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in Health &middot April 17, 2020

Describing Pain Levels to a Doctor

A key part of living with chronic pain is describing pain to a doctors which can be surprisingly difficult. I still find it hard, and I’ve been doing it since 2001! With that in mind, I’ve written this post about describing pain levels to a doctor. I’m specifying doctors in this post because getting people in your life like a partner or family member to understand your pain is a different situation from explaining it to your doctor.

For one, describing pain to a doctor is for a completely different purpose. It can be to make them believe you, to explain how things have changed (positively or negatively), or to get a diagnosis. Mainly, it’s important to describe your pain accurately because different types of pain can mean different things, like aching vs. sharp. Wherever you are in your pain journey, I hope that you find this post helpful!

As a reminder, I am not a doctor. I am a chronic pain patient, and I have a lot of experience being in pain, but I don’t have a medical degree. Additionally, this post contains affiliate links. Thank you for supporting Kate the (Almost) Great!

Contents hide
Basic Terms for Describing Pain to a Doctor
How To Use Comparison for Effectively Explaining Your Pain
The Dreaded Out-of-10 Scale for Describing Your Pain
Text reads: Describing pain levels to a doctor, www. kate the almost great .com (end text). Describing pain to doctors can be difficult. In this post, long-time chronic pain patient Kate the (Almost) Great helps you prepare to do that with words to use, ideas to help you explain your pain, and, of course, the dreaded out-of-10 pain scale.

Basic Terms for Describing Pain to a Doctor

Aching or dull: It is very annoying that these are the two best ways to describe my pain when it feels like these two words minimize pain. But that isn’t necessarily the case! I would describe this as a soreness. Sometimes I’ll describe my arthritis pain as aching but strong to emphasize that it’s a lot of pain. For me, if my pain is aching or dull, it doesn’t necessarily have one strong point where the pain is the worst.

Sharp: Pretty much what it sounds like! For me, sharp pain is intense, like it takes your breath away, and it is involved with a smaller area than aching pain is.

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Cramping: In this purpose, cramping pain is the kind that feels there’s a knot in the area where you’re feeling it. Maybe it’s because I associate cramping with periods (because cramps come along with periods), but when I have cramping pain, it’s pain that feels tense in the muscles specifically.

Shooting: When I have shooting pain, it has a starting point and it radiates from that point. Generally, it can radiate a long distance or a moderate one. When I’ve dislocated my knee (something that used to have allll the time, but that is thankfully not a regular occurrence any more), the pain has been shooting down my lower leg until the joint is put back in place.

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Throbbing or pulsating: This could be described as a shooting pain that shoots to a short distance and bounces back to the starting point. Like, a really short distance. When I’ve had ovarian cysts rupture – a highlight of my endometriosis experience – after the initial rupturing, I feel throbbing pain. The rupturing itself is a sharp, stabbing pain, and then the recovery is throbbing. It’s very painful, and when using shooting a short distance as an explanation for throbbing, I would say that pain post-rupture is shooting one to two inches and bouncing back. Another word to describe this type of pain is pulsating.

Stabbing: Stabbing goes along with “sharp” to me, but to me, they’re not the same thing. I’m not sure if this will make sense, but to me, while you can’t stabbing pain without it also being sharp, you could have sharp pain not be stabbing. Another way to describe stabbing pain is by comparing it to some other terms; I think of stabbing pain as sharp throbbing. To me, throbbing pain has rounded edges, while stabbing is very angular.

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Text reads: tips for explaining your pain, www. kate the almost great .com (end text). describing pain to doctor, describing pain levels, chronic pain, chronic illness, describing pain, how to describe pain, explaining pain, how to explain pain, rheumatoid arthritis, RA, arthritis, rheum, fibromyalgia, fibro, endo, endometriosis

Heavy: Heavy pain is like there’s a weight on it, whether on the area that is feeling that pain (like if it’s swollen) or on you overall, like in the pit of your stomach. Maybe heavy pain is pain that feels foreboding emotionally. I also associate heavy pain with throbbing, but like with sharp and stabbing, I feel like throbbing doesn’t have to be heavy, but heavy pain is almost always also throbbing.

Burning: This is a whole other type of pain compared to what I’ve described so far! Burning pain is hot, and it can be hot metaphorically or literally. When I’ve experienced burning pain, it has been post surgery when nerves were healing, and that pain was burning. It felt hot inside, but that area wasn’t hot to the touch, which is a symptom of inflammation.

Stinging: In my experience, stinging pain is like burning but down a couple of notches or like burning but not as sharp. It can be really intense as it is, and it’s not the exact same experience as burning (which is why it has its own entry), but it is very similar.

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How To Use Comparison for Effectively Explaining Your Pain

In recent years, I started comparing my pain when describing what I’m feeling to doctors. This isn’t something I necessarily do when I’m not at an appointment related to pain – for example, when I’m at the hematologist for my chronic anemia, they ask pain levels, but they care a lot more about my fatigue levels. But if I’m going to the rheumatologist or a joint specialist like my foot/ankle doctor, it’s a lot more important.

When I say “compare,” I mean comparing your present pain levels to previous pain experiences you’ve had. This can be specific or more general. A general example is, “My current pain is a 6, and an 8 is an ovarian cyst rupturing.” That is an experience I have had multiple times, and it’s in my medical chart, so my doctors can check and confirm that I’ve had that. I try to keep it a simple comparison (ovarian cyst rupturing) so that it’s not distracting from the point of the appointment. I try to use more general examples for general appointments like with my primary care doctor or for the unfortunate ER appointment. In ER appointments, it’s extremely important to explain my pain quickly and concisely, as 95% of the time that I’m there, it’s for something causing pain.

A more specific comparison would be using an experience that applies to that specialty. For example, when I see my knee doctor, I can compare my knee pain to various knee problems that I’ve had over the years. He has done 2 surgeries on the same knee, each surgery being for different things. When I see that doctor (which I thankfully haven’t needed to do for a while), I can compare my pain level at that time to my pre- or post-surgery pain levels.

Now that we have discussed words you can use for describing pain to a doctor and the tool of comparison for describing your pain, let’s talk about the most common way to explain what you feel: the annoying out-of-10 pain scale.

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Describing pain to doctors, kate the almost great .com

The Dreaded Out-of-10 Scale for Describing Your Pain

Easily the most common question I get from medical professionals when I have any appointment is how much pain I have out of 10. In my opinion, the out-of-10 pain scale is extremely annoying. Assigning numbers to my pain doesn’t provide a good description of it. Adjectives are a much better fit since there are different types of pain that could be the same number. For example, one day my pain could be a 6/10 and be dull and achy but the next day it could be a 6/10 and be burning and stinging. In both cases, I strongly believe a 6 is the right number, but the pain is very different. How can those numbers be accurate, then?

Additionally, we have no way to know if each number means the same thing to each person. And there’s no way to tell! Plus, we haven’t all experienced the same things, so we can’t all imagine the same type of pain and what of that would be a 10 (or any other number in the scale). Some hospitals or medical offices have descriptive words or phrases with the faces of an out-of-10 pain scale, but even then I’ve seen different descriptions for the same number. In some places, “mild pain” might be a 4, but in others, it’s a 2.

Plus, as I mentioned, different types of pain can be the same number, which is why all of those words I list at the beginning of this post are so needed. My pain might be a 6/10 and be achy or burning or stinging or whatever (you get the idea). But when describing my pain in each of these situations, I would without a doubt label them all a 6/10. These different situations generally mean different types of things are causing the pain, but it doesn’t change the fact that a doctor would ask me what number I would assign to my pain first and foremost. I’ve had some doctors then ask me to describe the pain, but others leave it at a number.

I don’t have a solution for replacing the out-of-10 scale or else I would be including it here. But I’m including these comments because I want to explain why it’s so important to describe your pain beyond numbers. Maybe if you use a number beyond 10 (even just out of 20) you can get more specific – 18 out of 20 seems like a more specific number than 8 out of 10.

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What are your tips for describing pain to a doctor?

Like this post? Check out:

How Arthritis Affects the Body, Why Is Endometriosis Misdiagnosed?, Chronic Illness Advice: Resources for the Newly-Diagnosed Patient, Arthritis Glossary: Frequently-Used Terms

Strategies to describe your pain, kate the almost great .com
8 tips for describing your pain to doctors, kate the almost great .com
How To Describe Your Pain Effectively Strategies That Can Help!
How to explain your pain levels to doctors
Kate Mitchell

Kate Mitchell is a blogger, chronic illness patient, and advocate who helps people understand chronic illness and helps chronic illness patients live their best lives.

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Reader Interactions

Comments

  1. Maryse S. Marius says

    April 20, 2020 at 6:17 pm

    Hey Kate!
    Very interesting article- it’s a unique one! These are wonderful tips which will help us explain our pain more accurately, with more descriptive words- instead of “it hurts quite a lot”.

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    • Kate says

      May 5, 2020 at 4:00 pm

      Exactly! Because “it hurts quite a lot” might be right, but it’s not always helpful when talking to medical professionals.

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  2. Katie says

    April 25, 2020 at 8:00 pm

    This is very helpful. The nuances really make a difference. Having the right language is so important.

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    • Kate says

      May 5, 2020 at 4:00 pm

      So glad it was helpful!

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      Reply
  3. LJ says

    September 21, 2020 at 2:32 am

    This is really great, thank you! I feel as though people who have chronic pain will completely relate to the verbiage you used. Every descriptive made me say “Yes, I know how that one feels and know exactly how she’s differentiating between them!” We don’t often come across something that so fully describes what we all feel at different moments.
    Stay Well!

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  4. Jen Atwood says

    May 30, 2021 at 10:45 pm

    Excellent article! I have difficulty answering the current pain level question at doctor visits because I have multiple chronic pain disorders…sometimes I answer with the highest number of the bunch, others an average. I also appreciate it when they ask for the pain level at the beginning and at the end because many of us can change quite quickly, especially when under stressful situations. I look forward to reading your blog now that I’ve discovered it!

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  5. Janet Jay says

    July 8, 2024 at 11:31 am

    This subject is so important to talk about– I wrote a piece a couple years ago about pain scales that seemed to resonate with a lot of people. I think we’re all struggling to find our way on this, and the more we demand alternatives, hopefully, the more normalized it’ll become.

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    • Janet Jay says

      July 8, 2024 at 11:33 am

      Huh, did the link not work? Sorry about that. Either way, mine is at https://www.janetjay.com/using-pain-scale-1-10-to-explain-your-pain/ if you’re interested. Thanks again for keeping this in the conversation.

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Week 19 of #2026Weekly I’m not going to lie - my Week 19 of #2026Weekly 

I’m not going to lie - my life now focuses even more on maintaining my body. Trying to avoid foot surgery + keep my bone density up so I don’t break another bone for a while on top of all the other things I do to manage my 10+ illnesses … it’s a lot of work. I did go to actual work this week lol but my camera roll is all chronic illness stuff this week. 

1️⃣ The machine that will hopefully prevent surgery!!! Every day, I do 40 minutes of this ultrasound machine (20 min on 1 fracture, 20 min on the other) and it will speed up healing 🤞🏻🤞🏻🤞🏻 
2️⃣ Continuing my exercise routine per my endocrinologist. Up to 30 minutes of Pilates 4 days a week … and since I don’t do exercises requiring pressure on my feet, the cast comes off. 

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1️⃣ Looking at an at-home ultrasound treatment machine 
2️⃣ Kate’s cast next to her yoga mat 

#Osteoporosis #RheumatoidArthritis #ChronicIllness #ChronicPain
I personally have rheumatoid arthritis, fibromyalg I personally have rheumatoid arthritis, fibromyalgia, and Sjögren's syndrome, which makes 3 forms of arthritis.⁣
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May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
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Like, comment, and share to spread awareness 💖 ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: Fact or Fiction? Let's Check! ⁣
Fiction⁣
Arthritis means only 1 thing.⁣
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There are over 100 kinds of arthritis, including osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, and more!⁣
katethealmostgreat⁣
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#ArthritisAwareness #RheumatoidArthritis #Fibromyalgia #SjogrensSyndrome #Arthritis
SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣ ⁣ I sh SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣
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I share my personal health experiences online, which I find it somewhat easy to do because I've been talking publicly - albeit to a smaller audience - since my health problems started in 2001. ⁣⁣⁣
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If you share something online, you need to be prepared for people to ask questions or argue with you. Should they? No. Will that stop them? Also do. ⁣
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That's one of the reasons that talking online about what can be trauma is not easy or for everyone. That's why it's important to practice self-care and to consciously think about what you want to share online before you do it. ⁣⁣⁣
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For example, I generally only talk publicly about a health situation once it has passed, especially if it's an emergency. I also make sure that I'm in a good place mentally before I talk about it. That way, I don't share things I'll regret sharing publicly later. It also helps me be less anxious about sharing these details.⁣⁣⁣
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And I don't share everything! There's lot of stuff that I haven't talked about not only online but with people in real life. It might seem like I share everything I've experienced, but I don't. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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Week 18 of 2026 Weekly 1️⃣ Cross-stitch and IVIG Week 18 of 2026 Weekly 

1️⃣ Cross-stitch and IVIG 
2️⃣ Another trip to the foot doctor. We’re officially in Try To Avoid My 6th Foot Surgery mode 🤞🏻 
3️⃣ At least there were lilacs?

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.

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IDs: 
1️⃣ Looking down at Kate’s lap. Tubes are coming out of her shirt. She’s working on a cross stitch.
2️⃣ Kate takes a selfie in a doctor’s office. She’s wearing a lilac mask.
3️⃣ A lilac bush

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FAQ: Have I Tried Yoga for My Pain? This is a se FAQ: Have I Tried Yoga for My Pain? 

This is a series where I answer questions I frequently get about my rheumatoid arthritis. I am not a medical professional and this is not medical advice - just saying the truth about my body in particular. 

Video: Kate speaks to camera. There are captions. A black text box reads “FAQ: Have I Tried Yoga for My Pain?” 

#RheumatoidArthritis #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
May is Arthritis Awareness Month, which is the per May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
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Like, comment, and share to spread awareness 💖⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: Fact or Fiction? Let's Check! ⁣
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Arthritis can affect anyone at any age, including kids as young as 3.⁣
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I’ve been on IVIG since September. So what does su I’ve been on IVIG since September. So what does success look like? ⁣
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*This is all just for me and my case!*⁣
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1️⃣ I haven't gotten sick at all since I started, not even a cold. ⁣
2️⃣ My lungs are clear of any ground glass opacities, which was what pushed us over to finally doing IVIG regularly. ⁣
3️⃣ We feel better about saying that I don't have any infections. Because symptoms are often signs of the body fighting an infection, we couldn't always trust that I wasn't sick because I didn't have symptoms. ⁣
4️⃣ Because of all of this, we're increasing my next Rituxan dose! This will mean better RA symptoms and hopefully no new illnesses for a few years.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: A bunch of IVIG supplies, including a pump. ⁣
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Week 17 of 2026 Weekly 1️⃣ Making some real progr Week 17 of 2026 Weekly

1️⃣ Making some real progress with this cross stitch
2️⃣ Walking casts have multiple uses, including holding down your mat! (Don’t worry - I only did broken-foot-compatible things) 

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.

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IDs:
1️⃣ An in-progress cross stitch. You can see that Kate stitched 2 bears.
3️⃣ A walking cast lies on a black yoga mat 

#CrossStitching #CrossStitcher #RheumatoidArthritis #Osteoporosis #LoopsAndThreads
Can we talk about fatigue for a sec? ⁣⁣⁣ ⁣ Fatigue Can we talk about fatigue for a sec? ⁣⁣⁣
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Fatigue is so much more than being tired. It's sleeping 10 hours at night and then struggling to stay awake during the day. It's trouble focusing because, even though you just had 3 cups of coffee, you're thinking about sleep. It's needing to factor rest in during the day because you have plans at night. ⁣⁣⁣
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It's a lot. ⁣⁣⁣⁣
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It's no secret that I have multiple chronic illnesses. But did you know that all of them - all 11+ of them - have fatigue as a symptom? Sometimes the fatigue is worse than the pain and, uh, I live with a lot of pain.⁣⁣
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This picture was taken when I was super anemic and waiting for 4 iron infusions. Now, months later, I can see it. And I also don't know how I got through the months of that anemia. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣.⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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