Kyra

potsyndrome hashtag performance

#POTSyndrome highlights the challenges of Postural Orthostatic Tachycardia Syndrome, a disorder affecting blood circulation, leading to symptoms like dizziness, fatigue, heart palpitations, and impacting daily life and activity levels.
I’ve come a long way since 2020. Sometimes, I can’t believe it was six years ago. I’m so glad I was diagnosed, put on the right meds, and made the lifestyle changes necessary to improve my symptoms. I still don’t donate blood 🩸#fyp #foryoupage #dysautonomia #potsyndrome #pots #fainting #dysautonomia #chronicillness #invisibleillness #chronicallyill #healthissues #potsawareness #dysautonomiaawareness
Anyone who has ever suffered from a migraine I am so sorry. Migraines are no joke especially when they are paired with a POTS episode or diagnosis. I have shared tips on how I handle my migraines now, and it has helped me tremendously. But wow … in the end of 2020 it was rough. #fyp #foryoupage #dysautonomia #potsyndrome #pots #fainting #dysautonomiaawareness #chronicillness #invisibleillness #migraine #migraines #potsawareness
it could happen to anyone. #chronicillness #chronicallyill #pots #potsyndrome #spoonie #illness #healthtok #chronicillnessawareness
I use a lot of other lifestyle changes but these are quick and easy ways to help with my symptoms. @Waterboy drink mixes have been a help in my journey to eliminate sugar while staying hydrated! I hope this helps some of you!! #fyp #foryoupage #dysautonomia #potsyndrome #pots #fainting #dysautonomiaawareness #chronicillness #invisibleillness #potsawareness #symptommanagement #dysautonomia
I have been obsessed with the versatility of the @Waterboy brand!! If you have a chronic illness and are pretty physically active or just somewhat physically active this is a huge help! Much love for all of you!!💙 #fyp #foryoupage #potsawareness #dysautonomia #dysautonomiaawareness #fainting #chronicillness #invisibleillness #hydration #pots #potsyndrome #Fitness #chronicallyill #awareness
I wish I was healthy enough to “care less” about what I do with my body. People seem to confuse having to do/not do certain things to manage a chronic illness and someone just taking care of themselves. It is not the same. #fyp #foryoupage #dysautonomia #potsyndrome #pots #awareness #fainting #dysautonomiaawareness #chronicillness #invisibleillness
They have me for at least two more years😂                                   #chronicallyill #potsyndrome #fyp #mcas #pots #fypage #dysautonomia #chronicheadaches #crps #syncope #invisibleillness #chronicpain #diagnosis #childrenshospital
Having a chronic illness doesn’t mean you can’t go out, have fun, and eat what you want for a night. @Waterboy ‘s weekend recovery mix truly helps to prepare me for nights like these! #fyp #foryoupage #dysautonomia #potsyndrome #pots #fainting #chronicillness #invisibleillness #chronicallyill #dysautonomiaawareness #potsawareness
#chronicallyill #potsyndrome #fyp #healthissues #mcas #pots #fypage #dysautonomia #chronicheadaches #invisibleillness #syncope #chronicpain #diagnosis #insurance #deductible #ivfluids
Safe to say I will never be getting a iron infusion again.               #chronicallyill #potsyndrome #fyp #mcas #healthissues #syncope #dysautonomia #chronicpain #pots #fypage
#chronicallyill #potsyndrome #fyp #healthissues #pots #mcas #fypage #dysautonomia #chronicheadaches #syncope #diagnosis #medicalhumor
My Heath has definitely transformed my life in ways I never would have imagined.  #chronicallyill #potsyndrome #fyp #mcas #pots #fypage #dysautonomia #chronicheadaches #crps #syncope #invisibleillness #chronicpain #diagnosis #medicalhumor
like why is my heart beating so hard it’s not that serious!  #pots #potsyndrome #potsie #spoonie #chronicillness #chronicallyill
Replying to @Scott Chegg health update and grwm!! #pots #potsie #spoonie #potsyndrome #health #chronicillness #chronicallyill #grwm #lifeupdate #healthupdate #nyc
#chronicallyill #potsyndrome #mcas #fypage #chronicheadaches #crps #fyp #syncope #dysautonomia #chronicpain #pots #invisibleillness #diagnosis
Dani had EVERY SYMPTOM of POTS and MCAS resolve within six months of joining Immune Resilience 🤯 This was after over a decade of struggling with endless chronic symptoms that kept getting worse and worse, despite trying a variety of diets, supplements, and medications. This is why we are proud to say we are the most comprehensive, holistic program for people struggling with symptoms of MCAS and POTS that exists, anywhere! Interested in joining Immune Resilience in January? DM for a link to a discovery call to make sure it’s a good fit. Want to become a competent clinician working with complex cases like Dani’s or understanding the deeper nuances of health? Jen is still accepting just a few new mentees- consult groups start 1/10. Info in bio, DM with questions. #potsyndrome #posturalorthostatictachycardiasyndrome #mastcellactivationsyndrome #mastcellactivationdisorder
forgot to hit 60s + cried #kellysweeneychoreo @Kelly Sweeney @tate mcrae #tatemcrae #tate #tatemcrae #tatertots #tatertot #tatemcraetour #sportscar #kellysweeney #momtok #MomsofTikTok #momlife #eds #ehlersdanlos #ehlersdanlossyndrome #ehlersdanlosawareness #ehlersdanlossyndromecheck #zebra #pots #potsawareness #potssyndromeawareness #potsyndrome
My illness gave me a passion I would have never found otherwise🤍 #chronicallyill #potsyndrome #fyp #healthissues #pots #fypage #invisibleillness #art #collegeartstudent #mcas #dysautonomia #chronicheadaches #syncope #diagnosis #crps #chronicpain #mcas
Please share if you are unable to donate anything helps during this time, the go fund me link is in my bio all proceeds will go directly to rent and utilities to keep the roof over our heads thank you for reading ❤️ #potssyndrome #potsawareness #potsyndrome #gofundmehelp #gofundme #greenscreen
•Yes, I actually did get my license taken 3x before I turned 18 - was going for a world record (not really)  •TikTok actually figured out the Dx, not me or my doctors.  •Yes, I did want to join the National Guard, but my recruiter said and I quote, “You wouldn’t even make it through the MEPS exam” BEFORE I was diagnosed with EDS   •I had my son 2 years out of high school. I was 19 & turned 20 two months later  •Yes, my spine is actually broken in 2 places & is full of abnormalities  •I did have more than 250 appointments last year. Put in perspective, there’s an average of 260 weekdays in a year.  •All dis is true. And the last slide wasn’t a joke. Lmk #tacobell #momtok #MomsofTikTok #momlife #eds #ehlersdanlos #ehlersdanlossyndrome #ehlersdanlosawareness #ehlersdanlossyndromecheck #zebra #pots #potsie #potsielife #potsawareness #potsyndrome #potssyndromeawareness #humortiktok #copingmechanism #copingskills

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