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Chronic pain

Your pain is real, and so is your life beyond it. You deserve to be believed, supported and cared for.

⏱ 8 min read📑 11 sections📚 16 sources✅ Reviewed October 2026

By the numbers

How common chronic pain is.

United States

24.3%of U.S. adults had chronic pain (pain on most days or every day in the past 3 months) in 2023 (CDC, National Health Interview Survey).
8.5%of U.S. adults had high-impact chronic pain in 2023, meaning pain that limited life or work activities on most days or every day (CDC).
51.6 millionU.S. adults (20.9%) had chronic pain in 2021 (CDC, MMWR 2023).

World

1.71 billionpeople worldwide have musculoskeletal conditions, such as low back pain, neck pain and osteoarthritis (WHO, 2022).
#1Musculoskeletal conditions are the leading contributor to disability worldwide (WHO, 2022).
160countries where low back pain is the single leading cause of disability (WHO, 2022).
570 millionpeople worldwide were living with low back pain (WHO, 2022).

By age & sex

12.3%of U.S. adults aged 18–29 had chronic pain in 2023 (3.0% high-impact) (CDC).
18.3%of adults aged 30–44 had chronic pain in 2023 (4.9% high-impact) (CDC).
28.7%of adults aged 45–64 had chronic pain in 2023 (11.3% high-impact) (CDC).
36.0%of adults aged 65 and older had chronic pain in 2023 (13.5% high-impact) (CDC).
25.4% vs 23.2%Women were more likely than men to have chronic pain in 2023 (high-impact: 9.6% vs 7.3%) (CDC).

These numbers show that chronic pain is one of the most common health experiences there is. If you live with it, you are far from alone.

What is chronic pain?

When pain sticks around for months or years. Tap any card.

Most pain is short-lived. You twist an ankle, it hurts, it heals and the pain fades. Chronic pain is different: it is pain that lasts for more than three months. It can be there all the time, or it can come and go.

Pain experts describe pain as an unpleasant experience of both the senses and the emotions. It is always personal, and it is shaped by the body, the mind and the world around you. A person’s own word that they are in pain should be respected.

Living with pain is not only a body experience. It touches your mood, sleep, work, relationships and how you see yourself. That is why caring for your mind is part of caring for your pain.

⚡ Chronic painPain that lasts more than three months, steady or on and off.
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Chronic pain can follow an injury or surgery, come with a condition like arthritis, or appear without a clear cause. Sometimes the original injury has healed, but the nervous system keeps sending pain signals. That does not mean the pain is “in your head”. It means the body’s alarm system has become extra sensitive.

Common kinds

  • Back and neck pain
  • Headaches and migraine
  • Joint pain, such as arthritis
  • Nerve pain (burning, tingling, shooting)
  • Pain after an injury or operation that never fully settled
  • Widespread pain with tiredness, as in fibromyalgia
Pain does not need a scan result to be real. If it hurts, it hurts, and you deserve care.
⏳ Short-term vs long-term painShort-term pain warns and heals. Long-term pain can outlast the injury.
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Short-term (acute) pain is a useful warning. It tells you to protect an injury while it heals, then it fades. Chronic pain keeps going past the normal healing time, often for months or years.

Pain usually has a protective job. When it lasts a long time, though, it can get in the way of daily life, work, friendships and well-being.

This is why chronic pain often needs a different plan than a fresh injury. Ask your clinical provider what that plan looks like for you.
🧬 Pain is always personalBody, mind and life all shape how pain feels.
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The International Association for the Study of Pain says pain is always a personal experience. Biology, thoughts and feelings, and life circumstances all play a part. People also learn what pain means through their own life experiences.

What this means for you

  • Two people with the same injury can feel very different pain
  • Pain can be real even when tests look normal
  • Stress, sleep and mood can turn pain up or down
  • Your own description of your pain matters
Saying the mind affects pain is not saying pain is imaginary. All pain, even a stubbed toe, is processed by the brain.
👥 Who it affectsPeople of every age, though it becomes more common with age.
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In 2023, about 1 in 4 U.S. adults had chronic pain. It was more common in older age groups and slightly more common in women than men. About 12 in 100 adults aged 18 to 29 had it too.

Around the world, conditions like low back pain, neck pain and osteoarthritis are the leading contributor to disability.

See “By the numbers” at the top of this guide for more.
Living with a long-term health condition, fatigue or an invisible illness? See the “Living with chronic illness” guide. For pain linked to stress and body symptoms, see “When the body speaks”.

Pain, the brain and the stress cycle

Why pain, worry and low mood can feed each other, and where to break the loop.

Pain is not just a signal from the body. It is something the brain makes sense of, using information from the body, your memories, your emotions and what is going on around you. That is why the same pain can feel worse on a stressful day and easier when you are calm or absorbed in something you enjoy.

How the cycle can turn

  1. Pain flares up.
  2. You feel worried, frustrated or scared about what it means.
  3. Stress makes muscles tense and keeps the body on alert, so pain feels sharper.
  4. You do less, sleep worse and see people less.
  5. Your body gets weaker and stiffer, and your mood drops.
  6. Low mood and poor sleep make the brain more sensitive to pain, and the cycle turns again.

The hopeful part is that a cycle can be interrupted at any point. Calming the stress response, moving gently, improving sleep, staying connected and treating low mood can each loosen the loop, even if the pain does not disappear.

🚨 An over-sensitive alarmLike a car alarm that goes off when someone walks past.
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With long-term pain, the nervous system can become over-sensitive. It sounds the alarm more easily and more loudly, even when there is little or no new damage. Learning about this can make pain less frightening and movement feel safer.

Things that can turn the alarm up

  • Fear that pain means harm
  • Long periods of not moving
  • Poor sleep
  • Stress and worry
“Hurt does not always mean harm.” This idea can make it easier to move again, step by step.
🌬️ Calm the alarmSlow breathing tells the body it is safe.
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When you are stressed, breathing gets fast and shallow and muscles tighten. Slow, deep breathing helps switch the body toward “rest” mode, which can soften tension and help you stay in control when pain is strong.

Try this

  1. Sit or lie in a comfortable position.
  2. Breathe in gently through your nose for a count of 4.
  3. Breathe out slowly through your mouth for a count of 6.
  4. Let your shoulders drop as you breathe out.
  5. Repeat for 2 to 5 minutes.
See the Breathing basics guide for more exercises you can use during a flare.
🎨 Shift your focusAbsorbing activities can turn the pain volume down.
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The brain has limited attention. When you are absorbed in music, a game, a craft, a show or a good conversation, there is less room for pain to take center stage. This is not pretending the pain is gone. It is giving your brain something else to hold.

Ideas

  • Calling a friend
  • Listening to a favourite playlist or podcast
  • Puzzles, drawing, knitting or building something
  • Watching birds, clouds or the sky
🧠 Notice your thoughtsSome thoughts turn up the pain alarm.
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Thoughts like “This will never get better” or “I can’t cope” are very understandable when you hurt. But they can raise stress and make pain feel bigger. Learning to spot these thoughts and answer them more kindly is a key part of talking therapies for pain.

Kinder ways to talk to yourself

  • “Hurt does not always mean harm.”
  • “I can do one small thing right now.”
  • “This is a flare. I have got through flares before.”

Pain, mood and sleep

How pain affects your mood and sleep, and when to reach out.

It is normal to have hard feelings when you live with pain. Frustration, sadness and worry are part of being human in a hard situation. But sometimes these feelings settle in, grow heavy and start to take over.

🌧️ MoodLow mood, worry and irritability are very common.
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People with a long-term health condition, including pain, have a higher risk of depression. When both happen together, each can make the other feel worse.

Chronic pain is also linked with anxiety, irritability and mood swings. Being in pain wears down your patience and your coping reserves, just like being very hungry or tired does.

Depression is treatable, even when you live with pain. Feeling low is not something you just have to put up with.
🌙 SleepPain makes sleep harder, and poor sleep makes pain feel worse.
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Pain can make it hard to get comfortable, and it can wake you in the night. Then, after poor sleep, the brain is less able to dial pain down, so the next day can hurt more. This loop is one of the most common parts of living with pain.

Gentle sleep habits

  • Go to bed and get up at about the same times
  • Keep naps short, or skip them if they keep you up at night
  • Keep the bedroom cool, dark and quiet
  • Try pillows or positions that support sore areas
  • Wind down with slow breathing or a calm activity
If sleep problems keep going, tell your clinical provider. Talking therapies for sleep can help, even when you live with pain. See the “Insomnia & trouble sleeping” guide.

Experiences people often describe

  • Big changes in sleep or appetite
  • Constant worry about your health or the future
  • Feeling guilty or like a burden to others
  • Feeling irritable or snapping at people you love
  • Feeling sad, empty or hopeless most days
  • Losing interest in things you used to enjoy, even things your body still allows
  • Pulling away from friends and family
  • Thinking that life is not worth living
Having some of these experiences doesn’t mean you have depression or anxiety. Social media videos that list “signs you have X” are not a diagnosis. Only a qualified professional can assess what’s going on for you, so please talk to your clinical provider or therapist.

Some of these experiences, like tiredness, poor sleep and trouble focusing, can come from pain itself, from low mood, or from both. That is one more reason to talk openly with your care team about how you feel, not only how your body feels.

If you are thinking about suicide or feel you can’t go on, call or text 988 (U.S.), or text HOME to 741741. If a life is in danger, call 911.

Common flare triggers

What can set off a flare or make pain worse, and what helps. Tap a card.

A flare is a time when pain or other symptoms get worse than your usual. Some flares have a clear trigger. Many people find that stress, sleep, activity levels, illness and even the weather can play a part.

Often there is no clear trigger at all. A flare can happen for no reason you can find. It is not your fault, and it doesn’t mean you did something wrong.
🎢 Doing too much, or too littlePushing hard on a good day, or resting for days, can both lead to more pain.
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Pushing yourself too hard or too fast, or suddenly starting a new activity or exercise, is a common reason for a flare. But doing too little matters too. Long stretches of rest can leave the body stiffer and weaker, so everyday tasks hurt more.

What helps

  • Break tasks up with short, frequent rests
  • Build up new activities slowly
  • Keep up gentle activity during a flare instead of long bed rest
  • See “Pacing and flare plans” for how to find your baseline
🌋 Stress and big emotionsWorry, conflict and upsetting news can turn the pain volume up.
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Emotional stress is one of the most common flare triggers. Research reviews also link ongoing stress with more severe chronic pain. Stress tightens muscles and keeps the nervous system on alert, so pain signals feel louder.

What helps

  • A therapist can teach skills for living with pain and stress (see “Approaches that can help”)
  • Plan extra rest around stressful events
  • Talk it through with someone you trust
  • Use slow breathing or a short body scan when you notice tension
Stress doesn’t mean the pain is “in your head”. It means your mind and body are connected.
😴 Poor or changed sleepA rough night, or a new sleep schedule, can make the next day harder.
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Not getting enough sleep, or changing your sleep schedule, can set off a flare. Poor sleep is also one of the key things researchers say keeps chronic pain going. Pain can make sleep hard too, so the two can feed each other.

What helps

  • Keep a steady wake-up time, even after a bad night
  • Keep naps short and early
  • Tell your clinical provider if pain often keeps you awake. The Sleep & mental health guide has more ideas.
  • Wind down with something calm in the hour before bed
🌦️ Weather and temperatureSome people notice more pain when the weather turns cold, damp or changes fast.
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Weather or temperature changes are listed as a flare trigger for some long-term pain conditions. Not everyone notices this, and the science is still unclear, but many people say a cold snap or a stormy week makes them ache more.

What helps

  • Check the forecast and plan lighter days when bad weather is coming
  • Dress in warm layers, and keep a heat pack handy
  • Move indoors when it’s too cold or wet to walk outside
  • Note the weather in your pain diary to see if it’s a pattern for you
🤒 Illness and routine changesA cold, an injury, travel or a disrupted routine can knock you off balance.
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Being ill or injured, or a big change to your daily routine, such as travel, a new job or a house move, can bring on a flare. The body is already working hard, and the usual habits that keep you steady can slip.

What helps

  • Ask your clinical provider before changing anything in your treatment plan
  • Keep a few anchors in place: meal times, a short walk, bedtime
  • Lower your expectations while you recover
  • When you travel, pack the things that soothe you, like a heat pack or a favourite pillow
Use the “Pain & mood diary” worksheet to spot your own triggers, then add them to “My flare plan”.

Pacing and flare plans

Steady beats boom-and-bust. Plan ahead for bad days.

Many people with pain fall into a “boom and bust” pattern. On a good day they do everything they couldn’t do before, then crash for days afterward. Pacing means doing a steady, planned amount each day, even on good days, so you have fewer crashes over time.

📉 Boom and bustOverdoing it on good days, then crashing.
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It makes perfect sense to want to catch up when you feel better. But pushing too hard often leads to a flare, then days of rest, then even more to catch up on. Over time, the good days can get fewer and the bad days longer.

Signs you might be in this pattern

  • You avoid activity for days, then do a lot at once
  • You often feel much worse a day or two after a busy day
  • You stop only when the pain forces you to
This is not a willpower problem. It is a very common pattern, and it can be changed.
⏱️ How to paceFind your baseline, then build up slowly.
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Steps

  1. Pick one activity, like walking, cleaning or computer work.
  2. Notice how long you can do it on a typical day without a flare afterward. That is your baseline.
  3. Start a little below that amount.
  4. Take a short break before you need one.
  5. Every week or two, add a small amount if your body allows.
  6. Do roughly the same on good days and bad days.

Helpful tricks

  • Break big jobs into parts across the week
  • Plan rest as an activity, not a failure
  • Swap between sitting, standing and moving
  • Use a timer so you stop before the pain stops you
Physical and occupational therapists can help you build a pacing plan that fits your life.
🪫 If effort makes you crash a day laterFor some conditions, building up is not the right first step.
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Some people, for example with ME/CFS or long COVID, get much worse 12 to 48 hours after physical or mental effort. This is called post-exertional malaise. For them, pacing means staying inside a personal “energy envelope” first, rather than adding more each week.

If this sounds like you, talk with your clinical provider before increasing activity. The “Living with chronic illness” guide has more on fatigue and energy budgeting.
🧯 Flare planA ready-made plan for bad days, written on a good day.
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Flares can be scary, and it is hard to think clearly when you are in a lot of pain. Writing a plan ahead of time means you don’t have to make big decisions in the middle of it.

A flare plan might include

  • Early warning signs that a flare is starting
  • Kind words to read to yourself
  • Tasks you can drop or hand off
  • Things that usually soothe you (heat, rest positions, breathing, a calm playlist)
  • What your clinical provider has advised for flares
  • When to call your provider or get urgent help
  • Who to tell, and what to ask them for
Use the “My flare plan” worksheet and keep a copy where you can find it fast.

Approaches that can help (and the honest evidence)

Talking therapies, mindfulness, movement and learning about pain. Tap any card.

Non-drug approaches are an important part of caring for chronic pain. They rarely make pain vanish, and it is fair to say so. What they often do is help people cope better, move more, sleep better, feel less distressed and get more of their life back.

For treatment of the pain itself, please talk with your clinical provider. The approaches below are meant to work alongside the care you get from your health team.
💭 CBT for painLearning skills to change the thoughts and habits that make pain harder.
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Cognitive behavioral therapy (CBT) for pain teaches practical skills: spotting thoughts that raise stress, pacing activity, solving problems, relaxing the body and slowly returning to things you value. It does not say your pain is imaginary. It helps you handle real pain with less suffering.

Honest evidence: a large 2020 review of research found CBT gives small benefits for pain, disability and distress compared with usual care. Small can still matter in daily life, and some people benefit much more than others.

What it can look like

  • Homework like activity diaries and practicing skills
  • One-to-one, in a group or online
  • Weekly sessions for a set number of weeks
🧭 Acceptance & commitment therapy (ACT)Making room for pain while moving toward what matters.
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ACT helps people stop fighting every moment of pain, which can be exhausting, and instead focus on living by their values. It uses mindfulness, noticing thoughts without being ruled by them, and setting small, meaningful goals.

Honest evidence: ACT is widely used for chronic pain, but a large 2020 review found the research quality was still too low to be sure how much it helps. More good studies are needed.

A simple ACT question: “If pain were not in charge today, what small thing would I do that matters to me?”
🧘 MindfulnessNoticing the present moment with curiosity instead of struggle.
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Mindfulness means paying attention to the present moment, including body sensations, without judging them. With pain, it can help you notice the difference between the raw sensation and the worry layered on top of it.

Honest evidence: research suggests mindfulness meditation may improve people’s ability to cope with pain. In a trial of adults with chronic low-back pain, a mindfulness-based stress reduction program improved function and pain compared with usual care.

A 3-minute body check-in

  1. Sit or lie comfortably and close your eyes if you like.
  2. Notice your breath without changing it.
  3. Gently scan from head to toes, noticing what you feel.
  4. If you meet pain, describe it in plain words: hot, tight, dull, sharp.
  5. Breathe toward that area, then widen your attention to the whole body.
🚶 Gentle movementWalking, stretching, yoga, tai chi or water exercise, built up slowly.
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When you hurt, resting can feel safest. But too much rest can make muscles weaker and joints stiffer, which can add to pain. Gentle movement, built up slowly, is safe for most people and can ease pain over time.

Honest evidence: yoga and tai chi have reasonable support for some conditions, such as low-back pain and knee arthritis. Evidence varies by condition and is still limited for some.

Ideas to try

  • Beginner yoga or tai chi classes
  • Chair-based stretches
  • Short walks, adding a minute or two each week
  • Swimming or exercises in warm water
Check with your clinical provider or a physical therapist about what is safe for your condition, especially after an injury or surgery.
📚 Learning how pain worksPain neuroscience education explains why pain can persist.
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Pain neuroscience education teaches how the nervous system creates pain and how it can become over-sensitive. Understanding this can make pain less frightening and movement feel safer.

Honest evidence: reviews of studies suggest it can help with pain, understanding, function and worry about pain, especially when combined with exercise or physical therapy.

Learning that pain is shaped by the brain does not mean it is “made up”.
🛁 Relaxation & everyday comfortsSmall, safe ways to soothe the body.
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Relaxation methods like slow breathing, guided imagery and progressive muscle relaxation can help calm the stress response and lower tension. Many people also find comfort in warmth, gentle massage, music or time in nature.

Try

  • A guided relaxation recording before bed
  • A warm (not hot) bath or a heat pack, if your provider says it’s okay
  • Music you love
  • Sitting outside for a few minutes
Self-management courses teach many of these skills together. Ask your provider or local hospital if they run one.
Many people do best with a mix of approaches. A pain management program may bring together talking therapy, movement and education under one team.

Myths and facts

Clearing up common misunderstandings. Tap any card.

❌ Myth: “If there’s no clear cause, it’s in your head.”Fact: Pain can be real and persistent even when tests look normal.
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Pain without a clear physical cause is often linked to changes in how the nervous system processes signals. The pain is real. Emotional and psychological factors can affect it, just as they affect all pain, but that does not make it imaginary.

❌ Myth: “Rest is always best.”Fact: Gentle, gradual movement often helps more than long rest.
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Short rests during a flare are fine. But long periods of rest can weaken muscles and stiffen joints. Building up gentle activity slowly, with pacing, is safe for most people. Check with your clinical provider about what suits your condition.

❌ Myth: “Talking therapy means they think I’m making it up.”Fact: Therapy helps you cope with real pain and its effects on life.
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Pain affects mood, sleep and relationships, and talking therapies are one way to ease that load. They work alongside medical care, not instead of it.

❌ Myth: “Feeling low is just part of being in pain.”Fact: Depression is common with long-term pain, and it is treatable.
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People with long-term health conditions, including pain, have a higher risk of depression, but it is not something you just have to accept. Getting help for low mood can also make it easier to manage your physical health.

❌ Myth: “Young people don’t get chronic pain.”Fact: Chronic pain affects people of all ages.
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Chronic pain becomes more common with age, but it affects younger adults too. In 2023, about 12 in 100 U.S. adults aged 18 to 29 had chronic pain.

❌ Myth: “They look fine, so it can’t hurt that much.”Fact: People show pain in many ways, and some hide it well.
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Pain experts say a person’s own report of pain should be respected, and that words are only one way of showing pain. Many people with chronic pain learn to keep going and look “fine” on the outside.

How to support someone in pain

For family and friends: what to say, how to help, and caring for yourself too.

When someone you love lives with chronic pain, it can be hard to know what to say or do. You may feel helpless, worried or even frustrated at times. These feelings are normal. What helps most is usually simple: believe them, listen and ask what they need.

👂 Believe and listenBeing believed is one of the biggest gifts you can give.
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Pain experts say a person’s own report of pain should be respected. You don’t need to see it to believe it.

Helpful things to say

  • “I believe you.”
  • “That sounds really hard.”
  • “What would help most today?”
  • “You don’t have to explain. I’m here.”

Things to avoid

  • “But you look fine.”
  • “Have you tried just…?” (unless they asked for ideas)
  • “My cousin had that and got better with exercise.”
  • Comparing their pain to yours or others’
Ask before giving advice: “Do you want ideas, or do you just want me to listen?”
🧺 Practical helpSpecific offers are easier to accept than “Let me know.”
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  • “I’m going to the store. What can I pick up for you?”
  • Cook a meal that freezes well
  • Drive them to an appointment and help take notes
  • Help with paperwork or phone calls
  • Plan low-energy hangouts, and don’t take cancellations personally
Keep inviting them, even if they often say no. Being included matters.
🐢 Support their pacingHelp them keep a steady pace, even on good days.
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Boom-and-bust patterns are common with chronic pain. On a good day, it is tempting for everyone to pack in as much as possible. Steady, planned activity usually leads to fewer crashes.

Ways to help

  • Build breaks into outings and family plans
  • Celebrate small, steady progress
  • Don’t pressure them to “make the most” of a good day
  • Offer to take over a task when they need to stop
🫶 Caring for yourselfSupporters need support too.
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Supporting someone long-term can be tiring and lonely. You may grieve changes in your relationship or your own plans. Looking after yourself is not selfish. It helps you keep going.

What helps

  • Join a caregiver support group
  • Keep up your own friendships and interests
  • Take regular breaks and accept help from others
  • Talk to a counselor if you feel overwhelmed
See the “Caregiver stress & burnout” guide for more support and ideas.

How community helps

You don’t have to do this alone.

Talking with people who live with similar pain can be a huge relief. They understand without long explanations, and they often have practical tips that only come from experience. Peer helplines, support groups and hearing other people’s stories can help you feel understood.

👥 Support groupsIn person or online, for your condition or for pain in general.
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Support groups bring people together to share experiences, tips and encouragement. Many are run by condition-specific charities or hospitals. Group therapy for pain is also offered by some clinics.

Finding one

  • Ask your clinical provider, hospital or pain clinic
  • Check libraries, community centers and faith groups
  • Look for a national organization for your condition
  • Try online groups if travel is hard
Look for groups that feel hopeful and kind. If a group leaves you feeling worse each time, it is okay to try another.
📱 Online communitiesConnection from the sofa or bed on low-energy days.
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Online groups can be a lifeline when leaving home is hard. They can also bring misinformation or products that promise cures. Stay curious and careful.

Stay safe online

  • Be wary of anyone selling a “cure”
  • Check health advice with your clinical provider
  • Protect your personal details
  • Take breaks if scrolling makes you anxious
🎓 Self-management coursesLearn skills alongside others who get it.
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Self-management courses teach day-to-day skills like pacing, goal-setting, relaxation and talking with providers. They are often run in small groups, which adds the benefit of meeting others.

Ask your provider, local hospital or community health center whether a course is offered near you or online.
🏃 Moving togetherGentle group classes add company to movement.
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Yoga, tai chi and water exercise have some support for certain pain conditions. Doing them in a class adds friendship, routine and encouragement.

Ideas

  • A beginner or chair-based class at a community center
  • A walking group that goes at an easy pace
  • Warm-water classes at a local pool
Tell the teacher about your pain so they can suggest gentler options.

When and where to get help

Signs it’s time to reach out, and how to get the most from appointments.

It is a good idea to talk to your clinical provider or a therapist if pain is getting you down, if worry is taking over, or if you are struggling to cope with daily life. You don’t have to wait until things are very bad.

Reach out soon if

  • You are pulling away from everyone
  • You are using alcohol or other substances to cope with pain or feelings
  • You feel sad, hopeless or numb most days for two weeks or more
  • You feel you can’t keep going
  • You have lost interest in nearly everything
  • Your pain suddenly changes or gets much worse
📋 Before the visitWrite things down so nothing gets lost.
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Appointments can feel rushed, and it is easy to forget what you meant to say. Speaking up for yourself is called self-advocacy, and it is a skill anyone can learn.

Bring

  • A short pain diary (when pain is worse or better, sleep, mood)
  • How pain affects daily life: work, sleep, chores, family
  • Questions you want answered
  • What you have tried and how it went
  • Your top 2 or 3 concerns, in order of importance
Use the “Doctor visit prep” worksheet and share it from your phone.
🎯 Describe the impactExplain what pain stops you doing, not just a number.
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Pain scores from 0 to 10 are useful, but they don’t show the whole picture. Telling your provider what you can’t do anymore helps them understand how serious things are.

For example

  • “I can’t sit for more than 20 minutes, so I had to stop driving to work.”
  • “I haven’t been able to pick up my grandchild in months.”
  • “I wake up 4 or 5 times a night from pain.”
❓ Questions to askIt’s okay to ask until you understand.
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  • What do you think is causing this?
  • What are my options, including non-drug options?
  • What are the pros and cons of each?
  • What should I do during a flare?
  • When should I contact you, and when should I get urgent help?
  • Could talking therapy or a pain management program help me?
  • Can you write that down for me?
You can ask the same question twice. You can ask for simpler words, a referral or a second opinion. That is not rude. It is how good care works.
🧑‍🤝‍🧑 Bring a support personA second pair of ears can help a lot.
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Pain and tiredness can make it hard to listen and remember. A trusted friend or family member can take notes, remind you of your questions and help you speak up.

Before you go, agree

  • Anything private you’d rather talk about alone
  • What you want from the visit
  • Whether they should speak, or just listen and take notes
💬 Mention your moodYour feelings are part of your health.
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Many people only talk about the body at medical visits. But low mood, worry and poor sleep are common with long-term pain, and they can be treated. In some places, primary care and mental health providers work together as a team, which is called collaborative care.

You could say

  • “Could I talk to someone about how I’m coping?”
  • “I’m worried all the time about my health.”
  • “The pain is getting me down. I’ve been feeling low most days.”

Where to start

  • A pain management clinic or program
  • A support group for your condition
  • A therapist or counselor, ideally one who works with chronic pain
  • Your primary care provider or specialist
Feeling dismissed by a provider? See “Invisible illness and not being believed” in the “Living with chronic illness” guide for words you can use.
If you’re in crisis, call or text 988 (U.S.), or text HOME to 741741. If a life is in danger, call 911. Outside the U.S., findahelpline.com lists free helplines by country.
Living with chronic pain takes courage every single day. Reaching out for support is part of that courage.

📝 Worksheets for this guide

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Sources

  1. Centers for Disease Control and Prevention (CDC), National Center for Health Statistics (2024). Chronic Pain and High-impact Chronic Pain in U.S. Adults, 2023 (NCHS Data Brief No. 518)
  2. Centers for Disease Control and Prevention (CDC), MMWR (2023). Chronic Pain Among Adults — United States, 2019–2021
  3. World Health Organization (WHO) (2022). Musculoskeletal health (fact sheet)
  4. Pain (journal), via PubMed Central (NIH) (2020). The revised International Association for the Study of Pain definition of pain: concepts, challenges, and compromises (Raja, Carr et al.)
  5. National Institute of Mental Health (NIMH) (2024). Understanding the Link Between Chronic Disease and Depression
  6. Cleveland Clinic. Chronic Pain: What It Is, Symptoms, Treatment & Management
  7. Cleveland Clinic. Fibromyalgia
  8. Dorset County Hospital NHS Foundation Trust. Managing Acute Flare-up of Chronic Pain (patient leaflet)
  9. Nijs & Reis (peer-reviewed) (2022). The Key Role of Lifestyle Factors in Perpetuating Chronic Pain: Towards Precision Pain Medicine (Journal of Clinical Medicine)
  10. Centers for Disease Control and Prevention (CDC). Manage ME/CFS
  11. National Center for Complementary and Integrative Health (NCCIH, NIH). Chronic Pain and Complementary Health Approaches: Usefulness and Safety
  12. National Center for Complementary and Integrative Health (NCCIH, NIH). Mind and Body Approaches for Chronic Pain: What the Science Says
  13. Cochrane Database of Systematic Reviews (Williams, Fisher, Hearn & Eccleston) (2020). Psychological therapies for the management of chronic pain (excluding headache) in adults
  14. Physiotherapy Theory and Practice (Louw et al.), via PubMed (2016). The efficacy of pain neuroscience education on musculoskeletal pain: a systematic review of the literature
  15. Peer-reviewed review, via PubMed Central (NIH) (2023). Pain neuroscience education in patients with chronic musculoskeletal pain: an umbrella review
  16. NHS (UK National Health Service). 10 ways to reduce pain

This guide is for education and self-care. It is not a diagnosis or a substitute for professional care. Please talk to a counselor or clinical provider about your health. Reviewed October 2026.

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