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.
Dear New York Community- We need urgent action now to persuade New York Governor Kathy Hochul to sign our ME/CFS bill into law! Take action now! Thanks to you and the #MEAction community, bill A7712B/S6928B, which provides for a myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) education and outreach program in New York, finally passed both the