longcovid hashtag performance

neck and joint pain gone and mental clarity came back #longcovid #covid #nicotine #nicotinepatch

A cautionary tale 🤍 #covid19 #longcovid #chronicillness

#Stitch with @zach #mask #masks #maskup #wearamask #flu #influenza #rsv #birdflu #covid #covid19 #covidー19 #covid_19 #longcovid #longcovidawareness #foryoupage #fyp #greenscreenvideo

yeah i’m back on my masking soap box again (i say as if i ever left) friendly reminder that you can always pick up a mask and start wearing it again at any time!!! literally right now!! today!!!! #covid #chronicillness #longcovid #disability

& I don't think it will ever be the same. Maybe one day, but I'll keep praying. ❤️‍🩹 #longcovid #cdiff #severecdiff #bacterialinfections #mecfs #pots #dysautonomia #floxed #fqtoxicity #fqt #levaquin #neuropathy #tremors #medicalgaslightingneedstostop #healthiseverything #faith #chronicillnessawareness

It should be common sense that chronically ill people are worthy of proper care and respect, but that seems to be lost these days. #chronicillness #potssyndrome #disabilitytiktok #disabilityawareness #longcovid

Replying to @Tamara Abroad like genuinely. lie. you can literally just lie and avoid the conflict all together. #covid #longcovid #chronicillness #disability

Replying to @boogalooboogz #longcovid #longcovidawareness

“Long Covid can’t be that bad!” Really? Try being bed bound for 2.5 years and losing everything you are! #longcovid #longcovidawareness #longcovidrecovery #chronicillness #chronicillnessawareness #chronicallyill #chronillnesswarrior

We told you #chronicillness #longcovid #epilepsy #mecfs #potssyndrome #myalgicencephalomyelitis #dysautonomia #autoimmunedisease #hashimotos #disability #disabled

Every time I went to the ER feeling like I was dying and thought they would help me, but instead they said I just had anxiety and all my bloodwork looked normal! #longcovid #longcovidawareness #longcovidrecovery #chronicillness #chronicillnessawareness #chronicallyill #chronillnesswarrior

obviously we always stay masked, but chains make it something exciting, and not just a necessity!!! the creators i bought from are @kristina @✨️ fairy 🍉 and @🦷 Tooth and Spell 🌙!! 🥰😷🥰 #covid #longcovid #chronicillness #disability #disabled

This is a very small depiction of the last 4 years. After each Covid I got, things got worse. We got married right before the first Covid I had…. so our marriage has not been easy! After becoming bedbound after the 3rd time I got Covid with “Long Covid” we continued to fight for treatments and doctors. We spent over 30k and I still was not better! Finally we found an amazing doctor and a treatment that would treat the core issue! AJ relapsed after 5 years which made the treatment much harder. I am still doing the treatment (8.5 mos in) but he is now sober and we are both healing! #longcovid #longcovidawareness #longcovidrecovery #chronicillness #chronicillnessawareness #chronicallyill #chronillnesswarrior #sober #relapse #addictionrecovery

honestly the amount I’ve seen in the last year is wild, I need to talk about histamine more because it’s fascinating and can be so helpful for some people 🥹 this was very simplified down and these symptoms can truly mean so much but something to know 🩵#histamine #mcas #pots #longcovid #dietitian #nutrition #lowhistamine #histamineintolerance #pmdd

it’s that simple!!! and if you’re not already, it’s a great place to start making a difference right now!!! #covid #longcovid #disability #disabled #chronicallyill

MIGRATING TO @ valeries_voice on IG - 🔗 ON MY PAGE 🤠👍 hi pals if you’re like wait is Valerie posting an Old Video yes yes i am i shall be repurposing some old content that did well in the next two weeks in hopes that it will 1) once again do well so yall see it and 2) yall see where to find me from now on in the likely and unfortunate event that this app gets cancelled later this month 🥴🥴 #longcovid #covid #chronicillness #chronicallyill

🥶😵‍💫🫠 #chronicillness #foryou #fyp #medicalbills #insurance #viral #chronicillnessawareness #longcovid #mcas

#stitch with @Josh McGough MD MS best post-ER care for someone with #LongCovid: a really top-notch Long Covid clinic (like Mt Sinai’s or Yale’s) or specialists/sub-specialists on university hospital Long Covid teams. Many of these conditions run in clusters/comorbidities, so sub-specialists & specialists tend to know who’s best to refer someone to bc so many of their patients also have that comorbidity (like my rheumatologist has so many EDS & fibro patients that he can spot POTS & refer them to a good POTS specialist). It’s good for patients to research providers in advance (publications, webinars, advocacy, etc). As for us patients with chronic conditions, if we’re in the ER it’s bc something else is going on (but all comorbidities need to be considered), we’re experiencing new symptoms our doctor wants us to get checked out, or we’re in such a bad flare we can’t make it through the night or weekend. Either way, we don’t want to be there & we know the ED staff doesn’t understand us. If someone is new to a condition, ofc they’re going to be scared & nervous! Have you ever stood up, felt your body swell with a seltzer sensation, begin to see stars, then wake on the sidewalk? Because that’s alarming. That doesn’t mean they need psych. It means they need elevate their feet & get a lot of saline & magnesium. Just because you can’t see the cause of their symptoms doesn’t mean the symptoms have no cause. Nervous system dysfunction is weird & unpredictable & if you think it’s overwhelming to acutely treat, imagine living with it chronically, while half of the medical world doubts that it’s even real. As someone waits to get into sub-specialty or specialty care, encourage them to get involved with disease advocacy (LC advocacy, POTS advocacy, etc). We prescribe it to most of our patients bc it is one of the most effective ways to provide support, a sense of purpose, hope, and community. Patients can learn so much from advocacy groups, including discovering providers who may be appropriate to treat them. #ChronicIllness #Fibromyalgia #POTS #LearnOnTikTok

#onthisday #fibromalgia #longcovid #chronicpain #sauna

That’s the way I like it! So grateful for a doctor who is helping me fully heal and doesn’t gaslight me! #longcovid #longcovidawareness #longcovidrecovery #chronicillness #chronicillnessawareness #chronicallyill #chronillnesswarrior

C0ngr3ss can suck it ❤️ Find me on YT Shorts and Bluesky 🦋 Also on RedNote but still learning Mandarin so give me a minute 🤣 Same username everywhere! #fyp #autisticadult #longcovid #chronicillness