People with seizures should not cook all alone. Its good to see someone was watching over her. My mom also get seizures. Once while cooking she got a seizure and she accidentally fell on the burner. It burnt half her face. So please never allow such people to cook all alone. Its very dangerous for them mostly.
@@courtney_wanna_sleep thanks for asking. She is ok. This incident happened in 2013. The scars are still there. Much to public disgrace. She feels so depressed looking at her face even now. How a beautiful face got ruined. Always make sure such people take meds on time and are never left to themselves
Fuckin hell, the way this escalates from autopilot movements that could be mistaken for absentminded fidgeting to full on seizing, it must be so strange to experience and to watch back
Yes it is hard for me to watch the video. I’ve only watched it a handful of times it bothers me a lot. I recently had a severe seizure totally blacking out and dropped all my food I had in my hands, took three weeks to recover from. I will do a follow up video
@@aprilshealthmore8048damn I have seizures where I seize on the ground. But movements mistaken as random fidgeting is got to be one of the cruelest seizures
I bite my tongue everyday due to sleep seizures. The worst were when I had a spinal fracture and a severe injury on my chin. I woke up in the morning only to find, I was almost paralysed and bled severely
My husband used to have seizures, a brain scan found lesions on his temprule lobe, he had surgery nearly 30yrs ago to remove them, another surgery 6mths llater and hes been fit free for 29yrs. Without the surgery I would have lost him n our children grown up without a dad. Look after anyone you know who has seizures, time is precious.
@@charmed0009 Absolutely. And, for your information, dogs can have seizures, too. Almost all mammals can have epilepsy, and I've seen a cat personally with a TC seizure. Right in front of me. They know.
@@charmed0009yeah, that's pretty scientifically established actually. Whether this dog barked because of the seizure, I don't know.. but they can absolutely tell. It's why they can be trained as seizure alert dogs. They can tell right before the start of one.
I suffer from seizures and its scary. There was one time where I had one in the shower, and I didnt know what happened until I woke up at the hospital, seizures are not something to be took lightly.
I used to suffer from seizures too...until my tumor got taken out a couple years ago...one year I had 7 seizures on that same exact day (Christmas eve morning)
I do not take showers alone someone has to be with me and I use a shower chair, I couldn’t imagine having one in the shower I am so sorry that happened to you. I think that’s one of my biggest fears is being in the shower and it happening. Thank you for sharing.
I had a seizure in the shower recently as well. My mum heard a thud and then splashing around, thinking it was my younger sister playing so she went to check and there I was seizing on the ground. My first ever seizure. I was so confused because one minute I was hopping into the shower and the next, my mum was on the phone crying. Apparently when I had my seizure I came around for a second, said "Mum?" and then had another. I'm absolutely scared of being left alone at this point but I just moved out of my parents place 😥
@@aprilshealthmore8048 I had seizure in the shower a few years ago and didn't know it. I went to work the next day and couldn't bend or stoop. I bent over to pick something up and couldn't get back up. My hip and back hurt like hell for over a week. I finally asked my now ex husband if he remembered anything happening. The only thing I remember is not feeling like myself and forcing myself to take a shower that night. When I do feel a seizure coming on in the shower, I knock on the wall because I can't speak. He said he heard me knocking the wall. He came in there and I had soap all over me. He said I slipped out his hands twice and hit my hip hard on the lip of the shower. He dragged me to the bed soaking wet and soapy. I didn't remember anything. The only way I know I've had a seizure if I'm missing a chunk of time or being 1 place and then another and not remembering how I got there or someone tells me.
@@aprilshealthmore8048 I pray that Jesus heals u n others who go thru epilepsy.dont worry trust God n pray ..I really was astonished as a lump disappeared by God's grace from my father's neck from behind of neck..God is gracious n trustworthy n listens to our prayers!I was astonished at the miracle!!pls pray ..u are miracle might be a prayer away,God knows
I wish these things never existed. I literally just had 3 today and 10 last month. I have multiple auras/seizures every month. Had one behind the wheel that caused a bad car accident. Only if ppl knew understood our pain and sufferings. First thing ppl think that medicine helps. In my case, medication doesn't seems to help. I pray that someway somehow a natural cure can take these seizures away from all of us. 🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽
I'm 58 and have seizures since I was 11. Meds don't work for me either. I have had some success with the vagus nerve stimulator implant but have never been seizure free. I have partial complex seizures.
When I am about to seize I become confused and very uncoordinated as well sometimes. A few times ago my mother said she knew because I was passing my fork and knife back and forth between hands because I couldn’t figure out how to cut my food properly. I kind of remember passing them back and forth because my hands were weak and wouldn’t turn correctly. And also one time I was about to get in the shower and when I turned the water on I just stood there having a small one (which I do remember staring at the water coming down and hitting the tub for a long time) but my mother came in and got my on the couch because she never heard me physically get in the shower but only turn the water on.
Thank you for sharing, it is very scary. I can’t stand when it happens. Takes me so long to recover as well afterwards I’m sure you can relate. Thank you for sharing.
My grandma had these when I was younger and I wish I had known what it was back then. Her cancer was too far along by the time they found it. Thank you for sharing your vulnerable experience to help educate people. Knowledge saves lives. ❤
I have bipolar and other horrid mental health conditions, but Jesus christ my heart goes out to those with epilepsy. I can't imagine the horror yall feel. I hope you can find the answer, there is one.
Thank you for saying being epileptic is a living nightmare, but I know being bipolar is no walk in the park either as both my mother and sister were bipolar.
I go through this with my autistic son and he is non-verbal. So I never know how he feels before or after the seizures. Sad thing to go through, my heart goes out to everyone that goes through these seizures. It’s so hard to watch 😢. Nice to read comments of how ppl feel before and after though. I wish my son could tell me.
I’m sorry to hear about your son, I’m so happy that I posted this video and it at least helping someone else brings me joy - that was my whole point of posting it
Father, I ask for Your intervention with her, and those in this comment section, that are experiencing similar episodes! Your Word declares: "... with His stripes we are healed." (Isaiah 53:5). We believe and claim it! We ask that the compromised area causing interruption with brain activity, be normalized, for Your honor and glory in Jesus Mighty Name! 🌹
That looks so terrifying when they are standing up, im so sorry, my brother had a sezuire this morning we are at the hospital now 😔 he fell out of the chair and started puking blood and shaking for about 5 mins.. untill the ambulance showed up Edit: dang that was only a month ago that was his second seizure, now he’s had 12
I’m so sorry to hear this !!! I pray your brother gets settled and thank amen care of ! Recovery ❤️🩹 isn’t fun either. It takes time and I feel like I have after shocks from mine !!
My daughter had a seizure on Friday we aren’t 100% what caused it until she sees the neurologist but she was spaced out completely (eyes wide open) her body went limp and she wouldn’t respond when I talked to her and she was like this for a good 5 minutes or so then her eye on her left side started twitching and she was kicking her left leg as well but only one side was like this . I didn’t know what was going on at the time . When we took her to the doctor she had a 101 temp they thought it was febral but because she was twitching on one side they don’t know so I’m going to schedule a appointment with the specialist It’s super scary
There is no cure for myoclonic seizures. These are non-epileptic in nature, but just recently I have found out that actually, I have focal seizures as well as my clinic. I am getting help, but I get them due to the illness I have, thank you so much for your comment this is why I made this UA-cam channel because I do believe a lot of people suffer with rare things that aren’t talked about.
my brother have seizure... it's starting when he confused,not sleeping well, looking bright light on eye's, too much sound on ears...then start seizure.. mostly 10 second to 30 seconds
Have had my 3rd already. The first two hurt for me that’s for sure and the recovery phase really does suck. Takes like 3 days to get your screws back n’ tightened
@@manaia759ive had them for 10 years now and id like to say yea the after math of most types of seizures do hurt. I have all kinds and ive had my face ripped open, teeth broken, nose broken, plenty of stitches, black eyes, horrible bruises. The list goes on. Seizures in the shower, on the stairs, on the road and no one even stopped i was on the road until my friends got back from tim hortons. Epilepsy is terrifying.
as a person with epilepsy i have these as well mine start off as a staring seizure then i get up and roam around and i got lost in a airport once because of it. i also have jerking seizures in my sleep and i had one so bad once that my foot knocked a hole in the wall
I'm a little concerned my seizures might be coming back. I don't know what its like to have one since the last time I had a bad one was when I was little. What was this seizure like for u? Update 10 days later. They came back and they are pretty bad but I'm recovering :)
I was in sixth grade and there was a girl with a helmet on. She had a seizure in front of me. I cried for weeks and had nightmares. I always give seizure warnings now and despise the flashing lights of police cars. I later met a nice girl who got them too. She couldn't drive. I drove her to a lot of places and helped her. I miss her. Her name was my middle name, but she was very religious and didn't like me because I was an atheist. I miss you, lizzy. I'm not a devil worshipper, ok? I have no car again but I can still help. I hope you got on keto like I said to do. Love you. ❤
I’m wishing the best for you :( I’m sorry you have to go through this my daddy is 55 and he just started having seizures. He takes 3000mg keppra and another medication I forgot. He got them out of no where. His seizures are grand mals. Please take care of yourself.
I've just started dealing with this in 2021, and my seizures range from (complex focal seizures) to (grand mal tonic clonic seizures) and (absence seizures)..... I'm hoping for the best for myself and that i can find the right meds to control them
3000mgs is a lot of medicine, i can’t function properly on just 1000, he must be either sleeping so much of the day or suffering so much keppra rage :/
Seeing someone have a seizure is the worst feeling in the world. You’re helpless to help them. You just have to make sure they are safe and comfortable till it passes. I watched my grandfather an my husband and I still cry seeing them.
Wait a minute this happens to me too. I noticed things have changed a little since I don't fall to ground and shake up. My head tilted up and down like this too.
It was probably because I saw her head snap into place while she was looking down, and that probably made her kind of dizzy. Also, I heard a pop sound exactly when her head snapped into place. All of this is just my evidence
Hello! I am still struggling with the myoclonus. My medical team is doing all they can to help my nervous system, I have an auto immune disease called chronic inflammatory demyelination poly neuropathy it’s very comparable to Multiple sclerosis! I appreciate you and your comment.
@@aprilshealthmore8048 I really hope someone caught you so you don’t hurt your head :/ I could never record my dad when he has his seizure I get too scared and find it a bit rude
@@nothanks6931 my team of neurologists told my family to record me when I have them so they can see what they look like since they’re non epilepsy- it is scary since then they haven’t recorded anymore nor do I want to see myself again like that. Thank you for sharing about you dad. He’s got a real good child like you to be there for him.
Actually I want to say truth I came here just for a knowledge to know what this disease is but after watching your video I literally got goosebumps. I even couldn't sleep a night as I was very scared. Hope no one else faces this in the life and hope u get well soon❤️
I'm so sorry you have to go through this. Please get a service dog that will alert you to the upcoming seizure so you can sit down and wait it out. Good luck and may God bless you.
@@aprilshealthmore8048 We really don’t know. But they do start out as more of a focal seizure and then it gradually goes into more of a myoclonic seizure. But whenever I’m asleep I do know that I have clonic seizures. Weird isn’t it how mine differ from when I’m asleep compared to when I’m awake
@@aprilshealthmore8048 I do have multiple heart heart issues such as a slow in(e)jection fraction ( how fast blood goes in and out of my heart ) I have a right bundle branch block ( when my heart might shut off for a split second and then beat back into place ) and then I have a exit sticky valve which basically means that sometimes not all the blood that’s supposed to be ejected comes out because the valve didn’t open all the way. And all of these aren’t specifically a major issue, they shouldn’t be underlooked either because all of these things can turn bad if something small even happens. So I go to the heart doctor once a year for a rhythm check, ekg, and echocardiogram. And then of course I was diagnosed with epilepsy when I was 10 years old.
My dad had just experienced this last month, we were both at my school just going to an open house meeting to see my teachers. We started walking to one of my classrooms but we couldn’t find it. We went to the janitor to see if she could lead us there. That’s when the seizure began, he was about to ask and then he froze, couldn’t speak, couldn’t hear, and couldn’t move. It scared me to death and the janitor thought he was having a heart attack. Luckily he seems to be doing a lot better now that he is on meds.
My first cousin get them real bad. He hospitalized every single time.he is slow to come around.. i hope they can invent things that will actually help. Bless her heart..❤😊
I go through this everyday I even ended up driving to another state because you are literally space out completely and it's very confusing in your brain.
Yeah...I kinda hated when youll get spaced out and everything cause sometimes when I'd try to explain why I was being weird or something...no one would believe...like in 6th grade 5 years ago...I had a seizure and the teacher took me outside and asked me why I did that and I told her a seizure...she wouldn't believe me we almost argued...
Every time I have seizures it’s mostly from lack of food, energy or coolness I can’t stand the heat, if I haven’t ate it’s hot and I have no energy I feel very distant then my eyes just open up and I realize I had a seizure
The fidgeting at the beginning stages of a myoclonic seizure kinda seem like the brain running a few automatic settings before freezing up and needing a hard reboot
I learned a lesson today. Those behaviors are also exhibited in people who use hard drugs and begin “tweaking”. Traditional I would see a shopped with those behaviors and assume they used drugs. I had no idea. I’m so ashamed.
My son had mild seizure-like movements of eyes rolling back in head. He was only about 1yr old. Did it caouple more times once with motherinlaw. Made appt with dr who referred him to specialist. They did I think a ekg? Then they were supposed to flip him over and do backside but he woke up on sedative and didnt want to give him more since he was so little. They didnt see anything on test. Not much theyvan do. Grade school-he had a fullblown seizure! Got up from chair, did a face forst body slam to floor!. Carpet softened blow. He laid there about 5 min and jerked all over, face sideways on cheek. I waited by his side till it stopped. I told him we were going to ER and he got very agitated which is common side effect, confusion, memory loss. He insisted on shower but I stood in doorway in case of falls. ER dr said granmal seizure but nothing they can do if they see no actual seizure. Daughter is RN and recomended pediatric neurologist. He tested him, thought he had Syncope=light headed when getting up from chair. He was his dr many years till he was 20 then he had to seek a dr for adults. That dr gave him meds. He has yet to set up with one. No meds for past few years. He is diagnosed with add-hadd
It’s definitely in his best interest to seek medical attention for the seizures. I really hope that the video encourages people to do more about the seizures. It is very frustrating. My heart goes out to you for your son.
I had a friend who had seizures. Was cooking, fell onto the stove and was badly burned. Spent the rest of his young life in the nursing home he had worked in.
I experienced my younger uncle having a seizure. While he was showing me his Ninja Turtles toys. I originally thought it was a joke (I was 7-8) and he was just laying on his chair eyes closed completely shut down for 2 minutes. I started to cry then went to my mum and nanny and showed them. After maybe 5 minutes an ambulance came and saved my uncle. It was a horrible day
my son has cp and epilepsy he has what they call tonic clonic seizures and is loaded up on medication and had a vegal nerve stimulator put in 2019 it helps bit he still has seizures. i pray for every one that goes through this has a safe and healthy life ... God Bless
@@wendijones5942 remember that you're an angel and God never gives us more than we can handle. All things happen in his time. We just need to trust in him. I'm praying for you.🙏✌️💖🦋
As a seizure patient as long as I stay on DAILY meds twice daily I have been great! If my meds are NOT in my system at my 4 month blood work my drivers license gets taken away for 6 months or until I’m 6 months free of seizures. Yes, this really sucks but after having a grand mal seizure I don’t mess with my seizures anymore
Sister Faith, you made my demons revel in anger. Where has this term "maladaptive day dreaming" been? Where have these words been to counter the strongest demon I have ever faced? All within this video. I'm just blown away. God will reward you greatly for this one. Thank you so much. Something that's been consuming my soul for so long is now identified, explained, and answered with divine wisdom. I'm in debt to you
Could a complex partial person get this type of seizures too? I think I got this several times even while driving my car. I had to stop for a while to let go
I worked 28 of my last 30 years as a welder like this. For the same company. I would have these small seizures that would cause me to freeze and stare. Drool would come out of my mouth. I would see peoples mouth moving in slow motion but couldn't hear any words that were spoken or the sounds of any machines running. Like someone flipped a switch to stop all sounds but everything continued to work. I would eventually stop and stare at a person or an object. If there was liquid in my bladder I would start urinating on myself with no control to stop it or move. I had only 3 full blown seizures in my 30 years working for the company..All of which I never knew happened until I was being loaded in the back of an ambulance with huge knots on my head from whatever my head hit something. I learned to keep extra clothes at work in case I urinated on myself because I had no way to get home..if you're an epileptic they take your driver's license away. I was fortunate to have a friend who I gave money to to pick me up everyday and was extremely dependable. If he was going to be off on vacation I had to make other arrangements to get to work. Sometimes I had to hide in the building and get locked inside the building and sleep at the company without anyone knowing it because most of the people didn't care if I needed a ride. Some actually liked seeing me struggle. Epilepsy also affected my memory. Before I left my job everyday I had to write down what I was doing so I would know where to begin the next day. Losing track of tools and things was another big issue I battled with. I would set things down no remembering where I left them. That is another area my "Job log" came in handy. I could look in the book where the last job was that I used that tool. New people's names would take me a while to learn. Our company had an employee high turn over rate which made it quite different for me. The good thing was once I was set up to do a job I did the same job for a few days. Another big plus for me was I am very gifted at repairing all kinds of manufacturing machines. No one else there was. If a machine had problems I could quickly diagnose it, order the parts and fix the machines. My boss kept me because he knew I would have problems keeping a job elsewhere. Not too many businesses want epileptics as an employee. 30 Years went by, my boss passed away and I was tired of fighting the epilepsy monster in my brain. I knew it was time to go file for my disability because now my body was also worn out..My Dr. said I was truly an inspiration to him because he never believed I would last as long as I did working.
I must say first of all, I appreciate you sharing your story, and I want to say you’re a very courageous and strong person and this is probably one of the best comments I’ve actually received out of the thousands of comments that I have received and what I hope helps you is that you’re not alone and I too worked over 23 years And I just really appreciate you sharing your story. I really hope that it makes a difference knowing that you’re not alone. I really hope that you are stable and that you’re doing good?
My sister has grand maul seizures it takes so much out of her takes her days to recover from it. If she misses one dose of her meds throughout the day she will have one. It is very scary
One of my sons had seizures since or before birth. Blood all over his baby bed. I know he had at least one seizure standing up. Hes been in pain for a long time, 50 years.
Once a year I'll end up with seizures in the middle of the night but 20 years ago it happened in the day and was immediately taken to the hospital that time i was only 5 years old it's so scary that sometimes i think i might die 😅
I can Relate here i was Diagnosed with Epilepsy when I was 4years old I'm 60 now and live alone it terrifies me when I go into the Kitchen with hotplates and Boiling water so i stopped Boiling water amongst other things that many people take for granted God bless
I had something like that today but I don’t know what it was, I was shaking uncontrollably but I could still see and hear everything around me, but I couldn’t talk and every once and a while it would stop for a bit but started again and I passed out for a bit, I was at school and it was the end on my first class and my teacher walked me to the nurse and honestly I don’t remember walking there like at all but when I was sitting in the back I felt like I was going to pass out again and I tried to tell the nurse but I couldn’t talk at all, and I passed out but the nurse thought I was faking it so I got sent back to class and had to go the whole day barely being able to walk
I have those too, usually after ptsd episodes, those are probably large scale (non verbal) panic attacks. You can have conscious seizures but they’re usually smaller scale or absent seizures. during my panic attacks my head felt and sounded like static and my hands locked in place for over an hour after.
my first ever and last seizure ever was in elementary school when i was in grade 1 i got it unexpectedly my teacher knew something was wrong so she called my mom early, at that point it started to kick in.. i cried while my mom carried me still having the seizure
They can come out of nowhere at anytime...most times with no warning very unsafe to be left alone cooking or bathing...in Jesus name miracles happen all the time ❤️🙏❤️ o
I’ve had seizures. With all the tests they can’t induce them or figure out why they happen. I’ll be at work and I’m going at 100mph then all the sudden I wake up to emt around me and I’m on a floor. They ask if I knew where I was, I saw a box with my company name on it and said the name. I really didn’t know where I was or why. I was asking my mom to call my sons mother so she could get him from daycare while I was in hospital. I was so confused that I didn’t remember that my sons mother had passed away 4 months before. Took a good couple days to get the fog out. I also have fainting spells without seizures, have had episodes where I wake up in my sleep with no ability to breathe. Like my throat is closed. To the point they had me wear a heart monitor as I slept because they didn’t know if I was having heart issues or strokes or something while I slept. They think it’s stress. Lack of good sleep etc. that my body gets overloaded and overwhelmed and it shuts down. Idk. It’s scary though and am not on medication because I’m not diagnosed epileptic. They also don’t want to give me anything for my anxiety because the withdrawals from those meds when I stop can cause seizures. So I just live with it. I’ve lost my license for periods now f time after seizures until medically cleared but have no diagnosis to collect when I can’t work.
Look into neurogenic orthostatic hypotension I’m not a doctor, but my daughter has heart issues and it took many years for them to find it and it’s very hard because it’s with the brain activity and you are correct stress can do this, but I wouldn’t give up don’t give up on you. Another reason why I posted this video because it took them years to figure out what was going on with me. I appreciate you sharing your story.
Sorry but if that'd been my son youd of heard a weird sound in his voice, and he'd of fell and busted his head on the floor, he's had them 28 yrs, both shoulders need surgery, which I'm scared to death when he gets it done, broken collarbone, and busted head several times. My son convulses very badly, and they started in infancy as febrile then absence seizures, then grand mal at 12. So she's lucky if that's as bad as it.gets I pray it gets no worse.
I'm sorry you have to go through that, I hope you get better.
Get better? Bro she got epilepsy there ain't no curing that💀
@@Guy.WhoAsked so? Some people can make it less common or even make it go completely by finding different lifestyles or taking pills
@@IAm-zo1bo sometimes when i come home to an empty house i have bad thoughts of coming home to him lifeless
Neuralink might be the cure
@@stachu1027 empty house? What do you mean
People with seizures should not cook all alone. Its good to see someone was watching over her. My mom also get seizures. Once while cooking she got a seizure and she accidentally fell on the burner. It burnt half her face. So please never allow such people to cook all alone. Its very dangerous for them mostly.
I don’t cook alone anymore
I’m so sorry your mom also suffers from seizures.. it’s so tough
I hope your mom is feeling weel now
@@courtney_wanna_sleep thanks for asking. She is ok. This incident happened in 2013. The scars are still there. Much to public disgrace. She feels so depressed looking at her face even now. How a beautiful face got ruined.
Always make sure such people take meds on time and are never left to themselves
I wish you the best! May your mom have better health
Fuckin hell, the way this escalates from autopilot movements that could be mistaken for absentminded fidgeting to full on seizing, it must be so strange to experience and to watch back
Yes it is hard for me to watch the video. I’ve only watched it a handful of times it bothers me a lot. I recently had a severe seizure totally blacking out and dropped all my food I had in my hands, took three weeks to recover from. I will do a follow up video
@@aprilshealthmore8048damn I have seizures where I seize on the ground. But movements mistaken as random fidgeting is got to be one of the cruelest seizures
@@snakyYT dislocated my shoulder twice from seizures and bit my tongue. My thoughts are ever with those who suffer from this debilitating malady.
I bite my tongue everyday due to sleep seizures. The worst were when I had a spinal fracture and a severe injury on my chin. I woke up in the morning only to find, I was almost paralysed and bled severely
I can relate to first experiencing autopilot and then having seizure while working
My husband used to have seizures, a brain scan found lesions on his temprule lobe, he had surgery nearly 30yrs ago to remove them, another surgery 6mths llater and hes been fit free for 29yrs. Without the surgery I would have lost him n our children grown up without a dad. Look after anyone you know who has seizures, time is precious.
I always do that before I have a seizure fumbling around and doing weird stuff. Usually at that point I’ve already blacked out
Bro got his screen glitched
@@watercuphealthy 💀
Sometimes I walk around my appartment for nothing before a seizure , my hands become stiff and I smell a weird odor
@@vincentbougie7776I've never had a seizure but I have all that symptoms and sometimes my head shakes by itself idk what it is tho
I honestly thought you were just cleaning your stovetop very thoroughly. So sorry you're dealing with this. All the best..❤
The dog was barking because it knew
@@charmed0009 Same way you know looking at her.
@@charmed0009 Absolutely.
And, for your information, dogs can have seizures, too. Almost all mammals can have epilepsy, and I've seen a cat personally with a TC seizure. Right in front of me. They know.
They can smell that their owner is about time go through a medical episode.
@@charmed0009yeah, that's pretty scientifically established actually. Whether this dog barked because of the seizure, I don't know.. but they can absolutely tell. It's why they can be trained as seizure alert dogs. They can tell right before the start of one.
Yes, I've seen dogs like that, they warn their owner to lay down and get ready...just amazing. @@a_diamond
I suffer from seizures and its scary. There was one time where I had one in the shower, and I didnt know what happened until I woke up at the hospital, seizures are not something to be took lightly.
I used to suffer from seizures too...until my tumor got taken out a couple years ago...one year I had 7 seizures on that same exact day (Christmas eve morning)
@@Maryann2024 omg I feel so bad! I just have focal seizures randomly (,like when I stand up to fast
I do not take showers alone someone has to be with me and I use a shower chair, I couldn’t imagine having one in the shower I am so sorry that happened to you. I think that’s one of my biggest fears is being in the shower and it happening. Thank you for sharing.
I had a seizure in the shower recently as well. My mum heard a thud and then splashing around, thinking it was my younger sister playing so she went to check and there I was seizing on the ground. My first ever seizure. I was so confused because one minute I was hopping into the shower and the next, my mum was on the phone crying. Apparently when I had my seizure I came around for a second, said "Mum?" and then had another. I'm absolutely scared of being left alone at this point but I just moved out of my parents place 😥
@@aprilshealthmore8048 I had seizure in the shower a few years ago and didn't know it. I went to work the next day and couldn't bend or stoop. I bent over to pick something up and couldn't get back up. My hip and back hurt like hell for over a week. I finally asked my now ex husband if he remembered anything happening. The only thing I remember is not feeling like myself and forcing myself to take a shower that night. When I do feel a seizure coming on in the shower, I knock on the wall because I can't speak. He said he heard me knocking the wall. He came in there and I had soap all over me. He said I slipped out his hands twice and hit my hip hard on the lip of the shower. He dragged me to the bed soaking wet and soapy. I didn't remember anything. The only way I know I've had a seizure if I'm missing a chunk of time or being 1 place and then another and not remembering how I got there or someone tells me.
I came here after getting one patient case today to know more info like this cases ..thank you for uploading this , be safe
I’ve had one about two weeks ago. Extremely severe I’m still having muscle soreness
Me when I try to lie:
@@aprilshealthmore8048 I pray that Jesus heals u n others who go thru epilepsy.dont worry trust God n pray ..I really was astonished as a lump disappeared by God's grace from my father's neck from behind of neck..God is gracious n trustworthy n listens to our prayers!I was astonished at the miracle!!pls pray ..u are miracle might be a prayer away,God knows
@@shashikala3807 If he exists then he gave her epilepsy.
@@simianto9957 you’re wrong, sorry
I wish these things never existed. I literally just had 3 today and 10 last month. I have multiple auras/seizures every month. Had one behind the wheel that caused a bad car accident. Only if ppl knew understood our pain and sufferings. First thing ppl think that medicine helps. In my case, medication doesn't seems to help. I pray that someway somehow a natural cure can take these seizures away from all of us. 🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽
I couldn’t agree more. I think you for sharing your story and keep fighting. That’s all we can do. I’ll be posting it updated video shortly.
@@aprilshealthmore8048 ur welcome
I'm 58 and have seizures since I was 11. Meds don't work for me either. I have had some success with the vagus nerve stimulator implant but have never been seizure free. I have partial complex seizures.
What does the aura feel like
Auras are hard to explain...closest thing I can describe it it feels like dejavu
When I am about to seize I become confused and very uncoordinated as well sometimes. A few times ago my mother said she knew because I was passing my fork and knife back and forth between hands because I couldn’t figure out how to cut my food properly. I kind of remember passing them back and forth because my hands were weak and wouldn’t turn correctly. And also one time I was about to get in the shower and when I turned the water on I just stood there having a small one (which I do remember staring at the water coming down and hitting the tub for a long time) but my mother came in and got my on the couch because she never heard me physically get in the shower but only turn the water on.
I can relate to these symptoms very much so and I appreciate you sharing your story. Thank you.
I have had such experience, it is so scary...
Sad for you, i hope you feel better now
I had 2 back in November and it’s scary as hell, I’m so sorry you go through this❤️😭
Thank you for sharing, it is very scary. I can’t stand when it happens. Takes me so long to recover as well afterwards I’m sure you can relate. Thank you for sharing.
YNt u y⁸⁸⁸⁸⁵
My grandma had these when I was younger and I wish I had known what it was back then. Her cancer was too far along by the time they found it. Thank you for sharing your vulnerable experience to help educate people. Knowledge saves lives. ❤
I have bipolar and other horrid mental health conditions, but Jesus christ my heart goes out to those with epilepsy. I can't imagine the horror yall feel. I hope you can find the answer, there is one.
You don’t feel it when it’s happening and can’t explain what you saw or felt till you quit seizing out.
#PleaseStayStrong
Thank you for saying being epileptic is a living nightmare, but I know being bipolar is no walk in the park either as both my mother and sister were bipolar.
I go through this with my autistic son and he is non-verbal. So I never know how he feels before or after the seizures. Sad thing to go through, my heart goes out to everyone that goes through these seizures. It’s so hard to watch 😢. Nice to read comments of how ppl feel before and after though. I wish my son could tell me.
I’m sorry to hear about your son, I’m so happy that I posted this video and it at least helping someone else brings me joy - that was my whole point of posting it
This is the same with me ❤ bad day yesterday.
So glad I found these videos on UA-cam, it truly helps to read everyones comments.
My friend a couple days ago had a seizure right in front of me. She was doing the same thing (looking up at the ceiling)
i was shaky a bit, i was expecting a jump scare... glad nothing like that happened.. but oh no, so sad to see u had gone through that =(
Father, I ask for Your intervention with her, and those in this comment section, that are experiencing similar episodes! Your Word declares: "... with His stripes we are healed." (Isaiah 53:5). We believe and claim it! We ask that the compromised area causing interruption with brain activity, be normalized, for Your honor and glory in Jesus Mighty Name! 🌹
Amen
That looks so terrifying when they are standing up, im so sorry, my brother had a sezuire this morning we are at the hospital now 😔 he fell out of the chair and started puking blood and shaking for about 5 mins.. untill the ambulance showed up
Edit: dang that was only a month ago that was his second seizure, now he’s had 12
hope he recovers soon🤞
@@justsmilereadingthis thank you
I’m so sorry to hear this !!! I pray your brother gets settled and thank amen care of ! Recovery ❤️🩹 isn’t fun either. It takes time and I feel like I have after shocks from mine !!
@@aprilshealthmore8048 thank you ❤️🔥
12 seizures? how thats not possible
I noticed the head movement when she first opened the microwave…that looks like how I look before it starts
Thank you for sharing !
Me too x
The dog barking was a sense of it coming on
They bark like that every time I have one , so true ! Good note
As someone who had seizures I can confirm this is what its like
My daughter had a seizure on Friday we aren’t 100% what caused it until she sees the neurologist but she was spaced out completely (eyes wide open) her body went limp and she wouldn’t respond when I talked to her and she was like this for a good 5 minutes or so then her eye on her left side started twitching and she was kicking her left leg as well but only one side was like this . I didn’t know what was going on at the time . When we took her to the doctor she had a 101 temp they thought it was febral but because she was twitching on one side they don’t know so I’m going to schedule a appointment with the specialist
It’s super scary
Thank you for sharing your story about your daughter ! Definitely needs to see a neurologist as well hoping docs can get to the bottom of them.
This helped me see what I do. I know nothing about them or even what I was doing until now. Glad you got it in tape. I hope there is a cure.
There is no cure for myoclonic seizures. These are non-epileptic in nature, but just recently I have found out that actually, I have focal seizures as well as my clinic. I am getting help, but I get them due to the illness I have, thank you so much for your comment this is why I made this UA-cam channel because I do believe a lot of people suffer with rare things that aren’t talked about.
my brother have seizure... it's starting when he confused,not sleeping well, looking bright light on eye's, too much sound on ears...then start seizure.. mostly 10 second to 30 seconds
???
so many things can be dangerous for her - i never thought about it - even taking a bath or driving - holding a baby …….
I hate that feeling like “restless legs” but all over the body, it’s just indescribable. (Well maybe I did lol)
I get the full blown seizures and they suck. I've never even heard of this kind of seizure. The brain is a trip
Me too I get the full blown ones too
Sorry for my ignorance but do seizures hurt?.. again sorry if this is a rude question
Generally no, people often aren't conscious of them happening.
Have had my 3rd already. The first two hurt for me that’s for sure and the recovery phase really does suck. Takes like 3 days to get your screws back n’ tightened
@@manaia759ive had them for 10 years now and id like to say yea the after math of most types of seizures do hurt. I have all kinds and ive had my face ripped open, teeth broken, nose broken, plenty of stitches, black eyes, horrible bruises. The list goes on. Seizures in the shower, on the stairs, on the road and no one even stopped i was on the road until my friends got back from tim hortons. Epilepsy is terrifying.
as a person with epilepsy i have these as well mine start off as a staring seizure then i get up and roam around and i got lost in a airport once because of it.
i also have jerking seizures in my sleep and i had one so bad once that my foot knocked a hole in the wall
Seizure disorder is a challenge
I have these seizures as well, I never remember, just extremely tired. Showed this to my best friend, and she said this is what I do as well.
Thank you so much for sharing, this was my whole reason for posting this video is to bring awareness
I'm a little concerned my seizures might be coming back. I don't know what its like to have one since the last time I had a bad one was when I was little. What was this seizure like for u?
Update 10 days later. They came back and they are pretty bad but I'm recovering :)
The dog already realised something is wrong
I was in sixth grade and there was a girl with a helmet on. She had a seizure in front of me. I cried for weeks and had nightmares. I always give seizure warnings now and despise the flashing lights of police cars. I later met a nice girl who got them too. She couldn't drive. I drove her to a lot of places and helped her. I miss her. Her name was my middle name, but she was very religious and didn't like me because I was an atheist. I miss you, lizzy. I'm not a devil worshipper, ok? I have no car again but I can still help. I hope you got on keto like I said to do. Love you. ❤
keto kills. that's devil-worshipper diet for real
and I have nothing against your religion Atheist
I’m wishing the best for you :( I’m sorry you have to go through this my daddy is 55 and he just started having seizures. He takes 3000mg keppra and another medication I forgot. He got them out of no where. His seizures are grand mals. Please take care of yourself.
Damn, I’m 20 and started getting them February last year. I take 500mg.
Im 25 and taking 1500mg (3 tablets) of levetiracetam twice daily, looking into surgery options.
Im 38 and I've had 7 or 8 now bout once a month. Weird to start happening out of the blue.
I've just started dealing with this in 2021, and my seizures range from (complex focal seizures) to (grand mal tonic clonic seizures) and (absence seizures)..... I'm hoping for the best for myself and that i can find the right meds to control them
3000mgs is a lot of medicine, i can’t function properly on just 1000,
he must be either sleeping so much of the day or suffering so much keppra rage :/
Awwww bless you hun 😘 My heart goes out to you xx
Seeing someone have a seizure is the worst feeling in the world. You’re helpless to help them. You just have to make sure they are safe and comfortable till it passes. I watched my grandfather an my husband and I still cry seeing them.
Wait a minute this happens to me too. I noticed things have changed a little since I don't fall to ground and shake up. My head tilted up and down like this too.
It was probably because I saw her head snap into place while she was looking down, and that probably made her kind of dizzy. Also, I heard a pop sound exactly when her head snapped into place. All of this is just my evidence
The brain is an amazing organ
nah bro where’s the seizure we got clickbaited
I'm also suffering from this 😭
I’m so sorry. It’s so hard on a daily ! Prayers 🙏🏼
@@aprilshealthmore8048 I get seizures on sleep only
I hope shes okay!
Hello! I am still struggling with the myoclonus. My medical team is doing all they can to help my nervous system, I have an auto immune disease called chronic inflammatory demyelination poly neuropathy it’s very comparable to Multiple sclerosis! I appreciate you and your comment.
@@aprilshealthmore8048 I really hope someone caught you so you don’t hurt your head :/ I could never record my dad when he has his seizure I get too scared and find it a bit rude
@@nothanks6931 my team of neurologists told my family to record me when I have them so they can see what they look like since they’re non epilepsy- it is scary since then they haven’t recorded anymore nor do I want to see myself again like that. Thank you for sharing about you dad. He’s got a real good child like you to be there for him.
@@aprilshealthmore8048 have you tried cbd or weed
@@stringbender3 yes 👍🏼
Actually I want to say truth
I came here just for a knowledge to know what this disease is but after watching your video I literally got goosebumps. I even couldn't sleep a night as I was very scared. Hope no one else faces this in the life and hope u get well soon❤️
I'm so sorry you have to go through this. Please get a service dog that will alert you to the upcoming seizure so you can sit down and wait it out. Good luck and may God bless you.
I wish I didn’t have seizures. Most of the time I get a warning. Once it happened while driving so I don’t drive anymore.
I have ones similar to this. My head jerks around and my arms and legs shakes and tremors.
What are your seizures called?
@@aprilshealthmore8048 We really don’t know. But they do start out as more of a focal seizure and then it gradually goes into more of a myoclonic seizure.
But whenever I’m asleep I do know that I have clonic seizures. Weird isn’t it how mine differ from when I’m asleep compared to when I’m awake
@@yourwitchbesti Do you have any underlying issues that are causing them ?
@@aprilshealthmore8048 I do have multiple heart heart issues such as a slow in(e)jection fraction ( how fast blood goes in and out of my heart ) I have a right bundle branch block ( when my heart might shut off for a split second and then beat back into place ) and then I have a exit sticky valve which basically means that sometimes not all the blood that’s supposed to be ejected comes out because the valve didn’t open all the way. And all of these aren’t specifically a major issue, they shouldn’t be underlooked either because all of these things can turn bad if something small even happens. So I go to the heart doctor once a year for a rhythm check, ekg, and echocardiogram.
And then of course I was diagnosed with epilepsy when I was 10 years old.
My dad had just experienced this last month, we were both at my school just going to an open house meeting to see my teachers. We started walking to one of my classrooms but we couldn’t find it. We went to the janitor to see if she could lead us there. That’s when the seizure began, he was about to ask and then he froze, couldn’t speak, couldn’t hear, and couldn’t move. It scared me to death and the janitor thought he was having a heart attack. Luckily he seems to be doing a lot better now that he is on meds.
My first cousin get them real bad. He hospitalized every single time.he is slow to come around.. i hope they can invent things that will actually help. Bless her heart..❤😊
That would be very scary that's one of my fears
I go through this everyday I even ended up driving to another state because you are literally space out completely and it's very confusing in your brain.
Yeah...I kinda hated when youll get spaced out and everything cause sometimes when I'd try to explain why I was being weird or something...no one would believe...like in 6th grade 5 years ago...I had a seizure and the teacher took me outside and asked me why I did that and I told her a seizure...she wouldn't believe me we almost argued...
@@Maryann2024 Yes nobody understands how your brain responds when you have a seizure.
Every time I have seizures it’s mostly from lack of food, energy or coolness I can’t stand the heat, if I haven’t ate it’s hot and I have no energy I feel very distant then my eyes just open up and I realize I had a seizure
Yes 🙌🏼
Thank goodness whoever was filming had the sense to stop and go to her aid. ❤
Waking up from a seizure is so scary and confusing. Especially if you’re alone.
Jesus Christ. I was waiting for a dog seizure. That is what a searched for.
If someone falls make sure they don’t hit their head hard against the floor. It’s good to learn what to do if someone is having a seizure
The ending was so creepy and scary to watch
"Im not acting at all and dont mind the cameraman"
The fidgeting at the beginning stages of a myoclonic seizure kinda seem like the brain running a few automatic settings before freezing up and needing a hard reboot
You should see about a seizure dog. It could alert to the chemical changes in her body before she seizes, so she could sit down and avoid accidents.
I also have petite mal seizures and I remember when I had an episode just like this. Only it included a kitchen knife.
Oh my !! Glad you’re ok !
@@aprilshealthmore8048 yeah I was fine. My mom was supervising me so nothing happened
Filming this lady at the stove that is having a seizure seems sick! Help her!
God bless you. I’ve had seizures for about eight maybe nine years now so I know what you’re going through.
I learned a lesson today. Those behaviors are also exhibited in people who use hard drugs and begin “tweaking”. Traditional I would see a shopped with those behaviors and assume they used drugs. I had no idea. I’m so ashamed.
My son had mild seizure-like movements of eyes rolling back in head. He was only about 1yr old. Did it caouple more times once with motherinlaw. Made appt with dr who referred him to specialist. They did I think a ekg? Then they were supposed to flip him over and do backside but he woke up on sedative and didnt want to give him more since he was so little. They didnt see anything on test. Not much theyvan do. Grade school-he had a fullblown seizure! Got up from chair, did a face forst body slam to floor!. Carpet softened blow. He laid there about 5 min and jerked all over, face sideways on cheek. I waited by his side till it stopped. I told him we were going to ER and he got very agitated which is common side effect, confusion, memory loss. He insisted on shower but I stood in doorway in case of falls. ER dr said granmal seizure but nothing they can do if they see no actual seizure. Daughter is RN and recomended pediatric neurologist. He tested him, thought he had Syncope=light headed when getting up from chair. He was his dr many years till he was 20 then he had to seek a dr for adults. That dr gave him meds. He has yet to set up with one. No meds for past few years. He is diagnosed with add-hadd
It’s definitely in his best interest to seek medical attention for the seizures. I really hope that the video encourages people to do more about the seizures. It is very frustrating. My heart goes out to you for your son.
The only seizures I’ve seen I have to catch them from falling.
This is the biological equivalent of a infinite feedback loop
I had a friend who had seizures. Was cooking, fell onto the stove and was badly burned. Spent the rest of his young life in the nursing home he had worked in.
I do that same crumb sweep on my stove..❤
I experienced my younger uncle having a seizure. While he was showing me his Ninja Turtles toys. I originally thought it was a joke (I was 7-8) and he was just laying on his chair eyes closed completely shut down for 2 minutes. I started to cry then went to my mum and nanny and showed them. After maybe 5 minutes an ambulance came and saved my uncle. It was a horrible day
Really scary & sad. My heart breaks for people like this.
I've seen this happen amongst my students. Scary
my son has cp and epilepsy he has what they call tonic clonic seizures and is loaded up on medication and had a vegal nerve stimulator put in 2019 it helps bit he still has seizures. i pray for every one that goes through this has a safe and healthy life ... God Bless
God bless your son
@@aprilshealthmore8048 thank you so much :)
God bless you sweetheart. You're just trying to be you and you're amazing!
Hopefully a cure will be found someday. God bless all of you with this ailment. ❤
@@wendijones5942 remember that you're an angel and God never gives us more than we can handle. All things happen in his time. We just need to trust in him. I'm praying for you.🙏✌️💖🦋
As a seizure patient as long as I stay on DAILY meds twice daily I have been great! If my meds are NOT in my system at my 4 month blood work my drivers license gets taken away for 6 months or until I’m 6 months free of seizures. Yes, this really sucks but after having a grand mal seizure I don’t mess with my seizures anymore
God bless her
I'm sorrt you are going through this. Thank you for sharing this, this helps me to understand my loved one better.
Yeah there are several types of seizures. I've never seen this one before. Bless her heart hope you get better!!
Sister Faith, you made my demons revel in anger. Where has this term "maladaptive day dreaming" been? Where have these words been to counter the strongest demon I have ever faced? All within this video. I'm just blown away. God will reward you greatly for this one. Thank you so much. Something that's been consuming my soul for so long is now identified, explained, and answered with divine wisdom. I'm in debt to you
Could a complex partial person get this type of seizures too? I think I got this several times even while driving my car. I had to stop for a while to let go
You would definitely discuss with your doctor
I am so glad the camera man didn't continue filming. I hope that they helped keep this lady safe.
I worked 28 of my last 30 years as a welder like this. For the same company. I would have these small seizures that would cause me to freeze and stare. Drool would come out of my mouth. I would see peoples mouth moving in slow motion but couldn't hear any words that were spoken or the sounds of any machines running. Like someone flipped a switch to stop all sounds but everything continued to work. I would eventually stop and stare at a person or an object. If there was liquid in my bladder I would start urinating on myself with no control to stop it or move. I had only 3 full blown seizures in my 30 years working for the company..All of which I never knew happened until I was being loaded in the back of an ambulance with huge knots on my head from whatever my head hit something. I learned to keep extra clothes at work in case I urinated on myself because I had no way to get home..if you're an epileptic they take your driver's license away. I was fortunate to have a friend who I gave money to to pick me up everyday and was extremely dependable. If he was going to be off on vacation I had to make other arrangements to get to work. Sometimes I had to hide in the building and get locked inside the building and sleep at the company without anyone knowing it because most of the people didn't care if I needed a ride. Some actually liked seeing me struggle. Epilepsy also affected my memory. Before I left my job everyday I had to write down what I was doing so I would know where to begin the next day. Losing track of tools and things was another big issue I battled with. I would set things down no remembering where I left them. That is another area my "Job log" came in handy. I could look in the book where the last job was that I used that tool. New people's names would take me a while to learn. Our company had an employee high turn over rate which made it quite different for me. The good thing was once I was set up to do a job I did the same job for a few days. Another big plus for me was I am very gifted at repairing all kinds of manufacturing machines. No one else there was. If a machine had problems I could quickly diagnose it, order the parts and fix the machines. My boss kept me because he knew I would have problems keeping a job elsewhere. Not too many businesses want epileptics as an employee. 30 Years went by, my boss passed away and I was tired of fighting the epilepsy monster in my brain. I knew it was time to go file for my disability because now my body was also worn out..My Dr. said I was truly an inspiration to him because he never believed I would last as long as I did working.
You are an inspiring and courageous man. Thank you for posting!
I must say first of all, I appreciate you sharing your story, and I want to say you’re a very courageous and strong person and this is probably one of the best comments I’ve actually received out of the thousands of comments that I have received and what I hope helps you is that you’re not alone and I too worked over 23 years And I just really appreciate you sharing your story. I really hope that it makes a difference knowing that you’re not alone. I really hope that you are stable and that you’re doing good?
Wow watching someone have a seizure is scary it made my heart drop. Im sorry for what you're going through
Get better soon, god bless you❤
I knew someone who had seizures till she hit middle school, so I know this sucks for you. Hope you get better❤
My sister has grand maul seizures it takes so much out of her takes her days to recover from it. If she misses one dose of her meds throughout the day she will have one. It is very scary
That has to be a scary terrible thing to go through. I hope there is something that can help you.
One of my sons had seizures since or before birth. Blood all over his baby bed. I know he had at least one seizure standing up. Hes been in pain for a long time, 50 years.
I googled porygon and saw the seizure episode. Crazy she’s wearing the same colors
Once a year I'll end up with seizures in the middle of the night but 20 years ago it happened in the day and was immediately taken to the hospital that time i was only 5 years old it's so scary that sometimes i think i might die 😅
I can Relate here i was Diagnosed with Epilepsy when I was 4years old I'm 60 now and live alone it terrifies me when I go into the Kitchen with hotplates and Boiling water so i stopped Boiling water amongst other things that many people take for granted God bless
My Dog suffers from them once in awhile. It is different in Dogs, but the reaction is the same. It is hard, but I hope everything goes well for you
❤wow never knew pre symptoms. Read comments.
Thank you for sharing.
May God bless and heal her. She must have a loving family. ❤
I'm having these since childhood and i was normalising it until i see ur video. Btw tc
I suffer from myoclonus generalized epilepsy. It's awful. I wish there was a remedy.
Thank you for sharing
See a Craniosacral therapist. A top class one. Read Thomas Attlees book - Craniosacral therapy integration. Will change your life 🙏
I had something like that today but I don’t know what it was, I was shaking uncontrollably but I could still see and hear everything around me, but I couldn’t talk and every once and a while it would stop for a bit but started again and I passed out for a bit, I was at school and it was the end on my first class and my teacher walked me to the nurse and honestly I don’t remember walking there like at all but when I was sitting in the back I felt like I was going to pass out again and I tried to tell the nurse but I couldn’t talk at all, and I passed out but the nurse thought I was faking it so I got sent back to class and had to go the whole day barely being able to walk
I have those too, usually after ptsd episodes, those are probably large scale (non verbal) panic attacks. You can have conscious seizures but they’re usually smaller scale or absent seizures. during my panic attacks my head felt and sounded like static and my hands locked in place for over an hour after.
@@sherry.blossom9866 I'm sorry to hear that. If I may ask, do you have those panic attacks as a result of the war?
I pray that you get better, I’m going through seizures as well
my first ever and last seizure ever was in elementary school when i was in grade 1 i got it unexpectedly my teacher knew something was wrong so she called my mom early, at that point it started to kick in.. i cried while my mom carried me still having the seizure
They can come out of nowhere at anytime...most times with no warning very unsafe to be left alone cooking or bathing...in Jesus name miracles happen all the time ❤️🙏❤️ o
I definitely don’t shower Nor cook anymore alone
I’ve had seizures. With all the tests they can’t induce them or figure out why they happen. I’ll be at work and I’m going at 100mph then all the sudden I wake up to emt around me and I’m on a floor. They ask if I knew where I was, I saw a box with my company name on it and said the name. I really didn’t know where I was or why. I was asking my mom to call my sons mother so she could get him from daycare while I was in hospital. I was so confused that I didn’t remember that my sons mother had passed away 4 months before. Took a good couple days to get the fog out. I also have fainting spells without seizures, have had episodes where I wake up in my sleep with no ability to breathe. Like my throat is closed. To the point they had me wear a heart monitor as I slept because they didn’t know if I was having heart issues or strokes or something while I slept. They think it’s stress. Lack of good sleep etc. that my body gets overloaded and overwhelmed and it shuts down. Idk. It’s scary though and am not on medication because I’m not diagnosed epileptic. They also don’t want to give me anything for my anxiety because the withdrawals from those meds when I stop can cause seizures. So I just live with it. I’ve lost my license for periods now f time after seizures until medically cleared but have no diagnosis to collect when I can’t work.
Look into neurogenic orthostatic hypotension I’m not a doctor, but my daughter has heart issues and it took many years for them to find it and it’s very hard because it’s with the brain activity and you are correct stress can do this, but I wouldn’t give up don’t give up on you. Another reason why I posted this video because it took them years to figure out what was going on with me. I appreciate you sharing your story.
Sorry but if that'd been my son youd of heard a weird sound in his voice, and he'd of fell and busted his head on the floor, he's had them 28 yrs, both shoulders need surgery, which I'm scared to death when he gets it done, broken collarbone, and busted head several times. My son convulses very badly, and they started in infancy as febrile then absence seizures, then grand mal at 12. So she's lucky if that's as bad as it.gets I pray it gets no worse.