Caring for the M.E. Patient
Caring for the M.E. Patient by Jodi Bassett, published by Lulu.com in 2011, is an illustrated guide that provides essential information on the neurological disease M.E. This edition spans 162 pages and is written in English. The book is designed for M.E. patients, their friends and family, partners, carers, and doctors, offering insights sourced from leading experts in the field.
Readers will find a comprehensive overview of M.E., distinguishing it from conditions like chronic fatigue syndrome (CFS). The book emphasizes the importance of understanding the basic facts about M.E. to better support those affected by the disease. With contributions from various experts, including a foreword by Dr. Byron Hyde, this resource aims to enhance awareness and advocacy for M.E. patients, while also addressing the challenges faced by those misdiagnosed with CFS.
Official synopsis Publisher
Essential information on the neurological disease M.E. sourced from the world’s leading M.E. experts. Suitable for M.E. patients, their friends and family, partners, carers or doctors. The book includes a foreword by international M.E. expert Dr Byron Hyde. M.E.is a distinct neurological disease and is not at all the same thing as ‘CFS.’ Learning the facts is not time-consuming or complicated. Supporting your ill friend or family member or patient more fully by being aware of the basic facts of M.E. could make all the difference in the world to them. This book shows you how. Jodi Bassett is the founder of the international M.E. charity, HFME. Jodi contracted M.E. in 1995 when she was just 19. HFME contributors also aim to advocate for those non-M.E. patients who have been given the always meaningless ‘CFS’ diagnosis, and subsequently denied correct diagnosis and treatment.
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