Ginger Savely - Morgellons: The legitimization of a disease: A Factual Guide by the World’s Leading Clinical Expert

Disclaimer: The information in this book is not intended as a substitute for medical counseling. The author does not assume liability for any loss, damage, or injury caused or alleged to be caused directly or indirectly by the information contained in or omitted from this book.

Copyright 2016 by Virginia Riley Savely

Library of Congress Cataloging-in-Publication Data is available on file.

All Rights Reserved. No part of this book may be reproduced in any manner without the express written consent of the author, except in the case of brief excerpts in critical reviews or articles.

In an effort to keep sales prices down, this book has been printed in black and white. Please visit www.gingersavely.com/morgellons-book to access color versions of all photographs.

Cover design by Ruben de Haas
Cover photo credit Denise Moudree

ISBN
E-Book: 978-0-9979200-0-0
Pap erback: 978-0-9979200-2-4

Printed in the United States of America

Travis Wilson was one of many orphan patients abandoned by the health care system because he did not have the good fortune to contract a known and socially accepted disease. To Travis, for the loss of his young life, and to the many other Morgellons patients who have suffered in isolation and fear, I dedicate this work.

There is a rapidly growing interest in Morgellons disease as evidenced by the fact that research papers on the topic have been among the most highly accessed scientific research on the Internet for the past few years. As director of the Charles E. Holman Morgellons Disease Foundation (CEHMDF), I hear from 5 to 10 new patients daily who have symptoms consistent with the disease and who have hit brick walls trying to access medical care.

In our early years, the CEHMDF would field calls from hostile doctors, disgruntled that we were validating the symptoms reported by Morgellons patients. Today we hear more often from doctors who are baffled and at a loss to know what to do for the patients presenting to their practices with the debilitating symptoms of this new and misunderstood disease. As more and more research is published in the medical literature, Morgellons disease is slowly gaining acceptance as an infectious disease despite an unusually fierce opposition that strives to keep it tucked away and dismissed as purely psychiatric in origin.

Dr. Ginger Savely was the first pioneering medical provider to take her Morgellons patients' symptoms seriously and work to legitimize the disease. She took on this very challenging patient population and stood by them in their darkest hours. Dr. Savely listened to her patients and looked at the blatant objective evidence. She was the first to speak out publicly about this serious health crisis and she has continued throughout the years to stand up for the reality of Morgellons disease through her numerous published articles, interviews, and presentations at medical conferences. Dr. Savely has been a lifeline for hundreds of suffering people who have lost their way and given up hope of ever receiving medical attention for their unusual and agonizing symptoms. She has worked to educate her peers and has been committed to helping her patients.

At a time when interest in Morgellons disease is at an all time high, this detailed first-hand account of the Morgellons journey is a much-needed resource. With clarity, personal style and years of experience, Dr. Savely has taken on a challenging and highly controversial subject. Using up-to-the-minute scientific findings, color photographs and sweeping examples she has illuminated the path to recognition of this debilitating and disfiguring disease, previously orphaned by the medical community.

We have come a long way against great odds on our journey to legitimize Morgellons disease. Dr. Savely paved the earliest path on the rockiest road to make this progress possible. I have no doubt that Morgellons disease will eventually be fully recognized worldwide by health agencies and the medical community at large because the scientific evidence has reached an undeniable point. I firmly believe that in time the truth will prevail.

This book provides long-awaited answers to the vital questions being posed by thousands of patients and clinicians about this unthinkable disease. In reading Dr. Savelys poignant narrative, you will learn to separate fact from myth and rumor from reality. This book will be a valuable resource for Morgellons patients and their families and friends and will serve as a guide for clinicians who are open-minded and committed to the health of their patients.

Cindy Casey-Holman, RN
Director, The Charles E. Holman Morgellons Disease Foundation www.MorgellonsDisease.org

Never doubt that a small group of thoughtful, committed citizens can change the world;
indeed it's the only thing that ever has.
Margaret Mead

In 2003 I was working as a primary care nurse practitioner in a family practice clinic in Austin, Texas. A few years earlier I had become interested in treating Lyme disease after my teenage daughter became very ill with it. Lyme disease, a tickborne infection caused by the bacteria Borrelia burgdorferi , is most commonly seen in the northeastern United States but cases have been reported in all 50 states. By 2003 about 30% of my patients were Lyme disease patients because as I became more interested and knowledgeable about the disease, people who suspected that they had it began to seek me out.

One of my Lyme disease patients had previously been diagnosed with ALS (amyotrophic lateral sclerosis), a progressive and fatal neurodegenerative disease involving gradual atrophy of muscles of the body. When he first became ill he had been an active young man who led hikes through the mountains in Colorado. By the time I saw him he was expected to live no longer than another year. I began treating him with antibiotics after discovering that his Lyme Western Blot blood test was positive. Almost miraculously, he slowly began to improve.

Jim Bergamo, a news reporter with an Austin TV station, caught wind of the story of this young man who was improving from an incurable condition, and thought it would make a compelling human-interest story for the evening news. He and his crew came to my office and taped a TV news segment about this ALS patient, his illness and my treatment of him. As Jim left the office and thanked me for the story I said, If you think this was interesting youve GOT to come back and do a story on Morgellons disease!

Of course, I had to explain what I meant by this because at that point no one had heard of Morgellons (pronounced with a soft G) disease. I explained that a dozen or so of my Lyme patients had mysterious, spontaneously appearing, slow-healing lesions with unusual colored filaments embedded in and/or extruding from their skin. Other doctors had diagnosed these patients with Delusions of Parasitosis but I was beginning to have some success treating them with antibiotics. Their symptoms were varied, unexplainable and bizarre. I knew these patients were not delusional because I had observed the filaments myself using lighted magnification. I had tried to extract the embedded filaments but since they were firmly and deeply attached my attempts to remove them caused patients deep, radiating pain.

I had learned from my colleague William Harvey, M.D. of Houston, TX (now deceased) that there was a name for the filament condition Morgellons disease. The name was given by a microbiologist in Pennsylvania whose 3-year-old son had the symptoms. So, Jim Bergamo and his team returned once more to my office to make what was to become a powerful, award-winning news segment about Morgellons disease. The day after the segment aired, dozens of people began calling my office, excited to know that there were other people with their unusual symptoms and that there was actually a name for their condition.