#pwms — Public Fediverse posts
Live and recent posts from across the Fediverse tagged #pwms, aggregated by home.social.
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There’s nothing truly like an Occupational Therapy appointment to make you face your challenges. It’s so much easier to just feel sad and useless. #MultipleSclerosis #PwMS #venting
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CW: #MultipleSclerosis Infusion
I have my twice yearly #rituximab infusion for MS tomorrow. I’ve loaded up on snacks and I’m gonna charge my Switch, grab a book and download some tv. I’m lowkey stressed about it. Writing codes at the Co-Op backwards and shit.
Last 2x I ended up in urgent care because the directions about getting checked out for issues after infusion are pretty scary. Here’s to me knowing what to expect and not having issues this time! #rituxan #pwms #fuckMS -
If you have any kind of #neurological condition (e.g. #pwME, #pwFM, #pwMS, etc.) or are a #carer for someone with such a condition, please consider completing the anonymous 2024/5 survey.
Powered by #SnapSurveys:
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If you have any kind of #neurological condition (e.g. #pwME, #pwFM, #pwMS, etc.) or are a #carer for someone with such a condition, please consider completing the anonymous 2024/5 survey.
Powered by #SnapSurveys:
-
If you have any kind of #neurological condition (e.g. #pwME, #pwFM, #pwMS, etc.) or are a #carer for someone with such a condition, please consider completing the anonymous 2024/5 survey.
Powered by #SnapSurveys:
-
If you have any kind of #neurological condition (e.g. #pwME, #pwFM, #pwMS, etc.) or are a #carer for someone with such a condition, please consider completing the anonymous 2024/5 survey.
Powered by #SnapSurveys:
-
If you have any kind of #neurological condition (e.g. #pwME, #pwFM, #pwMS, etc.) or are a #carer for someone with such a condition, please consider completing the anonymous 2024/5 survey.
Powered by #SnapSurveys:
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CW: Photo w IV/Multiple Sclerosis
It’s infusion day! Glad I have support, FMLA, snacks and a #NintendoSwitch. #MultipleSclerosis #pwms #infusion #rituximab #rituxan #gaming
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CW: #MultipleSclerosis Stuff
Before my diagnosed medical treatment for #MS I have to get my bloodwork done. And even though I intellectually understand that #rituxan kills off part of my immune system, it’s still alarming to see it in my lab results. #PwMS #MultipleSclerosis #chronicillness #rituximab
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Gosh, I’m grateful got #Valium. That was the easiest MRI yet. Hope the results are as straightforward and good. #MultipleSclerosis #MRI #claustrophobia #pwms
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Hello #PWMS, #Researchers #FediScience #Neuros
UPDATE UPDATE UPDATE
I’ve seen several hashtags using variations of #MultipleSclerosis, #MS, #RRMS, #SPMS, #LifeWithMS, #PPMS #MSRunner. Etc.
Can we use
👉🏼 #MultipleSclerosis 👈🏼 AND #MSChat
for #MS related stuff
AND STILL use a subtopic hashtag to introduce folks to the wide variety of topics and interests.
I hoping we get some #researchers, #scientists, and #neuros in the loop.
Thank for boosting.
❤️Anne
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Hello #PWMS.
UPDATE UPDATE UPDATE
I’ve seen several hashtags using variations of #MultipleSclerosis, #MS, #RRMS, #SPMS, #LifeWithMS, #PPMS #MSRunner. Etc.
Can we use
👉🏼 #MultipleSclerosis 👈🏼 AND #MSChat
for #MS related stuff
AND STILL use a subtopic hashtag to introduce folks to the wide variety of topics and interests.
I hoping we get some #researchers, #scientists, and #neuros in the loop.
Thank for for your suggestions, past boosts of my posts and following me.
❤️Anne
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Hello #PWMS
I’ve seen several hashtags using variations of #MultipleSclerosis, #MS, #RRMS, #SPMS, #LifeWithMS, #PPMS #MSRunner. Etc.
Can we try consolidating under #MultipleSclerosis AND #MSChat For all things #MultipleSclerosis related
AND still use a subtopic hashtag to introduce folks to the wide variety?
I hoping we get some of the post bird #researchers, #scientists, and #neuros in the loop.
Thank for for your past boosts of my posts and following me.
❤️Anne
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Hello #PWMS, #Researchers #FediScience #Neuros
UPDATE UPDATE UPDATE
I’ve seen several hashtags using variations of #MultipleSclerosis, #MS, #RRMS, #SPMS, #LifeWithMS, #PPMS #MSRunner. Etc.
Can we use
👉🏼 #MultipleSclerosis 👈🏼 AND #MSChat
for #MS related stuff
AND STILL use a subtopic hashtag to introduce folks to the wide variety of topics and interests.
I hoping we get some #researchers, #scientists, and #neuros in the loop.
Thank for boosting.
❤️Anne
-
Hello #PWMS.
UPDATE UPDATE UPDATE
I’ve seen several hashtags using variations of #MultipleSclerosis, #MS, #RRMS, #SPMS, #LifeWithMS, #PPMS #MSRunner. Etc.
Can we use
👉🏼 #MultipleSclerosis 👈🏼 AND #MSChat
for #MS related stuff
AND STILL use a subtopic hashtag to introduce folks to the wide variety of topics and interests.
I hoping we get some #researchers, #scientists, and #neuros in the loop.
Thank for for your suggestions, past boosts of my posts and following me.
❤️Anne
-
Hello #PWMS
I’ve seen several hashtags using variations of #MultipleSclerosis, #MS, #RRMS, #SPMS, #LifeWithMS, #PPMS #MSRunner. Etc.
Can we try consolidating under #MSChat For all things #MultipleSclerosis related and still use a subtopic hashtag to introduce folks to the wide variety?
I hoping we get some of the post bird #researchers, #scientists, and #neuros in the loop.
Thank for for your past boosts of my posts and following me.
❤️Anne
-
Hello #PWMS
I’ve seen several hashtags using variations of #MultipleSclerosis, #MS, #RRMS, #SPMS, #LifeWithMS, #PPMS #MSRunner. Etc.
Can we try consolidating under #MultipleSclerosis AND #MSChat For all things #MultipleSclerosis related
AND still use a subtopic hashtag to introduce folks to the wide variety?
I hoping we get some of the post bird #researchers, #scientists, and #neuros in the loop.
Thank for for your past boosts of my posts and following me.
❤️Anne
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Feeling pretty solid and human about 48 hours after my #rituxan infusion for #MultipleSclerosis. Here’s to hoping I stay relapse free for another six months! #ChronicIllness #MS #PwMS #rituximab #MSSucks
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It is almost funny how I thought I was not going to be anxious about my #rituxan infusion today. I almost made it to go time without an #anxiety spike, but the IV steroids put an end to that dream. #MultipleSclerosis #MSSucks #pwms #rrms #ChronicIllness #AnxietyDisorder #infusion #rituximab
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Med appointment today for #multiplesclerosis. I’m so lucky to have the family medical leave act to back me up for the amount of time I have to take for appointments because of my #MS. How do folks without #FMLA manage? #chronicillness #pwms #familymedicalleave
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I survived my first infusion! Woohoo!!! Was gone 7 hours total. I’m home now and I’m going to nap and hydrate and keep my fingers crossed for no side effects. #multiplesclerosis #pwms #rituximab #rituxan #fums
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Fuuuuuccckkk. First #rituximab infusion ever is today. In an hour. I’m so nervous and all my psychosomatic bs is in full effect. #rituxan #multiplesclerosis #pwms #ms
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CW: MS & Infusions
I’m scheduled for my first #rituximab infusion on June 13. It’s gonna take 4-6 hours. Any fun tips on how to pass the time enjoyably? #infusion #multiplesclerosis #pwms #ms #rituxan
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CW: MS and 🩸
Day two of a mild #multiplesclerosis flare up. I forgot that #menstruation makes it worse, too. Woohoo! Having so much fun right now. 🙄🤬 #fums #pwms
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CW: Multiple Sclerosis and Anxiety
I can go long periods without my #multiplesclerosis really impacting me, but today it’s rearing its ugly head. Manifesting in some vertigo and tingling in my hands and feet. I’d forgotten how much high anxiety levels can trigger MS. The past week has been ridiculous and my #anxietydisorder is definitely a factor in how I feel today. Luckily I can take the majority of the day off work to recoup. #chronicillness #fums #pwms #rrms
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CW: Multiple Sclerosis Rant
I’m so fucking angry. For the first time since diagnosis I have new lesions. Nearly eight years with nothing new on my #MRI and suddenly multiple new lesions. I’ve had a day to sit with it so I no longer feel like I’ve been punched in the gut. But even still. I’m so disappointed. I’d almost tricked myself into believing it was going away. Fuck you, MS. #fums #rrms #ms #multiplesclerosis #pwms #chronicillness #brainlesions
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New research on potential influence of gut bacteria on #multiplesclerosis. I find this interesting. Maybe it will lead to new treatments for those of us with #ms? #PwMS #chronicillness
https://pubmed.ncbi.nlm.nih.gov/36604748/ -
CW: Multiple Sclerosis
I am so frustrated by the tingly and numbness that I’ve had recently. Shooting down my arms to my fingertips. It was getting better and then I got #covid and it’s now much worse. Anyone else with #multiplesclerosis deal with this and find something that makes it go away? Usually I just wait it out. #fums #PwMS #numbness #chronicillness
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If you don't have a neuro already, then going through your general practitioner and working your way into a referral is your best move, but it looks like you've already done that.
I know some #PwMS just go straight to the ER... but it's the worst time of the year to do that, and, well, there's a Tripledemic on right now...
I'm sorry you're going through all that. You need relief! Sending you healing wishes that symptoms subside quickly!
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I vote that every time I’m too sick to work for a few days that I get to have the #WorldCup to keep me company. Can we make that an official thing?
Then again, I got through my first major bout with #multiplesclerosis by binging Game of Thrones. So maybe just stuff I find engaging to watch is fine…)
#worldcup2022 #distraction #covid #covidthoughts #PwMS -
@ahimsa_pdx I believe this is true for #PwMS (people with #MS/#MultipleSclerosis)
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I seem to be in the minority, but I vastly prefer #PwMS (person/people-with-multiple-sclerosis) over #MS (Microsoft?) or the lengthy #MultipleSclerosis.
I think I picked up that terminology habit from the ms-selfie newsletter - a good resource if #PwMS haven’t heard of it. With the caveat that the author is a UK neurologist, so not always applicable: https://open.substack.com/pub/gavingiovannoni
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My first #FollowBackFriday! If you’re a professional #VideoGame or #ttrpg #GameDev definitely say hi. Amateur too, as I’m not terribly professional most of the time anyways.
Also people in the #queer community, #PwMS / #MultipleSclerosis, or #GuildWars2 addicts. You’re my people.
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CW: Multiple Sclerosis
I am so frustrated by the tingly and numbness that I’ve had recently. Shooting down my arms to my fingertips. It was getting better and then I got #covid and it’s now much worse. Anyone else with #multiplesclerosis deal with this and find something that makes it go away? Usually I just wait it out. #fums #PwMS #numbness #chronicillness
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CW: Multiple Sclerosis
I am so frustrated by the tingly and numbness that I’ve had recently. Shooting down my arms to my fingertips. It was getting better and then I got #covid and it’s now much worse. Anyone else with #multiplesclerosis deal with this and find something that makes it go away? Usually I just wait it out. #fums #PwMS #numbness #chronicillness
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CW: Multiple Sclerosis
I am so frustrated by the tingly and numbness that I’ve had recently. Shooting down my arms to my fingertips. It was getting better and then I got #covid and it’s now much worse. Anyone else with #multiplesclerosis deal with this and find something that makes it go away? Usually I just wait it out. #fums #PwMS #numbness #chronicillness
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CW: Multiple Sclerosis
I am so frustrated by the tingly and numbness that I’ve had recently. Shooting down my arms to my fingertips. It was getting better and then I got #covid and it’s now much worse. Anyone else with #multiplesclerosis deal with this and find something that makes it go away? Usually I just wait it out. #fums #PwMS #numbness #chronicillness
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Med appointment today for #multiplesclerosis. I’m so lucky to have the family medical leave act to back me up for the amount of time I have to take for appointments because of my #MS. How do folks without #FMLA manage? #chronicillness #pwms #familymedicalleave
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Med appointment today for #multiplesclerosis. I’m so lucky to have the family medical leave act to back me up for the amount of time I have to take for appointments because of my #MS. How do folks without #FMLA manage? #chronicillness #pwms #familymedicalleave
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Med appointment today for #multiplesclerosis. I’m so lucky to have the family medical leave act to back me up for the amount of time I have to take for appointments because of my #MS. How do folks without #FMLA manage? #chronicillness #pwms #familymedicalleave
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Med appointment today for #multiplesclerosis. I’m so lucky to have the family medical leave act to back me up for the amount of time I have to take for appointments because of my #MS. How do folks without #FMLA manage? #chronicillness #pwms #familymedicalleave