A quiet truce after an MS relapse is like letting go, not fighting harder
I tune in to hear, 'Maybe healing isn’t always a sprint toward normal'
November feels like an inhale that hasn’t yet decided whether to sigh or sing. The mornings are quieter now, the air cooler, and for the first time in months, I also feel more peaceful.
On the other side of a recent relapse with relapsing-remitting multiple sclerosis, facing trauma head-on, a change of address, and a second dose of rituximab, my body has finally stopped sounding alarms. There have been no more falls, no dragging of drop foot, no struggles with spasticity, and no food making a quick exit before it can provide nourishment. There’s a strength returning to my legs and my life — a steadiness that had been absent for years.
What surprises me most isn’t the improvement itself; it’s how calm everything feels. No fireworks, no dramatic turning point, just a gradual unclenching of a white-knuckled fist and the laying down of grit. I’m not waiting for the next symptom or setback. I’m not forcing myself to fix, prove, or outrun anything. It’s as though my body and I have called a quiet truce.
The resilience in letting go
Multiple sclerosis (MS), in its strange way, has always been the teacher of tempo. It taught me that the body doesn’t move on a calendar and certainly not on your desired schedule. It moves in rhythms, cycles, and sometimes pauses. There were years I mistook that slowness for failure. I pushed harder, thinking forward momentum was the only proof of living.
But lately, I’m tuning into what my nervous system has been whispering all along: Maybe healing isn’t always a sprint toward normal. Perhaps it’s a slow, steady return to belonging in the present moment and within your own skin. For once, I’m not measuring progress by what I can do, but by what I no longer need to fight.
For most of my life, I believed strength meant holding on for dear life. Holding my body upright when it faltered. Holding relationships together when they were slipping. Holding plans in place as if sheer willpower could rewrite biology or circumstance. Letting go felt like failure and a kind of giving up that I swore I’d never do.
But somewhere in what has been the most trying year of my life thus far, between losing what I thought I couldn’t live without, and regaining a semblance of peace I feared I’d never feel again, I’ve started to see it differently. There’s a unique grace in release. It isn’t about indifference; it’s about trusting that not everything I set down will shatter and that some things are meant to find their own shape without my grip trying to fight the mold.
Living with MS has made me a reluctant expert in surrender. Each relapse, each recovery, each new adaptation is a small rehearsal in relinquishing control. I used to brace against every shift, tightening around what I couldn’t keep. Now I’m learning to meet change with softer hands.
Maybe resilience isn’t about how tightly we can hold things together, but how gently we can let them go. Because when I stop resisting the rhythm of the endings, the pauses, the slow re-beginnings, I’m realizing I’m making space for something steadier to grow into my life.
Trust feels quite a bit different these days. To me, it used to mean confidence in a plan, the right medication, and the correct sequence of steps to keep everything from unraveling. Now, it’s something quieter, and less about control and more about communion. I am trusting that my body knows when to fight and when to rest. I am trusting that slowing down isn’t the same as falling behind. I can trust that peace can coexist with uncertainty; that even when the future feels unmarked, everything can still turn out good.
Every evening, I step outside and watch the light change. The trees let their leaves go without panic, the sky takes its time shifting from vibrant colors to gray, and the air smells like something closing and something beginning at the same time. I think of how much of my life has been spent rushing to the next phase, the next scan, the next milestone, and the next sense of safety. Lately, I’m learning to let go, to linger, and to savor the time I have in the now.
Maybe this is what healing looks like in the quiet between seasons; not a finish line, but a gentler rhythm, a deep breath that says you don’t have to fight to be alive.
Note: Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Multiple Sclerosis News Today or its parent company, Bionews, and are intended to spark discussion about issues pertaining to multiple sclerosis.
Fran
This is one of the most profound writings I have come across in my over 25 years in dealing with MS. I can't thank you enough for taking the time to find these words. This will be added to that toolbox of items to inspire me in those days when MS is more difficult to handle. I am grateful.
Lisa Bowser
Thank you for your article! I feel at peace myself currently. I just recently got off of my MS medication as it was making me very sick. I feel very calm about my decision, and am trusting God entirely with the outcome. I feel better mentally than I have since I started taking medication 24 years ago. I'm not sure why, but I do. Have a blessed day and be a blessing!
Libbie Frank
Thank you for a beautifully written article, and for the reminder that "peace can coexist with uncertainty. "
MADELINE l NEWTON
now i wonder if we caused our selves to get this thing they call MS for we always wanted to do everything by ourselves and to just keep on pushing to get it done ...for that is how i was ,especially after getting married and having children for he was a truck driver and gone a LOT so i felt like i had to do it all ...i know yours was a different life but it does go along with we wanting to get it done and to do it by ourselves...just saying ...loved reading your story ...stay strong and enjoy life more that you have slowed down ...enjoy life...i know i am now more ...have a great day and many more ...especially the Holidays ...
Tom A
Beautiful writing that seems to catch the true meaning of MS that takes long to develop. We want to know. We are programmed to "fix it", which is what nearly all people set out to do, in one form or another, if they are not ignoring. But MS has a unique way of letting us know, over time, that sometimes there is nothing that you can do. One has to learn to be happy with that (at least sometimes) or, be miserable much of the time.
Stephanie
Thank you so much for this wonderful piece. Reading it during this difficult time is a great comfort.
Merlene
This article rang so true. I have navigated my MS journey for 55 years. Professing to others the elimination of stress. Now that I am in a progressive stage, I have been letting go each day of things I could navigate and control. You are right that a sense of peace of body and mind accompanies my daily routine. I still think of how the disease will progress and can I meet the challenge. .... but I want to trust it will be OK. I have a great support family. So I know that I am not alone. Thank-you for writing my thoughts on paper.