Sly Saint
Senior Member (Voting Rights)
Jeremy Jeffs is a filmmaker and photographer whose experience of living with ME/CFS inspired him to talk to and photograph others with the same illness. Here nine people reveal the devastating difficulties the condition brings – including their struggles to be believed by medics, to get a diagnosis, to access support, and simply to keep going.
Myalgic encephalomyelitis, known as ME, as well as chronic fatigue syndrome (CFS), is a doubly invisible illness. Not only are the symptoms hard to see, but the disease also attracts little understanding from the public and, at times, the medical profession. This leads to people with ME experiencing prejudice and disbelief, making them feel stigmatised and isolated.
I live with ME myself and for the past two years I’ve been meeting with, talking to and taking portraits of people who also contend with ME every day. Some have ME so severely that they are confined to bed, some are able to work part time, and many others struggle to simply keep up with a basic existence.
The lived experience we share has enabled me to connect and build a relationship with each person. Their words and portraits bring an identity and a visibility to an unseen community, demonstrating the range of people living with ME and the often devastating impact it has on their lives.
Living with ME | Wellcome Collection
Portraits and interviews by Jeremy Jeffs
real photos of real pwME