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You are here: Home / Coping / Talking With Your Doctor About Pain

Talking With Your Doctor About Pain

Last Updated: April 1, 2016

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

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Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

 

How to Talk to Your Doctor About Pain

by Jim Sliney Jr, RMA

Talking about your pain is one of the most challenging conversations you will ever. You are bound to have it with your doctor, or with friends and loved ones, and each time you do it’s going to be unpleasant. Why? Because to everyone but you your pain is invisible and as a result, people just don’t get it.

Explaining your pain to your Doctor is more than just unpleasant, it’s difficult and it’s a very high stakes conversation. If you don’t convey your experience correctly the road to cure, management or treatment can be longer than it needs to be.

I don’t want to diminish the value of having the pain talk with loved ones but because of the impact it can have on your entire approach to medical care I’m going to focus on how to talk to your Doctor.

Explaining pain to your doctor is a high stakes game. Share on X

Doctors rely heavily on signs. Signs are things they can test and measure objectively, like blood tests, electrocardiograms, MRIs and blood pressure measurements. In contrast, pain is a symptom.

Symptoms are subjective effects that only the patient experiences. Because they are subjective, it is not always easy for a Doctor to understand or interpret symptoms. Fortunately there is language you can use to make your subjective symptoms more objective. Let’s call this pain language “FLIC” (Frequency, Location, Intensity, Characteristics).

How to talk to your doctor about pain

FREQUENCY: How Long Has This Been Going On?

Headaches that happen intermittently every day, versus ones that occur persistently all night long are approached differently by your Doctor. Being able to tell your Doctor how long or how frequently your pain presents itself goes a long way to solving the mystery of cause and a subsequent treatment plan. The simplest way to look at the frequency of pain is to measure how long it lasts, or its duration.

You can have acute pain which is short in duration, or chronic pain which is long in duration. Hitting your thumb with a hammer produces acute pain. The pain from fibromyalgia is chronic pain. Once the duration is determined there are other accepted terms you can use to fine tune the frequency and duration of pain:

  • Intermittent – not continuous / occasional (e.g. back pain can be a chronic condition that comes and goes intermittently)
  • Sporadic – occurring irregularly or randomly (e.g. cluster headaches can be sporadic, happening at unpredictable intervals)
  • Predictable – foretold on the basis of experience or scientific reason (e.g. every time it rains the pain in my neck increases in intensity)
  • Flair-up – a sudden occurrence or worsening (when your intermittent or sporadic or predictable pain is suddenly present or suddenly worse than usual)
  • Constant – happening all the time (e.g. the pain in my shoulder joints is always present)
  • Acute recurrent – this happens in short duration but happens again and again, like migraine headaches
  • Chronic progressive – pain of long duration that continues to change and evolve, like degenerative nerve pain

LOCATION: Where Is Your Pain? / The Mcgill Pain Questionnaire

Where does it hurt? Pain conversations may start just like that. There is a common graphic of a unisex human figure with a back view and a front view. Doctors may instruct you to mark on such a drawing where your pain is being experienced.

Doctors may even request you to note a difference between pain that is on the surface and pain that is under the surface. This tool comes from the McGill Pain Questionnaire which includes other measurements, but the front and back of the unisex human figure is the most recognizable.

If you don’t happen to have a figure to draw on remember terms like, front, back, on the surface, under the surface, deep and shallow, however it should be easy enough to find the McGill Pain Diagram online and print it out.

INTENSITY: The Wong-Baker Faces / Scale of 1-10

the Wong Baker pain scale

 

The Wong-Baker Faces scale was originally devised to help children express the kind of pain they were experiencing. Most of us have seen this scale before (six faces ranging from a happy face to an upset, crying face) and it is very easy to use but its limitation is that it only addresses pain intensity.

The Wong-Baker Faces scale works the same way that the “1-10 Pain Scale” works, with ZERO being no pain and TEN being the worst possible pain. Take some time to think about where your pain falls on this scale. It is perfectly fine to say that your pain falls within a range of scores.

Where does it hurt is only the beginning of the pain conversation. Share on X

IF YOU’D LIKE TO HAVE A LAUGH ABOUT PAIN FOR A CHANGE WATCH COMEDIAN BRIAN REGAN TRYING TO EXPLAIN HIS PAIN IN THE HOSPITAL

CHARACTERISTICS: The Neuropathic Pain Scale

Knowing the Frequency, Location and Intensity of pain is very important, but to anyone living with chronic pain, there are still more ways to talk about it. The Neuropathic Pain Scale uses the same ONE through TEN model (when ONE is none and TEN is the most possible) to measure other aspects like:

  • Sharpness – a stabbing pain like an exposed nerve
  • Hotness
  • Coldness
  • Dullness – a deep pain, maybe throbbing, like swelling from an infection
  • Sensitivity to contact – does it hurt when clothes brush against it, when you poke it?
  • Itchiness

Being able to provide characteristics like this will help your Doctor understand the cause of your pain.

In addition, a discussion of the characteristics of your pain should include what treatments make it feel better or feel worse. Does your pain respond well to warm compress or aspirin? Have you found that hot showers make you feel worse? This can help your Doctor rule out certain treatments thus saving you time and frustration.

Knowing how to talk to your Dr about pain will really help your treatment. #chronicpain Share on X

If you don’t have this information prepared when you go to see your Doctor you will probably spend a good portion of your visit trying to figure all this out. That cuts into the time you could spend asking important questions, and getting better quality information and instructions.

Also, under such circumstances it is possible that your pain will be misrepresented. So when you are preparing for a visit with your Doctor prepare your FLIC ahead of time. You will be able to give your Doctor the kind of highly specific information they need to help diagnose or treat your pain which could get you the help you need faster.

 

Bibliography & Resources
  •  www.merriam-webster.com for basic definitions
  • https://www.painedu.org/nipc-resourcenter.asp an excellent source for information, tools and the pain assessment scales mentioned in this article

Jim Sliney JrJim Sliney Jr has been a Registered Medical Assistant for twenty years and has worked in research and a variety of environments providing care to patients. He works with non-profit organizations as a writer of educational material and a promoter of self-advocacy. His consultancy bridges the gap between rare and under-served diseases and the companies that make the products or services that can help them. Jim is currently studying Creative Writing at Columbia University, is excited to someday teach writing, and is working on his first novel.

 

Related Posts:

  • 7 Tips for Better Doctor Visits
  • The Chronic Pain Scale: Communicating Your Chronic Pain
  • 3 Steps to Choosing the Right Doctor
  • Are You Making Your Healthcare Appointments Work for You?

4 Comments Filed Under: Coping, Tips and Tricks, Treatment Tagged With: communication, dealing with doctors, doctors

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. LouisVA says

    April 2, 2016 at 11:53 am

    I would like to add chronic, severe pain does have some objective signs (a) high blood pressure & (b) high heart rate.

    Reply
    • Jim Sliney Jr says

      April 3, 2016 at 1:54 am

      Hi LouisVA,

      That is an excellent point! I agree that pain will increase blood pressure and heart rate. I will be sure that appears in future editions. Thank you.

      In my experience, blood pressure is a sign that doctors rarely attribute to pain since hypertension is so prolific.

      Reply
  2. ChronicMom says

    April 1, 2016 at 1:33 pm

    This is really helpful. I’ve always been terrible at describing pain and where it’s located, and when I go to the doctor I’m even worse at it because of my doctor anxiety.

    Reply
    • Jim Sliney Jr, RMA says

      April 1, 2016 at 5:22 pm

      I’m so glad this article has given you a valuable tool Chronicmom! It’s always so dreadful when you have to explain your pain. I had to find some new perspectives.

      Reply

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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