For an academic audience, I have written this presentation as a rigorously researched autoethnographic case study in which I use journal entries, calendar notes, emails, physician referrals, therapist notes, and text messages as evidence to tell my story of being a chronic pain researcher-turned-patient. Possibly the most important part of the presentation is my discussion of the social phenomena that played important roles in my healing. I demonstrate how models for understanding, and clinical guidelines for treating, chronic pain are inadequate, and how minimizing contact with medical doctors may have been the best thing to do—even in Germany, where the concept of psychosomatic illness is relatively widespread. I compare my own journey to the literature on chronic pain–patients’ experiences and ultimately merge my own experience with that literature to suggest how clinicians can change their behaviors to positively impact their patients’ chronic pain. Ultimately, my experience healing from disabling widespread pain illustrates how misguided most clinical practice guidelines for chronic pain treatment are and how the biopsychosocial model needs to be understood differently to truly help patients heal.
If you can attend the conference in June, I would love for you to hear my presentation. If not, you can always request that I speak with your own team of healthcare professionals. Simply request a workshop or training here.
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