Myelin Moxi

Myelin Moxi This page is about roller skating and how I use it to combat Multiple Sclerosis. I share my tips, tricks, falls and progress along both journeys.

Oh honey šŸ’• 2025 taught me things about myself, showed me what it means to advocate for myself, showed me what I was capa...
01/21/2026

Oh honey šŸ’• 2025 taught me things about myself, showed me what it means to advocate for myself, showed me what I was capable of in many aspects and encouraged me to keep my head up high despite all the challenges I endured.

This MRI was from the end of last year and I finally got to see a visual of my brain instead of trying to interpret text with language I don’t understand. What you see in the video is literal highlights of my brain lesions—they sparkle like the night sky ✨

As I say all the time, MS looks different on everyone. My doctor(s) have told me that the amount of lesions (and their placements) should have me in a much worse condition, and yet somehow I’m living a normal life. This really helps me maintain the idea that mindset is literally everything, and that I can continue to defy these odds by doing what makes me happy: roller skating through life, one sparkle at a time

✨New beginnings✨the beginning of this year has taught me to cater to myself and begin again.  No true New Year’s resolut...
01/11/2026

✨New beginnings✨the beginning of this year has taught me to cater to myself and begin again. No true New Year’s resolution, only to do more of what makes me feel good (like roller skating) and doing less of what doesn’t make me happy, whether it be frequenting people, places and things that don’t serve me).

I’ve enjoyed the time of self reflecting and finding my way back to myself and the things I enjoy and roller skating definitely made the cut. Cheers to a new perspective of growth, my boyfriend and I finding our way back to each other for the good, and getting a good grasp on what makes me, me. 🧔 2026 is looking good so far

Happy World MS Day! I’ve been MIA lately because, well, it’s not a pandemic anymore and life is calling me in so many di...
05/30/2025

Happy World MS Day! I’ve been MIA lately because, well, it’s not a pandemic anymore and life is calling me in so many different directions that I simply don’t have as much time to skate anymore like I did in 2020. Nonetheless, MS is an everyday thing that I always have to make time for, regardless of life circumstances.

If you’re new here, I was diagnosed with Tumefactive MS almost 8 years ago and have been rolling with the punches ever since. My journey started with numbness and tingling in my hands and feet when entering a hot vehicle in the middle of Texas summer. I saw a neurologist who prescribed me every medication under the sun until I found one that worked for me—now I’m on Ocrevus, which has been working wonders for the past 4 years.

MS looks different for everyone; some of us are rolling on skates while some of us may roll on a different set of mobility wheels, but regardless of what part of the journey you’re on, we’re all rolling towards the same outcome: to find a cure to end MS forever 🧔

Ocrevus infusion: ā˜‘ļø let’s be real for a sec. The whole insurance + medication process is a WILD ride. Not only did I ch...
04/10/2025

Ocrevus infusion: ā˜‘ļø let’s be real for a sec. The whole insurance + medication process is a WILD ride. Not only did I change insurance plans, I initiated the process with my Ocrevus provider in late January and didn’t get a full confirmation until April 2! 😤

Needless to say, I stood on business and get my infusion on time. Cheers to another protected 6 months to keep rolling. 🧔

Day 16/365: Night skates never hurt anybody 🤭 here’s a cute bail
03/16/2025

Day 16/365: Night skates never hurt anybody 🤭 here’s a cute bail

Day 14/365: Ok! So those shin stretches and exercises I’ve been doing have been really helping! I actually prepped last ...
03/14/2025

Day 14/365: Ok! So those shin stretches and exercises I’ve been doing have been really helping! I actually prepped last night and it felt amazing.

and I returned to our old stomping grounds as we ā€œconditionā€ to skate the Walk MS Dallas event in April! It felt so good to be back in the environment that started it all and made me fall in love with my wheels all over again. 🧔 What place made you fall in love with skating?

Happy MS Awareness month! I love being vulnerable and real about my diagnosis and talking about MS with anyone and every...
03/03/2025

Happy MS Awareness month! I love being vulnerable and real about my diagnosis and talking about MS with anyone and everyone. My favorite thing is to connect with other people living with MS and instantly feeling that sense of camaraderie, that exhaling feeling of no longer being alone in this very moment 🧔

To kickstart this journey of spreading the word, I’d like to share with my new followers a little bit about my diagnosis and what this funky two-letter word is all about it. Firstly, hi! I’m Kaci! I live with Multiple Sclerosis and having a great time! šŸ˜… Multiple Sclerosis, or MS, is an autoimmune disease that attacks health nerves in the brain and spinal cord. The damage to the nerves is the immune system mistaking healthy myelin sheath for ā€œbad guysā€ and eating away at the fatty coverings protecting the nerve itself (think of rags chewing through a wire and leaving it exposed).

The ā€œexposed wiresā€ then have difficulty relaying appropriate signals from the brain, leading to strange happenings in the rest of the body. Symptoms typically associated with this are numbness/tingling in extremities, balance and gait problems, cognitive issues like thought processing/decision making, vision issues, sometimes speech problems, incontinence, nerve pain and even memory loss.

MS looks different on everyone! While two people may experience a handful of similar symptoms, the journeys are not the same and do not have the same outcome. There is not a cure for this lovely anomaly as we know it, but we are able to slow the flare ups/progression/disability of this disease with disease-modifying therapies, or DMTs. MS can affect anyone no matter race, gender or background. It is NOT contagious and is a lifelong illness that affects everyone differently.

Thanks for coming to my TEDtalk šŸ™ŒšŸ¾ If you or someone you know is newly diagnosed, or suspects that MS could be a factor, don’t hesitate to reach out to the MS Society to speak to an MS navigator and discuss your options. 🧔

It’s ok not to take a giant leap of faith in order to achieve your goals. The small steps it takes to get there equal up...
12/17/2024

It’s ok not to take a giant leap of faith in order to achieve your goals. The small steps it takes to get there equal up to the big leap. Goals are suppose to be bite-sized to be manageable and reachable.

It’s also ok to work hard towards the goal and take breaks to keep going. Give yourself a rest and recover from the hard work you put in. When you get back to it, you’ll be better prepared to continue on to greatness. 🧔
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Plants + skates make the best dates! I’m still high on my skate-cation in downtown Ft Worth and visiting this amazing pl...
11/22/2024

Plants + skates make the best dates! I’m still high on my skate-cation in downtown Ft Worth and visiting this amazing plant store on the way! I wasn’t able to wear my skates inside, but having them leashed on my back was still a badge of honor šŸŽ–ļø there’s nothing like exploring your metroplex on roller skates

I finally skated downtown Ft Worth, y’all! šŸ˜ Much different than skating Dallas due to all the cobblestone terrain (whic...
11/14/2024

I finally skated downtown Ft Worth, y’all! šŸ˜ Much different than skating Dallas due to all the cobblestone terrain (which wasn’t my favorite) but I conquered it, just like old times. It was so good to be outside on my wheels reliving those summers with my favorite peeps 🧔 .vixen I’m looking at you! šŸ˜‚

To many more seasons of reigniting your love for a hobby that brings you to life
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