From: felix de fries
<felix.defries@bluewin.ch>
Subject: The new nitric oxide research: A silent revolution in the
AIDS- and cancer medicine
Zurich, 14th January 2002
To those affected
their doctors and carers
to scientists, institutions and media
in developed and developing countries
The
Silent Revolution in AIDS- and Cancer-Medicine
Ladies and Gentlemen:
In an interview
that he gave recently to the German magazine Raum + Zeit (Space
+ Time), Heinrich Kremer, M.D., answered various questions on AIDS,
its causes, the history of this clinical syndrome, the postulated HIV
retrovirus, and antiviral AIDS therapy.
Based on findings from new
NO research, evolutionary biology, and cancer research,
Kremer introduces in this interview a basically new understanding
for immune-deficiency and the emergence of cancer cells and
explains how these diseases could be treated successfully through therapy
involving cell symbiosis and redox harmonization.
As the medical head of a
specialized clinic for young drug addicts (German
federal government pilot study in Brauel, Lower Saxony), Dr. Kremer
became intensively engaged in examining the causes of AIDS and possible
therapies since diagnosis of the early cases. After leaving federal
service (1988) due to differences over medical and professional ethics,
he published various essays on AIDS that we have provided to you since
the early 1990s. ("Have Gallo and his Colleagues manipulated the HIV
Antibodytest to order", "15 Years of AIDS" (co-authored
in 1998 by Prof. Alfred Hässig),
and "Answers to Questions on HIV and AIDS and the administration
of AZT raised by Dr. Thabo M. Mbeki" (2000) all available at
www.virusmyth.com.
Doctor Kremer has now
presented his most recent findings on the functioning
of the human cell and the immune system in a scholarly book entitled
"The Silent Revolution in AIDS and Cancer Medicine", which
has been published in German by the
Ehlers Verlag at the end of last year. (www.ehlersverlag.de)
We are looking out now to
find an english or american publisher for this work
of 530 pages. The enclosed index of the book shows the various topics
treated.
Study Group AIDS therapy
Felix A. de Fries
Attachments:
The
interview from Raum+Zeit (November/December 2001)
- the
index of the book "The Silent Revolution in Cancer- and AIDS-Medicine
- therapy
recommendations
MD Heinrich
Kremer: The Silent Revolution of the AIDS-and Cancer-Medicine
About this
book:
The author, Heinrich
Kremer, M.D., experienced physician and clinical researcher, describes
here worldwide for the first time how and why a cell transforms itself
into a cancer cell, what the real causes of the so-called AIDS disease
are, and that cancer and AIDS are results of energy exhaustion in the
immune cells. Some 20 years of meticulous research work stand behind
these findings. It comprises the most important scientific
publications of orthodox medicine in the field of immune systems and
cell research since the end of World War II.
Dr. Kremer’s book points
out the absurdity of the HIV thesis and supports his skepticism
scientifically. However, the fact that this work refutes the
prevailing scholarly opinion of a mysterious AIDS-causing virus that
nobody has been able to demonstrate to date is but one aspect of the
book’s aspects. More essential is the fact that Dr. Kremer presents
a consistent therapeutic concept of global evolutionary medicine
substantiating for the first time that cancer and indeed all its forms
and AIDS can not only be stabilized but healed.
ISBN 3-934196-14-6
Contents
Overview
I. A
Disastrously Wrong Decision
20 years abuse of nitric gas as a sexual doping agent – the
apparently mysterious results
II.
The Sensational Discovery
Gaseous nitric monoxide as a bio-energetic regulator within and
between living cells – the gas
war between humans and microbes
III.
The AIDS Puzzle
Why AIDS Diseases were misinterpreted – the inhibition of the
gas defence is the cause of
acquired immune deficiency
IV.
AIDS is Not a Transmittable Disease
Opportunistic infections and Kaposi’s sarcoma were well known
before the AIDS era – a variety
of causes trigger the same immunity answer as programmed
by evolutionary biology
V.
The Challenge of Previously Valid Immunity Theories
How acquired immune deficiencies actually develop
VI.
The Most Successful Fusion of Evolutionary History
How the micro-gaia milieu functions – the vital role of the
mitochondria
VII.
Collective Tunnel Vision
Why "HIV characteristics" really are the results
programmed by evolutionary biology
and not specific causes of strong and/or continuous immune
stress – and what the "HIV test" really measures.
VIII. The
Solution to the Cancer Puzzle
Why normal cells develop into
cancer cells – the cancer cells’ degeneration
into embryonic properties is based on inactivation of mitochondria
programmed by evolutionary biology
IX.
HIV/AIDS Medicine Runs Amok
Why AIDS medicine causes AIDS and cancer as well as
degeneration of muscular and nerve
cells: the explanation of how AZT, Bactrim, and their
ilk actually work.
X.
The Monumental Rethinking Task
The elementary professional error of AIDS and cancer medicine
– why patients die from
chemotherapeutic poisoning
XI.
The Lifesaving Knowledge of Healing
On the practice of diagnosing, preventing, and treating AIDS,
cancer, and other systemic diseases
– compensating rather than eliminating
XII.
Resistance against Mass Poisoning in Africa
The international initiative of President Mbeki – answers
from the South African government’s
open discussion on causes of AIDS in the West and developing
countries, on non-toxic prevention of and therapy for AIDS, on
AZT’s real active mechanism and the globalized epidemic terror of physicians
and the media – the international HIV cartel’s refusal to join
the discussion and the disinformation campaign it launched
Literature
Index by
Subject
Seminars
with Dr. Kremer for Patients and Therapists
Overview
of Illustrations Tables
Chapter
IV:
- Disease model of the retrovirus AIDS theory Table I
- Actually observed clinical manifestations after strong or
continuous immune-cell and/or
endothelial cell stress due to different or combined causes
Table II
Chapter
V:
- Dual strategy as an immune system response Table III
Chapter
VI:
- Fusion model of primeval bacteria with proteobacteria for nucleus formation
and development of proto-mitochondria (eukaryote cell symbiosis)
1.5 – 2 million years ago Table IV
- Alternating switch between OXPHOS and aerobic gycolysis, physiological
and patho-physiological cell models Table V -
Compensated / decompensated oxidative and nitrosative cellular
stress Table VI
- Cell symbiosis and cell dyssymbiosis depending on NO and ROS production
Table VII
- Clinical examples of cell dyssymbiosis resulting from type-1
over-regulation or type-2 counter-regulation Table VIII
Chapter
VII:
- The HIV phantom –
virtual computer presentation of the so-called HI virus
according to speculative assumptions Table IX
- Experimental findings of the Montagnier team as counter-evidence
against the disease theory that
"HIV causes AID and AIDS" Table X
- Experimental findings of the Gallo team as counter-evidence
against the disease theory that
"HIV causes AID and AIDS" Table XI
Chapter
VIII
- Model of the
mitochondria sluices Table XII
- The mitochondria’s sluice rhythm Table XIII
- Programmed cell death in metastatic cancer cells after transfer of
a functioning iNOS gene Table XIV
- Programmed cell death in metastatic cancer cells after repeated injection
of synthetic lipo-peptides (LPS analogs) and induction of the iNOS
enzyme into the iNO synthesis Table XV
- Examples of how disease and fatality rates continued to decline in
infectious diseases in the
mid-19th to 20th centuries Table XVI
Chapter
X
- Characteristic
laboratory findings on increasing wasting syndrome: indicators for
type-II counter-regulation of cell dyssymbiosis in systemic
diseases (e.g., "HIV positive", AIDS, cancer, sepsis,
trauma, burns, operations, Crohn
syndrome, colitis ulcerosa, chronic fatigue syndrome,
over-trained athletes) Table XVII
