CFS Unravelled

Get Well By Treating The Cause Not Just The Symptoms Of CFS, Fibromyalgia, POTS And Related Syndromes

Dan Neuffer

• Publisher: Elednura Publishing
• Year: 2017
• ISBN:
  9780987509826
• Edition: 1
• Topic: Medicine
• Subtopic: Diseases & Allergies

Is reading yet another book on How To Treat all your CFS/Fibromyalgia/POTS symptoms REALLY going to create lasting change?

How can you recover from Fibromyalgia or Chronic Fatigue Syndrome (ME/CFS), POTS or Multiple Chemical Sensitivities (MCS) if you don’t even know what is causing the illness or why it perpetuates?

Whilst it has long been officially recognised that this syndrome is a neurological illness, treatments focus has still been on the severe physical dysfunctions that lead to the symptoms.

So forget the old concept of just symptom treatments, or looking for the next “CFS cure” or “Fibromyalgia breakthrough”. People all over the world have been recovering from this syndrome for many decades and now you can learn HOW and WHY some people have success whilst others who seemingly try the same strategies, don’t.

“What makes CFS Unravelled unique is that it breaks through the noise and focusses you on the underlying dynamics that the medical research communities have wrestled with for many decades. Understanding this is key for you to regain your health!”

Professor Kati Thieme, PhD

“recipient of the 2008 International Award for Fibromyalgia Research”

In this book you will learn:

• How the symptoms are created & what treatment options are available
• How the symptoms and dysfunction are all connected
• What strategies to explore and tailor to address the root dysfunction for a lasting and robust recovery
• How to best approach your recovery so you have practical steps to take you forward.

Clearly for an illness described as a neurological condition, the focus has to be on how to effect neuroplasticity to regain your health from CFS & Fibromyalgia (including POTS, MCS etc).

By understanding the dynamics of this illness as explained in the book, you will finally be able to understand WHY treatments you have tried in the past didn’t have a lasting effect. You will even learn why treatments that weren’t helpful, could be key in your recovery once you adjust your approach to the framework outlined in the book.

You can also listen to in-depth interviews with people that have recovered from Fibromyalgia/CFS/POTS/MCS on cfsunravelled.com. With a deeper understanding from the book, you will finally understand how and why they recovered from chronic pain and all the other symptoms.

 

Part One:
Introduction

 

Chapter 1

Naming Convention

“What's in a name? that which we call a rose
By any other name would smell as sweet.”

- William Shakespeare

Much contention surrounds the names given to this illness—not only about whether each is appropriate, but whether different names describe different illnesses altogether.

The names include Chronic Fatigue Syndrome (CFS), Myalgic Encephalomyelitis (ME), Fibromyalgia or Fibromyalgia Syndrome (FMS), Systemic Exertion Intolerance Disease (SEID), Postural Orthostatic Tachycardia Syndrome (POTS), Chronic Fatigue and Immune Dysfunction Syndrome (CFIDS), Multiple Chemical Sensitivity (MCS) or Electromagnetic Hypersensitivity (EHS) and sometimes other names are used for early expressions of the illness, such as Post-Viral Fatigue Syndrome (PVFS).

Other conditions such as Gulf War Syndrome (GWS) and Complex Regional Pain Syndrome (CRPS) or Reflex Sympathetic Dystrophy Syndrome (RSD) also likely fall into the same spectrum of illness, but include specific triggers and secondary dysfunctions that make them more uniquely identifiable (similarly to POTS and fibromyalgia where specific symptoms can be dominant).

I believe that none of these names are fitting, as most are based on symptoms and not on cause. I also believe that, despite their varied symptoms, these illnesses all share the same cause. Even if you disagree with me, I ask you to keep an open mind whilst you read this book and try to follow my reasoning.

For simplicity’s sake, this book will refer to this illness primarily as Chronic Fatigue Syndrome (CFS). Please forgive me if this is not the name you believe to be correct. Also, instead of ‘patient’ or ‘sufferer’, I will use the term ‘person experiencing Chronic Fatigue Syndrome’ (PEC), since thinking of yourself as a sufferer is ultimately not helpful

 

Chapter 2

Getting Started On The Right Foot

Why is it that, at a time when all the answers are supposedly at our fingertips, we often cannot get straightforward answers about our health?

Why is it that, when the medical industry and list of medical research organisations are bigger than ever, an illness like CFS is still ‘a mystery’?

I believe the answer involves three main factors:

1. The complexity of the illness.

2. The tendency for medical research to be highly specialised and focussed as opposed to looking at illness as a whole.

3. The years of unjust labels applied to people with CFS that have strained the relationship between patients and the medical community, making communication even more difficult.

Writing this book has been a challenge. Whilst health care professionals can benefit from it, my aim is to explain this illness to people experiencing CFS (PECs).

If you are a PEC, you may have very little medical knowledge, or you may have spent years reading and experimenting. The one thing you may have built up is scepticism. That’s why I have gone into some detail to show how the dots are connected in my hypothesis. If you can’t see how the illness works, you won’t act on the conclusions. And if you don’t act, you won’t benefit from the knowledge. I hope I have struck the right balance between detail and clarity.

Over the years, I have heard PECs criticise the conclusions and treatments of researchers and practitioners from around the world. The problem is that many valid and important ideas represent only part of the puzzle of CFS. To get well, you must have the full picture and understand all the steps required for recovery.

At this point, I’m going to ask you to clarify what you believe about CFS. Write down your answers to the questions below. If you don’t know the answer, write your best guess, or write, “I don’t know.”

1. What is the central cause of CFS?

2. What are the main things you need to do to recover from CFS?

3. Has doing these things led you to a full and permanent recovery?

Since you’re reading this book, I expect your answer to Question 3 to be “No.” This does not mean that your beliefs are all wrong, but they are probably incomplete. Your answers are the start of a framework that you can fill in as you read this book.

Treating problems in isolation doesn’t work. Neither does treating secondary problems alone. You must treat the root cause and address your own personal triggers of the cause.

You must also treat things in the right order. It’s a bit like cleaning the house for an important dinner guest: If you vacuum before you wipe the crumbs off the table, you won’t end up with a clean floor.

The mechanism of this illness is complex—complex because the human body is complex. Researchers, doctors, and PECs often get lost in the details and never see the big picture.

It is the big picture that CFS Unravelled is written to deliver - a big picture made of many individual puzzle pieces. I have sought to make the picture detailed enough for you to be confident that it is correct, so you can gain the confidence to start taking more focussed action to recover from this dreadful illness now.