Is the Cause of Cancer a Common Fungus?
by Dr Tullio Simoncini (oncologist)

According  to this hypothesis based on years of scientific and clinical research,  the cause of cancer is infection by a common fungus, Candida albicans.  The good news is that it can be treated with a powerful antifungal  agent that can't be patented (For treatment regimes see end of article).
My idea is that cancer doesn't depend  on mysterious causes (genetic, immunological or auto-immunological, as  the official oncology proposes), but it results from a simple fungal  infection whose destructive power in the deep tissues is actually  underestimated.
The  present work is based on the conviction, supported by many years of  observations, comparisons and experiences, that the necessary and  sufficient cause of the tumour is to be sought in the vast world of the  fungi, the most adaptable, aggressive and evolved micro-organisms known  in nature.
I  have tried many times to explain this theory to leading institutions  involved in cancer issues (the Ministry of Health, the Italian Medical  Oncological Association, etc.), elaborating on my thinking, but I have  been brushed aside because of the impossibility of setting my idea in a  conventional context. A different, international audience represents the  possibility of sharing a view about health which differs from what is  widely accepted by today's medical community, either officially or from  the sidelines…
In  considering the biological dimensions of the fungi, for instance, it is  possible to compare the different degrees of pathogenicity in relation  to the condition of organs, tissues and cells of a guest organism, which  in turn also and especially depend on the behaviour of the individual.
Each  time the recuperative abilities of a known psycho-physical structure  are exceeded, there is an inevitable exposure, even considering possible  accidental co-founders, to the aggression — even at the smallest  dimensions — of those external agents that otherwise would be harmless.  In the presence of an indubitable connection between patient morale and  disease, it is no longer legitimate to separate the two domains  (allopathic and naturopathic) which are both indispensable for improving  the health of individuals.
 Flaws in mainstream theories on cancer causation
When facing the most pressing contemporary medical problem, cancer, the first thing to do is to admit that we still do not know its real cause. However treated in different ways by both official and alternative medicine, cancer has an aura of mystery that still exists
around its real generative process…
In  agreement with the most recent formulation of scientific philosophy,  which suggests a counter-inductive approach where it is impossible to  find a solution with the conceptual tools that are commonly accepted,1 only one logical formulation emerges: to refuse the oncological principle which assumes that cancer is generated by a cellular reproductive anomaly.
However,  if the fundamental hypothesis of cellular reproductive anomaly is  questioned, it becomes clear that all the theories based on this  hypothesis are inevitably flawed. It follows that both an  auto-immunological process, in which the body's defence mechanisms  against external agents turn their destructive capacity against internal  constituents of the body, and an anomaly of the genetic structure  implicated in the development of auto-destruction are inevitably  disqualified.
Moreover,  the common attempt to construct theories about multiple causes that  have an oncogenic effect on cellular reproduction sometimes seems like a  concealing screen, behind which there is nothing but a wall. These  theories propose endless causes that are more or less associated with  each other; and this means in reality that no valid causes are found.  The invocation in turn of smoking, alcohol, toxic substances, diet,  stress, psychological factors, etc., without a properly defined context,  causes confusion and resignation, and creates even more mystification  around a disease which may turn out to be simpler than it is depicted to  be.
As  background information, it is important to review the picture of  presumed genetic influences in the development of cancer processes as  they are depicted by molecular biologists. These are the scientists who  perform research on infinitesimally small cellular mechanisms, but who  in real life never see a patient. All present medical systems are based  on this research, and thus, unfortunately, all therapies currently  performed.
The  main hypothesis of a genetic neoplastic causality is essentially  reduced to the fact that the structures and the mechanism in charge of  normal reproductive cellular activity become, for undefined reasons,  capable of an autonomous behaviour that is disjointed from the overall  tissular economy. The genes that normally have a positive role in  cellular reproduction are, then, imprecisely referred to as  "protooncogenes"; those that inhibit cellular reproduction are called  "suppressor genes" or "recessive oncogenes". Both endogenous (never  demonstrated) and exogenous cellular factors — that is, those  carcinogenic elements that are usually invoked — are held responsible  for the neoplastic degeneration of the tissues...
From  a very superficial analysis of the presumed oncological picture,  however, it seems to be clear how the assertion of all this unstoppable  genetic hyperactivity can do nothing more that unveil the abysmal  stupidity that is at the basis of this way of conceiving things. All  those who work in the field do nothing but repeat the stale litany of  reproductive cellular anomalies on a genetic basis.
It  is better to look for new horizons and conceptual instruments that are  capable of unearthing a real and unique neoplastic aetiology.
Back to taxonomy
In order to find the possible carcinogenic ens morbi on  the horizon of microbiology, it appears useful to return to the basic  taxonomical concepts of biology where we can see, incidentally, the  existence of a noticeable amount of indecision and indetermination.
Already  in the last century, a German biologist, Ernst Haeckel (1834–1919),  departing from the Linnaeian concept that makes for two great kingdoms  of living things (vegetable and animal), denounced the difficulties of  categorising all those microscopic organisms which, because of their  characteristics and properties, could not be attributed to either the  vegetable or the animal kingdom. For these organisms, he proposed a  third kingdom, Protista (protists).
"This  vast and complex world includes a range of entities beginning with  those that have sub-cellular structure — existing at the limits of life —  such as viroids and viruses, moving through the mycoplasms to, finally,  organisms of greater organisation: bacteria, Actinomycetes,  Myxomycetes, fungi, protozoa and perhaps even some microscopic algae."2
The  common element of these organisms is the feeding system, which, being  implemented (with very few exceptions) by direct absorption of soluble  organic compounds, differentiates them both from animals and vegetables.  Animals also feed as above, but especially by ingesting solid organic  materials that are then transformed through the digestive process.  Vegetables, by utilising mineral compounds and light energy, are capable  of feeding by synthesising the organic substances.
The  contemporary tendency of biologists is once again to pick up, though in  a more sophisticated way, the concept of the third kingdom. One goes  even further, however, arguing that within that kingdom, fungi must be  classified in a distinct category. O. Verona 3 says that if  we put multicellular organisms provided with photosynthetic capabilities  (plants) in the first kingdom and the organisms not provided with  photosynthetic pigmentation (animals) in the second kingdom — and  organisms from both these kingdoms are made of cells provided with a  distinct nucleus (eukaryotes) — and, furthermore, if we put in another  kingdom (protists), those monocellular organisms that have no  chlorophyll and have cells that are without a distinct nucleus  (prokaryotes), the fungi can well have their own kingdom because of the  absence of photosynthetic pigmentation, the ability to be monocellular  and multicellular, and, finally, their possession of a distinct nucleus.
Additionally,  fungi possess a property that is strange when compared to all other  micro-organisms: the ability to have a basic microscopic structure  (hypha) with a simultaneous tendency to grow to remarkable dimensions  (up to several kilograms), keeping unchanged the capacity to adapt and  reproduce at any size. From this point of view, therefore, fungi cannot  be considered true organisms, but cellular aggregates sui generis with  an organismic behaviour, since each cell maintains its survival and  reproductive potential intact regardless of the structure in which it  exists. It is therefore clear how difficult it is to identify all the  biological processes in such complex living realities. In fact, even  today, there are huge voids and taxonomical approximations in mycology.
Fungi characteristics
It is worthwhile to examine more deeply  this strange world, with such peculiar characteristics, and try to  highlight those elements that somehow may be pertinent to the problems  of oncology.
1) Fungi  are heterotrophic organisms and therefore need, as far as nitrogen and  carbon are concerned, pre-formed compounds. Of these compounds, simple  carbohydrates, for example monosaccharides (glucose, fructose and  mannose), are among the most utilised sugars. This means that fungi,  during their life cycle, depend on other living beings which must be  exploited in different degrees for their feeding. This occurs both in a saprophytic way (that is, by feeding on organic waste) and in a parasitic way (that is, by attacking the tissue of the host directly).
2) Fungi  show a great variety of reproductive manifestations (sexual, asexual,  gemmation; these manifestations can often be observed simultaneously in  the same mycete), combined with a great morphostructural variety of  organs. All of this is directed toward the end of spore formation, to  which the continuity and propagation of the species is entrusted.
3) In mycology, it is often possible to observe a particular phenomenon called heterokaryon,  characterised by the coexistence of normal and mutant nuclei in cells  that have undergone a hyphal fusion. Nowadays, phytopathologists are  quite worried about the creation of individuals that are genetically  quite different even from the parents. This difference has taken place  by means of those reproductive cycles, which are called parasexual.  The indiscriminate use of phytopharmaceuticals has in fact often  determined mutations of the nuclei of many parasitic fungi with the  consequent creation of heterokaryon — and this is sometimes particularly  virulent in its pathogenicity.4
4) In  the parasitic dimension, fungi can develop from the hyphas more or less  beak-shaped, specialised structures that allow the penetration of the  host.
5) The  production of spores can be so abundant as to include always, at every  cycle, tens, hundreds and even thousands of millions of elements that  can be dispersed at a remarkable distance from the point of origin 5 (a small movement is sufficient, for example, to implement immediate diffusion).
6) Spores  have an immense resistance to external aggression, for they are capable  of staying dormant in adverse conditions for many years while  preserving unaltered their regenerative potentialities.
7) The  development coefficient of the hyphal apexes after the germination is  extremely fast (100 microns per minute under ideal conditions) with  ramification capacity, thus with the appearance of a new apex region  that in some cases is in the neighbourhood of 40–60 seconds.6
8) The shape of the fungus is never defined, for it is imposed by the environment in which the fungus develops.  It is possible to observe, for example, the same mycelium in the simple  isolated hyphas status in a liquid environment or in the form of  aggregates that are increasingly solid and compact, up to the formation  of pseudoparenchymas and of filaments and mycelial strings.7
9) By  the same token, it is possible to observe in different fungi the same  shape whenever they must adapt to the same environment (this is called dimorphism).  The partial or total substitution of nourishing substances induces  frequent mutations in fungi, and this is further proof of their high  adaptability to any substrata.
10) When  the nutritional conditions are precarious, many fungi react with hyphal  fusion (among nearby fungi) which allows them to explore the available  material more easily, using more complete physiological processes. This  property, which substitutes co-operation for competition, makes them  distinct from any other micro-organism, and for this reason Buller calls  them social organisms.8
11) When  a cell gets old or becomes damaged (e.g., by a toxic substance or by a  pharmaceutical), many fungi whose intercellular septums are provided  with a pore react by implementing a defence process called protoplasmic flux,  through which they transfer the nucleus and cytoplasm of the damaged  cell into a healthy one, thus conserving unaltered all their biological  potential.
12) The phenomena regulating the development of hyphal ramification are unknown to date. 9  T h e y consist of either a rhythmic development or in the appearance  of sectors which, though they originate from the hyphal system, are  self-regulating , 10 that is, independent of the regulating action and behaviour of the rest of the colony.
13) Fungi  are capable of implementing an infinite number of modifications to  their own metabolism in order to overcome the defence mechanism of the  host. These modifications are implemented through plasmatic and  biochemical actions as well as by a volumetric increase (hypertrophy)  and
numerical hyperplasy of the cells that have been attacked.11
14 ) Fungi  are so aggressive as to attack not only plants, animal tissue, food  supplies and other fungi, but even protozoa, amoebas and nematodes.  Fungi hunt nematodes, for example, with peculiar hyphal modifications  that constitute real mycelial criss-cross, viscose or ring traps that  immobilise the worms. In some cases, the aggressive power of the fungus  is so great as to allow it — with only a cellular ring made up of three  units — to tighten its grip, capture and kill its prey within a short  time, notwithstanding the desperate struggling of the prey.
From  the short notations above, it therefore seems fair to dedicate greater  attention to the world of fungi, especially considering the fact that  biologists and microbiologists constantly highlight large deficiencies  and voids in all their descriptions and interpretations of fungi's  shapes, physiologies and reproductions. So the fungus, which is the most  powerful and the most organised micro-organism known, seems to be an  extremely logical candidate as a cause of neoplastic proliferation  [cancerous growth].
Imperfect fungi (so  called because of the lack of knowledge and understanding of their  biological processes) deserve particular attention, since their  essential prerogative sits in their fermentative capacity. The greatest  disease of mankind may therefore hide within a small cluster of  pathogenic fungi, and may after all be located with just some simple  deductions able to close the circle and provide the solution.
Candida albicans: a necessary and sufficient cause of cancer
Considering that among the human  parasite species the Dermatophytes and Sporotrichum demonstrate an  excessively specific morbidity, and that experience shows that  Actinomycetes, Toluropsis and Histoplasma rarely enter the context of  pathology, the Candida albicans fungus clearly emerges as the sole candidate for tumour proliferation [cancers].
If  we stop for a second and reflect on its characteristics, we can observe  many analogies with neoplastic disease. The most evident are:
1) ubiquitous attachment — no organ or tissue is spared;
2) the constant absence of hyperpyrexia;
3) sporadic and indirect involvement of the differential tissues;
4) invasiveness that is almost exclusively of the focal type;
5) progressive debilitation;
6) refractivity to any type of treatment;
7) proliferation facilitated by multiplicity of indifferent co-founders;
8) Symptomatological basic configuration with structure tending to the chronic.
Therefore,  an exceptionally high and diversified pathogenic potentiality exists in  this mycete of just a few microns in size, which, even though it cannot  be traced with the present experimental instruments, cannot be  neglected from the clinical point of view. Certainly, its present  nosological classification cannot be satisfactory because, if we do not  keep the possibly endless parasitic configurations in mind, that  classification is too simplistic and constraining.
We therefore have to hypothesise that Candida,  in the moment it is attacked by the immunological system of the host or  by a conventional antimycotic treatment, does not react in the usual,  predicted way but defends itself by transforming itself into ever  smaller and non-differentiated elements that maintain their fecundity  intact to the point of hiding their presence both to the host organism  and to possible diagnostic investigations.
Candida's behaviour may be considered to be almost elastic. When favourable conditions exist, Candida thrives  on an epithelium; as soon as the tissue reaction is engaged, it  massively transforms itself into a form that is less productive but  impervious to attack: the spore. If, then, continuous subepithelial  solutions take place, coupled with a greater areactivity in that very  moment, the spore gets deeper into the lower connective tissue in such  an impervious state that colonisation is irreversible.
In fact, Candida takes  advantage of a structural interchangeability, utilising it according to  the difficulties, e.g., in feeding, to overcome its biological niche.  In this way, Candida is free to expand to maturation in the  soil, air, water, vegetation, etc. — that is, wherever there is no  antibody reaction. In the epithelium, instead, it takes a mixed form,  which is reduced to the sole spore component when it penetrates the  lower epithelial levels, where it tends to expand again in the presence  of conditions of tissular areactivity.
The  initial mandatory step of an in-depth research endeavour would be to  understand if and in which dimensions the spore transcends, what  mechanisms it engages to hide itself or, again, to preserve its  parasitic characteristic, or if it has available a neutral quiescent  position which is difficult or even impossible to detect by the  immunological system. Unfortunately, today we do not have the  appropriate means, either theoretical or technical, to answer these and  similar questions, so the only valid suggestions can come solely from  clinical observation and experience. While not providing immediate  solutions, these sources can at least stimulate further questions.
Assuming that Candida albicans is  the agent responsible for tumour development, a targeted therapy would  take into account not just its static and macroscopic manifestations but  even the ultramicroscopic ones, especially in their dynamic valency,  that is, the reproductive. It is very probable that the targets to  attack are the fungi's dimensional transition points in order to perform  a decontamination with such a scope as to include the whole spectrum of  the biological expression — parasitic, vegetative, sporal and even  ultradimensional and, to the limit, viral.
If  we stop at the most evident phenomena, we risk administering salves and  unguents forever (in the case of dermatomycosis or in psoriasis), or  clumsily attacking (with surgery, radiotherapy or chemotherapy)  enigmatic tumoural masses with the sole result of facilitating their  propagation, which is already heightened in the mycelial forms. Why, one  may ask, should we assume a different and heightened activity of Candida albicans,  since it has been abundantly described in its pathological  manifestations? The answer lies in the fact that it has been studied  only in a pathogenic context, that is, only in relation to the  epithelial tissues.
In reality, Candida possesses  an aggressive valency that is diversified in function in the target  tissue. It is just in the connective or in the connective environment,  in fact, and not in the differentiated tissues, that Candida may  find conditions favourable to an unlimited expansion. This emerges if  we stop and reflect for a moment on the main function of connective  tissue, which is to convey and supply nourishing substances to the cells  of the whole organism. This is to be considered as an environment  external to the more differentiated cells such as nervous, muscular,  etc. It is in this context, in fact, that the alimentary competition  takes place.
On  the one hand, we have the organism's cellular elements trying to defeat  all forms of invasion; on the other hand, we have fungal cells trying  to absorb ever-growing quantities of nourishing substances, for they  have to obey the species' biological imperative to form ever larger and  diffused masses and colonies. From the combination of various factors  pertinent to both the host and the aggressor, it is possible to  hypothesise the evolution of a candidosis.
First stage: Integer epitheliums, absence of the debilitating factors. Candida can only exist as a saprophyte.
Second stage: Non-integer  epitheliums (erosions, abrasions, etc.), absence of stage debilitating  factors, unusual transitory conditions (acidosis, metabolic disorder,  and microbial disorder). Candida expands superficially (classic mycosis, both exogenous and endogenous).
Third stage: Non-integer epitheliums, presence of debilitating factors (toxic, stage radiant, traumatic, neuropsychic, etc.). Candida goes  deeper into the subepithelial levels, from which it can be carried to  the whole organism through the blood and lymph (intimate mycosis).12
Stages  one and two are the most studied and understood, while stage three,  though it has been described in its morphological diversity, is reduced  to a silent form of saprophytism. This is not acceptable from a logical  point of view, because no one can demonstrate the harmlessness of the  fungal cells in the deepest parts of the organism.
In fact, the assumption that Candida can  behave in the same saprophytic manner that is observed on integer  epitheliums when it has successfully penetrated the lower levels is at  least risky, because the assumption would have to be sustained by  concepts that are totally aleatory (i.e., dependent on chance). In fact,  we are asked not only to accept a priori that the connective environment is (a) not suitable to nourish the Candida,  but also at the same time to accept (b) the omnipotence of the body's  defence system towards an organic structure that is invasive but that  then becomes vulnerable once lodged in the deeper tissues.
As  for point (a), it is difficult to imagine that a micro-organism so able  to adapt itself to any substrata cannot find elements to support itself  in the human organic substance; by the same token, it seems risky to  hypothesise that the human organism's defence system is totally  efficient at every moment of its existence. As for point (b), the  assumption that there is a tendency to a state of quiescence and  vulnerability in the case of a pathogenic agent such as fungus — the  most invasive and aggressive microorganism existing in nature — seems to  carry a whiff of the irresponsible.
It  is therefore urgent, on the basis of the abovementioned considerations,  to recognise the hazardous nature of such a pathogenic agent which is  capable of easily taking the most various biological configurations,  both biochemical and structural, regardless of the conditions of the  host organism. The fungal expansion gradient in fact becomes steeper as  the tissue that is the host of the mycotic invasion becomes less  eutrophic and thus less reactive.

Benign tumours
To that end, it seems useful to consider  briefly the "benign tumour" nosological entity. This is an issue that  always appears in general pathology but is brushed aside most of the  time too easily, and it is overlooked because it usually doesn't create  either problems or worries. It constitutes one of those underestimated  grey areas seldom subjected to rational, fresh consideration.
If  the benign tumour, however, is not considered a fully fledged tumour,  it would be advantageous, for clarity, to categorise it in an  appropriate nosological scheme. If it is thought that, instead, it fully  belongs to neoplastic pathology, then it is necessary to consider its  non-invasive character and consequently to consider the reasons for  this. It is in fact evident how in this second scenario, the thesis  based on a presumed predisposition of the organism to autophagocytosis,  having to admit an expressive graduation, would stumble into such  additional difficulties such as to become extremely improbable.
By  contrast, in the fungal scenario, the mystery of why there are benign  and malignant tumours is exhaustively solved, since they can be  recognised as having the same aetiological genesis. The benignity or  malignancy of a cancer in fact depends on the capability of tissular  reaction of a specific organ expressing itself ultimately in the ability  to encyst fungal cells and to prevent them from developing in  ever-larger colonies. This can be achieved more easily where the ratio  between differentiated cells and connective tissue is in favour of the  former.
Situated  between the impervious noble tissues, then, and the defenceless  connective tissues, the differentiated connective structures (the  glandular structures in particular) represent that medium term which is  only somewhat vulnerable to attack because of an ability to offer a  certain type of defence. And it is in these conditions that benign  tumours are formed; that is, where the glandular connective tissue is  successful in forming hypertrophic and hyperplastic cellular embankments  against the parasites. In the stomach and in the lung, instead, since  there are no specific glandular units, the target organ, provided with a  small defensive capability, is at the mercy of the invader. 
Furthermore,  it is worth mentioning how several types of intimate fungal invasion do  not determine the appearance of malignant or benign tumours but a type  of particular benign tumour (specific degenerative alterations), as is  the case with some organs or apparatuses that do not have peculiar  glandular structures but nevertheless are attacked in their connective  tissue, although in a limited way. In fact, if we consider multiple  sclerosis, SLA, psoriasis, nodular panarthritis, etc., the possible  development of the fungus in a three-dimensional sense is actually  limited by the anatomic configuration of the invaded tissues, so that  only a longitudinal expansion is allowed.
Going  back to the precondition of areactivity that is necessary for  neoplastic development in a specific individual, it is permissible to  affirm how in the human body each external or internal element that  determines a reduction of wellbeing in an organism, organ or tissue  possesses oncogenic potentiality. This is not so much because of an  intrinsic damaging capability as much as a generic property of favouring  the fungal (that is, tumoural) flourishing. Then the causal network so  much invoked in contemporary oncology, which involves toxic, genetic,  immunological, psychological, geographical, moral, social and other  factors, finds a correct classification only in a mycotic infectious  perspective where the arithmetical and diachronic summation of harmful  elements works as a co-factor to the external aggression .
Conventional treatments vs antifungal therapy
With the theoretical basis of the tumour/fungus  equivalency demonstrated, it is clear how this interpretative key  offers a long series of questions concerning contemporary therapies,  both oncological (used without reference indexes) and antimycotic  (utilised only at a superficial level). Which path is best to walk  today, then, when faced with a cancer patient, since the conventional  oncological treatment, not being aetiological, can only occasionally  have positive effects and most of the time produces damage?
In  the fungal perspective, in fact, the effectiveness of surgery is  noticeably reduced because of the extreme diffusibility and invasiveness  characteristic of a mycelial conglomerate. Surgery to solve the problem  is therefore tied to the case; that is, to conditions in which one has  the luck to be able to remove the entire colony completely (which is  often possible in the presence of a sufficient encystment, but only  where benign tumours are concerned).
Chemotherapy  and radiotherapy produce almost exclusively negative effects, both for  their specific ineffectiveness and for their high toxicity and  harmfulness to the tissues, which in the last analysis favours mycotic  aggressiveness.
By  contrast, an antifungal, antitumour-specific therapy would take into  account the importance of the connective tissue together with the  reproductive complexity of fungi. Only by attacking the fungi across the  spectrum of all its forms, at points where it is most vulnerable from  the nutritional point of view, would it be possible to hope to eradicate  them from the human organism.
The  first step to take, therefore, would be to reinforce the cancer patient  with generic reconstituent measures (nutrition, tonics, regulation of  rhythms and vital functions) that are able to enhance the general  defences of the organism. 
Concerning  the possibility of having available pharmaceutical cures, which  unfortunately do not exist today, it seems useful, in the attempt to  find an antifungal substance that is quite diffusible and therefore  effective, to consider the extreme sensitivity of Candida towards sodium bicarbonate (i.e., in the oral candidosis of breastfed babies). This is consistent with the fact that Candida has an accentuated ability to reproduce in an acid environment.
Theoretically,  therefore, if treatments could be found that put the fungus in direct  contact with high sodium bicarbonate (NaHCO3) concentrations, we should  be able to see a regression of the tumoural masses. And this is what  happens in many types of tumour, such as colon and liver — and  especially stomach and lung, the former susceptible to regression just  because of its "external" anatomic position, and the latter because of  the high diffusibility of sodium bicarbonate in the bronchial system and  for its high responsiveness to general reconstituent measures.
By applying a similar therapeutic approach,  it has been possible in many patients to achieve complete remission of  the symptomatology and normalisation of the instrumental data.  It is important to emphasise that these cases are just an example of  what could be a new way of perceiving the complexity of medical  problems, especially in oncology. [Reports of seven cases of patients,  several of whom have been documented for 10 years following sodium  bicarbonate treatment, are summarised in the complete article at the web  page
http://www.curenaturalicancro.com/simoncini-writes.html  ; NEXUS Editor]
Critical considerations
It seems appropriate to analyse,  in a critical and self-critical spirit, what may emerge in neoplastic  pathology that is new and concrete. If we closely observe the proposed  therapeutic approach, it is possible to see that, independently of its  real effectiveness, it has value as an innovative theory. First, it  challenges the present methodology and especially its assumptions.  Second, it offers a concrete alternative proposal to a mountain of  conjectures and postures that sound authoritative but are too generic  and therefore ineffective.
The  identification of one tumoural cause, even with all the possible  general provisos, would represent a step forward that is indispensable  for escaping that passivity determined by a lack of results, and which  is responsible for medical behaviours that are based too much on faith  and not enough on real confidence. Given, therefore, that an  unconventional medical approach can benefit some patients better — from  any point of view — than the official treatments, and since valuable  results can be demonstrated, this should stimulate us to pursue further  research while avoiding patronising postures that are both limiting and  non-productive.
We  can therefore discuss whether or not sodium bicarbonate is the real  reason for the recoveries or if, instead, those recoveries are due to  the interaction of a number of conditions that have been created, the  results of unidentified neuropsychical factors, or maybe the results of  something totally unknown. What is beyond question, however, is  the fact that a certain number of people, by not following conventional  methods, have been able to go back to normality without suffering and  without mutilation.
The  message of this experience is therefore a call to search for those  solutions that are in accord with the simple Hippocratic obligation to  man's "well-being"; that is, we must be stimulated to a critical  evaluation of our contemporary oncological therapies which indubitably  can guarantee suffering. When we group together both malignant tumours  that are occasionally or never healed (such as lung and stomach) and  tumours that border with benignity (such as the majority of thyroid and  prostatic tumours, etc.) or put them together with those that have an  autonomous positive outcome notwithstanding chemotherapy (i.e.,  infantile leukaemia) — all of this appears to be devious and misleading,  having only the purpose of forging a consensus that would otherwise be  impossible to obtain with intellectually ethical behaviour.
The  fact that modern medicine not only cannot offer sufficient  interpretative criteria but even uses dangerous methodologies that are  also harmful and meaningless — even if carried out with good faith — is  something which must push us all to search for humane and logical  alternatives. At the same time, it is necessary to carefully,  open-mindedly and logically consider any theory or point of view that is  dared to be advanced in the battle against that monstrous and inhuman  yoke that is the tumour.
To  this end, a note of acknowledgement is to go to all those who are aware  of the harmfulness of conventional therapeutic methods and constantly  try to find alternative solutions. People like Di Bella, Govallo and  others, although guilty of utilising the same inauspicious principles of  official medicine (thus showing an excessively conformist mindset), are  actually using common sense by trying to relieve the suffering of  cancer patients through the use of painless methodologies, and in some  cases are able to achieve remissions, even though they're in the dark  about the real causes of
cancer.
In  an alternative perspective, then, it would be necessary to conceive a  new approach to experimentation in the oncological field, setting  epidemiological, aetiological, pathogenic, clinical and therapeutic  research in line with a renewed microbiology and mycology that would  probably drive us to the conclusion already illustrated: that is, the  tumour is a fungus — Candida albicans.
The  possible discovery that not only tumours but also the majority of  chronic degenerative disease could be reconciled to mycotic causality  would represent a qualitative quantum leap, which, by revolutionising  medical thinking, could greatly improve life expectancy and quality of  life. Such reconciliation might include a wider spectrum of fungal parasites (for example, in diseases of the connective tissues, multiple sclerosis, psoriasis, some epileptic forms, diabetes type 2, etc.).
In closing, considering that the world of fungi — those most complex and aggressive micro-organisms  —has  been bypassed and left unobserved for far too long, the hope of this  work is to promote awareness of the hazards of these micro-organisms so  that medical resources can be channelled not up blind alleys but towards  the real enemies of the human organism: external infectious agents.
Addendum: A Note on Cancer Treatment
The implications from my hypothesis that cancer is a fungus which can be eradicated with sodium bicarbonate are that:
1)  eighty years of genetic study and application has been for nothing,  especially considering that the genetic theory of cancer has never been  demonstrated;
2) the loss of millions, if not billions, of lives with all the suffering has been for nothing;
3) the billions of dollars spent on chemotherapy medicine, radiotherapy, etc. has been for nothing;
4) the recognition and prizes given to eminent researchers and professors has been for nothing;
5) the oncologist could be replaced by the family doctor; and
6) the pharmaceutical industry will incur tremendous financial losses (sodium bicarbonate is inexpensive and impossible to
patent).
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, an enema 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). (Note that  sodium bicarbonate should not be used as a cancer preventive.)
It  is important to treat each type of cancer with the right dosage. For  phleboclysis (drip infusion), 500 cc given in a series of intervals — 5%  strength on one day and 8.4% the next — is required, depending on the  patient's weight and condition; the stronger dose may perhaps be needed  in cases of lung and brain cancers according to the tumour type (primary  or metastatic) and size. 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 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 cancers (melanoma, epithelioma, etc.), a 7% iodine tincture should  be spread on the affected area once a day, 20–30 times consecutively in  one sitting, with the aim of producing a number of layers of crust. If,  after one month of treatment, the first crust is gone and the skin is  not completely healed, then the treatment should be continued in the  same manner until the second crust forms, heals and then comes loose  without any assistance. (The procedure is also applicable for treating  psoriasis.) After this treatment, the cancer will be gone and stay away  forever.
For more information, see "Protocol Treatments with sodium
biocarbonate solutions" at http://www.curenaturalicancro.com/cancer-therapy-simoncini-protocol.html  and FAQ sections at
By Dr Tullio Simoncini (oncologist) © 2007
Email: t.simoncini@alice.it
Website:
Nexus Editor's Note:
Due  to space constraints, we are unable to reprint Dr Simoncini's paper in  full. To download the complete paper including case study summaries, go  to the web page http://www.curenaturalicancro.com/simoncini-writes.html
Endnotes
1. Feyerabend, P.K., Contro il metodo ("Against Method"), Feltrinelli, Milano, 1994, p. 26
2. Verona, O., Il vasto mondo dei funghi ("The Vast World of Fungi"), Edizioni Nuova Italia, Firenze, 1973, p. 1
3. op. cit., p. 2
4. Rambelli, A., Fondamenti di micologia ("Basics of Mycology"), Edizioni Guida, Napoli, 1972, p. 35
5. op. cit.
6. op. cit., p. 28
7. Verona, op. cit., p. 5
8. Rambelli, A., op. cit., p. 31
9. op. cit., p. 28
10. op. cit., p. 29
11. op. cit., p. 266
12. op. cit., p. 273
About the Author
Based  in Rome, Italy, Dr Tullio Simoncini is a medical doctor and surgeon  specialising in oncology, diabetology and metabolic disorders. He is  also a Doctor of Philosophy. An humanitarian, he is opposed to any kind  of intellectual conformity, which he sees as often based on suppositions  without foundation or, worse, on lies and falsehoods. 
Dr  Simoncini regularly attends medical conferences and does interviews to  explain what's wrong with conventional cancer theories and treatments,  to present his fungal theory of cancer and to describe case studies  involving patients healed with sodium bicarbonate, a powerful  antifungal. His book, Cancer is a Fungus: A revolution in the therapy of tumours ( Edizioni Lampis), is available in Italian, Dutch and English from the website http://www.cancerfungus.com .
For  more information on Dr Simoncini's theory, therapy and case studies,  and to view interviews and testimonials, visit the portal website
Edited From – NEXUS New Times Magazine AUGUST–SEPTEMBER 2007 
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http://www.alternative-cancer-care.com/Cancer_Fungus.html
http://www.doctorfungus.org/Thefungi/img/candida.jpg
https://newsline.llnl.gov/articles/2008/may/images/05.16.08/fungus.jpg 
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