Julie Laffin
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Life as art: healing from CFS, FMS, and MCS
How does one go from twelve years in a wheelchair and mostly bedridden to walking, world traveling, working, and riding a bike?
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Chicago Tribune features chemically sensitive artist
The Chicago Tribune presents an inspiring account of one woman's struggle to overcome severely isolating and disabling chemical sensitivity.
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Interview with performance artist Julie Laffin
Moving Beyond MCS, a blog about recovering from environmental illness, has published an interview with performance artist Julie Laffin that explores how her work has evolved due to her illness.
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(dis)abling conditions: curated by Julie Laffin
Julie Laffin will be "Skyped" in to this year's disability-themed Site Unseen show in Chicago to help spread awareness on environmental illness. The show is presented by The Chicago Department of Cultural Affairs.
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She Speaks in Metaphors (I Understand)
My doctor (one of them) says my entire left side is jammed. It's like shrink-wrapped plastic wrap, tight and brittle but it should be like one large, flowing, unified teardrop. It should have coherence and flexibility and it should breathe.
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Artist Blogs About Life with Severe MCS and Advanced Neuro-Lyme
PlanetThrive.com's newest guest blog post is by Julie Laffin, a Chicago-based performance artist who writes of her struggles with severe chemical sensitivity and advanced neurological lyme disease.
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Julie and her environment:
"...the woman in the pictures was her friend and collaborator, Clover Morell;...she could not go because of her illness. What illness could keep someone out of the Czech Republic, I wondered?"
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