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.

Australia’s Biggest Blood Pressure Check is on this May.Around 7 million Australians have high blood pressure, and nearl...
01/05/2026

Australia’s Biggest Blood Pressure Check is on this May.
Around 7 million Australians have high blood pressure, and nearly half don’t even know it. It remains the single biggest preventable risk factor for stroke, heart disease, kidney disease and dementia.

The thing is, high blood pressure often has no symptoms. But it is preventable and treatable.

Don’t wait. Get checked this May. Know your numbers. It could save your life.
Please share this important message onto your page. You may know your numbers, but there are millions of people who don't. Thanks in advance!
https://strokefoundation.org.au/what-we-do/prevention-programs/abbpc

ABBPC 2026 is proudly supported by:
Major Sponsors: Kieser Australia Servier and AstraZeneca and Supporting Sponsor: Pure Australia

30/04/2026

Have your friendships changed since your stroke?
James was in his 20s when his stroke turned life upside down. Along with everything else, his friendships shifted too. Some people stayed. Some didn’t. And some connections changed in ways he never expected.

He talks honestly about what that’s been like, the awkward moments, the distance, the people who showed up, and the ones who couldn’t. It’s real, and it’s something a lot of people don’t talk about enough.

Friendships after stroke can look different. And that doesn’t always mean worse. Sometimes it means deeper. Sometimes it means finding your people in new places.

A big thank you to James for opening up and sharing this part of his story so honestly. And to Hailey, a childhood stroke survivor, for leading such a thoughtful and real conversation.
Watch their full conversation here: https://strokefoundation.org.au/media-centre/stroke-stories/the-takeaway-talking-about-friendships-after-stroke-with-james-kirkwood
If you feel comfortable, we’d love to hear from you, comment below and share your experience - it may help others.

29/04/2026

“Hi, I’m a stroke survivor and I’m part of the team helping shape a new online resource to support confidence after stroke.

Recovery isn’t just physical. It’s also about confidence, identity, and figuring out how to move forward in a way that works for you.

This project matters to me because I know how much that part gets missed.

We’re looking for people to try the website and give honest feedback—what works, what doesn’t, what actually helps, and what’s missing.

This is your chance to shape something that could genuinely support other people after stroke.

If you’re interested or want to know more, you can check it out here:
https://strokefoundation.org.au/what-we-do/research/research-projects/digital-solutions-to-improve-health-self-efficacy-after-stroke

Would love to have you involved.” - Saran

28/04/2026

A recent story out of Adelaide shows why speaking up matters.
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Shane, who uses a wheelchair, was stopped from being picked up in a designated disability zone because the car didn’t have a permit, and his mum was threatened with a fine.
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He didn’t stay quiet.
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Shane shared his experience. He spoke up about safety, dignity, and the barriers people with disability face every day. And people listened.
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The response was swift. An apology. A review. A conversation about doing better. This is what advocacy looks like.
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It’s not always loud, sometimes it’s simply saying, “this isn’t right.”
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Because change doesn’t happen without people who are willing to call it out.
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For many in our stroke community, advocacy becomes part of life after stroke. Whether it’s navigating access, being understood, or pushing for better systems.
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Tell us about your experience - we're pretty sure that you'll have had an experience of barriers in your way.

Hi, my name is Lou. I’m a young stroke survivor of 3 years, and I’ve lived here in Victoria for the past 10 years. Befor...
27/04/2026

Hi, my name is Lou. I’m a young stroke survivor of 3 years, and I’ve lived here in Victoria for the past 10 years. Before I moved here, I had lived in London for about ten years (I’m originally from the UK) a full decade of becoming me in my twenties and a year of my thirties unfolded there in London: many strong friendships were forged over several pints, late buses home, love, heartbreak, and reinvention. London shaped me. I felt strong there. Established. At home.

We had only just landed in London that very morning. On tenth December 2022, right off a long-haul flight from Melbourne and straight out of Heathrow onto the Piccadilly line to Finsbury Park tube station, we were greeted by our dear friend, Gaby. Weary-eyed and wired all at the same time in that strange way only jet lag can produce. The winter morning light felt sharp and so familiar to me as we headed out, shivering from head to toe, for a walk through Finsbury Park Nat, my partner; Gaby; Ellis, Gaby’s dog; and I trying to shake the travel from our bodies. It feels kind of symbolic in hindsight: walking off the distance and arriving properly.

I was buzzing. It was my belated 40th birthday celebration weekend with my London family in my city. I remember thinking how lucky I was.

Back at Gaby’s kitchen, each stuffing our faces with a bacon butty, the house warmed quickly with anticipation of the party that was to be that night. Our coats are over chairs, chatter, and plans. Nat and I went for a token jet lag sleep. We woke 2 hours later and started to get ready. I was dressed for the party properly dressed. Not ‘trackies from a flight’ dressed. Celebratory. Nice shirt on, hair styled, ready, ready. Nat popped out with her brother, Dan, and his fiancée, Ellie, to grab some drinks for the evening. And then something shifted.

Pins and needles in my left leg with a strange fizzing. At first it felt like one of those fleeting travel sensations dehydration, tiredness, altitude residue. We’d only landed hours before. It was easy to rationalise.

But my body was already in crisis. Gaby saw it in my face before I understood it myself. Something wasn’t right. She ran into the street in the hope that Nat was there.

The moment Nat saw me, she knew (an ED nurse through and through), confirmed by the second opinion from Ellie (a GP). No hesitation. She called 999. They didn’t answer....
Read what happened next: https://young.strokefoundation.org.au/stories/a-life-recalibrated

Do you know our mission?We’ve put it on a t-shirt - just in case you missed it.Spotted out in the wild today, our Stroke...
24/04/2026

Do you know our mission?
We’ve put it on a t-shirt - just in case you missed it.
Spotted out in the wild today, our Stroke Foundation team out and about, bringing our Strategy 2027: Stronger Together to life.

By 2027, we’re working toward:
Fewer strokes by reducing risk factors like high blood pressure and increasing awareness
Better outcomes through access to evidence-based stroke care in every community
Stronger recovery by expanding support, services, and rehabilitation for all
https://strokefoundation.org.au/about-us/strategy #
This is what advocacy in action looks like.

Lena, "Stroke doesn’t always look the way we expect, and it doesn’t only happen to “other people.” I definitely didn’t t...
23/04/2026

Lena, "Stroke doesn’t always look the way we expect, and it doesn’t only happen to “other people.” I definitely didn’t think it would happen to me.

The shock of being told I had had a stroke is unexplainable. I sat in the emergency room with my husband repeating, WTF, over and over again. How could this possibly have happened to me? I was 50 at the time and in the best physical shape of my life. Health and fitness were my passions, and I lived accordingly.

The blood clot that entered my brain happened on a Saturday night, and I didn’t recognise it as a stroke. I felt spacy and disconnected, and I was struggling to formulate what was going on in my brain into words. I couldn't remember the ritual my daughter and I shared at bedtime, and it scared her. I told her I was ‘fine, just tired’ and went to bed.

I went to the hospital the next morning, still not thinking it was anything serious. I felt okay, just a little ‘wobbly’. So when the CT scan confirmed I had had a stroke and I was admitted to hospital, I was in disbelief. That shock continued as I grappled with the idea that ‘someone like me’ could have a stroke. It didn’t feel fair and certainly didn’t make sense.

A week later, I was back in the emergency room. It was Easter weekend and the last place I wanted to be, but I was experiencing symptoms and had started to panic that I was having another stroke. In hindsight, it was likely symptoms of the first stroke, but at the time I didn’t have the knowledge or understanding of how I might feel or what recovery was going to look like.

Three months after the stroke, I had surgery to close a PFO (Patent Foramen Ovale), which the neurologists and cardiologists determined was the likely cause of the clot reaching my brain. A PFO is a small hole in the heart that can allow blood to move from the right to the left side and travel to the brain. I had never heard of a PFO, and the thought of heart surgery created another level of anxiety.

I’m not sure I ever fully comprehended exactly what my body had been through, and I think I was in denial for a really long time. I had trouble talking about the stroke, and there was a sense of shame attached. I went through periods of anxiety and panic, scared that it could happen again at any time.

I sought therapy and introduced mindfulness into my day to support my mental and emotional health. As an active, busy mum and coach running my own business, I struggled with the limitations that stroke fatigue and reduced energy brought. Stroke fatigue is incredibly challenging because it doesn’t seem to follow a pattern, and no one can see what you are going through. I also found it really hard to explain.

I had a hard time asking for help, and because I didn’t have any severe physical disabilities, I didn’t feel deserving of support. I felt like there were other people who needed it more, but with the encouragement of a friend who worked in brain injury, I found support through SHIU (State Head Injury Unit). They helped me to better understand what was happening in my brain and why things felt different. They introduced me to pacing, gave me someone to talk to who ‘got it’, and helped me figure out some goals and a way forward.

I was frustrated, but I tried to return to my life at a slightly slower pace, telling myself that I was okay, that it could be worse, and that I was one of the lucky ones… but I didn’t allow myself to grieve or feel sad over what was essentially the loss of my identity.

About a year after my stroke, I fell into what I would describe as burnout, or possibly depression. My body stopped me in my tracks again.

This time, I paid attention. I realised I needed to take time to truly heal and to feel my way through it. I stopped working with clients altogether and focused on my family and myself. I had to learn to say no to many things to reduce the busyness, and to manage my energy so I didn’t burn out from everyday tasks. But most importantly, I had to learn to let myself feel sad, and to accept that it was okay not to always be the strong one. I had to grieve who I was before the stroke in order to accept the life that was now mine.

I am still a work in progress, but two years on, things are looking much better. Instead of trying to return to the old version of myself, I have been creating new experiences. I now volunteer at Riding for the Disabled, prioritise myself and my family, and enjoy the calm and quiet of nature as much as possible. My approach to exercise has shifted in a healthier direction, and I am present in a way that may not have happened without the stroke.

I have adopted a slower pace of life, and mindfulness is now a regular part of my day. The stillness I practise has helped me rediscover who I am at my core, outside of my roles and the ‘doing’ that once defined my life.

If there’s one thing I would want others to take from my experience, it’s to listen to your body, even when the signs feel subtle or don’t quite make sense."

From Skye, "Being part of Australia’s first Mobile Stroke Unit (MSU) team was honestly a dream come true.It felt like we...
22/04/2026

From Skye, "Being part of Australia’s first Mobile Stroke Unit (MSU) team was honestly a dream come true.

It felt like we were part of something really important - a huge step forward for stroke care in Melbourne. To be there from the beginning, helping roll it out and seeing it come to life… I feel incredibly lucky.

Every call-out was different, but there was always an urgency to each case

The MSU is dispatched alongside a regular ambulance crew, who usually arrive first. When we get there, we take a handover from the paramedics and start assessing the patient straight away.

From there, it’s all about teamwork.

The nurse begins their assessment and links in with a neurologist via telemedicine. If needed, the neurologist can assess the patient remotely. If a scan is required, we bring the patient onto the MSU, where the radiographer has the CT scanner ready to go.

We run a CT scan on board, review the images in real time, and make a treatment decision - all before we’ve left the patient’s house.

If treatment is needed, we start it immediately.

Everything is happening at once - monitoring the patient, preparing scans, communicating with the hospital, and updating the family. It’s fast, focused, and incredibly collaborative.

The difference this makes is huge.

We’re treating people where they are; at home, at work, at the shops - sometimes just minutes after their stroke begins.

And you can see the impact right in front of you.

I’ve watched patients who couldn’t move or speak start to regain movement on the way to hospital. Their speech becomes clearer. Their face starts to return to normal.

It’s hard to describe how powerful that is to witness.

Those moments stay with you. They remind you exactly why this work matters.

I’ve always been drawn to fast-paced environments. I started in emergency nursing and then moved into ICU - so working on the MSU felt like coming home to that kind of environment.

But it’s different out there.

You don’t have a full hospital team behind you. It’s just the MSU crew and the paramedics on scene. You have to make quick decisions with limited information, trust your skills and knowledge, and trust each other.

That trust in your team becomes everything.

It’s not for everyone. Some incredibly skilled nurses prefer the structure of hospital settings. But for me, I loved it.

There are so many moments that stay with me.

One that stands out is a man who was completely paralysed down one side and unable to speak when we arrived. After his scan, we identified a large clot and immediately started clot busting medication before taking him to hospital for further treatment - and after his procedure, he high-fived the team with the arm that had been paralysed.

He went home three days later, moments like that never leave you.

But one of the hardest parts of the job was seeing people who came to us too late.

Not because they didn’t care, but because they didn’t know.

I’ve seen families do what they thought was the right thing, putting someone to bed to rest, not realising they were having a stroke. By the time help was called, the window for treatment had passed.

That’s why awareness is so important.

Knowing the signs. Acting quickly. It can change everything.

Continuing the Work....

Now, in my role with Stroke Foundation, I’m focused on something just as important - making sure people receive the best possible care when they get to hospital.

Through the Stroke Centre Certification program, we’re working to ensure hospitals meet high standards of care. When a hospital is certified, it means patients and families can trust the level of care they’ll receive.

For me, a good outcome is simple.

-Every paramedic equipped with the tools and knowledge to assess and treat stroke early.
-Technology supporting faster diagnosis and decision-making.
-Hospitals continuing that care with the right systems and staffing in place.

Because every person deserves the best chance of recovery.

And as I’ve seen firsthand - those first moments can change everything."

21/04/2026

Nine years after her stroke… she moved her thumb.
Nine years.
We’re often told recovery “plateaus.”
But stories like this remind us that progress can still happen - even years later.
When you decide to work towards something, when you set a goal that matters to you, long term change is possible.
And at the same time, it’s important to remember this is your journey.
You get to decide what you want to work on.
You get to decide what matters.
And it’s also okay to accept where you are.
There is no one right way to do recovery.
But sometimes… a small movement can mean everything.

Does stroke recovery feel overwhelming - like the road ahead is just too big? In her poem, Voula reflects on a powerful ...
20/04/2026

Does stroke recovery feel overwhelming - like the road ahead is just too big? In her poem, Voula reflects on a powerful lesson from life after stroke: you don’t have to “eat the elephant” in one bite. It’s about small steps - one moment, one effort, one win at a time. Because progress isn’t always loud. Often, it’s quiet, steady, and deeply personal… and those small steps matter

Voula, “3 years on I keep repeating to myself that you are stronger and resilient than the stroke
In my head I tell myself a tip...

In difficult times, move forward in small steps.
Do what you have to do, but little by little.
Don't think about the future or what may happen tomorrow.

Wash the dishes.
Remove the dust.
Write a letter.
Make a soup.

You see?

Advance step by step.
Take a step and stop.
Rest a little.
Praise yourself.

Take another step.
And then another.
You won't notice, but your steps will grow more and more.

And the time will come when you can think about the future without crying.”

Today is my 10-year stroke anniversary - this is what I have learned.  When people talk about stroke recovery, they ofte...
17/04/2026

Today is my 10-year stroke anniversary - this is what I have learned.
When people talk about stroke recovery, they often focus on the things you can measure; therapy hours, milestones, goals.

And yes, those things matter. But for me, there’s something just as important. Something quieter.

It’s not about being positive all the time. It’s not a personality trait. And it’s definitely not a burst of motivation that comes and goes.

It’s something deeper - a foundation that shapes whether I keep going, especially when things get hard - it is self-belief.

In the early days after my stroke, I didn’t have that belief.

I borrowed it.

I borrowed it from my physio, my occupational therapist, my speech pathologist - people who could see potential in me before I could feel it myself.

I borrowed it from my family, sitting beside me, showing up, quietly believing that I was still me. At that stage, I wasn’t driving my recovery. Other people were holding that belief for me. But things change. You leave hospital. Therapy becomes less frequent.

People around you start to think you’re “better.” And that’s when something shifts. Because this is where recovery becomes yours.

If you believe you can still improve, you keep going. You keep trying, adapting, pushing forward - even when progress feels slow.

But if you start to believe you’ve reached your limit… you can stop before you’ve really had the chance to see what’s possible.

I believe that belief, or lack of it, can change everything.

Living with stroke isn’t just physical; there’s fatigue, frustration, and grief for who you used to be. Moments where you question yourself. Without self-belief, those moments can feel like proof that you’re failing. With it, they become part of the process.

Some days I move forward.
Some days I don’t.
And I’ve learned that both are part of recovery.

Brooke, "I believe that stress caused my stroke.I own gyms. I’ve always been fit, strong, and busy - the kind of person ...
16/04/2026

Brooke, "I believe that stress caused my stroke.
I own gyms. I’ve always been fit, strong, and busy - the kind of person who doesn’t stop.

In January, I was completely fine. Healthy. Busy. But I’d had a really stressful week. I remember thinking - something is going to give.

But you don’t think it’s going to be a stroke; maybe you’ll get sick or burn out.

I got home from work, had a shower, sat on my bed to do some emails… and when I tried to stand up, I couldn’t.

My body just didn’t respond.

I ended up falling asleep. When I woke up, I had pins and needles, and my legs felt strange - floppy. It honestly looked like something was really wrong, but at the same time, I didn’t take it seriously.

I still went to my hairdresser appointment, I caught up with friends, and we were literally laughing about my “dead leg.”

By Friday night, one of my friends got worried and said we should go to Emergency.

We got there and it was full - so we left.

The next day was my son’s birthday. Life kept going, so I ignored my symptoms.

Sunday, I went to the gym and saw Ryan, a PT who had a stroke a few years ago. He took one look at me and said, “I wouldn’t muck around - get to the hospital.” I only found out later that I had some of the same symptoms that he had.

Still, my first thought was… how embarrassing if it’s nothing? I felt like a hypochondriac.

But I went.

And that decision changed everything.

At the hospital, they were great. Because of the numbness, they were initially looking at things like MS. Then they told me it was a stroke.

I immediately thought my stroke must have been triggered by stress, and even though I don’t have that as the cause – in my bones, I know this is why.

I was in the hospital for about five or six days. I couldn’t write. My head felt heavy. My body wasn’t doing what I told it to.

And then there was the loss of independence; I couldn’t drive for six weeks. I have three kids - 8, 11 and 14. I run three businesses. Suddenly, I was relying on other people to get me around, to help with everything. That was one of the hardest parts. I remember thinking - if you had to go through this alone, it would be so isolating.

Recovery has been a process. I still have foot drop; I walk with a limp - but it’s getting better.

I do physio. I go to the gym. I take it day by day.

That’s all you can do.

Looking back, I honestly don’t think I would have gone to hospital if it wasn’t for Ryan.

In that moment, having someone say, “this isn’t right,” made all the difference - because I couldn’t see it myself.

Thank you for saving my life, Ryan. I owe you one!"

Address

461 Bourke Street
Melbourne, VIC
3000

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Telephone

+611800787653

Website

https://informme.org.au/, https://young.strokefoundation.org.au/, https://enableme.

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