Pain Exchange

• The Future of PAIN: A Conversation with Karen Davis

  In this episode of Pain Exchange, our host and IASP’s Publications Manager/Editorial Assistant for PAIN, Dr. Renee Chasse, speaks with Dr. Karen Davis, Editor-in-Chief of PAIN, about the 2025 supplemental issue highlighting the 50th Anniversary of the journal. In this commemorative supplement, Karen decided to forgo looking into the past 50 years and, instead, look ahead at the next 50 years of the field, recruiting some of the field’s top minds to hear their thoughts on the future of pain research. Listen to this episode to hear more about the supplemental issue, Karen’s view on the future of the journal, and some of the most powerful innovations at the journal thus far. The views and opinions expressed by those interviewed are solely their own and do not necessarily reflect the views or opinions of IASP. This episode was produced by Peter DelGobbo, who also composed the theme music.

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• De-Stigmatizing Lipedema: A Conversation with Jonathan Kartt

  In observance of #PainAwarenessMonth, this inaugural episode of Pain Exchange follows IASP’s Publications Manager, Dr. Renee Chasse, as she speaks with Jonathan Kartt, the CEO of the Lipedema Foundation, about the disease and the Foundation’s work in spreading awareness about lipedema. Lipedema is a chronic medical condition, primarily affecting women, characterized by symmetric, often painful, buildup of adipose tissue (fat) in the legs, and sometimes the arms and lower mid-section of the body. Although the condition was first described in the 1940's, many research questions remain unanswered. Listen to this episode to hear more about this under-studied disorder, its connection to the pain field, and what researchers can do to incorporate lipedema research into their current programs. This episode was produced by Peter DelGobbo. The views and opinions expressed by those interviewed are solely their own and do not necessarily reflect the views or opinions of IASP. More information about the Lipedema Foundation is available on their website: https://www.lipedema.org/

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