fear seizures all these years. I found that when I had a fear seizure I became afraid of whatever I was thinking about at the time. I had no idea it was affecting me that way. I'm well on my way to fixing that now.

I wake up every night from 2-3am, and am awake for the rest of the night. For me it's caused by the CSF pressure thing.

I've had vivid dreams both on Trileptal and Lamictal. I wake up from them and I have to sit and think for a few minutes about whether they really happened or not.

I don't have a rise in temp or heart rate, but do have extremely variable blood pressure - again, that's from the CSF pressure in my skull.

Temporal lobe epilepsy is crazy-making. If IT doesn't make us crazy, the meds will. Thing is, we're not nuts. We just have siezures and it and the meds mess with our minds.
 
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Hi Rag

Welcome, you'll find a wealth of information here.

Have you browsed tle on YouTube? There are some excellent videos on T L E there, especially those on God. Don't be put off by the term "God" but search out those vids in particular -they are from a series by a doctor whose name I've forgotten - and show people describing euphoric experiences very much like yours.

A lot of interesting things happen during nocturnal seizures, not least of which is graphic dreaming and bodily movement. I have nocturnal seizures too, but am so late for work it's not funny (yes, nocturnal seizures again - slept through the alarm). I'll catch up with this later today my time.

My guess from what you've described sounds typical of tle, especially left T L E (where the euphoric experiences come from). Have you had any tests yet? It is hard going to a doctor with this stuff, lest they detain you under the Mental Health Act (as we say where I live).

I accidentally ended up with my Neurologist due to something else, and self-diagnosed my E with some help from everyone here and other sites on the internet. My neuro was convinced enough to order an EEG during which I seized, and voila! Diagnosis. I'm one of the lucky ones! Gather as much info and advice as you can, before presenting your symptoms to a doctor who might think you have a mental illness and send you on the wrong path. Beware the dragons *wink*
 
I have had some of the symptoms youre having. I was having complex partial seizures prior to getting my first VEEG done a few weeks ago. I was taken abruptly off all medications the day I was admited. The next day I started having seizures where I would get the funny feeling, aura, then my hands and feet would go numb and would get pin and needles feeling all in them. My head would then turn to my right, and my right side of my body would start to jerk. During the jerking, the numbness would get worse and go from my hands and feet to my face, where the roof of my mouth would feel so weird that it felt like a million needles would be poking at it. My whole face was numb like that. After the seizure ended, the numbness would fade as time went on. I was aware of what was all going on during the seizure too. which was new for me. I never before remember what took place during my seizures. For me, my dr said there were areas of spikes on the VEEG indicating I had epilepsy, but he said the seizures I was having, was coming up as non epileptic seizures. I was sent to a psych dr, who ruled out the stress seizures that my dr said I was having. I was put on another medication along with the Keppra XR that the dr had me stay on. Since then, Ive had the numbing feelings come and go. I have left temporal lobe epilepsy.
 
Thanks for the replies so far, everyone who's posted. :)

In hindsight, I hope I haven't given a misleading impression of how serious things are by posting all the symptoms I'd ever had in my lengthy essay! Some of them haven't happened so often, or haven't affected me recently, though the weirdness is indeed ongoing. I was just thinking earlier this morning shortly after I woke up (having got something like a decent night's sleep this time and not had any symptoms I was aware of) that maybe I tended to worry unduly and was going to have to be careful in talking about it not to make it appear worse to others than it actually was; or that maybe I was imagining at least some of it. (A common thought that strikes me, except when it's actually happening and there is no possibility of rationalising symptoms!)

I must have gone into early AM snooze mode while pondering this (and feeling, so far as I could tell, absolutely fine) because the next thing I knew I was snapping awake with a jerk, and a weird sounding groan that seemed not to be at all of my volition, and for a while after I woke (they began before) had rather vivid images in front of my eyes. They gradually faded, but I could see them for quite a while afterwards, especially if I closed my eyes; even after I was properly awake and alert, and the initial weird feeling in my head that I had when I first awoke subsided. It was a rather mild experience, and not very serious in the overall scheme of things (I didn't even get the raised temperature and palpitations this time). But it did serve as a timely reminder that I do get these weird symptoms rather a lot, and they're not going away any time soon that I can see, so perhaps trying to minimise them into irrelevancy isn't the best approach!

It's funny though, as I tend not to see myself as being particularly ill in general, and don't get the experience of headaches, nausea, pain, collapsing or behaving oddly in public and the attendant embarassment, other health problems, etc, that a lot of other people posting here seem to. It makes me keep wondering just how seriously I should take it, and whether I'm worrying unduly, when I see other people who I know get issues that I don't have to worry about expressing concern. But maybe, as the old allegory goes, it's simply the case that our own burden, however heavy it may be, is often easier to bear than that of others? *ponders*

Now for some specific responses:

but mine is not like fear of something its more like Ive accepted disaster will happen and am becoming at peace with it if that makes sense.
Actually mel, you may have put that better than I did, because this really does sound familiar. The fear thing, when I still get it, seems to be nearly always these days to be entirely phsyiological/part of the seizure, rather than my response to experiencing it. I've pretty much come to accept that if it happens, it happens, and there's not much I can do about it - hence the odd feeling I often have of being detached from the experience itself. I can have a very intense, overwhelming sense of fear, and yet instead of experiencing panic am irritated, or bored, or wryling hoping it will hurry up and finish, and stop bothering me. I think if I actually did panic, it would make it worse; with resignation it seems at least managable, if unpleasant.

The first year after my diagnosis i was scared to sleep I just knew I would die from this-now it doesnt scare me so bad but it has taken alot from me.
I used to worry about it a lot more too, for similar reasons. :) Funny how it's possible to become used to such things...

I've had the sense of overwhelming terror - I was like a deer in headlights. But no physical symptoms with it - just fear. I actually get those quite often.

I've also felt a sense of detachment from what's around me. I sometimes wonder if that's related to the constant pain that I'm in from the elevated CSF pressure in my head (IIH). I've read that epilepsy can cause it, too.

I've been afraid of going to sleep. I think it was because of the fear seizures all these years. I found that when I had a fear seizure I became afraid of whatever I was thinking about at the time. I had no idea it was affecting me that way. I'm well on my way to fixing that now.

I'm sorry you get those a lot still :( Fortunately that kind, which I would classify as probably the scariest kind when they get bad *well, what is more scary than fear itself?* seems to have become pretty uncommon for me lately (I'll probably have one myself tonight now I've said that though!). Do you mind if I ask whether they tried making psychiatric diagnoses on the basis of you reporting the fear symptoms? It seems like an easy (and therefore typical) line of mistaken thinking for the medical profession to want to go on...

Temporal lobe epilepsy is crazy-making. If IT doesn't make us crazy, the meds will. Thing is, we're not nuts. We just have siezures and it and the meds mess with our minds.

I'm SO glad I don't seem to get the same things in the daytime, or it might really begin to make me question my sense of reality and/or sanity. It does to an extent anyway, but more in the sense of how often I feel compelled to ask myself: "What? Did that really just happen? :O "

This is a big reason why I haven't sought treatment or pushed as hard as I might for some kind of firm diagnosis; I've been rather concerned that the effects of the medication (at least with my particular symptoms, I can't speak for anyone else's of course) might be worse than continuing untreated. Do you feel your quality of life has improved overall since you started the meds, or would you say it's more like switching one set of issues for another? (I appreciate this may be rather a difficult call to make!)

Have you browsed tle on YouTube? There are some excellent videos on T L E there, especially those on God. Don't be put off by the term "God" but search out those vids in particular -they are from a series by a doctor whose name I've forgotten - and show people describing euphoric experiences very much like yours.
That's interesting information actually, with all the looking up of various things I've done to try to get some insight I'd never really considered youtube! I will definitely take a look at some point - do you know of any specific ones you could link? :)

My guess from what you've described sounds typical of tle, especially left T L E (where the euphoric experiences come from). Have you had any tests yet? It is hard going to a doctor with this stuff, lest they detain you under the Mental Health Act (as we say where I live).

I accidentally ended up with my Neurologist due to something else, and self-diagnosed my E with some help from everyone here and other sites on the internet. My neuro was convinced enough to order an EEG during which I seized, and voila! Diagnosis. I'm one of the lucky ones! Gather as much info and advice as you can, before presenting your symptoms to a doctor who might think you have a mental illness and send you on the wrong path. Beware the dragons *wink*
I was rather concerned about them trying to make a psychiatric diagnosis from the begining; it didn't really encourage me to give a full description of symptoms, to say the least! The first time I got to see a neurologist, quite a few years ago now, I was both trying to ignore the weirder symptoms and had convinced myself that some of them were due to something else. My father had a thyroid problem, so I'd managed to get myself thinking that this might be related to the palpitation and raised temperature part of it. I was quite surprised, therefore, when I was referred to the neurologist (though I suspect I knew deep down that it probably wasn't the issue). As I avoided talking about quite a lot of what are probably the more distinguishing symptoms, they can perhaps be forgiven for being a bit confused about how to diagnose me. I ended up being hooked up to an ecg which I had to take home and wear for a day several times, had blood and urine tests etc; then they gave me a load of gallon bottles which they wanted me to pee into at night. Apparently this was to rule out some kind of obscure adrenal gland condition, which even they didn't appear to think I had to begin with. (I think the ECG must have found something out of the ordinary while I was sleeping, though I didn't have particularly bad symptoms at the time I FINALLY got to see the neurologist.) This had dragged on for some time and a lot of pointless and repetitive proceedures without really getting anywhere, and I finally rebelled at the "carrying around gallons of piss and stashing them in your house" stage and decided to just forget about the whole thing and see if it went away on its own.

It didn't, so when I finally went back again I'd done some research and decided I probably didn't have much options but to report more of the symptoms I was actually having in order to have a chance of getting an accurate diagnosis instead of being pushed from pillar to post forever. Unforntunately when I finally got to see the neurologist after about 6 months of waiting, he seemed more interesting in holding a telephone conversation with AN Other about his 11 year old son's important football match, which took up about two thirds of the "consultation". He considerately devoted the remainder to ignoring what I actually said as though I was speaking in an obscure dialect of Serbo-Croat, and boorishly reiterating his devoutly held opinion, evidently developed on the basis of a cursory scan of my notes just before I entered the room which left him none the wiser about what it might be, that it was "probably nothing serious, you need to stop worrying about it". I think I probably needed to be rolling on the floor to be more interesting than his son's sporting endeavours, to be perfectly honest. After this edifying experience, and having discovered that treatment options were possibly going to be counterproductive in any case, I haven't been back (this is years ago now).

I do find myself wondering, incidentally, how many other people have experienced this kind of medical obnoxiousness and unprofessionalism while trying to get diagnoses for a confusing set of symptoms which are fairly embarassing to talk about. My impression is that it might not be that uncommon... :(

I have had some of the symptoms youre feeling, aura, then my hands and feet would go numb and would get pin and needles feeling all in them. My head would then turn to my right, and my right side of my body would start to jerk. During the jerking, the numbness would get worse and go from my hands and feet to my face, where the roof of my mouth would feel so weird that it felt like a million needles would be poking at it. My whole face was numb like that. After the seizure ended, the numbness would fade as time went on. I was aware of what was all going on during the seizure too. which was new for me. I never before remember what took place during my seizures. For me, my dr said there were areas of spikes on the VEEG indicating I had epilepsy, but he said the seizures I was having, was coming up as non epileptic seizures. I was sent to a psych dr, who ruled out the stress seizures that my dr said I was having. I was put on another medication along with the Keppra XR that the dr had me stay on. Since then, Ive had the numbing feelings come and go. I have left temporal lobe epilepsy.
It sounds like the medication withdrawl may have caused problems you didn't have before... :( With all those symptoms, and an existing diagnosis of epillepsy, do you know what on earth they thought the seizures were, if they weren't epileptic? It sounds like he wanted to diagnose something psychological because he was having trouble interpreting his readings, and didn't want to admit to being less than perfect, and therefore tried to pin the blame on you, though it could be I'm reading too much into that. ;)

The numbness has usually been a fairly mild symptom me, and tended to be more like a distant impression of numbness than actually felt as a definite physical sensation though. Can I ask how they diagnosed TLE if you weren't normally aware of what was going on before this? I've perhaps seen conflicting information about thism but I was getting the impression that some degree of seizure awareness was rather common with temporal lobe symptoms (and maybe even the main problem, given that this awareness is often of altered states of being or percieving things that are not there) and physical symptoms less common.

Thanks for sharing anyway, to you and everyone who has. I've read quite a bit of helpful stuff here!
 
Do you mind if I ask whether they tried making psychiatric diagnoses on the basis of you reporting the fear symptoms? It seems like an easy (and therefore typical) line of mistaken thinking for the medical profession to want to go on...

I didn't tell doctors about the fear seizures until I finally landed in an epi's office. The doctors to that point thought I was nuts when I described some of the other stuff, and I was beginning to think I was nuts, too. Finally one of the neurologist that I saw suspected seizures and sent me to an epi. I told the epi pretty much everything, and he knew right away it was temporal lobe seizures.
 
Rag-that was something i did also was to just feed my doc bits and pieces because i just knew the real truth would be too bizarre! Memory loss was my main concern way back then and I figured I could just handle the rest.But now that Ive realized Im not the same person I used to be and im not happy and im just a fat,bitter, crazy woman i figured what the heck? Might as well let it all spill,which I did Monday at my appt with fillin epi.Wow-here I thought this was such a major breakthrough for me opening up,and he discounted most of my symptoms,as I said in a different post,as not being related to epilepsy.Ive been reading a few articles that has discussed the emerging thought that there is an interictal personality and psychosis related to temporal lobe epilepsy.I guess that we have become different people with different events that occur but not in the immediate realm of a seizure,but seizure related nontheless.Not every doc believes this,some just thin its mental illness coinciding with epilepsy but symptoms sound familiar to me
 
It sounds like the medication withdrawl may have caused problems you didn't have before... :( With all those symptoms, and an existing diagnosis of epillepsy, do you know what on earth they thought the seizures were, if they weren't epileptic? It sounds like he wanted to diagnose something psychological because he was having trouble interpreting his readings, and didn't want to admit to being less than perfect, and therefore tried to pin the blame on you, though it could be I'm reading too much into that. ;)

The numbness has usually been a fairly mild symptom me, and tended to be more like a distant impression of numbness than actually felt as a definite physical sensation though. Can I ask how they diagnosed TLE if you weren't normally aware of what was going on before this? I've perhaps seen conflicting information about thism but I was getting the impression that some degree of seizure awareness was rather common with temporal lobe symptoms (and maybe even the main problem, given that this awareness is often of altered states of being or percieving things that are not there) and physical symptoms less common.

Thanks for sharing anyway, to you and everyone who has. I've read quite a bit of helpful stuff here![/QUOTE]

I was dx with Epilepsy when I was 18 months old. I was having seizures prior to that, but my parents never thought at the time they were seizures. I was seen by a pediatric neurologist when I was alittle girl. I had tons of EEG's, MRI's and all came back saying I slowing in my Left Temporal Lobe. When I was first dx'd with Epilepsy, I wasnt on any medications and was having alot of seizures. I was put on numberous medications. Depekote, phenobarbatrol, Carbotral, TONS OF THEM! My mom knows all the medications Ive been on. Ive had grand mals, and complex partial seizures prior to them doing my VEEG. They have tried to take me off my medications before, and I went for 10 days with no seizures, then on the 11th day, I had seizures that wouldnt stop. My dr at the time was scared they werent going to get them to stop. But luckly they did. My last grand mal that I know of was in 2000 when I went out with a girlfriend and spent all night out. Since then, I was put on carbotral and Keppra and it took control of my seizures. When I went in for the VEEG, and was off all medications for 40 hours, and started having the seizures where I was aware what was going on during the seizures, my mom was so confused as to why i was having these new seizures Ive never had before. I was always having complex partial seizures before that and I was never consious through out them to remember what happened. It wasnt til after I was released from the VEEG that I started to google information about seizures and found that if youre abruptly taken off medications, you can have experience different seizures than what youre use to having. So that explains what took place during the VEEG. I was off my medications for 3 1/2 days and then put back on Keppra XR.

My dr said with the results of the VEEG, he saw the areas that indicated I had epilepsy, I just wasnt having the grand mal seizure like he wanted me to have. He said I "out grew" them, and was left with small seizures. But after saying that, he said he thought they were stress related. We spoke to him the day after I was released, because I woke up and about two hours after, I had 6 seizures in about half an hour. It scared my mom and husband, so we contacted him, and he said during that phone call that the seizures I had could possibly be simple partial seizures that were too deep within the brain to be detected on the VEEG. Once he said that, it all started making sense. I went to the psych dr that he referred me to, just to point out to them both that these were not stress related seizures. After seeing the psych dr, she said I was a very "balanced out person" and in her eyes, she thinks the seizures that I experienced during the VEEG, were simple partials. She asked all her questions, trying to get any information on how stress my life is and ended the appointment saying she doesnt think what took place was stress seizures. Even after a week of being put back on the Keppra XR, and not adding another medication to it, I was experiencing the numbness and tingling sensations, sometimes during the days, but alot of it was going on in the middle of the nights, with the jerking movements of my right side of my body. It wasnt til around 2 weeks after I came home, that I had what my mom thinks was a complex partial seizure. I dont recall what took place during the seizure and came to, looking to my right, and had a very bad headache. So, once we notified the dr about this, he said he was going to add vimpat to my Keppra XR. Since, then the numbness and tingling has come and gone, but I am thinking its getting better with controling the seizures. Its the side effects of the Vimpat that we are focusing on now, making sure they dont get worse.

My dr even said he wished he would have kept me in the hospital alittle longer to see what the VEEG results would have come up with. I told his nurse about me getting off my medications years ago and going 10 days with no seizures, but apparently he wasnt aware of this information til the day after I came home from the VEEG and had the 6 seizures within that half an hour and was told this information by my mom on the phone. He told her if he would have known this, he would have left me in the hospital longer to see if the seizures would have progressed more and kept me off my medication longer instead of putting me back on the medication so soon.

My next appointment to see him isnt til May 25th.
 
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I'd never really considered youtube! I will definitely take a look at some point - do you know of any specific ones you could link?

Here is the first of Neurologist Ramachandran's series for T L E and God:


Other suggestions will come up, too.

I was rather concerned about them trying to make a psychiatric diagnosis from the begining; it didn't really encourage me to give a full description of symptoms, to say the least!

As mentioned before, I was already in the care of a neuro. At the time my E symptoms hit with a vengeance, I'd been on her waiting list for a couple of months as a dementia client (you wouldn't believe how long it took me to remember the word "dementia" LOL). I had been investigated for possible TIA immediately prior, and in the course of that, TL atrophy was found. I knew what that meant, as it was found in a report five years earlier, but that neurologist didn't put it in writing, only told me "you have the brain of a much older person", and "you'll probably need another scan in five years". No doctor will follow that up without a written report, so thanks for nothing Mr Useless A/Hole Neuro. My GP thought for five years I had made that up; now he knows different.

My GP and I have worked together on some very difficult and unusual problems over 15 years, so have a good working relationship. If we didn't have a level of trust, or I had to go to "any old doctor at a clinic" I doubt I'd have described my tle symptoms either. They would have thought I was mentally ill. In fact, I was starting to think I was mentally ill. Constant "white noise" - visually and aurally - of various volumes/levels was the hardest to take and to explain, until I tuned in my new DVD player. So many symptoms, it's hard to list here. I can't remember seeing numbness on a T L E list anywhere, but I get a lot of that, including simultaneous numbness of both hands.

Eventually, I took a list of tle symptoms, and wrote next to them whether or not I experience them, and specifically what my experiences are. At my next appt with the neuro, after she said "I think you have depression" and I argued the point, I replied, "No, I think I have temporal lobe epilepsy". She asked me to convince her. I read from my list of symptoms. She asked me some questions, I responded honestly, and she booked an EEG on the spot. It just happened that the EEG had an appt free that day, and as I live a fair way away and have to take a day off work, I took that appt. Aside from the convenience, I wanted to know now! I seized under the EEG.

So my point there was to gather your information before you present it. Sometimes making a case before you go to the doctor does make you look like a hypochondriac, but if you have something that they are not familiar with, you can lead them in the right direction - in this case, to a neuro.

FYI, I have bilateral tle but predominantly right, and am highly photosensitive. I also suffer very debilitating migraines which it's fair to say are constant (current one, despite Topamax for 15 months, is 6 weeks old). I believe in prevention rather than cure (pain relief doesn't work for me), but life has been better on Tegretol; however, still seizing.

they gave me a load of gallon bottles which they wanted me to pee into at night. Apparently this was to rule out some kind of obscure adrenal gland condition

Hyper-parathyroidism? I went through that, too. What a joy, having days worth of stale urine in those bottles *not* Mine was because I make so many kidney stones.

Continue researching, don't worry so much about your symptoms - they're normal for E's - and collect data for your doctors. Good luck with it all!

cheers
 
New symptoms... hoo-ray! :(

Fisrtly, a big thank you to everyone who's responded in this thread. I have been reading, just didn't have anything specific I wanted to say back before! It's actually given me a lot to think about.

One thing I hadn't really realised is that the difficulty in getting accurately diagnosed for TLE symptoms might be commonplace, even once you got as far as the neurologist; though I knew there was a tendency, due to the nature of the symptoms, to have the doctors want to attribute them to some kind of mental illness. I imagine a lot of TLE sufferers who do have pre-existing signs of mental illness, or have gone too far down the road of doubting their sense of reality as a result of the symptoms, are going to face an uphill struggle in getting the organic nature of their problems recognised. :( Does anyone have any thoughts on what it is about epilepsy (especially TLE symptoms) that seems to cause doctors to be so reluctant to diagnose, even perhaps go into "denial" mode when faced with what ought to be a fairly clear list of symptoms?

On to my main point. I actually had a new symptom last night (can we say "yay"?) and wanted to see what people thought. At least, I had a symptom that I don't remember having before, though it is possible that I experienced something similar and didn't want to think about it. I have been paying closer attention since I've been posting here, as opposed to trying to forget about them as fast as possible as I usually do; and was thinking it might be a good idea to keep some kind of diary to help me track and remember symptoms, as people have advised. (Incidentally, can anyone tell me about how they keep their diaries? When do they write them; do they use a specific format; what kind of information do they regularly include, etc? I can think of a lot of things I could potentinally mention, but don't want to be writing lengthy essays on the topic every day!)

Anyway, back to the thing I wanted to ask about. I was woken several times around dawn - silly me for having a late night - with familiar seizure symptoms (raised heart rate and temperature, sometimes with weird feelings, as described earlier). They were relatively mild and commonplace in most respects, and wouldn't ordinarily be serious enough for me to pay much attention to due to the fact that I get those kinds of symptoms so often. However, one thing did happen with the first of these that bothered me quite a bit. I was wide awake, feeling my heart pounding and trying to shake off the weird feelings I was getting (a combination of lurching disorientation and the familiar peculiar warm floaty feeling), feeling rather irritated; when I noticed that something very strange had happened to my vision. I can remember what I saw quite clearly but am going to struggle to describe it. The best I can come up with is to say that my perspective was heavily blurred and distorted, especially around the middle of my field of vision. It was a bit like having a large magnifying lens with thick glass held in front of my face and looking through it, or a glass bottle. (I actually tried looking through a glass bottle a while ago, to check that it bore comparison!) Perhaps a photographic fisheye lens is closest actually, though I've never tried looking through one directly. There was also a slight shimmering, uncertain effect, as though the nature of the distortion was constantly changing (a bit like when a lens is being focused?) Anyway, I daresay that if anyone has had similar experiences they will know what I'm talking about.

This continued for maybe around 30 seconds after I was otherwise fully conscious and alert - I spent most of this time looking around the room to check that I really was seeing what I was seeing, thinking "What? This can't be true!" while otherwise feeling relatively alert and normal, though the strange feelings and rapid heartbeat were also persisting during this period. As I said, I've never experienced this kind of weird and vivid visual disturbance while wide awake; and unlike many of the other symptoms, it's not one I could really be aware of if it took place during sleep.

Has anyone else (particularly TLE sufferers, of course) had this kind of thing happen? I've heard of various visual effects, but I've tried to describe this one as well as I feel I can right now based on what I actually experienced. It was really disconcerting, and not a little scary!
 
I'm so glad you are going to keep a seizure journal. They are so useful. It's how I figured out most of my triggers, like lack of sleep, stress, alcohol, and caffeine.

Here's a thread that gives lots of seizure diary formats and options: http://www.coping-with-epilepsy.com/forums/f23/seizure-journals-10776/

The coke bottle vision could be lots of things, like a migraine aura, or it could be a seizure that is a form of Alice in Wonderland Syndrome. I have this sometimes. Something looks REALLY BIG. Or time, speed, and space warp. It's very strange feeling. It only lasts a few seconds and then poof! It's back to normal. Here's more about it:
http://www.aiws.info/
http://en.wikipedia.org/wiki/Alice_in_Wonderland_syndrome
http://www.medterms.com/script/main/art.asp?articlekey=24174
http://thetartan.org/2009/1/19/scitech/healthtalk

About what made docs doubt my sanity and think my seizures were actually me, nuts. I have typical TLE synmptoms. The first two neurologists I saw thought I was just a hypochondriac. one actually laughed at me. Probably didn't mean to, but he did nonetheless. That's when I found out that even many neurologists are not well educated when it comes to seizures. They just don't know what they look like, and are not able to make a proper diagnosis. After those two I was lucky enough to see an epi (seizure specialist). He knew what was going on first visit, and told me I had possible temporal lobe epilepsy, and scheduled a bunch more tests. Eureka! Finally someone who knew what they are doing.

It's even worse with primary care physicians. Their first instinct is to refer a person with TLE symptoms to a psychiatrist, for treament of mental illness. The psychiatrist more often than not will diagnose it as a mental disorder and prescribe drugs, none of which help seizures.

Once in awhile a good primary care physician, psychiatrist, general neurologist comes along and they DO recognize the seizures. I have no idea what percentage of physicians are those savvy docs and what someone's odds are of seeing one.
 
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I agree with everything Endless said.

There are also tle sufferers who describe their sight suddenly going "as if I was swimming underwater with my eyes open". It sounds as if your experience was like that.

I only have periods where both eyes blur (aside from what I need my glasses for).

The more I read how much trouble others had, the more grateful I am that my scans were taken, my atrophy was known, and I was in the care of a neuro before the worst of my symptoms hit. Six months later, and I could have been a psych patient.
 
a lot of that sounds very familiar to me
another way I like describing that floaty/basic/buzzy feeling is kind of like an overdose of goosebumps
typically goosebumps might be on the neck, arms, head and then subside after a few seconds (I guess)
but sometimes it's like I'll get that feeling all over my body intensely, and like it's over-goosebumpy to the point of having like, a higher voltage static cling all over my body
and it won't just subside
it'll linger and swell to the point of getting scary
at the onset for a while it'll feel nice, but then itll get weird with that weightless sensation
but overall your experiences ring true to a lot of mine
 
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