#Chronic Migraine

[spacefae]

I reblogged this and then found out this morning that my migraine medication was denied by insurance. I've been on it for 4 months, no problem. I'm currently waiting for the doctors to authorize or for an alternative to be given. This is the first time in my life that my migraines haven't controlled my daily life. I'm so angry.

[sketchjay]

Migraines are so odd, like wdym I have a headache and now I'm temporarily blinded

[chronicallydragons]

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

[disabled-bug]

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.

[raging-guanche]

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

[s-ccaam-era-crepe]

i think everyone who's ever had migraines should be financially compensated forever btw

[johnlennonirl]

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

[thebibliosphere]

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.

[chronicallymistreated]

People only have so much patience for those of us with chronic illnesses, chronic pain, and or mental health difficulties.

At the beginning there is so much support (or at least more support) but when they realise you're not recovering as quickly as they'd like... you get avoided, isolated, told you're exaggerating, etc. They seldom think about how those of us with chronic issues feel. How overwhelming it is to deal with everything day in and day out. There is so much anxiety, depression, grief, etc when dealing with chronic issues regardless of what they are.

If you're even more isolated because people refuse to see how much you're struggling or you're not recovering "fast enough" for the people around you just know you're not alone! There are so many of us in the same boat too

[drifting-bones]

they should invent walking that doesn't make you feel like you're going to keel over and die

[gabbagepatch]

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.

[chronically-ill-and-feral]

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.

[blitzsicedcoffee]

Me: I'm feeling so creative today! I wanna draw, I wanna write, I wanna create! I wanna play games!

My disability: mhmm thats great but I have strict plans for you to have a six hour long migraine where you're crying in bed and so nauseous you can't eat anything. Sooooooo.

[tofu-bento-box]

perhaps i am simply a delicate spoiled houseplant but i don’t think having a fun productive day should give you multi-day hangovers

[disabled-bug]

disabled people when their disability disables them

[raging-guanche]

my mom just got mad at me because "i have to rest every time i do the littlest thing even eat" is almost like youre chronically fatigued when you have chronic fatigue