Living with Lyme Disease is an easy to use self-help guide of holistic techniques to address some of the common symptoms and challenges of Lyme disease. Written by Helene Brecker, an Energy Medicine Practitioner who struggled with losing muscle strength in her legs and the ability to walk along with cognitive changes all stemming from a tick bite. The book offers techniques to empower the individual to help themselves in their own healing with the tools they have on hand - their hands. Part I offers some theories of Chinese Medicine, explains the modalities being used, and provides definitions of terms. Part II lists the systems affected and various energetic techniques to work with those challenges. The mental or physical challenges being faced are easily located and have descriptions of the techniques and how to work with them. Illustrations accompany verbal descriptions. As Donna Eden puts it, "Helene Brecker was one of the 100,000 people each year whose symptoms could not be controlled by medication. I have watched her healing unfold, and it has been a poignant victory of the human spirit using human ingenuity to tackle an enormous challenge. Her body was her laboratory, the canvas on which she painted a moving picture of her return to health. Like many who have overcome a terrible disease after conventional remedies have not worked, she is passionate - in the tradition of the "wounded healer" - to bring what she has learned to others. This book not only describes her journey back to health, it leaves markers on the path that others can follow."

Learn to live a rich, vital, and meaningful life despite Lyme disease or chronic illness.

A collection of poetry based on the author's experiences of living with Lyme Disease. This work highlights Lyme Disease. It is a personal account of what it is like to live with Lyme Disease.

As an avid outdoorswoman with a passion for health and fitness, Kristy could never have imagined that she would lose everything she knew and loved on a hike that was meant to bring her peace. After setting up camp one night, she realized she was covered in ticks. One tick in particular would change her life forever. Eventually, Kristy’s mobility became impaired, and she experienced a significant loss of cognitive function. This, along with a host of other ailments, would lead her to seek treatment outside of the country. There she would learn about Lyme disease and the many other infections she had acquired. Kristy would soon discover that she had also developed other significant health issues as a result of being misdiagnosed. She would eventually decide that—due to the unjust treatment of Lyme patients by the medical community—she could either choose to be a victim or rise to the challenge. In an effort to heal on all fronts, she sought treatment, help, and support from multiple sources. Healing and enlightenment came to her in surprising ways. She would eventually learn a truth about herself that would turn her life upside down. Finding this truth would help her take control of her future and see every aspect of her life in a different light. This realization showed her a way of life that was more fulfilling than she had ever imagined possible. Kristy discovered that when you’re stripped of what seems most important in life, you have the ability to see things more clearly than ever before. She may be living with Lyme forever, but Kristy is thriving in life like she never dreamed possible.

NEW YORK TIMES EDITORS’ CHOICE • In this vulnerable, insightful memoir, the New York Times columnist tells the story of his five-year struggle with a disease that officially doesn’t exist, exploring the limits of modern medicine, the stories that we unexpectedly fall into, and the secrets that only suffering reveals. “A powerful memoir about our fragile hopes in the face of chronic illness.”—Kate Bowler, bestselling author of Everything Happens for a Reason In the summer of 2015, Ross Douthat was moving his family, with two young daughters and a pregnant wife, from Washington, D.C., to a sprawling farmhouse in a picturesque Connecticut town when he acquired a mysterious and devastating sickness. It left him sleepless, crippled, wracked with pain--a shell of himself. After months of seeing doctors and descending deeper into a physical inferno, he discovered that he had a disease which according to CDC definitions does not actually exist: the chronic form of Lyme disease, a hotly contested condition that devastates the lives of tens of thousands of people but has no official recognition--and no medically approved cure. From a rural dream house that now felt like a prison, Douthat's search for help takes him off the map of official medicine, into territory where cranks and conspiracies abound and patients are forced to take control of their own treatment and experiment on themselves. Slowly, against his instincts and assumptions, he realizes that many of the cranks and weirdos are right, that many supposed "hypochondriacs" are victims of an indifferent medical establishment, and that all kinds of unexpected experiences and revelations lurk beneath the surface of normal existence, in the places underneath. The Deep Places is a story about what happens when you are terribly sick and realize that even the doctors who are willing to treat you can only do so much. Along the way, Douthat describes his struggle back toward health with wit and candor, portraying sickness as the most terrible of gifts. It teaches you to appreciate the grace of ordinary life by taking that life away from you. It reveals the deep strangeness of the world, the possibility that the reasonable people might be wrong, and the necessity of figuring out things for yourself. And it proves, day by dreadful day, that you are stronger than you ever imagined, and that even in the depths there is always hope.

Now completely revised and updated-the bible for the thousands who contract Lyme disease each year Lyme disease, transmitted through the bite of a tick, is one of our nation's fastest-growing epidemics. Since Coping with Lyme Disease was first published in 1993, the number of sufferers afflicted by this debilitating condition has grown alarmingly. Every chapter has been thoroughly revised and new information about the long-term neurological effects of Lyme disease and congential and chronic versions of the illness has been added. This comprehensive guide includes - basic prevention tips - a detailed catalog of the physical and psychological symptoms to look for - a complete look at the medical and home care options and insurance policies available to patients - a special discussion of Lyme's effects on women, children, and the elderly - an expanded resource guide, with listings of news publications, state-by-state support groups, and special family services This fully updated third edition informs readers of the latest medical findings in diagnosing and treating Lyme disease-providing crucial information about newly discovered Lyme-related illnesses, electromagnetic procedures, clinical and antibiotic therapies, and curative nutritional products now on the market. A longtime bestseller, this authoritative book is an essential tool for all Lyme disease sufferers.

A Best Book of the Year: Real Simple, Entropy, Mental Floss, Bitch Media, The Paris Review, and LitHub. Time Magazine's Best Memoirs of 2018 • Boston Globe's 25 Books We Can't Wait to Read in 2018 • Buzzfeed's 33 Most Exciting New Books • GQ Best Non Fiction Book of 2018 • Bustle’s 28 Most Anticipated Nonfiction Books of 2018 list • Nylon’s 50 Books We Can’t Wait to Read in 2018 • Electric Literature’s 46 Books to Read By Women of Color in 2018 “Porochista Khakpour’s powerful memoir, Sick, reads like a mystery and a reckoning with a love song at its core. Humane, searching, and unapologetic, Sick is about the thin lines and vast distances between illness and wellness, healing and suffering, the body and the self. Khakpour takes us all the way in on her struggle toward health with an intelligence and intimacy that moved, informed, and astonished me.” — Cheryl Strayed, New York Times bestselling author of Wild A powerful, beautifully rendered memoir of chronic illness, misdiagnosis, addiction, and the myth of full recovery. For as long as author Porochista Khakpour can remember, she has been sick. For most of that time, she didn't know why. Several drug addictions, some major hospitalizations, and over $100,000 later, she finally had a diagnosis: late-stage Lyme disease. Sick is Khakpour's grueling, emotional journey—as a woman, an Iranian-American, a writer, and a lifelong sufferer of undiagnosed health problems—in which she examines her subsequent struggles with mental illness and her addiction to doctor prescribed benzodiazepines, that both aided and eroded her ever-deteriorating physical health. Divided by settings, Khakpour guides the reader through her illness by way of the locations that changed her course—New York, LA, Santa Fe, and a college town in Germany—as she meditates on the physiological and psychological impacts of uncertainty, and the eventual challenge of accepting the diagnosis she had searched for over the course of her adult life. A story of survival, pain, and transformation, Sick candidly examines the colossal impact of illness on one woman's life by not just highlighting the failures of a broken medical system but by also boldly challenging our concept of illness narratives.