Juliet Chenery-Robson is a freelance photo-journalist and editor in the UK. She had to put aside her career and become a full time caretaker when her daughter developed ME at age 13.
Robson has spent the past 10 years raising awareness for ME. She describes an all too familiar experience with doctors:
[pullquote align=”full” cite=”” link=”” color=”#E7453A” class=”” size=””]Instead of taking it seriously and demanding more research, they try to airbrush it out of existence with antidepressants and talking therapies in the hope it will disappear like a puff of smoke. For most – those who’ve been ill for years and are not getting better – it won’t.[/pullquote]
Out of these harrowing experiences, Chenery-Robson has created this stunning photo series on ME.
![a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.](https://www.meaction.net/wp-content/uploads/2024/06/Severe-ME-Artists-Project-2024-1200-x-630-px-1-300x158.png)
Severe ME Artists Project 2024
Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by
1 thought on “Portraits of invisible illness”
I’m so sorry, Juliet for your daughters illness. You beautiful photographs say more than words ever could.
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