In a nutshell, pain neurophysiology education is the type of treatment for chronic pain that changed my life and inspired me to become a physical therapist.
I’ve mentioned it in passing on this blog, but I decided it’s high time I give the topic its own post.
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In my series “How a physical therapist helped me through my lowest point,” you can read the story of how my life had ground to a halt because of chronic pain, until I finally met Tim, a physical therapist who had studied with Neil Pearson.
Tim treated my pain in an entirely different manner than all the physical therapists and doctors I’d seen previously.
He explained to me that after all my body had been through– running 45 miles a week, only to develop compartment syndrome and barely be able to stand, to live like that for two years, and then to undergo surgery– my nervous system had gotten confused.
All the pain doctors hadn’t been able to explain– it wasn’t because I was crazy.
In fact, the reason I was feeling all this pain was because my body was trying to protect me.
My nervous system had decided the world was a dangerous place. It was tired of me taking chances– it didn’t want to have to deal with another injury. So it was making everything hurt. It was making me feel as though I were made of glass.
But I wasn’t made of glass, Tim assured me. My body was strong; it was capable. And this attempt on the part of my nervous system to protect me had over-served its purpose.
Tim explained that the surgery I’d had for compartment syndrome had been successful, and despite how much my legs might hurt at times, I wasn’t going to be able to bring it back just by walking down the street.
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The pain neurophysiology approach worked when nothing else had, because it gave me a real explanation for the pain that actually made sense.
Before that, all the physical therapists I’d seen (and I’d seen a lot) had taken one of two approaches:
A) You have some underlying soft tissue problem or scar tissue or whatnot that we have to fix with a special treatment, or
B) I can’t really find anything wrong with you, so the pain must be in your head and you should probably see a psychologist.
Neither of these approaches ever made a difference for me.
The “special treatments” for the hidden, subtle issues in approach never fixed anything or reduced my pain (except temporarily, because I felt like I was doing something). And approach B never fixed anything, because ultimately these problems were not reflective of my overall mental health.
Instead, I learned, my pain was the result of a specific phenomenon that occurs within the nervous system: central sensitization.
Basically, the underlying principle here is that the more practice the nervous system gets at sending signals, the better it will get at sending those signals. And that is true of pain signals, along with everything else.
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Coming up, I’m going to be providing a lot more explanations, linking to great resources, and also quoting excerpts from articles that I think explain things really well.
And I’ll be telling my own story, when it comes to my struggle to understand my body, and learning to deal with central sensitization.
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For now, I want to leave you with two posts I wrote on some of the main concepts I learned through my experience with PNE:
Understanding pain as your body’s alarm system
Understanding pain as an overprotective friend
These posts tie in a couple of anecdotes from Neil Pearson and Lorimer Moseley that I found particularly helpful. (Let me say, once again, that I am so, so grateful for their work!).
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I hope you find this post, and the related articles I linked to, to be helpful! I’m really excited about the things I plan to write about in the future, and I hope you stay tuned!
u2hearts
February 8, 2017 at 6:51 amI think you providing resources for people is an amazing thing. I’m happy to say pain is the one symptom I don’t normally have with MS but I know many who do.
sunlight in winter
February 8, 2017 at 12:37 pmThank you so much 🙂 I really appreciate that.
u2hearts
February 8, 2017 at 6:51 amI think you providing resources for people is an amazing thing. I’m happy to say pain is the one symptom I don’t normally have with MS but I know many who do.
sunlight in winter
February 8, 2017 at 12:37 pmThank you so much 🙂 I really appreciate that.
Zoe
February 9, 2017 at 4:33 amThis post is inspiring. Congrats for your dedication and i am glad you like it this thing so much! lookig forward to your new ‘root posts’ my dear
sunlight in winter
February 9, 2017 at 4:41 amThanks so much! I’m looking forward to your future posts as well 🙂
Zoe
February 9, 2017 at 4:33 amThis post is inspiring. Congrats for your dedication and i am glad you like it this thing so much! lookig forward to your new ‘root posts’ my dear
sunlight in winter
February 9, 2017 at 4:41 amThanks so much! I’m looking forward to your future posts as well 🙂
sunlight in winter
October 25, 2017 at 2:35 pmHi Virginia, would you mind emailing me at sunlightinwinter12@gmail.com? I’d be happy to answer your question in that format. Thanks!
sunlight in winter
October 25, 2017 at 2:35 pmHi Virginia, would you mind emailing me at sunlightinwinter12@gmail.com? I’d be happy to answer your question in that format. Thanks!