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#Mswarrior Reel by @ms.and.me (verified account) - Comparing this to the video of me walking 5 years ago, I'm blown away by how far I've come with my walking. I'm way steadier, stronger and my gait has
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@ms.and.me
Comparing this to the video of me walking 5 years ago, I'm blown away by how far I've come with my walking. I'm way steadier, stronger and my gait has improved so much. Plus, this video was taken after a 2-week illness, so that's a definite win. It's been such a journey getting to this point. At one time, walking unaided was a distant and unachievable dream. Now, walking unaided is the norm. Sure, every day is different. One day I wake up and think "yes I'm going to walk today." Another day I'll decide that a day resting is more for me. With MS there is no rhyme nor reason, just knowing my body and my limits is enough. But, If I can make this progress, you can too - just dream big, stay hopeful and keep pushing forwards ✹ (Apologies for the wobbly background, apparently my phone's focus is a bit off when I'm more than 30cm away 🙄) . . . . . #mswarrior #msawareness #chroniccondition #spoonielife #mswalking
#Mswarrior Reel by @kerryriches23 (verified account) - On World MS Day, I'd like to share my first symptoms that I experienced 17 years ago. These symptoms prompted me to book my first appointment with my
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@kerryriches23
On World MS Day, I'd like to share my first symptoms that I experienced 17 years ago. These symptoms prompted me to book my first appointment with my GP on 2nd August 2008, which started the journey of my multiple sclerosis diagnosis 🧡 What were your first symptoms??? Xx #worldmsday #happyworldmsday #fyp #multiplesclerosis #MS #disability #mobilityaiduser #disabled @worldmsday #disabilityawarness #relapse #inclusion #diversity ##mswarrior @mssocietyuk
#Mswarrior Reel by @medicalmedium (verified account) - Repost from @wild.blueberry.dreams ‱ 2 Years MS Medication Free! đŸ€Ż When I was first diagnosed, I was told I'd be on medication for the rest of my li
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@medicalmedium
Repost from @wild.blueberry.dreams ‱ 2 Years MS Medication Free! đŸ€Ż When I was first diagnosed, I was told I’d be on medication for the rest of my life. I broke down crying in my doctor’s office. It didn’t feel right, but after a scary episode of double vision and a week in the hospital, I was afraid—so I said yes to meds. But deep down, I knew there had to be another way. 10 months later, everything changed. After committing to @medicalmedium protocols, a follow-up MRI showed something unexpected: improvement. The large demyelinating lesion on my brain stem—the one that caused my double vision—had remyelinated so well, my doctor had trouble even finding it. That gave me the courage to go deeper. Going off my MS medication wasn’t a decision I made lightly. I worked closely with my doctor to come up with a plan to taper off as I supported my body through @medicalmedium protocols. Being on a med that lowered my immune system no longer resonated with me—especially after learning from @medicalmedium that the true root of MS is Epstein-Barr Virus and toxic heavy metals. Today, I’m proud to say it’s been 2 full years off MS medication. Do I still have a diagnosis? Yes. And I still have a few other brain lesions that remain unchanged. But I continue to work on my healing every single day. After 3.5 years of this journey, I’ve learned that healing isn’t about perfection—it’s about commitment. It’s about listening to your body, trusting your path, and showing up again and again. If you’re navigating decisions around medication, I see you. It’s not always clear or easy. Bring what resonates to your doctor and work together to find what’s best for you. Sending love, strength, and hope to everyone walking this healing road—you are not alone. Remember, the future is bright 🧡 #multiplesclerosis #healingms #mswarrior #msawareness #msrecovery #autoimmunehealing #medicalmedium #healingjourney #naturalhealing #ebvhealing #rootcausehealing #trustyourbody #medicationfree #healing #healingtaketime
#Mswarrior Reel by @nicolepedra (verified account) - What other things do you hate hearing? . . . #chronicillnessawareness #spoonie #chronicillness #multiplesclerosis #multiplesclerosisawareness #mecfs #
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@nicolepedra
What other things do you hate hearing? . . . #chronicillnessawareness #spoonie #chronicillness #multiplesclerosis #multiplesclerosisawareness #mecfs #mswarrior #invisibleillness #mentalhealth
#Mswarrior Reel by @beatingmyms - Life before my diagnosis was constant DOING. Life after the diagnosis is practicing "BEING." It's not because I have symptoms - it's because I want
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@beatingmyms
Life before my diagnosis was constant DOING. Life after the diagnosis is practicing “BEING.” It’s not because I have symptoms — it’s because I want to prevent them. I’ve learned to take breaks even when I don’t feel like I need them
 and to take naps when possible. Thanks to MS, I learned how to slow down. At one point, I had no choice. It is a scary diagnosis
 but we have to believe that we have some control over the prognosis. It starts in the doctor’s office, but it doesn’t have to end there
 ✹ Healing continues with the choices we make every day. What are you struggling with right now? 🧡 #ms #lifewithms #multiplesclerosis #mswarrior #msawarness
#Mswarrior Reel by @meg.winje - 5 years ago, my body started whispering
 and then it started screaming. Shortly after graduating college, I came home from a trip feeling off. Lighth
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@meg.winje
5 years ago, my body started whispering
 and then it started screaming. Shortly after graduating college, I came home from a trip feeling off. Lightheaded. Dizzy. I told myself it was nothing. But it didn’t go away. Within a few weeks, new symptoms kept piling on— ‱ Numbness spreading across the left side of my face and scalp ‱ Numbness in my right foot ‱ Subtle balance issues ‱ A level of fatigue I couldn’t explain Something was wrong—and I could feel it. I had never even heard of Multiple Sclerosis when I finally got the diagnosis. What I learned quickly is this: MS doesn’t look one way. It depends on where damage shows up in the brain or spinal cord—so symptoms can be wildly different from person to person. After countless appointments, bloodwork, MRIs, and even a second opinion, it was confirmed: This was my reality. But this wasn’t the end of my story—it was the beginning of a much deeper one. I share my journey because I know how confusing, isolating, and scary this phase can feel. If you’re navigating chronic illness, healing, or learning how to trust your body again—you’re not alone. Follow along as I share what I’ve learned about strength, resilience, and building a life that feels good in your body @meg.winje ❀ #wellnessjourney #holistichealth #healingjourney #chronicillness #healthjourney #mswarrior #healthtips #realfood #mystory
#Mswarrior Reel by @thatpatchlady - This technology did not happen by accident. The founder of this company watched his mother struggle with MS and refused to accept there was nothing h
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@thatpatchlady
This technology did not happen by accident. The founder of this company watched his mother struggle with MS and refused to accept there was nothing he could do. He spent 14 years researching the brain and nervous system connection and used his background in coding to develop a technology that supports mobility, stability and inflammation without drugs, chemicals or anything entering the body. He built this for her. đŸ„č The Liberty patch works through a patterned ridge surface like a QR code that activates the skin receptors and sends signals directly to the brain to re-synchronize the nervous system. No pills. No injections. No side effects. Nothing entering your body. Ever. Just a patch that gives your nervous system the input it needs to support your body every single day. This is what it was created for. If you or someone you love is living with MS please reach out. I want to help. 💜 👇 Comment PATCH If you’d like to watch the video where he talks about this, say VIDEO #multiplesclerosis #MSawareness #MSwarrior #nervoussystemhealing #naturalhealing
#Mswarrior Reel by @naturallywithjo - I didn't realize these were MS symptoms at the time. Double vision. Numbness and tingling. Fatigue. Brain fog. Looking back, the signs were there.
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@naturallywithjo
I didn’t realize these were MS symptoms at the time. Double vision. Numbness and tingling. Fatigue. Brain fog. Looking back, the signs were there. #multiplesclerosis #msawareness #chronicillness #mswarrior #invisibleillness
#Mswarrior Reel by @webmd (verified account) - Daniel Matterson was diagnosed with MS at age 23. At first, depression set in, but he was determined to be defined as a doctor and a dad, not by his c
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@webmd
Daniel Matterson was diagnosed with MS at age 23. At first, depression set in, but he was determined to be defined as a doctor and a dad, not by his condition. Watch more by tapping the link in our bio.
#Mswarrior Reel by @kad21 (verified account) - Come and walk a day in my shoesđŸ€” I try not to let these comets get to me but some days it does my head in that people think they can make comments l
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@kad21
Come and walk a day in my shoesđŸ€” I try not to let these comets get to me but some days it does my head in that people think they can make comments like life isn't had enough already🙄 #multiplesclerosis #disabled #mswarrior
#Mswarrior Reel by @pehota (verified account) - See you at the @chimarathon! 💙🧡 I wanted my nails to reflect how much work I put into this training cycle and have a tie to MS with the ribbon. The
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@pehota
See you at the @chimarathon! 💙🧡 I wanted my nails to reflect how much work I put into this training cycle and have a tie to MS with the ribbon. They match my race day outfit and any time I need a boost, I’ll look at my hand, see the MS ribbon, and remember why I’m doing this! What do you think of how they came out with the stars and ribbon?! Let me know below! #nails #runningcommunity #trending #vlog #bts #beauty #running #runnersofinstagram #runnergirl #marathon #training #marathontraining #chicagomarathon #multiplesclerosis #mswarrior #msawareness #spoonie #chronicillness #chronicillnessawareness #trending #race #raceday #nailinspo #marathonnails
#Mswarrior Reel by @chass_mshealing - ✹ "PPMS is part of my story, not the end of it." #multiplesclerosis #mshealing #mswarrior
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@chass_mshealing
✹ “PPMS is part of my story, not the end of it.” #multiplesclerosis #mshealing #mswarrior

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