#transepilepsy

[maxrqstuff]

I only saw an Anti under this tag #transepilepsy

So wanned to make some positivity ❣︎❣︎ As a Transepileptic person myself ^•^

Purple: Epilepsy

Yellow: Neuro Disability and support to every epileptic person

Purple: Transhood

Lightning: extreme Neurosignals

Blue: Nervesystem

-❥-ミ★-☾☼-𓆝-⚘❀-༒-✌︎︎-☞︎-☮︎︎-𖤍-𖣊-❣︎--☆彡-❥-

I also made a alt transnarcolepsy flag :3

Black: Seconds of Sleep

Dark Blue: Deep Sleep/-yness

Blue: Transhood

Light Blue: Struggle to stay awake

Clowd: Sleepyness

zZ: Sleep

-❥-ミ★-☾☼-𓆝-⚘❀-༒-✌︎︎-☞︎-☮︎︎-𖤍-𖣊-❣︎--☆彡-❥-

Stay safe y’all (¯ ³¯)♡

Don’t let Antis get to you ❣︎❣︎❣︎

Remember nothing is forever, so all the hate will be over one day ❣︎ And we can happily live fulfilling lives and being able to transition ❣︎❣︎

[whatevenisexisting]

The fact that there are people who want to have Epilepsy and read tips on it will never not disgust me. Like seriously. Y’all are fucking ignorant, ableist, and your identity is NOT in good faith.

Why? Because as someone who actually has epilepsy, it DOES hurt for me to see some people on tumblr want this damn condition. As I’m struggling to get through a work week, as I’m finally realizing I need accommodations, as I’m feeling frustrated because I haven’t had a seizure since April 19th, and I already had two this month.

Remember y’all, when you have a seizure, out goes your ability to drive for at least a few months. Put yourself in a small town with no public transit, rely on family to get literally ANYWHERE - and then tell me you’re “transepileptic”.

I wasn’t planning to ever drive again, but that decision DOES affect my life and let’s say I chose to drive once it was legal. Well, in my state I would have been able to drive by July but BAM. There it goes again.

Have a seizure, and you cannot drive. Now you have to find other ways to get EVERYWHERE you can’t walk to. And if it’s pouring like it is for me today? Yeah, your choice is either walk in the rain and get soaked, take an Uber for a ride that’s only 5-10 minutes and easy walking distance, or stay home.

Not everyone can rely on family or friends every single time they need to go somewhere, remember that.

And I know I’m focusing on this part but it’s just ONE aspect.

I mentioned I had a rough week at work and I did. Have fun dealing with post-seizure depression and just overall triggered depression as you work for a suicide hotline. Have fun not being able to tell 99% of your coworkers WHY you are struggling so much this week because you can’t even the say the name of your condition (and as a side note, your mom hates this and doesn’t understand - she thinks it just means you’re ashamed even though you aren’t), so yeah, they respect that and it’s your right but it would be easier to talk to them if they KNEW. But you don’t, because you barely accept your condition to begin with. (The five stages of grief? Yeah, apply them here and put yourself permanently in between denial and acceptance, also anger and depression, and have a jolly good time.)

Oh don’t forget needing time off work! Because if you’re lucky like me, you’re going to be exhausted the next day and will need to sleep all day! Which means using a sick day, and in America most people are LUCKY to get two weeks. My friend’s partner gets five days. Total. Of paid time off and sick COMBINED. So yeah, have a blast balancing what little sick time you get with needing to care for your body because sometimes you cannot recover quickly for them! You likely don’t know that tonic clonic used to be called grand mal (don’t worry most people without epilepsy don’t know this and you know you don’t have epilepsy soooo) but with grand mal, you might end up in the hospital because you can injure yourself! Any seizure that involves convulsions puts you at risk of physical (even mental, if you hit your head and get a concussion) injury, but I’m sure you haven’t thought of that part, have you?

Or maybe you have and you still want a condition that severely impacts people’s lives and can kill them, in which case you’re just ableist lmao, and insist that me being against people outright SAYING they’re faking a disorder is somehow transphobic or I’m “using the same talking points” as people against the trans community. Like stop stop STOP.

You know what the difference here is? Trans people didn’t choose to be trans, they can’t always come out of the closet because it’s NOT SAFE which surprise, might have a significant impact on their mental health. They don’t have a choice but to be closeted. Staying closeted STILL comes with consequences though. Coming out of the closet might come with consequences. There’s a reason trans people have such a high suicide rate.

As for the “talking points”…that’s just stupid because you people KNOW and SAY you don’t have this condition. You give each other “tips” for doing these symbols, or should I say FAKING the symptoms.

Me talking about the REALITIES of living with a disability is a desperate attempt to get you to stop romanticizing them. Me talking about the TRUTH of living with something like in my case epilepsy, is a desperate attempt to make you realize it’s NOT something you want.

I’M the one who didn’t have a goddamn choice for this condition. JUST LIKE trans people don’t have a choice to be trans and cis people don’t have a choice to be cis.

YOU fucking DO have this choice. YOU have the choice to get off Tumblr, out of this horrible echo chamber and ask yourself why the fuck you’re ASKING for TIPS FOR HAVING A SEIZURE.

Like for real, get off this hellsite and THINK about what you’re absorbing. This. Is. Not. Healthy.

And no, I don’t give a shit if you’re ~also disabled and okay with this~ because it’s not okay lmao. Like these are not good faith identities. Period. These people romanticize serious conditions, play into the idea that people with disabilities are faking theirs (especially if they suddenly become able to do things - “oh, jessy can do that, why can’t you?” Disabled people hear that enough already), and simply ignore the reality.

Ugh. I’m only writing this because Tumblr is a blog and a safe space to write, my therapist is sick today and can’t do a session with me, and I woke up still pretty sad and frustrated and then I thought of “transabled” people and decided to rant. Going to keep this public for now, might make it private later.

[blissfuloverdose7]

hey ya’ll! I made a transepilepsy flag

as someone with cis-epilepsy, I totally dig that transepilepsy is valid too. So, I whipped up a flag for those who identify that way❤️

[antiradqueer]

I was trying to search for epilepsy flags and I found like 3-4 transEpilepsy flags. What the actual fuck is wrong with transId’s? Like I get they are weird and are honestly probably delusional but SHIT. As someone with epilepsy why the fuck would you want epilepsy? 😭😭 I’ve literally had so many issues due to my seizures and I only developed epilepsy a few years ago. I wish radqueers would get some sense knocked into them -_-

.

[maxrqstuff]

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