Stroke Foundation

Stroke Foundation The Stroke Foundation partners with the community to prevent stroke, save lives and enhance recovery.
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We do this through raising awareness, facilitating research and supporting stroke survivors.

24/03/2026

“I’m fine.”
Sometimes, that’s the easiest thing to say after a stroke.
Many people mask how they’re really going. You might not want to worry others. You might feel pressure to “be back to normal.”

Or maybe it’s just hard to explain what’s going on inside.

Mel, a survivor of 5 years says, “Because the truth is… what others see on the outside rarely tells the whole story.”

“You can often be misunderstood - and the explaining alone can be exhausting.”

“Sometimes, masking just feels easier than trying to find the right words.”

But inside, there might be fatigue, anxiety, frustration, grief… or all of it at once.

Masking can help you get through a moment - but over time, it can be exhausting.

It can leave you feeling isolated, misunderstood, and like you have to carry everything on your own.

Mel also says, “And recovery? It doesn’t follow a schedule - no matter how much people expect it to.”

“Some days you move forward, some days you don’t - and both are part of the process.”

You don’t have to do it alone.

It might help to:

• Share honestly with someone you trust
• Let people know what you need (even in small ways)
• Connect with others who understand life after stroke
• Take the pressure off needing to be “okay” all the time

You’re allowed to have hard days. You’re allowed to be real about how you’re feeling.

It’s okay not to be okay - you don’t have to carry it alone.

P.S. This video isn’t about stroke recovery - but it speaks to the experience of masking. Thanks to thesbloke (Instagram) for making this reel.

23/03/2026

A stroke can happen to anyone - anywhere and any time.
But it doesn't always look the way you expect.
If you don't know the common signs, you might miss the chance to save a life.
Remember F.A.S.T.
Face - is one side drooping
Arms - Can they lift both arms
Speech - Is it slurred or hard to understand?
Time - Call 000 immediately
A stroke is always a medical emergency. Don't wait.
Remember - around 30% of strokes happen to people of working age. Stroke doesn't discriminate.
Please share. Not enough of us know the signs.

From Sarah, "It was a Monday morning, and I was 29. My partner woke up to me having a seizure. I wasn’t very responsive,...
19/03/2026

From Sarah, "It was a Monday morning, and I was 29. My partner woke up to me having a seizure. I wasn’t very responsive, so an ambulance was called. From there, my life shifted in ways I couldn’t have imagined.

I have no memory of those first hours, but I’ve been told I was confused - at one point thinking I was in Ireland! My dad, seeing that I wasn’t myself, pushed for an MRI. After a lot of convincing, the doctor finally agreed. Living rurally, the nearest MRI was a 1.5-hour drive away. We had planned to go the next day, but I started vomiting on the way home and still couldn’t make sense of what was happening. We ended up doing the MRI that afternoon.

The people reviewing the scan wouldn’t tell my dad or my partner what they’d seen. They only said, take her straight to emergency. That was the first sign I was in serious trouble. From there, I was flown from Dubbo Hospital to RPA, where I spent a week or more, and then back to Dubbo Hospital before moving to Lourdes Rehabilitation for about 3–4 months.

Recovery was overwhelming. I had short-term memory loss, cognitive challenges, and my independence was gone. I was off work for 14 months - I had been a domestic violence case worker, and returning wasn’t easy. My confidence had taken a hit, and it felt like I’d lost the skills and energy that had once defined me. On top of that, my seizure meant my license was suspended, making life in a rural area even harder.

Even with virtual therapies and one-on-one support to finish my diploma in community services, recovery was isolating and, at times, incredibly depressing. I spiraled. For the first 1.5–2 years, I had PTSD - I dreaded Sunday nights, being alone, and every hospital visit triggered anxiety.

Now, nearly three years on, I feel more like myself. I have a son who’s about to turn one, and he’s made the world feel right again. Pregnancy after stroke was its own challenge, but I wouldn’t change a thing.

The Invisible Effects

Many people assume recovery is straightforward if someone “looks fine.” But living with an invisible disability is far more complex than appearances suggest.

For me, that includes fatigue, guilt, depression, memory loss, slower processing, anxiety, emotional sensitivity, self-doubt, and sensory sensitivities like bright lights or loud environments. There’s also the lifelong impact of medications and the different approach to pregnancy and birth.

The biggest misunderstanding I face is people assuming I’m “fully recovered.” Sure, I’m okay most of the time, but that 10% that isn’t okay consumes all of me. When I struggle, people can think I’m being “difficult” or “overly emotional,” instead of recognizing there’s a real, invisible reason behind it.

Daily Life After Stroke

Invisible challenges seep into every aspect of life. Returning to work was daunting. I had lost my confidence, my sense of thriving. Socially, I went through a spiral — relying on alcohol to give me courage, which led to blackouts and added complications with medications. Large social environments became overwhelming, so I limited myself and significantly reduced alcohol.

Strategies That Help

Managing an invisible disability requires systems and routines. At work, I rely heavily on post-it notes, emails instead of casual conversations, and cross-referencing calendars and diaries. I take my time completing tasks, and I’ve learned it’s okay to ask for help or step aside when needed.

It’s all about creating supports that allow me to keep advocating for others - my clients, my family, and myself - while acknowledging my own limits.

What I Wish People Understood

Be kinder. Be understanding. Look beyond the surface. Just because someone seems “fine” doesn’t mean they aren’t struggling. Invisible effects mean a lot of silent suffering, often because we don’t want to appear dramatic or burdensome.

Living with an invisible disability after stroke is complex, isolating, and exhausting. But three years on, I feel grounded in a positive place. I’ve learned to advocate for myself, create routines that support my brain, and prioritize my mental and emotional health.

Recovery isn’t linear. Some days are good. Some days are incredibly challenging. But with support, patience, and kindness - both from yourself and others - life after stroke is still a life worth living."

National Close the Gap Day is a reminder of what’s possible when we listen, learn, and act together. Aboriginal and Torr...
18/03/2026

National Close the Gap Day is a reminder of what’s possible when we listen, learn, and act together.

Aboriginal and Torres Strait Islander peoples hold deep knowledge, strength and resilience. Closing the gap means walking alongside communities, listening to what matters, and supporting solutions led by community.

Everyone deserves equitable access to treatment and care.

By working together, we can improve care, strengthen outcomes, and create a future where everyone has the opportunity to live well.

Once you have had a stroke, knowing how to stand up for yourself within the health system or daily life really matters. ...
18/03/2026

Once you have had a stroke, knowing how to stand up for yourself within the health system or daily life really matters. Top advocate and survivor Adrian O'Malley has shared his top tips to help you advocate for yourself effectively.
https://ow.ly/3ai750XWt0b
Picture by Chris Lane via the Leader

This is a fact that shocks people - and it should. In Australia, stroke kills more women than breast cancer and more men...
16/03/2026

This is a fact that shocks people - and it should.
In Australia, stroke kills more women than breast cancer and more men than prostate cancer.
Yet many people don’t realise that a stroke is an attack on the brain, cutting off oxygen and causing brain cells to die.
Even more concerning, only 66% of Australians can name at least one sign of stroke.
So how many people are missing the signs - and not getting the life-saving treatment they need in time?
Please help us change that. Share this message with your friends and followers and help raise awareness in your community. When it comes to stroke, there is no time to lose.
https://strokefoundation.org.au/about-stroke/learn/signs-of-stroke

From Cheyanne, "It was January 2023, just weeks before my 24th birthday.We’d been out yabbing that day, enjoying the sun...
12/03/2026

From Cheyanne, "It was January 2023, just weeks before my 24th birthday.
We’d been out yabbing that day, enjoying the sun. When we got home, I bent down to put our daughter to bed. As I stood back up and took a few steps, I suddenly felt really faint and collapsed.

When I came to, I was lying on the floor and the whole room was spinning.

At the time, I honestly thought I’d just overdone it - too much sun, not enough food, exhausted from being a mum. I went to bed thinking I could sleep it off.

But the next day, I knew something wasn’t right.

My fiancé would ask me simple questions like, “Where are the keys?” and I couldn’t answer properly. I kept responding with things like, “Yeah okay,” even though in my mind I knew exactly what he was asking and I knew the answer. It was like my brain and my mouth weren’t connecting.

I noticed my face had drooped slightly, especially around my mouth. My speech wasn’t slurred, but my left arm and leg felt extremely heavy and weak. I couldn’t lift them properly.

We went to our local hospital, but the CT scan didn’t show anything. At first, they weren’t sure what was happening. They mentioned seizures. Even an insect bite.

My younger sister kept saying she thought I’d had a stroke, but I didn’t believe it.

I was young. Strokes don’t happen to young people… right?

I was transferred to a hospital an hour and a half away. After waiting three days for an MRI, they confirmed I’d had a cerebellar stroke.

That’s when they discovered the cause - I had an undiagnosed hole in my heart. A blood clot had passed through and travelled to my brain.

It was terrifying. Completely unexpected. And it changed our lives in an instant.

Racing Was My Life - Before my stroke, racing was everything.

Weekends at the track. Late nights working on the car. The adrenaline. It wasn’t just a hobby - it was our life. It’s what we did together as a family.

After my stroke, racing suddenly felt so far away. Like something, I might never get back.

I was still at every meeting. I’m part of the Modified Sedans SA committee. I did social media, crewed for my fiancé and my dad, helped wherever I could. But deep down, I thought that might be the only way I’d ever be involved again.

That’s when calisthenics became such a huge part of my recovery. Racing felt impossible. Calisthenics gave me something to focus on. It gave me a team again. Training. Coaching. Competing solo. It gave me purpose.

Now, whether it’s a lap on the track or stepping onto the stage, I don’t take any of it for granted. I know what it feels like to almost lose it.

Being a Mum Kept Me Going - There were days I felt scared, frustrated, and completely exhausted.

Then I’d look at her and remind myself - I didn’t have the option to give up.

I wanted to be present for her. I needed to be present for her. I wanted her to grow up with her mum still able to live life fully.

And I wanted her to see strength.

Not the kind where everything is perfect - but the kind where you keep showing up even when it’s hard.

Learning to Trust My Body Again - Returning to driving wasn’t just physical.

Physically, I had to rebuild strength and coordination on my left side.

Mentally, I had to learn to trust my body again. After a stroke, you don’t just bounce back. You question everything.

Emotionally, I had to accept that racing wasn’t something I could just jump straight back into.

That’s why calisthenics meant so much to me. It kept my mindset strong while I worked toward my bigger goal - getting back in the race car.

It helped me feel like I was moving forward instead of just waiting.

The Racing Community Carried Me - it blew me away.

Drivers, crews, people I’d only met briefly - they reached out. It reminded me how strong our speedway family really is.

When your whole world changes overnight, having that kind of support is everything.

What surprised me most was how many people genuinely cared.

It reminded me that I wasn’t doing this alone. My family wasn’t doing this alone.

Getting back behind the wheel was emotional. I thought it would just be excitement. But it was everything at once - nerves, adrenaline, gratitude… and a little bit of fear.

There were moments when I genuinely didn’t know if I’d ever sit in a race car again.

So when I finally climbed back in, put my hands on the wheel, and felt that familiar seat around me… it hit me hard.

The sounds. The atmosphere. It felt like coming home.

I remember sitting there with tears in my eyes and my heart in my throat thinking, “This is what I fought for.”

It wasn’t just about driving again. It was about getting a part of my life back that I thought I’d lost forever.

The Small Wins Matter Most - People see the big moment - for me, it was returning to racing.

They don’t see what recovery really looks like behind closed doors.

They don’t see the frustration. The tears. The days when you feel trapped inside your own body.

Some days the win wasn’t walking further or getting stronger.

Some days the win was getting dressed without crying because I couldn’t remember how to put my pants on properly. Or because my body just wouldn’t cooperate.

Those small, invisible wins are what built me back up.

And that’s what I’m most proud of - that I kept going, even when the progress felt small.

My Goals Look Different Now - Of course, I still want to win. That competitive side of me isn’t going anywhere.

But now it’s about more than trophies.

Every lap means something.

I want to show people the behind-the-scenes side of racing - the hard work, the setbacks, the rebuilds, the comebacks. I want to connect more, because now I understand how much community matters.

My biggest motivation?

Proving to myself that I wouldn’t give up. I would be kind to myself, but I would keep making incremental improvements.

Life can knock you down in the worst possible way. But you can still find your way back.

To Other Young Survivors - Especially Mums - Recovery isn’t linear.

You can have an amazing day where you feel strong and hopeful, and the next day feel like you’ve gone backwards. That doesn’t mean you’re failing.

That’s recovery.

You’re never too young. Too broken. Too far gone to rebuild your life.

Sometimes the dream feels so far away it’s overwhelming. But you can’t fix everything overnight.

Sometimes the biggest achievement is just getting out of bed. Making the bed. Having a shower. Getting through the day.

That’s where it starts.

If you keep showing up, even in the smallest ways - you can get stronger.

You can find yourself again.

And you can still chase the life you thought you’d lost, even if it looks different. "
Cheyanne Richter Uren s15 Modified Sedans SA

After his stroke, Matthew didn’t just focus on his own recovery - he set out to change recovery for others. He received ...
11/03/2026

After his stroke, Matthew didn’t just focus on his own recovery - he set out to change recovery for others.

He received a Stroke Foundation Future Leaders Grant to develop virtual reality (VR) tools that help people with aphasia practice real-life conversations in a safe space.

Imagine being able to step into a virtual café, order a coffee, respond to small talk and practice your speech - before doing it in the real world. That’s exactly what Matthew’s research is building. A space where people can rebuild confidence, reduce anxiety and rehearse everyday moments that can feel overwhelming after stroke.

Because when you’ve lived it, you understand how big those “small” moments really are.

His work is proof that lived experience doesn’t just shape recovery - it can transform it.

Read Matthew’s blog and see how technology is helping change the future of stroke rehabilitation.

https://strokefoundation.org.au/media-centre/stroke-stories/using-technology-to-change-stroke-recovery-because-i-ve-lived-it

10/03/2026

There isn’t one path in stroke recovery.
Recovery looks different for every person. For some, progress is big and visible. For others, it’s quiet, steady, and made up of small wins that only they truly understand. Every improvement - big or small - matters.
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Your recovery is about you. Where you want to go. The goals that matter to you. The support around you. And your access to the services and information you need along the way.
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Recovery is a team effort. The right team - health professionals, family, friends, and peers who truly get it - can make all the difference.
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It might not look like what you imagined. It might not follow the timeline you hoped for. But that doesn’t mean it isn’t progress. Keep going.
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Connect with others who understand. Reach out to StrokeLine 1800 787 653 for information, support and guidance.
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You don't have to do this alone.

From Brian, "Having a stroke changes your life in ways that are hard to explain. It affects your body, your emotions, yo...
09/03/2026

From Brian, "Having a stroke changes your life in ways that are hard to explain. It affects your body, your emotions, your independence, and even your relationships. Doctors and researchers know a lot about strokes, but they can’t always fully understand what it’s like to live through one every day.

That’s why I believe survivors like me need to be part of the research process. Our experiences give a perspective that no textbook or lab can teach. When I get involved - from helping shape the questions researchers ask, to giving feedback on the results - I know the research is more likely to focus on what really matters to people like me.

For example, I can speak about things that aren’t always obvious in a hospital or clinic: gaps in rehab services, the mental health support that’s missing, or how hard it can be to communicate with doctors and therapists.

Being part of research also means I can help make it more accessible. Fatigue, mobility issues, trouble speaking or thinking clearly, and transport difficulties - these are real barriers. I can tell researchers what changes might help someone like me participate. That could be adjusting schedules, simplifying forms, or thinking carefully about how data is collected.

I can also help make research more respectful. Sometimes questions or study topics can feel intrusive or even trigger painful memories. By sharing my perspective, I help make sure participants’ rights, privacy, and emotional wellbeing are protected.

Being involved in research is empowering. It turns me from a passive subject into an active partner. I get to help shape the future of stroke care, and my voice matters. Working alongside researchers helps build respect and understanding between survivors and the medical community, and breaks down the traditional hierarchy where only “experts” make the decisions.

Over time, these partnerships can grow into advisory panels or ongoing survivor groups that continue to guide research. Survivors also bring stories and real-life experiences that make findings easier to understand and apply. We help translate research into everyday language, teach communities, and champion better care and policies.

Most importantly, survivors bring fresh ideas and a reality check. We remind researchers what life is really like after a stroke. We can suggest new ways to measure recovery, highlight challenges that haven’t been studied yet, and inspire solutions that are practical, creative, and grounded in real life.

Being part of research doesn’t just help science - it helps people. It makes studies more relevant, care more effective, and recovery more achievable. And that’s why our voices matter. "
Want to explore becoming a research partner?
https://strokefoundation.org.au/what-we-do/research/participate-in-research

05/03/2026

From Hailey, "Dear little stroke warriors and the families who love them.
I am writing to you as someone who once stood exactly where you are now: a little stroke warrior who grew up.

Keep going, and find a life full of meaning, purpose, and fulfilment.

Before anything else: you are still you. Not broken. Not alone. You are strong, clever, funny, kind, and full of possibilities.

Having a stroke so young can feel overwhelming, confusing, and at times - unfair. You might wonder why your body feels different, why things take more effort, or why no one else seems to be struggling the way you are.

Some days you might feel so proud of how far you’ve come and the strong person you are. Other days you might feel a huge sense of tiredness, sadness, or frustration. All of that is okay. Every feeling is valid, and you are allowed to feel what you feel.

I won’t pretend the road is easy. Growing up after a stroke often means learning things in new ways and thinking outside the box. Some days might feel like the pieces don’t quite fit together - but you will get there.

And I promise you this: there is so much life waiting for you. Your story does not end with stroke, and it does not define the incredible things you will achieve.

You will find strengths you didn’t know you had. You will meet people who truly see you. You will discover ways of doing things that are uniquely yours.

The challenges you face now may one day become the very things that make you compassionate, determined, creative, and brave.

I am so proud of you for showing up, for trying again in a different way, for not giving up, and for doing hard things on days when others don’t see how hard they are.

You don’t have to be “inspiring” or “strong.” You just need to be yourself, and that is already enough.

To the families: thank you for the endless love you show, the patience, advocacy, and quiet courage you show every day. Your belief matters more than you know. The safety you create gives these kids room to grow, heal, and dream big.

And to all of you together kids, siblings, parents, carers: I know things might feel heavy with so many unknowns, but please know this - life after childhood stroke can be meaningful, joyful, and rich.

Just because it may look different to what you pictured does not mean less. It simply means different...

Keep going. Keep hoping. Keep being proud of how far you’ve come.

With understanding, care, and belief in you, from a grown-up who once walked this path."
- Hailey (I had a stroke at 6 years old)

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Stroke Foundation

The Stroke Foundation is a national charity that partners with the community to prevent, treat and beat stroke. We stand alongside stroke survivors and their families, healthcare professionals and researchers. We build community awareness and foster new thinking and innovative treatments. We support survivors on their journey to live the best possible life after stroke. We are the voice of stroke in Australia and we work to:


  • Raise awareness of the risk factors, signs of stroke and promote healthy lifestyles.

  • Improve treatment for stroke to save lives and reduce disability.

  • Improve life after stroke for survivors.