The Lady's Handbook for Her Mysterious Illness: A Memoir

The Lady's Handbook for Her Mysterious Illness: A Memoir

by Sarah Ramey

Narrated by Eileen Stevens, Sarah Ramey

Unabridged — 13 hours, 16 minutes

The Lady's Handbook for Her Mysterious Illness: A Memoir

The Lady's Handbook for Her Mysterious Illness: A Memoir

by Sarah Ramey

Narrated by Eileen Stevens, Sarah Ramey

Unabridged — 13 hours, 16 minutes

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Overview

"A best memoir of 2020" -BookPage

The darkly funny memoir of Sarah Ramey's years-long battle with a*mysterious illness that doctors thought was all in her head-but wasn't.*A revelation and an inspiration for millions of women whose legitimate health complaints are ignored.


In her harrowing, defiant, and unforgettable memoir, Sarah Ramey recounts the decade-long saga of how a seemingly minor illness in her senior year of college turned into a prolonged and elusive condition that destroyed her health but that doctors couldn't diagnose or treat. Worse, as they failed to cure her, they hinted that her devastating symptoms were psychological.
* * *The Lady's Handbook for Her Mysterious Illness is a memoir with a mission: to help the millions of (mostly) women who suffer from unnamed or misunderstood conditions--autoimmune illnesses, fibromyalgia and chronic fatigue syndrome, chronic Lyme disease, chronic pain, and many more. Ramey's pursuit of a diagnosis and cure for her own mysterious illness becomes a page-turning medical mystery that reveals a new understanding of today's chronic illnesses as ecological in nature, driven by modern changes to the basic foundations of health, from the quality of our sleep, diet, and social connections to the state of our microbiomes. Her book will open eyes, change lives, and, ultimately, change medicine.

Editorial Reviews

Publishers Weekly

★ 01/27/2020

In this illuminating debut memoir, musician Ramey offers an account of a mysterious illness that plagued her for more than a decade, beginning when she was in college in the early 2000s. Ramey recounts years struggling with excruciating pain, at times being unable to rise from bed. She pursued multiple medical treatments, but her pain persisted; when she turned to alternative approaches such as acupuncture and positive thinking, she found some relief, but also what she felt to be a New Age tendency to blame the victim. Though this medical saga is disturbing in the many miscalculations her doctors made, Ramey’s hilarious and upbeat sense of humor lightens even the direst of circumstances (a surgeon who performed the wrong surgery on her is dubbed Dr. Oops, and others merit such glib monikers as Dr. Vulva, Dr. Paxil, and Dr. Bowels). As Ramey relentlessly researched her own ailment, she learned that millions of women with such conditions as chronic fatigue, fibromyalgia, chronic Lyme disease, and other illnesses had also been ignored, mistreated, or belittled by conventional medicine. Ramey was eventually diagnosed with complex regional pain syndrome, and here she argues for more compassion among doctors and better treatment, and highlights reasons why some research has trouble securing funding (vaginal diseases, for example, are “too unpalatable for any awareness campaign, too unsexy to start a blog”). Ramey’s uncanny grit and fortitude will deeply inspire the multitudes facing similar issues. (Mar.)

From the Publisher

Sarah Ramey’s candor in discussing more than a decade of pain, confusion, and dismissal by countless doctors is matched by compassion for herself and every woman who has been told that her symptoms are only in her head, even when she knows her body is screaming. This is a book for anyone who has ever asked a question that didn’t have an immediate or easy answer, anyone who has worried about themselves or a loved one who isn’t getting better—despite following all the experts’ advice—and anyone interested in their own health, public health, or medicine. In other words, it’s a book with something resonant and useful for all of us. It’s also, not incidentally, a terrific read.”
—Chelsea Clinton, co-author of The Book of Gutsy Women: Favorite Stories of Courage and Resilience


"By making The Lady's Handbook for Her Mysterious Illness so smart, funny, and engaging, Sarah Ramey has found a way to turn life-saving medicine into a delicious read. I've given this book to so many people and they've all come back with overwhelming gratitude."—Ann Patchett, author of The Dutch House

 
“Sarah Ramey is a person of uncommon wit, bravery, compassion, honesty, and intellect. Every one of those qualities is on full display in this unflinching, important, and stunningly written memoir, which gives voice to millions of women whose experiences and pain have been ignored and minimized.”
—Ed Yong, author of I Contain Multitudes: The Microbes Within Us and a Grander View of Life
 
“With brilliant storytelling, Sarah Ramey tells of her experience with a mysterious illness while weaving in a practical roadmap for the woman who is overwhelmed, confused, depressed, desperate, and suffering with confusing symptoms. As she undertakes her heroine’s journey through her relationship with her body, she reclaims her power and comes home to herself—because in the end, it’s getting back into our bodies that allows us to become free. A masterwork and a page-turning, fantastic read.”
—Alisa Vitti, author of In The FLO and founder of FLO Living

“A visceral, scathing, erudite read that digs deep into how modern medicine continues to fail women and what can be done about it.”
Booklist, Starred Review
 
“Illuminating . . . Though this medical saga is disturbing in the many miscalculations her doctors made, Ramey’s hilarious and upbeat sense of humor lightens even the direst of circumstances . . . Her uncanny grit and fortitude will deeply inspire the multitudes facing similar issues.”
Publishers Weekly, Starred Review

“Astonishing, thorough and revelatory, a valuable resource for WOMIs and those who seek to understand and treat them. . . This book is a rallying cry to all other women whose illnesses go untreated but also to the general public on the need to make our medical system more responsive to chronic illness. Ramey’s memoir will lift you up by taking you down into the depths of despair that she experienced; you will be as inspired as you are educated about topics such as autoimmune disease, the endocrine system and the ways that society and gender affect them.”
America

Library Journal

03/01/2020

Blending medical writing and memoir, journalist Ramey's first book presents snapshots of her life navigating chronic pain, searching for a name for her condition, and struggling to be understood by physicians. Ramey recounts years of embarrassment and shame, experiencing aches, fatigue, and brain fog, living in near isolation as friends drifted away. Similar to Maya Dusenbery in Doing Harm, Ramey relates how women are more likely to be misdiagnosed and mistreated by doctors and to live with misunderstood conditions, especially autoimmune diseases. Interweaving clinical research with personal stories, the book follows Ramey as she moves from doctor to doctor, surgeon to surgeon, undergoing invasive tests and examinations in a decades-long pursuit of a diagnosis of fibromyalgia or ME/CFS. This is not always easy reading, and it shouldn't be—Ramey reiterates that the U.S. health care system is not designed with women in mind. She concludes with personal health advice. VERDICT Though dense at times, this work is among the few about understudied chronic conditions that primarily affect women, and the little attention they receive. For those living with invisible illnesses who have been told they don't look sick, and fans of the podcasts This Is Not What I Ordered and No End In Sight.—Stephanie Sendaula, Library Journal

Kirkus Reviews

2020-01-12
A memoir that explores the idea that women with chronic illnesses need to rally for appropriate medical care.

Making her book debut, Ramey, a writer and musician (known as Wolf Larsen), recounts, with captivating zest, a sorry tale of suffering from a cluster of symptoms that defied diagnosis. "I thought I was the strangest medical case on the East Coast," she writes, only to discover many others like herself. She was "a woman with a mysterious illness," a WOMI, chronically exhausted, aching, "likely in possession of at least one autoimmune disease," and likely to go from physician to physician in search of understanding. The daughter of physicians, Ramey began her quest for help believing unquestioningly in "Magical Pillthink," the notion "that if something is wrong, there is always a quick fix." She visited countless specialists and was treated with a host of medications that sometimes temporarily relieved symptoms, but more often not. She experienced "extremely bad—and often explicitly abusive—medical care," including botched surgeries. The author began to research her condition on her own, making some startling discoveries: the rise of autoimmune diseases in the last 30 years; the significance of the intestinal microbiome to digestive health and fatigue, aching, and "brain fog"; the role of antigens in producing an overactive immune response; physical and emotional traumas that can trigger WOMI symptoms; and microglia, tiny immune cells that protect the brain and nervous system that can become inflamed in response to a variety of stressors. Repeatedly prescribed antidepressants from frustrated doctors, Ramey indicts the medical establishment for its "contempt for women, and for the feminine," and recommends the new approach of functional medicine, which holds that "diet, lifestyle, and attitude are the cornerstones of health" and incorporates "testing, treating, and stabilizing" the four systems involved in "modern chronic illnesses:" the gut, liver, immune system, and endocrine system. Finally, her condition improved through common-sense changes: "Sleep, movement, a nontoxic environment, and a well-nourished psyche," Ramey concludes, are the basic needs for recovery.

Impassioned testimony of a fight for health.

Product Details

BN ID: 2940169298499
Publisher: Penguin Random House
Publication date: 03/17/2020
Edition description: Unabridged

Read an Excerpt

1

Dear Reader,

There may exist a graceful and elegant way to begin one’s gynecologic and colorectal memoir, but it never does spring to mind.

Let us start then with a story. We can travel back to where it all began, and for a moment leave the particulars behind. That sounds much nicer—lovely even—considering it all began so many years ago with a cool, luxuriant swim in Walden Pond.

~

I remember it well. The heat was heavy, I was a summer student at Harvard with no air-conditioning, and Walden beckoned for the reasons it always will. Though I suppose the busloads of tourists beached on the imported sand should have sounded some instinctive alarm when I arrived, they didn’t. I walked right on past and made my way to the side of the pond where the water was still and the snorkelers out of sight.

I remember walking into the water. I remember floating on my back. I remember the coolness and the peace and the poetry of the place, and I remember feeling like I couldn’t ask for anything more.

The next day in the emergency room, I had quite forgotten all of that.

A urinary tract infection, known as a UTI, is a very painful but easily treatable infection of the urethra. Most people describe it as “peeing broken glass,” and I would have to agree with most people.

But my ER doctors patted me on the back as they ordered up the standard antibiotics and I bounded off to the pharmacy, clutching my prescription, counting the minutes in the twenty-four hours they told me it would take to go away.

Fifty-six hours later, I was back in the emergency room. It had not gone away.

In fact, it did not go away for six months. “How strange,” the college physician said as he took my history. I had never been sexually active, which made things particularly challenging, both diagnostically and emotionally. I was a senior in college, and it was my time. I even had the right person picked out.

But the UTI stayed. We joked and called it my PUTI, or permanent UTI, and I laughed along with the rest. But in private, in the bathroom, I was profoundly unamused.

~

This prologue is typical of women like me. A simple and innocuous medical event—often with a gyno or gastro tilt—that should have resolved simply, but didn’t. She thinks it is just another one of life’s ups and downs, when in fact Up is about to become a distant memory.

There is a secret society of sorts that no one—not even the members—has heard of. We don’t look alike, we don’t dress alike, and we’re from all over. There is no secret handshake, no meeting place, no cipher.

We are the women with mysterious illnesses, and we are everywhere.

~

When I went home for Christmas just outside of Washington, D.C., my parents—who are both top-notch physicians—made an appointment for me to see Washington’s preeminent, top-notch urologist.

Dr. Damaskus said I seemed like a nice, normal young woman who would probably like to get back to the business of being able to pee and have sex freely, and he saw no reason why he couldn’t make that happen. He determined I no longer had an active infection—and then proposed a procedure, to be done right there, that day, in the office. As he described it, he would insert a small instrument into the urethra, rip it, and this would solve the problem.

I frowned.

But Dr. Damaskus assured me it was the only option, should I want a normal life again—the gentle ripping, he explained, was more of a light stretching of the tissue, and it would interrupt the muscle spasm and break the cycle of pain. He handed me a paper gown.

I’m almost nostalgic for my naïveté. I took the gown, steeled my nerves, saddled up, and put my feet in the stirrups.

The procedure began benignly enough with a small swabbing of topical lidocaine, but in the next step a device not unlike a very small car jack was inserted in the urethra and then ratcheted out several notches until the urethra, as promised, tore. It was a blinding pain that no amount of lidocaine would dull. He peeked over the paper blanket and asked if I thought he had gone enough notches. I was crying too hard to do anything but nod. He went one more notch.

Dear, patient reader, I have not forgotten about you, or our purpose here—or the cautionary voice in the back of my head whispering something about too much information. But I think this history is important. So before we move out of this reverie, let me come quickly to the end of the beginning of our story.

That night, after Dr. Damaskus sent me hobbling back on my way, intuition’s warning bell finally took up its low, steady thrum. I sat silently through dinner, and put myself to sleep early. Something was not right—something flulike, but menacing, was starting to bristle. Everything hurt, not just my urethra. My ears hurt. My teeth hurt. I fell asleep, my hands clenching and unclenching of their own accord.

When I woke, I was on the floor, quaking with rigors, drenched in sweat, and making a very bad noise. My mother was calling the hospital and dragging me toward the car. I had become septic, an infection of the bloodstream that would have ended badly if my mother weren’t such a top-notch physician. We were at the hospital in minutes.

I was not witness to the miraculous save, but I heard all about it when I woke up. Top-shelf, nuclear-grade antibiotics pumped into me by the gallon, and it seemed like every doctor at Sibley Memorial Hospital (except one Dr. Damaskus) came to sit by my side, making sure the doctors’ daughter pulled through. I was extremely well taken care of. I was going to live. It would all be all right.

By the next day, everyone had gone back to their private practices, wishing me well, which I very much appreciated. The only problem was (and I hated to be a stickler)—I wasn’t all right. I was still aching all over, badly, even though the infection was gone. I had a fever every afternoon, and intense pain all down my legs. The broken-glass pain was starting to radiate out to the surrounding muscles in the vagina, rectum, and bladder. My bowels seized up and stopped working. I itched.

“Strange,” my doctors murmured, making notes. “How very strange.”

They ran dozens of tests, but everything came back negative. At a loss (and at my insistence), they sent me back to school with painkillers and portable IV antibiotics. They said it would slowly all start to get better, and I believed it. When had my body ever done anything but get all better? I was ready to get back to the business of peeing and expressing my sexuality freely. I would carry my little IV from class to class if that’s what it took.

But my body did not get better.

Class after feverish class, night after achy night, and morning after urethrally excruciating morning, I could not deny: it was getting much worse.

And in the most mysterious ways.

I was on so many medications and getting so sick so fast, it was like a rabbit hole had opened up beneath me—that I was falling slowly past the clocks and the candlesticks, and that my parents and doctors were peering over the edge, quietly watching me float down and away.

~

The entire point of The Lady’s Handbook for Her Mysterious Illness is this:

It would have been helpful to know what a well-trafficked rabbit hole that was.

~

The unfortunate but innocuous series of medical events.

The gallons of antibiotics and fistfuls of painkillers.

The severe digestive issues, gynecologic issues, joint pain, itching, and fatigue.

The referrals, the specialists, the puzzlement.

The growing doctor-patient antipathy.

The dramatic health avalanche.

The clocks. The candlesticks.

The despair.

I thought I was the strangest medical case on the East Coast.

I was wrong.

~

Seventeen years later, I have become a well-known woman with a mysterious illness.

In the early years of this distinction, other women with mysterious illnesses would frequently introduce themselves to me, often at the most unexpected moments—at weddings, in elevators, or leaning across a bank of guests at a crowded Thanksgiving table—all wanting to discuss their own mysterious maladies. I just had to speak the words Candida or Subclinical Hypothyroid—or the most potent of all, Gluten—and three heads would rubberband in my direction. They either knew a woman with a mysterious illness, were married to a woman with a mysterious illness, or were themselves a woman with a mysterious illness. While other people grilled kebabs, we would speak discreetly and in low tones about constipation. When the daiquiri pitcher appeared from the kitchen, we would duck our heads to discuss whether or not daiquiris were gluten-free. At elegant cocktail parties, women were constantly pulling me into corners to talk about their vaginas.

You most likely know one of us already—a coworker, an aunt, a sister—some beleaguered old girl endlessly dealing with her health issues. She’ll be reluctant to talk about the particulars but noticeably lacking in a solid diagnosis. Most people privately agree she actually suffers from an acute case of hypochondria.

This woman may not know it yet, but she is in the club.

~

WOMI.

wo.mi | whoa-mee | noun

A woman with a mysterious illness.

~

I had to make this word up myself. I would have preferred a committee, or a wealthy patron—whoever is in the business of naming—to do it for me, but no one volunteered. I’d also have preferred something more dignified than WOMI—something with gravity, preferably in the Latin. Something that provoked the right response, which in my case is, “Holy fucking shit.” But because there is no name for what’s wrong with me, people don’t say holy fucking shit. They ask if I have tried green juice or positive thoughts.

Having a word helps.

Either way, I am sure you know a WOMI already. A spouse, a little sister, a cousin.

The signs are unmistakable. She is exhausted, gluten-free, and likely in possession of at least one autoimmune disease. She is allergic to ____ (everything), aching from tip to toe, digestively impaired, and on uneasy terms with her reproductive system. She is addled, embarrassed, ashamed, and inflamed.

She is one of us.

~

The following scene is unfolding in an office in your town every day, perhaps right now at this very moment:

Jane Doe crosses her ankles in the waiting room, absently turning the pages of People magazine. She looks around often—now at the oversize clock, now at the receptionist, now at the generic watercolors on the walls.

“Ms. Doe,” a flat voice calls out. “Dr. Bowels will see you now. Second door on the left.”

Jane takes a seat in the doctor’s office, regarding the diplomas on the wall. On the desk stands a life-size replica of the human intestinal tract. When Dr. Bowels bustles in, he introduces himself as he looks over her chart for what is clearly the first time.

“Now, Ms. Doe,” he says cheerfully. “What can I do for you?”

The interaction begins very seriously, a furious scribbling of notes, a furrowing of the brow, a lot of nodding. The usual diseases are ruled out and Jane confirms she has been tested, twice, for everything under the sun. Her primary symptoms are severe constipation, distention, and pain in the lower left quadrant of her abdomen. As the doctor pages through her thick medical file, Jane takes the opportunity to share some of the stranger nonbowel symptoms she has experienced—aching in the bones, fatigue, itching, unexplained gynecologic symptoms, memory problems, lower back pain—but the words are scarcely out of her mouth before she wishes she had kept her addenda to herself. She can see the red flags rising behind his eyes, and the note taking slowly tapers off. Before she knows it, where once Sherlock Holmes scribbled furiously, hot on the trail, bent on solving her mystery—he now leans back in his swivel chair, tip of his pen in the corner of his mouth, checking his watch. His look is saturated with understanding, for he has solved the case.

What we have here is not a rare, tropical disease, Watson. What we have here is an unhappy woman, badly in need of an antidepressant.

~

Six years went by before I was aware of the proverbial Jane Doe.

And again, I come from a family of excellent doctors. My mother, my father, my stepfather—even my grandmother was a famous endocrinologist. I am the absolute last person who should have walked off a medical cliff without so much as a Wile E. Coyote deadpan to the camera.

But this is how it always begins. The appointment with Dr. Bowels will likely be followed by a similar experience with Dr. Vulva, only to be repeated with Dr. Rheuma, who sends her on to Dr. Uro, and then Dr. Neuro, followed by Dr. Thyro, then possibly Dr. Chiro, and finally cycling back to Dr. Bowels. Since no lightbulbs have gone off over anyone’s head, off she goes to Dr. Freud.

This long and expensive chain of events is not only common for this type of patient—it is the norm.

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