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ME/CFS & MCS: Emily Lim Rogers

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Manage episode 346317313 series 3341885
Konten disediakan oleh The Chemical Sensitivity Podcast. Semua konten podcast termasuk episode, grafik, dan deskripsi podcast diunggah dan disediakan langsung oleh The Chemical Sensitivity Podcast atau mitra platform podcast mereka. Jika Anda yakin seseorang menggunakan karya berhak cipta Anda tanpa izin, Anda dapat mengikuti proses yang diuraikan di sini https://id.player.fm/legal.

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.

Emily Lim Rogers

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.

Support the show

Thank you very much to the Marilyn Brachman Hoffman Foundation for its generous support of the podcast.
If you like the podcast, please consider becoming a supporter!

Follow the podcast on YouTube! Read captions in any language.

Please follow the podcast on social media:
Facebook

Instagram
X
BlueSky
TikTok
Sponsorship Opportunites

Are you an organization or company interested in helping to create greater awareness about Multiple Chemical Sensitivity and Chemical Intolerance and/or looking for sponsorship opportunities? Please email us at info@chemicalsensitivitypodcast.org

  continue reading

Chapter

1. ME/CFS & MCS: Emily Lim Rogers (00:00:00)

2. Opening clip from Emily. (00:00:05)

3. Aaron introduces the podcast and episode. (00:00:18)

4. Emily explains ME/CFS. (00:04:00)

5. Emily discusses her health status and conditions she has that are associated with ME/CFS. (00:06:18)

6. Emily explains that MC/CFS is a gendered illness and that many people with the condition are women. (00:09:03)

7. Emily discusses the role of chemicals in our everyday environment that contribute to illnesses like ME/CFS. (00:12:58)

8. Emily explores HIV/AIDS activism and how it influenced people who are activists focused on ME/CFS. (00:20:00)

9. Emily talks about the challenges that people with ME/CFS face when trying to advocate for greater awareness and recognition of the illness. (00:25:00)

10. Emily discusses impacts of capitalism on people with chronic illness, including ME/CFS and MCS. (00:30:00)

11. Emily talks about long COVID and how it may lead to wider understanding and acceptance of ME/CFS and other illnesses. (00:36:56)

12. Aaron concludes the episode. (00:41:08)

61 episode

Artwork
iconBagikan
 
Manage episode 346317313 series 3341885
Konten disediakan oleh The Chemical Sensitivity Podcast. Semua konten podcast termasuk episode, grafik, dan deskripsi podcast diunggah dan disediakan langsung oleh The Chemical Sensitivity Podcast atau mitra platform podcast mereka. Jika Anda yakin seseorang menggunakan karya berhak cipta Anda tanpa izin, Anda dapat mengikuti proses yang diuraikan di sini https://id.player.fm/legal.

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.

Emily Lim Rogers

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.

Support the show

Thank you very much to the Marilyn Brachman Hoffman Foundation for its generous support of the podcast.
If you like the podcast, please consider becoming a supporter!

Follow the podcast on YouTube! Read captions in any language.

Please follow the podcast on social media:
Facebook

Instagram
X
BlueSky
TikTok
Sponsorship Opportunites

Are you an organization or company interested in helping to create greater awareness about Multiple Chemical Sensitivity and Chemical Intolerance and/or looking for sponsorship opportunities? Please email us at info@chemicalsensitivitypodcast.org

  continue reading

Chapter

1. ME/CFS & MCS: Emily Lim Rogers (00:00:00)

2. Opening clip from Emily. (00:00:05)

3. Aaron introduces the podcast and episode. (00:00:18)

4. Emily explains ME/CFS. (00:04:00)

5. Emily discusses her health status and conditions she has that are associated with ME/CFS. (00:06:18)

6. Emily explains that MC/CFS is a gendered illness and that many people with the condition are women. (00:09:03)

7. Emily discusses the role of chemicals in our everyday environment that contribute to illnesses like ME/CFS. (00:12:58)

8. Emily explores HIV/AIDS activism and how it influenced people who are activists focused on ME/CFS. (00:20:00)

9. Emily talks about the challenges that people with ME/CFS face when trying to advocate for greater awareness and recognition of the illness. (00:25:00)

10. Emily discusses impacts of capitalism on people with chronic illness, including ME/CFS and MCS. (00:30:00)

11. Emily talks about long COVID and how it may lead to wider understanding and acceptance of ME/CFS and other illnesses. (00:36:56)

12. Aaron concludes the episode. (00:41:08)

61 episode

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