#I’m having symptoms again
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#did you miss meee#I’m having symptoms again#traumacore#traumacore edit#vent art tw#traumacore collage#trauma#sa#tw#sa art#tw sa#neglect
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hi so our last post died, and things have gotten kinda worse with the arrival of our other cat, my elder brothers homelessness, and the racial abuse getting hurled my way
we’re two disabled black lesbians trying to navigate employment discrimination and the American healthcare system, and tbh we’re losing. we originally had to split everything between 6 people, but due to my brothers getting evicted, everything we have (and everything we don’t) also goes to them
like last time, I’m still waiting for a doctor but recently they told me to call back in November. I’ve been calling since April. I believe the stress of everything is causing a flare up of something and I have no idea how to manage it, on top of my new seemingly random food sensitivities that keep popping up. I’m exhausted all the time and sometimes can’t even get out of bed.
on a brighter note, my girlfriend applied to five jobs, but their phone was shut off this morning so it’s urgent that they pay their bill.
we were able to get some necessities early last month due to peoples help, but we can’t make it stretch with 8 people. it’s a shitty situation all around and I wish we didn’t have to ask but until my gf can get a job and I can find out exactly what’s wrong with me, this is literally all we have.
I’m not gonna link my PayPal anymore because people are harassing me with my deadname
my cashapp is $silvertheestallion and my gfs is $Peachjammn
my Venmo is cherryadventure2
thank you so much for reading
#this ask isn’t money related but if anyone has fibro or just burning chronic pain can I ask how did you know? I’m trying not to just say#oooh I have this but idk when I look at the symptoms it relates to me. I’ve found help in the fibromyalgia subreddit but I don’t know if it#is it not and I really don’t know if I can get to my doctor#I’ve been in pain for months. and nothing helps long term#and ik I should try and find a differnt doctor but I am trying#and it’s the same radio silence for months only to be told oh try again next month and I feel like going insane#I should prolly make this it’s own post
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Uh oh Sun is dying
And he’s known for awhile
#sundrop#fnaf daycare attendant#moondrop#fnaf sun#mad scientist au#lol drawing Freddy was the main reason I put this part off for so long#i need to not look at this any longer I’m gonna start hating it#so like sun made sentient plants in the hope of finding a cure#hope it’s not too subtle again#also even before moon was a thing sun was loosing memories#the symptoms have slowed with moons infection#but they’re still progressing#cw cancer#tw cancer#comic#my comics
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chronic pain vent in tags feel free 2 ignore
#EVERY time i flare up#i go down a rabbit hole of fibro comorbidities and remember i have literally all of them#almost every single tender point and textbook symptom#per the american college of rheumatology or whatever#panic disorder and migraine and mdd and a cocktail of other shit#every single one#can’t afford a doctor#anyone in a financial position to help me get a diagnosis/treatment doesn’t gaf#mom thinks all my problems are because i’m lazy unmotivated on my phone etc etc#i get treated like a dumb kid whining for attention anytime i mention my chronic pain#i’m so miserable#and then what do i do because im in pain! i relapse 🥰#i relapse over and over and over again 🥰🥰🥰#this shit is so stupid it’s almost funny#it hurts to breathe it hurts to move it hurts to lay down#gary i need a salary#tw vent#tw chronic pain#tw relaspe
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for like 2 days now i’ve been feeling like i’m getting sick but this has gotta be the most slow burn cold ever bc it’s taking FOREVER to actually kick in all the way what the hell
#it’s so weird like the few symptoms i have are making it pretty obvious it’s not just allergies#but nothing is intense enough for me to actually FEEL sick yet ya know?#plus they keep coming and going. like i’ll feel fine one hour and the next i feel weird again#what is going ONNNN#i just want it to happen already bc well.#i’m a freak who gets turned on by having a cold#sue me
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I would love to understand why my brain and body are desperate to not shower in the safety of my own home but perked up at the offer to go shower at the gym that’s full of people I don’t know and men who could pin me and locker rooms with open doorways and less control over cleanliness than I can get in my own apartment. Something something the years of swim practice and swim meet locker room showers being safe I guess?
#I’ll allow it#I’ll even encourage it if it can help me get over 6 miles walked per day again#but can I please fucking shower? I feel so gross#I have never in my life had as hard a time showering or bathing as I have this year and it’s been killing my self esteem#I feel like everyone knows I’m gross and I KNOW I need to shower#it’s important#and I don’t want my hair greasy or anything#but I go out of my way to avoid it except for an occasional hair wash or body shower when I need to go to an event#and it’s driving me CRAZY#cleanliness is really really next to godliness in my family and also I know everyone in the world views hygiene as a moral issue#and I CAN SHOWER I did it for YEARS I even did it daily for years I used to be SO good at always always doing at least the minimum#even if sleep deprived or sick#but now it’s like I’m stuck SCREAMING and slamming my palms bloody in a containment cell somewhere in the center of my concept of a body#BEGGING to just stop being so gross and to do a daily face routine and use lotion and keep my teeth healthy and keep my hair clean#and it doesn’t even matter#I’m so ashamed all the time#but my brain doesn’t give a shit about it anymore#it views the endless shame as a lesser evil and god I hope I figure out how to get that stopped#I don’t even get triggered in the shower!!! I don’t know what’s wrong! my brain just does everything it can#to keep me from undressing and showering#no matter how much I hate it#and this is so tmi sorry oh god#I’ll probably delete this later#but#shh katie#add to journal#is it the dissociation? is it the adhd? is it the ptsd?#FINALLY my POTS symptoms chill out for the winter and now THIS?
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The pain, the despair, the unmitigated agony of seeing one of your fave fanfic writers move onto another fandom, seemingly never to return.
#stinks to see how many rrr fans have dipped out#on the one hand: I totally get it cuz it’s a single movie and maintaining unlimited enthusiasm for it indefinitely#is an unreasonable expectation#BUT ON THE OTHER HAND!#I’m autistic and actually can maintain unlimited enthusiasm for something pretty much for life lmfao so I can’t relate#I also just feel sad to see how fandom culture moves so much quicker now#cuz there’s a constant never-ending deluge of ‘content’ assailing us from all sides#at all times#so it’s very easy to just burn through something and move onto the next thing#like fast food#not to get snooty about it but it does just feel like another symptom of the ever-increasing SPEED of consumption culture#and the shortening of attention spans that coincide with that#idk at the end of the day I’m just weird for forming lifelong attachments to films & shows#that I rewatch over and over again forever instead of getting into new stuff#so I secretly wish everyone in my fave fandoms could be like me and we could exist in a non-commercial state of suspended time forever#I can dream
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the christmas ruiner ➡️🧍🏼🐈⬛
#text tag#my mom really still thinks i’m getting on a plane on friday despite my refrain of ‘mac is sick. even if his symptoms do go away soon#i can’t leave him due to the chance of his getting worse again bc i can’t pay for a new flight and vet bills’#this’ll be my first time away from family for the holidays and honestly surprised by how much i’m grieving all the christmas stuff#i have a week and a half off work and the manuscript i’m supposed to be working on is late (classic) so………………#2024 really ending as the year of ‘take what you want and pay for it’#(post-christmas with mage will be nice. seeing firebird after many months will be nice. am just real sad)
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I finally got my period today 6 whole days late which is the latest I’ve ever been besides well you know. Once.
#I took 2 very clearly negative pregnancy tests in this time so I wasn’t really worried about that but the wait was still brutal#I’m very regular and the last two months have just been completely whack#when my thyroid was messed up I got one like 4 days late which was a symptom before it got diagnosed#I might need to check in there again#but like also last month was superrrr stressful and I got 2 way too close together#so I think my ETA was way too early on this one because it was based on the last cycle length yknow#so maybe being super later this month was actually just pushing it back in a normal range?#probably gonna give it another month to see if it just stays consistent again
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starting any new medication with intended or unintended mental effects is so weird. it’s not exactly like waking up with a whole new brain but it definitely feels like my mind got reformatted. this latest nervous system one is doing some what it’s supposed to physically (thank god) but it’s definitely doing… something to my thinking patterns and emotional responses. i’m not sure what. it has some overlap with the symptoms of an early manic upswing in the sense that the “regard for consequences” segment of my brain is sending an out-of-office message, so i thought it was that at first, but that’s definitely not it. but. something.
#and it’s NOT good for my job or relationships until i learn to manage it#and before you point at me the ‘girl you are experiencing a category 5 fandom event’ is a symptom and not a cause#maybe the hyper focus that tech bros abuse this thing for is just misfiring??#it’s like the brain fog moved from inside to outside??#i’m clever again but can’t see the road ahead or the people around me#i mean ‘nice’ is a deeply ingrained habit i’m not telling anyone to fuck off#my sister gave me extremely good news and i AM happy for her so that cracked through it!#but i have never thought ‘i don’t care’ in my life before unless i was manic lol#maybe posting into the void will shake it off#my exciting mental health#the symptoms
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narcolepsy is hilarious, I fell asleep but my brain didn’t do it all the way so I kept doing my tasks. Finished several quests in Skyrim, made a cup of tea, and fed my cat (I’m assuming I also gave her her pill but I can’t verify that like the other things). Was awoken by a call from my mum about the puppy she’s driving 7 hours for. I was in the middle of a fight in Skyrim and have no memory of the things I did. felt like I was back in school leaving class with a notebook full of notes and no memory of doing it. One time a teacher stopped me on my way out and thanked me for my insight on something, I still don’t know what I said but it was good I guess. Sleep me is more well spoken than awake me was something I learned.
#Baked talks#disabilty#funny disabled things#narcolepsy#i don’t know if this is a common symptom or if I’m misdiagnosed even tho all my sleep studies come back with narcolepsy#But who knows brains are silly#I often wonder if it’s actually something else cause certain symptoms don’t line up right but then again the same illness can present#Different in different people because again brains are very silly#I also have a mass in my brain but last we checked (10 years ago) it’s wasn’t growing Should probably get it checked out#Mri scans are expensive tho and my insurance hates paying for them yay Medicaid
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Oh please please please don’t let me have covid…
My body genuinely cannot take another round of it. Especially not just 7 months after the first time.
#my test is negative luckily but I am going to test again tomorrow#I do not feel right and it doesn’t feel like a normal flare up#plus I have a dry cough#which is a chronic symptom I haven’t had for a while#I’m genuinely so scared
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redditors and fakeclaimers in general are losers. you could be the "perfect" archetype of a system and theyd still find a way to fakeclaim you, dont take their opinions to heart. its rough, and easier said than done, but YOU know your experiences better than some asshole on one of the social media apps.
i hope you have a good day :>
Thank youuu
I feel like the whole “fakers/disordered” shit is very similar to the whole “truscum/tucute” arguments on tumblr/reddit that went on in the late 2010’s
#rusty speaks#system tag#love notes#they have a very similar vibe#Ik this is probably gonna be reposted to some subreddit(s) but idc at this point#the arguments on whether certain systems are faking their symptoms or not is stupid as fuck#like y’all don’t know someone’s day to day experiences other than what they post on social media#like yeah I make joke posts about my disorder and so do others#that doesn’t mean I don’t experience the disorientation and anxiety and anger and distress that others with the disorder feel#also I’m cross faded as hell again so I’m more honest that usual#I felt so anxious and stupid switching out with my Husk alter last night while at my friend’s place#I was trying to signal to my bf that we switched but he wasn’t getting it until we locked in enough to text him what was going on#I still feel so bad about telling a woman during an NA meeting “wow! you’ve been sober longer than I’ve been alive!!’’#and hearing “you’ve already told me that’’#shit made me wanna kill myself highkey#anyways toodles or whatever#I need to start writing in a diary again low-key
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I ate half a serving of some really really good pesto pasta in the evening. Just rocketed out of bed at 3 AM after an hour or so of intense rounds of pain and I’m not going to go into details but holy shit I wish I never ate more than a couple bites of it and just brought a smoothie or soup to the restaraunt instead this is AWFUL. Literally hauled myself into the bathtub with warm water just to breathe.
#will I take a sick day at work#probably not because I really need to hear those meeting discussions this week#will I have a carousel of unpredictable symptoms the rest of the night? possibly#oh my god. oh my god.#it was the best pesto pasta I ever had. it’s becoming the worst pesto pasta I’ve ever had. I am so sad#me: DO I HAVE FOOD POISONING????#also me: has a known GI condition that is the much more Occam’s razor answer to what caused this situation#and yet somehow still me: DO I SUDDENLY HAVE LACTOSE INTOLERANCE???#girl. it’s 4 am. meditate yourself to fucking chill in this bathtub.#then see if you can go back to sleep#anyway. lessons are being learned#I don’t have any idea what happened but it was sooooooooooo rich and I’m guessing it was too much fat or too much fiber or both#brb about to look up almond and pesto sauce nutrition labels#health#future me I hope this never happens to you again#gastroparesis#if I’m taking a warm bath in the middle of my worst POTS flare since 2017-2018#you know how bad I must feel to make that worth it lol
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6 weeks of breathing clean air, I still miss the smoke…..
🏝️🤙🏄🏾♀️🏄🏼♂️💔
#seemed appropriate to use t swift lyrics since I associated so many of her songs with them &haven’t been able to listen to any of them sinc#I don’t even want to say their names#if you know you know#purging them from my life has been depressing as hell#I’m so fucking sick of behind the scenes bullshit ruining my favourite ships#this is the THIRD TIME this has happened to me btw#I’ve genuinely been in mourning#I’m not even exaggerating when I say that finale triggered a days long anxiety attack for me#it’s so ridiculous how something that wasn’t even real caused me to have physical symptoms of distress but it’s true#my heart wouldn’t stop racing. chest was tight. started shaking a few times. felt lightheaded. couldn’t sleep. eating made me sick#it was awful#but now I’ve mostly moved on to anger#I’m angry at a lot of people involved for different reasons#I’m also angry because I’ve lost my inspiration to write#I was solely committed to writing about them the past few years and now that they’re over I have no desire to write for them or another shi#I’m crushed that I’ve lost my joy for writing those ficlets but it’s too painful now. probably always will be tbh#feeling pretty lost creatively…#thank god I made a new friend on here before shit hit the fan#she and I have been venting out our sadness and frustrations together and it’s helped a lot#I hope everyone else in the fandom was able to find support like I did#I know my exit from the fandom was abrupt but I had just finished watching and was reacting purley on raw emotion#but I still think it was my best way to cope with it all#apologies for the rant and to everyone following me who don’t know wtf I’m talkimg about but I was thinking about them today#and I needed to unload a bit#I’m not going to tag anything but I do miss this fandom terribly#I’m still at a point where I don’t want to hear anything about this show or ship ever again… but yeah… I really miss those good times#take me back to the season 3 hype#THIS is the bad place#personal#laura says things
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one thing abt being disabled/chronically ill that some people don’t get is that sometimes body maintenance that ensures you have the absolute minimum amount of function can also be something that takes away a lot of control and autonomy. you can argue till the cows come home that making those decisions to try and help yourself (or realistically to try to make sure things aren’t worse than they already are) is something that exhibits control and autonomy and stuff, but they can be so limiting in practice because they’re things that take up so much time but have to be done to do anything else
#i have to sleep a lot. i’m at the point where functioning requires 8 hours of sleep if not more#I should probably be getting 10+ but i’m a student and i work so 8 is the minimum. but then also getting ready for bed is a whole process s#the whole thing can take 10-12 hours depending how much im sleeping. just to make sure i can do anything#that is time in my day i cannot use for anything else. it’s not ‘oh but i can push through it’ because i can’t without spending the next da#lightheaded and nauseous and vaguely dizzy and with such intense brain fog I can’t think with my fatigue so bad i genuinely don’t know how#get myself to work a lot of days. my abled peers don’t have to deal with this at all. they have unlimited study time if they want to#and yeah it is a choice i’m making that’s true i could just not do. except i would lose my job and fail out of college because i would not#be able to get to classes or do my homework or think. but being told ‘but you are making choices about your life’ when i have lost so much#of what i used to be able to do because i am spiralling down and continuing to get worse is so.#literally last year i would wake up at 6:30 and then go to school till 3 and then go to my internship until 10 and get home at 11 and be in#bed anywhere from midnight to two in the morning and then wake up the next day and do it all again. i graduated with a 3.9 gpa and made it#into my top college while dealing with my cancer symptoms and then the two surgeries about it#but now i lose half my day to just making sure i can get out of bed. i can’t go anywhere because my body is physically too exhausted#any extra time goes into doing homework or occasionally time to myself#not decimating my health by doing minimum body care responsibilities isn’t freeing. occasionally i have a good day which is freeing but tha#usually goes into just. other things outside class or work or eating. I don’t go do something for myself or go do something fun on good day#because I still can’t. good days just mean i don’t want to lie down on the pavement when i’m going somewhere#I just. I don’t magically have control over my life because i try to get enough sleep. i lose half my day to doing that and ultimately it’s#just a bodily function that would have to happen anyway#this is a vent post im just having a really hard time right now because it feels like im in exponential decline. it was nowhere near this#bad last semester. my grades are tanking and i have no free time because anything outside of sleep is either work or school#vent tw#yall can rb this just ignore my tags completely#disability#chronically ill#i keep trying to explain to people how pots works because that’s all logical but there’s no way to explain what it’s doing to my body or ho#i feel all the time. the last time i felt this bad was when i had a bad flu or immediately after surgeries because i don’t react well to#anesthesia and always come out of them feeling like shit. and now i just feel like this all the time and it’s only getting worse#I can’t even stay up late anymore because my body feels like it isn’t counting the sleep even if I get 8 hours#I can deal if I have a free day the day after but that just leaves Friday and Saturday nights and I usually still have to do homework
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