#LivingWithMS
MRI RESULTS. GOOD NEWS! ❤️

Four tiny new lesions over three years, none appearing active. My neurological exams remain stable, and we’re continuing Kesimpta.

MS still kicks my ass some days, but today I’m celebrating.

I’m stable, y’all!

#MultipleSclerosis #LivingWithMS
November 3, 2026 at 7:25 PM
"But the worst part? It’s not the symptoms. It’s the looks..it's the #gaslighting of the #disabled .. #doctors, relatives, strangers. Everyone’s an expert until u ask them to live a week in your ruined skin.": buff.ly/6ayKim3

by livingwithms
#MS #disability #ChronicIllness #MedicalGaslighting
If You Could See MS – Part 2 The Horror Sequel You Can’t Unsee
Part 2 of “If You Could See MS” drags you deeper into the neurological horror of living with multiple sclerosis. Raw, furious, and darkly funny—this isn’t feel-good fluff. It’s blood, spoons, and…
buff.ly
October 9, 2026 at 7:30 AM
Ever wonder what a tonic spasm actually feels like? This graphic breaks down the unique experience, from the initial ‘clamp’ to the slow ‘unwind.’ Awareness stays with you throughout. Let’s make this invisible symptom visible. #TonicSpasm #InvisibleIllness #NeuroTwitter #LivingWithMS #EndTheStigma
September 30, 2026 at 5:10 AM
Life suffering from Multiple Sclerosis can be so difficult, it’s hard enough without the financial worries.
The GOOD NEWS is you may qualify for disability benefits!
A compassionate attorney explains
See if you're eligible today!
#FightingMS #MSWarrior #LivingWithMS
www.brrlaw.com/practice-are...
Multiple Sclerosis and Qualifying Disability Benefits
An advanced case of MS will have a good chance of qualifying for Disability benefits. A winning disability attorney with over 30 years experience explains how.
www.brrlaw.com
March 4, 2026 at 6:55 PM
A new project is exploring how women living with MS experience menopause, aiming to identify gaps in care and support.

Research in this area is still limited, so this study will help improve understanding and future support. 💜
ms-uk.org/news/new-pro...

#MSUK #MSResearch #LivingWithMS
New project to explore how women with MS experience menopause
ms-uk.org
April 15, 2026 at 1:16 PM
Waiting room time. I had my MRI yesterday, today my sister has hers! #livingwithMS #MSsisters
January 30, 2024 at 4:27 PM
March 7, 2025 at 4:45 PM
MRI came back with nothing new! No news is good news #livingwithMS
January 23, 2025 at 5:02 PM
garytrente.com

Halcyon is a 5” x 7” drawing showing a human silhouette merged with a tree, half full of leaves and half bare. It reflects my experience living with Multiple Sclerosis—strength and struggle in one. #Halcyon #LivingWithMS
April 27, 2026 at 11:25 PM
Hush is a series of nine small charcoal, ink, and pencil panels. These drawings are a reflection of my life with MS—an honest look at solitude and the spaces we occupy inside ourselves. #Hush #FigurativeArt #MonochromeDrawing #LivingWithMS
April 10, 2026 at 5:56 AM
Today is World MS Day - help raise awareness as people navigate Multiple Sclerosis together.
#WorldMSDay #MSHeartChallenge #MSIreland #LivingwithMS #LightUpForMS

www.ms-society.ie/
https://worldmsday.org/
May 30, 2025 at 9:00 AM
I purchased a #mooncool TK-Pro electric trike last night. Should have it by the weekend. Can't wait. Hoping it will be the thing that helps me stay active. #MulipleSclerosis #LivingWithMS
July 23, 2025 at 9:12 PM
Join The Coalition!💫 Mitzi Joi Williams, an accomplished neurologist, shares her expertise on multiple sclerosis.
Be sure to SHARE and SUBSCRIBE.
youtu.be/WbkOq91QT68?...

#MSStrong
#ThisIsMS
#EndMS
#LivingWithMS
#atl #thenerdyneurologist #Atlantabariatricsurgeon
The Coalition with Dr. Shani Belgrave: Demystifying Multiple Sclerosis with Mitzi Joi Williams, M.D.
YouTube video by Dr. Shani Belgrave
youtu.be
August 12, 2025 at 11:43 AM
#LivingWithMS

It’s the old story, Lydia. Invisible symptoms are among the heaviest we carry - fatigue, numbness, pain, etc.

People who say “Oh yeah, I’m tired too” don’t know the difference between ordinary tiredness & clinical fatigue
February 4, 2025 at 6:27 PM
Love this💪🏽
My health and career imploded a little over a decade ago and I am so thankful that I could hit the reset button and journey on this arduous task of reinvention.
Its been one H.E.🏑 🏑 of a ride.
Cheers🥂
#selfcare #selflove #chronicillness #MS #livingwithMS #doctorsofbluesky
An old friend said something really encouraging to me today, she said-

“Thank goodness we have the option to change in life.”

Just because one path in life didn’t work out the way you hoped, that doesn’t mean you’re a failure. ❤️
December 29, 2024 at 7:14 AM
I’m new to the #MultipleSclerosis community and eager to learn! 💜🧠

✨💡 If you are #LivingWithMS - what do you wish people without MS understood?

🔬💬 If you work in #MS advocacy, research, or support - what do you wish you had known when you first started?
February 4, 2025 at 5:30 PM
Every decision becomes a calculation.

And most people never see that part.

#multiplesclerosis #ms #mscommunity #livingwithms #mslife #invisibleillness #mssymptoms
April 11, 2026 at 4:04 PM
This was the hardest part.

Not the diagnosis…

what came after.

Part 4 of my MS story.

#multiplesclerosis #ms #mscommunity #livingwithms #mslife #mssupport #msawareness
April 10, 2026 at 10:03 PM
And you just sit there trying to find it again.

People think you’re distracted.

But your brain just… stopped.

#multiplesclerosis #ms #msbrainfog #mscommunity #livingwithms #mslife #mssymptoms
April 10, 2026 at 11:32 AM
This is when it stopped being confusing…

and became real.

I finally understood what I was dealing with—
but I wasn’t ready for it.

Part 3 of my MS story.

#multiplesclerosis #ms #mscommunity #livingwithms #mslife #mssupport #msawareness
April 9, 2026 at 10:03 PM
But MS doesn’t always show up the way people expect.

And just because it’s not visible…

doesn’t mean it’s not real.

#multiplesclerosis #ms #mscommunity #invisibleillness #livingwithms #mslife #mssymptoms
April 9, 2026 at 11:32 AM
The first neurologist I saw…

made everything feel worse.

No clarity.
No reassurance.
Just fear.

Part 2 of my MS story.

#multiplesclerosis #ms #mscommunity #livingwithms #mslife #mssupport #msawareness
April 8, 2026 at 10:03 PM
So you stop explaining.

Not because you’re okay—

but because it’s easier than trying to make people understand

#multiplesclerosis #ms #mscommunity #invisibleillness #livingwithms #mslife #mssupport
April 8, 2026 at 4:06 PM
This is how it started…

I knew something was wrong.
But no one could see it.

And that messes with you more than anything.

Part 1 of my MS story.

#multiplesclerosis #ms #mscommunity #livingwithms #mslife #mssupport #msawareness
April 8, 2026 at 12:03 AM