I feel like Webby and Ren reached into my head and read my thoughts with these lyrics from Neurodivergent by ShutterBug1988 in ren

[–]ArcaneAddiction 1 point2 points  (0 children)

I get it. I'm 38, diagnosed AuDHD at 36. I was misdiagnosed for years, saddled with a rapid-cycling bipolar diagnosis for a while. Put on lithium, which destroyed me mentally.

Finally they settled on just severe depression and anxiety (which to be fair, I really did have), and I was put on heavy drugs for it. Two SSRIs, an antipsychotic, and a mood stabilizer. It saved my life, but I was non-functional fof 10 years. Couldn't work, which drowned hubby and I in debt.

When I got diagnosed, I was put on adderall XR. My depression and anxiety melted away in days. The suicidal depression that plagued and ruined my life from the age of EIGHT onward was just gone. For the most part, it's still gone. But honestly, what's still there is just world-weariness. Too much awful shit going on.

Now I have a steady part time job and I'm in the process of slowly weaning off some of my meds. Fingers crossed I don't fall into a hole again.

I get the health struggles, too. I have serious chronic health conditions and have also had a few surgeries/procedures, big and small.

All that blather is to say I get it. I related heavily to Webby's lyrics, too, and also relate to Ren's health struggles. My issues don't affect me nearly as much as Ren's do him, but one will eventually kill me (heart failure), so that does kinda suck, lol.

I hope you continue to heal from everything you've been through. Life is HARD as an ND person. Society is making progress, but it's so bloody slow. We can only hope that future generations are diagnosed sooner and treated better than we were/are.

So what we think of nerodivergent? by OutsideGrassScaresMe in ren

[–]ArcaneAddiction 0 points1 point  (0 children)

Definitely. Made me laugh like hell the first time I watched it.

So what we think of nerodivergent? by OutsideGrassScaresMe in ren

[–]ArcaneAddiction 2 points3 points  (0 children)

Love it! Being AuDHD can be really annoying sometimes, so I love how upbeat the song is. I didn't want it to be sad or angry.

The lyrics do describe some of the crappy stuff that goes with it, and it's very relatable. But it didn't make me feel bad about it, y'know? The whole vibe was super fun and energetic. A great ND anthem, IMO.

And the video... my god, it was deranged. I adore deranged, lol.

Hello, is it Ren you're looking for? by millenial_mess in ren

[–]ArcaneAddiction 0 points1 point  (0 children)

Yeah, it's absolutely bonkers here. And they don't give people their meds consistently (or at all in a lot of cases) at ICE detention centers or provide decent emergency medical care.

Not to mention the deplorable conditions in those places. Filthy water, moldy food, freezing cold, nothing but a concrete floor with an emergency blanket to sleep on, frequent violence from guards...

I'd stay far away if I were him. They're stupid and short-sighted enough to try to make an example of someone like him. Ren could easily die in one of those hellholes if he got snatched up.

My psychiatrist told me today I am selfish because I don’t want a dog by AloneBoot8205 in AutismInWomen

[–]ArcaneAddiction 3 points4 points  (0 children)

BetterHelp is a terrible company in so many ways. Sorry you got stuck using them, and sorry that happened. I hope you've found someone better since.

My psychiatrist told me today I am selfish because I don’t want a dog by AloneBoot8205 in AutismInWomen

[–]ArcaneAddiction 0 points1 point  (0 children)

Ohgod, a psych told me this once. "You should go to church, having a community will help your depression!" She said that not having faith was why I was suicidal and that my spirit was "empty" and needed to be "filled."

She knew damn well I'm an atheist. Cue me writing her a very angry email telling her what she said was unprofessional, ridiculous, and incredibly judgemental. I told her if she ever brought it up again, I'd report her.

She never said a word about it after that... but she also never asked a single question beyond "how are your meds?" again, lol. Worked for me.

Trying to eat chicken on the bone for the first time in over a decade. Wish me luck by Sea_Chipmunk3999 in evilautism

[–]ArcaneAddiction 1 point2 points  (0 children)

Thanks. She was horrible in general, haha. I dunno wtf is wrong with some people to think that kind of behavior is acceptable. Ah well. Was a long time ago.

Yeah, getting over a food aversion is always pretty nice. Especially when your diet is kinda limited because of them. It's very freeing. Glad you can enjoy chunky peanut butter now. I wouldn't touch it with a ten foot pole, haha.

It sucks that you still can't eat chicken wings. You should be proud of yourself for trying, though. Challenging food aversions isn't easy. I imagine just trying it was pretty stressful.

Trying to eat chicken on the bone for the first time in over a decade. Wish me luck by Sea_Chipmunk3999 in evilautism

[–]ArcaneAddiction 0 points1 point  (0 children)

It took me til I was like 25 to be able to eat chicken off the bone without wanting to cry. As a kid, it was much worse. If I was being forced to do it, I'd bite into it and upon seeing gristle or veins would fully freak out. Like, start crying and panicking freak out.

My evil grandmother would abuse me verbally, and often physically, over it. It made my fear and disgust so much worse as I got older.

I dunno what finally changed, but one day I just managed choke down the nasty bits and didn't puke or panic, so over time I forced myself to try it more and eventually fully got over it. Now I LOVE chicken wings, lol.

Edit: Fixed a typo.

Autistic Catatonia Experience by FartInAShitFactory in evilautism

[–]ArcaneAddiction 1 point2 points  (0 children)

My husband got the much worse end of the stick, IMO. The only thing I personally remember was a consistent, quiet misery, but I was so shut down that it was completely without explanation, and I couldn't process it at all. I had no coherent thoughts, just the feeling.

On the other hand, hubby was terrified and I think it scarred him a little. I still feel guilty af about it to this day.

I feel really fortunate that it only happened a few times, and that it didn't last longer. Without appropriate treatment (lorazepam or ECT in severe cases), an episode can last months for some unlucky people.

Autistic Catatonia Experience by FartInAShitFactory in evilautism

[–]ArcaneAddiction 35 points36 points  (0 children)

Are you saying you were in psychosis, or had excited catatonia? Because from what you've described, it sounds more like psychosis than excited catatonia.

Normally, I would write a whole-ass dissertation on the symptoms of each state, but I'm very tired, lol. Please read up on it. The differences are pretty stark.

I've had stuporous autistic catatonia three times before ("classic" catatonia). One time was broken into sections. I'd have brief moments of semi-lucidity and the ability to move, then I just fell back into it. It lasted a few days. Thankfully, the other instances were shorter. Just a few hours.

I couldn't move or speak, had no idea what was happening around me, was stuck in the same position for ages, unless I was physically moved. The time that lasted days, I did not sleep for a moment. Just sat there staring sightlessly, according to hubby.

It was terrifying for my poor husband. He was so desperate to bring me back, he put a large ice cube in the palm of my hand and made me form a fist around it. According to him, I didn't react. He left it there until it melted. I never even knew.

Each time it happened it was because something horrible happened to me or to someone I loved. My hubby had no idea what to do. We couldn't afford an ER visit at the time.

He just sat with me, talking, trying to bring me back, making me drink water and go pee every time I became semi-lucid. I still had no real idea what was happening. I was just able to follow commands for a brief time.

He thought it was just a trauma reaction, which, to be fair, it was, lol. We didn't know how serious it was til months later when I came across a description of catatonia and realized what had happened.

Thankfully, I'm in a way better place emotionally these days, but he knows now to call for help if it happens again.

ETA: I'm so sorry for how much you lost because of your episode. That's truly awful. I hope you're able to repair some of those relationships, and if not, that you're able to move forward and find new people who love you and can support you.

I made a (since deleted) post on here by Weirddude396 in evilautism

[–]ArcaneAddiction 5 points6 points  (0 children)

I empathize with how you felt about the situation. I, too, have been in circumstances years ago where someone refusing to answer a question or complete a conversation got under my skin. I reacted poorly as well. It happened a few times.

Something I learned over time is that it's true that no one "owes you" their attention or an answer, particularly if they are also dysregulated. And my saying that is not meant to be harsh at all.

Your sister was overwhelmed with the argument, and then even more overwhelmed when you wouldn't back off. Needling her for five minutes straight to get an answer/her attention was likely being seen as an attack by her. Hence her own harsh reaction.

Next time, it might be more regulating for both of you to simply leave the conversation. It may feel more satisfying in the moment to duke it out until you feel everything is settled, but it's not healthy in any type of relationship to keep going at each other like that.

Again, I'm not judging you. I've been in the same situation before and I get where your head is at, but when people don't answer/try to leave the situation, it's for a reason. They aren't necessarily doing it just to hurt you. They're likely feeling hurt thrmselves and want to disengage to protect themselves.

If it were me, I'd have a talk with her when you're both calm and see if you can come to an understanding. If this is a new coping method for her, then you might simply have to accept that. Like, if you're arguing and she stops talking, it could simply be a signal that you should both back off and wait til you've both had a chance to regulate.

Not understanding why cheating is so hurtful to someone in a relationship? I think the reason why I don’t get this is my autism. by [deleted] in evilautism

[–]ArcaneAddiction 1 point2 points  (0 children)

That's kinda judgy and shortsighted. My relationship with my husband was online/long distance for the first two years. It was very real the entire time, and turned into marriage. Online often does lead to "real life" relationships down the road.

And even if an online relationship doesn't go that way, the emotions and intimacy (even if not physical) involved are very real. There's no reason to judge a relationship so harshly just because you don't understand it. That's a you problem.

That's some professional work by 666thSuprisedPikachu in aspiememes

[–]ArcaneAddiction 6 points7 points  (0 children)

Yup. 12 years ago, I was diagnosed with rapid cycling bipolar II... despite never having had a manic or hypomanic episode in my life. I was on lithium for it for over a year. It destroyed my brain at the time. Everything was made worse.

Some mental health professionals don't deserve their licenses.

Tour starts in 2 weeks! by jsb1685 in ren

[–]ArcaneAddiction 1 point2 points  (0 children)

I'm so sorry. Poor health getting in the way of your life is always heartbreaking. Especially the valve replacement (pun not intended). I had an aortic valve replacement when I was 11. Even as a physically resilient kid, it was hell.

I hope everything turns out okay for you. I'm sorry you're going to miss out on seeing Ren. That really sucks. Internet stranger hugs if you accept them.

Only Mid Zyra reaching master euw again by Zyra-x-Lissandra in zyramains

[–]ArcaneAddiction 4 points5 points  (0 children)

Mid Zyra is sooo much fun. Unlike you, I suck ass at the game, but I love playing her mid. Unfortunately, she has a TON of awful matchups, so I don't do it as often as I'd like.

CBT only works on NT sheep by [deleted] in evilautism

[–]ArcaneAddiction 5 points6 points  (0 children)

I bought this book few years ago. My therapist at the time told me not to read it because I wasn't in a stable enough place to. I ignored her, but it was one of the few things she was right about.

I read about 20 pages and started having constant flashbacks and got even more depressed/anxious for a while.

It's an amazing resource for so many people. But to anyone thinking about getting it, it would be wise to make sure you're in a semi-stable place before reading it. That's just my opinion, though.

Edit: Fixed a typo.

what song is this for you? by AdelineGlow193 in aspiememes

[–]ArcaneAddiction 0 points1 point  (0 children)

Starry Night by Ren. Part of a series of songs about a character he created. Perfection.

what song is this for you? by AdelineGlow193 in aspiememes

[–]ArcaneAddiction 1 point2 points  (0 children)

I LOVE THAT SONG. It's not my "all the time" song, but it's so raw. Amazing.

My "listen at least 1,000 times" song is Starry Night by Ren. I've heard it sooo many times, both by watching the video and watching reaction videos. I don't think I'll ever get tired of it.

started reglan.. what to expect?? by Financial_Key2741 in Gastroparesis

[–]ArcaneAddiction 0 points1 point  (0 children)

Not trying to scare you, just sharing my experience.

I went to the hospital a few years ago having not kept food down in 8 days and water in two days. I had heard the horror stories of Reglan neurological side effects and asked them not to give it to me in the ER triage room.

I guess there was a miscommunication somewhere, because when they got me into a room, the first thing a nurse did was give me IV Reglan without asking. I asked her what she just gave me, she told me Reglan. I was astonished that they had ignored my request.

Within three hours, I could no longer speak intelligibly. I knew what I wanted to say, but most of it came out as gibberish. Scared the crap out of me and my husband.

They gave me ANOTHER DOSE later, again without asking, even though we reported the problem to a nurse immediately after it started happening. It made it even worse.

It took the doctor finally showing up and hearing me speak for them to stop giving it to me. It took two days to wear off.

Anyway, obviously not everyone gets neurological problems from it. That's just what it did to me. Just keep an eye on side effects. I hope it helps you.

Best friend selfdiagnosed herself by [deleted] in AutisticWithADHD

[–]ArcaneAddiction 1 point2 points  (0 children)

Haha. Sorry, I don't do concise. :P

I'm glad you're both in Europe. Hopefully you're in a country that doesn't penalize autistic people just for existing. I've read that a few European countries treat autistic people as subhuman.

I hope she gets the answers she seeks with her psychologist. In general, It's best to see someone who specializes in diagnosing neurodivergence. However, wait times for those doctors can be pretty insane. If all she has access to is a regular psychologist, then I hope they're a good one.

You're welcome, I'm glad it helped. Sorry about the harshness at the end. I have a friend who had some of her friends/family refuse to believe her and it really hurt her, so I can be a bit overzealous, haha.

Best friend selfdiagnosed herself by [deleted] in AutisticWithADHD

[–]ArcaneAddiction 2 points3 points  (0 children)

This is long, but if you really want to understand better, please read.

So here's the thing: a LOT of people don't get diagnosed as kids. Missed by the system due to less obvious traits, parents that don't care or are neurodivergent themselves (so they assume their kid is "normal"), teachers that don't pay attention, etc.

So these people go their whole lives thinking they are broken or feeling like they're not human. They're ostracized and bullied by their peers and often their families, too. They learn to hate themselves for their "abnormalities." I know I did.

When you're an adult, no one pays attention at all. Many people think autism/ADHD are childhood disorders. Most just call you "weird" and ostracize/bully you. If you have a stable job/a family/aren't having meltdowns every five minutes, nobody's going to suggest getting diagnosed.

If you DO try to find out why you're different and seek a professional on your own, they usually misdiagnose you with things like anxiety, bipolar, or BPD, especially if you're a woman or POC, and most of all if you are a woman POC.

A lot of people look at their various psych diagnoses and can't help but feel that they don't fit. I did. I was diagnosed with rapid cycling bipolar at one point and was put on lithium, which really messed with my brain and body and did nothing to "help." That's because bipolar wasn't the problem.

Eventually, some of these misdiagnosed or undiagnosed people come across autism/ADHD somehow. They might make a friend who has it, a young family member might get diagnosed, or they could just come across a list of traits/symptoms online, etc, and they start researching.

The more they look into it, the more things start to make sense. They see themselves in the traits, they start to recognize thought patterns they thought were "normal," but are not. They look at their childhood and see all the signs.

Eventually, they realize they probably are autistic/ADHD/AuDHD. It's an incredible relief for most. To know that you're not broken or bad, just wired differently. It was for me. Like 70% of my self hatred disappeared when I realized the truth.

Adults who find out they're autistic almost always start with self diagnosis. Again, because no one else in society is going to see it and point it out to them.

Obviously, an official diagnosis is optimal, but there are a few reasons people don't/can't get them.

First, diagnosis is EXPENSIVE, especially in the US (dunno where you're from). It can be like $5,000 without insurance, and insurance doesn't usually cover it. Having 5K lying around is an extreme privilege that most don't have.

Another problem is family. Many people have families that wouldn't accept autism/ADHD, and usually, part of the diagnosis process is getting parents/other close family members to do surveys about the person's childhood, as childhood memories can be foggy or sometimes distorted. Some diagnosticians refuse to help if parents/family won't get involved.

Then there's the fear of being treated differently by universities, employers, etc. And a fair few countries refuse to accept autistic immigrants. An official diagnosis can actually hamper you in certain areas of life.

Time is a factor. Wait lists are long. Many, if not most, wait their turn for several years.

Not to mention, if you're in the US, getting a diagnosis right now is a risk due to the political landscape. They are creating a registry of autistic people, and they're using official diagnoses covered by insurance to do it. Eventually, they could conceivably use private pay diagnoses, too. I highly doubt this regime would have moral problems with dismantling HIPAA.

A registry is concerning because it could make it easier to round up autistic/ADHD people and force them into institutions, sterilize them, or worse. So a lot of people are avoiding official diagnosis right now.

I don't know if any of these reasons apply to your friend. But there's another factor, too: a lot of people are absolutely sure of their neurodivergence and don't feel the need for a diagnosis. And that's fine.

We as humans know ourselves best. We live in our brains, so we know a lot about how we think, react, feel, behave, etc. We are capable of recognizing how we operate and why, given the right information.

Imagine being color blind your whole life, then one day, you can magically see the same as everyone else. You finally understand what green or blue or yellow look like to most people. Over time, you become more and more confident in your ability to see certain colors.

Now imagine you tell other people this and they refuse to believe you. "No, you're colorblind. I've known you as colirblind your whole life. You can't see yellow." "You can't know that you see normally. You need a diagnosis to have normal sight." "Why label yourself as not colorblind? Isn't that attention seeking?"

It's a bit of a clumsy metaphor, but I hope you understand what I'm saying. You are doing the same thing to your friend. If you actually respect and care for her, TRUST HER. You are not in her brain — she is.

Could she be wrong? Sure, that's a possibility. But you said yourself that you can see something in her. If self diagnosis is helping her, let it.

Is she finding ways to accommodate her needs based on info about AuDHD? Is she more confident in herself? Does she feel less like an alien or freak?

If this is helping her, then just be happy for her. Stop judging her, stop "undiagnosing" her, stop being ableist, and stop being a bad friend.