Undiagnosed Mini Strokes At Night (no Epilepsy)
Jul 20, 2015
Almost 2 years ago, my wife started having, with what acts like, Mini Strokes. She has had over 60 of these events with varying severity. Sometimes she has quick recovery, sometimes it takes days.
Loss of movement is always on her left, her eating is affected, her left eye, left face drooping, left arm, left leg. Just like a TIA, this can affect her for a short time and mostly resolve itself within a couple hours or take days to resolve. CT Scans show nothing and stroke doctor says they are not strokes. Our neurologist says she is not an epileptic per some tests she did. Her blood tests show no STDs. She does not have Celiacs disease either.
She does have several health conditions but the doctors are stumped.
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I posted in epilepsy earlier. I couldn't find the sleep boards. I am suspicious I have epilepsy but I wanted to see if anyone else has experience with this. I have severe sleep myoclonus that occurs every night all night. It causes me and jerk and I usually see a flash of light and hear a clicking sound. This occurs over and over so I hardly ever sleep. Does anyone have any experience with this?
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Hallo - my husband was taken into hospital a few days ago with a ?heart attack - but that (thank God) was not proven. They said it could be angina. But the next day after having been given Amitriptyline he showed the symptoms of a mini stroke and I couldn't understand what he was saying because of slurred speech. The GP (when he was discharged) said it was highly unlikely to be a stroke and he blamed this drug - as did all the hospital doctors.
This is very odd to me and can I ask whether it could be true? He hadn't been on the drug prior to admission, so I don't know why on earth they gave it to him in hospital.
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After a very painful kidney stone problem and thus being told I have Bilateral kidney stones; I have just been diagnosed with Primary hyperparathyroidism. The docs want to operate to remove the faulty gland(s) but I am very concerned about the procedure in the UK which does not seem to include the mini op or MIRP operation. Has anyone had this type of surgery in UK(either mini or other) and what were your experiences? I am wondering if I should travel to Florida for it?? I also have low vit D and they want me to take vit d supplements. I think this is dangerous to elevate my calcium level even more?
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I'm 15 years old, the first time i tried weed was when i was 13. i have started smoking weed a lot more when i was 14 , i always got nervous to speak in front of a large group like a school presentation, but that nervous became more serious turned into anxiety, i just went to doc. today, my anxiety gets so bad at school i ask to go home because of it i look for every chance i can get to "escape" the uncomfortableness. i won't even read out loud at my own desk. i don't know if weed caused this because i love weed. i'm not a person that freaks out if i don't have it but if its in my face ill hit it. i went to a physiatrist for my first time she said i need to go to the docs.(which i did). IDK for sure but i think the doc. will give me med. i am just wondering if i can still smoke weed and take the med. without having my mini "heart attack''.
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I've had migraines a good chunk of my life and I haven't had one in roughly 9 months but I have been experiencing almost like mini migraines? in that I experience pain very similar to a migraine but without the aura or having to lie down or take it seriously. I guess these could be tension headaches, but I'm not sure? I've also been experience other symptoms, including: ear pain, sensitivity to light/sound, ringing in the ears, and various pains all over my body. these symptoms can happen with a migraine but lately they've been constant and if not, happening often enough that I'm noticing. I've had a brain scan and nothing. I don't think it's ever been like this before and I'm curious as to what it could be? As in, a starting point. I do have migraine medication but all it does is put me to sleep, it doesn't help with the pain. Not sure if that matters.
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I took Cerazette for 9 days, felt so ill i came straight off it. Anxiety attacks, racing heart, was off work for 8 weeks it was a nightmare. its now 3 months on, my periods are getting somewhat back to normal, but i've been left with a fast heart rate. I've been rushed to A&E a few times its been so fast i thought i was having a heart attack. i'm now on beta blockers to keep it under control until it's investigated. its ok sat down, but if i try and walk or do anything it goes through the roof.
I've heard of other women that have had this but i'm desperate to find out whether it will eventually go back to normal on it's own or has it left me with long term issues.
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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 have been on the combined pill (Gederal) for a couple of years now but my doctor wants to change me to the Mini Pill (Cerelle). My Combined pill is perfect so i don't want to change. I mentioned that i had one migraine with visual disturbance and she explained to me that even one of these migraines is a reason to come off the combined pill. The combined Pill regulated my periods but she explained that this mini pill is now going to make me irregular.
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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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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'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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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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