Women turning pain into art

女性将痛苦变成艺术

The Conversation

社会与文化

2025-01-06

26 分钟
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单集简介 ...

Chronic illness - and the pain it often brings - affects millions globally. But while women are more likely to experience chronic pain, they’re less likely to receive adequate treatment. Ella Al-Shamahi speaks to two women who have transformed their experiences with pain and chronic illness into powerful creative expression. Polly Crosby is a British author living with cystic fibrosis. Feeling invisible in the stories she grew up reading, she was inspired to write The Vulpine, a young adult novel deeply rooted in her personal experiences: the protagonist’s condition closely reflects Polly’s own. Polly is dedicated to portraying characters with disabilities and chronic conditions authentically, without invoking pity or hero-worship. Lavi Picu is a Romanian-Canadian interdisciplinary artist and Lyme disease advocate. She uses painting, drawing, and poetry as therapeutic tools to manage her condition while raising awareness for chronic illness. Lavi's art acts as a visual aid to, in her words, "make the invisible visible". Produced by Emily Naylor Image: (L) Polly Crosby credit Archant. (R) Lavi Picu courtesy of Lavi Picu.)
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  • This BBC podcast is supported by ads outside the uk.

  • I'm Ella Alshamahi and this is the conversation from the BBC World Service, the program that amplifies women's voices, which is really just a fancy way of saying we get two talented women from different countries who share an expertise, bring them together and see what happens.

  • Chronic illness and the pain it often brings affects millions globally.

  • But while women are more likely to experience chronic pain, they're less likely to receive adequate treatment.

  • Today I'm speaking to two women who have transformed their experiences with pain and chronic illness into powerful creative expressions.

  • Joining us in the studio is Polly Crosby, a British author living with cystic fibrosis.

  • Her upcoming young adult novel, the Vulpine draws from her own experiences and those with chronic conditions.

  • And Lavi Pickle is a multidisciplinary artist originally from Romania, now based in Canada.

  • She wants to make, in her words, the invisible symptoms of chronic illness visible.

  • Polly Lavi, welcome to you both.

  • Thank you.

  • Thank you for having me.

  • Lavi, how has Lyme disease and lupus shaped your life?

  • So Lyme disease and lupus are two autoimmune diseases that can wreak havoc throughout your body because they can affect multiple like organs or they can create a lot of problems within your body and they have a lot of overlap, overlapping symptoms, which makes them very difficult to diagnose.

  • Um, in here in Canada, for example, the system, it's a bit faulty.

  • And for Lyme disease, let's say the two tier tests that most of the doctors are relying for are showing false negatives.

  • And while you are reassured by your doctor you do not have Lyme disease, the bacteria continues to wreak havoc within your body.

  • And most of the Lyme sufferers are.

  • It takes about at least one year and a half to two years and a half to get a diagnosis, a proper diagnosis.

  • I'm one, let's say one of the happy cases.