tokgauge
EN
EnglishEspañolPortuguêsFrançaisDeutschItalianoBahasa IndonesiaTürkçeРусскийไทย

#dysautonomia

88 clips from 30 authors · 122M total views. Every clip opens with its own counters and comments.

I get 10 days with no nose hose:) #pots #posturalorthostatictachycardi — @sara.helenn43.5M0:11@sara.helennhow i handle fainting in public 🚑🫀 #posturalorthostatictachycardiasynd — @karinadrury26.8M1:01@karinadruryHe really is my everything❤️ he’s truly incredible with my dysautonomi — @eviemfitness11.1M0:54@eviemfitness@AYBL Fainting episode in the gym due to Dysautonomia (VVS & POTS) 🩵 @ — @eviemfitness9.2M1:22@eviemfitness⚠️may be hard to watch⚠️#fypシ #spoonie #chronicillness #chronicpain #p — @tanzchelsea6.5M0:18@tanzchelseaGracias a todos los extraños que aplaudieron sin saber mi historia y a — @ivon.ars6.5M0:17@ivon.ars#greenscreen #fypシ #inpatient #hopital #spoonie #bloodinfection #bacte — @tanzchelsea2.9M0:08@tanzchelseaReplying to @sophia My experience with dysautonomia: 1️⃣ my symptoms, — @carolinecrayy2.8M8:11@carolinecrayy#fyp #moonlightsonata #mcas #sicktok #zebrastrong #genetics #spoonie # — @tanzchelsea2.7M0:41@tanzchelseaI had been doing really good for about 3 months. But the last few days — @traceydferrin2.3M0:42@traceydferrinDo you know of anyone experiencing this? Send it to a friend or tell u — @berneruppercervicalchiro1.3M2:04@berneruppercervicalchiro#fypシ #spoonie #chronicillness #chronicpain #paintok ##chronicwarrior — @tanzchelsea1.1M2:58@tanzchelseaI’m back! Update on whats been going on with me and why I’ve been gone — @kaya.mieko1M5:05@kaya.miekoI thought all of this was normal. I thought it was just me. Turns out… — @kelssyyy_604K1:11@kelssyyy_This is a total game changer! Introducing the all-in-one Rollator and — @kaya.mieko488.7K2:54@kaya.miekothe more you know 💭 #pots #dysautonomia #ChronicIllness #tachycardia # — @kelssyyy_398K@kelssyyy_Hate this illness 🥰 #viral #foru #trending #fyp #video #family #tik_to — @jay_new718245.1K0:06@jay_new718Over a year ago I went to the Keiser Clinic in Chelsea, Michigan for t — @kristicreatesofficial210.6K1:31@kristicreatesofficialInspired by the og baby formula girl @Caroline Cray ✨ #mcas #autoimmun — @rylie_shaw210.2K1:11@rylie_shawDoes this happen to you during hot showers? #dysautonomia #hotshower # — @doctormyro198.3K0:26@doctormyroStory time… 🧠 #POTS #potssyndrome #spoonie #dysautonomia #posturalorth — @kristicreatesofficial185.6K2:41@kristicreatesofficialwill keep going!! Practice makes better. ⭐️ Even since last year, I’m — @faythegay173.2K2:44@faythegayDo you crash after eating? Yes there can be a blood sugar component to — @thetracyrodriguez172.8K0:59@thetracyrodriguezlots of love for my fellow chronic illness girlies🧂🤍 #potssyndrome #dy — @mimithemortician161.6K1:17@mimithemorticianReplying to @madsmads17 I wish I was exaggerating but at this point we — @thekaitjustice159.4K1:09@thekaitjusticeSome people I see in clinic describe a very specific type of “bloating — @dr.zac.spiritos156.4K0:09@dr.zac.spiritosI’ll never learn 🙄🤷‍♂️ #viral #foru #trending #fyp #tik_tok #family #v — @jay_new718149.2K0:10@jay_new718the more people are aware if it the sooner itll get recognized and soo — @elizabethfortmeyer146.7K0:14@elizabethfortmeyerJust want to say thank you! #lymedisease #dysautonomia #bartonella #ma — @christinaasmr77K@christinaasmrAsk someone with hypermobile Ehlers-Danlos syndrome and MCAS, “What do — @dr.zac.spiritos65.3K0:07@dr.zac.spiritosYes, people with hEDS can have joints that bend, pop, sublux, and disl — @dr.zac.spiritos59.2K0:07@dr.zac.spiritosOne of the stranger phenomena I’ve seen with MCAS is reactive hypoglyc — @dr.zac.spiritos55.7K0:11@dr.zac.spiritos2 ans depuis mon diagnostic « officiel » 🫠 #dysautonomie #dysautonomia — @lilisemood34.9K9:11@lilisemoodPot is not in your head, it is a physiological response to the body be — @doctorbengalyardt34.7K1:12@doctorbengalyardtThis is how I exercise safely with POTS without triggering a crash. 💪🏼 — @kristicreatesofficial30.9K1:20@kristicreatesofficialYou’d be surprised how many things can agravate POTS that you don’t kn — @allirose81926.6K1:01@allirose819Replying to @𝓐𝓼𝓱𝓵𝓮𝔂𝓔𝓵𝓲𝔃𝓪𝓫𝓮𝓽𝓱 if you have autoimmune diseases or cancer — @thekaitjustice26.1K0:23@thekaitjusticeIs it Dysautonomia? For many people it can take years before they get — @jbirdfit22.9K7:45@jbirdfitPOTS is typically a problem of the autonomic nervous system. The heart — @drsiyabmd21.9K1:42@drsiyabmdThis is one of the adaptive workouts that has allowed me to stay more — @michelleyoung21.8K0:56@michelleyoungOne thing that is almost part and parcel of MCAS is an incredible reac — @dr.zac.spiritos21K0:10@dr.zac.spiritosIt’s an uphill battle #hypermobility #ehlersdanlossyndrome #mcas #dysa — @drgracedpt15.2K1:01@drgracedptWhen someone is in an MCAS flare, one of the first questions I ask is: — @dr.zac.spiritos13.5K0:09@dr.zac.spiritosYou’d be surprised how many things can agravate POTS that you don’t kn — @allirose81912.7K1:31@allirose819Replying to @Matthew Stone #dysautonomia #nervoussystemhealing #pain # — @drgracedpt11.5K1:19@drgracedptI wanna know! #potssyndrome #POTS #spoonie #posturalorthostatictachyca — @kristicreatesofficial11.4K0:07@kristicreatesofficialPOTS girlies wearing compression shorts under everything 🤭 #fyp #POTS — @allirose81911.1K0:08@allirose819non negotiables for dysautonomia #chronicillness #posturalorthostatict — @karinadrury7.6K1:06@karinadruryOnce you diagnose MCAS, that can actually be the easy part. The harder — @dr.zac.spiritos7.4K0:11@dr.zac.spiritosPots should not take almost 6 years to get a diagnosis, your doctor do — @doctorbengalyardt7K0:59@doctorbengalyardtPot is not from your brain pot is not from your anxiety. Pot is not ma — @doctorbengalyardt6.8K1:02@doctorbengalyardtyou get it if you have chronic illness #chronicillness #dysautonomia — @karinadrury6.5K0:07@karinadruryPOTS is a terrifying condition, but you CAN put symptoms into remissio — @drmarybethhealth6.3K0:06@drmarybethhealthReplying to @Montauk Project Daughter get to swimming and winning! #PO — @bonniedoes5.4K2:24@bonniedoeswas too funny to not join in 🤠 #pots#potssyndrome #dysautonomia #tachy — @kaylamae55005.1K@kaylamae5500Replying to @the sperm that won #dysautonomia #compression #compressio — @irisolympia4.9K1:51@irisolympiaApparently POTS is just ✨white woman laziness✨ with a side of tachycar — @rachaelinarkansas4.7K8:24@rachaelinarkansasOne of the more frustrating things I see in MCAS is how difficult it c — @dr.zac.spiritos4.3K0:10@dr.zac.spiritosGrieving the girl I was before POTS while learning to love the girl I’ — @mandy.stucker4K@mandy.stuckerI have POTS and this is what I did at the gym today not medical advice — @kristicreatesofficial3.4K0:55@kristicreatesofficial

Top authors

@sara.helenn — TikTok avatar@sara.helenn1 clip@karinadrury — TikTok avatar@karinadrury3 clips@eviemfitness — TikTok avatar@eviemfitness2 clips@tanzchelsea — TikTok avatar@tanzchelsea4 clips@ivon.ars — TikTok avatar@ivon.ars1 clip@carolinecrayy — TikTok avatar@carolinecrayy1 clip@traceydferrin — TikTok avatar@traceydferrin1 clip@kaya.mieko — TikTok avatar@kaya.mieko2 clips@berneruppercervicalchiro — TikTok avatar@berneruppercervicalchiro2 clips@kelssyyy_ — TikTok avatar@kelssyyy_3 clips@kristicreatesofficial — TikTok avatar@kristicreatesofficial10 clips@jay_new718 — TikTok avatar@jay_new7182 clips

Related tags

#pots#chronicillness#potssyndrome#spoonie#posturalorthostatictachycardiasyndrome#mcas#mastcellactivationsyndrome#heds