This blog is my outlet for my adhd, autism, depression, anxiety, chronic illness, and ptsd among a few other things. If there are things that are triggering to you or need me to tag certain posts, just ask and I’ll certainly do that
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@thehappywords
This blog is my outlet for my adhd, autism, depression, anxiety, chronic illness, and ptsd among a few other things. If there are things that are triggering to you or need me to tag certain posts, just ask and I’ll certainly do that

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A trend in the "nobody cares about me" crowd that they probably don't want to hear about but needs to be said anyway is that maybe sometimes people do care about you, you just won't let them.
If you alienate everyone close to you by demanding their time and energy but still complain that nobody cares about you because they aren't doing enough, that is actually a you problem.
Until YOU internalize what healthy love is, you won't feel loved no matter what anyone around you does. And in the process of yelling about how unfair it is you're harming the people who actually give a shit. Sometimes.
And this obviously (but stating anyway cuz Tumblr) isn't everybody who feels like nobody cares. But it is a trend I have seen in numerous people. It is, kinda, hard to care for someone if they're aggressive and hard to be around on a chronic basis.
It's disordered behavior, too, but that doesn't mean you have a free pass to lash out at people. It is your responsibility to evaluate reality vs. your trauma in relationships and not make it other peoples' jobs to emotionally regulate you for you.
OH, ALMOST FORGOT, ALSO VERY IMPORTANT:
While relationships should be a relatively equal amount of give and take, you doing things for others that they never asked for nor expected of you and then being angry when they don't give 150% back is also a problem. It doesn't mean you're a nice person who's selfless and always giving to others. It means that you're not practicing healthy boundaries and you need to learn that Being Useful doesn't make people love you any more. If you unbalance the scale it isn't fair to come back at people with resentment when they practice healthy boundaries, i.e. respecting their own needs and limits and not centering you in every part of their lives.
I actually highly recommend looking into codependency if this is a thing for you.
VIOLATING YOUR OWN NEEDS AND BOUNDARIES DOES NOT MAKE YOU LOVABLE; YOUR RESENTMENT IS A BURDEN TO OTHERS.
btw it's so fucking stupid you can be anxious physically in your body even after you've decided mentally you don't care. I'm supposed to be in charge here
"It doesn't matter if you're autistic, people will dislike you if you don't act normal-" yeah we noticed. The problem at hand generally isn't that we don't know that people judge individuals who fail to fit in, it's that fitting in isn't always a choice people can effectively make
And here you are, continuing on, despite how hard it's been lately. Proud of you.

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"it's just growing pains" -> "you're too young for that to hurt that bad" -> "you just need to get in better shape" -> "welcome to being old, everyone is in pain"
hey. look at me. if you think you have a low pain tolerance because things that don't seem to bother other people much (headaches, period cramps, walking a certain distance, etc) hurt you enough that you have trouble functioning or need a break or just want to curl up into a little ball and stop because it hurts too bad or it's distracting you? that's probably not you reacting more strongly to the same amount of pain. you're probably experiencing more pain than everyone else, and you shouldn't ignore that, because you deserve medical care and support
general tips for tapering off meds as someone who has done it both safely and unsafely before:
⭐ DISCLAIMER: this is for harm reduction purposes only. if you want to come off a medication, it is best to do so with a trusted professional.
unfortunately, not all professionals know how to properly taper and may put you in danger. some may deny assistance entirely. please advocate for yourself/bring someone with you, or seek better care.
please do NOT rely solely on this post to do a self taper. i am a patient, may be wrong, and do not know you. if you can't access professional assistance, do your own research before doing anything.
- check if your medication has a withdrawal syndrome. learn about the symptoms and watch for them as you taper. if you begin to experience moderate or severe withdrawal, return to the previous dose at next dosing and reassess the tapering schedule.
- start low and go slow. the higher your dose and the longer you've been on the medication, the smaller the dose reductions will be and the less frequently you reduce the dose.
- how your dose was increased does NOT translate to how it should be decreased. tapering depends on the medication, current daily dose, and how long you've been on the medication.
- make a schedule and stick to it. do not rush. depending on your situation, it can take anywhere from days to years to come off a medication. days if you've only been on it for a short time or are on a low dose, years if you've been on it for years, and weeks to months in most other cases.
- instant release is NOT the same as extended release. instant release medications are released into the bloodstream much faster than extended. extended stays in the blood for longer. generally, you will be tapering more slowly on an ER med than an IR one.
- signs you're tapering too fast are: feeling sick, heart rate and blood pressure changes, issues with temperature regulation, distressing mental health symptoms like severe depression or anxiety, erratic mood, hallucinations, delusions, paranoia, severe insomnia
- normal changes as you taper down: mild changes in mood, energy, sleeping habits, appetite; these should fade as your body readjusts to the lower dose. if they do not go away after tapering ceases, contact a professional.
And as for the question of whether or not to taper, here are some reasons people choose to taper down or off:
The meds are causing side effects that cannot be tolerated
The meds are reducing quality of life instead of enhancing it (ex: being overly sedated or stimulated)
The meds are not effective or not effective enough to warrant the risks
To lower the risk of complications from long term medication use (ex: movement disorders from taking antipsychotics)
To avoid the withdrawal syndrome
The meds interact with other medications they are on, or are going on
The meds are too expensive
To learn to cope without medication
Psych meds have helped some, but there are also many more who find them not worth the risks or cost.
While I always hope people can safely taper down with a doctor, I know this is not always possible.
If you need to come off a medication for your health but lack support, self-tapering is an option. But it's risky, and can lead to crisis or hospitalization if done incorrectly.
If you choose to self-taper, if you do nothing else, please take it slow and stay safe! Do your own research!
Are you on psych meds? (read all options)
yes; they help me and i want to stay on them
yes; they only help a bit but i dont mind taking them
yes; they dont help me and i want to come off
yes; they cause me side effects and i want to come off
yes; they dont help/cause side effects but my psych refuses to take me off them
yes; i have mixed feelings about my meds
no; i dont take meds but i want to
no; i dont take meds and i have mixed feelings about them
no; i used to be but i am not anymore (by choice)
no; i used to be but am not anymore (by circumstance)
no; i am not on psych meds and dont plan to be
dont know why i need to say this but airing out someone else's med issues and criticizing them for not adhering to safe practices was NOT the point of this post in the fucking slightest.
this post is about keeping people as safe as possible in risky situations, not publicly shaming them and using them as an example of what not to do.
even the most perfect tapering schedule can still result in severe instability. it's not the expected result, but it is a possible one in some situations. it all depends on the individual and what they're on.
Life in an Autism World
in me there are two wolves:
the emotionally sensitive autism and the emotionally numb autism.
I’m sure many of us can relate lol

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If you're comfortable accusing anyone of faking disability, you're not a real ally to disabled people
One time when I was a kid a group of girls and I had to treat another student for hypothermia by ourselves because she had so many invisible health issues that the adults we asked for help didn't believe us. The student in question was actively hallucinating. When I finally ran for help the people I grabbed were slow as shit to respond, casually joking about how "dramatic" the person in question was.
The kid was picked up by an ambulance 30 minutes later.
Now as an adult working in security I get SO MANY folks- upper-middle aged mostly- coming to me to 'rat out' people they think are faking it.
I was once sent into a bathroom because a client demanded that the "fucker won't get out, so good drag them out"- I was NEVER going to do that, so I did a wellness check instead. You know who it was? A person recently released from the hospital after a car accident. They had a hole in their skull and major hearing loss. They couldn't answer the owner because they couldn't HEAR the owner.
Another time about a homeless man who got around town by kicking the ground from his wheelchair. "You know he doesn't actually need that thing, his legs work fine, it's just for pity points"- Oh, so he's not paralyzed, his wheelchair is performative? Funny story Dale, I actually know that guy, he was backed over by a truck and has chronic pain from his shattered pelvis. But sure, let's make him stand up and walk everywhere so nobody feels too bad for him and tries to help him or something.
"She doesn't need that scooter, I've seen her get out of it."
"Look how fat he is, because he just rides around and refuses to get up."
"She doesn't really need that cane- she comes here without it all the time"
Sincerely, truly, from the bottom of my heart- as someone who isn't physically disabled but hears this shit all the time- fuck off
Dear everyone, forever,
If you care at all about people who have anxiety, autism, OCD, CPTSD, or any other number of "ruminating," "nervous," and "catastrophizing" conditions or dispositions, you need to abandon this phrase and others like it IMMEDIATELY:
"I need to talk, give me a call."
The PROBLEM isn't the request, it's ambiguity and unnecessary room to worry. Here's a little help, for the confused and ambiguous communicating types:
❌ "We need to talk."
✅ "Can we talk? I've been thinking about what you shared last night and I'd like to tell you more about my perspective."
❌ "Have you looked at your email yet?"
✅ "Did you see the email about the flight change? We'll need to update our plans."
❌ "Please come see me sometime today."
✅ "Do you have time to swing by my office and to go over the report? I have some feedback before it gets sent out."
❌ "Give me a call when you have a sec."
✅ "Can you call me so we can talk about when to meet to plan the presentation?"
❌ "When can we talk?"
✅ "When can we catch up? I miss you!"
GUESS WHAT???? Being kind not cryptic does mean saying/typing/sending MORE words vs. less. And that's fine--just say/type/send them. Your choice to take 2 minutes instead of 15 seconds will be a HUGE weight of mental load off your anxious receiver. You may save them hours or days of ruminating/worrying/obsessing.
This is especially important if you have power over them, aka, you are a boss/teacher/parent. Especially because some of these same folks won't feel comfortable saying back to you, "about what?" they'll just go on worrying until you say more. Even if they know they shouldn't. Even if they try their best to "assume positive intent." Even if they take anti anxiety or other mental health meds to help.
INTERESTINGLY, I have also heard people who say they cannot stand it when someone does this to them DO IT TO OTHERS because they forget that it sounds cryptic as fuck and they only remember their own firsthand experience. You may know that when you texted "When can we talk?" you are happily reaching out to chit chat, but they might hear it as "something's wrong in our relationship and it's so bad I'm not going to say it until we talk" and then they are wracking their brains to figure out "what they did wrong" when the answer is literally fucking nothing.
Clarity is kindness.
Taking 2 minutes and using a few more words can truly make all the difference to someone else.
one of the hardest things to learn as a depressed former Gifted Kid™ is that half-assed is better than nothing. take the 50%, 40%, even 20% job. scrubbing your face is better than not taking a shower at all. picking up your clothes is better than never cleaning. nibbling on some bread is better than starving.
DO THINGS HALFWAY. NOW YOU’RE 100% BETTER OFF THAN YOU WERE BEFORE.
One of my college professors used to say “anything worth doing is worth doing poorly.” I didn’t understand that for years because I didn’t do anything poorly, I couldn’t do anything poorly, I had to Do Everything Perfectly.
But brushing your teeth for 30 seconds is better than not brushing them at all when that 2 minutes seems exhausting. Doing ten minutes of yoga is better than 10 minutes of sitting when 30 minutes of cardio sounds impossible. Changing my clothes is good when a whole shower is impossible. Standing on the porch for a few minutes is worth it after being in the house for three straight days because I don’t have the energy to go anywhere.
Anything worth doing is worth doing poorly… because doing it poorly is better than not doing it.
someone please hit me over the head with this post every day for like the next week thanks. a mention, a reblog with text, a message, something.
You must understand that perfectionism isn’t striving for excellence, it’s a crippling fear of being flawed and therefore worth abandonment or punishment. It’s a kind of psychological avoidance. You’re avoiding fear and failure , not embracing the thing you want to do bc if it was about the thing you want to do you’d be fine with partial victory.

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see my problem is if i “listen to my body” it literally only wants to lie down and take naps, all the time
i truly am exhausted by how hard life is as a high support needs / severely disabled person with no caregiving support or real treatment.
wanna go somewhere? sorry, you cant Walk or Open Doors.
wanna make some original art? nope, your arms are Too Weak. but you can do this simple craft if you want. at least there's that.
wanna eat? ahah, well. wouldn't you love that. Stomach Pain and Dizziness. cant cook and cant even eat a snack. Starve.
wanna lay down and rest? everything from the waist down is going to feel like it's in a vice. like someones squeezing your spine from the inside.
sit instead? ahah oh... dear... didnt you hear me before? spine vice.
wanna chat with a friend? there's no one around!
wanna watch a show or play videogames? photophobia and brain fog. push through if you want but you'll regret it.
wanna play with your cat? you cant even keep up with him.
wanna sleep? you'll need to spend 6 hours going back and forth between your bed and the couch because staying in one position for too long is excruciatingly painful
want a moment of peace and comfort literally ever? well you are shit out of luck. you will never feel comfortable again. your pain is permanent.