Doctor Tullio Simoncini
THE WHOLE THERAPY
If 40, 30, or even 20 years ago it was still possible to somehow
convince people of the goodness of official oncology and of its
results, today, after results that are as continuous as they are
inane, although trumpeted regularly by the media, nobody accepts
being seduced by words, about hypotheses and promises that are
undelivered and undeliverable, any longer. The painful awareness,
which almost everyone has experienced, of the miserable end of
this or that relative, friend, or acquaintance, is associated with
We must surrender to the evidence that contemporary oncology is
incapable of giving us the answers and the necessary to those who
are cancer patients and that therefore it is our moral and ethical
obligation to try to find the correct solution for the gravest
and most painful disease of our time.
Cancer is a fungus
For about 100 years, the fundamental theory behind cancer has been
based on the hypothesis that it is a malfunctioning of the genes.
This point of view implies that cancer is intracellular. My point
of view however is that cancer is a fungal infection, and therefore
an extra cellular phenomenon.
In the plant world, cancers are caused by a fungal invasion, and
it is possible to argue that the same thing happens in human
beings. Fungi are always involved in cancers: they are found
both in vivo and in the post-mortem examination*.
However, scientists believe that they develop after the onset of
the illness. My opinion is that they come before it: they produce
the cancer, blunt the immune system and then invade the entire
Each type of cancer is caused by fungi of the Candida species,
as also referenced by other research*, and the histological configuration
is a result of the defence reaction of a tissue against the invasion.
In time, the tissue gets exhausted and produces only undifferentiated
A cancer could be termed a ‘solid abscess,’ where the
colonies form the centre, and host cellular reaction is all around.
Traditional anti-fungal drugs are ineffective in treating tumours
because the solid colonies can be attacked only on the surface
of their volume, and after the first administrations they become
A solid infection is much more powerful than a bacterial one. That
is why simple fungal infections can last forever.
I have identified the substances uniquely able to penetrate these
volumetric infections: for cancer of the internal organs it is
sodium bicarbonate; and the best substance to eliminate skin cancer
is iodine tincture, particularly when it is spread onto the growth.
There are many publications that describe the effectiveness of
sodium bicarbonate on cancer*, but the conclusions drawn in them
are invariably wrong because they assume intracellular, rather
than antifungal action.
My methods have cured people for 20 years. Many of my patients
recovered completely from cancer, even in cases where official
oncology had given up.
The best way to try to eliminate a tumour is to bring it into contact
with sodium bicarbonate, as closely as possible, i.e. using oral
administration for the digestive tract, enemas for the rectum,
douching for the vagina and uterus, intravenous injection for the
lung and the brain, and inhalation for the upper airways. Breasts,
lymph nodes and subcutaneous lumps can be treated with local perfusions.
The internal organs can be treated with sodium bicarbonate by locating
suitable catheters in the arteries (of the liver, pancreas, prostate,
and limbs) or in the cavities (of the pleura or peritoneum). It
is important to treat each type of cancer with the right dosage.
For a phleboclysis, 500 cc at 5% or 8,4% is required; for external
administrations it is enough to taste if the solution is salty.
Sometimes it is judicious to combine different administrations.
For each treatment, take into consideration that tumour colonies
regress between the third and fourth day and collapse between the
fourth and fifth, so that a six day administration is sufficient.
A complete, effective cycle is made up of six treatment days on,
and six days off, repeated four times. The most important side
effects of this care system are thirst and weakness.
For skin cancer, a 7% iodine tincture should be spread on the affected
area, 20-30 times once a day, with the aim of producing a number
of layers of crusts. After this treatment, the cancer will be gone
and stay away forever.
This therapy is also applicable in paediatric oncology, provided
the dosage is adjusted and revised according to the weight and
age of the infant, as well as the type of neoplastic formation.
Several well-documented clinical cases, examined before and after
sodium bicarbonate treatments, were reported on and outlined
I wrote a book entitled ‘Cancer is a Fungus’ published
in Italian, Dutch and English, thanks to the help of family and
friends. Video footage of patient testimonials is also available
on the internet site mentioned above. My deep wish is to make this
therapy available to all humanity. In order to do so I must carry
on my research. This research is done privately, since I have received
no response from official institutions — despite having published
the results of the well-documented and successful clinical cases
I have treated. It is my firm hope that soon, the fundamental role
of fungi in the development of neoplastic disease is acknowledged,
so that it is possible to find, with the help of all existing forces
of the health establishment, those anti-mycotic drugs and those
systems of therapy that can quickly defeat, without damageand suffering,
a disease that brings so much devastation to humanity.
When compared with the whole universe of fungi forms mycetes that
are pathogenic for humans are not very numerous.
They usually cause diseases called mycosis, which are commonly
divided into superficial (when the infection is limited to the
cutis, body hair, hair of the head, and nails) and deep (when the
infection attacks internal organs such as lung, intestine encephalus,
bones, and others). The fungi are generally classified as:
1. dermatorphytes, causing afflictions that are typical of the
2. sporotrichum schenckii, which are also almost exclusively located
on the epidermis
3. Criptococcus neoformans, responsible for a diffused infection
of the lung (the organisms are inhaled with dust) as well as chronic
4. Histoplasma capsulatum, which in humans produces the nodular
cutaneous form, mucous form, the pulmonary form, and the systemic
5. Actinomycetes, with pathogenic action on the cutis, lungs, and
6. Chrysosporium parvum (causal agent of the adiasphyromycosis),
a cosmopolitan disease where the respiratory tract constitutes
the primary and only localization of the infection
7. Aspergillus fumigatus, cause of the Aspergillosis, whose most
frequent location is in the lungs, followed by a secondary location
in the cerebrum and in the kidneys
8. Paracocci dioides brasiliensis, which causes the paracoccidioidomycosis,
a primary pulmonary infection that can become diffused in immuno-depressed
9. In recent years, Pheoiphomycosis ialiphmycosis, pennicilinosis
(marneffei), zigomicosis and other rare mycotic infections are
acquiring more and more importance since they can be responsible
for pathological scenarios that are sometimes very serious because
of the compromised conditions of immuno-compromised patients.
10. Candida, both as Albicans and as any other pathogenic stock
which afflicts the cutis, nails, internal mucus membranes (oral
cavity, vulvar vaginitis, urethritis, balanitis, perianal infection),
bronchi and lungs.
Candida is also responsible for causing generalized forms of septicemia
of remarkable gravity.
The gravest disease of humanity is, therefore, hidden within this
grouping of fungi. Some further analysis will make it easier to
identify the cause.
Dermatorphytesand sporotrichum are responsible for a morbidity
that is too specific. We know from experience that Actinomycetes,
Criptococcus, Hystoplasm, Chrysosporium, Paracoccidioides and other
causal agents of Pheoiphomycosis ialiphmycosis, pennicilinosis,
zigomicosis are very rarely part of a pathological context. Finally,
Aspergillus can be considered a variation of Candida. Only one
of the six kinds described above remains as the sole responsible
agent for tumors: Candida.
CANDIDA AND CANCER ALWAYS CONCURRENT
There are a large number of works that document the constant presence
of the mycetes in the tissues of cancer patients, especially in
In recent years, we have observed a crescendo of voices addressing
this terrible fungus to the point of defining it as 'the most important
and most urgent problem that oncology has to solve'.
The following figures concerning the coexistence of Candida and
cancer have been collected by several authors:
R.L. Hopfer: 79%
U. Kaben: 80%
W. T. Hughes: 91 %
T.E. Kiehn: 97%
The percentages observed are truly impressive, especially when
considering the difficulty of seeing Candida in the organic materials
to be examined. This was also reported by R.S. Escuro, Z. O. Karaev,
and T.J. Walsh.
The positive results quoted allow us to confirm that Candida is
always present in the tissues of cancer patients. Not only that,
but Candida species represent today, according to several scholars,
the first cause of morbidity and mortality in patients affected
by neoplasias of the hemolinphopoietic system.
O. Uzun even analyzed all data from 1974 to 1999 concerning the
presence of candidosis in patients and the prognostic factors including
predictable elements of mortality and came to the conclusion that
the global rate of mortality in cancer patients varies between
33% and 75% and that this is independent of the type of infecting
The phenomenon is usually interpreted as a consequence of the
weakening and of the exhaustion of the organism because of neoplastic
lesions. Conversely, we have to believe that the aggression of
Candida takes place in the carcinogenic sense after the superficial
pathogenic phases - that is, the classic epithelial candidosis
- in several stages:
a) rooting in the deep connective tissue (in the various organs)
b) expansion with evoking of an organic reaction that attempts
to encyst the fungin colonies, with the outcome being the formation
c) growth both in the surrounding tissue and remotely (metastasis).
d) progressive exhaustion of the organism with consequential global
organism invasion. This is the stage that is most commonly observed
and that is considered 'opportunistic'
In summary, Candida is not a post hoc but an ante hoc cause.
Tumors are perceived as one phenomenon.
Tumors are one phenomenon, but there are many types. Why?
According to official views that see genetic alteration at the
basis of neoplastic development, it is possible that the alteration
can manifest itself in any environment with all possible typological
From the microbiological point of view, instead, it is always Candida
that invades various anatomical parts, evoking different reactions
as a function of the organs it feeds on. These behaviors are a
function of the quantity and quality of the affected tissues. An
organ whose connective tissue has been invaded defends itself with
cellular hyper-productions that attempt to encyst the fungin colonies
which are trying to completely colonize the organism.
It is in this way that the whole histological variety of neoplasias
can be explained. The histological variety appears not to be influential
in the determination of the cause, which is always and only Candida.
It is in this way that during a neoplastic event some genes can
be hyper-expressed - that is, amplified - in a defensive effort
determined by hyper-productive needs of the tissue. This reaction
is normal and not anomalous at all.
Consider the following example. If we take an inert thorn, for
example that of a sea urchin, and we inoculate it first in the
skin, then in the bronchi, the bone, brain and in other body areas,
we evoke an immune response of a cellular type tending to encyst
the thorn, that is, to form some kind of a cocoon in which to enclose
By the same token, the immune system interprets fungin colonies
beyond a certain dimension as extraneous foreign bodies stimulating
an encystment reaction that is produced with the type of cells
of the invaded tissue.
The thorn or the fungus can therefore cause, according to the case,
an epithelioma, an adenocarcinoma, an osteosarcoma, a gliobastoma,
and so on.
In the first moments of the invasion, the organism is able to
send mature cells to contain the proliferating fungi: this is the
phenomenon of a differentiated tumor. As the colonies become more
powerful, and tissues are exhausted, cells become more and more
immature up to anaplasia.
Furthermore, the ratio between differentiated tissues and connective
tissue existing in an organ determines the reaction capability
and thus the degree of malignancy of a neoplasia. The fewer noble
cells there are, the more malignant and invasive the tumor becomes.
So, on the one hand we have noble tissue which cannot be attacked
(muscles and nerves), and on the other the simple connective tissue.
The glandular tissue which is halfway between these two elements,
just because it is provided with that complex structure that confers
to it a certain ability of encysting the fungi, can oppose their
invasion by producing the phenomenon of the benign tumor. For example,
if we consider the thyroid, we can see how in this gland neo-formations
can take any graduation of malignancy even when they possess benign
histological characteristics, as is the case for capsulated follicular
carcinoma, long ago called metastasizing benign adenoma.
This can happen because the concept of a 'benign tumor' does not
have an absolute value. In this case, even if it is true that fungin
cells cannot normally go through the differentiated cells barrier,
that does not mean that under particular conditions they cannot
It is for this reason that such neo-formations are considered 'odd'
in oncology. But such oddities can be easily explained with the
interpretation key of fungin infection. When the glandular tissue
is exhausted, the benign tumor becomes a malignant one.
For all intents and purposes, it is always the same Candida attacking
different tissues, each time adapting itself to the type of environment
it finds. The specifications usually assigned to the various candidas
(Candida Albicans, Krusei, Parapsilosis, Glabrata, Tropicalis and
others) underestimate the fact that they all come from one single
progenitor which, when it genetically mutates to attack the host,
transforms itself into this or that stock.59
R.L. Hopfer for example found no less than four different Candida
species in the post-mortem cultures of a leukemia patient.
N. Aksoycan demonstrated that seven different stocks of Candida
actually have the same antigenic structure.
F.C. Odds reports how the same Candida stock can colonize different
anatomical areas at different times.
J. Hellstein has found the common clonal origin in Candida Albicans
for both commensal and pathogenic stocks.