#Chronic Migraine
Explore tagged Tumblr posts
Text
yes but it goes like this: "um no i'm not that ill i'm just lazy and i need to push through"
*pushes through*
"am i dying right now why do i feel like this"
"oh maybe i actually am sick"
"no, this cannot be true, everyone was always saying that i'm just lazy - i am imagining these symptoms right now, i need to collect myself and stop being silly"
*dissociates*
*does another thing*
"yeah now i'm already dead"
*waits until it gets a 1% better*
"yeah i'm not that sick, i was able to dissociate and do the thing so that means i'm healthy and i just want attention, i'm completely healthy i should do this and this and this now"
*failes to do anything cause i did too much and i can't move from pain*
"i'm just lazy i should kill myself"
#chronicillness#chronic illness#chronically ill#invisible disability#disabled#disability#chronic pain#chronic migraine#chronic fatigue
503 notes
·
View notes
Text
yeah...
#chronic life#chronic illness#chronically ill#chronic pain#chronic fatigue#spoonie problems#fibromyalgia#myalgic encephalomyelitis#chronic migraine#multiple sclerosis#MS#CFS
25 notes
·
View notes
Text
Chronic migraine haver Darry going to work despite the blurry vision
Chronic migraine haver Darry trudging up and down the ladder slowly because his head is pounding something awful
Chronic migraine haver Darry who’s boss calls Soda the moment he notices Darry not working as hard
Chronic migraine haver Darry almost crying from relief when his boss sends him home
Chronic migraine haver Darry who gets basically carried into the house, all his strength zapped
Chronic migraine haver Darry who has to sit on the dark, bathroom floor in case he needs to throw up
Chronic migraine haver Darry who lets out a big sigh when Ponyboy put a cold wash cloth on his eyes
Chronic migraine haver Darry with a heating pad on his back, muscles so tense he can barely move
Chronic migraine haver Darry falling asleep with his head in Soda’s lap while he was massaging his head and neck
Just chronic migraine haver Darry
#the outsiders#darry curtis#ponyboy curtis#sodapop curtis#chronic migraine#sickfic#kinda#pushing my problems onto fictional characters
29 notes
·
View notes
Text
Being 90% bedridden feels like torture if I love being productive. I'm reading more books lately to stop being online all the time, but I'm barely able to focus and after a few hours I'm unable to focus at all. I'm basically dissociating for a large portion of my day. I could watch TV and such, but I'm just 'consuming' and I feel empty when I do this for a long time.
I need to reframe my thinking on 'productivity', 'usefulness', 'wasting time', but it's really hard. I see people enjoying their life, the world keeps spinning and I'm just alone in the same bedroom. It's lonely, isolating and everything I do feels useless.
I feel like entertainment is never meant to be watched for 24/7, it's meant to be a treat after a day of productivity.
#chronic illness#chronic pain#disability#disabled#chronic migraine#fibromyalgia#gastroparesis#chronic fatigue#migraine#bedridden#feeling alone
20 notes
·
View notes
Text
me with the chronic pain, desperately wanting to do so many things but being physically unable to, going blind from the headache, genuinely scared i'm dying right now because of how bad the pain is:
"i'm so LAZY, i just make this all up because i want attention, i only need to motivate myself, why am i so lazy i should kill myself, i'm completely healthy i'm just too stupid to motivate myself, these symptoms are just my hallucinations, i have delusions because i want attention, i should kill myself if i can't even work while being completely healthy"
#chronicillness#chronic illness#chronically ill#chronic pain#chronic fatigue#chronic migraine#invisible disability#gaslighting#medical gaslighting
23 notes
·
View notes
Text
anyone else ever wish they could lie down harder? Like, I'm already horizontal, but I need more horizontal. I need to be absorbed by the floor. I think that would fix me
#My orthostatic tolerance is currently zero#POTS#postural orthostatic tachycardia syndrome#me/cfs#fibromyalgia#chronic illness#disability#migraine#gastroparesis#chronic pain#chronic fatigue#chronic fatigue syndrome#myalgic encephalomyelitis#spoonie#mast cell activation syndrome#MCAS#dysautonomia#chronic migraine#joint pain#hEDS#ehlers danlos syndrome#hypermobility#hypermobile ehlers danlos#interstitial cystitis
34K notes
·
View notes
Text
I’m so proud of people living with chronic health conditions. That shit is HARD. Idk who needs to hear this, but if no one else has said it: I’m proud of you. You’re sticking it out through so much pain and grief. That’s no small feat.
Every small thing you do for yourself health adds up. The grief is heavy and it comes from a place of love. The grief knows the pain is wronging you.
I’m proud of you. I hope on the good days you can be proud of yourself.
Keep going.
#chronic illness#disability#chronic pain#spoonie#ibs#chronically ill#gerd#pots#arthritis#spoonie life#chronic illness blog#chronic health issues#chronic fatigue#chronic health problems#chronic disability#spoonie stuff#spoonies#encouragement#endometriosis#disability pride#proud of you#fibromyalgia#postural orthostatic tachycardia syndrome#irritable bowel syndrome#gastroesophageal reflux disease#gastrointestinal#uplifting words#chronic health tag#chronic migraine#autoimmune disease
5K notes
·
View notes
Text
friendly reminder you dont need a diagnosis to be in disability spaces, as an example im in constant pain and fatigue, have migraines every week and my joints hurts to a point I can't write, but since familiar gaslighting/medical trauma and the fact that im an indigenous, brown skin fat man a diagnosis is fucking hard (but im in my way! :)) , but i still deserve a safe space to talk about my experiences and to feel valuable and supported.
never feel like youre interrupting someone's space or that you shouldn't be here cause you dont have a diagnosis, disabilities existed before diagnosis
#fatphobia#disabled pride#disabled community#actually disabled#pro self dx#pro self diagnosis#chronically ill#chronic migraine#chronic illness#chronic pain#chronic fatigue
7K notes
·
View notes
Text
i think everyone who's ever had migraines should be financially compensated forever btw
#camera talks#disability stuff#this is for my chronic migraine girlies (gn) <3#i think we should all get 1 million million dollars everyday actually#this is the worst fucking night of my life (everytime i have migraines) (specifically rn tho)#chronic pain#chronic migraine#migraines#chronically ill#disabled#disclaimer because idk I’ve got a lot of notes on this#I have diagnosed chronic migraines. I used to have them 5-6 times a week#now with medication on a good week I’ll only be affected 2-3 days#on bad weeks it’s much worse#anyways don’t doubt my condition I know what I’m talking about thx
32K notes
·
View notes
Text
Yesterday the 12th of May was Fibromyalgia awareness day. I'm a little late uploading it, but spreading awareness is being done nonetheless. Lots of love for my chronic pain people!! <3
#fibromyalgia#fibromyalgia awareness#chronic illness#chronic pain#disabled#disability#disabled artist#chronic fatigue#chronic fatigue syndrome#hidden disability#invisible disability#spoonie#chronic migraine#migraines#artist
28K notes
·
View notes
Text
Have you ever vomited so hard you not only wrecked your throat but dislocated your collarbone?
How about a migraine so bad it triggers your mast cells into a pre-anaphylactic reaction and you start breaking out in hives all over your body?
Yeah. Me neither until 4 o’clock this morning.
New level of hell unlocked.
And the migraine is still ongoing. I’m just no longer blind and dry-heaving.
I hate this.
#chronic health tag#chronic migraine#tw vomit#tw body injury#my collarbone is back in but everything hurts so bad#if I can’t keep this water down I’m heading to the ER
4K notes
·
View notes
Text
Legit one of the hardest lessons I had to learn. Being exhausted it okay.
46 notes
·
View notes
Text
It's odd getting diagnosed. I've waited YEARS for the 'right' one to be given. I lost count how many times i cried & begged for help, medical care, further testing. The isolation of illness, quiet suffering. Then, one day its as if im going to get answers, finally. Within all the fuckery they go "you have ___" the relief of that wasn't really any weight off, I felt nothing. "Yeah that makes sense" i remember the neuro staring at me waiting for some sort of reaction but I didn't have any.
And then it came. It went from a diagnosis to "if you get worse, get in touch" but what i heard was "we don't care until you are worse, we will do little intervention to stop you from getting worse, but please, dont stop living your life"
They really did say 'go about life as normal' completely ignorant of my normal, despite the long list of symptoms I've described, written notes that are in my file. But *hooray,* I'm back waiting again!
So now? I wait, trying to go about life as normal, wondering how I will even notice getting worse, cos no-one ever believed me before, why would they now?
forever the pessimist, especially when it comes to healthcare
#chronic life#chronic illness#chronically ill#chronic fatigue#chronic pain#spoonie problems#fibromyalgia#myalgic encephalomyelitis#chronic migraine#multiple sclerosis#chronic disability#disability
23 notes
·
View notes
Text
they should invent walking that doesn't make you feel like you're going to keel over and die
#disability#disabled#physically disabled#me/cfs#myalgic encephalomyelitis#joint pain#joint problems#cripple punk#physical disability#mobility aid#cane user#mobility aid user#ow my joints#chronic fatigue#chronic pain#chronic illness#chronically ill#chronic migraine#long covid
4K notes
·
View notes
Text
Listen guys, you don't need to look nice to go outside. Your health is more important than appearances.
I just went on a walk in my pajamas, greasy hair in a shitty bun, acne, and a pair of new balance sneakers. Cars passed by and I said hi to everyone who passed. Did I feel self-conscious? Of course, but it was worth it.
Now I feel a lot better, because I didn't A. Overextend by forcing myself to shower/get dressed/put on concealer beforehand or B. Avoid doing anything because I felt like a mess.
Go outside and be however you are. It's not your job to look good to random strangers, you deserve to go outside.
#someone get me a cookie for walking with a migraine#i feel very brave#disability#disabled#hearing impaired#meniere's disease#chronic illness#hard of hearing#chronic disability#chronic pain#chronic migraine#chronically ill#invisible illness#illness mention#invisible disability#disability pride#blurb#exercise#accessibility
2K notes
·
View notes
Text
this is the picture I show any doctor when I have to go.
Anymore, when I get asked about my pain, I just hand the doctor my phone. I've been at a constant 8 on the chronic illness side of the picture for a year and a half now. I hate it but I thought this could be useful. I straight up got the off of Google so I am unsure who to credit for the original but I have been a great help to me so I wanted to share.
3K notes
·
View notes