American breakdown Our ailing nation, my body's revolt, and the nineteenth-century woman who brought me back to life

A writer and social worker charts her harrowing descent into mysterious physical illness. What is now more popularly known as chronic fatigue syndrome was a complete anomaly to Lunden when, in 1989, at age 21, she became ill six months after relocating from Canada to Maine. Her symptoms included lassitude, exhaustion, headaches, and deep depression. A mononucleosis diagnosis brought little relief since her chronic weakness persisted so intensely that she could barely hold a pen to write in her diary. In 1988, the "wicked flu that never went away" received its official name: chronic fatigue syndrome. With limited resources for regular physician visits, the author became disheartened and even suicidal. At 26, Lunden discovered the biography of mid-19th-century diarist and social critic Alice James, sister to novelist Henry and psychologist William, who developed a fatigue that crippled most of her bodily systems. Lunden drew immediate correlations between James' debilitating medical ailment--first misclassified as hysteria, then neurasthenia--and her own ordeal. With a detective's persistence, the author began intensive research into potential causes, including chemical toxins and stress emergencies. She dug into the work of immunologists, toxicologists, and infectious disease specialists, past to present, who studied CFS, and her investigation broadened her perspective about not only overlooked medical ailments, but the current problematic state of American health care in general. Throughout, Lunden deftly interweaves her story with that of James. After producing such an exhaustive survey of disease and disorder, the author's cynicism is understandable, and she criticizes physicians who dismissed her with depression, just as James' doctors had mischaracterized her symptoms as female hysteria. Lunden shines a sobering light on CFS, its evolution and misinterpretations, and its increasing prevalence within the general population. Blending theory and memoir, the author personifies her struggle for wellness and its associated costs and consequences. An alarming chronicle of catastrophic chronic illness and a passionate plea for health care reform. Copyright (c) Kirkus Reviews, used with permission.