Today, one of my second graders was working on shape name recognition, and we got to this picture of a pyramid shape with a wide-ish base. When he saw it, his eyes lit up and he turned to me with a huge grin on his face, pointed at it, and said "When the teacher forgets to assign homework" before bursting out into hysterics, covering his mouth and giggling.
I don't understand what happened except this kid CLEARLY knows about the strong comedic and memeable value of mathematical shapes and emotions that I, an old millennial, cannot comprehend
I did, however, try to recreate this moment as the meme this child must have seen in his head
maybe he was thinking of the dancing triangle meme??
i have seen this gif with that exact caption before. this is absolutely the one he was thinking of
That kid saw one of the simplest geometric shapes and said that's blorbo from my memes 👍
i saw a couple pictures with the phrase “headphones/music on, world off” and i know the pictures were from like 2014 but i never saw that phrase before and i thought it was genuinely cute! and also im forcibly making myself emo and i thought drawing a cute girl who is more emo than i would ever be would be fun! she doesnt have a name yet :3 i hope u guys like it !!!!
Hi there! I got tired of seeing my condition (that impacts my literal every day life) being left out or forgotten about during discussions about disabilities, so I made my own post about it! Let's go!
First Off! What the heck is epilepsy? Epilepsy is the fourth most common neurological disorder in the world, and it's a chronic medical condition. Epilepsy is a brain disorder that causes recurring, frequent, triggered, and unprovoked seizures to occur.
The official Epilepsy Foundation describes seizures as follows: "Seizures are sudden surges of abnormal and excessive electrical activity in your brain, and can affect how you appear or act. Where and how the seizure presents itself can have profound effects...Seizures involve sudden, temporary, bursts of electrical activity in the brain that change or disrupt the way messages are sent between brain cells. These electrical bursts can cause involuntary changes in body movement or function, sensation, behavior or awareness." (Source link)
Sounds like a lot of fun right? This is our life. Even with medication, we can be VERY limited to what can be safe for us. Seizure medications are NOT a cure, they only exist (at least as of now) as a tool to help have your seizures less often, or be triggered less intensely. Even on medication, seizures can still happen.
If you have epilepsy as a child like I did, it impacts your entire growing and developing experience. I spent MANY times as a child in and out of hospitals, neurologist and specialist offices, an getting so many EEG tests done. The pain of scrubbing the glue out of your hair for DAYS is horrible.
At a young age my seizures were so frequent and serious, it impacted my brain's ability to retain information. I had to re-learn the names of things at age 8 and 9. I had to re-learn HOW TO READ at age 10. I had to be home schooled because the public school system of my state at the time refused to work with me. I have VERY distinct and vivid memories of crying over my little baby ABC's book that I needed as a 4th and 5th grader. I knew I should've known this by this age. I knew that at one point I already did, and it was TAKEN FROM ME.
As an adult, I'M NOT ALLOWED TO DRIVE A CAR. And I can NEVER go to see a movie in theaters or go to see concerts or live music. There are entire TV shows I don't get to see. I can't go to clubs, arcades, dances, or raves. I miss out on A LOT of fun things. I always do, and I'm WELL AWARE of the fun I'm missing out on. The social, casual, and fun life experiences I'll never get to have. That WE'LL never get to have. And oh yeah! Seizures can KILL SOME OF US. Yep.
And the list goes on, and every person with epilepsy experiences it differently. There are multiple different types of seizures you can have, they're NOT always convulsing on the floor. For example, I have complex-partial-myoclonic-seizures. Meaning my muscles DO twitch when I have seizures, but I'm not always completely unconscious and sometimes I'm even able to stay sitting up. However, I'm still very "off" and can't focus or remember much for a good while after the fact. I can't talk or communicate during one, even with my slight bit of consciousness.
My experiences are not universal, I just wanted to talk about it and bring it up. It helps to talk about it even a little bit.
Here's more about different kinds of seizures.
Here's more about common seizure triggers.
Here's more about CORRECT seizure first aid.
And here's more general information/resources.
Please stop leaving us out of disability awareness. Please stop ignoring us or saying we're "not really disabled" or anything else like that. Please. Why does it always feel like the only people who care about epilepsy, are people WITH epilepsy? We're so tired of being ignored by others who don't have our condition.
If you're an epileptic person reading this, I see you. I love you. You're so strong, we all are. I believe in you, I believe in us. We're so much stronger than we get credit for, and it's going to be ok. Your anger and frustration are valid. Your emotions and struggles are real. You're valid, and I see you. Hang in there, we got this.
imagine if doorways grew back like scabbed over with fresh drywall and you had to keep carving them back out with a jabsaw to keep the doorway clear etc
Imagine if the membranes recoiled in pain every time you did this. Imagine if over time, some doorways became accustomed sensation. Imagine that very rarely, some even seemed to enjoy it.
*sleepover host voice* imagine if you two went to sleep
why are people even fucking with gatcha games the wikipedia random article button is $0 and i just rolled a 10th century byzantine encyclopedia on my 17th try
