seen from Yemen
seen from United Kingdom
seen from China
seen from China
seen from United States
seen from China
seen from Tajikistan
seen from United States
seen from United States
seen from T1
seen from Germany
seen from Netherlands
seen from United States
seen from China
seen from China
seen from Canada
seen from Türkiye
seen from Poland
seen from France
seen from China
My favorite YouTuber posts every Friday, so I’ve formed a nice ritual where every other Friday when I have to do my biologic injection I watch that week’s video while I wait for the shot to get to room temperature. It calms me down and makes having to stab myself a little less terrible. I’m glad that there are small ways that can make living with chronic illness more bearable.
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
question for people with (nr)/axSpA: does stiffness make it uncomfortable the first few moments after laying down? i’ve been experiencing this for so long and it’s not particularly painful but it’s fucking annoying
the long-awaited (by me) info sheet on ankylosing spondylitis symptoms, research, and myth debunking is now available! send it to your friends, your enemies, your chronic illness groupchats, print it out and staple it to your local telephone polls - and please let me know if this is helpful, if you have questions, and if there’s anything you think should be added!
https://docs.google.com/document/d/1LLfI4ACQyiiLViyqVO030cTalZAFGfmu8n5-KuLzrrg/edit
what your doctor didn’t tell you about ankylosing spondylitis by mac @crippleprophet note: this is a living document, so I will be updatin
a cousin of mine told me she’s “so sorry to hear” that i have to use a walker now and i know she means well but using a walker has been a life-changing positive change in my life so getting pitied for it makes me so uncomfortable
Confession #4,590
I got diagnosed last year with AxSpA and fibro but that may have been wrong and now I'm back to not being sure why I am in constant pain. I've had to be off my NSAID for 3 days and I'm already in excruciating pain all because I have to go for an MRI tomorrow to see if I actually do have AxSpA. If that wasn't enough I have to move out of my house asap and it gets worse - now I can't apply for skills tests so I can get my dream job far away from retail because I need a fucking contact address.
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
Once again it seems I am the only patient under 40 in the rheumatologist’s office fun fun fun
bawling my EYES out. while my rheumatologist is still unclear on my diagnosis, she wants me to try humira to see if it helps and i finally feel like i’m being taken seriously, like she actually wants to figure out my condition
my girlfriend, doing her med school rheumatology unit feedback after they perpetuated the myth that ankylosing spondylitis has a 3:1 male:female incidence rate: and of course i’m going to mention the bullshit about AS—you don’t happen to have that citation, do you?
me, already pulling up the google doc: oh of course i do
