Epilepsy :: Seizures? Vary From Short Shakes To Full Blown Unconsciousness
Jan 14, 2014
I have had what we believe to be seizures for three years now. They vary from short shakes to full blown unconsciousness and full body convulsions. The EEG would cost me over $2,000 USD to have done and I just do not have the money. The seizures started March 16th, 2011 from head trauma sustained at the police department. The fragment of bone has embedded itself into a small part of my brain where if I am touched the wrong way there I will lose consciousness.
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By now some of you will know that I love mirt. but alas although it instantly lifted my depression and made me feel alive, I am now experiencing sporadic full blown rages! I have never in my 55 years been an angry person in fact I am too placid most of the time. I have now had 5 rages since being on mirth for four weeks, today I was practically ejected from my chemist because of my behaviour. All because they couldn't find my prescription! I contacted my doctor and said my rage frightens me, I even cry angry tears after each incident. I have now been told to stop taking mirtazapine with immediate effect! Alas start venlafaxine (spelt wrong) tomorrow! No tapering...just stop!
Cannot believe my luck. Did anyone here experience unnatural rages?
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For nearly a year now I have been having these symptoms, which are really starting to affect my life and college work.
Start off first with zoning out of conversations and just not being quite with it.
Then comes loss of consciousness and eyelid fluttering.
Then confusion, wandering round, verbal aggression (not screaming or anything, but apparently I can be quite rude)
Then I come round, just feeling tired.
Altogether (apart from tiredness) this can last anything up to an hour. I don't remember anything of these, and all the information has come from witnesses. I have had an EEG and MRI, which were clear. So why am I still having these?
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About 10 years ago I had something that resembled a stroke. I felt really strange that day and thought I needed to dilate my veins, i reasoned a run might help. After running about half a mile half the side of my body tensed or stiffened up; my head locked to one side, my arm curled in, my fingers curled in, the same side's leg stiffened and it was hard to walk. This lasted for something like 4 hours, and since then I've had trouble concentrating on things and the left side of my head/brain feels like numb/inflamed. I went to the ER and they gave me an MRI and said I had a brain cyst.
I always thought it was a stroke and I got some degree of damage, but a recent MRI doesn't show evidence of a stroke (but the pineal cyst is still there). So if it wasn't a stroke then what was it? Does this sound like an asymmetric tonic seizure?
I've had some other incidents that I thought were panic attacks where my vision goes dark, my hearing goes away and have to fight to not black out. Is my pineal cyst causing me seizures? I don't shake though.
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I am looking for information. My Mom has been diagnosed with Seizures about 10 - 15yrs. ago. She has been on different medications- currently taking Carbamazepine 500 mg A. M. and 400mg P.M. her doctor is starting her on Depakote with 250 mg twice a day then 500mg twice a day. She also sleep walks and high anxiety.
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My son has been having episodes at school, he explains then as he stares, and he can't hear anything, but he can remember what's happened and he can see and move his hands, he doesn't think he could stand or anything though. He is 10 years old and has recently moved schools, He has only noticed these episodes at his new school for the last few months and he had not experienced one at home until the other day when he said he opened the cupboard and just stared at the cups for a while. He also says he doesn't know when it starts or when it is happening but knows when it has finished that it has happened. He is going in for an EEG in a few days, I am a stressed mother who doesn't like waiting :/ Does this sound similar to any seizures anyone else has had?
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I think I been having seizures, I fall to the ground and start shaking a lot, when I was a child I did have seizure I did faint a lot but that had stop at the age of five, I told my mom because one time my friend was about to call 911, is it possible for me to start having seizures again?
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I've had epilepsy all my life. I find the stress has really brought my seizures on a lot. Relationships has anyone had problems with their seizures in a relationship.
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I have been suggested 500 mg depakote.Very scared of weight gain..
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I am a 27 year old male and about 3 months ago I started having seizures. The first 2 were about 2 months apart and both times! paramedics were called and I was taken to the er. Both these times my heart rate was high around 140 and my oxygen was low. After blood and urine tests I was told my potassium was low and I was given fluids and potassium pills and ativan. After the first seizure I got a ct scan at the er and an eeg and an mri a couple weeks later. My neurologist cannot figure out what could be causing them. After the second seizure I was given keppra in an iv at the er and the put on it daily. After a little more than a week on keppra I broke out in a rash. My doc then put me on trileptal, 300mg twice a day slowly stepping up to 600 mg twice a day. Before I got to the full dosage of the trileptal, two days ago I had another seizure. This time it did not last as long and I did not go to the er. My heart was racing for about 30 minutes after and then I was fine. I go back to the neurologist next week and I would like to try more testing instead of simply throwing medicine at the problem. Any ideas what could be the cause of all this?
I will add that I see a psychiatrist and I am on 20mg of prozac and 30mg of remeron for depression and anxiety. Also, my potassium has been checked in between and even before the seizures and it was always normal. Any information would be greatly appreciated. Thanks.
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I seem to have this seizure type thing only when I am on transport and sun is flashing through the trees.
my senses all disappear, I blackout for about 30-40 seconds then jolt back into reality, I sometimes involuntarily scream when I jolt back because its scary.
I have been tested for epilepsy and have come back clear, is it possible to have only sunlight induced epilepsy.
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I've noticed for years that if I lay down when I feel an aura coming on, no matter how intense it gets, I won't black out & go into a full blown T/C. Usually after a T/C my brain seems to.....how should I say.....reset itself as far as "knowing" how intense the last aura was....with every C/P I have they get more & more intense every time I have one until I would black out from one and end up in a T/C. Strange thing though, I've noticed that everytime I'm sitting or standing after they get so intense, I'd fall and go into one. If I lay down on the floor, after awhile, no matter how intense the C/P (AKA aura as far as I'm concerned) gets, it suddenly goes away after a bit. Anyone else ever notice this? Why could this be? I've tried to ask a handful of Neuros. but they NEVER give me time. Everything is "You have any seizures lately? Let's get a blood level. OK see me in ___ months." And that's pretty much the extent of the visit! They NEVER want to let me ask anything else (I've seen 7 or 8 in my life, so I don't think things are any different anywhere. And I'm not the only one I know who gets this attitude.) Anyone have any idea WHY this "pattern" would happen? Could it be more oxygen getting to the brain? More blood?
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Been on too many different kinds of medication for my seizures from 3yrs to now. Is there any other options besides having surgery to possibly them
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My mom has seizures but the doctors say nothing shows on the test they run.
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A month ago I was fine, no pain, no aches, nothing.
Then a small burning ache started in a precise spot on my right thigh.....then my breasts started to hurt.....then my elbow on my right arm..... Both sides of my ribs under my armpits.....my shin on my left leg and my inner thigh......then my whole left arm from wrist to armpit.
I feel like I've just been punched all over!
Blood Tests - normal
Urine test - normal
Stool sample - normal
ECG - normal
The pain isn't all the time, but in short sharp or short burning aches, it's stopping me from sleeping properly and its sometimes really scary when I get a sharp pain in my chest and left arm. It takes my breath away sometimes
I also get these strange "rushing" feelings in my chest/head when I lay down to sleep at night. Its almost like the rush you get when something makes you jump, but it lasts only a few seconds then it's gone. But I can have 3 or 4 of them in a row. But of course it's quite scary when you've no idea what they are.
Been in and out of doctors for weeks now and spent nearly £100 on prescriptions that haven't helped.
Been put on Amitriptyline 10mg for the pains but no change yet after a week, will keep taking for now though.
Im not convinced it's Fibromyalgia, but my doctor isn't the easiest to talk to.....
If anyone has any insight and can help me understand this all or maybe has any ideas please comment.
I'm 28, only other issue is PCOS but that doesn't give me much hassle.
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My whole body shakes from lithium. Dr decreased my dose today down to 600 mg a day. Does anyone know of any essential oils that would help with this until my lithium levels decrease.
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Am I the only one? After having a seizure I can't talk right.
It is as if I have lost the ability to talk, and if I am able to talk, It is very slurred. Finding the right words are hard for me to find For at least an hour after having a seizure. Does anyone else face this problem?
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I was diagnosed with epilepsy about a year ago. I have for the past 3 year had strange eye sight. When i spoke with my neurologist she had never heard of it before. The only way that i can describe it is the vision you get after about 2-3 pints. I have been to the opticians and my eyes are perfectly fine. It is worse when i am outside and can make me feel dizzy and light weighted. Any advise would be appreciated. It makes me not want to go out.
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I have been put on Epilim 1g for the past few months for hemiplegic migraines which is helping massively however I'm only 26 and recently got engaged and would love a glass of wine or two. I asked my neuro and he said it would be fine but I just wanted to know If anyone else drinks alcohol on epilim?
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Has anyone had or have a short cervix? If so how short and what did your doctor tell you or recommend?
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I'm a 19 yr old female. So after some google searches i finally found out what I have, LPR. I was a tightlacer, i used to eat a lot of black pepper on food everyday, and drink yerba mate with lemon juice everyday, and lots of fruits, as most fruits are acidic it has certainly helped with the development of my LPR. I thought i just had allergies issues due to excess mucous, cough, sinus pressure and feeling weak. And a strange burning throat while or after eating with difficult swallowing, that time id get short of breath sometimes but it wasn't common at all, and heartburn i think i had about 5 or 6 episodes in months/years , not a complain at all, is very rare. While i didn't know what i had and kept tightening my conical corset, eating right before going to sleep with the corset on, always laying after eating because i was feeling unwell, then i developed harsher symptoms: more constant sinus pressures, throat pain, lump feeling while trying to swallow, shortness of breath, dizziness, phlegmy throat, non productive cough, one congested nostril, etc. i searched about it and found out about LPR, did all the diet changes needed, no more caffeine from yerba mate, no more peppers/chili/cinnamon/dairy/artificial sweetener full of acid preservatives, no more eating close to bedtime, no more most fruits only banana and persimmon which i don't know its ph but i don't want to stop it because it sweetens my acai bowl with frozen banana and frozen acai blocks. I've been to a ENT here but they don't even know much about LPR in the US, let alone in Brazil. She prescribed me 40 mg prilosec 30 min before breakfast everyday . I started it on April 1st and i know it will take months to see a improvement. And i really don't like taking meds, one side effect of this PPI is a fat liver and i've been eating clean 4 years straight, i never drank, never smoke, dont eat added sugars, wheat, vegetable oil, processed foods, i only eat home cooked whole meals i really don't want to rely on this PPI for a long time, i want the surgery which she told me never would prescribe me it... Ive had some improvements since diet changes, my sore throat is gone, burning throat not as common as it was before, post nasal drip gone too just not phlegmy throat , voice loss was gone, lump feeling in throat was gone too. But i still have bad symptoms that are making my life miserable, my shortness of breath now is more constant and happens several times everyday, its worse when i stand up and i get a bit dizzy too and my vision darkens too for few seconds, i always have this mucous in my throat, throat burning while eating, its hard to swallow, not that i feel the lump i just feel my throat is tighter now, and sinus pressure. I could really live with those throat symptoms, but this shortness of breath is driving me crazy and making me miserable, its horrible, i know its due to LPR and maybe a hernia i dont know, but as i used a conical corset for 2 years very constantly and very tight on my rib area i think it maybe must have done something to my lower lungs, besides making my diaphragm breathing difficult and squeezing my stomach. I have difficult breathing IN , no wheezing sounds at all.
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