spms hashtag performance
#spms explores themes of self-expression, mental health, creativity, humor, empowerment, connection, personal stories, trends, community, challenges, dance, art, individuality, authenticity, inspiration, positivity, support, awareness, entertainment, and passion.
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Its giving get knocked down and slowly get back up again. Its giving self compassion. Its giving showing up daily, even if that means showing up .25% one day and 50% the next. No one said its easy, its hard either way. But, you do have a choice in the matter. So whatcha gonna pick today? #chronicallyill #chronicillnesslife #livingwithms #thisisms #lessonslearned #mswarrior🧡 #msstrong #theliftcollective #mslife #msawareness #mindsetmatters #mssymptoms #msrelapse #setbacksandcomebacks #sickdoesnthavetolooksick #chronicillnesssupport #chronicillnesscommunity #ms #patientleader #rrms #spms #ppms #multiplesclerosis
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19 years…half my life…with MS My MS anniversary was Dec 5. I spent it at the neurologist. Ever since then I’ve been in a healthcare twilight zone that is #chronicallyill folks are realllll familiar with. I’m tired of advocating for myself. I’m tired of trying to ‘prove’ that these are very real issues in a 15 minute appt with a new provider so they can determine how sick I am. I’m tired of living with this illness for 19 years and being treated like I’M unsure of how I feel. I know doctors are in the middle just as much as patients are, in a horribly failing healthcare system AND I can be upset with my care and limitations of the system we are all trying to operate in. The benefit of so much experience with MS is knowing that this is a passing blip of time. Its knowing that I can meet these challenges (even tho I hate having them). It’s knowing it will all pass, maybe a bit slower than hoped, but regardless it will pass. Same for you if life is lame right now, just keep showing up and taking care of you. THAT’S what matters. No LIVE this week or next. I gotta regroup and rebalance after this chaos. I am planning on sending email updates and sharing actual fun and informative things in my newsletters so sign up for those if you’re missing out on our weekly lives. 🧡 #chronicillnesslife #thisisms #livingwithms #msrelapse #mssymptoms #hopeisadiscipline #ms #rrms #spms #ppms #chronicillnesscommunity #chronicillnesssupport #mslife #sickdoesnthavetolooksick #msawareness #theliftcollective #msstrong #mswarrior🧡 #lessonslearned #19yranniversary #multiplesclerosis #patientleader #invisibleillnessclub
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Actual comments i get almost daily on post. What are uninformed strange comments you get? #ms #multiplesclerosis #chronicillness #bedbound #fyp #ppms #rrms #spms #bekind #Paralyzed #Wheelchair #MSWarrior #behindthesmile
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This was then confirmed by a neurologist. The MRIs (brain & spine) along with my presenting symptoms were what got me diagnosed. I have a pinned video talking about the symptoms that prompted me to go to the doctor 🧡 #multiplesclerosis #mswarrior #multiplesclerosiswarrior #thisisms #mstok #msawareness #mslife #multiplesclerosischeck #multiplesclerosistiktok #mssucks #mssucksbutimstillfabulous #chronicallybadass #autoimmunedisease #rrms #spms #ppms #CapCut
1.6k
#onthisday Happy to report in the year since I posted this, Botox in my leg has helped a TON #multiplesclerosis #mswarrior #multiplesclerosiswarrior #thisisms #mstok #msawareness #mslife #multiplesclerosischeck #multiplesclerosistiktok #mssucks #mssucksbutimstillfabulous #chronicallybadass #autoimmunedisease #rrms #spms #ppms
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It’s gonna be one of those days #multiplesclerosis #mswarrior #multiplesclerosiswarrior #thisisms #mstok #msawareness #mslife #multiplesclerosischeck #multiplesclerosistiktok #mssucks #mssucksbutimstillfabulous #chronicallybadass #autoimmunedisease #rrms #spms #ppms #MemeCut #memenatal #MemeCut #memenatal #Meme #MemeCut #memenatal
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