Befriending The Wolf: The Guide To Living And Thriving With Lupus by Milly DiericxBefriending The Wolf: The Guide To Living And Thriving With Lupus by Milly Diericx

Befriending The Wolf: The Guide To Living And Thriving With Lupus

byMilly Diericx

Paperback | September 6, 2016

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This book was created to help fellow Lupus sufferers manage their condition and live happy, fulfilling lives. It's a compendium of proven resources and methods to feel better, giving honest reviews of various healing techniques in their effectiveness with alleviating the symptoms of Lupus and other autoimmune disorders. Filled with healing methods, tips and emotional release exercises,Befriending The Wolf: A Guide to Living and Thriving with Lupuslooks at the condition from physical, mental, emotional and energetic points of view, offering a menu of empowering choices so everyone can find their own personal path to wellness.
Milly Diericx was diagnosed with Lupus Erythematosus Systemicus in 2001. Her diagnosis inspired her to search for alternative means of dealing with this condition. She is now a dedicated therapist, teaching proven methods that bring solace and hope to others. She lives in Mexico City with her family.
Title:Befriending The Wolf: The Guide To Living And Thriving With LupusFormat:PaperbackDimensions:162 pages, 8 × 5 × 0.68 inPublished:September 6, 2016Publisher:Morgan James PublishingLanguage:English

The following ISBNs are associated with this title:

ISBN - 10:1630478741

ISBN - 13:9781630478742

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Read from the Book

25th December, Christmas Day. My spinal cord was inflamed and horribly painful, the fever was back to alarming temperatures, my whole body arched in spasms, and I could not deal with the pain anymore. My mother searched frantically for medical help. The only doctor available was a geriatrist whose older patients tend to get sick in winter, so he hadn't left for the holidays. My husband was still in the city, so my parents took me to the doctor's office. He only agreed to see me on Christmas Day because my symptoms were so serious. When he saw me, doubled over in pain, sitting in a wheelchair, unable to move, burning with fever, he was appalled. I sat there listening while my mother recounted the week's events. Listening to the story, I could not believe it had taken this long to see a doctor. By his face, I could tell that the doctor couldn't believe it either. In my mother's voice, I could hear despair, guilt, helplessness. He could hear it too because he didn't say anything to the fact that we had waited this long. He just uttered the ominous pronouncement, "I think she has lupus, an incurable disease, and by your account, she has an incredibly virulent attack. She has only a couple of days to live." Merry Christmas! was my only coherent thought, or the only one I remember. Silence reigned. Everyone was in shock. It took a few minutes to sink in. They had to ask the question, of course: "Doctor, is there anything you can do?" He prescribed prednisone (or cortisone) in massive doses, not with a lot of hope, but he had to do something. When the initial shock wore off, depression set in and the next weeks were a blur. My parents called my husband with the news and he came back immediately, but I don't really remember him being there, nor do I remember my children being there, or the nurse that was hired the next day to care for me. All I remember is the void, a huge dark void that had become my entire existence.After a diagnosis of impending death, when you don't die immediately, there follows an endless pilgrimage of doctors, tests of all sorts, second opinions, and general despair and confusion. My family was going berserk, taking me to specialist after specialist, looking for that person who would say something different, something they wanted to hear. They were in a panic. I was still in shock and so darn sick that I honestly could not give a damn. I felt like a piece of driftwood in an angry sea. Decisions were made for me, I was never consulted, almost ignored, and it was just fine-I had no energy to think, let alone decide. Appointments, doctors, tests all went by in a blur. The inevitable conclusion was the same: I had systemic lupus erythematosus, an incurable and often lethal disease, and the attack was so virulent and aggressive that I would most likely die very soon. Actually, the doctors did not understand how I was alive still. They just flooded my body with huge amounts of cortisone, transplant strength immunosuppressants, quinine (Plaquenil), and kept me quiet. Time would tell.

Table of Contents


The Essential Triad

What Color Is Your Reality?

Chapter 1 Solving the Mystery

My Story

Ignorance Is Bliss

"I Think She Has Lupus"

Turning Point

From Last Rites to Recovery

Chapter 2 Finding Answers

Discovering Myself through Research

Changing Paradigms

Defining Lupus in My Own Terms

Choosing the Path to Wellness

Identify Your Triggers

Life Situations and Physical Exertion

Hormonal Fluctuations

Spiritual Wellness

Chapter 4 Taking Control of Your Health

Exercise Your Ability to Choose

Cultivate Stick-to-itiveness

Keep Your Thought Patterns Positive

Set Small Goals

Stop the Emotional Roller Coaster

What is the worst the can happen?

What can I do about it at this time?

What am I really afraid of?

Chapter 5 Vanquishing Negative Emotions

The Physical and Mental Level of Emotions

Identify Negative Emotions

Change the Beliefs That Feed Your Thoughts

Choose Happiness

Liberate Negative Emotions

Orient your body and your life

Chapter 6 Staying Well, Living Life

Tips for Minimizing Physical Symptoms

Alternative Treatments, Therapies, and Diets

Balancing Your Body's Chakras

Chapter 7 Adieu and Godspeed



About the Author