EDUCATIONAL ARTICLE

Living with Persistent Pain

By David Hennessy, Clinical Psychologist

Living with persistent pain can involve much more than finding a way to reduce symptoms. Pain may affect how you sleep, move, work, connect with people and think about the future. Ordinary tasks can require planning that other people never see.

There is no single formula for managing this. A useful starting point is to consider what would make everyday life more workable: a steadier routine, support with difficult emotions, an activity you miss, or a clearer plan for harder days. These goals can sit alongside appropriate medical treatment and the wish for pain relief.

This article explores practical ways of living with ongoing pain. For an overview of the website’s pain resources, visit the Chronic Pain hub.

David Hennessy, Clinical Psychologist at Hennessy Clinical Psychology in Varsity Lakes.

Pain Is Real, and Its Effects Are Personal

Persistent pain, also called chronic pain, is pain that continues or returns for more than three months. It may accompany an ongoing health condition, follow injury or surgery, or continue without a clear explanation for all its features. Different mechanisms can contribute, and they do not operate in the same way for everyone. [1], [2]

Pain is a real sensory and emotional experience influenced by biological, psychological and social factors. Recognising these influences does not mean pain is imagined, caused by a poor attitude or explained entirely by stress. A person’s account of their pain deserves respect. [1]

Understanding your own condition matters more than fitting every experience into one explanation. Ask your healthcare team what is understood, what remains uncertain, and whether there are particular precautions relevant to you. New symptoms still deserve assessment.

The related article How the Autonomic Nervous System Responds to Pain explores pain-related bodily responses. Here, the focus is on the choices and adjustments involved in daily life.

Living Well Can Include More Than Pain Relief

Pain relief is a reasonable goal. It is also possible for some aspects of quality of life to improve while pain continues. Having both aims allows room for treatment and for the life happening around it. [2]

Consider what you would like to be easier or more available. Perhaps you want to sit with your family at dinner, return to a hobby in a modified way, or get through appointments with less disruption afterwards. These are useful goals even if they do not change a pain rating.

A practical question is: What would make this week a little more workable? The answer might involve doing something differently, asking for help, or reducing a demand. Living well should not become another standard you are expected to meet perfectly.

Acceptance and Action Can Work Together

Acceptance involves acknowledging what is happening now, including pain, frustration and limitations, so that choices can be made from that starting point. It can coexist with seeking treatment, requesting a second opinion or advocating for better support. [3]

You might acknowledge, “Standing is difficult today,” and then arrange a seat so you can join a family activity. The limitation remains real; adapting the activity makes another option possible. Acceptance does not require liking the situation or deciding that nothing can change.

Acceptance of pain is associated with less interference in everyday functioning. This does not mean that a person’s attitude determines their disability, or that accepting pain will make it disappear. [4]

Some days, action may mean practising a skill or trying an adapted activity. On other days, it may mean resting, setting a boundary or arranging a medical review. The useful question is whether a response fits your health needs, circumstances and priorities.

Finding a Workable Rhythm of Activity and Rest

When pain eases, it can be tempting to catch up on everything. If this is followed by a prolonged increase in symptoms, life may become a cycle of pushing hard and then needing substantial recovery. Other people find that uncertainty gradually leads them to do less. Neither pattern is a personal failing.

Pacing involves planning manageable amounts of activity and recovery, rather than repeatedly reaching exhaustion. It may include dividing tasks, alternating demands and asking someone else to share the load. A health professional can help tailor this to your condition. [5]

For example, preparing a meal could involve sitting for some tasks, choosing a simpler recipe or spreading the preparation across the day. These are illustrations rather than a prescribed schedule. The right approach depends on what your body can manage and what support is available.

Use a Flexible Plan Rather Than Automatic Increases

A plan should be reviewed against its effects. If an activity repeatedly causes marked or delayed worsening, discuss this with your treating team rather than automatically adding more. Rest, rehabilitation and activity need to fit the particular condition. There is no universal timetable that everyone should follow. [2]

Pacing can protect space for enjoyable activities as well as essential jobs. Otherwise, limited energy can become entirely absorbed by chores and appointments.

Rebuilding Confidence With Everyday Activities

It is understandable to feel cautious when movement has hurt before. In some musculoskeletal pain conditions, fear of pain can contribute to avoiding activities and losing confidence. That is one possible influence, rather than an explanation for every person’s pain or disability. [6]

Where an activity is medically appropriate, a physiotherapist, occupational therapist or other treating professional may help you find a manageable way to approach it. This could involve changing the movement, using equipment or trying a smaller part of the task. Appropriate precautions still matter. [5]

For someone who misses gardening, the first useful change might be a raised planter or help with lifting. For someone returning to study, it might be seating, shorter sessions or accessible materials. The aim is to find a workable way to participate, with room to adjust if the approach is not helping.

Preparing for Pain Flare-Ups

A flare-up is an increase in symptoms beyond their usual level. It can be unsettling, particularly when no clear trigger is apparent. Familiar flares do not necessarily mean new injury or that previous progress has been lost. They also should not be used to explain away new or concerning symptoms. [2], [7]

A plan made with your healthcare team can reduce the number of decisions required on a difficult day. It may cover:

  • Which tasks can be shortened, postponed or shared.
  • Which comfortable positions, movements or other agreed strategies may help.
  • How to use medicines according to the prescribed plan.
  • Who to contact if symptoms change or the usual plan is not enough.

During a familiar flare, adjust demands and use the strategies agreed with your team. Where suitable, retain small parts of your routine and some contact with other people. Review the plan if it repeatedly leaves you unable to manage. [7]

A brief record can help you discuss patterns without needing to monitor every sensation. Sometimes no single cause becomes clear.

Making Room for Sleep and Emotional Wellbeing

Sleep deserves attention in its own right. When persistent insomnia accompanies chronic pain, cognitive behavioural therapy for insomnia (CBT-I) can improve sleep. Pain may change less, so better sleep should not be presented as a guaranteed route to pain relief. [8]

If nights remain difficult, ask about assessment rather than relying only on general sleep tips. Your clinician can consider pain, medication effects and other possible sleep problems.

Frustration, sadness, worry and grief can arise when pain disrupts life. Psychological support may help with distress and the effect pain has on everyday activities. Benefits vary, and improvements are often modest rather than complete. [9]

A brief relaxation or grounding practice may be worth trying if you find it comfortable. It need not become another task to perform correctly. If focusing on bodily sensations makes you more distressed, discuss alternatives. Emotional care can sit alongside physical treatment without making you responsible for controlling every symptom.

Relationships, Work and a Sense of Yourself

Unpredictable pain can make commitments difficult. Other people may see what you manage at one moment without seeing the preparation, discomfort or recovery around it. Discussing practical needs can be more useful than trying to make someone fully understand every sensation.

For example: “I would like to come, but I need a seat and the option to leave early.” Or: “I can do this part of the job, but I need help with the lifting.” These are ways of making participation more workable, not promises about what you will always manage.

If pain is affecting employment, speak with your treating team about suitable adjustments. These might involve duties, hours, equipment or the working environment. What is feasible will depend on the job, your condition and available support. [10]

Changes in capacity can also bring grief about familiar roles. You may still value being a parent, friend, worker or creative person while expressing that role differently. The broader article Living With Long-Term Health Conditions explores adjustment and identity across different health conditions.

Money, housing, culture, caring responsibilities and access to services also shape what is possible. A useful plan needs to fit these realities. [2]

Working With Your Healthcare Team

Bring a specific everyday concern to an appointment: what you are finding difficult, what you have tried, and what you would like help with next. A short note may be easier to use than trying to recall everything during the consultation.

Psychological approaches such as cognitive behavioural therapy (CBT) and acceptance and commitment therapy (ACT) may support coping, emotional wellbeing and participation. They complement appropriate medical and rehabilitation care. They do not establish the cause of pain or require pain to be psychological in origin. [9], [11]

ACT can help people relate differently to difficult thoughts and feelings while taking steps towards what matters. The amount of benefit varies between people and pain conditions. [3], [11]

For information about the practice’s support options, see Psychology and Chronic Pain. Changes to prescribed medicines should be discussed with your prescriber rather than made on the basis of an educational article. [10]

When Pain Needs Medical Review

Seek medical advice when pain changes significantly, your usual plan stops being adequate, or symptoms are increasingly affecting sleep, mood or daily functioning. Ongoing pain does not prevent another health problem from developing. [10]

Seek urgent assessment for new weakness, loss of bladder or bowel control, rapidly worsening severe pain, or pain accompanied by fever or significant injury. These examples are not a complete checklist. [12] For a medical emergency, call 000.

You can ask your treating team to clarify which changes need prompt attention in your particular condition. This can help distinguish an agreed response to familiar symptoms from situations that require reassessment.

Choosing One Useful Next Step

You do not need to reorganise your whole life at once. Choose one concern that matters now: simplifying a demanding task, arranging a review, planning for a flare or reconnecting with someone in a manageable way.

Notice whether the change helps and what it costs in effort or recovery. Keep it, adapt it or seek advice. On a difficult week, maintaining essentials may be enough. Your worth does not depend on how active, productive or positive you can be.

Frequently Asked Questions About Living With Persistent Pain

Can I enjoy something and still be in significant pain?

Yes. Enjoyment and pain can occur together. Managing a social visit or enjoying a moment does not show how severe your pain is, what it took to participate, or how you may feel afterwards. A person’s report of pain should be respected. [1]

What if I have tried pacing and it has not helped?

Ask your treating team to review the plan, including the task, recovery time, equipment and demands around it. A plan may need changing, and persistent worsening may need reassessment. Difficulty with pacing does not show that you have failed or are not trying hard enough. [2], [5]

Do I need to feel ready before making a small change?

Not always. An appropriate, manageable step can sometimes be taken with uncertainty or discomfort present. It should still respect your health needs and medical advice. The step might be asking for assistance rather than increasing activity. [3]

How can I tell whether an approach is helping?

Agree on outcomes that matter to you, such as a more manageable task, better sleep or less disruption from distress. Consider benefits alongside fatigue, symptom worsening, cost and effort. Bring that information to a review so the plan can be adjusted. [2]

Related Services and Information

Find the main pain information pathway and details about psychological support.

Explore the primary hub for pain information, psychological support and related resources.

Read about psychological support for pain-related distress, coping and everyday functioning.

Related Educational Articles

These articles offer further understanding of bodily pain responses and adjustment to ongoing health conditions.

Explore pain-related autonomic responses, arousal and protective behaviour.

Read about emotional adjustment, changing roles and identity across long-term health conditions.

References and Resources

  1. Raja, S. N., Carr, D. B., Cohen, M., Finnerup, N. B., Flor, H., Gibson, S., Keefe, F. J., Mogil, J. S., Ringkamp, M., Sluka, K. A., Song, X.-J., Stevens, B., Sullivan, M. D., Tutelman, P. R., Ushida, T., & Vader, K. (2020). The revised International Association for the Study of Pain definition of pain: Concepts, challenges, and compromises. Pain, 161(9), 1976–1982. https://doi.org/10.1097/j.pain.0000000000001939
  2. National Institute for Health and Care Excellence. (2021). Chronic pain (primary and secondary) in over 16s: Assessment of all chronic pain and management of chronic primary pain (NICE Guideline NG193). https://www.nice.org.uk/guidance/ng193/chapter/recommendations
  3. McCracken, L. M., & Vowles, K. E. (2014). Acceptance and commitment therapy and mindfulness for chronic pain: Model, process, and progress. American Psychologist, 69(2), 178–187. https://doi.org/10.1037/a0035623
  4. White, K. M., Zale, E. L., Lape, E. C., & Ditre, J. W. (2025). The association between chronic pain acceptance and pain-related disability: A meta-analysis. Journal of Clinical Psychology in Medical Settings, 32, 448–459. https://doi.org/10.1007/s10880-024-10061-1
  5. Better Health Channel. (2025a). Treating persistent pain. Department of Health, State Government of Victoria. https://www.betterhealth.vic.gov.au/health/conditionsandtreatments/Treating-persistent-pain
  6. Vlaeyen, J. W. S., & Linton, S. J. (2000). Fear-avoidance and its consequences in chronic musculoskeletal pain: A state of the art. Pain, 85(3), 317–332. https://doi.org/10.1016/S0304-3959(99)00242-0
  7. Queensland Health. (n.d.). Your guide to managing flare ups [Patient information sheet]. Statewide Persistent Pain Management Network. https://www.health.qld.gov.au/__data/assets/pdf_file/0023/730850/7_Managing_flare_ups.pdf
  8. Selvanathan, J., Pham, C., Nagappa, M., Peng, P. W. H., Englesakis, M., Espie, C. A., Morin, C. M., & Chung, F. (2021). Cognitive behavioral therapy for insomnia in patients with chronic pain – A systematic review and meta-analysis of randomized controlled trials. Sleep Medicine Reviews, 60, Article 101460. https://doi.org/10.1016/j.smrv.2021.101460
  9. Williams, A. C. de C., Fisher, E., Hearn, L., & Eccleston, C. (2020). Psychological therapies for the management of chronic pain (excluding headache) in adults. Cochrane Database of Systematic Reviews, 2020(8), Article CD007407. https://doi.org/10.1002/14651858.CD007407.pub4
  10. Better Health Channel. (2025b). When do I need to see my doctor about persistent pain?. Department of Health, State Government of Victoria. https://www.betterhealth.vic.gov.au/health/conditionsandtreatments/when-do-i-need-to-see-my-doctor-about-persistent-pain
  11. Ye, L., Li, Y., Deng, Q., Zhao, X., Zhong, L., & Yang, L. (2024). Acceptance and commitment therapy for patients with chronic pain: A systematic review and meta-analysis on psychological outcomes and quality of life. PLOS ONE, 19(6), Article e0301226. https://doi.org/10.1371/journal.pone.0301226
  12. National Institutes of Health. (n.d.). Pain. https://health.nih.gov/health-topics-a-z/pain

Australian Resources

Educational Disclaimer

This article provides general educational information. It does not diagnose the cause of pain or replace individual medical assessment, psychological care or rehabilitation advice. Pain conditions and support needs differ. Discuss activity, treatment and medication decisions with your treating healthcare professionals.

Enquiries and Appointments

If persistent pain is affecting everyday life and you would like psychological support, you are welcome to enquire about an appointment. Care is tailored to your circumstances and goals, alongside other healthcare where appropriate.

David provides psychology for adolescents and adults in Varsity Lakes on the Gold Coast, with telehealth available across Australia. You can read about David’s approach before making contact.