God I feel like shit, why do I feel like shit
-Person with the "I feel like shit" disorder.

shark vs the universe

titsay
noise dept.
we're not kids anymore.
Show & Tell
Alisa U Zemlji Chuda
h
Monterey Bay Aquarium
d e v o n
$LAYYYTER

Kaledo Art
dirt enthusiast
Today's Document
Xuebing Du

#extradirty

Andulka
Cosmic Funnies

ellievsbear
"I'm Dorothy Gale from Kansas"
seen from Malaysia

seen from United States
seen from United States

seen from Malaysia

seen from Malaysia

seen from United States
seen from United States

seen from Germany

seen from Malaysia
seen from United States

seen from Malaysia

seen from United States

seen from United States
seen from United States

seen from Malaysia
seen from United Kingdom

seen from United States
seen from Azerbaijan
seen from United States
seen from Malaysia
@tizzychardia
God I feel like shit, why do I feel like shit
-Person with the "I feel like shit" disorder.

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
I hate being chronically ill what the FUCK do you mean I have fatty liver at 21 years old. IM 140 POUNDS.
Thank you Familial Hypercholesterolimia. As if I didn't have enough on my plate, and my plate is already PORTIONED, mind you.
I basically have to find a way to power through starvation until I'm at like 100 pounds or else I'm going to have a heart attack or a dead liver because of my LDL. Genuinely FUCK my biological parents for having all these genetic problems and choosing to have a kid anyways. What the fuck is wrong with you two.
Insert Jeopardy music here
Alright folks, what is causing the sudden, massive wave of nausea after weeks of no symptoms?
A: The crab I ate earlier and other food related sickness.
B: My yearly April POTS flare.
C: Anxiety.
D: GERD flare.
E: Might just need to shit.
F: Unlocking yet another bullshit "no cure" comorbidity of some kind.
Stay tuned for the answer, folks. I'm 99% sure I'm going to end up vomiting within the next hour.
Edit:
Aaaand folks we're back after the 14 minute break with our answer. Let's go down the line.
If you answered B, D, or F, you were incorrect. This was surprisingly not a chronic illness related event.
If you answered C, you were incorrect. The sheer force of what exited my body could not have been caused by anxiety alone.
If you answered E, you were incorrect. While I did end up shitting, it did not alleviate the nausea.
This means that if you answered A folks, you were correct. This was either the result of a mild, unknown seafood allergy, the crab being parasite ridden, binge eating, or all of the above. We are currently waiting on confirmation from the other party who ate the same crab, to determine if this result is due to parasites or something personal to my body.
That's all folks, thanks for playing. My nose burns and I am ready for bed.
Doctor appointment days fell like filler episodes. Can't do anything at all leading up to it because you've gotta conserve your energy, and it just feels like you're wasting your day.
Couldn't do anything yesterday because I had to save energy for a dentist appointment today, and I can't do anything tomorrow either because I'll need to save up energy again for a cardio appointment on Friday. I've spent the whole week just stalling and doing a bunch of fuckin nothing.
The cardio appointment itself is bullshit. I see the actual doctor once a year, the doctor who previously told me POTS isn't diagnosable, and the extent of it is just:
"You still having symptoms?" "Yeah." "Symptom treatment and meds working?" "Yeah." "Any questions?" "Nah." "Ight see you in a year."
This is honestly the best way I've found to explain POTS to people who don't absorb medical information well. Unfortunately, I have to portray myself as William Afton to get my point across.
Springlock suit.
We are constantly inside a springlock suit.
During the day, when we are wearing compression gear, hydrating, intaking sodium and electrolytes, taking medication, regulating our body temperature, taking breaks, eating smaller meals, managing our diet; all of those symptom management tools are metaphorically winding the springs inside the springlock suit to keep the animatronic parts coiled back.
But if we move too much, if we get hurt, if we neglect to manage our symptoms, aka not winding the springs, we flare. The springs snap back and impale us with metal from every possible location on our body, and we get stuck for an extended period of time.
My friends don't really do well with medical terminology, and we all tend to find it a bit depressing, so this metaphor seems to help. If they ask how I'm doing today and I send a picture of Springtrap, they know I'm really going through it.

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
My body has decided that it is allergic to the sun. Not heat, just the sun specifically.
My heat intolerance has not been bothering me as much lately so I figured, hey, it's like 70 degrees outside, let me just step outside for 10 minutes and enjoy the air. Feel the sun on my skin for the first time in 2 years. Enjoy life. No risk of sunburn, I'm hydrated, I've got my ice packs and fan on me, we good.
My body is now boiling me alive.
Even ice feels hot on my skin.
Why body. Why.
You can handle 90 degree water but not 70 degree sunlight. What a picky bitch.
BREAKING NEWS!!: Average non psychotic singlet thinks they know when someone is faking said illnesses… totally not saneist behavior!
No clue where this is coming from but this is a wild thing to wake up to
But you do realize that the "non-psychotic singlet" thing just kinda makes you look a little stupid...right?
DID/OSDD are specified/unspecified dissociative disorders. Not psychotic disorders. You can experience symptoms that mimic or present like psychotic symptoms (actual psychotic symptoms are consistent with disorders such as schizophrenia, major depressive, schizoeffective) but DID/OSDD are not classified as psychotic disorders. The dissociative symptoms are simply similar to psychotic symptoms due to disruptions in reality.
Are you saying that if I AM psychotic, I have the right to comment on things in regards to DID/OSDD? Or do I have to be a "psychotic system" to truly speak my peace? Or maybe just a system without the "psychotic" attached to it, which would mean you adding "non psychotic" to your message would be pointless.
I don't think you even know what you want.
I feel as though I kind of know what I'm talking about here considering I've been professionally diagnosed with MDD for the last 7 years and experienced my own unfortunate states of psychosis and psychotic symptoms, but, to each their own, I guess. Professional diagnosis might be a foreign concept to you, so I don't take it personally.
Bringing up psychotic symptoms/disorders in the same context as dissociative symptoms/disorders makes you look like a fuckin nut, btw.
I don't know if this is a neurodivergent thing or something exclusive to the way my brain works, but I genuinely hate questionares with my whole heart because the questions/answers aren't specific or descriptive enough for me to give what I consider to be an "accurate answer."
At my last bloodwork appointment, they gave me a yearly depression screening paper. I already knew that my results were going to be a little wonky because I have a depressive disorder, but the questions and limited answers were genuinely pissing me off.
"Do you spend a lot of your time feeling tired or out of energy? A, not at all. B, several days. C, more than half the days. D, all the time."
Like, yes, D, all the time, but that's because fatigue comes with my Dysautonomia. That doesn't mean I'm depressed or suicidal, but these questions don't have the option to provide that context.
"Do you find it hard to communicate with others on how you feel? A, not at all. B, rarely. C, often. D, all the time."
It depends on what needs to be communicated and what feelings I'm trying to communicate. Am I communicating complex feelings or surface level feelings? Am I communicating these feelings with a stranger, an acquaintance, a friend, or a family member??? What exactly defines something as "hard"? Simply difficult or near impossible for myself??
Like I need context with the questions and the ability to provide my own contextual answers in order for me to feel satisfied with the questionare, because without appropriate context given or received, I will not trust the accuracy of the fucking results.
Hey I fucking hate this.
"Hi, yes, I need a refill for XYZ. I just looked at the date on the bottle, and it says to refill by literally 2 days ago, but surely you can still give me a refill because 2 days is not a substantial amount of time."
"Ahh, I'm sorryyyyy!! We actually can't give you a refill. You'll have to go back to your doctor and set up an actual appointment to renew the prescription. If you called two days ago, this wouldn't be necessary, but unfortunately, it expired."
"...Why are you not able to refill it now?"
"Well we can't tell if you're still taking the medication or if you still need it, so if you make an appointment with your doctor to confirm if you still need it, we can totally get you a refill! :)"
"So if I called literally less than 48 hours ago, you would have been completely under the assumption that this is a medication I still need. But now you are under the assumption that my chronic illness has magically cured itself within the span of two days, to where I need a doctors confirmation that my chronic illness, is still, in fact chronic, for you to do a refill."
"Yes :) my apologies."
"Jesus okay let me call my doctor."
Calls my fucking doctor.
"Hello doctor X, I would really appreciate it if you could renew my prescription for XYZ because I am pretty much out, and as you know, this medication depends on my ability to function."
"Hi! It's nice to hear from you again, but you will have to come in person and schedule an appointment for me to renew your prescription."
"Why. I'm pretty much housebound, and going to physical doctors appointments leaves me symptomatic for weeks. I would really like to avoid doing that since I'm being forced to attend holiday events soon, and I need all the energy I can get."
"I completely understand! Unfortunately, we can't tell if this is really you over the phone."
"....but you've heard my voice before. It's me. You know me."
"Yes, but that's not a form of reliable identification to ensure that you still need this medication, that you're renewing it for yourself and not someone else, not taking more than you should, abusing it, etc."
"...I can send you a photo of my ID."
"I understand your frustration, but that is still not a reliable form of identification. In-person identification is what is required."
"I can literally read off my damn social security number. My birth certificate. I can fax you a copy of my fucking taxes. Anything. I just need a refill. A refill that I would have had no issues with if I ordered it two days ago."
"Still unreliable. Would you like to set up an appointment for sometime soon?"
"...." *Literally vibrating with rage at this point.*
"...I have about 4 days left of my medication. When is the soonest you can get me in."
And this usually results in me having to wait an extra month, unmedicated, overly symptomatic and flaring by the time I have to physically go to the appointment, only to have to wait an extra few days for the pharmacy to actually have my meds, because these dumb fucking cunt ass bitches are convinced that either I'm not me, that my chronic illness has magically cured itself, or that I'm secretly a drug addict abusing my medication.
NAUSEA MEDICATION.
YALL ARE ACTING LIKE I'M ASKING FOR OPIOIDS.
KILL YOURSELF
Being chronically ill is having weird avoidances towards regular things because they remind you of symptoms and turn them into a trigger.
The visual disturbances that come with presyncope? I can't look at window/door screen because my eyes start fucking up. No flashing lights, no florescent lights, especially at night.
Can't be pitch black either. I always have my phone on night as a light source, I can't have my eyes open and staring at complete darkness because that is what I see before I pass the hell out.
I can't do complete silence. There needs to be some kind of humming, sound, music, noise happening at all times because if my body is left in complete silence, I can hear pressure in my head and the tinnitus starts kicking in.

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
Another part of being disabled/chronically ill that isn't talked about that much is how you just stop mentally aging, especially if you got sick in your teen years. You're stuck at the age you were during the year before you got sick because you get held back from the things that make you feel older.
Like I don't think I've mentally gotten past being 18. I turn 21 in less than a year. Like some of my friends are employed full time, some of my friends are in the army and navy, some of my friends are engaged, some of my friends are having babies, some of my friends have moved out and away from their parents, some of my friends are driving now, some of my friends party at clubs, they travel states, they go on big vacations, and I just never got to get to that point. All of the things that I should be doing for my age, I can't do, and it makes me feel like a fucking baby, dude.
Goodbye POTS summer, hello Ehlers Danlos winter.
Like omg!! My energy levels are back!! I have an appetite again!! Blood pooling is less frequent!
Unfortunately, chronic joint pain is now at an all-time high.
We can never win dude 💔
if your neuro diversity activism doesn't include people with psychosis then it's worthless I'm not sorry to say
Doing this cool new thing called deliberately ignoring my esophageal disease because I want to feel like a normal person again just for 20 fucking minutes before the excruciating nausea and pain kicks in
I know this is going to kill me in less than an hour but oh my god. It is so fucking horrible to be HANGRY all the time because you have to eat the same safe food every day so your stomach doesn't fuckin explode. Like I'm done. I don't care if I end up with EC or bedridden or have another flare. I just want one little taste of my life back.
I hate the culture shock that people get when they realize that someone's disability is actually disabling and not the watered-down romanticized/glorified tiktok version of whatever it is you're dealing with.

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
The monkeys paw is the equivalent to dealing with the side effects of a medication that's supposed to help with symptoms of your disability.
I take my Ivabradine, which helps slow my heart rate. Oops! No more functional vision for the next 10 hours. Every light I look at will make me motion sick. The walls are breathing. Fun.
Severe GERD is so embarrassing bc wdym I sneezed and it made me throw up a little