Added: 3 years ago
From: SmnthJeynes
Views: 49,148
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  • ummm... i really dont know what to say about this

  • poor baby god bless him and all others as well he doesnt have to have this problem or no one

  • I started crying cuz he's soo little that's rlly sad if u have it at that age

  • wow i have epiipsy too

  • YU HANDLED THIS REALLY WELL BUT NOT HOW MY MOM HANDLES MINE''!-...

  • Poor kid, hope they go away

  • poor kid i suffer epilepsy but my fits occur at night time more than day and sometimes early hours of the morning

  • god has them under there wings and they can soar

  • why did u put this video not hating just wondering...

  • It's videos like these that make me tear up at myself -- I don't think I could be as collected and patient a mother as you, even if I REALLY want to be. I would be so afraid. God bless you and your son -- how is he doing?

  • How brave mother you are!!! me and wife when my baby had this, we lost our mind and and i coldnt control my feeling i took him and and running out I didnt know what happen to me even i know very will this called Refractory epilepsy, but its really hard to see him doing like that

  • My daughter has febrile seizures, it is horrifying! She stops breathing and the works with hers though... yet they are still only febriles... I have had to administer CPR to her 2 times due to seizures and OMG it is terrible... hers are not usually short periods of time either... the first one she was out and could not speak for over 8 hours, the second was only a couple of hours but we now have rectal valum to give to her during the seizure.... God Bless you all for this vital information.

  • oooo i have tht to im 24 year old n i have tht bout u knw ur child have to take medication to control dnt worry ur child be goood

  • That's an adorable little kid...

  • y the hell were filming this in stead of helping him.

  • hugz n prayerz. hang in there lewis . i have seizures too ( complex partial seizures )

  • i dont see how yall can handle this. i know there really isnt much you can do about it other than meds that might help. but i have a 4 year old lil boy and if i had to watch him have a seizure i would break down and freak out. i give u and not just u but all the parents that have to watch their children put up with this major koodos for handling it as well as you do. i dont think i could handle it as well as you guys. im sorry for you that you have to go through this

  • Thats really sad :(

  • My son has epilepsy and doctors often ask us to film his seizures. Also posting them helps other parents like me to not feel so alone. when My son Oz was having seizures before his diagnosis of epilepsy these videos helped us to understand what to do and what to expect. There is nothing shameful or disrespectful about them. That you for posting this video. And God bless that sweet baby Lewis. He has helped our family.

  • please take that baby to the hospital

  • well even if shes filming it for documentary purposes , out of respect for her son ..she shouldnt be showing them to the public eye ..especially youtube. which will on bring hate comments and immature kids making fun of him..dont you think ,would you want videos of you having a seziure posted online

  • why is this uploaded on youtube?

  • To help others. if another parent is looking to learn about their Child ect.

  • why do ppl make these vides that is just mean

  • the typical generalize tonic clonic seizure.... i think you can give Carbamazepine on that kind of attack. if there are some side effects of the drugs, inform your pediatricain immediately. also avoid using erythromycin when having a carbamazepine medication cause the two drugs compete for metabolism by the liver.

  • you know why people share these video's? it's so that people can actually catch a glimpse of what it's like

  • My daughter has recently been diagnosed with a metabollic disease. Unfortunately she has absences and since a few days larger absences/epileptic seizures. Thank you for sharing your experiences so that I can get a better picture of my daughter and the things we probably will encounter in the future. God bless...

  • I don't understand why you have posted this on youtube.

    If my child was suffering like that then the last thing I would be doing is VIDEOING them.

    i would not want others to see them in that condition and i don't think that they would thank me for videoing their pain for anyone and everyone to look at on the net.

    Just don't get it.

    I am very sorry that this child is ill and i hope he gets the treatment he needs.

    Videoing him? Weird.

  • i see what your saying but it helps. in a weird crazy way it helps. my girl friend has Absence seizures. shes been having it for 19 years not and she just started to have this kind this year. now i did all my resurrect on it but reading it is not like seeing it. now you might say that he is in pain but he is not. at this oint he is not felling anything. its after. this person is posting a vid so people can see how one is.

    plz dont take it as suffering its more of a rebooting of the brain

  • That's horrible that you would actually exploit your helpless little boy to the internet having a seizure!

  • im 14 and i had a seizure on the bus the other day and one other time during a math test

  • Because you want to help others understand what one looks like! and if you need to show others e.g your doctor.

  • my daughter is 20 months old and has dravets syndrome.. she even had a fit similar to this but worse which lasted 4/5 hours and had to be admitted to picu.. bad times my hehart goes out to you

  • Thank you Mandy for your message. I cant imagine how terrifying the 4-5 hour seizure must have been. Lew has started on a cycle of seizures every 3-4 weeks and we have no idea why, his medication may need upping, we'll see.  I do hope your daughter's journey with dravets is as easy on you all as possible. Much love x

  • it was absolute torturous hell! believe me i wouldnt wish it on my worst enemy... she has all different sorts of fits and it is very difficult she has just had 9 siezures from monday to sunday just gone.. hope hes well for as long as poss xxx

  • my bro is 8 and has it but takes meds. scared us when he had his second because it was on christmas and every1 was freaking out!

  • poor babyy....god bless him and all the other children with the same problems.!!!

    u cant do anything when some body is having a seizure?????

  • So realy all you can do is make sure tey dontswollow their toune or hit their heads on anything hard

  • I got diagnosed was I was 8 and my seizures not controlled by medication until I was 21. The tongue swallowing claim is in fact a myth. Nobody can swallow their tongue. The only thing you can do is, like you said, move any objects away and pay close attention. Any seizure lasting less than 5 minutes is fine and they'll bounce back. More than 5 minutes and you need to call an ambulance. Mine lasted around 3 minutes, so I'd wake up and be fine about 3 hours later as if nothing happened.

  • @xXGaTaGaNgStErXx no.. unfortunately all you can do is watch and time. if under 4 minutes, ok. if over 4min 30 sec you should call an ambulance, especially with the ones that Lewis is having....

  • My little sister (10Years old) suffers from siezers as well. Ive never seen one (Im 23). I dont think Id be able to handle it. So Im thankful Ive never had to witness one. She used to have one every 4 or so months. But these past couple days shes had one right after the other. It really scares me. I was just trying to learn more about it. Im sorry for you little boys condition.

  • My daughter suffers from absent seizures, they are mild compared to this poor baby. I will keep him in my prayers. Never realized how much of an impact this has on all the family we feel horrible she has to have them . Started at age 2 she is now five. They are so scary god bless you.

  • God bless his heart! I just experienced one of these today and it scared the crap outta me!

  • god im 12 and this is really scary to me, to see a little kid or anyone having a seizure scares the crap out of me now and i hope the best with to everyone that does

  • My 3yr old daughter is suffering with seizures as well, since the age of 1. I know what you are going throught and hope it all works out in the end, stay strong and keep fighting!

  • This poor child he is suffering so bad, Out of all the people to make sick like this criminals and child molestors they choose this sall child

  • aww i feel sorry for this child.

    my lil brothers have seizures and it not a fun thing to see. but their body doesnt shake, only their eyes keep rolling to the back of their head and all they do is cry while goin through it

  • their eyes keep rolling to the BACK of the head? whoa. now i'm REALLY scared i'll be sure to keep 'em in my prayers. and the kid in the vid.

  • Holy crap that poor baby... :( I live with seizures too. I'm on 2000mgs of Depakote and 100mgs of Topamax a day. It certainly helps, even if it does seem to make me dumb when I try to talk to people. Do the doctors have your little one on anything? You can always friend me and PM me in the future about this.

  • Poor baby, and he smiled after it was all done. Thats a strong baby!

  • what did she watch

  • I remember how horrifying and painful it was for me the first time I watched my baby sister have a seizure. Mixed feelings about one being video'd and posted for the world to watch.

    God bless little Lewis and your family.

  • god bless u and ya child

  • i used to have seizures but i am on medication for it and i havent had one since 2001 and my ma took me to the hospital and they kept saying that it was breath holding spells!

  • i feel so sad for you to have to watch your baby go through this. Keep Strong Hun x x x

  • I have a 9month old daughter and I know as a grown man that loves his child I would hurt inside having to watch this happen to your baby

  • FOR INFORMATION - Lewis seizure protocol is rescue medication after a 5 minute seizure and hospital admission for any seizures following within 12 hours. He has no protocol for cluster seizures as he usually only has seizures once or twice a month.

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