Hi everyone! I recently heard from a reader who was looking for some suggestions on where to turn next, in terms of finding a medical professional to help him. He said he'd been struggling with central sensitization syndrome for three years now, and had yet to receive any significant help. I thought his advice might… Continue reading How to find help for Central Sensitization
I wanted to share a really important post with you all this morning, from the author of Chronically Undiagnosed. She's a therapist who is dealing with chronic illness. Recently, she wrote about her experience attending a chronic pain support group that incorporated some of the theories of modern pain science... but did so very badly.… Continue reading Too much of a good thing: when people don’t really *get* pain science
Using metaphors to explain how pain works One of the original reasons I started this blog was to get the word out about the various pain scientists and educators whose work has touched my life (including, but not limited to, Neil Pearson and Lorimer Moseley). From them, I've learned that pain isn't here to make… Continue reading The story of my wrist, and the pot of boiling water (Finally, my own pain science metaphor!).
Okay, so here’s the story of the time I thought I’d found the right person to help me, which of course, made it all the more disappointing when it didn’t turn out to be the case. In telling my story, I’m choosing to gloss over every little ache and pain I had; every time I… Continue reading The doctor who *almost* helped me (How I developed central sensitization, Part 6)
Whew. I have really enjoyed writing my more personal posts recently-- I love to tell a good story, and to feel as though my past experiences have some meaning. (And I've really appreciated all your kind words, comments, and shares!). But also, wow-- some of those posts were very emotional for me. Right now I’m… Continue reading Learning about central sensitization: the power of naming, and the future of pain treatment