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Episode 15: Creating Coalitions: ME/CFS & MCS. A Conversation with Emily Lim Rogers.
Manage episode 346317313 series 3341885
Thank you for listening to The Chemical Sensitivity Podcast!
New episodes twice a month. Subscribe for free where you get your podcasts.
If you like the podcast, you can support our work to help us continue creating greater awareness about MCS. Thank you very much! We really appreciate it.
In this episode, I’m speaking with Professor Emily Lim Rogers. Emily is a Disability Studies researcher and educator who specializes in Myalgic Encephalomyelitis, also known as Chronic Fatigue Syndrome or ME/CFS.
She is the Mellon Postdoctoral Fellow in Disability Studies in the Department of American Studies, the Program in Science, Technology, and Society, and the Cogut Institute for the Humanities at Brown University in Providence, Rhode Island, in the U.S.
In our conversation, Emily explores:
- The nature of ME/CFS.
- How people with ME/CFS and MCS struggle to have these illnesses understood and accepted.
- Online activism as a way for people with chronic illnesses to call for change.
- The impacts of capitalism on people with ME/CFS and MCS.
- How long COVID could potentially lead to more research and understanding about ME/CFS and MCS.
DISCLAIMER: THIS PODCAST AND WEBSITE DO NOT PROVIDE MEDICAL ADVICE
The information, including but not limited to, text, graphics, images, and other material contained on this website are for informational purposes only. No material on this site is intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health care provider with any questions you may have regarding a medical condition or treatment and before undertaking a new health care regimen, and never disregard professional medical advice or delay in seeking it because of something you have read on this website. No material or information provided by The Chemical Sensitivity Podcast, or its associated website is intended to be a substitute for professional medical advice, diagnosis, or treatment.
If you like the podcast, please consider becoming a supporter!
- Support the podcast.
- Find the podcast on Patreon.
- If you like, please buy me a coffee.
Follow the podcast on YouTube! Read captions in any language.
Please follow the podcast on social media:
Facebook
Twitter
Instagram
TikTok
Special thanks to the Marilyn Brachman Hoffman Foundation for its generous support of the podcast.
45 episoder
Manage episode 346317313 series 3341885
Thank you for listening to The Chemical Sensitivity Podcast!
New episodes twice a month. Subscribe for free where you get your podcasts.
If you like the podcast, you can support our work to help us continue creating greater awareness about MCS. Thank you very much! We really appreciate it.
In this episode, I’m speaking with Professor Emily Lim Rogers. Emily is a Disability Studies researcher and educator who specializes in Myalgic Encephalomyelitis, also known as Chronic Fatigue Syndrome or ME/CFS.
She is the Mellon Postdoctoral Fellow in Disability Studies in the Department of American Studies, the Program in Science, Technology, and Society, and the Cogut Institute for the Humanities at Brown University in Providence, Rhode Island, in the U.S.
In our conversation, Emily explores:
- The nature of ME/CFS.
- How people with ME/CFS and MCS struggle to have these illnesses understood and accepted.
- Online activism as a way for people with chronic illnesses to call for change.
- The impacts of capitalism on people with ME/CFS and MCS.
- How long COVID could potentially lead to more research and understanding about ME/CFS and MCS.
DISCLAIMER: THIS PODCAST AND WEBSITE DO NOT PROVIDE MEDICAL ADVICE
The information, including but not limited to, text, graphics, images, and other material contained on this website are for informational purposes only. No material on this site is intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health care provider with any questions you may have regarding a medical condition or treatment and before undertaking a new health care regimen, and never disregard professional medical advice or delay in seeking it because of something you have read on this website. No material or information provided by The Chemical Sensitivity Podcast, or its associated website is intended to be a substitute for professional medical advice, diagnosis, or treatment.
If you like the podcast, please consider becoming a supporter!
- Support the podcast.
- Find the podcast on Patreon.
- If you like, please buy me a coffee.
Follow the podcast on YouTube! Read captions in any language.
Please follow the podcast on social media:
Facebook
Twitter
Instagram
TikTok
Special thanks to the Marilyn Brachman Hoffman Foundation for its generous support of the podcast.
45 episoder
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