I hate being so self aware of my anxiety and chronic illnesses that it’s not even a surprise when it all flares up.
It’s more like:
oh so this is today’s shitshow?
okay thennn
seen from Germany
seen from Brazil
seen from United States
seen from Sweden
seen from United Kingdom
seen from Sweden

seen from United States
seen from Germany

seen from Australia
seen from France
seen from United States

seen from France

seen from Germany
seen from United States
seen from United States
seen from Australia

seen from Germany
seen from United Kingdom
seen from Yemen

seen from Germany
I hate being so self aware of my anxiety and chronic illnesses that it’s not even a surprise when it all flares up.
It’s more like:
oh so this is today’s shitshow?
okay thennn
Current Mood
wanting to rip out either my spine or nervous system
Little doodle I did between classes. I’m in the middle of the worst fibromyalgia flare I’ve had since I was diagnosed, and this is one of the first things that popped into my head. How pain pills don’t help us fibro patients.
[Archives] What the biggest cost of chronic illness really is, and how I try to manage it. Read it here: https://is.gd/illexpensive⠀ .⠀ .⠀ .⠀ .⠀ .⠀ #chroniclife #chronicpain #chronicdisease #chronicillness #invisibleillness #spoonie #spoonieproblems #spoonielife #spoonies #lupus #sjogrens #antiphospholipidsyndrome #epilepsy #awareness #lupusawareness #health #healthcare #flareups #meds #medications #doctors #hospitals #doctor #doctorfees #hospital #medicalbills #medical #illness #billstopay
When you feel that flare coming and you know there’s nothing you can do but ride it straight to hell.
Me after doing all the things during a low pain day
Trying to keep my shit together in public when a flare hits.