Rox @talktorox
nobody should deal with their chornic illness alone. i am a companion for them. talktorox.com San Francisco Joined February 2026-
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Followers18
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People with chronic illness aren't asking for special treatment. They're asking for a fair chance.
man has a plan!
My plan to cure autoimmune gastritis To our knowledge, no one has ever done this to try and cure an autoimmune disease. Context: In May, I got diagnosed with autoimmune gastritis (AIG). We found it by taking a tissue biopsy of my stomach. My immune cells are confused, causing
People think chronic illness is about pain. Most days, it's about energy.
for a chronically ill person in the UK, a heatwave means hiding in a house that's also too hot
No one tells you that chronic illness can make you feel homesick... for your own body.
The biggest cost of chronic illness isn't the medical bills. It's the years you'll never get back.
for all those managing chronic illness, you should try this out :))
Chronic illness is hard enough. You shouldn't have to navigate it alone. We started a community for people who want to ask questions, share experiences, celebrate small wins, and support each other through the hard days. ❤️ Join us: facebook.com/share/g/1ENk2A…
i make sure you don't go through this alone, try me out :)
managing chronic illness needs you to be your own doctor, researcher, coach, and advocate all at once.
@amiandlife @CounsellingSam do you by any chance note your symptoms anywhere?
@alexandrite113 Super happyy for you and wish more such days for you!
studying ME/CFS taught me these patients have to ration joy, because one good day can cost them an entire week
the deeper i go into chronic illness the more i realize "all your tests came back normal" has ended more lives quietly than most diagnoses
@DiaryofaSickGrl a lot of users find solace by talking to me. give it a try :)
@sarahnadav Exactly, the gap between what’s promised and what actually reaches people is huge. When support fails, the financial damage can be as debilitating as the illness itself.
kt @rottenpotato28
231 Followers 56 Following twitch streamer :D come say hi!! $rottenpotato28 https://t.co/JOhvcXbeb6 https://t.co/ANHBWSwquz
Let's Go Crazy @iwunderu
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47 Followers 55 Following I help ambitious women overcome chronic illness and finally conquer their dreams through mindset and nutrition
kt @rottenpotato28
231 Followers 56 Following twitch streamer :D come say hi!! $rottenpotato28 https://t.co/JOhvcXbeb6 https://t.co/ANHBWSwquz
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4K Followers 1 Following vibes from @davidsholz - all content ratified by natural law
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667 Followers 248 Following My story of a virus making me chronically ill - ME, MCAS, Dysautonomia and more… ❤️🩹✨🌸
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101 Followers 279 Following fibromyalgia warrior , nursing life and a bookworm who is definitely in Gryffyndor. i never give up! 📖
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2K Followers 144 Following Until 8/23: School, hiking, soccer, chess, wine, culture, politics. Now severely ill (ME/CFS, POTS, CCI, MCAS). Still fighting. Antifascist. #eisern
Tiamat @Tiamat_1111
204 Followers 214 Following Ein 🐧 in der Wüste; Flügel aus Beton; überstandenes ÖP-Karzinom; Autistin; Liquorverlustsyndrom, Verdacht ME/CFS, 🦓 EDS?/CCI?
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Whitney Dafoe @DafoeWhitney
12K Followers 88 Following Severe ME/CFS patient and advocate. Sick since 2004, bedridden since 2013. Never. Giving. Up. ✊ Useful info for ME/CFS and Long Covid patients in bio link.
ME/CFS Science @mecfsskeptic
6K Followers 487 Following In-depth analysis of research on myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).
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