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Kerry Walsh

  • Blog

    Racing the Clock or Learning to Breathe?

    When the Year Begins with Loss The first two months of this year have felt heavy. More loss.More hardship.More difficult news than I expected so early on. I won’t name names.…

    February 23, 2026
  • Blog SMA Awareness

    I’m Looking for Treatment — But I Feel So Alone

    There’s a part of this journey I don’t think many people talk about. Not the fear, not the uncertainty, not even the clinical science — but the isolation that comes with…

    January 19, 2026
  • Blog SMA Awareness

    When Awareness Meets Reality: Reflections on SMA, Privilege, and the Power of Early Diagnosis

    At KmotivationSA, I use my lived experience to spark meaningful conversations, challenge systems, and champion change. I write this reflection not only as someone living with spinal muscular atrophy (SMA), but…

    January 12, 2026
  • Blog SMA Awareness Updates

    When Accessibility Depends on Your Postcode: Why Disability Parking in South Africa Needs to Change

    In the 25 years I’ve lived with a disability, I have never received a parking ticket for using a disabled parking bay. Until this holiday. On a recent trip, I was…

    December 28, 2025
  • Blog

    Psychological Safety, Language, and True Accessibility: Why They Matter More Than We Think

    In a world that is constantly evolving, we talk a lot about inclusion, accessibility, and diversity but the real heart of these concepts often lies in something far more intimate: psychological…

    November 24, 2025
  • Blog

    Sometimes, You Just Want Someone to Understand

    I was watching Survivor the other night — a show that’s usually all about strength, strategy, and survival — when something completely different caught my attention. One of the players opened…

    November 10, 2025
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If my wheelchair could talk… oh, the stories it wo If my wheelchair could talk… oh, the stories it would tell! 😂♿

It would probably say:

“Watch the toes—I don’t reverse quietly.”
“Yes, I’m a wheelchair… but I’m also a handbag, table and coat rack.”
“That doorway is definitely narrower than it looks.”
“My battery percentage controls the entire mood.”
“Please don’t move me without asking—we’re a team.”
“And yes, Kerry is an excellent driver… most of the time!” 😜

Swipe through to see what else my wheelchair would say—and add your own in the comments! 💬

#IfMyWheelchairCouldTalk #WheelchairLife #DisabledAndProud #LifeWithSMA #DisabilityHumour #KmotivationSA #ChampioningChange
5 Tips on How I Stay Motivated During the Mid-Year 5 Tips on How I Stay Motivated During the Mid-Year Slump 💜

The middle of the year can feel heavy. The excitement of January has faded, life gets busy, and motivation isn’t always easy to find.

Living with Spinal Muscular Atrophy has taught me that motivation isn’t something you wait for—it’s something you choose, one day at a time.

✨ Remember your why.
✨ Celebrate the small wins.
✨ Give yourself grace.
✨ Focus on what you can control.
✨ Keep showing up.

This year has challenged me more than I expected, but it’s reminded me that resilience isn’t about never struggling—it’s about refusing to give up.

If you’re feeling stuck, this is your reminder: you don’t have to be perfect. You just have to keep moving forward. 💜

#MotivationMonday #MidYearMotivation #KeepGoing #SMAWarrior #DisabilityAdvocate #Resilience #KmotivationSA
People often read that quote as motivation. I rea People often read that quote as motivation.

I read it as reality.

Living with a progressive condition means I’m constantly aware that tomorrow isn’t promised to look like today. I don’t know how much strength I’ll have next month, next year, or even next week. Every new weakness is a reminder that time isn’t something I can take for granted.

That’s why I chase the moments.

I say yes to opportunities. I hug my people a little tighter. I work relentlessly toward my dreams. I fight for treatment. I speak up. I keep showing up.

Not because I’m trying to do everything…

But because I feel like I have so much life left to live before my body tells me I can’t.

If there’s something on your heart, don’t keep waiting for the “perfect time.”

Make the call.
Take the trip.
Start the dream.
Tell people you love them.
Fight for the life you want.

Because later isn’t guaranteed for any of us.

❤️ Don’t leave your life waiting for “someday.”
There are days when I wish I could go back and hug There are days when I wish I could go back and hug the little girl who wondered why her body was different.

The little girl who didn’t know what the future would hold.
The little girl who was scared.
The little girl who questioned whether she’d ever truly belong.

If I could speak to her today, I’d tell her this:

You are stronger than you know.

You will face challenges that most people will never understand. You’ll lose abilities you once had. You’ll fight battles behind closed doors. You’ll cry, you’ll grieve, and you’ll question everything.

But you’ll also discover a strength that can’t be measured by muscles.

You’ll find your voice.
You’ll inspire thousands.
You’ll build a life filled with purpose.
You’ll turn pain into advocacy and fear into hope.

I’m not doing this because it’s easy.
I’m doing it for the little girl who never imagined she’d make it this far.

And for every person who is fighting a battle they didn’t choose…

Keep going.

One day you’ll look back and realise you’re becoming the person your younger self desperately needed.

💗 This one’s for little me.

#DoingItForLittleMe #SpinalMuscularAtrophy #SMAAwareness #DisabilityAdvocate #KeepGoing #FindingMyFeet #KMotivationSA #RareDisease #HopeInTheJourney #ChampioningChange
🍫 Happy World Chocolate Day! 🍫 Today is the perfe 🍫 Happy World Chocolate Day! 🍫

Today is the perfect excuse to enjoy that piece of chocolate you’ve been thinking about… because calories don’t count on World Chocolate Day, right? 😜

Life can be busy, stressful, and sometimes overwhelming. That’s why it’s important to celebrate the little moments that make us smile—even if it’s just your favourite chocolate melting in your mouth.

For me, it’s a reminder that joy doesn’t always come from the big milestones. Sometimes it’s found in the simplest things: a good laugh, time with people you love, and yes… a piece (or two) of chocolate. ❤️

So go ahead—treat yourself without the guilt today.

🍫 Milk, dark or white… which one are you choosing?

#WorldChocolateDay #TreatYourself #FindTheJoy #LittleMoments #KMotivationSA #ChocolateLovers
🌈 July is Disability Pride Month 💙♿ For a long ti 🌈 July is Disability Pride Month 💙♿

For a long time, I thought disability was something I had to overcome before I could truly be proud of myself.

Living with Spinal Muscular Atrophy (SMA) has brought challenges that most people will never see. It has changed my body, taken away abilities I once had, and forced me to adapt in ways I never imagined. Some days are incredibly difficult, especially as my condition progresses.

But Disability Pride isn’t about celebrating the struggles.

It’s about celebrating the person I have become because of them.

Disability Pride Month is about recognising that disability is a natural part of human diversity. It’s about embracing our identities, challenging stereotypes, advocating for accessibility, and reminding the world that disabled people deserve the same opportunities, respect, healthcare, and inclusion as everyone else.

I’m proud of the resilience I’ve built.
I’m proud of every barrier I’ve helped break down.
I’m proud of every conversation I’ve started about accessibility.
I’m proud that my wheelchair represents freedom, not limitation.
And I’m proud that my voice continues to create change, even on the days my body won’t cooperate.

Disability isn’t something I hide.
It’s part of my story.
It has shaped my perspective, strengthened my purpose, and given me the opportunity to advocate for thousands of people who deserve to be seen and heard.

This Disability Pride Month, I hope you’ll take a moment to learn, listen, and help create a world where everyone belongs—not despite their disability, but with it.

Because disability isn’t the opposite of ability.
It’s simply another way of experiencing life.

💙 Happy Disability Pride Month.

#DisabilityPrideMonth #DisabilityPride #SMA #Accessibility #Inclusion #RareDisease #KMotivationSA #ChampioningChange
I don't want sympathy. I want a chance. Every day I don't want sympathy. I want a chance.

Every day, I wake up wondering what I'll lose next.

Will I still be able to feed myself?
Will I still be able to lift my arms?
Will I still be able to hold on to the independence I've fought so hard for?

Living with Spinal Muscular Atrophy (SMA) means watching your body slowly become something you no longer recognise. It's grieving pieces of yourself while you're still here.

For years, there was nothing that could stop this disease.

Now there is.

I'm not asking for a miracle.
I'm not asking to be "fixed."

I'm asking for the opportunity to access a medication that could slow the progression of my disease and give me more time—more time to work, to advocate, to love, to laugh, to make memories, and to continue living the life I've fought so hard to build.

I've done everything I can.

I've researched.
I've met with doctors.
I've made phone calls.
I've written emails.
I've refused to give up.

Now I need our medical system to do its part.

No one should have to fight this hard just for the chance to protect the life they still have.

I deserve treatment.
I deserve to be heard.
I deserve a chance.

And so does every South African living with SMA.

Please stand with me. Share this post, start the conversation, and help us remind those who make these decisions that behind every application is a person whose life matters.

Because access to life-changing treatment shouldn't depend on whether you can afford it. It should depend on whether you need it. 💜
A new month doesn't mean you have to have everythi A new month doesn't mean you have to have everything figured out.

It simply means you've been given another opportunity to keep going.

Whether June brought you victories, setbacks, unexpected challenges, or moments you'll always treasure, leave room for hope as you step into this new chapter.

Take life one day at a time.
Celebrate the small wins.
Be kind to yourself.
And remember that progress isn't always loud—sometimes it's simply choosing not to give up.

Here's to fresh starts, renewed strength, and finding joy in the little moments.

Welcome, July. Let's make it count. 💙

#HelloJuly #NewMonth #FreshStart #KeepGoing #ProgressNotPerfection #Motivation #KMotivationSA
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