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#psoriaticspondylitis — Public Fediverse posts

Live and recent posts from across the Fediverse tagged #psoriaticspondylitis, aggregated by home.social.

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  1. @samhainnight I am—I have to come off my meds for #PsoriaticSpondylitis for 10 days (5 before, 5 after) to vax, so I try to do them all at once.

    Good luck with MediCal—it’s a pain signing up, but it’s worth it. My m-i-law is on it. I love this state. ❤️

  2. The drug I take for #PsoriaticSpondylitis is nearly $9k a month from CVS Caremark. If it weren’t for insurance (which covers 80%), I’d just have to die. #BigPharma

    From: @cbarbermd
    med-mastodon.com/@cbarbermd/11

  3. I really really REALLY want an #UnfittedKitchen. When we first moved here, we rented an apt in San Diego w/ a huge kitchen. It had a big empty wall—I think most ppl put a kitchen table+chairs there, but I lined up tall industrial shelves instead, & I LOOOVED IT. It makes cooking so much easier, especially for someone like me, who has #PsoriaticSpondylitis (loads less bending/stooping). apartmenttherapy.com/unfitted-

  4. @dangerousmeta Good to know--thank you. I'll tell him. Has your wife had it? I had to come off my #PsoriaticSpondylitis meds for 2 full wks, which srsly sucked. I have to stop taking them 5 days before & 5 days after every COVID vax, too. BLEH.

  5. @Brian_Mahoney I never used cannabis when I was young--I tried it when I was 15 or so, & I hated the way it made me feel. But none of the meds I've used for #PsoriaticSpondylitis help me very much, so I started supplementing with gummies (with my docs' full approval) so that I can at least sleep at night, & they've REALLY helped.

  6. A mani recommendation!

    You guys know I have #PsoriaticSpondylitis , which is basically #PsoriaticArthritis that affects my spine & SI joints. Outside of that, it rly jacks w/ a couple of organs (liver & lungs) & my nails. Oh, my poor nails. They're a MESS--brittle, thin, weak, & w/ ridges that constantly split & bleed. I used to wear acrylic nails, but they're just so unhealthy. Plus, they're expensive & require a 3 hr round trip to have them done every month. +

  7. This is such an important thread.

    I have #PsoriaticSpondylitis . The drug I take for that costs apprx $10k /month—our health insurance covers 80% of that. Before #Obamacare , my illness would’ve been a pre-existing condition, & they’d have covered 0%. ZERO. None of my rheum appts would’ve been covered. No x-rays, no scans, no nothing. If a doc visit or procedure pertained to my illness, I would’ve had to have paid for it out of pocket—or simply skip it. #HealthInsurance mstdn.social/@mcnado/112078115

  8. A 🧵!

    I went back & forth about whether I should share this, bc it's not only gross, it's rly embarrassing. But it's common knowledge I have no filter. So. You may be wondering why I haven't shared any photos of the beautiful CA coastline. Well, it's because there aren't any. I think most of you know I have #PsoriaticSpondylitis . With PS comes #UlcerativeColitis . Fortunately #Rinvoq has had my UC pretty much under control for quite some time. But when Maddy & I were leaving SF, it decided to +

  9. I feel so, so rough today. So weary. I think I’ll share a photo of my sweet Teddi getting her ears scritchied & hit the hay. I hate this illness. #PsoriaticSpondylitis #DogsOfMastodon

  10. I switched ankylosing spondylitis/psoriatic spondylitis meds today. I've been on Cimzia for a few months; it didn't really help me. I started taking Rinvoq this morning. One pill a day instead of an injection every 2 wks--I like that. Pls cross your fingers this drug works. I'm running out of options. #worryandfear #fearandworry #psoriaticspondylitis

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