PSA ABOUT SEIZURES. AKA HOW TO HELP A SEIZURE PATIENT WITHOUT BEING AN ASSHOLE.
I just had a seizure in french class, so this is the part where I go over seizure first aid just in case somebody you know goes through what I do.
1. As soon as they start seizing get somebody to start a timer. If you don’t know the person call an ambulance. If you do know them, and know they have a seizure disorder call an ambulance anyways; unless they’ve previously told you otherwise. Don’t call the police. Police don’t know how to handle seizure patients. If you call the police that makes you an asshole. When the medics arrive tell them how long the patient has been seizing for, or how long they where seizing for if the seizure has stopped.
3. if they are seizing violently do not hold them down, seriously you can give them serious bruises or even break their bones
2. If they’re not seizing violently, turn them on their side, and try to get them in the position closest to shock position that you can. They’ll thank you for this if they throw up and don’t choke on their own vomit.
6. If possible put a pillow or soft object underneath the persons head. This will stop them from braining themselves on the floor, which is usually something we appreciate greatly. generally cracking our heads open is even less fun than seizing.
Do not, and i mean it do not put anything in their mouth. They’re not going to swallow their tongue, that’s not an actual thing. They may bite it, but that’s preferable to choking on whatever shit you put in their mouth. Just don’t do it.
4. If they wet themselves don’t tease them about it. don’t even mention it unless it’s to offer them a change of clothes. this isn’t a medical thing, this is just a “don’t be an asshole” thing.
Don’t hold them down
5. don’t be an asshole in general. sometimes seizures and bodily fluids come hand in hand. we know this. trust me.
Waking up from a seizure can be super scary, especially if the person has never had one before. Don’t let them sit up right away, and speak to them in as soothing of a voice as you can, and i mean like nature-documentary type soothing, that shit has got to be as calm as it possibly can be.
Don’t fucking hold them down you can break their fucking bones i’m not kidding
I may add more to this later, but my brain is fried because, you know, i just had a seizure.
seizures usually only last a few seconds to a few minutes so it is usually best to let the seizure run its course. because if you call an ambulance the seizure will more than likely have stopped before they got there.
CALL 911 FOR HELP IF:
it is their first seizure
A seizure lasts 5 minutes or longer (status epilepticus)
Repeated seizures occur without the person regaining consciousness
NEVER EVER PUT SOMETHING IN SOMEONES MOUTH WHO IS HAVING A SEIZURE!
Do not force anything, including your fingers, into the person's mouth. Putting something in the person’s mouth may cause injuries to him or her, such as chipped teeth or a fractured jaw. You could also get bitten.
November is Epilepsy Awareness Month. 1 in 26 people will develop epilepsy in their life time, I am one of those people. Epilepsy is the 4th most common neurological disorder and there is no cure.
I suffered my first epileptic seizure back in February at the age of 20, it took roughly 5 months for me to be diagnosed. Thankfully I was diagnosed and am able to control it with medication. Suffering a seizure is a horrible experience for all of those involved. The person having the seizure (depending on the type) is completely unaware of their surroundings and who is there. And for the people there it can be traumatic. My mum witnessed my second seizure and was frozen with fear at seeing me in that state. If I had been at home or out with friends when my seizures occurred who knows what would of happened.
My point to this post is to help raise awareness of epilepsy and the lasting effects it can have. There is also a thing called Sudden Unexpected Death in Epilepsy (SUDEP) which is not commonly discussed, even when someone is diagnosed with epilepsy the doctor (well mine did) avoids talking about it. SUDEP scares me on a daily basis and knowledge of basic seizure first aid can help prevent it.
For those of you who spend time with me (or anyone who spends time or knows of anyone who is living with epilepsy), whether at uni or in a social aspect, please make yourself aware of what a seizure looks like (mine is tonic clonic seizures), and what to do should I have one. One day it could save my life.