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Cancer is now officially cured after two weeks!

Written by Huib, published Friday December 30th, 2016

Suppose. You don’t feel well. You ignore it first, pretend to be able to go on with your busy life. It will go away, you think. But it doesn’t. There is even a swelling visible. So you visit your doctor, who sends you to the hospital. The specialists do their tests and you get the diagnose: cancer.

Imagination is more important than knowledge – Albert Einstein

Treatment starts while your outlook on life is completely upside down. What about that future you imagined? What about your job or company? Your family? You had a healthy life style and thought positively, so how could this happen to you?

Fortunately you don’t need to worry about finances or health care. You have paid your insurance fees and the doctors claim their hospital is the nation’s expert center on this specific type of cancer.

However, after two weeks your treatments and the payment for them stop. Why? Because the international Cancer Guidelines say so: “after two weeks of treatment, any lingering cancer symptoms are imaginary“.

The general response is that doctors don’t believe in cancer, after two weeks of treatment. But one honest doctor tells you that he will lose his job and license, if he actually tries to help you any longer. The fact that he does not speak up, reinforces the groupthink mechanism.

You start doing your own research and find out that these guidelines are drawn up by a profit-driven organisation, that has been proven to be corrupt, fraudulent and has ignored hundreds of peer-reviewed scientific articles which flatly contradict their claim. To no avail, because your doctors will simply label that ‘conspiracy theory’ and ignore it.

Apart from the fact that the swelling is still growing and you become bed-ridden, this verdict leads to a whole range of new problems. You are suddenly declared ‘fit to work’. You will lose any social benefits, your savings, your house, your friends.

If you’re a minor, your parents will be charged with “Munchausen by Proxy” and will lose custody over you. They will be blamed for ‘making you ill’ in order to attract attention. Judges will take this nonsense into account as ‘expert evidence’.

Your friends and family have a deeply rooted faith in the medical system, so they stop paying much attention to you. Instead, they call you lazy, a hypochondriac and a chronic attention seeker. Doctors agree and stuff you full of anti-depressant drugs. Which makes matters worse in 98% of the cases.

Any natural approach to cure cancer is ridiculed in the media, prohibited by the government or at least not covered by your insurance. The more you research, the more you find that rigged science is used to uphold these policies, which have already been proven to be fraudulent. The research that should have been done, is simply not funded.

Sounds absurd?

Now you will have a clue why people with Lyme are so upset and why they cry out for help and understanding. Why they commit suicide in alarming numbers.

They cannot do much themselves. They try to find treatments, to find the money to pay for them, to fight of all kinds of bureaucracy and sociale stereotyping, while they are hardly able to function anymore.

I found it shocking that most of them are even no longer able to read a book; no matter how badly they’d want to.

For me ‘Lyme’ is much more than just one of the many diseases that go around in our modern times. It is a multi-headed monster; a hidden parasitical disease showing a parasitical system with many faces. With the potential to transform the current medical system into something much more healthy.

The only thing needed to start this transformation is a collective willingness to engage and to learn. To get Lyme, before you get it.

I have heard many Lyme patients say, “I wish I had a cancer diagnosis because then I’d be taken seriously and I’d know if my prognosis was positive or grim. It’s the limbo that’s excruciating and where you lose family, friends and your life.”In 2017 I’ll make a series of short posts on these different yet interrelated topics. Let me know in the comments of my LinkedIn or Facebook post, if you find these posts helpful and what you’d like me to focus on next.

I do hope this post did not offend cancer patients. One of my best friends is currently dying from it. My intention with this blog post was to show you the absurd medical, social and legal status of Lyme.

I wish you a new year with compassion and understanding.

Huib Kraaijeveld

Author of ‘Shifting the Lyme Paradigm’ and founder of the On Lyme Foundation

First published: 30 December 2016 16:00

drs. Huib Kraaijeveld

In: Inspiration Lyme Nonsense Science

"This book perfectly describes the plight of millions of patients, who suffer from chronic Lyme Disease in many countries all over the world."
Prof. Christian Perronne, France

"This book is a gift of truth and passion to humanity."
Mia Morales, Lyme patient, USA

"I received the book exactly on the day that I had decided to end my life. Huh?! Yep. I am 35 years old years and have been ill for 19 years. Now I know why: Lyme. Everyone should read this book!"
Miranda, the Netherlands

"This book offers a new practical, human centered way of dealing with health information. It is also ringing a bell for the new time how to work together towards health and thriving."
Kim Schimmler, MD, Germany

"This pioneer's work made it perfectly clear that, when "i" becomes "we", even illness becomes wellness."
Frans Vermeulen, journalist, the Netherlands

"In his crucial work on Lyme disease, dedicated social researcher Huib Kraaijeveld does not pretend to have all the answers, but guides us towards asking the upsetting and essential questions."
Prof. Cees Hamelink, professor Communication Sciences & Human Rights, the Netherlands

"This book reads like a thriller! It touched me deeply and I am sure it will change the course of history."
Linda Graanoogst, journalist, the Netherlands

"Well, I am wiping my eyes and blowing my nose, while tears stream down my face. I guess that is a good sign. You hit the nail on the head claiming that Lyme survivors need 'understanding'. I would like my own partner to read this book."
Anodea Judith, PhD & author, USA

"What an awakening perspective! Huib has successfully set a quantum leap for understanding and managing Lyme disease by common people."
John Wong, bestselling author, Singapore

"A true and unpretentious caretakers' guide to understand Lyme. This book will help you to completely understand what your friend is going through; regardless of the symptoms they have. I wish it had been written ten years ago, because it can actually save lives!"
Cheryl Versalle, Lyme patient, USA

"This book actually speaks to people beyond its target audience (caretakers of people with Lyme Disease): people like me who are not travel companions, but to whom it is not hard at all to have or develop understanding and compassion. This makes the reach of this book bigger, much bigger if you’d ask me. I am amazed a book can do all of this!"
Saskia Steur, business blogger, the Netherlands

"This book reads like an exciting novel, were it not that it concerns a deadly serious issue. It calls to contribute and take care of each other and our world. Read, weep, feel and act!"
Manfred van Doorn, leadership expert, the Netherlands

"A creative and very intelligent vision to dive even deeper into the world of Lyme, to look at yourself, other people, but also the entire world around you."
Friend of someone with Lyme

"The book indicates that Lyme disease can be a sexually transmitted disease. This will cause a tidal wave of awareness all over the world. Like the child in the old fairy tale The Emperor’s New Clothes, who exclaimed: 'But the emperor is wearing no clothes!'"
Ola Aniel Petterson, STD campaign leader, Sweden

"What a brilliant sociological work! I am sure it will have much impact."
Professor Neuropathy, Germany

"This book is a big eye opener. Both for friends of people with Lyme disease as well as for people with Lyme. Or for any other health issues, for that matter."
Martin Möhrke, medical research leader, Europe

"I cannot read any other book for more than two minutes now, in this hell called Lyme. Yet yours I cannot stop reading! I should have put it away hours ago to clean the house. But I simply cannot stop."
Ineke, wife of a husband with Lyme, the Netherlands

"This book is a delight to read. It offers soft candlelight and warm campfire camaraderie on an often dark and lonely journey."
Laura Bruno, medical intuitive Lyme expert, USA

"A very honest and yet witty way of helping those with Lyme disease. This book is full of ideas on how to help your friend with Lyme, as a travel companion on this crazy journey called 'Lyme'."
Lisa Hilton, Lyme advocate, USA

"Both the personal experiences as well as the author’s sharp mind turn this into an incredibly inspiring book that raises the consciousness of its readers."
Kara, ex Crohn disease patient, the Netherlands

"Tempting, informative and eminently readable! Shifting the Lyme Paradigm is an absolute eye-opener for those who are not aware of what the journey of Lyme disease entails."
Terri Mackinnon-Cross, CEO WorldLymeDay.com, Canada

"This book gave us the recognition and acknowledgment, which were like a band-aid on an open wound."
Sara, Lyme patient, Belgium

"Very insistently written based on intensive, almost existential, personal experiences, this book also gives a clear overview of all relevant information for both patients and caretakers."
Jan Eendebak, former chairman Lyme Foundation STZ, the Netherlands

"A relief to read, written by an expert who shares his dedication to his own path with us, and brilliantly written."
Muna, mother of a daughter with chronic Lyme, the Netherlands

"Playful, frightening, informative and encouraging."
Merel, kinesiologist, the Netherlands

"This book made me realize that there is too little known behind the phenomenon Lyme. In a challenging manner the author provides understanding of Lyme disease and suggestions for tackling this disease. I have 'prescribed' this book to many of my patients and mostly astonishment was soon followed by recognition. An absolute must for anyone with (still) unexplained symptoms or the people close around them."
Duco Kanij, osteopath, the Netherlands

"This book guides you through the labyrinth of Lyme swiftly, while it took us YEARS to even get this far."
Eugenie van der Linden, ex-Lyme patient and therapist, the Netherlands

"This book is an absolute 'must read' for everyone! For patients, for family and friends, and for doctors who can finally learn that Lyme is more than what is written in their textbooks and that they should not be able to dismiss "unexplained" complaints as psychological too quickly!"
Anne Fierlafijn, MD, Belgium

"Shifting the Paradigm of Lyme is not like any other book on Lyme that I have read. It appeals to a higher consciousness, and is analytical in an introspective way that is pleasant to read. This book is a friendly and warm reminder that no Lyme patient is ever alone."
Thomas Grier, biologist, USA

"This book show how caring friends can intervene to provide succor and alliance ‘against the odds’ of a potentially serious and very complex illness that is still poorly understood by mankind."
Kenneth Liegner, MD, USA

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