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#msawareness — Public Fediverse posts

Live and recent posts from across the Fediverse tagged #msawareness, aggregated by home.social.

  1. The hardest part of supporting someone with MS is often the fear of saying the wrong thing. We’ve curated a guide to help you move past 'toxic positivity' and offer the quiet, practical presence your loved one actually needs. No pressure, just genuine connection.

    #MSAwareness, #CaregiverSupport, #InvisibleIllness, #SupportSystem, #Empathy

    Read more: mooddrafts.com/what-to-say-to-

  2. Ever wondered why the butterfly is the face of the MS community? It’s more than just a pretty symbol—it’s about the transformation we live through every single day. 🦋🧡 We've curated the ultimate guide to captions for your ribbons, ink, and advocacy posts. Check it out here:

    #MSAwareness, #MultipleSclerosis, #SpoonieLife, #MSWarrior, #OrangeForMS

    Read more: mooddrafts.com/orange-ribbon-b

  3. MS isn't always a 'brave journey'—sometimes it's just a 14th meltdown and a broken internal thermostat. 🌡️ If you’re done with the toxic positivity, these captions are for you. No filters, just the messy, wobbly truth.

    #SpoonieLife, #MultipleSclerosis, #ChronicIllness, #MSAwareness, #InvisibleIllness

    Read more: mooddrafts.com/ditch-the-fluff

  4. MS isn't always a 'brave journey'—sometimes it's just a 14th meltdown and a broken internal thermostat. 🌡️ If you’re done with the toxic positivity, these captions are for you. No filters, just the messy, wobbly truth.

    #SpoonieLife, #MultipleSclerosis, #ChronicIllness, #MSAwareness, #InvisibleIllness

    Read more: mooddrafts.com/ditch-the-fluff

  5. MS isn't always a 'brave journey'—sometimes it's just a 14th meltdown and a broken internal thermostat. 🌡️ If you’re done with the toxic positivity, these captions are for you. No filters, just the messy, wobbly truth.

    #SpoonieLife, #MultipleSclerosis, #ChronicIllness, #MSAwareness, #InvisibleIllness

    Read more: mooddrafts.com/ditch-the-fluff

  6. MS isn't always a 'brave journey'—sometimes it's just a 14th meltdown and a broken internal thermostat. 🌡️ If you’re done with the toxic positivity, these captions are for you. No filters, just the messy, wobbly truth.

    #SpoonieLife, #MultipleSclerosis, #ChronicIllness, #MSAwareness, #InvisibleIllness

    Read more: mooddrafts.com/ditch-the-fluff

  7. Posting for World MS Day isn't just about orange ribbons—it's about honoring the 'terms and conditions' of a body that moves at its own pace. Whether you're a warrior or an ally, your voice matters. Let's make the invisible visible. 🧡

    #WorldMSDay, #MSWarrior, #InvisibleIllness, #MyMSDiagnosis, #ChronicIllness, #MSAwareness

    Read more: mooddrafts.com/world-ms-day-ca

  8. Posting for World MS Day isn't just about orange ribbons—it's about honoring the 'terms and conditions' of a body that moves at its own pace. Whether you're a warrior or an ally, your voice matters. Let's make the invisible visible. 🧡

    #WorldMSDay, #MSWarrior, #InvisibleIllness, #MyMSDiagnosis, #ChronicIllness, #MSAwareness

    Read more: mooddrafts.com/world-ms-day-ca

  9. Posting for World MS Day isn't just about orange ribbons—it's about honoring the 'terms and conditions' of a body that moves at its own pace. Whether you're a warrior or an ally, your voice matters. Let's make the invisible visible. 🧡

    #WorldMSDay, #MSWarrior, #InvisibleIllness, #MyMSDiagnosis, #ChronicIllness, #MSAwareness

    Read more: mooddrafts.com/world-ms-day-ca

  10. Posting for World MS Day isn't just about orange ribbons—it's about honoring the 'terms and conditions' of a body that moves at its own pace. Whether you're a warrior or an ally, your voice matters. Let's make the invisible visible. 🧡

    #WorldMSDay, #MSWarrior, #InvisibleIllness, #MyMSDiagnosis, #ChronicIllness, #MSAwareness

    Read more: mooddrafts.com/world-ms-day-ca

  11. Let’s be real: living with MS isn't always an 'inspirational journey.' Sometimes, it just sucks. 🧡 We’ve curated a collection of captions that skip the toxic positivity and speak the unvarnished truth for World MS Day. Copy, paste, and be heard.

    #WorldMSDay, #MSAwareness, #InvisibleIllness, #SpoonieLife, #MSWarrior

    Read more: mooddrafts.com/ms-awareness-ca

  12. Thanks to @swisslet I saw this short video about fragments of daily lifes of MS diagnosed: https://m.youtube.com/watch?v=NJzyfR6dbT8
    I live with #sclerosismultiplex for 8 years and started blogging about it in #polish about health care garden. Short story, after 5 years it progressed but now, after medicine change, I hope it slowed. In summer I'll check it with magnetic resonance.

    #msawareness #multiplesclerosis #kesimpta

  13. Thanks to @swisslet I saw this short video about fragments of daily lifes of MS diagnosed: https://m.youtube.com/watch?v=NJzyfR6dbT8
    I live with #sclerosismultiplex for 8 years and started blogging about it in #polish about health care garden. Short story, after 5 years it progressed but now, after medicine change, I hope it slowed. In summer I'll check it with magnetic resonance.

    #msawareness #multiplesclerosis #kesimpta

  14. Thanks to @swisslet I saw this short video about fragments of daily lifes of MS diagnosed: https://m.youtube.com/watch?v=NJzyfR6dbT8
    I live with #sclerosismultiplex for 8 years and started blogging about it in #polish about health care garden. Short story, after 5 years it progressed but now, after medicine change, I hope it slowed. In summer I'll check it with magnetic resonance.

    #msawareness #multiplesclerosis #kesimpta

  15. Thanks to @swisslet I saw this short video about fragments of daily lifes of MS diagnosed: https://m.youtube.com/watch?v=NJzyfR6dbT8
    I live with #sclerosismultiplex for 8 years and started blogging about it in #polish about health care garden. Short story, after 5 years it progressed but now, after medicine change, I hope it slowed. In summer I'll check it with magnetic resonance.

    #msawareness #multiplesclerosis #kesimpta

  16. Thanks to @swisslet I saw this short video about fragments of daily lifes of MS diagnosed: https://m.youtube.com/watch?v=NJzyfR6dbT8
    I live with #sclerosismultiplex for 8 years and started blogging about it in #polish about health care garden. Short story, after 5 years it progressed but now, after medicine change, I hope it slowed. In summer I'll check it with magnetic resonance.

    #msawareness #multiplesclerosis #kesimpta

  17. So that was that. After 2 and a bit years of timing breakfast and dinners to accommodate #vumerity, last night, with some average tapas, I had me last 🤷
    Roll on #mavenclad on Monday.
    #drugfreeweekend
    #MSawareness
    #fuckMS

  18. So that was that. After 2 and a bit years of timing breakfast and dinners to accommodate #vumerity, last night, with some average tapas, I had me last 🤷
    Roll on #mavenclad on Monday.
    #drugfreeweekend
    #MSawareness
    #fuckMS

  19. So that was that. After 2 and a bit years of timing breakfast and dinners to accommodate #vumerity, last night, with some average tapas, I had me last 🤷
    Roll on #mavenclad on Monday.
    #drugfreeweekend
    #MSawareness
    #fuckMS

  20. It's MS Awareness Week! I am once again riding the Chesapeake Challenge in June. This ride is part of Bike MS, which raises money for multiple sclerosis research. I will be riding a metric century! My goal this year is to raise $1,000.

    These funds are needed now more than ever. Can you help me?

    events.nationalmssociety.org/p

    #MSAwareness #BikeMS #disability #fundraiser

  21. MS is highly prevalent in people in the #PNW so even if you don’t think you know anyone with MS, you probably do. #MSAwareness #MultipleSclerosis #FuckMS
    4/4

  22. Today I get to talk to my neurologist about my MRI results, get whatever labs they assign and assess my current treatment. With two new lesions showing in my #MRI I have no idea what to expect.
    #MSAwareness #MultipleSclerosis #FuckMS
    3/4

  23. This month marks nine years from the bout of optic neuritis that led to diagnosis. There is no cure for MS and every day of living with it is different. I’m lucky in that I currently go long periods of time without relapses. Not everyone is so lucky. And there’s no guarantee that my luck will hold.
    #MultipleSclerosis #MSAwareness #FuckMS
    2/4

  24. March is #MultipleSclerosis Awareness Month and boy am I aware right now. How many doctor’s office fish tanks have I sat in front of throughout my life?
    MS is a neurological condition where your own immune system attacks the myelin sheaths that protect your nerves. It can manifest for folks in any number of ways. For me, it has presented itself as optic neuritis, vertigo that lasts for weeks on end, intense numbness and tingling and pain from my rib cage down and more. #MSAwareness #FuckMS 1/4

  25. Coming to the end of another #MSAwareness week. MS affects over a million people in the US & their families, including mine.
    I'll be walking to #EndMS at #WalkMS #Pittsburgh Sun April 16th at Point Park. Please share & help if you can.
    mssociety.donordrive.com/index

  26. It's Multiple Sclerosis Awareness Week. Here's an inspiring blog post from a participant in a clinical trial for #MS.

    "I scored my clinical trial experience as a win because I gained a new network of professionals that provided useful tips that I continue to apply and shapes my life with MS for the better."

    momentummagazineonline.com/blo

    #MSchat #MultipleSclerosis #MSawareness #disability

  27. “Slurred speech, tingling face? OMG, are you having a stroke!?”
    No, I have multiple sclerosis. This is my normal. #MSawareness