We think my nephew might have epilepsy


Recommended Posts

So firstly, i think this post is more aimed at anyone who has or knows people that have epilepsy.

Well we THINK my 5 year old nephew may be having epileptic fits, but are not 100% sure. He will be sitting and\or running around like a normal child, then will suddenly stop. His eyes kind of glaze over, he goes red in the face and you can see that he cant move or control his limbs.

He then bursts in to tears and you can see he is absolutely scared ****less.

Afterwards though, he remembers what he was feeling. He says that it felt like ants running around his head and that his heart was going to pop out of his chest. He said that he sees strange things like the cusions on the seats being bigger than giants etc and lots of flashing lights like lightning.

My sister has taken him to the doctors and has shown the doctor a video of what is happening to him. The doctor said it looks like a fit of sorts, even though he is not on the ground throwing his body around like you would expect an epileptic to do, so has reffered him to a peadiatrician.

My mum works in a doctors and they said that it may be a fit, but not 100% epilepsy, as he likely wouldnt remember having the fit or the feelings of the fit after the event. So this leads us to believe he might have some kind of tumour or something :'(.

Of course this is ALL speculation, but i wonder if it sounds familiar to people or if someone might have ideas as to what it is... We currently have up to 3 weeks just for the appointment with the specialists to come through :(

i am epileptic my self, but my fits where not like that. Mine is under control with medication now. All i remember of mine is feeling sick and my vision going slow. Then the next thing i can remember is waking up in the back of an ambulance with my tongue being bitten all up.

Its not a nice thing to have happen at any age, but to a five year old is not fair at all. The National Society for Epilepsy http://www.epilepsysociety.org.uk/ they have info on there. And they have a forum as well. This might be a good place for your nephew's parents to look, they have a "for parents" section that might be able to help them. I hope they sort him out soon.

......

My sister has taken him to the doctors and has shown the doctor a video of what is happening to him. The doctor said it looks like a fit of sorts, even though he is not on the ground throwing his body around like you would expect an epileptic to do, so has reffered him to a peadiatrician.

....

"Grande mal" seizures where you shake about on the floor are not the only type of fit you can have and I think they are in fact quite rare. There is a of variety of types of fits, as crazy as it sounds.

Some people just glaze over and go "out of it" for a few seconds, then they are fine, for example, with no drama at all. I was once shown a video of someone having another type of fit where the man was standing and moving around in a strange manner, though he was not actually in control of his body and dropped the hot drink he was holding :/ The frequency of fits can vary as well, from very occasionally to every few seconds or minutes.

While this does sound a bit like a fit from what I know of them (as someone who of course is not a trained medical professional), obviously it could be caused by any number of things which will be why he's had this referral. I hope they can diagnose it quickly as that will hopefully enable treatment and reduce anxiety.

I believe medication can control it for many people but I've never really looked into the treatments for it. I think websites like the link posted will be your best bet for reliable information.

In the meantime, it might also be prudent for you all to research the best ways of coping with these fits so as to minimise harm and anxiety for your nephew..

Go see a neurologist or get a referral to see one. Its the best option. If a GP helps with diagnoses without a referal then you are just not getting the best possible treatment.

I was diagnosed with it. As to wether I actually have it or not is being debated right now with a neurologist. So if I have it, its been 10 years. I'm also on the lowest does of meds my neurologist has pretty much ever prescribed. So that said, I'm very lucky.

I do remember somewhat what happened before I had a grand mal some of which is characteristic of all people who've had such a seizure. I've had episodes. There's the obvious flinching of the arms - which you can't control. I used to think mind over matter, but its not so unfortunately.

Some of the symptoms you've described I know I've have had (and still sometimes do, for me its really the meds). I know I get the glazed eyes/look there's been the odd time where I've had it. I've actually had it to the point where I see some stars momentarily and I feel like I'm floating a bit and disoriented. But the rest, stopping and turning red doesn't sound like something I've experienced or familiar hearing w/epilepsy.

That said, tell his/her parents to see a neurologist. I got bounced around by GPs even though I asked before having the seizure that I see a neurologist. I was getting all kinds of these episodes sans seizure. Even if it isn't a brain disorder, the good thing is many also specialize or are quite familiar with muscular and neck/back problems too. This should help. Please tell them not to Google the diagnoses or look up in medical books.

Grand Mals hurt like a ******. I've never experienced as much pain in my life until the 3 or 6 months after it happened - i was still hurting for that long after. I'm glad I wasn't killed. Luckily too, *some* kids do outgrow it. I only got mine in early adulthood.

I wish the kid the best! Its a shame sometimes too....when you visit the Sick Kids hospital and see what hell those poor kids under 10 are going through. We should all feel fortunate for what we have.

Sounds like some sort of fit he might be having. Maybe an onset of the normal fit.

Have he been eating well enough? Drinking plenty water?

Absolutely eating and drinking fine.

i am epileptic my self, but my fits where not like that. Mine is under control with medication now. All i remember of mine is feeling sick and my vision going slow. Then the next thing i can remember is waking up in the back of an ambulance with my tongue being bitten all up.

Its not a nice thing to have happen at any age, but to a five year old is not fair at all. The National Society for Epilepsy http://www.epilepsysociety.org.uk/ they have info on there. And they have a forum as well. This might be a good place for your nephew's parents to look, they have a "for parents" section that might be able to help them. I hope they sort him out soon.

I have a video of the "fit". He certainly isnt himself and as Laura says below, he just seems to be acting strange and has no control of his body etc. :(

"Grande mal" seizures where you shake about on the floor are not the only type of fit you can have and I think they are in fact quite rare. There is a of variety of types of fits, as crazy as it sounds.

Some people just glaze over and go "out of it" for a few seconds, then they are fine, for example, with no drama at all. I was once shown a video of someone having another type of fit where the man was standing and moving around in a strange manner, though he was not actually in control of his body and dropped the hot drink he was holding :/ The frequency of fits can vary as well, from very occasionally to every few seconds or minutes.

While this does sound a bit like a fit from what I know of them (as someone who of course is not a trained medical professional), obviously it could be caused by any number of things which will be why he's had this referral. I hope they can diagnose it quickly as that will hopefully enable treatment and reduce anxiety.

I believe medication can control it for many people but I've never really looked into the treatments for it. I think websites like the link posted will be your best bet for reliable information.

In the meantime, it might also be prudent for you all to research the best ways of coping with these fits so as to minimise harm and anxiety for your nephew..

Thanks. I am sure its some type of fit, but to be honest im not sure what to research. We still dont have confirmation that he is fitting and we dont know if it would be epilepsy or some type of tumour etc...

What i was hoping is that someone might be able to say 100% sure, "thats what i have and it is connected to this". I guess thats kind of clutching at straws on my part :(

Laura is right. There are lots of types of seizures from the larger ones (Grand Mal) to smaller exhibiting ones (Petit Mal). Sounds like the Petit Mal is more like what he has. Also seizures have a post recovery phase canned "post ictal" where the patient just goes to sleep before awaking. Your neurologist needs to assess this in greater detail.

http://www.nlm.nih.gov/medlineplus/ency/article/000696.htm

Good luck Rich and my thoughts are with your nephew!

Laura is right. There are lots of types of seizures from the larger ones (Grand Mal) to smaller exhibiting ones (Petit Mal). Sounds like the Petit Mal is more like what he has. Also seizures have a post recovery phase canned "post ictal" where the patient just goes to sleep before awaking. Your neurologist needs to assess this in greater detail.

http://www.nlm.nih.gov/medlineplus/ency/article/000696.htm

Good luck Rich and my thoughts are with your nephew!

Thanks Barney. Yeah the "fits" last approximatly 5 - 10 minutes and afterward he spends about 5 - 10 minutes laid out exhausted. Then he suddenly gets up and runs around like a nutter as usual as though nothing has happened.

My sister wonders if it is related to tiredness as she is keeping a diary of the events and has noted that its usually between 5pm or 7pm in the evening and a couple of times at 7am. There have been a few times at mid afternoon and usually when he has been running around exhausting himself out.

Its so frustrating that we need to wait up to 3 weeks for the referral to go through and then only for him to be pre assessed before they start to really start to look in to it in more detail. I would say its worse because he is such a young child and is so scared. I mean i would be scared to have it happen to me, but for a child of his age to go through this must be devistating!

I have epilepsy since a year ago. It is a bitch and does alot of psycological damage (in my case)

Im the type that just knocks out and gets up without having any clue of what just happened (I wake up in the hospital or in my bed with a cut bleeding). Before each attack, I remember having strong conflicts with emotions (love or friends) or when Im thinking hard (my first attack happened a bit after playing Portal. I played Portal: Prelude yesterday, got a headache, got very scared, went to bed, and slept)

It is very very frustrating when you dont know what happens when you wake up. Im on my fifth. And, as a matter of fact, Im having a headache today now during class and Im pretty worried one might happen now. But oh well.....

Also on a sidenote, today at might Im going to play Portal: Prelude again and Im going to try again and see if I get use to it and can "fight" it somehow....It is not a good idea but oh well....It is very depressing and after passing your written exam but having being classed with epilepsy and not being able to take the drivers exam 100% since it is not legal to drive here (and besides while in a dri

I believe your nephew might not have it right now but will develop it further on in his young life

So firstly, i think this post is more aimed at anyone who has or knows people that have epilepsy.

Well we THINK my 5 year old nephew may be having epileptic fits, but are not 100% sure. He will be sitting and\or running around like a normal child, then will suddenly stop. His eyes kind of glaze over, he goes red in the face and you can see that he cant move or control his limbs.

He then bursts in to tears and you can see he is absolutely scared ****less.

Afterwards though, he remembers what he was feeling. He says that it felt like ants running around his head and that his heart was going to pop out of his chest. He said that he sees strange things like the cusions on the seats being bigger than giants etc and lots of flashing lights like lightning.

My sister has taken him to the doctors and has shown the doctor a video of what is happening to him. The doctor said it looks like a fit of sorts, even though he is not on the ground throwing his body around like you would expect an epileptic to do, so has reffered him to a peadiatrician.

My mum works in a doctors and they said that it may be a fit, but not 100% epilepsy, as he likely wouldnt remember having the fit or the feelings of the fit after the event. So this leads us to believe he might have some kind of tumour or something :'(.

Of course this is ALL speculation, but i wonder if it sounds familiar to people or if someone might have ideas as to what it is... We currently have up to 3 weeks just for the appointment with the specialists to come through :(

Sounds like what my soon to be g/f has. She doesn't cry after that, she just "spaces out" .

I have epilepsy since a year ago. It is a bitch and does alot of psycological damage (in my case)

Im the type that just knocks out and gets up without having any clue of what just happened (I wake up in the hospital or in my bed with a cut bleeding). Before each attack, I remember having strong conflicts with emotions (love or friends) or when Im thinking hard (my first attack happened a bit after playing Portal. I played Portal: Prelude yesterday, got a headache, got very scared, went to bed, and slept)

It is very very frustrating when you dont know what happens when you wake up. Im on my fifth. And, as a matter of fact, Im having a headache today now during class and Im pretty worried one might happen now. But oh well.....

Also on a sidenote, today at might Im going to play Portal: Prelude again and Im going to try again and see if I get use to it and can "fight" it somehow....It is not a good idea but oh well....It is very depressing and after passing your written exam but having being classed with epilepsy and not being able to take the drivers exam 100% since it is not legal to drive here (and besides while in a dri

I believe your nephew might not have it right now but will develop it further on in his young life

Hold on. You have been told you have epilepsy and you sound like its pretty out of control... Are you not on medication to control it? Im pretty sure also doing things to trigger a fit cannot be healthy on the brain at all :s

Sounds like what my soon to be g/f has. She doesn't cry after that, she just "spaces out" .

My newphew cries during and after. During the attack he cries in a strange way. As though he is crying but fighting or something, its hard to explain, but is not a usual cry. Its kind of like a squeek.

Afterward he does cry normally and relaxes... But he is 5, so you cant blame him for crying...

This topic is now closed to further replies.
  • Recently Browsing   0 members

    • No registered users viewing this page.
  • Posts

    • Thanks for the info, but I'm still not sure if I need this....
    • We check out the SKG PS700 Neck Massager by Steven Parker I was offered the chance to test out the SKG PS700 Neck Massager, and full disclosure, they let me keep it regardless of my findings. Anyway, I jumped at the chance due to my long hours sitting at my desk; I figured it could offer some neck pain relief. What's in the box: SKG PS700-2 Neck Massager Rechargeable Battery (inside massager) Type-C USB cable User Manual Quick Start guide 1-Year Warranty In short, everything you need to get started. According to the official listing, here are the key features: Biomimetic Kneading & High Torque Motor: Designed with innovative biomimetic kneading heads that perfectly simulate the touch of human hands. Powered by a high-torque motor, this massager delivers powerful and precise deep tissue relief to effectively target stiff neck muscles and release built-up tension Soothing Heat & Integrated Sound Relaxation: Experience the ultimate Relaxationation with our dual-action approach. The soothing heat function gently warms your neck, while the built-in sound Relaxation provides calming audio tracks, helping you achieve a state of mindfulness and mental tranquility during your physical massage Cordless Convenience & Travel-Ready & Father's Day Gifts: Crafted for maximum portability and ease of use. Its lightweight, cordless design allows you to enjoy a premium massage anywhere without the hassle of tangled wires-whether you're taking a quick break at your desk or winding down at home Versatile Relief for Home & Office: An essential wellness companion for office workers, gamers, frequent travelers, or anyone looking to integrate mindfulness into their daily routine. It seamlessly fits into your lifestyle, providing instant neck relief whenever and wherever you need it Safe & Premium Materials: Manufactured with high-quality, skin-friendly materials to ensure a safe and comfortable experience without irritation. SKG backs this device with dedicated customer service, making it a thoughtful tech-health gift for family and friends App & Bluetooth Music Control: Connect via Bluetooth to control your massage settings through the dedicated app and enjoy your favorite music during your massage session for a fully customizable and immersive relaxation experience Red Light Warmth Technology: Features advanced red light warmth technology that penetrates deep into neck muscles to enhance blood circulation and provide soothing comfort while relieving muscle tension and stiffness Design With all that out of the way, here are my own findings. SKG does not say what materials are used to make the neck massager. However, on the product website, it mentions "soft-touch silicone" with what looks like PU leather cushioning, with the rest being mostly made up of plastics. On the inside of the massager, there are two "biomimetic kneading heads" that are motorized for the different styles of massage, which are not actually listed at all in the paper user manual, but the standard included modes are: De-stress mode, Mediation mode, Relax mode, Shiatsu mode. The massager looks quite premium and is actually very comfortable to wear. This massager is small and light enough to go anywhere, as it doesn't get in the way of anything, so I was able to use it in the chair while writing this review. Unlike the back massager, SKG does not warn in the user guide not to use it for more than 30 minutes a day (or two 15-minute sessions). However, there is a long laundry list of important safeguards to consider before and during the use of the device, and it is warned that the neck massager is not waterproof. It also includes a 1,400mAh battery with a rated power of 14W and input of 5V, which is the standard for up to USB 3.0 power (although the Amperage is not mentioned at all). SKG does not say how long it takes to charge, but a quick calculation at 2A (if that is what it is) would mean it would take roughly 1.5 hrs to charge from empty. In any case, the light around the button changes from orange to green on a full charge. In addition, it is not possible to use the device while it is charging. On the right of the neck massager is the On/Off and modes button, which also acts as a joystick. You can operate all the modes directly from the power button, as well as the app, which I'll get into a bit later: Push up: Short press to adjust Heat levels On/Off button: long press Mode Switching: Short press (while in operation) ➕ Push left: increase Music volume ➖ push right: decrease Music volume Push down: Short-press to turn Music on or off The massager defaults to De-stress mode, and it is not stated anywhere if the neck massager has overheat protection. This time around, regarding heat, the only detail I could find is that it has "triple action soothing heat." The temperature stages are not listed anywhere in the paper manual, Amazon listing, or official website. The heat levels can be adjusted through the app or directly on the device using the joystick button. Usage There's also the SKG Health app, which makes using the massager far easier than feeling around for the button on the side of your neck. If the app is stopped, you are required to log in with a verification code over email, which I am not too pleased with, as this means it will only work that way for however long SKG decides to support it through said app. However, I was not able to get the app to connect to the OS500, which I have reported back to my contact. Bluetooth appeared to be working on the neck massager as it became available to pair with my phone, but the SKG app failed to discover it. Before I forget, there's also a switch next to the USB charging port to deactivate and activate the Voice Prompt, which, when enabled, audibly tells the user when switching intensities, modes, or connecting to the app and informs when the massages start and are completed. That said, on to my likes and dislikes, which are listed below. What I didn't like Unable to connect the Neck Massager to the app Use through the mobile app relies on continued support from SKG What I liked Can be used without the app Cordless use Light and comfortable to wear Heat is also quite comfortable Where to buy: According to the official website, this has an MSRP of $249.99, but is currently $50 (on Amazon). To sweeten the deal a bit more, there's also an in-page coupon that knocks a further $20 off the price. SKG PS700-2 Neck Massager for $179.99 on Amazon (was $199.99) Apply the in-page $20 off coupon for the final price of $179.99 Just like the back massager, this gets a confused thumbs up (due to the cost). However, I cannot rate it through app usage as it failed to connect. As an Amazon Associate, we earn from qualifying purchases.
    • This Samsung T7 external SSD deal lasts less than a day by Sayan Sen Recently we had covered some nice deals of internal NVMe SSDs which include the 4TB TeamGroup G50 for only $400, the WD_BLACK SN7100 2TB for just $243, as well as the Samsung 990 PRO 1TB for $370. If however you require an external SSD for portability and quick data transfers and have a budget of less than $200 the Samsung T7 1TB model is currently on a limited time deal at just $190, it's lowest price in nearly three months. The deal ends today so you better hurry if you need one (purchase link below). The T7 weighs in at just 72 grams meaning it should be fairly easy to carry around helping in the portability department. Via its USB 3.2 Gen 2 interface the T7 promises sequential read speeds of up to 1050 MB/s and writes of 1000 MB/s. It is also fairly robust with a drop protection of up to 2 meters, though bear in mind that this is not waterproof. For that you will have to choose the rugged T7 Shield. The technical specifications of the Samsung T7 1TB are given in the table below: Specification Value Model Code (1TB) MU-PC1T0T / MU-PC1T0H Interface USB 3.2 Gen 2 (10 Gbps) Dimensions (W × H × D) 85 × 57 × 8 mm Weight 72 g Sequential Read Speed Up to 1,050 MB/s Sequential Write Speed Up to 1,000 MB/s Drop Resistance Up to 2 m (6.6 ft) Encryption AES 256-bit hardware encryption Operating Temperature 0°C to 60°C Non-Operating Temperature -40°C to 85°C Humidity 5% to 95% (non-condensing) Shock Resistance 1,500 G, duration 0.5 ms, 3-axis (non-operating) Vibration Resistance 20–2,000 Hz, 20 G (non-operating) Get it at the link below: Samsung T7 Portable SSD, 1TB External Solid State Drive, MU-PC1T0T/AM, Gray: $189.98 (Sold and Shipped by Amazon US) Good to know This Amazon deal is U.S. specific, and not available in other regions unless specified. We only use first-party seller links (at the time of article publishing); ensure that you purchase from a first-party seller link only. Check out Today's Deals on Amazon | or our recent tech deals. Become a Prime member (for Students or SNAP) via Neowin Get Prime Access - Prime for half price (for qualifying Medicaid, EBT, SNAP) Subscribe to Prime Video, Audible Plus, Music Unlimited or Kindle Unlimited via Neowin As an Amazon Associate, we earn from qualifying purchases.
    • I just wish they would put more love into Virtual Desktops. There is just so much more they could do.
    • Sounds like you just skimmed over the review, I answer all those questions in it. Although I admit I did not test if DTS works over the headphones, when I get some time I will test this. My personal use case is more speaker-driven (I cover this in the review too).
  • Recent Achievements

    • Dedicated
      Almohandis earned a badge
      Dedicated
    • Dedicated
      JuvenileDelinquent earned a badge
      Dedicated
    • First Post
      DrWankel earned a badge
      First Post
    • Reacting Well
      DrWankel earned a badge
      Reacting Well
    • Week One Done
      Supreme Spray LV earned a badge
      Week One Done
  • Popular Contributors

    1. 1
      +primortal
      505
    2. 2
      +Edouard
      184
    3. 3
      PsYcHoKiLLa
      84
    4. 4
      Michael Scrip
      78
    5. 5
      Steven P.
      76
  • Tell a friend

    Love Neowin? Tell a friend!