
Headless Youth Podcast
Podcast by Headless Youth Podcast
A podcast about Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), mold avoidance, craniocervical instability, environmental degradation, and the epidemic of chronic illness.
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Episode from 2020 found in the archives, edited by Rene Joly. Walker and Lucas discuss Fallout New Vegas, mold avoidance in the Southwest, and Gulf War Syndrome.

A reading of Virginia Woolf's essay "On Being Ill" by Eva. #disability #VirginiaWoolf #chronicillness Art by Remedios Varo.

In 2018, after 16 years of suffering with the illness ME/CFS, Anne Örtegren died by physician assisted suicide. Anne was a fierce advocate for ME/CFS patients; she wrote for HealthRising.com about her experience with the disease and why the world needs to pay attention and fund research. She explained her choice to end her life in a final post titled "Farewell – A Last Post from Anne Örtegren." This bonus material episode is a reading of that letter. You can read along here: http://lobel.nu/anne.html. You can find Anne's other posts here: https://www.healthrising.org/authors/anne-ortegen/. Please listen and pay heed to Anne's final words, they are important. Here's an excerpt we'd like to highlight: "It would be easier to handle if there were breaks, breathing spaces. But with severe ME/CFS there is no minute during the day when one is comfortable. My body is a war zone with constant firing attacks. There is no rest, no respite. Every move of every day is a mountain-climb. Every night is a challenge, since there is no easy sleep to rescue me from the torture. I always just have to try to get through the night. And then get through the next day. It would also be easier if there were distractions. Like many patients with severe ME/CFS I am unable to listen to music, radio, podcasts or audio books, or to watch TV. I can only read for short bouts of time, and use the computer for even shorter moments. I am too ill to manage more than rare visits or phone calls from my family and friends, and sadly unable to live with someone. This solitary confinement aspect of ME/CFS is devastating and it is understandable that ME/CFS has been described as the 'living death disease'... ...If we knew there were relief on the horizon, it would be possible to endure severe ME/CFS and all the additional medical problems, even for a long time, I think. The point is that there has to be a limit, the suffering must not feel endless."

The final installment of the series "Many Seasons in Hell" with @death_denial subjects: -Knowing death, near death experiences -Possibility of cure, medical progress -Chronic illness experience across age and class -“If God is good, all things will be rectified” -Ways to endure and find strength within yourself -EPILOGUE edited by Rene Joly #mecfs #longcovid #pasc #mysticism

Many Seasons in Hell part V * War reading with chronic illness * Nazi defeat at Stalingrad * Hermann Goring and Elf ***** * Elves, faeries, various depictions * Matcha * Religion, spirit/soul, vs the material. Mind and matter * Nietsche’s illness, contextualizing his fixation on vitality * Religions and suffering; Christianity and Buddhism * Making sense of suffering, or the attempt to * Assisted suicide and religion * Buddhism and realms * Different conceptions of afterlife * Seeking spiritual guidance Edited by Rene Joly
Aloita 3 vrk maksuton tilaus
Kokeilun jälkeen 7,99 € / kuukausi.Peru milloin tahansa.
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