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Discovering the Power of Movement

When I was initially diagnosed with a musculoskeletal condition, I learnt quite quickly from practical experience that when I moved, my stiffness and pain were both much less. Full disclosure: I had always been a swimmer and a weightlifter before my chronic conditions made themselves known, so I wasn’t starting from scratch. Even so, I was so convinced movement was helping me, I did a twelve-month Fitness Coaching course to learn more. For the record, I am 70 years of age with three musculoskeletal conditions. 

Learning to Pace Myself

I also participated in a Chronic Pain Management Program at the Barbara Walker Pain Management Centre.  That was where I learnt about pacing our activity. Quite often patients may try to do what they did before their condition (or conditions) appeared. That can lead to increasing fatigue or even hurting ourselves.
Pacing is about determining our starting point then increasing what we do, usually at about 10% a week although this can vary from person to person. Of course, not forever – if I increased at 10% a week for 11 years, I’d be climbing Mount Everest now! I can assure you, I am not! 

Building my Routine

When I first started, I would do four small walks a day. Five minutes each.  I gradually increased each walk over time and decreased the number of walks per day to two or three, depending on the day and other commitments I may have. 
At one point each walk was about 12 minutes, three times a day. Before work, lunchtime and after work. Now in my eleventh year of managing my conditions, I walk four kilometres a day, my step goal is 7,500 steps per day and I do strength training three times a week. I still do not do the four kilometres in one walk: I may break it into two walks, sometimes three.  

The Importance of Strength Training

Strength training is very important to maintain not only bone density but also muscle strength. I have a damaged lumbar spine: I particularly work on my posterior chain (back muscles) strength to support my back and ensure I am mostly pain free. Although I design my own workouts, I do consult an exercise physiologist. 
When I first reintroduced strength training into my routine, I would do less steps on those days. Now, several years later, I no longer need to reduce my step goal on weights days.  

Movement for Everyone

Not everyone can walk and weightlift though! Musculoskeletal Health Australia and Epijoint are well aware of that and are promoting chair-based exercise: The World’s Biggest Sit In. Chair-based exercise is an inclusive, accessible form of physical activity suitable for everyone. It offers a range of benefits including improved cardiovascular health, enhanced strength, better flexibility, and increased bone density, all whilst keeping your movements safe and controlled. exercise 

Expert Evidence

Arizona-based chronic pain specialist David Tom, M.D. has said:
They see movement as medicine Depending on the severity of your condition, you may not be able to exercise with the intensity that you used to or want to. But if you’ve been avoiding exercise altogether, it’s time to start.
“We used to put patients on bed rest for pain. Not anymore,” says Dr. Tom. “Staying physically active is critical for pain management, as it releases endorphins which can improve your mood and even ease pain.” People who don’t move can get tight muscles, joint pain, muscle strain and spasms, which can worsen existing pain.
Source: 4 Resilient Ways To Cope With Chronic Pain 

Caveat:
Make sure you talk to your doctor/(s) and/or physiotherapist before using Movement As Medicine. My purpose is to provide my experience as encouragement from a practical perspective. To illustrate the value of moving. Having said that, not all conditions are the same. Different patients have different comorbidities, different degrees of severity: a host of clinical considerations. Always consult YOUR health care providers. 

Additional Information: 

Pacing for Beginners 

We Need Personalised Numbers 

Movement as Medicine 



Where my OA story Begins:

I have had osteoarthritis, OA, for about 20 years. It began to impact me after a career as a dancer in my early 20s, too many hours spent working in high heels, and genetics. Saddest day ever when I gave away all my heels I couldn’t wear.

I was active, had young kids, walked a lot and was very fit, but my feet were so painful.
No shoes seemed to be comfortable and the thought of going for a long walk became really impossible.

Impacts of OA:

OA started in my feet first and made it painful to walk, one of those things you tend to just put up with until it gets to the point you don’t want to do much of anything that involves using your feet!
Difficult as my jobs involved a lot of walking and standing. Some days were worse than others and you tend to put it aside when it isn’t in the forefront. Shoes became difficult to find as I looked for more comfy styles. Even then, shoes I had worn and then changed for a season, were so painful to wear again.

Doctors tend to be a bit dismissive and say, it’s just arthritis you’ll learn to live with it, take these medications. Sadly, most medications don’t agree with my body, so finding other ways to manage the pain and mobility issues had to be a priority.

Moving Forward:

Gentle is the answer, no strenuous exercising, as I paid for it for days afterwards. So, continuing to keep moving and moderating exercise or activities to suit the condition became priority.
Supplements were unsuitable, I have too many allergies, especially the ones with shellfish. I have tried everything.

OA then started in my hands, which being a cook and painter was very hard to take. I had to keep finding gadgets that could open jars, chop things, and stirring the Christmas cakes became a job for the Kenwood chef. I just couldn’t make the big wooden spoon mix the cake. That was a big disappointment for me.

I also do Aboriginal painting which became very painful. I persisted and found ways to manage by taking short breaks, where once I could sit and paint for hours. I love painting with a passion, so adapting was a must.

Keep moving it or you lose it is a very good reason to keep going, you do lose functionality if you don’t. I also have rheumatoid arthritis and taking steroids has caused osteoporosis, which I had no idea I had until I started breaking bones. In the space of 2 years, I went from being ok, to serious disease. Not a long time in which to lose that much bone, mainly in my feet, which has made my walking even harder, but you keep going, I refuse to give in.

Limited mobility and pain can feel like you want to give up, but keep moving in any way you can, it will help you regardless of age.

The World’s Biggest Sit In  – an exciting initiative to help you get moving!

If you want to join a fun event that will help you keep moving and gain some flexibility, join Musculoskeletal Health Australia’s World’s Biggest Sit In on the 26th of October 2025 at Rippon Lea Estate, Melbourne or join in virtually via Zoom – it’s ideal for anyone with OA or another musculoskeletal condition.

MHA are going for the WORLD RECORD for the largest 30 minute chair-based exercise class – so we NEED YOU!! It’s free to register, for more information visit: The World’s Biggest Sit In. 

 

 

 



Living with a musculoskeletal (MSK) condition often means managing pain, stiffness, fatigue, and reduced mobility. Chair-based exercise offers a safe and accessible way to stay active without putting excess strain on joints or muscles.

What does the research say?

Research shows that seated exercise can improve strength, flexibility, and balance, while also supporting independence in daily activities. For people with MSK conditions, it provides an adaptable alternative to traditional exercise—helping to reduce discomfort, enhance overall well-being, and build confidence to move in ways that feel achievable and sustainable. 

Chair-based exercise (CBE) provides a safe, low-impact alternative that is supported by emerging research. Studies have shown that chair-based programs improve muscle strength, balance, and functional mobility, which are essential for preserving independence and reducing the risk of falls Trials in populations with osteoarthritis have demonstrated that chair-based interventions, such can enhance mobility and reduce pain. In addition, structured CBE has been associated with improvements in psychological well being, sleep, and quality of life, highlighting its holistic benefits 

What are some of the benefits?

Chair based exercise has specific benefits as a training method:

Accessibility & Inclusivity: Ideal for those with limited mobility, health issues, or low fitness levels. More likely to be performed consistently and a great way to increase confidence

Improves Strength & Function: Ideal for those with limited mobility, health issues, or low fitness levels. It can also minimise load-bearing and reduce balance issues.

Boosts Mental & Physical Well-Being: Benefits can range from improved mood and sleep to better immune markers and memory even from short sessions.

Feasible Across Settings:Deliverable at home, in clinics, hospitals, or community centers; easy to scale and adopt.

Safety & Compliance: Low injury risk and high adherence across most population groups

It’s important to note that although chair-based exercise has been shown to be effective, it should, in principle, be a starting point for those with low baseline function and be a part of a fuller rejuvenation/rehabilitation process. Overall, chair-based exercise is an evidence-based, adaptable, and inclusive approach to keeping people with MSK conditions active. It enables safe participation in physical activity, supports symptom management, and promotes long-term musculoskeletal health!

Visit the MHA website to explore our collection of Chair-based exercise videos, designed for all fitness levels. Remember to listen to your body, go at your own pace, and avoid pushing beyond your limits. Your safety and wellbeing are always the top priority.   

 

 

References Cheung, C., Wyman, J. F., Resnick, B., & Savik, K. (2014). Yoga for managing knee osteoarthritis in older women: A pilot randomized controlled trial. BMC Complementary and Alternative Medicine, 14(1), 160. https://doi.org/10.1186/1472-6882-14-160

 Kim, S. H., & Park, Y. H. (2020). Effects of chair-based resistance band exercise on physical functioning, sleep, and depression in older adults living in long-term care facilities: A randomized controlled trial. Geriatric Nursing, 41(6), 733–739. https://doi.org/10.1016/j.gerinurse.2020.07.009 

Park, J., McCaffrey, R., Newman, D., & Cheung, C. (2017). The effect of chair yoga on biopsychosocial outcomes among older adults with lower extremity osteoarthritis: A pilot randomized controlled trial. Journal of Geriatric Physical Therapy, 40(2), 99–107. https://doi.org/10.1519/JPT.0000000000000080

 Sitjà-Rabert, M., Martínez-Zapata, M. J., Martín-Rodríguez, S., Fort-Vanmeerhaeghe, A., Rey-Abella, F., Romero-Rodríguez, D., & Bonfill, X. (2015). Effects of a chair-based exercise program on physical fitness in older adults: A randomized controlled trial. International Journal of Sports Medicine, 36(10), 799–804. https://doi.org/10.1055/s-0035-1548885  


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Exercising when living with chronic musculoskeletal pain can be challenging especially when you’re unsure which movements are safe or effective. Musculoskeletal conditions often cause pain, stiffness, and inflammation in the joints and muscles, making physical activity feel overwhelming. However, regular exercise can help to ease these symptoms, improve mobility, build strength, and support overall wellbeing. A good saying is…MOVEMENT IS MEDICINE! 

The key is to find the right type and level of exercise for your individual needs. It’s always best to work with your doctor, physiotherapist, or fitness professional to create a tailored program that suits your condition and goals. 

 

A Daily Dose of Movement

Aim to incorporate some form of movement into your day, consistency is important, even low intensity movement is good…every little bit helps! The most beneficial routines tend to include a mix of: 

  • Flexibility exercises: Stretching and range-of-motion activities help maintain or restore flexibility in your joints and muscles, reducing stiffness and keeping your body moving more freely. 
  • Strength training: Building muscle strength supports your joints, enhances bone health, and improves your ability to carry out everyday tasks. 
  • Aerobic fitness: Activities like walking, swimming, or cycling get your heart rate up, improving cardiovascular health, increasing endurance, supporting weight management, and lowering your risk of other chronic conditions like diabetes. 

The most important factor? Choose activities you enjoy. Whether it’s walking with a friend, joining a group class, or trying something new (like chair-based exercise), enjoyment boosts motivation and helps you stick with it. 

 

 Gentle Exercise Options

If high-impact activity feels out of reach, there are still plenty of ways to stay active: 

  • Low-impact aerobic activities – such as cycling, walking, and swimming 
  • Tai chi – gentle, flowing movements that promote balance and flexibility 
  • Chair-based exercises – a highly accessible and adaptable option 

 

Why try Chair-Based Exercise?

Chair exercises are ideal for people with limited mobility or those who struggle with balance. They allow you to strengthen muscles, improve flexibility, and boost circulation all while staying seated or using a chair for support. You don’t need any special equipment or a large space, making them a great option at home, at work, or wherever you feel comfortable. 

These exercises are inclusive and easily adaptable. You can adjust the intensity, duration, and frequency to suit your needs, and target different parts of the body. Chair workouts can even be combined with elements of yoga, Pilates, or Zumba for added variety and enjoyment. 

 

Get Started Today

Visit the MHA, World’s Biggest Sit In, website to explore our collection of chair-based exercise videos designed for all fitness levels. Remember to listen to your body, go at your own pace, and avoid pushing beyond your limits. Your safety and wellbeing are always the top priority.  

 


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Living with a musculoskeletal condition often means managing ongoing pain, fatigue, and emotional challenges. In those tough moments, it’s natural to want to retreat and rest, but it’s also where self-care becomes most important. 

The World Health Organization defines self-care as “the ability of individuals, families and communities to promote health, prevent disease, maintain health, and cope with illness and disability with or without the support of a health worker.” Self-care is about taking intentional steps to support your physical, mental, and emotional wellbeing. For people living with musculoskeletal conditions, this means learning what works best for your body and giving yourself the time, space, and support to do it. 

Self-care is empowering. It allows you to take an active role in managing your symptoms and improving your quality of life. Promoting self-care means equipping people with the tools, knowledge, and confidence to make informed decisions about their health.  

 Why does self-care matter?  

  • Daily symptom management: Practices such as gentle exercise, stretching, rest, and heat/cold therapy can help manage day-to-day symptoms, reduce flare-ups, and increase mobility. 
  •  Staying active and informed: Even small movements can make a difference – consider chair-based exercise as a starting point. Being empowered to understand your condition, and recognising which therapies or activities help, encourages consistent self-care practices and long-term health benefits. 
  •  Nutrition and energy: Eating well supports joint and bone health, reduces inflammation, and improves overall energy levels. Staying hydrated, choosing nourishing foods, and listening to your body are simple but essential acts of self-care. 
  •  Mental health and emotional resilience: Living with chronic pain can impact your mood, motivation, and relationships. Self-care also means taking time for mental wellbeing, whether that’s through mindfulness, relaxation, peer support, or connecting with others who understand your experience. Feeling confident in your ability to manage your health can help reduce feelings of stress, helplessness, or frustration. 

To support this, Musculoskeletal Health Australia (MHA) has developed a range of tailored self-care plans for specific musculoskeletal conditions. These plans are aligned with the International Self-Care Foundation’s Seven Pillars of self-care.  

The MHA Self-Care Plans provide practical guidance and condition-specific advice to help you better understand, manage your condition, and live well.   

Self-care plans available on the MHA website include: 

 Self-care is more than a routine; it’s a mindset. Embracing it fosters resilience, confidence, and a greater sense of control. By making space for your physical and emotional wellbeing, you’re taking powerful steps toward living your best possible life whilst managing your musculoskeletal health. And remember self-care is not selfish, it’s essential. 

 More to explore 

  Tiny Buddha 

  This information was developed for mental health professionals, however there are a lot of useful resources that are helpful for anyone wanting to learn more about self-care. 

  ReachOut 

  Musculoskeletal Australia 

  University at Buffalo, School of Social Work 

  This information was developed for students studying social work, and professionals working in the field, however there are a lot of useful resources that are suitable for anyone wanting to learn more about self-care. 

  International Self-Care Foundation 

  Mental Health First Aid USA, National Council for Mental Wellbeing 

  Healthline  

References 

(1) Self-care interventions for health, World Health Organization. 

 (2) Health literacy, Australian Commission on Safety and Quality in Health Care 

 

 

Contact our free national Helpline

Call our team if you have questions about managing your painmusculoskeletal conditions, treatment options, mental health issues, or accessing services. They’re available weekdays between 9 am-5 pm on 1800 263 265; email helpline@muscha.org or via Messenger.


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Breakthroughs and Beyond: CAR T therapy in SLE

By Alberta Hoi

For Lani Watson, living with lupus once meant she could barely walk across a room. Diagnosed in 2022, she battled constant fatigue, joint pain, a severe skin rash, and the feeling that her own body was attacking itself. But today, thanks to a ground-breaking treatment, Lani is back playing football and living symptom-free. Her remarkable recovery using CAR T-cell therapy made national headlines – and for good reason.

CAR T therapy, short for Chimeric Antigen Receptor T-cell therapy, is a new and powerful treatment that was originally developed to treat blood cancers. It works by taking a person’s own immune cells and genetically modifying them so they can hunt down and destroy harmful immune cells. Now, researchers are testing whether this same approach can help people with severe autoimmune conditions like lupus.

In lupus, the immune system mistakenly attacks the body’s own tissues, and a type of immune cell called the B cell plays a major role. These B cells produce damaging antibodies and trigger inflammation. The version of CAR T therapy used in Lani’s trial is designed to remove nearly all B cells from the body, even the deep-seated, long-lived ones that are hard to reach with standard treatments. The idea is to give the immune system a kind of “reboot”. After the old B cells are cleared out, new ones gradually return, but they tend to look and behave more like those seen in healthy people.

It’s easy to understand why this approach has sparked so much hope.  For patients like Lani, whose disease didn’t respond to regular treatments, CAR T therapy offers real hope. But as researchers involved in these early trials emphasise, it’s not a silver bullet – and it’s not for everyone.

There are several types of CAR T-cell treatments being developed, and each one works a little differently. Before someone can receive this therapy, they need to go through comprehensive assessments, including disease activity scoring, immunological testing, and screening for potential risks. Right now, CAR T therapy for lupus is still experimental and only available through clinical trials

For most people living with lupus, conventional treatments are still the mainstay of care. Medicines like hydroxychloroquine, corticosteroids and immunosuppressants help control flares, protect organs, and improve daily life. These treatments can have side effects, but they are often essential, and they work best when combined with regular check-ups and a strong relationship with your healthcare team.

CAR T therapy is a major medical advance, but it’s also a very intensive process and currently only offered to a select group of patients with severe, hard-to-treat lupus. Even when it works well, long-term monitoring is essential, just like Lani’s 15-year follow-up plan.

The future of lupus treatment is full of promise. But for now, staying connected to your lupus specialist, sticking to your treatment plan, and acting early when symptoms change remain the keys to living well.

Contact our free national Helpline

Call our team if you have questions about lupus, managing your painmusculoskeletal conditions, treatment options, mental health issues, or accessing services. They’re available weekdays between 9 am-5 pm on 1800 263 265; email helpline@muscha.org or via Messenger.


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Joe recently took a week off work. Mentally and physically, he’d hit a wall, and with his back pain much worse than usual, he knew he needed to step back, take a breath, and reset.

That wasn’t easy for him to do.

Joe felt like he didn’t have the right to feel off. Didn’t most people experience back pain? He told himself he needed to keep a lid on the pain he was feeling — to just push through, do better, try harder. There were people out there working long hours just to make ends meet, dealing with “real” struggles. He had a steady job, a roof over his head, a good family, and solid mates. So, what was his excuse for feeling like he couldn’t cope?

That guilt made things worse. He couldn’t let go of the (ridiculous and outdated) thought that men weren’t supposed to feel this way. He felt selfish for not just ‘pushing through’.

But when Joe finally brought up how he was feeling with his GP and then later his mates, he realised he wasn’t the only one who felt like this.

And just like Joe, a lot of us living with musculoskeletal conditions are running on empty and just trying to keep it together.

So, for anyone out there who needs to hear this, IT’S OKAY.

It’s ok to take a break or to rest. You’re not a machine. Take the time you need to recover, both physically and mentally, from the things that are affecting you. That way, if you do return to what you were doing, you’ll feel refreshed and better able to deal with everything.

It’s ok to say no. We all want to please others, to be the go-to guy, so sometimes saying ‘no’ can be a real challenge. But you need to weigh up how you’re feeling and all the things you have going on and decide whether you can take on something else. If you can’t, then say no. Importantly, don’t feel you have to apologise for doing so.

It’s ok to listen to your body. In fact, it’s necessary. Living with a chronic condition means that you need to be aware of how you’re feeling. If you’re tired, rest. If your back hurts, move. If you’re feeling sluggish, get some air. Try and listen to whatever your body is telling you- listen and take action.

It’s ok to talk about mental health. Actually, it’s vital that we do. The more we talk about mental health and how we’re feeling, the less stigma will surround it, leading to more people opening up about their mental health and getting help when they need it.

It’s ok not to be perfect. No one is, no matter how they appear at work, around mates, or on social media.

It’s ok to put yourself first. Sometimes we need to make ourselves our top priority– whether that’s physically, mentally and/or emotionally. You’ll be better able to help others when you’ve taken time to look after yourself.

It’s ok to have an untidy house/car/office. Or for the grass to need mowing. Or for pet hair to cover every surface of your home. Sometimes things get a little untidy as we prioritise our health and wellbeing over making the bed, cleaning the bathroom or putting away the dishes. And that’s ok.

It’s ok not to watch the news. Take time to unplug from the often-chaotic 24/7 news cycle and focus on the world around you, including you, your family and friends.

It’s ok to be kind to yourself. Our inner critic can be really loud at times. If yours is giving you grief, ask yourself – would you say those things to someone you love? The answer is probably no. So quiet that inner voice by making a list of three things you like about yourself, and keep it on your phone or stick it on the fridge. Remind yourself of these things regularly.

It’s ok to forgive yourself. We often beat ourselves up for the smallest of mistakes. If you made a mistake – (or are being super-critical of yourself) – look at what you did, learn from it and move on – or talk about it if this is proving difficult. Don’t just keep thinking about it – it’ll only drive you crazy, add to any unease you’re feeling and make you more unhappy.

It’s ok to not be ok and feel sad/angry/vulnerable. Your feelings are valid, and they matter. However, if you feel like negative feelings are taking over, talk with someone. A trusted friend or family member, or a healthcare professional. While it’s ok to feel like this from time to time, you don’t want to feel like this all the time. And you don’t have to. There’s help available.

It’s ok to cry. We all have difficult days, and crying can be an outlet when we feel sad, stressed, overwhelmed, scared, angry or in pain. So, let it out.

It’s ok to put your phone down. We look at them too often anyway, so put it away for an hour, a day, a week. Be present and be mindful of the people and what’s going on around you.

It’s ok to admit you’re struggling. And it’s ok to ask for help. It doesn’t mean you’re not a capable person. It just means that in this time and place, you need some help. And that’s fine. We all need help every now and then.

It’s ok to take your time. We don’t always have to be in a hurry. Make space to breathe and be still, meditate and be mindful.

It’s ok not to have all the answers. You’re not Google or ChatGPT. Saying ‘I don’t know’ is a valid and human thing to say.

It’s ok to put aside your ‘to-do’ list and be spontaneous. Lists can help us feel in control and organised, but sometimes it feels amazing to toss the list aside and just do something unexpected, just because you can.

It’s ok to do more of the things that make you feel good. Playing sport, catching up with your mates, picnics with the family, reading a book to your kids…whatever it is that makes you feel good can help you recharge your battery, reset and make you a happier person.

And remember, it’s ok to be you.

Contact our free national Helpline

Call our team if you have questions about managing your painmusculoskeletal conditions, treatment options, mental health issues, or accessing services. They’re available weekdays between 9 am-5 pm on 1800 263 265; email helpline@muscha.org or via Messenger.

Crisis support

If this article has raised some issues with you, there is help available. Contact Lifeline Australia on 13 11 14 for 24-hour crisis support and suicide prevention.

More to explore

 

 


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Why gout isn’t a joke

Meet Dave.
He’s 42, plays seniors footy on weekends, works hard during the week, and loves to have the occasional beer with his mates. A few months back, he woke up in the middle of the night with what felt like a red-hot poker stabbing his big toe. At first, he thought he must’ve knocked it at training. But it wasn’t going away. The pain was intense — it was so bad he couldn’t get his shoe on, let alone run onto the field.

Sound familiar?

For Dave — and thousands of men just like him—that burning pain turned out to be gout, a type of arthritis that often strikes in the prime of life. And while your mates might have a few “cures” to offer at training, this Men’s Health Week, it’s time we set the record straight: if you’ve got gout, talk to your GP or a health professional.

What is gout, really?

Gout is a form of arthritis. It’s caused by a buildup of uric acid in the blood, which forms needle-like crystals in the joints. The result? Sudden,gout severe pain, swelling, and redness — often in the big toe, but it can hit ankles, knees, fingers, elbows, or wrists too.

The pain is no joke. It can stop you in your tracks. Putting on socks, walking to the bathroom, or getting through a workday can become near impossible during a flare.

Why men should pay attention

Here’s the kicker — gout hits men harder and earlier than women. It’s most common in men between 30 and 45, often when you’re still feeling invincible. By the time people hit 65, the gender gap narrows, but for some, the damage can already be done.

It’s also easy to ignore. Maybe you think it’s just a footy injury, or something you ate. But repeated flares can lead to permanent joint damage, kidney problems, and serious pain if it’s not managed properly.

The triggers: what sets gout off

Several things can increase your risk of developing gout or triggering a flare:

  • Carrying extra weight
  • High blood pressure or heart disease
  • Drinking too much, particularly beer or spirits
  • Red meat, organ meats, and shellfish
  • Sugary drinks (including some “health” drinks high in fructose)
  • Dehydration
  • Diuretics (water tablets)
  • Crash dieting or fasting

Even stress and lack of sleep can play a part.

Spotting a gout flare

Gout can hit suddenly, often at night. You might feel:

  • A joint that’s hot, red, and swollen
  • Sharp, intense pain that wakes you up
  • Shiny or tight skin over the affected area

Getting the right diagnosis

You can’t diagnose gout just by Googling symptoms or taking your mate’s word for it. Your GP is your best mate in this situation. They may:

  • examine the joint
  • take a fluid sample to look for uric acid crystals
  • order blood tests or imaging

There are other conditions that mimic gout—getting the right diagnosis matters.

What helps

Step 1: Deal with the pain
During a flare, your doctor might recommend:

  • over the counter or prescription medications
  • rest
  • ice packs

Step 2: Prevent future attacks
If flares are becoming regular, or if you have kidney issues or uric acid lumps called tophi, you may need daily medication to manage uric acid levels.

What you can do

Managing gout is about much more than just the medicines. You can take real steps to stay on top of it:

  • Take your meds exactly as prescribed
  • Stay hydrated
  • Go easy on the booze
  • Avoid binge eating or crash dieting
  • Exercise regularly and lose weight gradually if needed
  • Use an ice pack during flares
  • Keep a food diary to spot triggers
  • See your GP regularly to monitor progress

Important: Diet alone usually isn’t enough. Many men with gout may need medication, even if they eat well.

The worksite wisdom trap

Your mates mean well — at work, at footy, at the pub. They’ll have plenty of advice, from Dad did this to Aunty swears by that. Some of it might help, and some of it mightn’t. But don’t gamble your health on backyard remedies.

Listen to the professionals
Your GP, a rheumatologist, or a dietitian can give you clear, evidence-based advice to help you get back to living pain-free.

The bottom line

Gout can be painful. It can also chip away at your quality of life, affect your work, fitness, and the things you enjoy most—whether that’s chasing the kids around, playing footy, or having a beer with your mates.

But it’s also very treatable.

This Men’s Health Week, don’t brush it off. If something’s not right—swollen joints, pain at night, flares that keep coming back — book that appointment. Take charge.

Because the strongest thing you can do isn’t just pushing through the pain — it’s getting the help you need to live better.

Your future self — and your joints — will thank you.

 

Webinar: Gout – Your questions answered

It’s not too late to register for tonight’s webinar, “Gout -Your questions answered” with expert presenter Professor Flavia Cicuttini. Register here. A recording of the webinar will be made available after the live session. Please email info@muscha.org to request the link.

Contact our free national Helpline

Call our team if you have questions about gout, managing your painmusculoskeletal conditions, treatment options, mental health issuestelehealth, or accessing services. They’re available weekdays between 9 am-5 pm on 1800 263 265; email (helpline@muscha.org) or via Messenger.

Crisis support

If this article has raised some issues with you, there is help available. Contact Lifeline Australia on 13 11 14 for 24-hour crisis support and suicide prevention.

More to explore



Jack Bobridge is sharing his story for Men’s Health Week
Professional cyclist racing on the road
Photo credit: Fanny Schertzer

Hi, I’m Jack. I’m 36 years old, originally from South Australia but now living in WA with my wife and our two amazing kids. I’m an Olympian and former professional cyclist, and these days I’m a bricklayer, small business owner, and someone learning to manage life with rheumatoid arthritis (RA).

If you saw me now – tattooed, outdoorsy, maybe covered in brick dust – you probably wouldn’t guess that not long ago, I was competing at the highest level in cycling. From 2010 to 2016, I raced professionally, living and training across the globe. Representing Australia at the 2008, 2012, and 2016 Olympics was something I’ll never forget – especially as cycling’s been passed down through my family for generations.

Cycling was my life. Every day was about pushing limits, eating clean, recovery, data, and performance. But just after I won the under-23 World Time Trial title, I started to notice something was off. At first, it was small things – stiffness in my elbows, soreness in my knees. But it got worse. Fast. Within weeks, I was in pain every day. I couldn’t explain it. I started seeing doctors, chasing answers. It took 18 months to get a diagnosis: rheumatoid arthritis.

That’s a long time to be in pain without answers. And I was one of the lucky ones – being a professional athlete, I had to get help. A lot of men out there, two-thirds according to the research, would rather push through or wait it out. I get it. We’re taught to tough it out. But let me tell you – RA doesn’t care how tough you are.

Getting diagnosed didn’t mean things got easier straight away. I was put on a medication that made me feel like I had chronic fatigue. I could barely function, let alone race. Eventually, I stopped taking it, and things began to improve. But those years were rough – not just physically, but mentally too.

When your body is your livelihood and it suddenly stops working, it messes with your head. I started drinking to numb the pain – not just in my joints but in my mind. And I can tell you now, alcohol only made things worse. RA and alcohol are not a good mix. It took me a while, but I’ve learned better ways to cope.

These days, my relationship with fitness has changed, too. No more endless hours on the bike. I stick to the gym with lighter weights, movement that keeps my joints strong without breaking me down. I also spend as much time as I can outdoors – scuba diving, boating, camping.

My mental health still needs attention, and that’s okay. I’ve stopped trying to go it alone. I’ve got a great support system in my wife and family. If I could give one piece of advice to men reading this: speak up. It’s not weak. The earlier you ask for help, the sooner you can get on top of things.

RA has also made me rethink my diet and how I live. I’m more conscious of what I put into my body – less acidic foods, more balance. I watch for personal triggers like big weather changes, which I feel often set off my flares. These days, I’m on a different medication, and I use prednisolone when flares hit. It’s not perfect, but it’s manageable.

There’s a big misunderstanding out there that RA is just a bit of joint pain. It’s not. It’s constant, it’s exhausting, and it can take over your life if you let it. But it doesn’t have to define you.

Today, life looks different, but it’s good. My wife and I run a coffee trailer and a bar-caravan for weddings and events. Bricklaying keeps me moving and outdoors, even if it’s a tough gig with RA. And I want to help others – especially young athletes, or any bloke battling musculoskeletal disease, chronic pain and mental health struggles.

If I could talk to my younger self, I’d tell him to take better care and ask for help sooner.

So, during Men’s Health Week, here’s my message to you:

If something doesn’t feel right – pain, swelling, fatigue – don’t wait. Don’t accept “it’s just a virus” or “it’ll pass” as the final word. Keep pushing for answers. Speak up. Get checked.

You’re not alone. And the earlier you act, the better your future will be.

Jack Bobridge is an Olympian, former professional cyclist, father, bricklayer, small business owner, and advocate for men’s health and rheumatoid arthritis awareness.


 

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By: Rob Chippendale

My name is Rob, I’m a member of Musculoskeletal Health Australia’s Consumer Advisory Committee, and I’d like to talk with you about my experience with exercise.

I have Scheuermann’s Disease in my thoracic spine, prolapsed discs in my lumbar spine, and palindromic rheumatism, which is a little like the evil uncle of rheumatoid arthritis. In this article, I’d like to share with you some of the steps I took to get myself into a regular exercise regimen, along with some suggestions that helped me when creating and implementing my exercise goals and plans.

I began exercising a number of years ago. I started out by speaking with my GP, rheumatologist and physio, as I wanted a better understanding of my body’s limitations, as well as what my expectations should be. From there, I drafted a plan and created a daily routine, then put it in place and began exercising!

If you are new to exercise or haven’t exercised in a while, I found a good starting point to be doing an audit of your past and current exercise patterns. For me, this included what exercises I had done previously, what I was currently doing, and what I would like to be doing in the future. I first did an audit like this a few years ago and was surprised at how much about exercise I was able to remember. I have found, though, that my balance wasn’t as good as it once was. To help with this, I sought the advice of my physio who introduced me to ‘proprioception exercises’. They are something that I would encourage everyone who is struggling with their balance to look at under the guidance of their healthcare team.

I exercise each day, no matter what. I begin by easing myself into my routine by stretching and thinking, and then I join my physio or a friend for exercise. I walk as far as I can each morning, go up and down some stairs, and always maintain focus on my long-term goals. Whoever I’m with will drive my mobility scooter as I walk beside them. It’s good to have other people involved with my exercise plans, as they’re able to give me the feedback I need and help keep me motivated.

As well as walking up and down stairs to exercise, I walk sideways and heel to toe as much as I can. I find it is important for me to be aware of how I’m walking and whether it is causing me pain. I listen to what my body is telling me, and rest when I need to. The old adage of “no pain, no gain” is better consigned to the distant past, as exercising should never cause unnecessary pain.

I’d urge everyone to speak to their GP and healthcare team, as I’ve done and continue to do. They are aware of my state of health and give me sound advice on pacing and what exercises I should or shouldn’t be doing. My GP and rheumatologist continue to give me valuable advice, and we regularly review my progress.

Rob’s Top Tips:

  • Start by writing down your exercise patterns – what you’ve done previously, what you’re doing currently, and what you’d like to be doing in the future. That way, you can revisit it and make changes as you think of things.
  • Set some goals and create an action plan to achieve those goals. You may want to do as I’ve done and formulate your plan with your GP, as they were quick to remind me that if I wanted to build up to walking a kilometre, I needed to aim for 500 metres first.
  • See your chosen healthcare professional regularly. I benefit from seeing my GP weekly. I’m able to answer his first question, which is usually “What exercises have you done in the last week?”, and then we discuss the coming week and what my goals are.

Exercise is a vital part of maintaining and improving both my physical and mental well-being, and it’s been working quite well for me. I’d encourage everyone to include their healthcare team, family and friends with them on their exercise journey to help manage their musculoskeletal health and overall wellbeing. I know having them involved helps me to feel safe, supported and accountable.

Over 400 years ago, Swiss alchemist and physician Paracelsus made a statement that gave rise to the concept that all medicines are capable of doing harm, but what matters is the dose. And so too, I believe it can be with exercise.

So, crawl before you walk, and walk before you run. You won’t finish until you start, and what you start, you should finish.

If you would like more information on exercise, musculoskeletal conditions or ways you can support your musculoskeletal health, call the team at Musculoskeletal Health Australia on the free, national, B.A.M. Helpline on 1800 263 265 or email helpline@muscha.org

 


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