This was me EXACTLY in school !! , I used to be terrified of reading out loud in front of the class , just in case I "blanked out" and everyone would just stare at me , which isn't much fun when your 8 !
@@kandiceashmichealson3944 You really should go to a doctor. I also had them all the time, until this year I had a tonic-clonic seizure and spent some days in the hospital because of the fall. I could have died. Now with the medication I am free of absences for all these months, and before it I had them around 3-10 times a day. The risk is something to take into consideration. Stay well!
There's a difference between daydreaming and absence seizures. With absence seizures, you're not aware that you 'spaced out' but with daydreaming you're fully aware
*Anyone else had those moments when you've had an absence and you end up just staring at someone, and you only realise once they start waving at you or asking what you're staring at?*
I have had epilepsy since i was 9 and I have missed so much school because I was having seizures about 100 times a day so I wasn't getting a chance to learn but 8 years later I have done my GCSE's and I am in year 12 and I am ready to come off my medication. Time and patience is key. Don't rush something you didn't plan.
There is this online chat room for teenagers with epilepsy to socialise and talk to other people who are going through the similar situations. I thought it was pretty cool and maybe you should check it out as well www.thetea-room.com/
@@steffipullely6907 Thank you! I really needed that because I have epilepsy but I don't actually know anyone else with it, so it makes me feel so different! Thank you so much!💜
My girlfriend had this problem. I tried this med on her. Its been one year and she is perfect. She is a medico and we have given it to hundreds of people now. And none has come back with a any complaint.
I have tonic clonic seizures and absences and I felt dizzy so sat down when the class was standing saying good morning and my science teacher yelled at me and just then had an absence I tried to explain but I got a lunch detention she didn't care
I’m not epileptic but I used to have absence seizures due to a different neurological condition. Thank you for raising awareness a lot of people don’t know this is a seizure and would look at me like they don’t believe me when I said I had seizures.
Found out that my spacing out moments were seizures when I had an episode in front of my doctor. I went there about my insomnia and headaches and left finding out I didn’t escape the epilepsy or cluster headache genes. It was only embarrassing when I had a seizure while looking in someone’s general direction and they thought I was staring at them. I still get episodes even in my twenties but it’s not as frequent.
I’m the same way as you. I have the same episodes where I space out, and feel like I’m going to get sick. I was diagnosed with seizures back in 2018. I take lamotrigine to control them. I just recently had a seizure. I was at work, and started spacing out. My manager called paramedics, and I was taken to the hospital. The thing that triggered my seizure was dehydration. This has happened to me in the past. Now I’m drinking a lot more water which will help
Have you seen a doctor or been diagnosed? If not then I recommend bringing up your suspicions because before I was diagnosed I thought something was wrong with me. The myoclonic seizures scared me before I was diagnosed because I thought maybe I had something like Tourettes or some reason why my body was randomly moving. I felt reassured after the diagnosis because I realised that there was nothing actually wrong with me, my brain was just a bit different
Well, hellø there, felløw human! Exact same with me. I had one huge seizure unexpectedly on my 18th back in March (I wasn’t diagnosed before then) but since I was 12/13 I have been getting myoclonic seizures and that is the most common with me (have them every day). I’m glad Ik what it is now and I’m so glad there’s people out there who know what it’s like- I got diagnosed 3 days ago btw lol x
I never really knew I had these until I was diagnosed in 2018. I would have these episodes where I would space out and become dizzy. They lasted for seconds. My parents and I never knew what was going on. One day I was getting ready for work, and I had an episode. My mom took me to the hospital, and the doctors ran tests. Everything looked normal, and then I had another episode. They ran an EEG, and low and behold. I was diagnosed with absence seizures.
I've had epilepsy since 2005, really struggling with support recently, wish people at my work would know what an absense seizure is insead of looking at me like im ignorant or stupid
I have these same seizures. I was diagnosed with them back in 2018. My family and I never knew I was having seizures. I would have these episodes where I would space out and become dizzy. One day I had one of these episodes, and my mom took me to the hospital. The doctors ran tests, did bloodwork, and everything was normal. Before we left, I had another one of these episodes. They ran more tests and did an EEG. Turned out the EEG results came back I was having seizures. I take Lamotrigine now to control them
i have to give my teachers a notice every year. incredibly annoying but it helps knowing both me and the teachers don't have to be as concerned about how to react when they happen
Schools think they are fake that your ignoring them or cocking an attitude. I have these hundreds a day I have had issues with school my whole life I have had this since I was 2 years old. People really need to acept this and don't judge or make fun can't help it.
Thank you for posting this. I have been battling epilepsy since a car accident about 10 years ago. I am just now being treated for it and seeing positive differences in my life. I am actually making TH-cam videos on the subject of my battles with TBI, epilepsy and myeloma. Mine are partial complex seizures and yes...embarrassing stuff happens. I am medicated for it and am eating ketogenically to try to control it. Absense seizures are so lame!!! This is well needed! Thanks for posting this...epilepsy sucks!
When I have one, I can’t see, like whenever you get up too quickly. I usually start panicking and crying after I have one, and I have trouble focusing for the rest of the day afterwards,,, maybe mine are a different type of absence seizure??
THIS HAPPENS TO ME EXACTLY ALSO. I thought it was severe Dissasociative episodes for a long time!!! This is insane. I haven't been officially diagnosed but my prescriber wants to send me to a neurologist. I'm worried because I started college recently and I'm worried about these things occurring. Since I havent been OFFICIALLY diagnosed, I'm worried they will just roll their eyes and tell me "oh well. Get back to me when you've actually seen a doctor"
@@hanahtherabbit14 I was looking into it more,, and I believe my case is simple partial seizures. The descriptions of it sound similar to what I’m experiencing. The symptoms are a little scary,, but it’s accurate to what I was explaining. But I don’t think I should self-diagnose myself haha. I would feel awkward bringing it up to my neurologist- you know,, because he diagnosed me and all. I don’t want to sound like I’m correcting him :(
Does it happen only normally when shifting positions/standing? And your vision seems to “cave in”? I’m not a doctor but look up Postural Hypotension. It’s simply a form of low blood sugar that can cause you to feel dizzy, lightheaded, or even faint upon standing. Look into it 🤞🏽
I too get absence seizures. Mine before were very short, but now they seem like they’re lasting longer. I recently had a seizure, and it took a little bit for me to get out of it. I no sooner found out that the reason it takes me so long to get out of it, is because of a thing called post ictal. What this is, the brain returns to normal after the seizure has occurred. I had learned that it could take minutes, hours, or even days before the brain returns to normalcy. There is confusion, and biting of the lip or tongue in this stage
The moment you have a absence seizure out in the football field and the game starts, next thing you know, everyone teleported but meanwhile you were froze.
Dray Crouse , I once had an absence seizure in the middle of a busy road. It was like the distance of the cars were two soccer fields away. Then I blink my eyes, and some cars are swerving around me beeping their horns. One car crashed into a wall, the people were OK.
Dray Crouse I play hockey and a similar thing happened to me. I’m a defence and one time I was in front of the net battling with a girl from the other team, next thing I know everyone’s on the other side of the ice.
I have burned my self w an iron....and stayed in the street the street after attempting to cross while cars tried to avoid hitting me...when I realized what was happening I freaked out
I remember having these seizures they can be very scary to stop suddenly not knowing why you keep on stopping what you were doing! I had them when I started preschool as a very young girl. Epilepsy runs in my family and one of my family members has bad epilepsy luckily I had only this type of seizure that they showed in the video or called petit mal or absence seizure. I had them a long time until like maybe 4th grade in school or so when they got cured. Most kids will outgrow this type of seizure but some still have it for a very long time luckily I outgrew mine and the medication helped get them better too. It's defiantly very embarrassing when these seizures happen! You could be hanging out with your friends like this video shows and a seizure strikes you and people look at you like what is wrong with you but overall great video and it defiantly helps spread awareness about these types of seizures!
My niece got diagnosed with Epilepsy back in January and she had an absence in the middle of a lesson and the teacher shouted at her for it and the worst part was is that they know she is Epileptic and that she was having an absence.
When I was younger I was having around 80 of these a day. One time in particular my family and I won’t forget I was crossing the road at a busy intersection with my younger cousin and mom neither of which realized I had stopped. My mom ran back and picked me up and ran as I was about to get hit by a large truck
I had a lot of them throughout the primary school up to the sixth grade. Both my parents and teachers used to say I was always in my world but i truly wasn't. It also used to be a constant complaint of the teachers, "i do not understand what is wrong with her she keeps staring out the window but when i ask her the questions she knows the answer." Truthfully nobody from my family gave it attention , they said I simply loved daydreaming. Thankfully though it stopped after the 7th year. I could never understand what they truly were before but know that i have searched into it more all my supposedly daydreaming started to make sense.
God, I hate that! If you know the material and your grades are fine, then WHO CARES if you're staring off into space?? I think teachers are mostly narcissistic egomaniacs who can't stand it when all eyes aren't on them.
Getting epilepsy after husband hit me in the head is scary now I'm 39 an it's been going on 7 years this has changed me but I push to understand an live my normal life
I need to send this to my friends so they understand, I haven’t been diagnosed yet but I get absences , my mom caught it, I went out for a minute, strange, tests on Oct 8th wish me luck ❤️😖
This hurts to watch. As a kid I was finally diagnosed at 6 after I had a spell and collapsed on the kitchen floor in front of my mom. Had been having trouble in school and always felt so embarrassed to be caught when I didn't know what I'd done. Honestly though I eventually outgrew it with meds as a teen I still will catch myself drifting and wonder if I'm actually really free. People don't realize the lasting damage these things do. Being scared and confused as a child certainly has its lasting effects. My love to those of you still fighting the battle.
when I was a baby i had a febrile seizures i stopped breathing and turned blue my mom gave me mouth to mouth and by the time the EMTS arrived i stopped seizing . In pre k i would get angry and punch any thing that was in front of me that is when it was suggested that my parents should take me to a therapist. 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 but have been seizure free since the age of thirteen and so was taken of meds which caused massive weight gain a hand tremor and memory loss. The point is meds are good up until a point an then it becomes a pill no pun intended. my triggers are flashing lights, specifically the transition from the out doors to inside a classroom getting too hot photo and recently sleep deprivation. my parents were told to treat me as a normal child and to see how fare I would develop and look at me now I have graduated high school with honors though I did hope for a regents diploma but after taking the algebra common core regent seven times starting out with a 40 and ending up with a 57 oh well. I start collage in July not august 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 and so i have all of the symptoms of Aspergers but lack any sort of understanding math as a result i have no understanding of money and never really learned my basic math facts.(i am just learning them now in college which for most Aspergers people they are gifted with math abilities )i also have orthotic because due to my seizures that i had straight feet at birth i also have a sensory processing disorder. i have low gross motor control and other motor issues as well. After my father died, 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 . i have been getting driving lesson and have 10 -20 seizures in the drivers seat. i take omega 3 cod liver oil liquid form as i can not swallow pills this helps decrease the too -small -to -medicate -seizures i have very small seizures that show up on the EEG as misfired neurons and the Dr. called them "flurries" 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 there own for me an absent seizure lasts 1 second with is rare but these flurries can last 5-10 minutes.
I was misdiagnosed with childhood absence epilepsy, and then misdiagnosed again but with benign rolandic epilepsy, and I have now been diagnosed with juvenile myoclonic epilepsy and they suspect I have another type, but I forgot the name of it
Its great to know that schools will be more alert with different kinds of epilepsy. Absense is the most hard to identify as a seizure. I have absense and before i was diagnosed i wasnt sure that they were actually due to epilepsy. It will be great if school children understood epilepsy as well as teachers :)
I have both absence and tonic-clonic seizures, and have since I was 13. It really makes my life a lot more difficult, but I'm on medicine for it. However, it hasn't been working much lately and I've been having many tonic-clonic seizures. I've also been having many absence seizures in the shower and it really sucks. I'm getting through it.
trying to get my partner diagnosed and I am in a state of frustration with nhs at the moment they are so intent that she makes up her seizures. her eyes roll back and her neck goes stiff, has hallucinations, nausea, wandering around, spins in circles, shouts out, swears a lot, severe anxiety and depression and suicidal tendences. I have seen a pattern of when these seizures happen and it always seems to be the afternoon of a thursday around 4pm never ealier or later and she also falls over alot during it... she also does this in the video so which or what is happening? she could be having non epileptic seizures as she is schizophrenic and hears voices which gets worse during these seizures as well... hmm?
I love it ....this way to teach kids about epilepsy is realy helpful to epiletic kids becuse it make them easy acceptabl by the other kids and not make fun of them....so keep up
I don't think I'm the intended audience here, but as a hypochondriac, this channels is currently proving very useful in helping me confirm that I'm most likely _not_ suffering from the ailments shown in the videos. Thanks
I think i have absence seizures. Sometimes when im just standing around, i feel like my soul has been taken out of my body, and i cant control anything for like, 0.5 seconds. I came to this video to see what it looks like. I dont wanna self diagnose, but im pretty sure i have absence seizures.
This girl at my school has this. Sometimes she'll stare at someone or something and we need to tell the teacher. Or if she falls on the floor and she's twitching I feel bad cause we can't touch her until she's done. But today I was looking around the room and she stopped and stared at me and I told the teacher and she said leave it and like 3 minutes pass and she's still staring at me then when I got up to tell the teacher and fell on the floor and started twitching. This went on for 6 minutes. We had to call the ambulance bc if it lasts more then 4 minutes she could die. It was scary. They rushed her to the hospital. Her mom told me she wouldn't stop twitching until she got to the hospital (the hospital is like 20-30 minutes away)
This is interesting, recently I had my first tonic clonic (I'm 31) I think they used to be called Grand Mal? But after seeing this, I've realised that I've been having this kind of seizures for a long time... Only my school just used to give me detention for not paying attention or day dreaming
This. I was an excessive daydreamer in elementary school and middle school. In High School, I just zone out in space. I got detention for the first and only time in 4th grade for daydreaming. If your teaching is too boring and/or uninteresting, my mind switches to daydream mode to keep itself entertained.
This is what happened to me when I was in jr. high and the public school kicked me out and sent me to a boarding school for 3 yrs. but as time went by I came back to the public school I was at in my jr. yr. and I went on to work in Special Ed. for 35 yrs. and I stood up for students who had neurology disorders.
usually when you're "reading" but not really reading, you're still able to move your eyes and stuff, it's just not processing. with absence seizures you have no control (except basic reflexes like continuing to stand/sit up if less severe). if you were to compare it to something, i guess it's more like when you're really tired and trying not to fall asleep, but you keep nodding off and your head jolts up when you realize you need to stay awake. you don't feel yourself or remember actually drifting off to sleep, you just suddenly realize you're not supposed to be.
As someone who has this kind of epilepsy, I would just like to clarify that these kinds of seizures are not always this quick. I have had absence seizures that literally lasted for either 30 minutes, or an hour or so. They come on with absolutely no warning, and you cannot be woken up from them. Said person just freezes up for an indefinite period of time. One tell that someone is having an absence seizure is obviously a completely blank expression, but(at least for me, not sure if this applies to everyone with this kind of epilepsy) another sign is repititious movements, such as moving your finger in a circle over and over again. This video does a great job of showing how sudden the seizures can come on, but I figured I should mention that the seizures can go on for *far* longer than just a few moments.
I get like this sometimes. Once I was out in a club dancing and next thing I used I had stopped in the middle of the dance floor and my friend was tapping me on the shoulder asking if I was ok and I continued dancing. Apparently I was “zoned out”
I do have this kind of epilepsy and once i was in class i think my teacher was calling me and the seizure started and when it ended i heard my teacher shouting my name. Everyone was looking at me like i was a alien...
I'm 19 now When I was 14 I had this seizure ar school and I'm presenting MY PROJECT I was so embarrassed that I had this and I BLANK OUT and my teacher ask "are you okay sweetie?" And I said oh oh yea! I'm fine! And later on when it is home time I didn't tell my mom because I don't want her to freak out and finally I continue the seizure till I'm 19 years old :( And can I have 5 likes for 5 years seizure? :(
There is this online chat room for teenagers with epilepsy to socialise and talk to other people who are going through these similar situations. I thought it was pretty cool and maybe you should check it out as well. www.thetea-room.com/
Have a question for the room...when a child, I had incidents where my mind would go completely blank for a split second (I assume). Usually it it was when a bright light would flash or perhaps catch me in the corner of my eye. On a couple occasions I'd be riding in a car and passing through trees so light-shadow-light in quick succession. It didn't effect me - my parents never noticed and I kind of thought is was normal. Oddly one of my children had the same thing....when he described them to me I remembered my own incidents. He says he thinks they are absence seizures...
Yeah I have also experienced this kinda seizure when the flash light or colour ful light catches the corner of the eye (my right eye) and it feels so freaked out but no one notices and after this thing happens I used to get some headaches or anxiety
I had my first seizure in 23 years last night, I'm almost 40 and I don't have any more .... I accidentally drank a low cal drink and know I had issues with aspartame when it first came on the market. I wonder if others have had similar issues?
@@therion8469 You know that seizures are literally your neurons firing wrong and that they're something you can't control? Maybe take your attitudes back to the middle ages, oh, wait, even they knew seizures weren't voluntary.
I hate these so much sometimes I wish I was just normal, and I could erase all the stupid memories of me at school and ppl staring at me and even I didn't know why they happened every time I think about it I feel like crying
Yes me too, I even peed to myself at some point after holding myself for too long then had a seizure. It was terrible but I still have them and facing the world to accept us and my family who are too African traditional
i have epilepsy its horrible as i cant even go swimming or something with my mates without my parents. when i was seven i managed to get rid of them for about a year but then they came back. i am now 13.
High humidity and low atmospheric pressure is the reason why people get seizures! I found out because my previous seizure was during when the hurricane and I googled it and found out. That's why places with high humidity such as The UK and Pakistan have the highest percentage of Epileptics.
My brother used to have absence seizures and they were really bad. We do not bother them when they are happening because the doctor said to wait until his seizures are done to bother him.
Im here in philippines 2004,(19 yrs old) that time when im surgery because of sinusitis turn to infection in my brain.. since im recover that dont know i why starting of epilepsy thru weekly,monthly,yearly until now im thnkfull to other doc. They help me to about the medical drugs... My last triger epilepsy is 2018, but before that yes im always feeling last past in aura seizure but bcause of medical turn to absences seizure now, 2018 2020 feel only absencea seizure, im using my drug in 2 a days everyday but now the here in whole world of covid 19 bcause of that im taking once a day for limit in buy supply in the drugs store. And also financial problem... Im sharing this my story life for asking for help in any for stop my sickness.. thank you for this day Godbless
Yes, there is. There is more seizures involved with epilepsy. Do you have any involuntary movements. Most people tend to mistake epilepsy for tics or Tourette's syndrome. Muscle contractions and other seizures are involved.
So I have an 8 year old son, he was formally diagnosed with this. It happens so many times during the day and has gotten to the point that when he blanks out, he wets himself (we homeschool thank goodness) I always hug him while it’s happening and I’ll ask him what he sees when it’s happening and he says he see’s his great grandma sometimes (he was around during her passing and it definitely took a toll on him emotionally). We just started ethosuximide. My biggest fear is him being stuck taking meds that “turn him into a zombie” he’s such an active child, full of life. I wish more than anything that I could do more...
I have had these seizures since I was 9 years old and when I was 18 they stopped, 31 years later the seizures came. Apparently the seizures were laying dormant until I was stressed out and they returned and I have the seizures for the rest of my life.
Thanks for sharing your story Jon, I'm sorry that your seizures didn't go away completely. Stress is quite a common trigger for seizures, although for many people, the cause is very difficult to determine. You can read more about that here: www.epilepsy.org.uk/info/triggers
I've had absence seizures before plus 2 breakthrough seizures which happened as a result of me forgetting to take my medication. I'm hoping to start having driving lessons in the near future, once I get checked up, as I haven't had any absences for well over a year now.
My friend has absence seizures that are just like this, one minute he will be fine the next he is staring into space my little sister has complex epilepsy and has atonic seizures my mum told me to just let my friend get on with the fit but if it lasts for longer than 1 minute I should call her and ask what to do
Ok ,so since my late 16s I frequently have this problem : Sometimes randomly I have strange feelings which is indescribable, its like things are coming closer, into more focus , deja vu etc when all of a suddem I go blank and there is loss of awareness and connection with the surrounding, I am not conscious or aware of anything its same like when a person sleeps then after few secs I return back from that blankness and then forget what I was doing that particular time and even what I did the entire day, I then try and start recalling which it takes me good 3 -4 mins to remember everything, sometimes I can control/ ward it off , other times it happens so frequently that by the end I get terrible headaches... My mother and sister tell me that I give a death /blank stare during that period Its been happening for 3 years now, then 3-4 days ago I had a full tonic- clonic seizure in the morning for the 1st time... my sister saw it , I was sleeping and suddenly I began jerking , My lips turned blue, eyes rolled to a side and I bit my tongue.. Of course I was unconscious after this , and don't remember anything of the seizure , my sister described it to me, only I had headache and body ache throughout the day and felt tired and sleepy I did go for an MRI , which came back normal Could someone please tell what is all this..it would be of great help ..
As someone who has absences sezuire this is so relatable i remember when i had one during a swimming race luckly i was doing backstrokes so when it happened i was just floating on the water and my brother got me out of the water if i was doing butterfly or front strokes i bet i would've drowned
I've had epilepsy since I was 7 years old so I've had it for 7 years now.. and it's tough to say the least. My first year I wasn't on medication so that was the worst year..my mum said she woke up screaming from nightmares for weeks because she was so terrified. Because I didn't have jsut absence ones I had; tonic clonic, absence, facial twitching also stress seizures so i faint in school alot and it tends to make me very weak etc and my parents use to count how many times they called any ambulance. They stopped counting after it got past the 300 Mark, that was when I was 9, I'm 14 now.
This was exactly me and still is me I hate having absence seizures I get so embarrassed thanks to my childhood neighbor I got diagnosed with epilepsy because she noticed that I blanked out a lot but now I’m on lots of meds I used to collapse to the ground and times and even drop things now I blank out sometimes even say random words when blanked out and do stupid things when I blank out like recently I was drawing and I blanked and Drew a line somewhere I wasn’t meant to I got mad at myself and scribbled it out since I didn’t have a rubber I hope it gets better for anyone who does have epilepsy you guys can do this you are strong ❤❤❤❤❤❤❤❤❤
Ashlee's Bathroom nice violin 🎻 you should get it checked out to calm your nerves about it if your worried but I was worried and i turned out to be healthy only I had epilepsy which doesn’t matter since I go about my life as normal 💕
@@Kiahboudreaufanning thanks for the advice, and I did go to the doctor. They ruled seizures out. They think it's a form of panic attack. It did only happen in stressful situations (like interacting with people I dont know).
I can’t tell if I have epilepsy or if I’m just casually zoning out but just not clarifying my surroundings after I come back in contact with people. My mom has seen me staring at nothing without me blinking and I can remember them so that’s why I think it’s just me zoning out.
I was diagnosed with epilepsy last month. I was a spacey kid who sucked at school but was otherwise bright. Now I wonder if it was absence seizures interfering with learning?
I had this when I was like watching some movies or in outdoor like in school days(when quarantine wasn't a thing) I always get a brain block is what I call, but then I still continue on what I remember. But I never had a a seizure before. Just this one because I swear I felt it.
Ok so I've suspected I've had a problem since I was about 5 at least. Now, I've gone to a neurologist who believes I am having absence seizures, but they're non-epileptic, and caused by abnormal brain tissue. Anyone else?
I think this has happened to me before. I don't remember any of what happened until my friend called me. I don't remember what we were previously talking about, what I was looking at, what I was thinking about.. nothing. Do these types of seizures have triggers? Because it happened after I went on about 4 very fast rides at a fair. Would that have caused it?
Hi there - all kind of things can be triggers for all kinds of seizures. Sometimes we just don't know what triggers them at all. You can read more about some common seizure triggers here: www.epilepsy.org.uk/info/triggers Hope that helps!
This is totally me! i had it since i was 2 my mom told me but i got this problem at young age so i don't feel weird or embarrassed it was like part of me but still it was difficult at sometime like crossing the road or get in the train before the door is closed😥
and how many parents would pass this off as..what was that, oh she is ok, see she cam back. I am an adult, and I have been sked not to drive, our son's aba therpaist asked me if I was ok 2x I only heard the second are you ok...Now I have to ask myself.... did I show signs as a Child and no one noticed? I also have Autisim. I also only had one EEG, and I hear that sizures may not occur during an EEG. so now They do a 72 hour home EEG. thank you for showing this video.
Some kid in my class just had one in 8th period an hour ago, me and him were messing around and he just dropped a tool in his hand and stared at nothing for 5 minutes
hi. I don’t know if it’s just a normal thing that happens to a lot of people, but, sometimes, when I see (maybe watching a music video) flashing lights, I find difficult to breath normally, like after a long running session.sometimes at school, I just went blank. My friends asked me if I was in stand-by, and I said, really confused, no. Or maybe I abruptly become really confused of what I am doing, of why I am in a place, or I freeze when I am standing up, or sitting on the couch or laying in bed... should I see a doctor? sorry for the mistakes but I am not an English speaking person…
This sounds unusual. It would definitely be worth speaking with your doctor. And if you possibly can, having someone take a video of you while it is happening could be really useful. This is our information about how epilepsy is diagnosed www.epilepsy.org.uk/info/diagnosis/diagnosing-epilepsy Kathy Epilepsy Action Helpline Team
This was me EXACTLY in school !! , I used to be terrified of reading out loud in front of the class , just in case I "blanked out" and everyone would just stare at me , which isn't much fun when your 8 !
I called it blanking out too omg!
i had absolutley no idea that this was a seizure i have them all the time
@@Ace96ify what???
I used to call them blanking out too 😂😂
@@kandiceashmichealson3944 You really should go to a doctor. I also had them all the time, until this year I had a tonic-clonic seizure and spent some days in the hospital because of the fall. I could have died. Now with the medication I am free of absences for all these months, and before it I had them around 3-10 times a day. The risk is something to take into consideration.
Stay well!
There's a difference between daydreaming and absence seizures. With absence seizures, you're not aware that you 'spaced out' but with daydreaming you're fully aware
It’s like you are dead but still alive
Ye
It just feels like blanking out, and ya kinda just snap into it, barely noticing that anything happened at all
@@welsh_ml5671is there only me who feels confused after it and don’t remember having one
I always have an absence siezure and everyone thinks it's staring at the.
*Anyone else had those moments when you've had an absence and you end up just staring at someone, and you only realise once they start waving at you or asking what you're staring at?*
Yep
Yea
Omgg like yes lol but I do it on purpose sometimes when they wave
Gladly not lol they will just think that im thinking something atm. My "blank out" face kind of looks like someone in deep thought. 😅
no thats just you having a crush if ur staring at a girl and ur a boy
I have had epilepsy since i was 9 and I have missed so much school because I was having seizures about 100 times a day so I wasn't getting a chance to learn but 8 years later I have done my GCSE's and I am in year 12 and I am ready to come off my medication.
Time and patience is key. Don't rush something you didn't plan.
Good for u! Hope your doing good
There is this online chat room for teenagers with epilepsy to socialise and talk to other people who are going through the similar situations. I thought it was pretty cool and maybe you should check it out as well
www.thetea-room.com/
Epilepsy is curable .For a sureshot remedy for epilepsy, e mail me sahil.steve198@gmail.com. We have cured hundreds of people of different age groups.
Peyton Mott I have Epilepsy too. Ever since I was a few months old.
@@steffipullely6907 Thank you! I really needed that because I have epilepsy but I don't actually know anyone else with it, so it makes me feel so different! Thank you so much!💜
2.00am watching people have seizures.... and I have school tomorrow...
Omg its 1am
@@zokaya10 lol we're the people in 2020
Wolfix Woods and me
Omg sameee but I have church for the first time in so long
Same
Who else finds it really embarrassing when it happens????
Me because of the looks others give me
me
Katie Powell me
Hmmm... that's incredibly bold. Every person's epilepsy is different. How are you sure your one remedy would help it?
My girlfriend had this problem. I tried this med on her. Its been one year and she is perfect. She is a medico and we have given it to hundreds of people now. And none has come back with a any complaint.
I had this in science and I fell for my stool and my science teacher stayed with me throughout of it
I have tonic clonic seizures and absences and I felt dizzy so sat down when the class was standing saying good morning and my science teacher yelled at me and just then had an absence I tried to explain but I got a lunch detention she didn't care
Contact this doctor directly on his WhatsApp number for your Total Cure. +2347030936239
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@@danielacamara2265 stop.
@@oliviawatkins673 that is well not right tbh
I’m not epileptic but I used to have absence seizures due to a different neurological condition. Thank you for raising awareness a lot of people don’t know this is a seizure and would look at me like they don’t believe me when I said I had seizures.
How did you get diagnosed?
Found out that my spacing out moments were seizures when I had an episode in front of my doctor. I went there about my insomnia and headaches and left finding out I didn’t escape the epilepsy or cluster headache genes. It was only embarrassing when I had a seizure while looking in someone’s general direction and they thought I was staring at them. I still get episodes even in my twenties but it’s not as frequent.
When having the absence seizure what are you thoughts while in it , are you like stuck in thought or is it just blank thought
I be stuck
I’m the same way as you. I have the same episodes where I space out, and feel like I’m going to get sick. I was diagnosed with seizures back in 2018. I take lamotrigine to control them. I just recently had a seizure. I was at work, and started spacing out. My manager called paramedics, and I was taken to the hospital. The thing that triggered my seizure was dehydration. This has happened to me in the past. Now I’m drinking a lot more water which will help
I had this loads of times as a child but it was never formally diagnosed.
Have you seen a doctor or been diagnosed? If not then I recommend bringing up your suspicions because before I was diagnosed I thought something was wrong with me. The myoclonic seizures scared me before I was diagnosed because I thought maybe I had something like Tourettes or some reason why my body was randomly moving. I felt reassured after the diagnosis because I realised that there was nothing actually wrong with me, my brain was just a bit different
Well, hellø there, felløw human! Exact same with me. I had one huge seizure unexpectedly on my 18th back in March (I wasn’t diagnosed before then) but since I was 12/13 I have been getting myoclonic seizures and that is the most common with me (have them every day). I’m glad Ik what it is now and I’m so glad there’s people out there who know what it’s like- I got diagnosed 3 days ago btw lol x
th-cam.com/video/lT3P6XHCtXg/w-d-xo.html.
@@wellhelltherefellwhuman4637 No need as I seemed to have grown out of it. I was very young at the time.
I never really knew I had these until I was diagnosed in 2018. I would have these episodes where I would space out and become dizzy. They lasted for seconds. My parents and I never knew what was going on. One day I was getting ready for work, and I had an episode. My mom took me to the hospital, and the doctors ran tests. Everything looked normal, and then I had another episode. They ran an EEG, and low and behold. I was diagnosed with absence seizures.
I've had epilepsy since 2005, really struggling with support recently, wish people at my work would know what an absense seizure is insead of looking at me like im ignorant or stupid
Or looking at u like u r ignoring them ...or intentionally do it to b passively combative
@Sian Vlog I'm also suffering from this since 2005. It's not cured yet. I have graduated and learn how to live with it.
th-cam.com/video/lT3P6XHCtXgc/w-d-xo.html.
th-cam.com/video/lT3P6XHCtXg/w-d-xo.html
I understand completely that happens to me on the daily
I have these same seizures. I was diagnosed with them back in 2018. My family and I never knew I was having seizures. I would have these episodes where I would space out and become dizzy. One day I had one of these episodes, and my mom took me to the hospital. The doctors ran tests, did bloodwork, and everything was normal. Before we left, I had another one of these episodes. They ran more tests and did an EEG. Turned out the EEG results came back I was having seizures. I take Lamotrigine now to control them
This happens to me always and I hate teachers call my name and ask me what they say. Like I have a problem okay? Not my fault
Exactly
Like..... they are already supposed to know what you have
i have to give my teachers a notice every year. incredibly annoying but it helps knowing both me and the teachers don't have to be as concerned about how to react when they happen
Gracia Mariola exactly
Therion84 stfu when people have this they blackout, they can’t hear, feel, think, or see anything for about 15 seconds. No it’s not their fault.
Schools think they are fake that your ignoring them or cocking an attitude. I have these hundreds a day I have had issues with school my whole life I have had this since I was 2 years old. People really need to acept this and don't judge or make fun can't help it.
i feel you. 😞
katiecash46 thank you
katiecash46 I feel you
katiecash46 or you could just pay attention 😒
@@therion8469 ... you’re an idiot.
It some times happens to me when I’m listening to someone talking and I just go blank every so often like I just go
Thank you for posting this. I have been battling epilepsy since a car accident about 10 years ago. I am just now being treated for it and seeing positive differences in my life. I am actually making TH-cam videos on the subject of my battles with TBI, epilepsy and myeloma. Mine are partial complex seizures and yes...embarrassing stuff happens. I am medicated for it and am eating ketogenically to try to control it. Absense seizures are so lame!!! This is well needed! Thanks for posting this...epilepsy sucks!
When I have one, I can’t see, like whenever you get up too quickly. I usually start panicking and crying after I have one, and I have trouble focusing for the rest of the day afterwards,,, maybe mine are a different type of absence seizure??
THIS HAPPENS TO ME EXACTLY ALSO. I thought it was severe Dissasociative episodes for a long time!!! This is insane. I haven't been officially diagnosed but my prescriber wants to send me to a neurologist. I'm worried because I started college recently and I'm worried about these things occurring. Since I havent been OFFICIALLY diagnosed, I'm worried they will just roll their eyes and tell me "oh well. Get back to me when you've actually seen a doctor"
@@hanahtherabbit14 I was looking into it more,, and I believe my case is simple partial seizures. The descriptions of it sound similar to what I’m experiencing. The symptoms are a little scary,, but it’s accurate to what I was explaining.
But I don’t think I should self-diagnose myself haha. I would feel awkward bringing it up to my neurologist- you know,, because he diagnosed me and all. I don’t want to sound like I’m correcting him
:(
Does it happen only normally when shifting positions/standing? And your vision seems to “cave in”? I’m not a doctor but look up Postural Hypotension. It’s simply a form of low blood sugar that can cause you to feel dizzy, lightheaded, or even faint upon standing. Look into it 🤞🏽
I get absent seizures. It really annoys me because they make me dizzy afterwards so If I'm running I sometimes fall.
th-cam.com/video/lT3P6XHCtXg/w-d-xo.html .
Seriously, that's me too.
I too get absence seizures. Mine before were very short, but now they seem like they’re lasting longer. I recently had a seizure, and it took a little bit for me to get out of it. I no sooner found out that the reason it takes me so long to get out of it, is because of a thing called post ictal. What this is, the brain returns to normal after the seizure has occurred. I had learned that it could take minutes, hours, or even days before the brain returns to normalcy. There is confusion, and biting of the lip or tongue in this stage
Scary
The moment you have a absence seizure out in the football field and the game starts, next thing you know, everyone teleported but meanwhile you were froze.
Dray Crouse , I once had an absence seizure in the middle of a busy road. It was like the distance of the cars were two soccer fields away. Then I blink my eyes, and some cars are swerving around me beeping their horns. One car crashed into a wall, the people were OK.
@@samanthapeters2972 That has always been my fear-having an absence on a road or near a train
Dray Crouse I play hockey and a similar thing happened to me. I’m a defence and one time I was in front of the net battling with a girl from the other team, next thing I know everyone’s on the other side of the ice.
Omg yes...teleported...that's a way of putting it
I have burned my self w an iron....and stayed in the street the street after attempting to cross while cars tried to avoid hitting me...when I realized what was happening I freaked out
I remember having these seizures they can be very scary to stop suddenly not knowing why you keep on stopping what you were doing! I had them when I started preschool as a very young girl. Epilepsy runs in my family and one of my family members has bad epilepsy luckily I had only this type of seizure that they showed in the video or called petit mal or absence seizure. I had them a long time until like maybe 4th grade in school or so when they got cured. Most kids will outgrow this type of seizure but some still have it for a very long time luckily I outgrew mine and the medication helped get them better too. It's defiantly very embarrassing when these seizures happen! You could be hanging out with your friends like this video shows and a seizure strikes you and people look at you like what is wrong with you but overall great video and it defiantly helps spread awareness about these types of seizures!
Kimberly Pa Ji
Literally, even when you feel like somethings wrong or can feel an episode coming, you still pretend that your fine
Thank you for this video. I’m a pharmacist and I had a difficult time visualizing this. Your video was very helpful. I appreciate all of your work.
My niece got diagnosed with Epilepsy back in January and she had an absence in the middle of a lesson and the teacher shouted at her for it and the worst part was is that they know she is Epileptic and that she was having an absence.
When I was younger I was having around 80 of these a day. One time in particular my family and I won’t forget I was crossing the road at a busy intersection with my younger cousin and mom neither of which realized I had stopped. My mom ran back and picked me up and ran as I was about to get hit by a large truck
I had a lot of them throughout the primary school up to the sixth grade. Both my parents and teachers used to say I was always in my world but i truly wasn't. It also used to be a constant complaint of the teachers, "i do not understand what is wrong with her she keeps staring out the window but when i ask her the questions she knows the answer." Truthfully nobody from my family gave it attention , they said I simply loved daydreaming.
Thankfully though it stopped after the 7th year.
I could never understand what they truly were before but know that i have searched into it more all my supposedly daydreaming started to make sense.
Mine didn't stop tho. But my parents and teachers had no idea what was happening
God, I hate that! If you know the material and your grades are fine, then WHO CARES if you're staring off into space?? I think teachers are mostly narcissistic egomaniacs who can't stand it when all eyes aren't on them.
Getting epilepsy after husband hit me in the head is scary now I'm 39 an it's been going on 7 years this has changed me but I push to understand an live my normal life
I hope you left him if he did that on purpose.
Bruhh, this happens to me all the time and my teacher is concerned.
I need to send this to my friends so they understand, I haven’t been diagnosed yet but I get absences , my mom caught it, I went out for a minute, strange, tests on Oct 8th wish me luck ❤️😖
@Sumoki oh my god, I forgot all about it. Well I got tests and they found it was actually due to severe anxiety. But I’m good now xx
This hurts to watch. As a kid I was finally diagnosed at 6 after I had a spell and collapsed on the kitchen floor in front of my mom. Had been having trouble in school and always felt so embarrassed to be caught when I didn't know what I'd done. Honestly though I eventually outgrew it with meds as a teen I still will catch myself drifting and wonder if I'm actually really free. People don't realize the lasting damage these things do. Being scared and confused as a child certainly has its lasting effects. My love to those of you still fighting the battle.
This happens to my 7 year old cousin all the time. Didn’t know absence seizures were a thing until today.
th-cam.com/video/lT3P6XHCtXg/w-d-xo.html
when I was a baby i had a febrile seizures i stopped breathing and turned blue my mom gave me mouth to mouth and by the time the EMTS arrived i stopped seizing . In pre k i would get angry and punch any thing that was in front of me that is when it was suggested that my parents should take me to a therapist. 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 but have been seizure free since the age of thirteen and so was taken of meds which caused massive weight gain a hand tremor and memory loss. The point is meds are good up until a point an then it becomes a pill no pun intended. my triggers are flashing lights, specifically the transition from the out doors to inside a classroom getting too hot photo and recently sleep deprivation. my parents were told to treat me as a normal child and to see how fare I would develop and look at me now I have graduated high school with honors though I did hope for a regents diploma but after taking the algebra common core regent seven times starting out with a 40 and ending up with a 57 oh well. I start collage in July not august 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 and so i have all of the symptoms of Aspergers but lack any sort of understanding math as a result i have no understanding of money and never really learned my basic math facts.(i am just learning them now in college which for most Aspergers people they are gifted with math abilities )i also have orthotic because due to my seizures that i had straight feet at birth i also have a sensory processing disorder. i have low gross motor control and other motor issues as well.
After my father died, 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 . i have been getting driving lesson and have 10 -20 seizures in the drivers seat. i take omega 3 cod liver oil liquid form as i can not swallow pills this helps decrease the too -small -to -medicate -seizures i have very small seizures that show up on the EEG as misfired neurons and the Dr. called them "flurries" 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 there own for me an absent seizure lasts 1 second with is rare but these flurries can last 5-10 minutes.
I was misdiagnosed with childhood absence epilepsy, and then misdiagnosed again but with benign rolandic epilepsy, and I have now been diagnosed with juvenile myoclonic epilepsy and they suspect I have another type, but I forgot the name of it
I've had them ever since I was a baby, I didn't know they were seizures though. I'd always remember feeling embarrassed for blanking out all the time
This year I will be turning 20 and I have been suffering from Absence Seizure as far as I can remember
Its great to know that schools will be more alert with different kinds of epilepsy. Absense is the most hard to identify as a seizure. I have absense and before i was diagnosed i wasnt sure that they were actually due to epilepsy. It will be great if school children understood epilepsy as well as teachers :)
They are not they think they are fake my whole life. And it's not. I can't. Help it
2015
I have both absence and tonic-clonic seizures, and have since I was 13. It really makes my life a lot more difficult, but I'm on medicine for it. However, it hasn't been working much lately and I've been having many tonic-clonic seizures. I've also been having many absence seizures in the shower and it really sucks. I'm getting through it.
do you still get them?
trying to get my partner diagnosed and I am in a state of frustration with nhs at the moment they are so intent that she makes up her seizures.
her eyes roll back and her neck goes stiff, has hallucinations, nausea, wandering around, spins in circles, shouts out, swears a lot, severe anxiety and depression and suicidal tendences.
I have seen a pattern of when these seizures happen and it always seems to be the afternoon of a thursday around 4pm never ealier or later and she also falls over alot during it...
she also does this in the video so which or what is happening?
she could be having non epileptic seizures as she is schizophrenic and hears voices which gets worse during these seizures as well...
hmm?
I love it ....this way to teach kids about epilepsy is realy helpful to epiletic kids becuse it make them easy acceptabl by the other kids and not make fun of them....so keep up
I don't think I'm the intended audience here, but as a hypochondriac, this channels is currently proving very useful in helping me confirm that I'm most likely _not_ suffering from the ailments shown in the videos. Thanks
I think i have absence seizures. Sometimes when im just standing around, i feel like my soul has been taken out of my body, and i cant control anything for like, 0.5 seconds. I came to this video to see what it looks like. I dont wanna self diagnose, but im pretty sure i have absence seizures.
Hey! Any concern with seizures MUST be checked by a doctor just to be sure
This girl at my school has this. Sometimes she'll stare at someone or something and we need to tell the teacher. Or if she falls on the floor and she's twitching I feel bad cause we can't touch her until she's done. But today I was looking around the room and she stopped and stared at me and I told the teacher and she said leave it and like 3 minutes pass and she's still staring at me then when I got up to tell the teacher and fell on the floor and started twitching. This went on for 6 minutes. We had to call the ambulance bc if it lasts more then 4 minutes she could die. It was scary. They rushed her to the hospital. Her mom told me she wouldn't stop twitching until she got to the hospital (the hospital is like 20-30 minutes away)
This is interesting, recently I had my first tonic clonic (I'm 31) I think they used to be called Grand Mal? But after seeing this, I've realised that I've been having this kind of seizures for a long time...
Only my school just used to give me detention for not paying attention or day dreaming
This. I was an excessive daydreamer in elementary school and middle school. In High School, I just zone out in space. I got detention for the first and only time in 4th grade for daydreaming. If your teaching is too boring and/or uninteresting, my mind switches to daydream mode to keep itself entertained.
These are not tonic clonic seizures.
They never said that. Read it again.
This is what happened to me when I was in jr. high and the public school kicked me out and sent me to a boarding school for 3 yrs. but as time went by I came
back to the public school I was at in my jr. yr. and I went on to work in Special Ed. for 35 yrs. and I stood up for students who had neurology disorders.
Does this have anything to do with blanking out while reading and not remembering anything?
usually when you're "reading" but not really reading, you're still able to move your eyes and stuff, it's just not processing. with absence seizures you have no control (except basic reflexes like continuing to stand/sit up if less severe).
if you were to compare it to something, i guess it's more like when you're really tired and trying not to fall asleep, but you keep nodding off and your head jolts up when you realize you need to stay awake. you don't feel yourself or remember actually drifting off to sleep, you just suddenly realize you're not supposed to be.
As someone who has this kind of epilepsy, I would just like to clarify that these kinds of seizures are not always this quick. I have had absence seizures that literally lasted for either 30 minutes, or an hour or so. They come on with absolutely no warning, and you cannot be woken up from them. Said person just freezes up for an indefinite period of time.
One tell that someone is having an absence seizure is obviously a completely blank expression, but(at least for me, not sure if this applies to everyone with this kind of epilepsy) another sign is repititious movements, such as moving your finger in a circle over and over again.
This video does a great job of showing how sudden the seizures can come on, but I figured I should mention that the seizures can go on for *far* longer than just a few moments.
@@cyuinanotherlife No worries! Pretty much, except you can't be "woken up" from them. You can only "wake up" on your own, once the seizure passes.
I get like this sometimes. Once I was out in a club dancing and next thing I used I had stopped in the middle of the dance floor and my friend was tapping me on the shoulder asking if I was ok and I continued dancing. Apparently I was “zoned out”
Learn more about epilepsy with Epilepsy Action’s range of
e-learning courses. learn.epilepsy.org.uk/
Epilepsy Action .
What
4th
My youngest son has absence seizures
My bf has seizures these videos r a lot of help! Thank u
I do have this kind of epilepsy and once i was in class i think my teacher was calling me and the seizure started and when it ended i heard my teacher shouting my name. Everyone was looking at me like i was a alien...
Hello dear I know someone who can help you with the cure. Add him up on WhatsApp +2348075354290
I'm 19 now
When I was 14 I had this seizure ar school and I'm presenting MY PROJECT I was so embarrassed that I had this and I BLANK OUT and my teacher ask "are you okay sweetie?" And I said oh oh yea! I'm fine! And later on when it is home time I didn't tell my mom because I don't want her to freak out and finally I continue the seizure till I'm 19 years old :(
And can I have 5 likes for 5 years seizure? :(
There is this online chat room for teenagers with epilepsy to socialise and talk to other people who are going through these similar situations. I thought it was pretty cool and maybe you should check it out as well.
www.thetea-room.com/
Since you are or you are almost 20, are you okay?
So you made us go through a “guilt trip” just to ask for likes? Get better or some shit but don’t beg for likes dude, sick or healthy
I dont tell any one either
Dude tell ur mom
Have a question for the room...when a child, I had incidents where my mind would go completely blank for a split second (I assume). Usually it it was when a bright light would flash or perhaps catch me in the corner of my eye. On a couple occasions I'd be riding in a car and passing through trees so light-shadow-light in quick succession. It didn't effect me - my parents never noticed and I kind of thought is was normal. Oddly one of my children had the same thing....when he described them to me I remembered my own incidents. He says he thinks they are absence seizures...
Yeah I have also experienced this kinda seizure when the flash light or colour ful light catches the corner of the eye (my right eye) and it feels so freaked out but no one notices and after this thing happens I used to get some headaches or anxiety
I had my first seizure in 23 years last night, I'm almost 40 and I don't have any more .... I accidentally drank a low cal drink and know I had issues with aspartame when it first came on the market. I wonder if others have had similar issues?
I'm an Epileptic Person, sometimes, I do experienced that.
that used to happen to me when I’d have to give presentations and stuff, and it still does, actually.
Just pay attention
@@therion8469 You know that seizures are literally your neurons firing wrong and that they're something you can't control?
Maybe take your attitudes back to the middle ages, oh, wait, even they knew seizures weren't voluntary.
@@therion8469JuST PaY AttEnTioN, dude if their neuroshitwhatchamacallit would just cooperate no? but no, it's not their fault they're not cooperating
I hate these so much sometimes I wish I was just normal, and I could erase all the stupid memories of me at school and ppl staring at me and even I didn't know why they happened every time I think about it I feel like crying
Yes me too, I even peed to myself at some point after holding myself for too long then had a seizure. It was terrible but I still have them and facing the world to accept us and my family who are too African traditional
i have epilepsy its horrible as i cant even go swimming or something with my mates without my parents.
when i was seven i managed to get rid of them for about a year but then they came back. i am now 13.
th-cam.com/video/lT3P6XHCtXg/w-d-xo.html
High humidity and low atmospheric pressure is the reason why people get seizures! I found out because my previous seizure was during when the hurricane and I googled it and found out. That's why places with high humidity such as The UK and Pakistan have the highest percentage of Epileptics.
My brother used to have absence seizures and they were really bad. We do not bother them when they are happening because the doctor said to wait until his seizures are done to bother him.
th-cam.com/video/lT3P6XHCtXg/w-d-xo.html
It’s more common in kids considering it’s like you stop did you don’t even notice when the seizure starts
I've had these since I was 7 and I was scaring my parents. I was told that I fell down the stairs at one point.
+Graycetube 1 I'm 24 now
Contact this doctor directly on his WhatsApp number for your total cure then. +2347030936239
Im here in philippines 2004,(19 yrs old) that time when im surgery because of sinusitis turn to infection in my brain.. since im recover that dont know i why starting of epilepsy thru weekly,monthly,yearly until now im thnkfull to other doc. They help me to about the medical drugs... My last triger epilepsy is 2018, but before that yes im always feeling last past in aura seizure but bcause of medical turn to absences seizure now, 2018 2020 feel only absencea seizure, im using my drug in 2 a days everyday but now the here in whole world of covid 19 bcause of that im taking once a day for limit in buy supply in the drugs store.
And also financial problem...
Im sharing this my story life for asking for help in any for stop my sickness.. thank you for this day Godbless
My mom has epilepsy and I notice this year that I think this happens to me are there any other signs
Yes, there is. There is more seizures involved with epilepsy. Do you have any involuntary movements. Most people tend to mistake epilepsy for tics or Tourette's syndrome. Muscle contractions and other seizures are involved.
every time I speak/chat with people I freeze which can't even control it and takes a while to either speak or think properly
So I have an 8 year old son, he was formally diagnosed with this. It happens so many times during the day and has gotten to the point that when he blanks out, he wets himself (we homeschool thank goodness) I always hug him while it’s happening and I’ll ask him what he sees when it’s happening and he says he see’s his great grandma sometimes (he was around during her passing and it definitely took a toll on him emotionally). We just started ethosuximide. My biggest fear is him being stuck taking meds that “turn him into a zombie” he’s such an active child, full of life. I wish more than anything that I could do more...
+2348148445027
Prayers to your son
I have this. The worst thing is that it can strike at any time
Omg i have this multiple times a day..... i thought i was just zoned out.... but.... idk know if i have to go to the doctor or somthing
Depends if you have other symptoms. I'd definitely suggest getting it checked either way. It could be ADHD, for example.
@@Vessecora I have already been tested for ADHD, ADD and autism.
I have had these seizures since I was 9 years old and when I was 18 they stopped, 31 years later the seizures came. Apparently the seizures were laying dormant until I was stressed out and they returned and I have the seizures for the rest of my life.
Thanks for sharing your story Jon, I'm sorry that your seizures didn't go away completely. Stress is quite a common trigger for seizures, although for many people, the cause is very difficult to determine. You can read more about that here: www.epilepsy.org.uk/info/triggers
I've had absence seizures before plus 2 breakthrough seizures which happened as a result of me forgetting to take my medication. I'm hoping to start having driving lessons in the near future, once I get checked up, as I haven't had any absences for well over a year now.
What is the seizure when people lose control of their body and start shaking or something?
Jeking seizures my sister gets those she is a diabilty
I have absence seizures and also drop seizures and we can't find a cause
My friend has absence seizures that are just like this, one minute he will be fine the next he is staring into space my little sister has complex epilepsy and has atonic seizures my mum told me to just let my friend get on with the fit but if it lasts for longer than 1 minute I should call her and ask what to do
This happens to me sometimes. I also start to feel off in really bad artificial lighting.
Contact this doctor directly on his WhatsApp number for your Total Cure . +2347030936239
My sorry ass teachers just thought I was on drugs. 🤔😑
A girl had one of these today but it lasted about 40 minutes straight without her responding
Ok ,so since my late 16s I frequently have this problem : Sometimes randomly I have strange feelings which is indescribable, its like things are coming closer, into more focus , deja vu etc when all of a suddem I go blank and there is loss of awareness and connection with the surrounding, I am not conscious or aware of anything its same like when a person sleeps then after few secs I return back from that blankness and then forget what I was doing that particular time and even what I did the entire day, I then try and start recalling which it takes me good 3 -4 mins to remember everything, sometimes I can control/ ward it off , other times it happens so frequently that by the end I get terrible headaches...
My mother and sister tell me that I give a death /blank stare during that period
Its been happening for 3 years now,
then 3-4 days ago I had a full tonic- clonic seizure in the morning for the 1st time... my sister saw it , I was sleeping and suddenly I began jerking , My lips turned blue, eyes rolled to a side and I bit my tongue..
Of course I was unconscious after this , and don't remember anything of the seizure , my sister described it to me, only I had headache and body ache throughout the day and felt tired and sleepy
I did go for an MRI , which came back normal
Could someone please tell what is all this..it would be of great help
..
You can have seizures if you have a temperature.
As someone who has absences sezuire this is so relatable i remember when i had one during a swimming race luckly i was doing backstrokes so when it happened i was just floating on the water and my brother got me out of the water if i was doing butterfly or front strokes i bet i would've drowned
I've had epilepsy since I was 7 years old so I've had it for 7 years now.. and it's tough to say the least. My first year I wasn't on medication so that was the worst year..my mum said she woke up screaming from nightmares for weeks because she was so terrified. Because I didn't have jsut absence ones I had; tonic clonic, absence, facial twitching also stress seizures so i faint in school alot and it tends to make me very weak etc and my parents use to count how many times they called any ambulance. They stopped counting after it got past the 300 Mark, that was when I was 9, I'm 14 now.
This was exactly me and still is me I hate having absence seizures I get so embarrassed thanks to my childhood neighbor I got diagnosed with epilepsy because she noticed that I blanked out a lot but now I’m on lots of meds I used to collapse to the ground and times and even drop things now I blank out sometimes even say random words when blanked out and do stupid things when I blank out like recently I was drawing and I blanked and Drew a line somewhere I wasn’t meant to I got mad at myself and scribbled it out since I didn’t have a rubber I hope it gets better for anyone who does have epilepsy you guys can do this you are strong ❤❤❤❤❤❤❤❤❤
Types of seizure like this are hard to realize if they are having seizure or they are just doing some funny things
My doctor thinks I'm having this type of seizures and this is exactly what I do. Should I be worried.
Ashlee's Bathroom nice violin 🎻 you should get it checked out to calm your nerves about it if your worried but I was worried and i turned out to be healthy only I had epilepsy which doesn’t matter since I go about my life as normal 💕
@@Kiahboudreaufanning thanks for the advice, and I did go to the doctor. They ruled seizures out. They think it's a form of panic attack. It did only happen in stressful situations (like interacting with people I dont know).
Interesting
I have absence seizures I had absence seizures at school and the teacher didn't even notice
I can’t tell if I have epilepsy or if I’m just casually zoning out but just not clarifying my surroundings after I come back in contact with people. My mom has seen me staring at nothing without me blinking and I can remember them so that’s why I think it’s just me zoning out.
Tell the neurologist.
I was diagnosed with epilepsy last month. I was a spacey kid who sucked at school but was otherwise bright. Now I wonder if it was absence seizures interfering with learning?
I had this when I was like watching some movies or in outdoor like in school days(when quarantine wasn't a thing) I always get a brain block is what I call, but then I still continue on what I remember. But I never had a a seizure before. Just this one because I swear I felt it.
Ok so I've suspected I've had a problem since I was about 5 at least. Now, I've gone to a neurologist who believes I am having absence seizures, but they're non-epileptic, and caused by abnormal brain tissue. Anyone else?
that is my school but we don't wear blue we wear green riverviewpriamy school
Struggling with seizures my whole life this is a little accurate
th-cam.com/video/lT3P6XHCtXg/w-d-xo.html
At school i randomly have an absence seizure but no one seems to notice
I think this has happened to me before. I don't remember any of what happened until my friend called me. I don't remember what we were previously talking about, what I was looking at, what I was thinking about..
nothing. Do these types of seizures have triggers? Because it happened after I went on about 4 very fast rides at a fair. Would that have caused it?
Hi there - all kind of things can be triggers for all kinds of seizures. Sometimes we just don't know what triggers them at all. You can read more about some common seizure triggers here: www.epilepsy.org.uk/info/triggers
Hope that helps!
Thats me everywhere i hate when i do that especially in school because i always have to lie i never say whats actually happened.
Rx tab albendazole 400mg, tab epiford cr 500mg, tab folvite 5mg, tab epsolin 100mg bd. Epilepsy stop medicine is ferrissium 5mg.
I was diagnosed with Disassociation Disorder but now I'm wondering if it was a misdiagnosis
Get a second opinion.
I was born prematurely because I had a seizure in the whom and I’ve had Epilepsy ever since
This is totally me! i had it since i was 2 my mom told me but i got this problem at young age so i don't feel weird or embarrassed it was like part of me but still it was difficult at sometime like crossing the road or get in the train before the door is closed😥
Dfrnce between lost in thoughts absent mindedly and absence seizures plz
I had epilepsy since i was 3 and I've still got it and im 39 now but it's not as bad as it was before
Lisa Rougier just stay off the caffeine and eat keto a News plant oils
I had this and fell over in a car park. I was out on my own at the time. My mum came and found me and took me to hospital
+2348148445027
and how many parents would pass this off as..what was that, oh she is ok, see she cam back.
I am an adult, and I have been sked not to drive, our son's aba therpaist asked me if I was ok 2x I only heard the second are you ok...Now I have to ask myself.... did I show signs as a Child and no one noticed? I also have Autisim. I also only had one EEG, and I hear that sizures may not occur during an EEG. so now They do a 72 hour home EEG. thank you for showing this video.
Some kid in my class just had one in 8th period an hour ago, me and him were messing around and he just dropped a tool in his hand and stared at nothing for 5 minutes
They aren't that short tho they're a few seconds longer
Um ya it might be be like that for. You but for me they are short only a few seconds we probably just have different types of epilepsy though
hi. I don’t know if it’s just a normal thing that happens to a lot of people, but, sometimes, when I see (maybe watching a music video) flashing lights, I find difficult to breath normally, like after a long running session.sometimes at school, I just went blank. My friends asked me if I was in stand-by, and I said, really confused, no.
Or maybe I abruptly become really confused of what I am doing, of why I am in a place, or I freeze when I am standing up, or sitting on the couch or laying in bed...
should I see a doctor? sorry for the mistakes but I am not an English speaking person…
This sounds unusual. It would definitely be worth speaking with your doctor. And if you possibly can, having someone take a video of you while it is happening could be really useful.
This is our information about how epilepsy is diagnosed www.epilepsy.org.uk/info/diagnosis/diagnosing-epilepsy
Kathy
Epilepsy Action Helpline Team
Well this would explain what I'm dealing with pretty well