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Ugh. All of my EEGs are Normal, routine, walking eeg and 3 day video monitoring .according to Neuro’s notes it slight asymmetric atrophy of the left hippocampus/mesial temporal lobe which is nonspecific” but she also said can be a result of the type of seizures that are happening. They know it’s not a psychological thing, they are actually from the brain but it’s always normal 😂 it’s very annoying and I’ve had like 12 different meds tried, including newer ones, but it still is happening, I’m kinda tired of the whole thing. The grand mal seizures seem to be less of an issue, but the others are like maybe once a week to a couple of weeks when I’m lucky. I just want them to figure out what is causing it and what to do about it.

Bulshit

I have a generic which makes me sick, doesn’t do what the drug is supposed to do at all.. currently waiting to get a refill from the manufacturer that works.

Oh my god this is my old neurologist!

If its 2 late but no too pyscho tropica emergency take it.

Dr Oyalo is trustworthy and doing great work with his product on autism kids. My daughter is a point of contact and her improvement in speech and other social activities (responding to name, no more hyper activity, bitting, tip toe walking) has been heart warming

Was misdiagnosed with adhd and was never diagnosed, amphetamines never helped, but when I got an injury and put on anti-epileptic pain management medication that my brain finally got fixed.

Alcohol does depress your central nervous system, and benzodiazapines also depress your central nervous system and are also prescribed for seizures ( I know a case where it is also prescribed for tardive dyskinesia).

But whenever you can do nothing guess wallah have margarita

Can I get married ? I got seizures I'm say to my girlfriend. She break up with me

can be cure if u understand the root cause

i have ran over 52 convicted criminals am i autistic or a wanted murderer

The Epilepsy program has been Interesting. I will follow the Doctor 's orders. Thank-You!

I got complex partial and secondary generalized tonic clonic. But my MRI and EEG return normal. But my neurologist still treats me as epileptic person. Its better to believe that I'm epileptic rather than let me suffer.

The staring thing is both for me. I have had adhd my entire life and I both daydream and have absence but haven't been diagnosed. Also just learned about myoclonic seizures because I've had the jerking problem since a very young age and never told anyone about it. I just hid when they were bad enough people would notice. Now as I'm 28 they are getting even worse and I'm going to finally see a doctor and get to the bottom of it. I use to get really sick ones as a kid too where I wanted to vomit, was sweating as I felt I was boiling and my entire body would become so heavy and lethargic that it was even hard to breath and then I would rapidly become confused and hazy and almost lose consciousness. All this I hid as a kid because I would feel them come on and would go hide. Dealt with it alone (really don't recommend as it's depressing and extremely hard and dangerous) but I'm finally going to speak up about it. I have 2 kids and want to make sure I'm ok for them. No idea what could have caused mine though because I haven't had seizures since birth. They just started one day before I was even a preteen. I'm curious how it all began

fear fear fear

epilepsy is because of too much sea salt and no body health. seizures because of the head are angry and they who get seizures are being alone and no pictures of human,animal,plant near them, that is to prevent to infected by seizures. picture for replacement the real one . soo you are not being seizure while the head are angry you are while near other soo you not hit by it. btw it only attack A,AB blood. O and B will be deaf ,blind ,and muted. if it what you are talking are schizophrenia it because of they swallow their tooth ,clean the poison of the tooth might will enough .they scared to dead and no one see and understand why they scared.it an image of black ghost that shown at when they fear dead when they feel cold water and wind and other thought that make them scared to dead. that ghost only able to defeat by asking him question nor command him.

Would you say for an epileptic a safe route would be to not pursue alcohol but other drugs but in the daytime hours as opposed to at night when sleep would be inhibited (hopefully sleep will happen in the nighttime)

Question my son is 3 just had a eeg was a 30min session results came back normal when should he take a second test

I've been having them since a baby. They are more of an annoyance than anything for me now.

with intranasal midazolam as compared to intravenous midazolam and intravenous diazepam..Read More from

Me who has both

Can people with absence seizures drive a motor vehicle?

Amazing grace as I am cured from epilepsy with herbs sent to me by a RUclipsr Dr Joe Herbal research .reach him and consider a good health from epilepsy .

i have TLE and adhd and the TLE seizures are focal aware. It seems like im spacing out to people around me. Im half aware of what is happening around me while Im also in half of a dream state with heightened senses like the taste of metal and a strong sense of deja vous. When i come out of it I probably look distressed. So while it is very similar to spacing out, its actuslly quite distressing and hard to explain to people that dont have this type of seizure.

my daytime eeg was normal, sleep deprived wasn’t. waiting to see a doctor, have been havinf strong déjà vu episodes for the last 4 years but they are getting worse and starting up again which is why i got the EEG. i’m a bit nervous

Sometimes when I feel stressed I just want to smoke it's a feeling and sort of a way I feel like I can ease the stress idk if I can still smoke some advice would be helpful.

Thanks to everyone taking their time to read this testimony on how my son was saved from Epilepsy . He was diagnosed three years ago, and he's 18, I have tried several treatments and medications, nothing was working out, this got me frustrated and depressed. I kept praying and finally God answered my prayers when someone from youtube introduced me to this herbal doctor, from Africa and gave me his contact details. I called and explained my son's condition after which I made an order for his herbal remedy, he asked for my address and the next day I got a tracking number for a parcel sent to me through DHL and I got some days latter. It was a liquid herbal medicine and a letter containing the instructions on how to use the herbs, I called him again to confirm and the next morning I started giving my son the herbs as instructed and after one week I noticed great improvement on my son and I continued until the herbs got finished and everything lasted for just one month and now my son is totally free from Epilepsy, doctors said he’s perfectly fine and there will be no more seizures. If you've been searching for a genuine solution for Epilepsy, connect with Doctor Solution on Whats App + 23 4 8 0 7 7 6 8 3 1 0 9 or ( solutionhealinghome@gmail.com)

How long after can it detect because I feel I’m having night ones but they are really rare and happen when sleep deprived

Plz. Sir. Help. Sir. Plz

If I haven't had a Seizure since 2013 or 2014 can I still have epilepsy

If you read Kathy Marshack' s books. She sais autism is lack of connection between emotional empathy and cognitive empathy. (Ee and ce). And me coming from a family with several high functioning autists (not myself) i have witnessed fullblown autistic behaviour behind the front door while the same person isnt doing that at work or with remote family and friends. And it was always difficult to convince people to believe the problems i had living behind that frontdoor as a kid. And then i read marshack and visited several meetings with other kids of autistic families (non autistic kids now adults) and we all came to the conclusion: they can do feel think communicate everything just not use ee and ce at the same time. So they make mistakes also in logical info processing because they cannot have logical deduction with cognitive info combined with emotional info. So thats why they cannot change perspective, think contextual, and tune into intrinsity of human info. It all makes sense to me but hard to explain to people who werent raised among autism. We kids of autism speak fluently their language but outside the home we interact in another way and we see the difference: they have empathy they think logically and can mentalize: just not while beeing emotionally connected: its either one system or the other if it has to be at the same time they have a temper or just blank out. I see it all the time. If you only know autistic people at the workplace you will never have this issue they are in cognitive logical mode . To me it makes sense that those two different types of braincircuits cause shortcircuits. I myself have absense epilepsy and my brain shortcircuits exactly in the brainpart that gets overloaded. due to meningitus as a kid. But if you must overuse a braincircuit that you had to built to bypass the lack of another (in autism the ce+ee connection): that will totally overuse some other part. Im just curious if autistic epileptics mostly have left or rightbrain shortcircuits or always different parts? PS about epilepsy occuring after puberty totallt fits with this ee ce theory: so the autistic person has a hard time developing EQ (emotional intelligence) where non autistic people go into a next level EQ at puberty, the autistic person cannot because so far he/she got away with bypassing ee-ce with rational mentalisation, but now in the next level cannot keep up. Add group vibes to the mix and your gone. You can never mentalize rationally several people at once: peergroups are unmentalizable for them. So you have emotional empathy 100% that doesnt mix with rational logic at the same time (it does in theory but not while engaging) so they cannot control it or mold it. Thats why they cannot hold two perspectives at the same time: as soon as they look from the others perspective they loose their own. And resonance: he thinks that i think that you think can only be done holding 2 perspectives simultaniously one in 'as if state' and one your own. They take the asif state even too literally. Anyway everything beyond two steps with more than one person simulatiously cannot be done quick enough with only ce. But you see some very high functioning autistic people finding ways even around that: I dont know how they do that, its rare but very interesting. So most autistic people dont grow their EQ at all after 12 years old. But there are some who are very low EQ for decades but then make a jump and have found a circuit around it and then become emotionally much wiser all of a sudden. But that is rare.

You can also just ASK them. If your having a daydream or a seizure I can tell you the experience is very different. I have both add and absense epilepsy and the difference is..... with one you are unconsious and with the other you are very much alive. Anyone who actuality TALKS with the person will know. If you ask an add person: what were you thinking of? and the person says: well I was thinking if bees can see more colours or if the other side of themoon is always dark.... So someone could be staring at a wall thinking: is that oker yellow or stone yellow? We can also zoom in at detailed close sounds and vision and a zoomed out blur and haze, but then your still aware of the sensory input even if it’s hard to discribe. I must say having movements isn’t really proving it’s not add, we move and tweak and twist often. We don’t ever sit still completely it’s hard to keep track of what all those limps are doing. If you ask and the person had no thoughts at all: that means that person does not have add. add people do not daydream without thoughts, it is not possible for an add person to have no thoughts. Let the person just draw the daydream on paper: you will know if we are dealing with real add in no time: If they ask for more sheets of paper that it is. We can make up a whole movie inside our mind including smell sound tactile feelings and references to other movies while in your head discussing the movie with an imaginary friend. Add people do not have the capacity to stare into the distance while thinking nothing. Unless we are overwhelmed and are spaced out... if the surroundings have flickering tl-lights and other people and an echo and you hear the ventilation or heater: living without filter and with our high sensitivity we implode sometimes, and that can trigger seizures. I sometimes think the fuse breaks because I have no off switch if that makes sense. But I don’t know any other add person with epilepsy so I’m just connecting dots that are only connected in my own particular case I guess. If the person is overwhelmed by overstimulance I would first ask how to help them, if they are not unconscious but are hearing everything in a blur than just saying ‘o well at least you don’t have a seizure, it’s just add overload’ seems very wrong to me. You can just get the child out of the overwhelming situation and buy them headphones and change the lights or allow them to wear a hoody with hat in class and take breaks.

I get pain in my sides and my belly and around my heart, and after its over i feel like i used some heavy druggs

I have absence seizures had them since I was little but never got diagnosed because my doctor at the time said they happen so fast and only lasts about 5-15 seconds. He also said it’s hard to notice when it happens unless it happens when someone is trying to talk to you and you don’t respond. I still get them along with myoclonic seizures usually before bed when I’m lying down trying to sleep they would always wake me up and it would happen multiple times before I actually get to sleep and sometimes it will happen during the day but rarely. I’ve been after my new doctor to send me for a CT scan or mri but he won’t do it

I was diagnosed with absence epilepsy when I was 8 or 9. I ended up accidentally making my elementary school teachers go through a training for it. I have been off meds since I was around 11 because I didnt really get seizures much anymore. It recently came back (last school year) and my parents don't believe that it came back. My brst friend has witnessed me have up to 5 a week at one point because it's so bad now. I think I can also feel my mind slowly begin to fall into a seizure as well because it becomes hard to focus and understand things.

I was born with epilepsy and cerebral palsy. I have a twin brother, i was born first. My brother was born with no problems. I take phenytoin for my epilepsy, as a child I was on phenabarbatone, then at 14 i was put on Epilim 500mg. Which caused me to gain lots of weight. I went to live in Canada for a few years where I was taken off eperlim & switched to phenytoin. Which I still take today. As a child I had grand mal seizures, which doctors said I would grow out of. Which I did, but I now have petit mal. It' feels weird when I have it, i can hear all thats going on around me, but ppl and any noise, sound much louder, plus it feels like I'm floating on water. Before the seizure I get the smell like burnt toast. I can have a seizure at any time, night or day. Unpredictable. I feel a little confused when I come round, which lasts for a couple of minutes, then I'm back with you again. Usually a cup of tea helps me recover. I read a lot of blogs where people who shared their testimonies kept mentioning Anti-seizure Herbal medication. I searched for a website I just followed the email address of Doctor Patrick that was shared on these testimonies; I got lucky when I got a reply from Dr. Patrick. I followed his instruction, used Herbal Medicine in less than 2 months, I was already cure because of the changes I was seeing. Within a period of 5 months, I was cured totally forever. I went back to my neurologist, I was checked up and marked epilepsy free. If you need his help you can Contact this herbal doctor via his email herbalmedicalhome@gmail.com and WhatsApp connection is +2348102558553 for help..

hi i’m rlly worried that i’m having seizures and unaware. because i’m having huge time gaps of my memory throughout the day for the last few months and i’m only 16. it’s like i go to the fridge to get juice and then i sit down but then my mom says she was talking tk me for like 2 mins and i am positive she didn’t speak to me of i didn’t hear her. or like i went to the kitchen to make tea and then my mom came and said why did i turn the light off and i have no recollection of ever turning off thy light but i would’ve had to do it like earlier

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yoga, breathing exercises and good diet would help a lot to cure epilepsy and seizures. exclude meat, smoking, alcohol , masturbation and include yoga,breathing exercises and vegeterian food diets to remove seizures and epilepsy. saying from my personal experience. and yes, dont hesitate ton share yuour problem to your parents, siblings and if possible doctors. i feel seizure when sttretching my chest without oxygen.

Excellent collaboration of data and personal clinical observations. It was fantastic how you were willing to voice your scientific imagination when putting your opinions forward. It was refreshing to see an epilepsy neurologist promote the social model of care in the management of seizures. Well done and I can only hope that researchers take on board your requests for appropriate experimental design. Thanks, you made my day 😁

My brotger is 22 years old.. One time before 5-6 years, we saw syntoms like epilepsy but doctor told us it is not epilepsy and his reports was normal that time... Now after 5year again that thing happen and his reports are normal now...so what are the possibility...it can happen bcz of any other reason or it is epilepsy?

Thank you, very helpful! Take care

DISAGREE! with marijuana laced with other drugs.

My son has seizures since he was 1yo and the doctor doesn’t believe he has epilepsy because she can’t see on the EEG. All the symptoms match with rollandic!

I really like the taste of alochol, so I do still drink but not a lot. I just have little tastes of drinks. Yesterday at a party I had 1 cider, maybe 2/5 of a beer and a tiny bit of vodka mixed in raspberry lucozade. I won't allow myself to get drunk ever I'll just enjoy tasting stuff

Absolutely brilliant, thank you so much.

When I was a baby I had a febrile seizure, I stopped breathing and turned blue. My mom gave me mouth to mouth and by the time the EMTS arrived I stopped seizing. As i grew from baby to toddler, my parents began to see that i was delayed. So I started early intervention at 3 years old I had occupational therapy and PT. In pre k I would get angry and punch any thing that was in front of me, after my parents had been observing me in a pre K class and talking to the pre k teachers it was suggested that my parents should take me to a therapist to rule out any behavior issues. He took one look at me and said that I was having seizures he then referred me to a neurologist. At the at the age of 5, I was diagnosed with Childhood Absence Epilepsy. i was put on Depakote for the next 9 years This is how Depakote affected me it caused massive weight gain, memory loss, a hand tremor a one point i stoped eating i had no appetite i was depressed. I was also on Clonidine guanfacine (mood stabilizer). Then when i was 10 i was on levocarnitine as I did not have too much vitamin A in body. My triggers are flashing lights, the transition from the out doors to inside a classroom, getting too hot and recently sleep deprivation. When i have an absent my pupils will go from normal to pin point this is the only physical sign. My seizures last one-second and happened every minute to every minute and a half. So there are 60 seconds in a minute and 24 hours in a day then I was having seizures every 1440 minutes or 86400 seconds, so in total I would have 86400 seizures per day before I was put on meds. My parents were told to treat me as a normal child and to see how far I would develop, and look at me now I have graduated High School with honors. I am in Collage as you can infer I was not expected to do much of what I just mentioned. The effects of my seizures is that I have Aspie like tendencies due to my epilepsy which I know is difficult to understand. to put it in simple terms as a result of my seizures my brain compensated and rewired itself. I also have severe deficits in Processing Speed, Perceptual Reasoning, and Working Memory, Upper Limb Coordination, Manual Dexterity, Fine Motor Skills, Hand Strength, Visual Perceptual Skills, and understanding meaning. When was 19, my father died, and it seems I have had a relapse if that is possible.I still have my absence seizure but it is not enough to put me on meds. When I was thirteen I had my last EEG and my seizures showed up as misfired neurons not seizure activity per say and the Dr. called them “flurries” at that time I was taken off of meds , so here is what my flurries are typically like: I will become very spacey, I can not interact with my surroundings, I also felt locked in to place. I am completely aware, my vision becomes like a tunnel, and thing start to move or vibrate on their own.

When I get absence seizures it happens many times throughout one day! But it doesn't happen every day and the eeg and MRI came back normal! I got them all the time when I was little