Managing thoughts and behaviors when living with chronic pain: lessons from a road trip

A lot has changed for me this past year. I’ve experienced successes I wouldn’t have imagined possible 6 years ago (heck, 3 years ago, or even just a year ago). But this most recent success is a pretty huge one for me. Even bigger than the long hikes, starting to run again, and snowshoeing adventures that have happened in this past year. You see,

Musings on the 2016 SDPain Summit (part 2)

This is part 2 of my initial musings on the 2nd annual San Diego Pain Summit, it has to be two parts because there was so much good stuff it was way too much to include in one post. Here’s Part 1 if you missed it which went over stress, motivational interviewing, acceptance, creativity, and being human. Awesome, right? On to


Labels, narratives, identity, and chronic pain

I have been thinking about the language we use with ourselves lately, particularly our self-talk and our labels. I’ve been thinking a lot about the words chronic, pain, and patient in particular. How does continually using, or hearing, these words reinforce our pain? Does being identified as a ‘chronic pain patient’ become an integral part of our identity that then makes it more difficult to change our

Improving communication, giving voice to those with chronic pain

In the last few months my readership has jumped a bit (thank you to everyone who has shared my posts or had recommended my blog to a patient, client, family member, or friend) so I wanted to take a moment to explain a bit about what I’m trying to do here. I’ve also been living without internet for nearly two


Acceptance: It doesn’t mean giving up or giving in

At some point along the way in writing this blog and trying to figure out this whole chronic pain thing, I went from learning about and understanding more about the science of pain to actually living what I know (well, mostly living what I know, I have my moments). I didn’t really notice it myself, at least not until it was