Contents
Preface
Foreword
General Questions About Cancer
Questions About the History of Mistletoe Therapy
Mistletoe as Medicinal Plant
Clinical Application of Mistletoe Therapy
Question About Immunology
Methods for Testing the Efficacy of Iscar
Results of Treatment with Iscar
Concurrent Therapies — Medicinal
Concurrent Therapies — Artistic Therapies
Biographical Work and Related Issues
Meaningful Combination with Orthodox Medicine
Meaningful Combination with Alternative Medicine
Nutritional Aspects
APPENDIX
Anthroposophical Medicine
Methods
Glossary
Preface
In view of the fact that it is now possible to receive
immune stimulating therapy with mistletoe in the US, Mercury Press thought it
advisable to make available introductory material accessible to the lay person.
Dr. Richard Wagner, who with his wife Elizabeth, has a very
active oncology practice in Germany, has also taken the time to write
extensively about his experiences and investigations. In this book he shares
with us 160 questions about treatment of cancer with the mistletoe preparation
Iscar available in the US from Weleda, Inc. in Congers, NY. (Iscador in Europe)
These questions were asked by his patients during his many years of practice
and he shares with us his answers.
It is well to bear in mind that the views he expresses are
the views of one very experienced physician who has treated and studied many
patients, however, that does not mean that what can be read here is dogma.
Treatment in anthroposophical medicine strives to be individualized treatment
and this means that other physicians may choose to vary what is suggested here,
in agreement with Dr. Wagner when he says that "immune stimulating therapy
cannot be a 'schematic therapy'. Only individualized therapy brings the desired
results."
For those to whom anthroposophical medicine is new there is
appended a brief discussion to familiarize the reader with some of the ideas,
methods and terminology of this human centered medicine initiated by Rudolf
Steiner with the help of Dr. Ita Wegman.
Scientific literature regarding mistletoe preparations is
available in the form of several compendia from Mercury Press, Spring Valley,
NY.
Foreword to the Present Volume
During the last eighteen years I have collected the
questions that patients have asked about my activity, first at the Filder
Klinik in Stuttgart, then in the Lukas Klinik in Arlesheim / Basel and finally
in my general practice in Stuttgart, and have attempted to answer them here in
a generally understandable manner.
There were some considerations for presenting a book in this
form. Even though there were already a whole series of comprehensive books and
accounts about anthroposophical therapy with mistletoe preparations (referred
to in the bibliography), I was, also as a result of discussion with many of my
patients, of the opinion that it would be meaningful to publish a short account
on therapy with Iscar. This book allows one to quickly inform oneself about
particular questions, which is useful for patients as well as for physicians
who are not yet familiar with mistletoe therapy.
One does not always have the time to study an extensive
account, but for those interested, references are made here to those books.
Those who want to understand the nature of anthroposophically extended
medicine, which is especially focused on anthroposophical cancer therapy here,
cannot avoid these more extensive discussions.
I hope that this little book can aid the understanding of
therapy with Iscar and can help interested colleagues and afflicted patients on
the often difficult path of cancer therapy.
General Foreword
Despite research and teaching about the causes of cancer and
the possibility of treatment having been pursued for many decades, the
resulting methods of contemporary oncology are only successful for a few types
of cancer.
Among these are specific kinds of childhood leukemia,
testicular carcinoma, specific subforms of mammary carcinoma and lung carcinoma
as well as Hodgkin's disease and ovarian carcinoma. However, recent
investigations show that, in the case of mammary carcinoma, only few patients
benefit from chemotherapy in a healing sense. It appears that only the interval
between an operation and the appearance of metastases is prolonged, but not
the total survival time.
Yet, with many other forms of cancer one has the impression
that the survival time of the patient cannot be significantly prolonged, either
by an operation, or by the succeeding therapies, such as radiation or
chemotherapy.
However, the survival period of the patient with a humane
quality of life is, according to my view, the only parameter against which a
therapy can be measured. It is unimportant that the patient shows reduced
tumor manifestation if this is not directly connected to a lengthening of survival
time.
Today we have indications that, even in epithelial tumors,
chemotherapy has a therapeutic effect only in a few cases and that the survival
period is in fact not lengthened.
The problems of modern medicine, in the form of side
effects, have increased, so that a great number of patients leave their primary
and secondary oncological therapy, and turn to alternative methods of
treatment.
The field of alternative methods of treatment is immense and
extends from thymic extracts, treatment with trace elements, various diets, ozone therapy, to mistletoe
extracts.
It is important to the publisher, to the Weleda
pharmaceutical company and to myself as author and editor of this series, to
explain, in general, the contribution medicine can make if extended according
to anthroposophical principles and, more particularly what contribution
mistletoe therapy, which has grown out of this approach, can make to contemporary
oncology.
It has to be stated clearly that this is not an alternative
ontological therapy, but rather that anthroposophically extended medicine can
only truly be an extension if it includes the medicine of natural science,
while using other forms of therapy and other medications in addition or as a
sole therapy.
For a description of anthroposophical medicine, its basic
concepts and terminology please see the appendix.
- Richard Wagner
General Questions About Cancer
Is cancer really an illness of our time?
If one surveys the history of medicine, one can observe that
every century has had its own unique challenge in the form of one or another
severe illness. One can look back at centuries that suffered the consequences
of such contagious diseases as the plague and cholera, but also to a time not
so long ago in which tuberculosis claimed many victims.
One has the impression that in our time the occurrence of
cancer is increasing dramatically, a fact that has been determined
statistically. This is not merely an apparent increase in the sense that,
through modem diagnosis, tumor illnesses are discovered in many living patients,
where a hundred years ago they would not have been discovered or named until
the patient had died.
Is cancer limited to a particular age group?
There are types of cancer that only appear in a particular
age group. At least this was so in the past. One could for instance be sure
that testicular cancer mostly appeared in the age group 30 to 35 and prostate
cancer mostly after the age of 60. Here too things have changed. We encounter
patients in practice who have testicular cancer at the age of about 80, and on
the other hand there are patients who have prostate cancer at about the age of
35. One also has the impression that cancer is becoming ever more chaotic in
character. In other words, cancer with metastases already appears in the
primary phase, without a prior period of latency.
Is cancer becoming more aggressive?
We encounter ever larger numbers of patients in practice
who, already at the diagnostic stage of the illness, have metastases in life
threatening areas, such as the liver or lungs. Thus one has the impression
that, besides the increasingly chaotic nature of cancer, its aggressiveness
has also markedly increased.
How does increased aggressiveness of the carcinoma affect
treatment with Iscar?
With many cancer patients one does not have time to choose
the right therapy at leisure. As one can see from questions that are addressed
later, a trial period is necessary in order to establish which mistletoe therapy
the individual patient reacts to best. Previously one had far more time to
choose the right preparation after a cancer operation and to study its
effectiveness on a patient.
Today there are increasing numbers of cancer patients for
whom there is only one chance to find the correct preparation. Due to the fast
progress of the illness the therapy simply has to work; there is no second
chance. This is especially true of pancreatic carcinoma, but also of all
carcinomas in the metastatic stage.
Is cancer treatment over once an operation and subsequent
therapies such as radiation or chemotherapy have been administered?
In my opinion real therapy only starts once primary therapy
has been concluded. By primary therapy we mean an operation and then, depending
on the stage it is at and also depending on the type of tumor, the subsequent
therapies, such as chemotherapy or radiation. These certainly are often
necessary. However, they only serve to eliminate the tumor and other possible
tumor manifestations. Contemporary clinical diagnosis cannot, however, detect
micrometastases. Many of these therapies are thus only carried out because of
the suspicion that there might already be micrometastases in the rest of the
body, for example when a lymph node has been affected in breast cancer.
Radiation and chemotherapy are then used to try and kill these off. Whether
this is successful or not is often questionable. If it were to succeed in every
case, no further metastasis would occur.
Furthermore, all these therapies deal only with the physical
manifestations of cancer. They do not consider the circumstances that led to
cancer. In our opinion it is essential that the causes of cancer are also
treated, and not only the physical results.
What are the causes of cancer?
There are many causes for the appearance of cancer. Today we
know that the development of cancer occurs in several stages, and that the
foundation for such an illness can already be laid in the earliest childhood.
It has for example been determined that cancer patients often lacked "nest
warmth" in childhood, in other words that these people often had to do
without the nurturing of their mother.
It is essential that, during childhood and youth, people
should be able to develop their creativity by means of a specialized pedagogy.
They should learn a healthy daily rhythm and, in their home environment, and
through the absorption of the emotional mood of their environment, learn to
distinguish between right and wrong.
Children must furthermore be encouraged to develop their
particular abilities and their personalities, so that they can meet the
challenges life will offer them.
From these short explanations one can already see how
manifold the possibilities for disturbance can be and also how important the
early years of a child can be. During the adult years there are many triggering
factors for cancer. Firstly there are the physical carcinogens, for example the
triggering of lung cancer by cigarette smoke and tar products.
An unrhythmical lifestyle often leads to regulatory
disorders on a cellular level, which after a while cannot be reversed. Rhythmic
disturbances which are triggered by influences such as hormone therapy, excess
nourishment, sleeping pills and other medications, lead to pre-cancerous conditions
which can become carcinomas.
As a whole, there is a gradual disturbance of balance
between biological regulation on the one hand and the degeneration of cells on
the other.
Rudolf Steiner explained that there is a constant struggle
for balance in the formative energies of the total organism, which is
controlled by the hierarchically arranged higher aspects of being discussed in
the appendix: the etheric body, astral body and spiritual Ego. Cell matter is
formed and differentiated by these higher aspects of being into muscle, nerve
or liver cells for example. These cells, which are equipped for their specific
purposes become tissues, organs and finally humans during embryonic
development. In the case of cancer the cells in predisposed areas withdraw from
the guidance of the higher aspects of being, and follow their own growth
patterns, which are alien to the human organism as a whole. In other words, the
tumor has a life independent of the organism.
In conclusion one can say that cancer often begins in the
earliest childhood and youth with a disturbance in the area of the
spiritual-emotional being. The different aspects of being can then over time
not fulfill their guiding role over the living body. Stress situations and
blows of destiny, but also illnesses caused by the excessive consumption of
refined food, have the same effect. This results in an overall weakness of the
immune system, as well as a certain blindness to harmful influences, which are
no longer noticed or reversible.
Control then lapses in a predisposed area of the body and an
emancipation of the cells is experienced. In other words, a malignant tumor
develops.
The weakening of the energies of formation on the one hand,
and the increased aggressiveness of the ensuing process due to influences of
the contemporary environment on the other, lead to the described cancer
process. Thus, to sum up, this process begins on the spirit-emotional level and
slowly invades the entire body.
What symptoms make possible the early detection of cancer?
Firstly, bodily elimination should be observed, for example
bleeding, which should always be investigated. Furthermore, changes in the skin
should always be monitored and inspected. Observing the whole person, one has
to determine whether the subject is a so-called pre-cancerous type, with a
predisposition to cancerous illnesses. In a case history one has to especially
note a lack of childhood illnesses, especially when no febrile conditions were
attained.
Sleep, digestive and liver function disturbances with
intolerance to certain foods, as well as constipation should be investigated,
as should be hormonal disturbances, fatigue and very slow recovery from
illness.
On an emotional level depression, difficulty in coming to
terms with problems, difficulty in expressing one's feelings and difficulty in
establishing contact with the environment, are significant. Lack of interest,
lack of initiative and lack of self-confidence complete the picture.
Of course it is very hard to only connect these symptoms
with cancerous illnesses, because fatigue for example is not only a symptom of
cancer, but also of many other diseases.
It is nevertheless important to bear cancer in mind in the
case of all these disturbances, because all those involved may not allow the
scales to fall from their eyes until cancer has already erupted, only then to
realize that cancer had already been building up for a long time.
Is it possible to treat a pre-cancerous person?
The concept
of 'pre-cancerous' is vague.
Many doctors understand it to mean that the physical and
psychological conditions have already changed. Orthodox medicine has a very
precise definition that states that a true preliminary phase of cancer presents
pre-malignant deformed cells.
If a pre-cancerous condition presents itself according to
this definition, I would already begin treatment with Iscar.
Of course it does not makes sense to only begin a therapy
once cancer has already manifested physically. In the case of a predisposition
it sometimes makes more sense to start treatment earlier.
On the other hand, it must be said that every mistletoe
therapy induces the production of antibodies. One has to imagine that every one
of us has individualized albumen and that the body does not tolerate foreign
albumen, but reacts to it by creating anti-bodies and eventually an allergy.
All mistletoe preparations contain plant albumen that can
lead to such blockages, if not to allergies. In the worst case a patient could
fail to react to a mistletoe preparation when it is most needed, i.e. when
cancer occurs.
I would thus not recommend the use of mistletoe preparations
for the mere improvement of immunity, or to overcome exhaustion.
Has mistletoe always been used for the treatment of cancer?
During the Middle Ages mistletoe therapies were used for
depression, high blood pressure and epilepsy. Only through the indications of
Rudolf Steiner did it become known that mistletoe could heal cancer. It was
then developed as an injection, whereas in the Middle Ages it was used as drops
or as a tea.
Can all doctors carry out treatment with mistletoe?
In principle treatment with Iscar can be carried out by all
doctors. However, the treating doctors should familiarize themselves with the
treatment. Nowadays there are unfortunately many doctors and therapists of
every kind who begin a mistletoe therapy with patients without familiarizing
themselves with the exact dosage instructions, or with the kind of mistletoe
therapy.
A warning must be leveled against unmonitored mistletoe
therapies, because the desired effect may not be achieved if it is not carried
out according to specific regulations and criteria.
All doctors can however inform themselves of the
possibilities of the therapy and its applications, and carry out treatment on
the patient. Basic information is given in this book.
Does treatment with Iscar make sense with all kinds of
tumors?
Treatment with Iscar should proceed with care in the case of
primary brain and spinal tumors, as well as metastases in the brain. First the
preparation should be taken orally, as drops. The dosage for this can be found
in the guidelines for Iscar treatment of malignant tumors.
Experienced doctors can try to introduce treatment with
injections, but the dangerous possibility of pressure on the brain due to
improved circulation must be considered. Only doctors with experience should
therefore try this treatment. For this reason brain carcinomas or metastases in
the brain are included as contraindications in the guidelines for Iscar.
Furthermore, in the case of leukemia, excluding
chronic-lymphatic leukemia, treatment should occur with utmost care. This
treatment may only be carried out by an experienced doctor.
The same holds true for granulomatous lymphoma (Hodgkin's
disease) and for non-Hodgkin lymphomas. Care should also be taken with
myelomas.
Are there contraindications for treatment with Iscar?
In the case of a known allergy to Iscar, treatment can only
commence after a very slow increase in dose. At temperatures higher than
100.4°F/38°C, treatment should be interrupted until the signs of inflammation
have subsided. Further contraindications are active tuberculosis, hyperthyroidism
with unbalanced metabolism, as well as primary brain and spinal tumors, unless
an experienced doctor carries out the treatment.
So far no effects are known which indicate that Iscar should
not be administered during pregnancy. Great care should be taken to administer
Iscar strictly according to prescription. This would for example be applicable
in the appearance of a mammary carcinoma during pregnancy. Because it is known
that mammary carcinomas during pregnancy are one of the most malignant, I would
already start with mistletoe therapy during pregnancy, after the third month at
the latest.
Questions About the History of Mistletoe Therapy
Since when has therapy with mistletoe been known?
Mistletoe was already known in ancient times. Virgil
described in the sixth book of the Aeneid how Aeneas, with the help of a golden
twig similar to a mistletoe twig, crossed through the underworld unharmed.
Further mentions of mistletoe are found, in a description by
Plinius, and also in the ancient Nordic song cycle, the Edda.
In the Middle Ages mistletoe was used for all kinds of
complaints, such as epilepsy, high blood pressure, stenocardia, asthma,
sterility, depression and sleep disorders. It was also against ghosts, and in
the folk usage of some peoples it possessed a mystical use: it was supposed to
protect against fire and illness, ensure a happy marriage for engaged couples
and bring luck.
What is mistletoe?
Mistletoe is a plant that lives on other plants, mostly
trees and bushes, as a semi-parasite. It draws water and mineral salts from its
host, but can photosynthesize by itself for the creation of carbohydrates, and
is therefore only a semi-parasite.
There are many hundreds of types of mistletoe, mostly in
tropical and sub-tropical areas. They differ in form, leaves, blossoms and
fruit.
In Europe there is only one type of mistletoe, the evergreen
mistletoe with white berries (Viscum album). Botanically there are three types
of mistletoe: deciduous, fir and pine mistletoe. Probably there are also
different types of deciduous mistletoe, due to a variation in constitution.
Mistletoe has its own growth rhythms. The berries that ripen
in November/ December are eaten by birds, mostly by the mistle thrush.
The seeds rapidly pass through the intestine of the bird,
then to fall on a branch to which they stick.
The mistletoe seeds, which are contained in the berries and
later stick to the branches, need light for their further development. Without
light they lose their ability to germinate.
The growth of the mistletoe sprout is very slow. The first
tiny leaves are only formed in the second summer, the buds only in the fifth
to sixth year. The plant only bears fruit at the end of the sixth to seventh
year. It takes seventeen months from the beginning of flower formation, for the
berries to ripen, while the rose for example only needs five months.
How is mistletoe harvested?
The mistletoe for use in the preparation of Iscar is
harvested twice a year, in June and in November/ December. Through a special
process the juice is extracted. The summer and winter juices are mixed in a machine,
so that the remedy contains extracts from all the parts of the plant: the
leaves, stalks, berries, seeds and flowers.
The remedy is obtained only through the special
manufacturing and mixing process of the prime substance.
Mistletoe is harvested from six different host trees: apple,
oak, elm, poplar, pine and fir. A different preparation is made from each type
of mistletoe.
Since when has the Iscar preparation been available?
The first Iscar guidelines are dated at July 1930. Dr. W.F.
Daems had, however, determined from the WELEDA archives that there had been
talk about an Iscar preparation since 1925.
Doctor Ita Wegman ordered the first mistletoe preparation,
based on indications by Rudolf Steiner, to be manufactured by a pharmacy in
Zurich in 1918/19. This was the preparation "Iscar".
On June 3rd 1907 Rudolf Steiner mentioned mistletoe for the
first time. He explained that mistletoe was a remedy in the same way as poisons
can be remedies.
How is Iscar manufactured?
As has been explained before, the various juices undergo a
mixing process, a so-called machine process. Special machines had to be
manufactured according to Rudolf Steiner's indications.
The first machine for the manufacture of Iscar was in
operation in 1922. This machine was developed further by Karl Unger, E.
Schickler and engineer P.E. Schiller. From 1933, A. Leroi also further refined
the machine developed by Kaelin, in Arlesheim.
The problem that arose in developing a machine process
involved the question of how the summer and winter juices should be mixed.
A machine that fulfilled these needs could only be built
with the development of new materials. No further details about the machine
process will be given here, as this can be studied further in the literature.
Mistletoe as Medicinal Plant
What substances does mistletoe contain?
It is known that mistletoe contains viscotoxins, lectins and
so-called Vester's proteins, as well as amino acids, alkaloids, polysaccharides
and vitamin C.
What are viscotoxins?
Viscotoxins are a group of at least five different proteins
with basic characteristics, which in a cell culture show a cytotoxic, or cell
poisoning effect.
Viscotoxins can attach themselves to nucleic acids, and are
amazingly heat resistant.
They are toxic, resulting in cell death in high doses. In
weaker doses in animal tests, hypertension, bradycardia and a
negative-inotropic effect on the heart muscle were observed. The growth of
human tumor cells is significantly inhibited.
What are lectins?
Lectins consist of a large number of substances which are
found in most living beings. They are types of protein, which can specifically
recognize and reversibly connect to particular free and cell membrane bound
sugar types. The lectins have the characteristic that they agglutinate the
cells to which they connect, for example erythrocytes, lymphocytes or malignant
cells. This can result in a toxic or hormone-like effect, even with very weak
doses.
The first observations about the existence of lectins in
mistletoe were made in 1956. In the meantime three other lectins have been
found. Mistletoe lectin I appears most frequently and is the most cytotoxic
lectin.
The total molecule of mistletoe lectin I has a strong
cytotoxic effect in cell cultures. It can however also stimulate the
immunological character of certain cells. The increase of lymphocytes is thus
stimulated and the immunomodulating characteristics have also been verified.
What can be said about the other constituents of mistletoe?
The so-called Vester's proteins are toxic for tumor cells,
and have a cytostatic effect. They also lead to thymus enlargement, which has
been verified by various investigations.
The alkaloids are also toxic for tumor cells, but their
further meaning is not yet clear.
The polysaccharides may have an immune boosting effect, by
the stimulation of the neutrophil granulocytes.
The amino acids, in this case for example arginine, are connected
to immune stimulation and thymus enlargement.
The vitamin C found in mistletoe could also be immune
stimulating.
As a whole mistletoe contains a rich mix of substances, and
added to these are further substances which only come into existence during the
preparation and fermentation processes.
Since when has mistletoe been investigated experimentally?
In 1906 Gaultier published a work about the blood pressure
lowering effect of mistletoe. In 1930 Kaelin published a work about the
treatment of cancer with Viscum. These works were the starting point for various
investigators who explored mistletoe therapies. In 1932 Madaus showed that the
application of freshly crushed mistletoe paste on a fresh wound prevents wound
healing by retarding cell multiplication. In 1936 Havas published results about
the effects of mistletoe extracts on the growth of plant tumors.
Koch found in 1938 that surface tumors in animals become
necrotic when mistletoe is injected into and around the tumor. Plenosol was
developed out of these experiments. In 1954 the Russian researcher Chernov
published a work about the efficacy of mistletoe against tumors near the skin.
Buhl showed the efficacy of Iscar in mice with tumors, when mice treated with
Iscar lived longer than control mice that were not treated. Vester identified a
protein complex in 1968, which had the highest tumor inhibiting and cytostatic
effect to date. In 1961 Miller showed a polysaccharide with a strong tumor
inhibiting effect. Franz and Luther showed the tumor inhibiting and immune
stimulating effects of mistletoe lectins between 1975 and 1985. Khwaja could
positively influence the survival time of tumor carrying mice through
alkaloid-like substances in 1980.
In this overview only some of the researchers who have a
strong connection to mistletoe have been given. Since then mistletoe research
has become extremely extensive.
Have animal experiments been done?
Since 1938 (Koch) there have been numerous animal
experiments on tumor carrying animals (mice, rabbits and guinea pigs).
Currently an attempt is being made to use tissue cultures, so as to avoid
animal experiments for ethical reasons.
For further accounts of the effects of Iscar on tumor
carrying animals, reference is made to the literature.
Clinical Application of Mistletoe Therapy
What results does one see with the application: mistletoe
therapy?
One sees a clear increase in the body's natural immunity in
the sense of immune stimulation, and furthermore a stimulation of the warmth
organisation. Many patients report a change in their warmth organism in the
sense that they are no longer cold and sometimes manifest a slight febrile
condition. Furthermore, there is an improvement in the general feeling of well
being and in productivity. Appetite and sleep improve, even when the tumor
cannot be reduced, or a further spreading of the tumor cannot be prevented. A
definite lessening of tumor-related pain can also be observed. The main effect,
however, lies in the inhibition of malignant growth, which is achieved without
affecting healthy tissue.
What illnesses can be treated with Iscar?
All malignant and benign growths, as well as malignant
illnesses and related disturbances of blood forming organs, excluding some
which have already been discussed, can be treated.
Bone marrow activity can be stimulated, and formation of
metastases can be inhibited. Defined pre-cancerous patients can also be treated
with Iscar.
What does pre-cancerous mean?
The defined pre-cancerous condition is, for example, cervical
dysplasia, craurosis vulvae, proliferative mastopathy stage III, papillomatosis
of the bladder, or polyposis of the colon, as is found in ulcerative colitis.
Another instance could be ulceration of the stomach.
Can sarcomas also be treated with Iscar?
Sarcomas are very malignant types of cancer. Of course they
can be treated with Iscar, but should also be treated with Cetraria, which is
made of Cetraria islandica, a type of Icelandic moss.
Can metastases also be treated?
Malignant primary tumors, and also metastases are the domain
of Iscar treatment. The treatment is often successful in preventing the spread
of metastases by stabilizing the process of metastasis.
It is understandable that every patient wants all metastases
to disappear. However, this is often an unrealistic wish. Patients
nevertheless often live longer with their tumor under treatment with Iscar than
when extensive orthodox therapy is given. Such treatment reduces the size or
number of the metastases, but taxes the immunity of the patient so much, that
there is no strength for fighting advanced tumor growth. From the point of view
of survival time, there is thus no advantage for the patient.
Containment of metastasis is often already a big
achievement.
Are metastases treated in the same way as primary tumors?
Metastases are basically treated in the same way as primary
tumors. That means metastasis of breast cancer in the liver is treated not as a
liver carcinoma, but as breast cancer.
What Iscar preparations are available?
Iscar preparations from the following host trees are
available:
a) Viscum mali
(apple tree mistletoe) – Iscar M
b) Viscum pini
(pine mistletoe) – Iscar P
c) Viscum
quercus (oak mistletoe) – Iscar Qu
d) Viscum ulmi
(elm mistletoe) – Iscar U
Why are metal additives used with Iscar?
Metal additives are included to achieve a stronger effect.
It is known from anthroposophical and homeopathic medicine that metal
additives can increase the effect on some organs.
What metal additives are used with Iscar preparations?
Silver carbonate, copper carbonate and mercury sulfate are
used.
What concentrations of metal additives are used in Iscar
preparations?
The metal additives are worked out at a dosage of 0.01 mg
per 100 mg fresh plant extract. They are used as homeopathically prepared
dilutions.
Can treatment with a mercury additive be carried out
simultaneously with an amalgam elimination treatment?
The metal additives are used in a homeopathic dosage, and
can never lead to a mercury accumulation in the patient. This preparation can
thus be used simultaneously with amalgam elimination.
Why is Iscar packaged in a series?
Series packs were developed to make dosing easier.
Generally the same dosage should not always be used, since
immune stimulation would decrease, because the organism becomes accustomed to
the stimulus.
For this reason the Iscar series packs begin with relatively
low concentrations, which are gradually increased, with the last three ampules
being those with the highest concentration. After a break a lower concentration
is started again. Series packs have proven themselves in practice.
Only experienced therapists should deviate from series
packs.
What series packs are available for Iscar?
For Iscar M, P and Qu the series packs 0, I, II and III are
available.
What concentrations do the Iscar liquid preparations for
oral use contain?
The Iscar liquid preparations contain three percent each in
Iscar M, P and Quercus. A one percent solution is also available for Iscar P.
What side effects are known?
A known side effect is the slight rise in body temperature.
This rise in temperature is a desired effect. There may be an inflammatory
reaction at the site of injection, which however may only appear with the
higher concentrations.
This is not an allergy. This reddening is completely
harmless and a sign that the patient is reacting to the dosage.
Can or should one do anything about the inflammation?
One should not do anything about the inflammation at the
injection site unless the patient is in great discomfort. In that case one can
apply compresses with Weleda Calendula Essence, Weleda Arnica Essence or with
Merculialis perennis 10% ointment. In the case of pruritus (itching) Combudoron
compresses have been helpful.
Are there any more serious side effects?
In the case of fever above 100.4°F / 38°C with a general
feeling of illness, or in the case of local reactions greater than 2 inches / 5
cm in diameter, the subsequent injection should only be given after disappearance of the symptoms. The concentration of the next injection
should also be halved. In unusual cases general allergic reactions can appear,
such as generalized itching, blister formation, chills, asthma and shock. In
these cases the preparation must, of course, be immediately discontinued and the
reaction treated. Desensitization must then be started.
Has death occurred due to Iscar injections?
Such cases are not known. In my own practice I have not
experienced any occurence of severe reactions in twelve years. At the most
there was an allergic reaction with asthma and low pulse. This could be
alleviated by treatment with calcium and anti-allergenic medications.
With the general increase of allergies one should, however,
be more prepared for the incidence of an allergic reaction with the use of Iscar
preparations. It would thus be prudent to do a preliminary test with a relatively
small dosage.
It is furthermore important to adhere to the guidelines for
therapy with Iscar and not to immediately begin with a high dosage.
If nodules form after injecting with Iscar, do these
dissolve again?
A large number of patients develop swellings and nodules at
the injection site after the first injections. After two or three series
packages these reactions disappear. Only a few patients develop hardening of
the subcutaneous tissue which dissolves very slowly. One must keep in mind that
the injection site should be changed frequently, so that the stimulus is not
always given at the same injection site.
What emergency facilities should a practice using Iscar be
equipped with?
In the case of severe reactions a venous line must
immediately be started in the patient. Plasma expanders, electrolyte solutions
and adrenaline are indicated. Then it must be determined whether
glucocorticoids have to be given intravenously, or whether calcium and
antihistamines are sufficient.
The practice should thus have adrenaline, cortisone and
antihistamines, and at the same time there should be the possibility to start
an infusion. The practice should also be able to supply oxygen.
These measures are not different from the treatment of
general allergic reactions that could arise from other medications. Every
medical practice should thus be equipped with these items.
Can Iscar be administered at the same time as chemotherapy?
Treatment with Iscar can and should be administered during
chemotherapy. During chemotherapy there is a decrease in white blood cells due
to the therapy. Iscar has a stabilizing effect on this situation.
However, the dosage will possibly have to be increased
during chemotherapy. There must, in other words, be stronger stimulation. The
need for this has to be determined individually. Generally the tolerance to
chemotherapy is improved by the simultaneous treatment with Iscar.
Can Iscar be administered in conjunction with hormone
therapy?
Iscar can be administered in conjunction with all hormone
treatments, both with oral medication, as well as medication which is injected
subcutaneously or intramuscularly.
Care should be taken not to inject Iscar near hormone
implants.
As many hormone therapies have a rhythm disturbing and
temperature decreasing effect, the use of Iscar is recommended.
Can Iscar be administered during radiation therapy?
Often it is said that Iscar should not be administered
during radiation therapy. This is not true. It is only important that Iscar is
not injected in the actual area that is being radiated. The injection should be
at least a hand's width away from the area of radiation.
Radiation therapy also has an immune depressing effect in
the patient, which makes therapy with Iscar essential. The side effects of
radiation, including excessive fatigue, can be lessened by the use of Iscar.
How should therapy with Iscar be administered?
There are two phases: an induction phase and a maintenance
phase.
It is necessary to estimate the reaction of the patient to
Iscar in the induction phase so as to avoid an initial reaction. One thus
begins with a weak preparation. The course of events during the maintenance
phase depends on the condition of the patient, what other therapies are being
administered (eg. chemotherapy or radiation therapy) and to what degree the
cancer has spread. During the induction phase one always begins with the dosage
0.01 mg and increases this very gradually until the individual dosage has been
achieved.
One should always begin with series 0, if possible without
metal additives. In the case of a definite reaction in the patient, series 0
should also be administered in the maintenance phase.
Patients who show no reaction to series 0 should go on to
series I. Series I is usually the recommended dose.
The administration of series II or series III should only be
attempted by experienced therapists and then only if there is definitely no
reaction in the patient.
What is meant by 'reactions' is explained later.
If there is absolutely no reaction, even with series III,
the type of Iscar should be changed.
How can one assess the individual
reactions of the patients?
The individual reaction dosage can be assessed by:
1. the
improvement of general well being and lessening of tumor related pain;
2. temperature
reactions, in the sense of a slight increase in body temperature;
3. improvement
of immunological status, which can be documented as an increase in the T helper
cells and a reduction in the T suppressor cells, as well as an increase in the
eosinophils and the absolute lymphocyte count;
4. local
inflammatory reactions up to a maximum diameter of 2 inches / 5 cm.
What
improvement in well-being can be achieved?
Improvement in well being is seen with an increase in
appetite and weight, a normalization of sleep patterns, a feeling of warmth,
increased productivity and a psychological improvement.
Many patients show an increased lust for life with the
treatment, as well as improved social integration.
A decrease in tumor related pain can also be expected, and
painkilling medication can be dramatically decreased.
Is it important to measure temperature?
In the early days of therapy with mistletoe, the measurement
of temperature was the only reaction, besides the local reaction, which could
be determined in patients. At the time it was a great undertaking even to carry
out a differential blood count.
Measuring is however only meaningful if the initial
temperature is measured in the morning before rising, and is monitored in the
late afternoon at about 6PM, after lying down for half an hour. If this rest
period is not adhered to it can easily be the case that movement temperature is
measured, which bears no relation to Iscar. Physiologically, the evening
temperature is somewhat higher than the morning temperature. The
temperature increase must therefore be at least 0.9°F /
0.5°C to really indicate a temperature reaction that is distinct from a mere
reaction to physiological activity.
Patients who can adhere to these criteria should measure
their temperature at the beginning of treatment with Iscar. It is important to
take into account what medication is being taken concurrently. Most painkillers
lower temperature, as do hormonal preparations.
Is it still meaningful to measure temperature?
In my opinion the measurement of temperature has lost its
meaning. It is now possible to measure the immunological phenomena in the
patient before and after therapy, which has more value than temperature ever
had.
If the patient is thus being treated by a doctor with the
necessary possibilities for monitoring, measurement of the temperature can be
omitted.
What can be understood by immunological status?
There is an increase in leukocytes and a change in
concentration of the individual leukocyte sub-populations in the case of
improved immunological status. An increase of granulocytes has for example been
noted, especially also of eosinophils. The immune system is very disharmonious
in most patients: the T helper cells are exhausted; the T8 suppressor cells are
massively increased; and the natural killer cells, which can directly kill off
tumor cells, have been massively decreased. A harmonization of this aspect indicates
an improvement in the immunological status.
For how long should Iscar be injected?
With most types of tumor one must take into account that 80%
of the relapses and metastases appear during the first two years after primary
therapy. It is therefore absolutely necessary that Iscar be administered for at
least two years.
After two years of therapy the treating doctor should decide
whether it is possible to introduce longer pauses between the series. This
depends on the individual risk, on the tumor size and on the risk of possible
metastasis.
How is treatment monitored?
Blood counts are obligatory. The examinations that should be
carried out are discussed further below.
Are there critical phases in mistletoe
therapy?
Critical phases in mistletoe therapy appear especially in
conjunction with immune suppressing therapies, such as chemotherapy, radiation
therapy and hormone therapy. Monitoring should be done more often in such cases
and therapy should be adjusted according to the immune status of the patient.
At times when the emotions or body are burdened, for example
with viral infections, the treatment should be intensified.
Therapy should be intensified in the case of loss of
employment and all strokes of destiny that are not overcome.
It is important that the treating doctor has detailed
knowledge about the circumstances of the patient to be able to assess the
existing risks.
How often should Iscar be injected?
As a rule Iscar is injected three times a week. After every
fourteen injections a week's pause is given.
In the case of a severe risk to the patient an injection can
be given every second day, with a three-day pause after every seven injections.
In the case of a satisfactory course the pauses are
increased over time. The pause of one week could thus be increased to two weeks
in the second year, and to three to four weeks in the third year of treatment.
Treatment should not, however, go below ten series (seven
ampules each) per year.
In special cases it might also make sense to administer
Iscar daily without pauses, as in the case of an advanced illness. However, if
the dosage is increased to such an extent, monitoring must be done regularly to
avoid over-stimulation.
How does desensitization work?
In the desensitization treatment 0.1 ml Iscar, of the
strength 0.001 mg of the type used, is injected, but without a metal additive.
The dosage is then increased daily by 0.1 ml, to a total strength of 1 ml. It
sometimes makes sense to divide this over a few injection sites.
It is important to keep in mind that this injection should
not be administered subcutaneously, but intracutaneously. When the patient can
tolerate 1 ml Iscar 0.001 mg, the next grade can be administered, in other
words Iscar 0.01 mg. This again starts at 0.1 nil.
Can one inject oneself with Iscar?
It is often asked whether patients can carry out therapy at
home, or whether it is necessary to come to the medical office.
There are different viewpoints on the issue.
For many patients it is completely impossible to appear at
the medical office every second day, or three times a week. For others it is
necessary to experience the therapeutic input of the doctor and to receive the
daily injection at the office.
An individual decision thus has to be made, whether the
patient carries out the therapy alone, or with the help of the doctor.
For normal therapy it has proven successful for patients to
inject themselves at home. The patient then just has to come in regularly for
monitoring. When injecting at home the patient should be careful to rest after
the injection. When the patient goes to the medical office to be injected, it
is frequently combined with going shopping, which does not, of course, enhance
the absorption of the remedy.
Should one inject in the morning or in the evening?
Actually one should inject early in the morning, especially
before ten o'clock, as the injection should be administered during the
ascending temperature curve.
There are however many patients who are very restless in the
morning, for example a wife with cancer who is restless due to the husband and
children leaving in the morning, and who cannot find the tranquillity to inject
early in the morning.
In this case it is better to inject in the evening when it
is peaceful, and then to have a long period of rest afterwards.
In my practical experience one cannot assume that the
efficacy of the evening injection is any less than that of the morning
injection. Much more important is the period of rest afterwards, which should
be about half an hour.
Are there special "tricks "for administering the
injection?
The injection should only be administered subcutaneously.
The preparation should not be mixed with other, not even homeopathic,
medications, unless it is the indicated metal additive.
The injection site should be close to the tumor or to the
endangered area. The distance should be 1-2 inches / 3 cm from the tumor and at
least 4 inches / 10 cm from malignant melanomas. This holds true only for
existing carcinomas that could not be removed by operation.
In the case of all other carcinomas one has to assume that
the injection should be administered where it is most practical. It is not
always advisable to inject at the operation site, because scarring or
lymphostasis sometimes hinders absorption.
We thus always recommend that the injection be administered
in the abdomen. Taking the belly button as the middle point of a circle, the
patient should inject, a hand's breadth from the belly button, around the
center. The skirt or trousers waistband area should, however, be avoided, to
prevent local irritation. The thigh can be used as an alternative. The upper
arm, especially in the case of operated mammary carcinomas, ought to be
avoided if possible.
How should one inject?
Injections should only be subcutaneous, which is under the
skin, at an angle of 45°. Many patients inject too superficially; in other
words one can see a slight bump on the surface of the skin after the injection
has been given. This results in the injection being too much in the region of
the hypodermic, where there are sensitive nerves; this results in increased
pain and also allergic reactions.
Can Iscar also be administered intravenously?
Only experienced therapists should administer an infusion
therapy with Iscar. This can be carried out in the case of increased tumor pain
or when there is advanced cancer, which cannot be arrested with the normal
therapy.
An indication for mistletoe infusion is, furthermore, very
low immunity, which, despite an increase in therapy, or change to another kind
of Iscar, cannot be improved.
There are particular guidelines for Iscar infusion, which
will not be discussed further here, because they are strictly for use by
experienced therapists. A strong allergic reaction should always be expected in
the case of an infusion, and therefore the treating doctor should be prepared
for emergency treatment, which includes intubation.
Can Iscar be administered into the body cavities?
In the case of an effusion, such as in the pleural cavity,
Iscar can be administered directly, for example after an aspiration. This
should only be carried out after treatment with subcutaneous Iscar has already
taken place. Iscar can also be administered intraperitoneally, for instance in
the case of ascites.
There are particular guidelines for these applications,
which should only be carried out by experienced therapists.
Why are mistletoe plants from different host trees used?
Rudolf Steiner gave indications for the use of mistletoe
plants from different host trees in the treatment of different tumor types.
Many other perspectives have arisen empirically. Until recently it was believed
that it is merely an anthroposophical idea that there is a definite difference
between, say, apple and oak mistletoe.
Today it can be verified by means of gas chromatography, and
by various other means of analyzing the contents of mistletoe, that these two
mistletoe types are quite different and contain different substances. The
experience of the doctor is thus needed for finding the right preparation for
the type of tumor.
Which host tree should be chosen?
Basically one should follow the scheme as contained in the
guidelines for treatment of malignant tumors with Iscar.
According to this scheme Iscar Qu is especially used in men,
whereas Iscar M is especially used in women. Metal additives are prescribed
according to homeopathic and anthroposophical principles, and differ according
to the type of tumor.
Iscar P should be administered in men and women according to
the type of tumor.
It is up to the experienced therapist to change the host
tree, which could, for example, mean using oak mistletoe in women; for this
there are specific indications.
How should the host tree be changed?
The host tree should be changed when, despite an increase in
dosage, for example from series I to II, or even III, there is no improvement
in quality of life, metastasis or immunological status. One can then, for
example, change from Iscar P to Iscar Qu. One must also be careful to start
again with series 0 or series I.
One can therefore not change from Iscar P series III to
Iscar Qu series III.
Special tests have been developed to determine which
preparation or host tree the patient reacts to best. This is necessary due to
the few criteria in terms of which it is decided what preparation should be
changed to, when, say, the efficacy of a preparation decreases over time. (Not
yet available in the US.)
Should one administer therapy already before the
operation?
Most patients unfortunately only arrive at therapy with
Iscar after an operation. It is desirable to administer
two series of Iscar before surgery, as this stimulates the
immune system. The operation could trigger a
spread of malignant cells. This may happen, especially in
the case of tumors that cannot be fully removed.
Is it advisable to postpone
the operation for four weeks so that a course of Iscar injections can be
administered?
This is an individual decision. One should bear in mind that
a mammary carcinoma has already been developing for two to three years before
it is discovered clinically. It is thus meaningless that some doctors fall into
a state of panic and book an operation for the next day, when one can assume a
long development period for the carcinoma.
The operation should, however, not be postponed for long,
because a tendency for metastasis must be anticipated. I would advise a
patient to undergo at least one series of Iscar injections, which takes 14
days. However, it is up to the individual to decide whether she/he can postpone
surgery for that long with the knowledge of having carcinoma.
Should the tumor markers be determined before an operation?
By 'tumor markers' we mean particular substances found in
the blood that are formed from possible tumor cells.
There is a rate of between 50 to 70 percent elevation with
most tumor markers, which means there are significant numbers of tumor
patients where the tumor markers do not indicate a possible cancer or
metastasis. However, tumor markers are positive in many patients and should
definitely be determined before an operation. If they decrease after the
operation one can reliably assume that metastasis has not occurred, as long as
the tumor markers remain within normal limits. If one had only determined the
tumor markers after the operation, one would not be able to determine whether
the tumor markers were indicative in the patient.
Can Iscar cause false
positives in the case of certain tumor markers?
There are numerous tumor markers. Until now only the (rather
outdated) tumor marker TPA has been shown to increase during Iscar treatment.
This tumor marker is a so-called "tissue peptide antigen". As tissue
stimulation occurs relatively frequently at the start of Iscar therapy, this
tumor marker can increase. This is however the only marker known to be elevated
with mistletoe therapy. As the TPA marker no longer plays a role in the
diagnosis of mammary carcinomas, this falsification is meaningless.
For how long should Iscar therapy be administered in the
case of a mammary carcinoma?
As mammary carcinomas often only metastasize late, a long
period of therapy is advisable. The minimum treatment period, I would say, is
five years. If there has been no metastasis and the immune status is favorable,
only seven series of Iscar injections should be given in the fifth year. The
treating doctor should decide whether there are risk factors in the individual
that require an increased period of therapy.
Are there carcinomas that have to be treated with Iscar
throughout life?
As soon as a metastasis occurs, therapy with Iscar may not
be stopped. The patient's response to the treatment has to be continuously
monitored, and possibly the host tree or the dosage may have to be changed. In
the case of malignant melanomas, skin and organ metastases have been described
after a lapse of 40 years. In the case of this type of carcinoma, therapy should
be continued for more than 20 or 30 years, and the frequency of therapy
individually determined.
How are Hodgkin's disease and non-Hodgkin lymphoma treated?
For treatment of these conditions we recommend the
preparation Iscar P with Mercurius viv. 6x series I. The dosage should not be
increased unless the immune system absolutely needs it. In the case of this
illness an increase of dosage should only be undertaken by an experienced
doctor.
Colchicum Rh D5 ampules should also be injected
subcutaneously twice a week as an additional treatment.
Is there a treatment
for plasmacytomas?
In terms of reducing the expansion of the plasmacytoma, the
results are not as successful as in the treatment of carcinoma. There are
however very good long-term results regarding pain therapy. It is thus
imperative to try Iscar P, possibly Iscar P with Mercurius vivus 6x, not
however above series I, and especially not above series II.
Are there details available about Iscar M 5 mg Special or
Iscar Qu 5 mg Special?
This is a new development in Iscar concentrations, with a
defined and stable lectin content. The total lectin content is 250 ng/ml for
Iscar 5 mg Special, and 375 ng/ml for Iscar Qu 5 mg Special.
A stable total lectin content in the preparations can be
assumed, this is achieved and controlled by means of the selection and mixing
of suitable mistletoe extracts.
Lectins are considered among the most interesting
ingredients of mistletoe today and are being investigated by many scientists.
Do the new Iscar preparations replace the old Iscar
preparations?
These new preparations can be considered as a further
diversification of the available Iscar preparations.
There is no need for patients, who are using other
preparations and are reacting well to them, to abandon these preparations.
What applications do you envision for Iscar M and Qu 5 mg
Special?
In my practice I have generally found it effective to put my
patients on the normal Iscar preparations. Exceptions are patients with tumors
that need speedy treatment, such as those who have pancreas carcinomas that
cannot be operated upon. These are immediately treated with Iscar Special.
A change to the Special preparation is only undertaken if it
is not possible to treat the patient with the normal preparations, in other
words if no improvement in quality of life or immunological status could be
achieved.
It is also used for patients who complain of severe pain,
for example due to bone metastases.
After observing more than one hundred patients in my medical
practice we have arrived at the following guidelines: patients in whom
metastasis has occurred during regular mistletoe treatment, as well as those
who arrived for therapy with already existing primary metastases, are being
treated with the Special preparations.
What results have been observed with the Iscar Special
preparations?
Surprisingly there have been many patients who were treated
with Iscar Special, where metastasis regression has occurred. Such regression,
and also remissions of other kinds, could not previously have been expected
with the other preparations, at least not to this degree.
It remains to be seen how this therapy will develop further.
Does the administration of Iscar Special differ?
Basically, before a first treatment with Iscar Special, one
package of an Iscar series from one of the host trees should already have been
administered, as the reaction to Iscar Special preparations can be quite pronounced.
Subcutaneous administration three times a week with 1 nil of
a series package is recommended. If there is a good reaction, one can change to
Iscar M or Qu 5 mg Special.
One ampule of Iscar M or Qu 5 mg Special should be injected
two to three times a week. No breaks should be taken.
It is in addition advisable to adapt the necessary dosage to
the reaction and the immune status of the patient.
This means that it is also necessary to monitor the
improvement of well being, the temperature reaction, the immunological status
and the local inflammatory reaction.
In the first year of treatment no pauses in therapy are
necessary. From the second year a pause of one week can be taken after every 16
injections.
Do the Iscar Special preparations have any unusual features?
Unusual features include especially the improved immune
stimulation, the reduction of existing tumor pain, as well as a clear
improvement in the warmth organism.
Which types of tumor react well to Iscar?
Studies show a significant improvement of patient survival
time due to treatment with Iscar in various stages of cervical, ovarian,
vaginal, mammary, stomach, bronchial and other carcinomas. All the above
mentioned carcinomas thus indicate the efficacy of Iscar treatment.
Unusual features exist in the treatment of Hodgkin's disease
and non-Hodgkin lymphomas, as well as in the treatment of leukemia and
plasmacytomas. This has already been discussed. Reference is made to the literature
regarding trials that have been done. (Available from Mercury Press)
Questions About Immunology
What is to be understood by the regulation of immunity?
Essentially the purpose of the immune system is to ensure
the integrity of the individual nature of the living organism. Without this
assertion of individual characteristics against foreign information carriers
positive development would be impossible. Evolution presupposes differences
between individuals, which are maintained throughout life by means of an active
immune system. In this context the regulation of immunological recognition and
of defense mechanisms is of central importance. There are two areas of immunological
regulation. On the one hand there is the auto regulation of the immune system,
which includes all influences that are generated in the immune system itself.
On the other hand there are regulatory influences that are generated in the
other systems of the organism, but which act in a regulatory way on the immune
system, such as hormonal or central nervous system influences, which emanate
from the pituitary gland.
The immune regulatory mechanisms become understandable only
by means of the developmental history of the participating cells, which can all
be traced back to a hematopoietic stem cell and which develop specific
functions by means of differentiation. The differentiation of the cells, their
multiplication and their functional actions are regulated by many factors,
which often includes a feedback mechanism that prevents an over-reaction.
Of central interest are the macrophages, the killer cells and
B cells, which group themselves around the granulocytes and mast cells. Their
interactions are regulated by cytokines, which are very differentiated.
What influence do emotions have on immune status?
Recently a new branch of research, namely
psycho-neuro-immunology, has been developed. This science shows that the brain
also participates in immune regulation. Previously it was already known that
strokes of destiny, which could not be fully overcome, or depressive states,
have a direct influence on the immune system. Today this can be demonstrated by
an examination of nerve activity.
What tests are used to determine immune status?
Determining immune status is based especially on the
differentiation of immune competent killer cells. The so-called T helper cells
and the T suppressor cells are clinically of special interest, as are also the
natural killer cells, which can work directly on tumor cells.
Where can such an immune status test be carried out?
An analysis of immune competent cells can be carried out in
every large laboratory with the necessary facilities. Any doctor treating a
patient can send a blood sample to such a laboratory for an immune status test.
In the case of already manifest cancer being treated with immunomodulation,
medical insurance would, as a rule, carry the costs.
What are helper cells?
T helper cells (characterized by the surface antigens T4)
are understood to be cells that have the task of recognizing an antigen that is
presented by a macrophage. The task of helper cells is also to activate B cells
to form antibodies via plasma cells, to activate T8 (suppressor) cells and to
activate macrophages to phagocytosis.
What are suppressor cells?
The task of suppressor cells, which are distinguished by the
surface marker T8, is the recognition and dissolution of target cells, the
presence of which is indicated by helper cells. Moreover, the task of
suppressor cells is the suppression of immune responses, and to thereby
counteract hyper-immunity. They also maintain tolerance of the "self' together with the helper
cells.
What is the lymphocyte transformation test?
The lymphocyte transformation test is a test that determines
whether immune cells are immunologically competent. Frequently, immunologically
competent cells multiply due to unspecific stimuli or medication. In other
words we find an increase of lymphocytes and T helper cells, with decreasing T
suppressor cells. It is also necessary to determine whether or not the cells
are actually active, that is whether they can recognize tumor cells and engage
in anti-tumor activity. Unfortunately there is often only a stimulation of the
cell count, without an increase in the aggressiveness of these cells.
The lymphocyte transformation test indicates whether
activity is indeed possible, not only by counting the cells, but also by
determining the development of aggressiveness in these cells.
This test should thus be done at intervals to establish
whether the cell counts, which have been achieved by the therapy, are
immunologically competent.
What clinical significance does immune status have?
Determining relative and absolute quantities of lymphocyte
subpopulations is not only meaningful for the diagnosis of immunological
illnesses, but also for therapy.
Defects in the defense system, determined in terms of the
shift of concentrations within the lymphocyte subpopulation, can be diagnosed
with this method.
Regular monitoring during treatment especially enables the
doctor to draw further conclusions from the parameters of the findings.
Immune suppression is a notable symptom of tumor illnesses
and is often indicated by an increase in T suppressor cells, a decrease in T
helper cells and a relatively low number of natural killer cells.
Immune suppression such as this is often found after
chemotherapy, radiation or cortisone treatment.
However, such changes can often already be observed before
clinical diagnosis of a carcinoma, and such a test can thus already be
implemented beforehand.
Frequently there is also a displacement of absolute cell
count in the lymphocyte subpopulation. Especially after chemotherapy or
radiation there is a decrease in the absolute lymphocyte subpopulation, besides
the decrease in the total leukocyte count.
What immunological results are known in treatment with
Iscar?
Effects on the thymus and spleen have been described in
animal and other studies. There is, furthermore, a stimulation of the T
lymphocytes and a harmonizing of the different lymphocyte subpopulations.
Investigations have also been done regarding the effect on B
lymphocytes, in other words, on the humoral immune reaction. The effects on
total lymphocyte counts, neutrophils and eosinophils have also been described.
The influence on the activity of granulocytes and on the activity of
macrophages has in addition been investigated, as has been the effect on
basophils and mast cells.
Furthermore, there are investigations concerning the
so-called peritumoral reactivity of the organism, in other words, concerning
the change of the tissue around the tumor, in which clearly discernable
inflammatory infiltrations can be positively evaluated.
How can the efficacy of Iscar be summarized in terms of immunological
parameters?
In many studies it has been proven that Iscar increases the
count of immune cells, which includes the total lymphocyte count, as well as
the granulocyte count. This leads to improved immune competence. Iscar has a
balancing effect by redirecting displaced immune cells, which should have a
regulatory function. The cytokines especially regulate the stimulation or
inhibition of the various cells involved in immune reaction, they become more
efficient with Iscar treatment.
One can assume that Iscar has a stimulating and harmonizing
effect on many cytokines. Overstimulation, which may also be due to tumor
related factors, is evened out by Iscar.
In conclusion it can be said that
Iscar heightens the
immunological competence of the organism, so that the tumor is recognized as an
enemy, and the dissolution of tumor cells can begin.
Often the tumor is masked, which means the immune cells can
no longer recognize it as such.
What are natural killer cells?
In terms of developmental history, natural killer cells are
older than T lymphocytes. As the name suggests, they have an important function
in fighting tumors. They also regulate B cell differentiation and hematopoiesis,
or blood formation.
What are macrophages?
Macrophages are the cells which provide the antigens that
sensitize T cells. They destroy viruses and tumor cells by means of chemotaxis,
enzymes or phagocytosis. They therefore play an important role in the cellular
fight against viruses and tumors.
What are B lymphocytes?
B lymphocytes are plasma cells that produce antibodies. They
are stimulated by antigens or degenerated cells. These antibodies serve as a
defense against infections, and produce antibodies due to the antigen stimulus
of tumor cells.
What are circulating immune complexes?
Circulating immune complexes come into existence due to the
reaction of an antigen to an antibody. Antibodies are produced in tumor
patients as a reaction against tumor cells. These antibodies, associated with a
tumor, can, together with corresponding antigen substances, create circulating
immune complexes. At a certain concentration these immune complexes are no
longer disturbed by macrophages. They then gather around the tumor creating a
barrier that prevents an active immunological reaction against the tumor cells.
They also block the macrophage function, thus immobilizing any effective
defense mechanism against tumor cells.
Methods for Testing the Efficacy of Iscar
How is therapy with Iscar tested?
There are completely different general criteria for the
assessment of reactions to Iscar. First a fever reaction should be observed,
and second a change in well being. Conclusions can also be drawn from the
differential blood count, the reaction of the eosinophils and the behavior of
the C-Reactive Proteins.
The Merieux Multitest and subcutaneous skin tests may also
be used to indicate reactions to Iscar.
The so-called LGL cells (large granular lymphocytes) are
particular immunological cells, which can be used to determine an immune
reaction.
Determining immune status is the most conclusive way of
evaluating a reaction to Iscar.
Is the measurement of fever sufficient?
Rudolf Steiner indicated that, without the appearance of
fever, mistletoe therapy has not been effective. It is thus desirable to
achieve a change in temperature in treatment with mistletoe. The problems that
arise with the measurement of temperature have already been discussed.
When temperature is measured certain minimum criteria have
to be adhered to.
There should be a temperature increase of at least
1.4°F/0.8°C, or even of 1.8°F/1°C. It is important to consider whether the
patient is taking painkillers or other temperature lowering medications.
It is also important to start the measurement of temperature
one week before treatment with mistletoe is commenced, so that there is a
baseline temperature curve.
A temperature increase of at least 1.4°F/0.8°C, which has to
be clearly distinguishable from the physiological temperature curve, can be evaluated.
The harmonizing of an otherwise chaotic temperature pattern
should furthermore be determined. Many cancer patients have rigid or chaotic
temperature patterns that can be harmonized with Iscar treatment.
What changes in well being can be achieved?
An improvement in sleep patterns, an increase in appetite,
as well as a significant decrease in tumor pain have been reported.
An increase in physical activity related to an improvement
of mood, as well as an improvement in mental activity, have also been reported.
Many patients no longer feel caught in the
"stranglehold" of cancer, but instead try to lead an active life
again.
One can however not assume that a sense of well being in a
patient can be used as the only criterion for determining dosage. Many patients
are, for example, undergoing concomitant therapy such as chemotherapy or
radiation, which negatively influences quality of life to a great degree.
What are "epileptiform reactions"?
In his medical work Rudolf Steiner frequently describes the
effect of mistletoe therapy on the human being, especially on the relationship
between the etheric body to the astral body. (See appendix) Steiner elaborates
that during certain mistletoe reactions the etheric body is too strong in
relation to the physical body, and cramp-like reactions can occur. He even
indicates that, precisely due to mistletoe therapy and the effect of mistletoe,
a strange feeling of falling can occur.
An attempt has been made in various investigations to
determine whether these reactions do in fact appear in patients. This reaction
could, however, only be determined in three of 116 patients.
One should perhaps expand the observation by taking into
account that many patients describe such a reaction as a circulatory problem,
or as an effect of chemotherapy or hormone therapy, whereas the effect may be
due to treatment with mistletoe.
However, this criterion seems to be too subtle to be used as
a measure of efficacy.
What meaning does the differential blood count have?
Carrying out a differential blood count before starting
therapy with Iscar, as well as during therapy, is seen as essential for
diagnosis, and cannot be omitted.
Such a differential blood count should be carried out on
every patient at the start of therapy. Based on this initial count, the
strength of treatment is determined and adjusted in the course of therapy.
Dosage has to be chosen in such a way that the total
leukocyte count increases during therapy. Leukocyte counts of at least 6000 are
desirable, but not often achieved by tumor patients.
During therapy leukocyte counts should thus rise to at least
6000, after which a stable dosage can be implemented.
Tumor patients undergoing chemotherapy and radiation often
have depleted leukocyte counts of 3000. An increase by 2000 would be necessary
to assume efficacy of the mistletoe treatment.
Overstimulation occurs in some patients. If the Iscar series
are increased too quickly, relatively high leukocyte counts can arise, which
should be reduced again.
How can leukocyte counts be interpreted?
A count of about 2500 peripheral lymphocytes is desirable in
cancer patients. However, it is important not to rely on the percentage value
of the total leukocyte count. A value of 44 percent leukocytes sounds very
good, but taking into account that 44 percent leukocytes are calculated in a
total of only 2500 leukocytes, the absolute counts would be quite low.
The goal of 2500 absolute lymphocytes should also be arrived
at in stages. Many cancer patients have lymphocyte counts of only 1000 to 1200
before treatment.
It is important not to stimulate too quickly. Therapy should
be administered gradually over three months from series 0, to series I, to
series II.
If the desired effect has not been achieved after three
months, dosage should be changed, or a different Iscar type used.
What can be said about eosinophils?
Today eosinophils are considered potent cytotoxic effector
cells that frequently appear in conjunction with allergic and tumor illnesses.
New investigations indicate that they are important defense cells against
tumors.
The functions of eosinophils are regulated by lipid and
protein mediators, which originate from mast cells or lymphocytes.
The major basic protein of eosinophils is especially
interesting for therapy, as it has a cytotoxic effect on tumor cells.
Eosinophile peroxidase, an enzymatic protein contained in
eosinophils, is very important due to its toxicity to microorganisms and tumor
cells.
An absolute count of 400 eosinophils is desirable to be
achieved through treatment.
Is the stimulation of eosinophils a factor for
prognosis?
Investigations of over 700 tumor patients have in fact shown
that if eosinophils can be increased, patients achieve longer survival periods,
despite advanced tumors. Tumor remission, that is a shrinking of the tumor
mass, may even be achieved.
Only very few patients with good clinical results have not
shown these effects.
In future special attention should thus be given to how the
eosinophils react. This gives an indication of how closely a tumor patient
needs to be monitored, and to what degree the patient needs to be immune
stimulated.
Machine counting of eosinophils is often incorrect and can
thus not be evaluated. One should make the effort to regularly count the eosinophils
oneself, to gain an exact indication of whether stimulation is in fact taking
place.
There have been cases where there was in actual fact an
eosinophil count of ten percent, whereas the microscope counted only one or
two percent.
Can C-Reactive Proteins indicate immune stimulation by
Iscar?
C-Reactive Proteins are so-called acute phase proteins.
The cytokine interleukin I, which is produced by monocytes,
stimulates the creation of C-Reactive Proteins. This occurs by means of the
effect of interleukin I on the hepatocytes.
It would be ideal to determine interleukin I levels, but
this is prohibitive due to costs.
The amount of C-Reactive Proteins formed can, however, serve
as a measure for the formation of interleukin I. By means of this measurement
it is thus possible to determine whether the patient's individually determined
dosage is in fact stimulating the production of interleukin I, and thus the
production of an immune regulatory substance.
An investigation of C-Reactive Proteins is relatively easy
to carry out. However, higher C reactive protein concentrations are measured in
the presence of bacterial infections, viral infections, non-infectious inflammatory
illnesses, as well as with heart attacks, pregnancy and after operations.
If there is no infection in the patient, no surgery in the
past three months and no pregnancy, C reactive protein levels can be used as a
method of diagnosis.
Keep in mind that normal concentrations lie between 10 to 40
mg/l and in exceptional circumstances even up to 60 mg/l.
This is a relatively sluggish system, so an increase up to
only 100 mg/l is actual proof that the patient is being immune stimulated
through treatment with Iscar.
As C-Reactive Proteins can easily be determined in practice,
it can be implemented as a parameter for immunity in infusion therapy.
A C-Reactive Protein (CRP) increase of only 50 mg/l is not a
meaningful indicator for improvement.
What is your opinion on using the Mirieux
Multitest for assessing efficacy?
Using the different skin tests to determine cell mediated
immune reactivity is based on the fact that a typical skin reaction of the
delayed type occurs after intracutaneous administration of antigens with which
the immune system has already come to terms. This is intended to serve as
measure for the actual functioning of cell mediated immune reactivity against
the respective antigens.
In large studies one can prove that the Multitest values
change depending on the stage of the tumor. The intensity of the skin reactions
also correlates with the survival period of the patients.
Also here it is important to note that the system is
relatively sluggish.
In our opinion the system cannot be used for determining
whether Iscar is in fact having a stimulating effect. At the most one can determine
how severely disturbed the immune status of the patient is.
Is it meaningful to determine the LGL (large granular
lymphocyte) cells?
LGL cells are immune competent cells, which can be made
visible by special coloring and measuring techniques.
LGL cells serve as a good parameter for determining the
efficacy of Iscar dosages. The relationship of dosage to efficacy can be read
clearly by means of LGL cells, during therapy with series I, series II and
series III.
The difficulty lies in finding a laboratory that is able to
make a reliable diagnosis. This is only possible in few laboratories.
What meaning does immune status have for treatment with
Iscar?
Cellular immune deficiency could be determined in most of
the patients. Depending on the stage of the illness and preceding chemotherapy
or radiation, immune deficiency could be observed in the reduced numbers of the
various lymphocyte subpopulations. Especially evident were the reduced numbers
of T lymphocytes or natural killer cells.
In the case of patients who had undergone chemotherapy or
radiation, B lymphocytes counts were also reduced.
Many tumor patients, or patients with metastases displayed
increased numbers of activated T lymphocytes and natural killer cells,
indicating that the immune system was still able to react in a meaningful way
to the tumor condition.
Careful analysis of the study reveals that the initial
immune status of patients is very varied.
In advanced tumor conditions the immune status can be poor,
but it can also be highly stimulated, possibly because the organism seems to,
"at the last minute", realize that it has to prevent further
spreading of tumor cells.
One can thus not at the outset assume that a severely ill
patient needs to be treated with a high dosage of Iscar, or a low dosage at the
start of a tumor illness.
Individual decisions have to be made about what strength of
treatment should be used for the individual patient.
It is important to know that every patient reacts
differently to chemotherapy and/ or radiation. One can therefore never predict
whether immune competence will be severely or minimally affected by the above
mentioned therapies.
In conclusion it can thus be said that immune stimulating
therapy cannot be a "schematic therapy". Only individualized therapy
brings the desired results.
What cell counts should be achieved in immune status?
Immunity often clearly reflects the stage of cancer, and
immunological tests during the course of cancer can give the experienced doctor
indications for determining the dosage.
Generally the results aimed for in immune profile should be:
1. The total
lymphocyte count should be about 2000.
2. The T4
helper cells should be between 42% and 46%.
3. The T8
suppressor cells should not exceed 23%.
4. The natural
killer cells should lie between 7% and 10%.
Activity should also be observed. An improvement in the
immunological status and in the results of the lymphocyte transformation test,
indicate an improvement of prognosis. The lack of improvement in a poor immune
system, or a worsening, indicate the beginning of metastasis or a progression
of the tumor illness.
Results of Treatment with Iscar
Are there clinical results for therapy with mistletoe?
To date there are more than 40 clinical studies of the
treatment of various tumors with Iscar. These are mostly retrospective studies,
but there are also prospective, randomized studies.
In retrospective studies an analysis is made a few years
after therapy, and the efficacy of the treatment is compared to data in the
literature. In prospective, randomized studies a study goal is determined,
therapy is established and the patient is randomized into a group. Neither the
doctor nor the patient knows whether the treatment is a placebo or active.
Based on many years of experience, anthroposophical doctors
are convinced of the efficacy of treatment with Iscar, and thus feel that it is
unethical to withhold mistletoe therapy from patients.
It is therefore out of the question that a patient who
appears for treatment should be refused such treatment, or be subjected to
randomization.
This reduces the possibility of carrying out randomized,
prospective studies.
Are randomized prospective studies necessary?
In my opinion such studies are not necessary, because
ethically they can only be carried out with great difficulty. It makes far
more sense to observe well-documented individual cases. This is done by
creating so-called "matched pairs", which means finding patients with
the same course of illness and the same starting point, and to document these
cases.
A well-documented individual course of illness says far more
about the curative possibilities of a preparation than big statistics in which
many patients have to be excluded due to detailed regulations.
Furthermore, most orthodox medicines in use today were
tested retrospectively.
What results are there for breast cancer in women?
Three studies were carried out at the Lukas Klinik in
Arlesheim. In a first study carried out retrospectively, of the 319 patients
who were adequately treated with Iscar, a higher number were still alive ten
years later, than those who were not adequately treated with Iscar (e.g. the
family doctor did not continue with treatment).
The figures for clinical stage I (breast cancer without
lymph nodes effected) were 65 percent and 38 percent, and for stage II (breast
cancer with lymph nodes effected) 33 percent and 17 percent.
A second study made a historical comparison between patients
who were treated adequately and over a long time, and those who broke of
treatment with Iscar after a short time.
The average survival time for patients who were adequately
treated with Iscar was almost twice as long as for those who were treated
inadequately.
A third retrospective study, also with recurrent and
metastasizing late stages, showed similar results.
The efficacy of Iscar treatment in mammary carcinoma
patients is clear in practice. In my own experience there are many patients who
definitely profit from the treatment, who certainly live longer with metastasis
than they would have without treatment.
What studies are available for other types of cancer?
Further studies have been done on ovarian carcinomas,
cervical cancer, colon and rectal carcinomas, as well as on bladder cancer.
There are also studies on lung, stomach, and skin cancer,
and on pleural carcinomatosis.
The studies have in common that patients treated with Iscar
live longer. In studies where well being is central, a definite increase in
well being was observed, especially in comparison to other therapies.
Recently there have been warnings about therapy with Iscar.
What is the background to this?
As more information becomes known about the immune system,
the resulting viewpoints diverge more and more.
Numerous immune stimulating substances, such as cytokines,
are produced in response to Iscar treatment. Recently so-called cytokine
receptors for different types of cancer have been found. For example, ovarian
and kidney carcinomas have such cytokine receptors, as do other types of
tumors.
Now the question is whether the increased cytokine
production with Iscar treatment can also lead to the stimulation of malignant
cells.
One must add that these effects have not been established in
practice, neither in the various studies nor in the various anthroposophical
clinics.
In fact, many patients treated for ovarian cancer showed a
longer survival period than is possible by means of chemotherapy.
Especially patients in whom orthodox medicine had failed
showed a longer survival period than is known in the literature.
There is thus absolutely no evidence that stimulation of
malignant cells occurs due to mistletoe extracts.
As recent investigations show, mistletoe preparations have a
harmonizing effect on the cytokines. This means that cytokine fractions,
decreased due to the tumor illness, were clearly increased, while on the other
hand the excess of excreted cytokines returned to normal.
One can thus assume that improved immunological competence
can be achieved by means of this process. Stimulation due to the harmonizing
process seems to be excluded as a possibility.
What are the results with malignant melanomas?
Malignant melanomas belong to a group of tumors that react
very well to immunomodulatory therapies. Already in early years trials were
done regarding immune stimulation with other medication, such as BCG.
A study at the dermatology university clinic in Basel,
Switzerland, shows a clear prolongation of survival for patients who are
treated with Iscar. This study is reinforced by other observations. A study on
melanoma patients was carried out in our own practice. There is an across the
board lengthening of survival period, and in the case of three patients there
was even a regression of metastases.
In this situation individualized treatment, not schematic
treatment as is carried out in studies, is important.
All patients are therefore treated individually according to
their immune status, which is especially essential in the case of patients with
malignant melanomas.
What are the results in the case of ascites with regard to
the administration of Iscar?
There have been many attempts to administer Iscar
intraperitoneally after ascites punctures (paracenteses) were carried out. The
aim is to inhibit the malignant cells responsible for the production of
ascites, and to limit the loss of energy in the patient due to frequent ascites
puncturing (paracenteses).
The difficulty lies in the fact that the abdominal cavity is
a relatively large area. The small quantities of Iscar that can be administered
are obviously not enough to have a huge effect. Higher concentrations should
not be applied, as this could lead to sub-ileus type reactions.
The administration of Iscar in body cavities may only be
carried out by experienced therapists.
What experiences are there with
intrapleural administration of Iscar?
It has proven very effective to administer Iscar in the case
of pleural effusions, after thoracentesis has been carried out.
Care must be taken that thoracentesis should not be carried
out completely, so that Iscar can mix with the
remaining effusion and act on the tumor cells.
It is important not to start with a dosage higher than 20 mg
Iscar of the desired type. 9 ml aspirate should be mixed with 1 ml Iscar and
re-administered.
Fever and pain can appear as side effects, and must be
discussed with the patient beforehand.
A preliminary treatment with subcutaneous injections must in any case have been carried out previously.
Often pleural effusions, due to adhesion of the pleura
layers, are successfully dried out by means of intrapleural administration.
What is the background to Iscar infusions?
As has been elaborated before, Iscar infusions should only be carried out by an experienced therapis. tThe practice has to be equipped
for emergencies, as allergic reactions cannot be precluded. Furthermore, it
should be possible to do a thorough immunological diagnosis, as
over-stimulation could otherwise occur.
Over-stimulation always leads to immune suppression, which
then remains for at least two months during which time tumor cells can increase
rapidly.
An uncontrolled administration of infusion therapy is thus
not advisable.
Despite the dangers infusion therapy with Iscar is sometimes
necessary. For more information reference is made to the literature. (Mercury
Press)
Generally it can be said that Iscar infusion therapy has the
following results:
1. increased
immune stimulation,
2. definite
decrease in pain,
3. tumor
recession is more frequent than with subcutaneous injections
Concurrent Therapies — Medicinal
Is other concurrent therapy with Iscar of value?
Therapy concurrent with Iscar is meaningful in the case of
tumor localizations or metastases, or in the case of general cancer symptoms.
There are for example particular medicines for hemostasis,
effusions, febrile conditions, bone metastases, and for regulating circulation
and intestinal function.
Medication for analgesia for acute or chronic pain may be
required. Skin reactions to radiation should also be treated.
What concurrent therapy can be used in the case of bone
metastases?
For bone metastases, in conjunction with Iscar treatment, an
ampule of Cerussite D8 every day or every second day, combined with
Pyromorphite D8 or Fluorite D6 as a subcutaneous injections is recommended.
These preparations are effective for the stimulation of bone formation and
against pain.
What concurrent therapies are meaningful for the treatment
of pain?
Iscar has a pain killing effect and may enable a reduction of analgesics.
In the case of a great deal of pain, Iscar infusions may be considered.
Different kinds of tumor pain have benefited from the following treatment:
1. Formica D3/
Formica D15 AA amp: daily one ampule subcutaneously.
2. Apis/Rhus
toxicodendron comp.: daily one ampule subcutaneously.
In the case of chronic pain conditions one to two ampules of
Aurum D301 Equisetum arvense D20 AA can be injected subcutaneously daily.
In the case of nerve pain the preparation Naja comp. has
proven effective. One to two ampules can be injected subcutaneously daily.
Is there a remedy for a skin reaction to radiation?
Weleda skin tonic and Lotio pruni comp. cum Cupro have
proven to be effective in the treatment of this condition. These remedies
should be applied frequently to the radiated areas to prevent skin reactions.
They have also proven effective in the prevention of bedsores in bedridden
patients.
Daily application of Quartz 1% oil in the area of an
operation or radiation has also proven to be beneficial. In the case of skin
reactions to radiation Combudoron liquid or gel is recommended for daily
application.
Is there a therapy for ulcerated tumors?
Calendula ointment 10%, Viscum pini Gel 10% or Viscum pini
5% ointment are effective in the treatment of this condition.
Is there a remedy for hemorrhaging?
To contain acute bleeding in tumor tissue Stibium metallicum
praeparatum D6 ampules have been especially effective. Two to five 1 ml
ampules or one 10 ml ampule should be administered daily. Intravenous
administration has been especially effective.
In the case of abdominal bleeding Stibium metallicum
praeparatum 0.4% suppositories are recommended. In the case of gynecological
bleeding Berberis Decoctum D3 ampules should be injected subcutaneously once or
twice daily.
What preparations can be used for the stabilization of
circulation in conjunction with Iscar?
For the treatment of circulatory disturbances, which are
relatively frequent in cancer patients, Cardiodoron is effective. 15 to 20
drops should be taken three times daily. Veratrum album Decoction D4, 20 drops
three times daily, also leads to a clear improvement in circulation.
Is liver treatment meaningful?
The liver is often severely affected in tumor patients. On
the one hand, it is a large organ with a clear immune function in the
reticulo-endothelial system. On the other hand, medication, either cytostatics
or painkillers, must be detoxified here, often leading to a severe burdening
of the liver.
Substances released in tumor breakdown are also a toxic
burden to the liver.
The following medications have been effective in relieving
the burden on the liver:
1. Carduus
marianus capsules: one or two capsules three times daily.
2. Hepatodoron
tablets: two tablets three times daily.
3. Chelidonium/
Curcuma capsules or tablets: one capsule three times daily.
What remedy is
effective for the regulation of digestion?
Digestodoron N tablets or drops is an effective remedy.
This medication leads to a clear improvement in the
secretion and motility of the digestive tract, as well as a reduction of
heartburn, nausea, bloating and diarrhea.
Fluid intake has a regulatory function regarding good
digestion.
A medicinal therapy without adequate fluid intake does not
seem to be effective.
Concurrent Therapies — Artistic Therapies
Are artistic therapies applied concurrently with Iscar
effective?
The treatment of a cancer patient must include the whole
human being. In other words it is not sufficient to only take into account the
physical well being of the patient in the use of the various therapies.
It is just as important to stimulate the patient emotionally
and spiritually.
In many patients, not only the physical well being, but also
the emotional and spiritual aspects have been disturbed.
The artistic therapies, especially curative eurythmy,
therapeutic painting and sculpture, speech therapy, music therapy, as well as
color and light therapy serve to alleviate these disturbances.
Is concurrent therapy with curative eurythmy effective?
Curative eurythmy is a movement therapy, which is always
determined by the doctor's diagnosis, and is carried out by a qualified
curative eurythmist in cooperation with the doctor.
A different understanding of illness and health is required
in the treatment of the ill organism by means of an artistic therapy.
Cancer patients experience in curative eurythmy that they
can actively contribute something to their healing process, that they are not
passively at the mercy of their illness. This immediately brings about an improvement
in well being.
The organic change enabled by curative eurythmy cannot be
easily detected by patients, due to the fact that it is a long-term therapeutic
process. During this process the diseased organ is treated by an actual restoration
of the organ function and form.
The lack of energy often experienced by cancer patients can
be reduced with eurythmy. The same is true for the loosening of rigid movement
forms. Increased activity gives confidence and strength, as well as the courage
to fight cancer.
Curative eurythmy can reduce lymphatic congestion, reduce
pain and increase the sense of inner strength, which is significantly depleted
in most cancer patients. Eurythmy is for many people a strange new way of
movement, but it can bring about the experience that one has strengths and
abilities one did not know existed. In eurythmy the emotional experience of
humans, which is ruled by the objective laws of language, is expressed in
movement formation.
In practice the effects of curative eurythmy have been
obvious. Many patients treated by us carried out this therapy concurrently with
their cancer therapy, many of whom immediately reported feeling better, that
they had more courage and that they experienced a decrease in all their
manifold complaints.
What meaning do artistic therapies have?
Artistic therapies should lead to a sense of unity in body,
soul and spirit of the patient.
One-sidedness should be counteracted, and the harmony of the
four aspects of being should be strengthened by means of such therapies.
The kind of therapy that is applicable has to be determined
on an individual basis. Besides curative eurythmy there are also music, speech,
painting and sculpture therapies.
Biographical Work and Related Issues
Is it significant to speak of "biographical work"
in a modern context? Is this method also used for therapy?
For a long time there was no awareness of the factors in the
patient's history which were related to the development of tumors.
Psycho-neuro-immunology has proven that emotional
experiences, which have not been dealt with, present a great risk in the
development of cancer.
Patients often develop cancer after a severe emotional crisis
or after a long depression. In our opinion it is therefore essential to
consider such individual factors.
A patient with a mammary carcinoma who is supported by her
husband has a much better prognosis than perhaps a patient with the same stage
of cancer, who is being beaten by her husband because she now only has one
breast. These are real examples from our practice.
It is clear that the above mentioned patient who is being
beaten needs concurrent speech therapy to enable her to change her situation,
or to get out of the situation.
Of course it is very hard for many patients to examine their
life and to bring on changes. Family structures are set and changes are not
always possible in this regard. The comfort of family members could possibly be
affected, which can bring about opposition. It is however essential to discuss
such factors with patients and to start an appropriate course of therapy.
This could take the form of biographical work, which shows
the patient the course of their life up to that point, and highlights
significant events. The patient and therapist together decide what changes can
be effected, with an emphasis on the future.
However, it could also be important for the patient to
undergo speech therapy, which would give the patient courage to live with the
illness and all its facets.
Psychotherapy is recommended only after the condition of the
patient has stabilized.
Psychotherapy taxes the patient heavily, because issues,
which have been suppressed for years or decades, are brought to the surface.
These would have to be worked through, which is not possible if the patient is
struggling with tumors, or as well as with chemotherapy or radiation also.
Speech therapy is recommended in such a case, which can,
when stabilization has set in, be carried over into psychotherapy.
Can the family help with therapy?
Family help can vary significantly depending on the
situation, but is always essential regarding a change in diet, which is
discussed later. It is also essential for the family to understand that tumor
patients have a different concept of time.
In many cases one must assume that, with the start of
metastasis, the dying process has begun, i.e. complete cure is no longer
possible. Family support and great sensitivity in accompanying the patient in
this difficult process, is thus needed. The family should not allow courage and
hope to fail.
Many tumor patients work for their families to the point of
exhaustion, until the start of their illness. Often it is not convenient for
the beneficiaries to now share the workload. Unfortunately for many families
the shock of tumor diagnosis is forgotten after a few months. Many react
strongly during primary therapy and the possible subsequent chemotherapy or
radiation therapy. Once the patient again fills their role in the family or in
the workplace, after conclusion of primary therapy, the cancer diagnosis is
forgotten and the patient is, once again, heavily burdened with
responsibilities.
Obviously a relapse into a situation, which in the first
place led to the illness, is very bad for the prognosis. However, a change in
the situation could lead to healing.
Should the patient always be told the truth with regard to
the prognosis?
Many studies have shown that patients can handle the truth,
whereas previously this had been strongly dis- puted. However, sometimes those
concerned find it is easier not to tell the patient the truth because they then
don't have to deal with the situation. In other words, many doctors and family
members prefer to withhold the truth, so that they don't have to deal with
reactions, such as despair, anger and bitterness on the part of the patient.
However, this, for example, often leads to a situation in
which both partners know the true situation, but are too scared to discuss it
with each other. The tumor patient does not want to burden anyone, and the
partner wants to protect the patient. The result is a lack of communication,
which can be a heavy burden in the last few months of the patient's life. This
is, however, precisely the time at which patients need their family and their
partner to come to terms with their destiny, and to organize the things that
are important to them.
Meaningful Combination with Orthodox Medicine
Can therapy with Iscar be combined with chemotherapy, hormone
therapy or radiation?
The reasons why Iscar therapy should always be carried out,
especially in the case of chemotherapy or radiation, have been discussed
earlier.
During chemotherapy the immune competence of the organism is
radically reduced, this needs to be balanced out by the use of Iscar. A
positive side effect of treatment is the stabilization of the leukocytes, which
means that chemotherapy, if necessary, can be carried out with success. Also,
the interruption of chemotherapy due to leukopenia, which is often necessary,
is prevented.
The information concerning radiation therapy has already
been given.
Injections can be administered up to the time of an
operation, but should be discontinued post-operatively for 14 days. This
prevents a possible interference with wound healing or infection. After a
14-day break the therapy can be restarted. In the case of sensitive patients
who have undergone a severe operation, a dose reduction may be necessary.
Does Iscar treatment work despite chemotherapy and
radiation?
If a patient has been treated extensively with chemotherapy
or radiation therapy, leukopenia can set in, which often remains for years.
Obviously the efficacy of Iscar therapy is reduced in such a situation, because
certain reaction systems have been hardened and significant results are no
longer possible.
But, even in such cases, it is often astonishing what can be
achieved with mistletoe therapy, especially in conjunction with an artistic
therapy, which would dissolve the mentioned hardening.
If a patient with metastases arrives for Iscar treatment
after many operations, a lot of chemotherapy and a lot of radiation therapy, it
is not realistic to expect great results from mistletoe therapy.
We would still recommend, that mistletoe therapy be started,
even if only the well-being is improved during the time left for the patient.
Are there special indications for treatment with Iscar in
conjunction with cytostatics?
Reactions to the various cytostatics are very individual. It
is not possible to predict how severely a patient will react to a cytostatic
combination.
Even the new Taxol therapy, which initially seemed to result
in severe side effects, is tolerated by many patients, with the most severe
problem being total hair loss.
It is also not possible to predict how severely a patient is
going to react to a specific combination in terms of the immunological burden.
This has to be determined individually.
If a patient is to receive Interferon in conjunction with
chemotherapy, should Iscar be administered anyway?
In my opinion Iscar should also be administered, but only in
conjunction with immune monitoring.
Chemotherapy results in severe immune deficiency, which
would probably not be corrected solely by the use of Interferon.
A combination seems promising, as the basis for treatment
with Interferon is completely different from treatment with Iscar.
The immune parameters should however be monitored to prevent
over stimulation of immunity. A combination therapy with Interferon should not
be attempted without monitoring immunity. The same holds true for Interleukin 2, Tumor necrosis
factor Alpha, Interleukin 1/6 and 11, and hematopoietic growth factors.
What painkillers should not be used?
Today many preparations of the Diclofenac type are
recommended, especially for the treatment of pain in bone metastases, such as
in the case of prostate carcinoma.
With the use of these medications it is important to know
whether the tumor is forming an inflammatory wall to encircle the metastases.
Investigations have shown that painkillers of the Diclofenac
type disproportionately concentrate in this inflammatory wall, thereby
disturbing the inflammatory wall.
Therapy with Iscar tries to stimulate such an inflammatory
wall, and tries to stimulate and activate the migration of immune competent
cells, such as eosinophils, into the inflammatory wall.
Pain therapy with Diclofenac preparations thus leads to a
disturbance of this immune reaction, and is therefore a contraindication for
the therapy with Iscar.
Centrally working analgesics such as Naloxone, Tramador, or
other such medications are preferred.
It has proven successful to let patients choose their own
pain therapy. Many of my patients, who have after all learned to inject
subcutaneously, have Tramador ampules at home, which can also be injected
subcutaneously. Patients can look after themselves very well in this way. Side
effects are relatively rare, especially if the effects of the preparations have
already been tested in practice.
Does hormone therapy represent a contraindication with Iscar
therapy?
All hormone therapies can be administered in conjunction
with mistletoe therapy. This holds true for oral applications and for forms of
therapy where implants are placed under the skin of abdomen, or are administered
intramuscularly by means of injections.
Hormone therapy can lead to temperature rigidity, which can
be balanced by means of mistletoe treatment, or with artistic therapies.
The physical effects of hormone therapy, or the effects on
the sexuality of the patient, are often severe, and should be addressed by
means of speech therapy.
Meaningful Combination with Alternative Medicine
What methods of alternative therapy can be used in
conjunction with Iscar?
The methods of so-called alternative medicine are manifold
and range from treatment with thymic extracts, enzyme preparations, vitamin
preparations and trace elements, to ozone therapy, various kinds of blood
cleansing and many alleged immune-stimulating methods. It is important to know
that mistletoe therapy is not an alternative therapy, but is included in the
framework of an anthroposophically extended therapy.
This means that an anthroposophical doctor who administers
mistletoe, is also trained as an orthodox doctor, and can also apply orthodox
medicine in the treatment of cancer.
Anthroposophical doctors treat patients from a different
understanding of the human being and of illness, using other medical therapies,
artistic therapies, and also Iscar. Anthroposophical medicine is thus not an
alternative to normal medicine, but an effective enhancement of existing
therapies.
Not all alternative therapies are suited for use in conjunction
with Iscar.
First, questionable therapies, which have financial gain
rather than treatment as a goal, should be avoided.
Many alternative therapies have an immune stimulating
effect, for example thymic preparations. In such cases it is important to determine
whether further immune stimulation is actually necessary, or whether there is a
danger of overstimulation in combination with Iscar.
Ozone therapy can also have an immune stimulating effect,
but, if the wrong dosage is chosen, can have an immune depressive effect.
Would you combine thymic preparations with Iscar?
Firstly, I would begin treating a patient with a mistletoe
preparation, because the efficacy of these preparations has been documented.
If, despite an increase in dosage and changing the type of
mistletoe, there is no immune stimulation and the tumor illness is advancing, I
would carry out treatment in conjunction with thymic preparations. It has to be
kept in mind that these are defined preparations containing defined substances.
What about a combination therapy with vitamin A?
Stimulation of cellular and humoral immunity is possible in
treatment with vitamin A. An increase in antibody production has been
documented with the use of vitamin A, and the development of cytotoxic T lymphocytes
and an increase in the activity of natural killer cells can be observed with
high dosages of vitamin A.
A direct effect can furthermore be seen in the
anti-proliferating effect against the actual tumor cells. In a study it could
be shown that bronchoscopically determined metaplasias in the bronchial mucous
membrane had decreased significantly in heavy smokers with the administration
of vitamin A.
There are also further studies about decreased hormone
levels in the case of metaplasias in the intestinal and urogenital mucous
membranes, which can be seen as the preliminaries to pre-cancerous changes.
What can be said about combination with vitamin C?
Experimentally numerous immunological reactions can be
achieved with vitamin C. An extreme deficiency of this vitamin leads, among
other reactions, to defects in cellular immunity.
The most meaningful observation however seems to be that,
with vitamin C, the transformation of amines to nitrosamines, and the amides to
nitrosamides by means of nitrites, can be slowed down or prevented. In animal
experiments these nitro compounds dissolve carcinomas of the liver, esophagus,
stomach, kidney and pancreas. It thus makes sense to administer high doses of
vitamin C in conjunction with Iscar.
Vitamin C can be taken in the form of ascorbic acid powder.
Three knife tips per day are considered sufficient.
Some patients with metastasizing tumors show that the
administration of vitamin C in conjunction with infusions results in a definite
stimulation in immunity.
What can be said about combination with vitamin E?
Vitamin E is especially effective as an antioxidant, and is
thus active with selenium in binding free radicals in cell membranes.
These free radicals appear increasingly as a result of
environmental pollution and can be a burden to the immunity of cancer patients,
but also to healthy individuals. Vitamin E thus helps to prevent pre-cancerous
conditions.
It has been proven in experiments that people with low
vitamin E plasma values have a higher risk of carcinomas. This is especially
true in combination with low selenium concentrations. Besides bronchial, stomach
and mammary carcinomas, for which a significant relationship with low vitamin E
plasma concentrations has been proven, colon carcinomas should also be kept in
mind. It has been difficult to prove a relationship between vitamin E levels
and colon carcinomas in studies, because frequency is significantly lower.
What can be said about trace elements?
Trace elements play an important role in all life processes
and are winning increasing importance in clinical oncology. They are used for
diagnostics, and are being administered more frequently to correct deficiencies,
or to achieve specific pharmacological conditions.
Selenium counts as one of the trace elements most essential
to life. About twenty years ago it was pinpointed as a possible environmental
protector against cancer. Large scale experiments on risk populations about
using selenium in cancer prevention are being completed.
Selenium is a requisite for normal cell growth, but slower
growth appears in the case of heightened concentrations, and irreversible cell
damage and eventual cell death in the case of very high concentrations.
Depending on the concentration, selenium is thus growth
substance and growth modulator, as well as cytotoxic agent.
Selenium influences the immune system. It stimulates the
formation of antibodies, modulates lymphocyte proliferation and improves the
activity of macrophages and killer cells. Selenium however does not turn around
the immune activity, and dosages in high sub-toxic quantities have an immune
depressing result. Epidemiological studies show an inverse relationship between
death due to cancer and local selenium quantities. These findings are supported
by the results of prospective studies, from which it is clear that low selenium
values in healthy volunteers are an indication for the heightened risk of
cancer.
In the face of these observations it is justified to accept
the therapeutic value of selenium for tumor patients.
The immunomodulatory basis of selenium is different from
that of Iscar and no overlapping occurs. A combination of selenium and Iscar
therefore seems effective. Very high concentrations of selenium however have a
cytotoxic effect.
What can be said about therapy with zinc?
Zinc is another trace element used relatively frequently in
the treatment of tumor patients.
Tumor growth is influenced by changes in zinc intake, with
growth speeding up with a surplus of zinc and slowing down with a depletion of
zinc. Even tumor regressions have been observed.
However, medicinal deprivation of zinc cannot be used for
treating cancer in humans, due to the severe side effects.
Whether the cytotoxic results of chemotherapy are altered
with zinc deprivation cannot be answered at this stage.
An inverse relation was observed between zinc concentrations
in the prostates of patients with prostate carcinomas, and the results of
therapy. Certain cytostatics results in a decrease of zinc in tumors.
As the serum zinc values are mostly low in cancer patients,
the question needs to be asked whether they will be normalized by zinc
supplementation.
One has to take into account that zinc can speed up tumor
growth and that low zinc levels are not the result of low zinc intake, but
rather the result of the tumor's need for high quantities of zinc. Zinc
supplements at sub-toxic levels administered in the drinking water of mice with
spontaneous mammary tumors resulted in a rapid acceleration of tumor growth.
In vivo zinc acted reciprocally with selenium, with the
anti-cancerous results of selenium completely cancelled by zinc. This confirms
the observations that there is a direct correlation between zinc intake through
nourishment, and the fatality of breast cancer.
A warning must thus be leveled against treatment with zinc,
as the zinc levels necessary for therapeutic purposes is not yet known.
Is treatment with iron dangerous for tumor patients?
The role of iron in tumor development is the subject of many
investigations. From these it follows that iron may be essential for life, but
that, in excess, it stimulates tumor growth. Excess iron is stored in the metabolically
active cell membranes of tumor cells, instead of in the cytosolic ferritin as
in normal cells. This enables the rapid growth of tumor cells. The iron content
of tumor cells varies considerably and depends on the type of tumor. For
example, breast tumors are often high in iron content.
Large quantities of iron can accumulate in tumors. In mice
with large mammary tumors the total iron content of the tumor exceeded that of
the liver.
As tumor growth is dependent on iron intake, iron
supplementation in anemic patients should be carefully evaluated.
For tumor prophylaxis the same holds true for iron as does
for zinc: chronic surplus, as well as chronic deficiency should be avoided.
Resistance to cancer is decreased organ-specifically in the case of chronic
iron deficiency.
Iron supplementation should, as with zinc, occur via diet
rather than medicinally. The absorption of both elements is especially
regulated by phytic acid, which is found in wholemeal products.
What other trace elements are important for therapy?
It is possible that chronic copper deficiency results in
weaker cancer resistance.
Until now copper supplements have seemed unnecessary, as
copper deficiencies were only observed in rare illnesses. Chronic copper
deficiency is especially linked to bone and joint illnesses, but copper
supplementation does not seem to be beneficial.
Magnesium stabilizes cell membranes, and a synergetic
interaction between magnesium, selenium and vitamin E can be assumed.
It is noticeable that subnormal magnesium concentrations
have been observed in almost all types of cancer, excluding melanomas.
General magnesium supplements cannot however be recommended,
as magnesium can accelerate tumor growth.
Nutritional Aspects
Can a specific diet be recommended for cancer patients?
There are many opinions about specific diets for cancer
patients, none of which are completely convincing. Without any intake of
nutrients, an existing tumor can be starved.
However, all tumor diets that aim to "starve the
tumor", or through the elimination of essential ingredients aim to
"dry out the tumor", lead to a considerable loss of vitality in the
patient, which often rapidly leads to tumor progression.
Tumor patients should follow these general criteria:
1. Mostly fresh
food should be used, and if possible no preserved food, preservatives or
artificial fertilizers.
2. No alcohol
should be consumed. Alcohol has a laming effect on the spiritual Ego, which is
probably the most important aspect of the human being. It furthermore affects
the liver, which in our experience is the most important organ in cancer
therapy.
3. Potatoes and
tomatoes should be considerably reduced in the diet of a cancer patient.
4. Joy and
rhythm in eating, and restfulness while digesting, should be observed. These
qualities are severely lacking in contemporary lifestyles.
Why should tumor patients not eat potatoes?
Potatoes are not real roots, but rather stalk growths, which
develop in the soil without light. If one exposes potatoes to light, they
become poisonous. Especially cancer patients should avoid young potatoes, as
they still have the potential to become poisonous. Rudolf Steiner elaborated
that potatoes belong to the group of plants known as nightshades, which burden
the digestive system and can lead to dullness and general lethargy. In other
words they don't stimulate restorative energies.
In experiments the poison solanin has been found in the skin
of potatoes. This poison is more evident in young potatoes, and recently the
suspicion has arisen that it may contribute to the formation of cancer.
It is important to know that in experiments on laboratory
animals with tumors, the tumors grew faster in the animals fed on a potato
diet.
Why should tumor patients not eat tomatoes?
Rudolf Steiner said that the tomato, according to its
nature, especially stimulates that "which is independent in the organism
and that which specializes". In today's medicine we know that rheumatic
and gout patients should not eat tomatoes. In the case of rheumatism and gout,
deposits are formed in the joints or in the muscles. One could perceive cancer
as an independent deposit in the organism. We can then understand why Rudolf
Steiner said that cancer patients should not eat tomatoes.
There are also animal experiments indicating that animals
with tumors, which are fed with tomatoes, develop significantly larger tumors
than the control group.
It is furthermore important to know that tomatoes, like
potatoes, also form the poison solanin.
Besides this, the proliferating growth, the love of muddy
ground, the ripening in darkness and the characteristic of the fruit to draw
the last strength out of the plant, place tomatoes in a particular category.
These characteristics are the reason why Rudolf Steiner urged cancer patients
not to eat this fruit. This does not mean that this fruit is forbidden across
the board. It can absolutely be recommended to healthy individuals. It is also
a misunderstanding that other nightshades should be avoided. Peppers for
example are important nutritious plants, as are cucumbers and pumpkin-type
vegetables, and should definitely be included in the tumor patient's diet.
What general guidelines should be observed in the tumor
patient's diet?
Today, together with nutrients, the human body absorbs
hundreds of different chemical substances, of which only a few serve as
nutrients for the maintenance of bodily functions.
Due to the possible causal link to malignant tumors,
mutagenic substances in foods should be especially monitored. Included are
plant additives, toxic molds that cause perishing, as well as mutagenic
substances that can arise in the preserving, processing and preparation of
foods.
The high possibility that foods could be contaminated with
persistent environmental poisons, such as heavy metals, pesticides or
radioactive nuclides, which all have mutagenic characteristics, is only
mentioned here.
Cancer patients should be especially careful about
environmental poisons in food, but also about the possibility of foods
poisoned with molds.
Molds are relatively widespread today and food contaminated
with mold should not only be thrown away, but should generally be destroyed.
Often it is not possible to see whether food is contaminated
with mold spores or filaments. The mold is only visible in one place, but will
have grown through the food and have resulted in spoiling. Cancer patients
suffer far more severely from the effects of ingesting mold.
Generally the consumption of food types that are more
frequently contaminated, such as moldy nuts or highly heated, grilled pickled food,
should be avoided. Food coloring should also be avoided.
Is there a link between nutrition and the immune system?
Nutrition, or individual nutrient substances, interact with
the immune system and can inhibit or stimulate its function. Conclusions can be
drawn from this for the treatment of patients with malignancies.
Different effects were found in the immune system with the
intake of specific substances, such as arginine, nucleotides and lipids. Many
more tests will be necessary to determine nutritionally induced effects on the
immune system with regard to specific clinical situations, such as burns,
lengthy operations, organ transplants or tumors. However, current studies
indicate promising results with immunomodulating diets.
In tests arginine clearly influenced immunity in the human
being. Furthermore, healthy volunteers who increased their daily arginine
intake showed significantly increased lymphocytic reactions to mitogens.
Post-operative patients, who received increased arginine by means of enteral
alimentation, also showed improved lymphocytic reactions to mitogens.
In animal tests the size and frequency of tumors could be
reduced by means of increased arginine intake. Animals inoculated with a virus
displayed longer latency periods regarding tumor formation and smaller tumors,
when fed on an arginine containing diet.
All studies so far indicate that arginine has an immune
stimulating effect. The improved function of lymphocytes and macrophages could
be important in improving immune function post-operatively, and in preventing
potential infectious complications.
It is important to know that high levels of arginine can be
detected in mistletoe.
Nucleotides can also influence tumor growth. In animal
experiments with induced T lymphocytic tumors, the tumors were dependent on
nucleotides for their full development.
Lipids are important nutrients in the reaction of the
organism to nutrient deficiency and stress. It has recently been discovered
that lipids, especially prostaglandins, play an important role in the immune
system.
In conclusion it can be said that immune competent cells
react differently according to whether the diet contains medium chain
triglycerides, omega 3 fatty acids and omega 6 fatty acids. Recent
investigations show that the immune system can be influenced therapeutically
and prophylactically with the administration of a special fat containing diet.
A diet can be put together in such a way that, mainly through
a change in the proportion of the different kinds of fats, the function of the
immune system is changed according to the need of the clinical situation.
Are there questions not yet asked in this context?
This small book contains the questions of many patients
about therapy with Iscar. Many questions of other patients or their doctors
have perhaps not been answered extensively enough, but for further information
reference is made to the literature.
APPENDIX
Anthroposophical Medicine
Anthroposophical medicine is the spiritual scientific
extension of natural scientific medicine.
It rests, in the assessment of health, illness and healing,
on the physical laws that are encompassed by the natural sciences, but also equally
considers the laws of life, emotion and spirit in their mutual dependencies.
Physical body, 'body' of life forces, 'body' of emotional experiences and
spiritual Ego are, according to anthroposophical knowledge, the four aspects of
being.
Aspects of being
| Physical body | inorganic,
material, "mineral" |
Etheric body (growth body)
| basis
for body of life forces, "plant-like" |
Astral body (emotions)
| basis
for organization of sensory experience and emotional life,
"animal-like" |
Spiritual Ego
| basis
for the spiritual individual, "human" |
With regard to matter and its laws, the physical body, which
humans, animals, plants and the lifeless mineral world have in common, can be
perceived directly by the senses.
The essential step from the inorganic nature of the mineral
to the organic nature of all living organisms is the result of the body of life
forces (etheric body), which allows the development of form to occur by means
of metabolism, growth, regeneration and reproduction.
Humans and animals have in common the body of emotional
experiences (astral body) as bearer of drives, instincts and inner sensing,
which also allows independent movement to occur.
The human being's consciousness of self and control of self,
the possibility to understand oneself as an individuality, as one who stands
consciously and responsibly in the world, is founded in its spiritual essence,
in the spiritual Ego. This is the essentially human, because it is the
spiritual dimension, from which the human being creates culture and learns in
the course of life.
The above-mentioned fourfold nature results in a
differentiated functional organization of the human being and the essential
laws of existence. The physical body is perceptible through the sense organs
while the three other aspects of being are not. They can only be recognized by
their effects in the domain of physical phenomena.
The working of the aspects of being in the human being's
physical body result in the morphological threefoldness of
the nerve-sense system with its center in the skull, but
functionally effective in the entire body;
the rhythmic system with its
functional center in the chest cavity; and
the metabolic-limb system which encompasses all metabolic
activity and willed movement, and which is centered in the metabolic organs of
the abdomen and in the limbs.
The physical three-foldness corresponds to a spiritual
three-foldness of the human being:
| nerve-sense system | carrier
of thought |
| rhythmic system | carrier
of feeling |
| metabolic-limb system | carrier
of will |
The three-fold organization is effective in the total
organism, in the organ systems, organs, tissues and cells, morphologically as
well as functionally. At each stage of life it experiences a corresponding
modification. The rhythmic system mediates between the two opposite poles of
the nerve-sense system and the metabolic-limb system, and creates health in
the sense of a delicate, ever newly created balance, which is a harmonious
working together of the aspects of being. A departure from the healthy central
point results in the manifold illnesses.
This conception of a physical-spiritual functional
organization, which recognizes the whole of the human as ensouled, makes
possible an all-encompassing view of physical, pathological and therapeutic
problems. The aim of treatment is thus based on the task of re-establishing the
harmony of energies.
Methods
Natural scientific and spiritual scientific methods are used
in anthroposophical medicine. Anthroposophical doctors are convinced that for
this purpose, besides a conventional natural scientific training, a training
based on Goethe's methodology for the understanding of life processes, is
necessary. Furthermore, training in meditative higher knowledge, or insight, is
necessary. Rudolf Steiner (1861-1925), founder of Anthroposophy, described
this in terms of Imaginative, Inspired and Intuitive steps to higher knowledge.
The results of the spiritual scientific research of Steiner are viewed as the
starting point for many diverse contemporary studies and research projects in
anthroposophical medicine. Natural healing methods, physiotherapy, phytotherapy,
homeopathy, psychotherapy and artistic therapies can now be understood with a
rational basis by means of the anthroposophical view of the human.
For the understanding of illness and for the finding of
cures it is necessary to do research using the above mentioned methods. To move
from pathology to therapy one needs to answer the question of how the organ
systems described above, and the aspects of being, come to expression in the
ill person, and with which curative means from the three natural realms, or
through which action of the human, a healing of the patient can be attained.
The understanding of the relationship between the human aspects and the natural
realms on the one hand, and the actions carried out by the human on the other
hand, are the essential foundations of therapy.
It is essential for the understanding of illness in terms of
anthroposophical medicine that physical changes are understood as the
expression of soul and spirit, which, in their changing interactions, can
reveal themselves as illness, or also as a healthy expression of life and
emotion. Psychiatric illnesses are also viewed and treated in their bodily
context, in an equivalent of the above-mentioned body-soul relationship. The
therapeutic measures adopted by anthroposophical medicine are also based on
these considerations.
Specific
methods of therapy have arisen, such as:
a) Medication
according to special pharmaceutical methods of production, as also determined
in the "Homeopathisches Arznei Buch" (HAB); or, for metal therapy,
the breakdown of substances through plants (vegetabilized metals); or the
application of rhythmic and other processes in the manufacture of specialized
healing plant substances, with the most well-known example being the
manufacture of mistletoe preparations for the therapy of tumor illnesses.
b) Procedures
for external applications, eg. metal containing ointments, rhythmic rubbing, or
oil dispersion baths.
c) Curative
eurythmy, a movement therapy founded by Rudolf Steiner, as well as artistic
therapies: sculpture therapy, painting therapy, music therapy and speech
formation as therapy, which all draw patients into an active, engaged
participation in their own healing process.
d) Psychotherapy based on the anthroposophical view of the
human and of illness, which is based on the spiritual scientific understanding
of biography, and the soul's development from the bodily to the spiritual.
The basis for understanding illness and medicine according
to anthroposophical medical methods, is contained in the book that Rudolf
Steiner wrote in collaboration with Dr. Ita Wegman: Fundamentals of Therapy: An Extension of the Art of Healing through
Spiritual Knowledge, (Mercury Press, Spring Valley, 1999).
It is therefore clear that mistletoe therapy cannot be
understood in isolation when speaking of anthroposophically extended medicine
in tumor therapy. Rather, other forms of therapy, e.g. art therapy, must be included
in the expanded view and the understanding of the human.
Only by treating the entire human as a unity of body,
emotion and spirit, can a tumor patient be successfully healed.
Richard Wagner, MD
Glossary
antihistamine: medication against allergic reactions
antigen: alien protein that causes the formation of
antibodies in the body, which then make the protein harmless
antibody: defense substance formed as a reaction to the
invasion of an * antigen in the blood serum
antibody formation: an immune reaction
anti-proliferative effect: acting against proliferative multiplication of tissue
ascites: abdominal dropsy; collection of fluid in the
abdominal cavity
bradycardia: slow cardiac activity, slow beating of the
heart
cell membrane: forms the cell surface; represents a barrier
through which some substances, eg. water, can move through, others eg. sugar,
not
chemotaxis: orientation movement triggered by chemical
stimuli
collum carcinoma: cervical cancer
colon carcinoma: cancer of the large intestine
craurosis vulvae: shrinking of the transitional mucous
membranes (in this case of the vagina)
(Breisky's disease) cytokine: * lymphokine
cytotoxic: cell poisoning, cell damaging
desensitization: artificial reduction of a specific
oversensitivity (eg. an allergy); it is possible to test which substance the
patient is reacting to; the patient is injected with the smallest quantities
that give a hardly discernable reaction, which is increased gradually, to
achieve insensitivity
differential blood count: counting white blood cells with an
isochromatic method
effector: substance that regulates an enzyme reaction
enteral: regarding the intestine
enzyme: organic compounds in living cells, which regulates
the metabolism of the organism
eosinophil: white blood cells colored with eosin (a red dye)
erythrocytes: red blood cells
esophagus: gullet
granulocytes: a type of white blood cell
hematopoiesis: blood formation
Hodgkin's disease: malignant lymphoma that probably arises
from the lymph nodes; malignant disease of the blood
hypertension: high blood pressure
hyperthyroidism: overactive thyroid
immune suppressant: medication that suppresses immune
reactions
immune system: a functional unity including immune cells,
other cells and organs, which preserves the individual structures and functions
of the organism by working together in the fight against foreign substances;
the thymus gland is essential for the immune system, as is the system
containing the liver, spleen, lymphatic system and bone marrow.
immune tolerance: the level beyond which an individual does
not react normally to an immunogenic stimulus, in other words does not respond
to an antigen by forming antibodies
inoculate: to bring pathogens, tissue, cell material into an
organism
inotropic: influencing the strength or contraction power of
the heart muscle; increasing: positively inotropic; reducing: negatively
inotropic
interleukin I: stimulates T and B lymphocytes
interleukins: signal substances for immune regulation
intracutaneously: into the skin
intraperitoneally: into the abdominal cavity
intubation: insertion of a tube, e.g. airway tube through the
nose or mouth
killer cells: sensitized T lymphocytes; excrete cell poisons
in the presence of cells containing foreign antigens (eg. transplanted cells,
tumor cells)
leukopenia: depleted total leukocyte count
"Leukotriene"/prostaglandin: prostaglandin
leukocytes: white blood cells; made up of granulocytes
(60%-70%), lymphocytes (20%30%) and monocytes (2%-6% of the blood leukocytes);
in infectious illnesses there is a gradual change in the leukocyte division,
which can be seen in the differential blood count, and which enables a
conclusion to be drawn about the illness
lymphocytes: white blood cells that originate in the stem
cells of bone marrow; formed in the bone marrow, lymph nodes, thymus and
spleen, and mostly end up in the blood via the lymphatic system
lymphokines: substances produced and excreted by the
lymphocytes, which activate other cells and influence their function for the
formation of various enzymes
macrophages: large * phagocytes
mastopathy: proliferating nodule and cyst formation, tissue
multiplication, processes of change in the mammary glands
metabolic: (self-explanatory in English)
metaplasia: curable change of differentiated tissue into
another type of differentiated tissue
mitogens: substances that effect cell division
mutagen: triggers mutation
mutation: change, alteration
neutrophile: easy to color with chemically neutral
substances, especially susceptible to neutral colorants, eg. of leukocytes
non-Hodgkin lymphoma: malignant lymphoma
papillomatosis: cauliflower-like growth
phagocytes: Cells that are free in the blood (white blood
cells), and are able to absorb and to make harmless alien substances,
especially bacteria, by means of * enzymes. According to place of origin,
prevalence and tasks, there are eg. histiocytes, monocytes, macrophages,
microphages
phagocytosis: dissolving and making harmless of alien
substances in the organism by means of phagocytes
plasma: 1. living substance
2. clottable body fluid, eg. blood plasma, muscle plasma, albumen
containing liquid gained by pressing live muscles
plasma cell tumor: multiple myeloma, Kahler's disease;
cancerous swelling in the bone marrow which originates from a single, malignant
degenerate plasma cell type (B cell of the immune system)
plasma expander: plasma substitute, solutions of natural or
synthetic colloids
pleura: covering of the
lung tissue
prospective studies: possibility; with regard to the future
prostaglandin: local
hormones that are biologically highly active and originate from the different
body tissues; very important for cell function and act as transmitters
proteins: general description of albumens
randomization: a selection that allows an exact calculation
of random dispersion, based on the probability of theoretical assumptions;
serves for the attainment of representability of random checks and experiments
reactive protein: a protein located in the liver which can
attain serum concentrations thousands of times higher than average by means of
increased synthesis, in the case of infectious and non-infectious, inflammatory
and dying off processes
receptors: reception devices of the organism for particular
stimuli
resorption: absorption of dissolved substances in the blood
and lymphatic system
reticulo-endothelial system: a cell system belonging to the immune system, which is also
described as resorbing inner surface of the body. Especially plays an important
role in healing chronic illnesses
selenium: important trace element; contained in bones and
teeth
"sistieren": (self-explanatory in English)
subcutaneous: under the
skin
sub-ileus: disturbance of the intestinal movement as early
symptom of intestinal obstruction
suppressor cells: suppress the immune reaction of other,
especially T helper cells
stenocardia (angina pectoris): heart complaint appearing as
labored respiration; due to a functional disturbance of the coronary artery,
which supplies the heart muscle with blood
T helper cells: lymphocytes
important for the regulation of immune reactions
tumor markers: substances traceable in the blood serum that
allow conclusions to be drawn about a particular tumor
This publication is an adapted translation
from the original German:
Krebs, 160 Fragen and Antworten zur Therapie mit Iscador®
published by Verlag Urachhaus, Stuttgart 1996
ISBN 0-929979-83-4
Copyright C 2000
by
MERCURY PRESS
Fellowship Community
241 Hungry Hollow Road
Spring Valley, NY 10977