#and i'm fatigued already
Explore tagged Tumblr posts
Text
existing is so damn tiring sometimes a lot of times
#i woke up 0.5h ago#and i'm fatigued already#it's not even like something happened there's no reason for me to feel this way and it makes me feel even worse#neverending cycle or some shit ig#i want to draw or write but my head's completely empty#and i don't have the time#god if you exist why did you make me such an annoying bitch#compulsively complaining even though there's nothing to complain about#i want a different brain ;w;
2 notes
·
View notes
Text
pest control TWO!!!!! heres the first one
adn heres the obligatory bonus bc i can't help myself :')
#i already threatened that little basard twice in these i may as well make good on it#pizza tower#peppino spaghetti#fake peppino#the noise#fp ''oh god wait that is not a real rat and also tastes awful'' moments. he doesnt actually have any interest in eating that thang ok#even if seeing a small scampering little guy like that WILL activate his prey drive without fail#peppino loves it he thinks it's the funniest shit in the world for fp to go after noise. so he is always encouraging this.#but anyway yeah. fp is *really* not the one noise should be worried about.#arting#pizzaposting#i still have lots of tag room thjis time so im gonna do some tangential nonsense rambling. e#fp gotta be like crazy good at hunting i think. not just for strength and predator instincts but also bc like#he doesn't have much in the way of a scent or body heat or anything that would give him away as an alive thing#not to mention he's uh... not particularly organically-shaped a lot of the time#so esp. to smaller prey that don't like... memorize a landscape; if he holds very still he's like completely undetectable#total ambush king. though i'm sure hes also very good at#persistence and pursuit hunting since he has peppino's speed and no way of getting muscle fatigue. ultimate beast#fortunately he doesnt care that much and doesnt really need to eat so hes not devastating the local ecosystem or anything#except for the rats.
881 notes
·
View notes
Text
Communicating with medical staff is its own special circle of hell. Do they even read your messages before they respond??? This can't just be my set of doctors, can it?
#I'd write it off if it only happened 2 or 3 times but holy shit it's all the time always#Sometimes they answer a question comically irrelevant to what I asked#This time a nurse stepped in to lmk that I can't have the labs I requested unless I'm currently experiencing fatigue#I let them know I have been for YEARS (they should already know this. It should be all over my charts)#and a DIFFERENT NURSE replies#saying sorry I read all your messages and labs and we can't run that test unless you're currently experiencing fatigue :/#And I have to wait up to a week sometimes for a responce!!!! Makes me want to scream
14 notes
·
View notes
Text
hey guys where should I go to get checked out for chronic fatigue syndrome...
#as somebody who's already got a fair share of chronic illnesses and such i don't take this lightly but ALSO#saldy my body seems to want to take everything it can get!! so ironically this would just fit perfectly and idk what else#but there's little to no informed online and despite knowing my medical history I'm not about to go to my GP#and be like 'HEY so i did some research AND how can i get evaluated for cfs thnx#me/cfs#cfs#chronic fatigue syndrome#also to those of you that have it#you don't happen to have a chiari malformations as well? I'm just interested if these maybe go hand in hand#thx#disability#diagnosis
44 notes
·
View notes
Text
so gonna be real I barely do life updates here anymore but I've got some bullshit coming up in my personal life that's not looking good. I said I was working on finding out what's wrong with my health from doctors and getting help for a bunch of stuff in my life in general and getting a support system and stuff and I was and it was going well and things were looking up
but now I've been forcefully inducted into some programme thing to push me into doing something I'm physically incapable of doing with my disability but it's apparently mandatory or I'll lose some of the support. I don't know why they decided I can when they know of my issues (and they haven't even recieved the form where they're supposed to be checking for my capability yet so wtf) but apparently there's no way for me to opt out and it's going to last for a year at least
and I've seen a lot of negative things about this program when I wasn't even seeking bad reviews, the majority is negative. so my life might be about to go to shit for a while and I'm already feeling miserable and it hasn't even started yet lol. this may genuinely badly affect my mental and physical health which I've been working so hard to deal with lately so it's very upsetting and stressful
I hope it's not going to take up all my time and I can still be as active as I want to be here because it's one of the things that actually brings some brightness to my life. I also hope all the stress it's going to put me through doesn't affect my behavior here and seep into what I do but I'll try my hardest not to let that happen because my blog is one of the very few positive things in my life atm
best case scenario is they realize I can't do this and take me off it but it's not looking good. that would be more likely in a perfect world where people could take invisible (well mostly invisible for me) disabilities seriously. because I'm not even that hopeful about the doctor stuff at this point, maybe it's just because it's taking so damn long for the referrals I need for them to check me out in the areas needed but I don't know if they'll even find out what's up with my chronic pain and or if I'll get a diagnosis
so yeah I think I'm actually just screwed and life is about to become even more painful and exhausting for me than it already is and a hell of a lot more stressful as a result but maybe if it leads to my health worsening like fainting in front of people again it'll be enough for them to see that this was a bad idea haha. I mean first of all my first meeting about this has been booked for me the day I'm literally taking an 24 hour ECG test because they won't even let the doctors try to finally find out what's wrong with me before pushing me to do this ffs
#delete later#I've already been struggling with terrible fatigue lately even worse than I usually have it#so I haven't been able to do so many of the things I love or talk to my friends here or anything f#because I'm so tired when I'm done with everything for the day#I'm worried that it's about to get so much worse because of this. I'm so stressed and upset#and that's without all the fucking physical pain that's going to make me miserable when it causes more flare ups#whatever. just thought I'd say because it's had me in an awful mood already and it hasn't even started#I really don't want that to seep into all my posts
14 notes
·
View notes
Text
Hahaha I can't eat at all today and I keep feeling like I'm going to throw up, why is my body this
#i'm gonna be real with yall#we're nearly at the point of me writing my gp and telling him that look#i haven't managed more than about 2-3 cups of food a day#and none of it can be meat-based or wheat based or dairy based so what keeps happening is i'm literally fucking starving#i don't know how to get to a point where i can eat and my nutritional levels are all low enough already before this started that#my doc wanted me on vitamin supplements which i haven't been able to source yet#so now that we're like a month into me being completely alienated from food i'm starting to have some real problems#cannot describe the level of fatigue and cognitive decline that's been happening for me and that's not including the physical decline#i've literally been huddled in the bathroom for like half an hour because i can't get my stomach to settle and i want to scream
10 notes
·
View notes
Text
Annoyed bc i'm just so so tired and can barely keep from falling asleep much less do anything but lie in bed.... Hmm i wonder.... *Checks blood pressure* *96/51* ... Yep that'd fucking do it :/
#and anything online and from dcotors is always “how to lower blood pressure” “what foods to lower blood pressure” “high blood pressure?”#and there's just nothing on how to raise blood pressure#“drink more fluids” yeah#i already am what do you think i'm doing??#increase salt? drink electrolytes?#it's just not doing anything#and low blood pressure is making me so fatigued i can barely sit up#and even when i do#I can't hold up my body#disability#chronic illness#disabled#chronically ill#low blood pressure#fatigue#rant#vent#how is this my life??#why is this my life??#cripple punk#tumblr
15 notes
·
View notes
Text
Chronic Pain/Fatigue & Cleaning
I generally clean in small, bite-sized amounts, spread across several days which makes it more manageable and allows me to stay on top of mess
Today however, I accidentally dropped some stuff, requiring me to use Henry Hoover, as it wasn't something a brush would clear up
The hoover/vacuum is like a final level boss fight when you have chronic pain and fatigue (for me)
It is SO HEAVY, even just pulling it around, not lifting with my arms. The back and forth across carpet feels like I'm scything grass, I'm using all of my weight to push forward and pull back the hoover head. Tilting my head down makes me feel dizzy, that feeling you might get on a rough boat trip.
Pain creeps in, crawling up my shins and wrapping around my shoulders
After I finished hoovering that small patch, I am sweating through my back, I can feel the beads slowly rolling down my neck & I can barely catch my breath. I feel irritated by the sweat, uncomfortable, unsteady on my feet, so I go back to my safe spot
I sit down, immediately my left arm and hand is tingling and burning, like when you've been lifting weights in repetition and the jelly-feeling comes on. Then it begins in my right arm & hand. There was still tingling in both hands 20-30 minutes later
I remember the before-times when I would dedicate my Sundays to cleaning, I could do it all in one day, preparing myself and home for the week ahead. That would mean dusting, polishing, hoovering, mopping, clearing dishes and so on
I can't do it like before. It makes me feel so useless & weak, another reminder that my body doesn't work like that anymore, that I'm not the same. It's frustrating to see the accumulation of "what I'd like to clean" and then realise the little amount I am actually able to and it makes me feel dirty. I can't remember when I was last able to clean my dishes
Oh to go back to before so I can just "be" without consequence
#chronic life#chronic pain#chronically ill#chronic fatigue#as if finding energy to shower isn't already hard enough on its own#chronic pain syndrome#joint pain#i'm in pain#chronic illness#fibromyalgia#myalgic encephalomyelitis#fibro#spoonie life#spoonie problems#no spoons#idk what this is
89 notes
·
View notes
Text
I need to get back into morning person mode. Morning person me was so productive and happy.
#I'm usually the opposite of a morning person#But those two months of starting work at 6am to escape the heat turned me into one#And I kept it up for almost the entire year to get up at 6am which even felt late for me#Because that was 7am in Germany when I'd been at work already for an hour just a month prior#And I had an hour long breakfast every day and didn't stress about being late and just enjoyed the morning#Went over some notes#And then in winter I got up slightly later because it was so dark#But I mostly kept it up for a year or so until I was back in Germany and finishing up my thesis and too fatigued#And then I had my depressive phase this year
7 notes
·
View notes
Text
one thing that's really fucked me up after becoming chronically ill is that my balance has become awful, like nowadays i have trouble walking in heels on uneven ground while younger me could do basically anything in heels, sometimes if i turn or stop too abruptly i nearly fall over, it's awful
#chronic illness#postural orthostatic tachycardia syndrome#pots#cfs#me/cfs#myalgic encephalomyelitis#chronic fatigue syndrome#idk which of my many illnesses is causing this tho#my eds probably makes it worse tho#but i don't think eds is the cause because it's genetic so i've always had it#i'm so sad that i have trouble in heels nowadays cause#1) they make me even taller than i already am which is fun#and 2) they look pretty and i have some that look really good with certain outfits
11 notes
·
View notes
Text
#kirby#daily kirby#my art#digital#hal laboratory#nintendo#favorites#saw someone I stopped following from some nebulous Bad Vibes say some real Dumb Crap that I'm so tired of hearing already.#so I gotta complain about it for a bit before I can wind down and sleep -n-#at least I'm only normal tired today instead of super double tired.#*normal-for-me tired#which is. much more than normal tired. as I have debilitating chronic fatigue.
76 notes
·
View notes
Text
the flu really starts hittin different on day seven of it
#that's when the ''THIS WILL NEVER END I WILL NEVER BE NORMAL AGAIN'' anxiety starts kicking in#right now my brain is in ''i want this to be over already so the fact that it isn't means I'm DYING'' mode#even though almost all my symptoms are gone and i'm just coughy and fatigued now#and even tho by this time next week i'll prolly be fine#anyways y'all!! please get your flu shots if you can!! i forgot and it is absolutely beating my ass rn. pls stay safe.
7 notes
·
View notes
Text
My sleep schedule this past week would bewitch some sleep scientists, I'm certain
#For the record:#Sat to sun 5am to 4pm#Sun to mon 3am to 3pm#Mon to tue 6am to 6pm#Tue to Wed 10am to 8pm#It is now thur 9am and I haven't slept and my current plan is to stay awake until I physically cannot anymore in the hopes of resetting this#I'm already starting to feel delirious but I'm hoping I'll somehow hold out till at least 6pm#And if you're wondering#Wow what has she been doing all day to need THAT much sleep aka almost 12 hrs every day for the past week#Absolutely nothing lads#Last time I left the house was the 2nd of March to go to a friend's bday dinner and since then I'm just existing#Gotta love chronic fatigue#At least I'm seeing daylight again today#Haven't in the last 3 days#If you made it this far in the tag rant ily and hope you sleep well tonight <3
8 notes
·
View notes
Text
why do we have summer already? last time i checked it was february
#im so tired#while i'm already chronically fatigued any temperature above 15C is sucking the remaining energy out of me#don't get me wrong i'm happy to have one warmer day and go out on the sun for a while#but soon i won't be able to sleep again and i'm gonna be a ghost for few months#and everything gonna be sweaty and ughh the horror of wearing less clothes or dying in jeans on 30 degrees#it cam stay how it is now fine but we can't have summer yet boys i can't take it
18 notes
·
View notes
Text
cried while doing my physical therapy, but i got through it. how i'm gonna be able to do these new exercises 3/4 times a day is beyond me, but i'm done for today. yay or whatever
#i thought this shit was supposed to get easier the longer you do it#feels like fucking torture#i feel so frustrated and useless not being able to do such easy looking movements#but ig that's the point#them being specifically made to strenghten parts of my body that are fucked#idk man it just sucks going through this 3/4 times a day and once a week with a pt#acupuncture two times a week#and regular therapy once a week#my chronic fatigue and chronic paint can't handle this pace i've broken down three times already and it's only been two weeks of this#that's on top of regular life shit and other doctor's appointments too#god i'm just so tired#*mina.txt#health cw
5 notes
·
View notes
Text
Bleh
#thinking about shit#getting really tired and stressed with everything going on#and I'm seriously starting to wonder if this is my next breaking point#and if I'm going to be forever worse bc I kept pushing myself with my me/cfs#that's the fucking scary thing about it; not knowing if I'm doing to accidentally do something wrong and make myself permanently worse#and I don't know how to explain these fears other than fucking terrifying#to literally be entirely unaware of the true limitations of your body and not knowing if you're going to make yourself worse by accident#I cannot wait for the move to be over#once we have a legal address together I can get on my husbands insurance and beg him to quit#I am incapable of working a traditional job as it is but I'm forced to because I have no other options#so I'm already pushing myself on a regular basis#and I fear every flare up is just going to be my new normal#and what if it is just a flare up? I have to keep working I have to do my job I have to do chores I have to pack#will working myself this hard during the flare up lead to something worse?#I can't do this anymore I just fucking can't#I can't stand not knowing if this past year is going to permanently incapacitate me#I'm already reliant on my husband for everything short of carrying me to the bathroom and wiping my ass for me#I hate not being independent and I hate the idea that I might be stuck in this much pain and this much fatigue for the rest of my f'in life
2 notes
·
View notes