This month, Valerie Free’s new book, Lighting Up a Hidden World: CFS and ME will be released to the public.
In 1990, Valerie Free was a vibrant, thirty-year-old woman: a court stenographer, wife, and mother. In July of that year, she came down with a sudden, flu-like illness and after months of unrelenting and bizarre symptoms was diagnosed with chronic fatigue syndrome (CFS). Despite the challenges posed by her health, her search for answers led her to write Lighting Up a Hidden World: CFS and ME — the result of decades of research and outreach to the chronic illness community. Valerie resides on an acreage with her family in Alberta, Canada.
From Free’s website:

The onset can be fast and shocking or slow and insidious. It can happen to anyone at any age. A flu, a vaccination, or an infection can be the innocent beginnings to the potentially life-long and disabling illness called myalgic encephalomyelitis (ME), which is more commonly known as chronic fatigue syndrome (CFS), or ME/CFS in North America. In the mid 1980s, the U.S. Centers for Disease Control (CDC) was called in by concerned doctors who were witnessing an influx of patients with a mysterious illness. Eventually the CDC labeled the condition “chronic fatigue syndrome” which turned out to be very misleading. Decades later, in 2016, health agencies are finally beginning to agree with international experts that ME/CFS is a serious, chronic, multi-system illness.  Through artwork, poetry, story-telling, and meticulous research, Lighting Up a Hidden World: CFS and ME takes readers into the fascinating, yet frightening, landscape of ME/CFS. Author Valerie Free shares her personal experiences and delivers illuminating first-hand perspectives from patients, caregivers, journalists, and medical professionals from within the global community in short easy-to-read segments. These stories reveal the disgrace, controversy and tragedy of worldwide neglect by political and health care systems, leaving ME/CFS research underfunded and millions of people marginalized, sick, and socially unsupported.
Lighting Up a Hidden World: CFS and ME advocates for those too ill to speak out, abounds with patient resources, and offers realistic hope for the future. People living with this illness, along with their family and friends, will find compassion and camaraderie in its pages. This book reaches beyond the ME/CFS community exposing the themes of human suffering, resilience, and the need for social change.

The importance of literature and qualitative research on revealing the insidious nature and prevalence of ME/CFS cannot be overstated.  Make others aware of Free’s debut by posting on Facebook, Tweeting, and informing others interested in ME/CFS about this new work.  Lighting Up a Hidden World should be available from booksellers all over the globe, including amazon.com, amazon.ca, and Barnes and Noble, later this month.
Learn more about other books, films, and television that discuss ME/CFS on MEpedia’s article.