GiGi
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(Questions in background - photos displayed) "The spirochetes that you can see on Darkfield - you have to use a marker, a serum marker, that stains them in a certain way. So then you can detect them, because they are very small and there are limits to the microscope. If you have the Rife microscope, you could certainly see them. The ......can blow it up this much more.
But also remember, the spirochetes are in three forms in the tissue. There are fully grown spirochetes, only present in an untreated patient. The moment you throw any treatment in there, they do two things: they either go inside the cell, called L-form: comes from the name Lister (Lister was a British microbiologist); they lose their ..... and shed their cell wall and their shape and they look like a little dot, like a little grain of sand inside the cell - you can no longer tell what it is. The other thing they do outside the cell is that they can encyst themselves within a fraction of a second --- when you put any toxin in there, they go into a cystic form.
The cystic form can withstand fire up to 1000 degrees, and basically the only thing that is going to survive after you are all gone is the spirochete cysts in you. That is the only way that we are going to be able to tell that you were there.
When you do Darkfield microscopy, there are two ways of looking -- on is the instant view that you get and the other one is to wait until the slide is outside the body, so the temperature is going to be sinking down from 37C to the room temperature of whatever - 19C; so the cell is going to become inhospitable for the bugs inside. So in their last attempt to try to survive, they come out of the dying red cells and white cells that are on your slide and trying to find a place to escape to where they can survive, and we can watch them do that. So one way of diagnosing is to wait for that moment, and it is amazing what comes out of the cells.
Gitte Jensen, who I mentioned before, she did a wonderful research project:
Little brief: knowledge that we have is that Red Blood Cells do not have DNA - they do not have a nucleus with DNA in it. So what she did, simply, is to look at whether a red blood cell is infected - is very simple - you just need to look for DNA in the red blood cells; if you find DNA in there, you know that it is foreign; it is alien. So she found that over a lifetime the DNA in our RBC is in a linear progression more and more and more toward the end of life. That's one thing she did. And another study she published was that there is a direct relationship between the subjective feeling of wellness and the amount of foreign DNA found in your Red Cells. Phantastic study. It simply shows that illness is nothing else, but an accumulation of foreign bugs in us.
She also found that the DNA in white cells; white cells do have a nucleus and have DNA in them, and the DNA in white cells and other body cells toward the end of our life is twice as long as it was when we were born. That means, at the end of our life, we are only half 'us' and half 'them.' That was a huge finding. That should have been on Time Magazine on the cover. It is a huge discovery! And of course Lyme Disease just being one of the many bugs that contribute to that. I apologize for not having here here - she probably would have come, I came too late to realize that she is an important person.
Here is a little bit of literature: 22% of horseflies, deerflies and mosquitos are infected with Borrelia and coinfections in endemic areas, which is now - the endemic area in the US is the US - so there is no illusion about that! And you have the paper somewhere in your handout, the cystic form ..........(I did this a year ago - it was just published by Bradford who we just mentioned, but now there are many papers out in good peer review papers confirming that there is this magical cystic form of Lyme Disease, which we still don't know how to treat.
It is assumed that metronidazole and tinidazole is cracking those cysts. I do feel it is an illusion by deluded researchers, because I remember sitting at the microscope in India (did years of research/treatment there) and we worked with metronidazole, everybody was on high doses of flagyl there, and it did not crack anything! So I think it is more like a well wishing right now. I do not believe that metronidazole or tinidazole will lastingly open the cysts up.
I think the solution will definitely be to change the inner environment, the milieu, so the cyst does not feel like hatching. C., do you know anymore hard scientific ------ ? (not understandable)
Just ask the question: Did you ever have a course of antibiotics in your life? That for me clarifies that issue, because all the experiments they did on the cystic form -- you give a patient one pill, and immediatley you have the cysts appearing everywhere in the body. That pretty much includes all of us here in the room.
There is also some fairly good biological research that shows that the amino acid cysteine is cracking the cysts. Easy to remember - cysteine - cysts. That is something that needs to be explored. We know from worms, from resisting worms that are much tougher than the spirochete cysts, that cysteine works brilliantly through a biochemical process; the cyst is made up of a certain material and it simply is reactive with cysteine. That has not been explored, but should be. (Question.) I don't know, I just know from worm cysts very well that it is highly reactive with the amino acid cysteine and is a big cyst breaker, in a gentle way."
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map1131
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Oh my goodness. I've posted lately about my darkfield experiences. My naturopath and I watched a bad guy break through the wall of one of my red blood cells. She freaked because she had never seen anything like it.
I was her first lyme patient (that she knew of), boy did she get an education on lyme from me. It was my job to teach her and I did. She was able to diagnose a woman that was ill and couldn't get any answers as to why she was ill from a long list of docs. When she looked at this womans blood with darkfield she told her, I know your twin sister. Her blood two weeks ago looks exactly like your. Finally this lady knew it was lyme.
This naturopath has another patient that is slowly dying. She has been told for 20 years she has MS. Ten years ago a doc did a WB and told her she was just alittle positive, so it's not lyme disease. Dumb@&!#. This naturopath had done everything to try to convince this woman she has lyme. She even had me come in and talk to the woman. This woman says it's not lyme, it's MS. She will be dead soon, that's how bad she is. We tried.
Gigi, I will print this and let my naturopath see it. It will help her with others. She has my darkfield on vhs tape.
Thanks, Pam
-------------------- "Never, never, never, never, never give up" Winston Churchill Posts: 6478 | From Louisville, Ky | Registered: Jan 2002
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could someone compare and contrast the role of cysteine mentioned in the conference with its other role, mentioned the abstract below, about hemolysis(destruction) of red cells.
secondly, would NAC, N-acetylcysteine do the same as cysteine, but only at a slower rate? i don't know. if NAC metabolizes to cysteine, then this would suggest that its a potential inducer of hemolysin; thusly, and hence red blood cell destruction.
lastly, consuming a lot, either of NAC and/or cysteine would necessitate taking a lot of vits. B12, Folate, B6, magnesium, and whatever else, to prevent formation of homocysteine.
in the medical abstracts section, i searched the word,'cysteine,' and found two relevant abstracts.
Any thoughts?
Title: Hemolytic activity of Borrelia burgdorferi. Authors: Williams LR, Austin FE Source: Infect Immun 1992 Aug;60(8):3224-30 Organization: Department of Microbiology and Immunology School of Medicine University of Louisville Kentucky 40292.
Abstract: Zones of beta-hemolysis occurred around colonies of Borrelia burgdorferi grown on Barbour-Stoenner-Kelly medium containing agarose and horse blood. Blood plates were inoculated with either the infective strain Sh-2-82 or noninfective strain B-31 in an overlay and incubated in a candle jar. Both strains of B. burgdorferi displayed beta-hemolysis after 1 to 2 weeks of incubation. The hemolytic activity diffused out from the borrelial colonies, eventually resulting in lysis of the entire blood plate. Hemolysis was most pronounced with horse blood and was less intense with bovine, sheep, and rabbit blood. Hemolysis was enhanced by hot-cold incubation, which is typical of phospholipase-like activities in other bacteria. Further characterization of the borrelial hemolysin by using a spectrophotometric assay revealed its presence in the supernatant fluids of stationary-phase cultures. Detection of the borrelial hemolytic activity was dependent on activation of the hemolysin by the reducing agent cysteine. This study provides the first evidence of hemolytic activity associated with B. burgdorferi.
Title: Incorporation of cysteine by Borrelia burgdorferi and Borrelia hermsii. Authors: Sambri V, Cevenini R Source: Can J Microbiol 1992 Oct;38(10):1016-21 Organization: Institute of Microbiology University of Bologna Italy.
Abstract: The growth rate of Borrelia burgdorferi and Borrelia hermsii in BSK II medium prepared with cysteine-free or cysteine-containing (0.185- 5.92 mM) CMRL 1066 medium was studied. In media with cysteine-free CMRL 1066, growth of borreliae was detectable, although it was reduced by approximately 80%. Bacterial growth was maximal when the concentration of cysteine in CMRL 1066 reached 1.48 mM, which represents the standard cysteine concentrations of the medium; higher concentrations inhibited the growth of borreliae. Cysteine incorporation, measured by the uptake of radiolabeled cysteine, showed that cysteine enters B. burgdorferi and B. hermsii cells by passive diffusion. Labeling studies of borreliae with [35S]cysteine indicated that B. burgdorferi has several cysteine-containing proteins, including ones at 22, 30 (OspA), and 34 kDa (OspB), whereas B. hermsii showed only two [35S]cysteine-incorporating proteins, at 22 and 24 kDa, which were exposed onto the outer cell surface. In addition, most of the cysteine-incorporating proteins could be biosynthetically radiolabeled when bacterial cells were grown in vitro with [3H]palmitate, and the differences in cysteine incorporation observed between B. burgdorferi and B. hermsii were found to be correlated with differences in lipoproteins.
Keywords: Bacterial Proteins, AN, Borrelia, DE, GD, ME, Borrelia burgdorferi, DE, GD, ME, Cysteine, PD, PK, Electrophoresis, Polyacrylamide Gel, Support, Non-U.S. Gov't, Medline File
Language: French Unique ID: 93121225
some things(not inclusive) that i get from reading the abstract just above:
1. Cysteine-free media growth of Bb reduced by 80% 2. 1.48millimoles of cysteine, the standard dose of cystein in the growth media maximized Bb growth. 3. a dose of cysteine in the media greater than 1.48millimoles inhibited Bb growth. 4. Bb just lets cysteine in freely(passive diffusion). No apparent resistance to keeping it out. This might imply that hooking up silver to cysteine might kill Bb. i could imagine that this silver-cysteine could also kill the person, as well--before, or after killing Bb.
Notes: a. A conversion/extrapolation formula for the corresponding human dose of cysteine exists for the 1.48millimolar dose in the media. Simplistically, this ``might'' be one basis for figuring one's dose of cysteine should they wish to take cysteine.
GiGi
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I want to emphasize here that Dr. K. was addressing mainly medical professionals, MD's and DDS's and Scientists/Researchers when he talked about Cysteine during this 3-day conference. He was not addressing do-it-yourself Lymies -- maybe a couple! So please take that into consideration.
I have posted many times that it is not advisable to take NAC without the guidance of a professional who fully understands what it does and when it can be and when it cannot and should not be taken. More clearly - it can readily take the "bad stuff" into the brain instead of out of the brain - . So please, do not play with NAC. The people who have taken it probably know what I am talking about.
Dr. K. said clearly addressing the people he knows in the audience that "cysteine" should be explored, meaning just that -- exploring it.
Topic Date Forum Infra-Red Sauna 16 May, 2005 Medical Questions can someone explain these tests to me? 03 March, 2005 Medical Questions NAC - should you take it? 02 August, 2004 Medical Questions HEAVY METALS 29 June, 2004 Medical Questions Glutathione update 30 May, 2004 Medical Questions
Posts: 9834 | From Washington State | Registered: Oct 2000
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Who is Dr. K? Or where online can I get info about the conference you're talking about?
Thanks for posting. It's very interesting, although I have to say that hearing that Flagyl probably doesn't break open the cysts as I thought it did, is discouraging.
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Areneli
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Please write who is Dr.K. Obviously he is a public person so you could give here his name.
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Boomerang
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quote:Originally posted by psano: Who is Dr. K? Or where online can I get info about the conference you're talking about?
Thanks for posting. It's very interesting, although I have to say that hearing that Flagyl probably doesn't break open the cysts as I thought it did, is discouraging.
I noticed that too....very frustrating.......
Our LLMD says Flagyl does the cyst busting...and it's been used for that for years. Stange report.
I don't know who that doctor is either? Please enlighten.
SForsgren
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I have the Dr. K protocol linked from my Protocols page below and you can also see my notes from the conference there. Additionally, the direct URL is www.neuraltherapy.com.
-------------------- Be well, Scott Posts: 4617 | From San Jose, CA | Registered: Jul 2005
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map1131
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IMO, Dr K and his reports and studies should be on every lyme or vector borne illness person's list as a must reading.
This doc has more insight into the big picture here and if he reports it, it's worth thinking considering.
Pam
-------------------- "Never, never, never, never, never give up" Winston Churchill Posts: 6478 | From Louisville, Ky | Registered: Jan 2002
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SForsgren
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A-a-men Pam. I have looked for information that made sense since last July and Dr. K has the most comprehensive approach in my opinion for those that want non-ABX routes or as an adjunct.
-------------------- Be well, Scott Posts: 4617 | From San Jose, CA | Registered: Jul 2005
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In my opinion, he is one of the last great doctors out there. I am so glad he exists and is so very passionate about his work.
Posts: 856 | From Texas | Registered: Jan 2005
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To your knowledge .. just talking about the cyst form here..I know there are many immune evading tactics of Bb -- but does it also form cysts in response to an active immune system (active against the particular Bb organism), and can (theoretically) those cysts be penetrated by front line immune cells?
Mo
Posts: 8337 | From the other shore | Registered: Jul 2002
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two problems w/rt the links i posted above, with the first being something having gone awry when i converted the originally posted, but extremely long url into the form expressed by http://www.tinyurl.com
secondly, i can't get into the medical abstracts again in order to convert the the two links. will do so when i'm able to get into the med.abstracts section of this site.
to find cysteine, go to medical abstracts,this section, then enter the word,'cysteine' in the search field. cysteine and hemolysin are mentioned in one of the first 4 links, pulled-up for your search.
posted
one possible explanation for the hypothesized positive effect of cysteine mentioned in the conference referred to:
in lymies, at least,cysteine induces hemolysin production according to the abstract pulled-up in the medical abstracts section of this site.
hemolysin destroys the erythrocyte, thereby leaving borrelia and babesia, at least temporarily exposed, free in teh blood stream. if exposed in the blood stream, then its "open season" on Bb and babs by the immune system, and/or antibiotics to which they are susceptible.
one amongst many downsides to destroying red cells would be the release of free iron,other forms of iron, and free copper, and other forms of copper into the blood stream. in turn, being free, these two elements will then promote/catalyze(?) free radical production, the extent to which would be dependent on, among many other variables, the dose of cysteine taken. in a very sick person, a small, moderate or large dose of cycteine for a period of time could get one a garaunteed 'spot o' tea' in the e.r., and/or the cardiac intensive care unit, i would think.
posted
just a note to say that i've edited my original post, by splicing two actual abstracts on cysteine into it.
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oxygenbabe
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Thanx for pulling this up as I didn't see it the first time around.
Finally someone saying what I always thought--that the idea that tini or flagyl busts cysts was just...a silly idea!!!! I never understood where this assumption came from.
Since flagyl works on h. pylori, though, I thought perhaps tini and flagyl have an inhibitory effect on flagella...including those of spirochetes. If you slow them down then maybe they are less effective, less able to wiggle through tissue and burrow in.
That was always my hypothesis. I wonder what Dr. K would think of that.
That data on rbc's is interesting.
Posts: 2276 | From united states | Registered: Jun 2004
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didn't either and/or both brorson&brorson, and dorward(?) publish abstracts on tinidazole's and/or flagyl's effects on at least two form of Bb ? best i recall, at lest one of their abstracts on in vitro effects addressed the one of the non-spirochetal forms.
whats the latest thinking on the effects of these two abx? who wrote on the effects on flagella? i've benefited significantly from these two abx.
i more or less answered my own question. its was almost rhetorical.
for now, i presume that amongst all other metabolic routes taken, the change from nac to cysteine is one such route; its almost a given.
the acetyl group of atoms(1)is hooked up to the nitrogen atom-end of cysteine. this group of atoms, is easily, either removed, attached to, and otherwise transferred/switched to different molecules, or the same molecule by enzymatic and non-enzymatic metabolic routes of the body.
in my most reductionist, non-cynical view, while nac may be found in the body(i don't know), making this commercially, serves the dual function of getting a patent on a product which, in this case, is an amino acid, cysteine.
the chemist puts the acetyl group of atoms on a molecule, and bingo!...the marketing dept. reports in the media significant results in conditions a-to-z...barney's testicles are f-i-n-a-l-l-y descending, and big bird had her very first period !
1)this is acetic acid, as found in vinegar for example, whose -COOH group of atoms is hooked up with the nitrogen in the cysteine.
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In reference to Dr K I'd like to mention DR Issels.
Josef issels was a huge influence on Dr klinghardt and I very impressed by DR Issel's work. For him integrative medicine meant having a dentist in his hospital!
With CFS/Lyme we have a chronic illness without signicant pathology as in Cancer, but apart from that his model is very useful for us.
From the 50's he was looking at Mycoplasma's in relation to chronic illness.
wallace www.issels.com HOLISTIC INTEGRATIVE APPROACH TO CANCER : THE ISSELS TREATMENT Ilse Marie Issels
Josef M. Issels, M.D., is remembered worldwide as the foremost pioneer of the holistic integrative approach to cancer and chronic degenerative disease.
He developed a very comprehensive logistic treatment system which he first published in 1953 and administered to approximately 15.000 cancer patients in the hospital and clinic he founded in 1951 at Lake Tegernsee near Munich/Germany. In 1970 the hospital was enlarged from 80 to 120 beds with extensive research facilities including a dental ward (for the diagnosis and treatment of focal infection) , immunological and microbiological departments where various vaccines were developed. Programs included research on pleomorphism (Enderlein), microbes in oncogenesis, for example mycoplasma (Gerlach), autologous vaccines (Issels), mixed bacterial vaccines (Coley), darkfield microscopy, hyperthermia etc. The facility provided state-of-the-art medical care in a resort setting.
It was the first hospital of its kind, designed for the immunobiological treatment of cancer patients who had exhausted conventional treatments. Over 90% of all patients were suffering from progressive metastatic cancer, and too often in the terminal stage. The massive confrontation with these patients posed new problems of therapy which had not been considered in classic cancer therapy, that is the treatment of the tumor alone. The possibility of daily clinical observation and comparison of similar incurable cases for months at a time - the research at the bedside - permitted new experience, centered on the body's natural defense, repair and regulatory mechanisms.
Dr. Issels summarized his conclusions from this experience in his holistic concept of the development of chronic degenerative disease and malignancy. It serves as the fundament for his comprehensive treatment strategy which attends to b o t h the disease symptoms and the causes and preconditions for the development of these symptoms. In the case of cancer the treatment is not only directed at the malignant tumor, but also at the correction of the preconditions for the formation of the tumor. It aims at the restoration of the natural defense, repair and regulatory mechanisms of the cancer afflicted person as a whole.
Research has shown that every vertebrate organisms is constantly threatened by cancer cells whose formation is a daily occurrence. Not every newly produced cancer cell leads to a tumor, as the body possesses a natural defense system. The system with the highest differentiation within the entity of the natural defenses is the cellular immune system. This has a homeostatic control function or immune surveillance according to the concept of Thomas. It is this system which differentiates between "self" and "non-self" and destroys alien or outlaw cells including cancer cells. Thus an intact immune system and intact regulation of physiological cell death (Villunger, Strasser) is capable of protecting the organisms from the development of a malignant tumor.
Dr. Issels differentiated between two causal complexes in the development of cancer, namely:
the factors which induce the transformation of a normal cell into a cancer cell, and those factors which impair the immune and regulatory systems to an extent that they cannot prevent cancer cells from developing into a tumor. According to Buttersack, Eppinger, Schade and others the defense potential is a multi-layered structure of numerous, very different functional systems embracing virtually the whole body. During the decades of treating advanced cancer, Dr. Issels observed the synergistic effect of treatment modalities that comprise all the defense zones.
Table 1 Interaction between the Neuro-Hormonal Control System and the Four Defense Zones.
Luckey and Schmid differentiate between four successive defense zones:
The adaptive "extracorporal defense zone". It consists of the physiological obligatory microflora on all epithelial surfaces with its autonomous defense function. It is responsible for the development of the "basic immunity of the organism" ( Gordon, Luckey and Miyakawa). The functional integrity of the other defense zones can only be guaranteed by a healthy eubiotic microflora. The functional integrity of the other defense zones can only be guaranteed by a healthy eubiotic microflora.
The constitutive "epithelial defense zone". It consists of all epithelial surfaces and performs defense, filtration, excretion and absorption (Carbonara, Crabbe, Heremans, Mitchison). The excretory function of this zone is of special importance for the elimination of metabolic and oncolytic toxins. A back flow of the waste products leads to a blockade of this system with all the consequences for the other zones, and thus to an impairment of the defense potential.
The constitutive "lympho-reticular defense zone". It consists of the "lympho-epithelial system" with the thymus, the Waldeyer's tonsillar ring, the Peyer's patches, the "lympho-retothelial system" such as the white pulp of the spleen, the lymphatic centers, the white bone marrow and the storage endothelia. The importance of this zone has been shown by the research work of Alexander, Good, Hellstrom, Klein, Nossal, Old, and others.
The constitutive "reticulo-histiocytary defense zone" . It is the pluripotent mesenchyme which embraces almost half of the body weight. It is also called the regulatory ground system (Pischinger) with its various functions such as the stem cell function; the transit function that intervenes between nerves, organ cellss, blood, lymphatic and intestinal cells; the homeostatic function; the defense, detoxification and storage functions.
These four defense zones are successive, are closely interrelated and - what is often neglected - they are under neuro-hormonal control. They do not only fulfil defense but also other vital functions.
The blockade of only one function of one of these zones, for example of the excretion belonging to the second zone, or even the blockade of the control system such as the diencephalon or the autonomous nervous system on its own, may contribute indirectly to a lowering of the defense potential.
The activities of the kybernetic synergism of the four defense zones are defined by some authors as the "big resistance". The resistance is a very complex mechanism which is not alone to be seen in the much discussed importance of the T-and B-lymphocytes. It is an accomplishment of the entire organism and therefore holistic.
To achieve optimal results treatment should cover all the defense zones including the control system whose importance has been shown by the research findings of psychoneuro-immunology.
The Issels Treatment comprises the person as a whole - body and mind. It is based on the concept of oncogenesis (Issels 1953) as outlined under table 2 :
TABLE 2 - Hypothesis of the Pathogenis of Cancer.
Pre-and post-natal endogenous and exogenous factors (I) can lead by mutagenic, toxic, sensitizing and neural effects via the transit mesenchyme to secondary damage (Roessle) (II) to organs and organ systems as well as to functional disturbances of the neural, hormonal, excretory and defense systems.
Affects on the detoxifying and excretory systems deteriorate the endogenous environment or "milieu" and can lead to complex metabolic disturbances which are common to all chronic degenerative diseases and vary according to constitution and disposition.
Further constant influence of the causal factors and the persistence of secondary damages can impair the defense, repair and regulatory mechanisms to an extent that produces an imbalanced condition which, in the case of a genetic predisposition, can gradually develop into a "tumor-milieu"(III). This constitutes a specific endogenous environment which provides the ideal medium for cancer cells, and microorganisms found in cancer, to thrive. From such pre-cancerous condition (III), when defense potency is lowered further, a malignant tumor may develop at the site of least resistance.
With the manifestation of the malignant tumor (IV) and its symptoms (V) the cancer disease enters the recognizable phase and conventional treatment starts with the weapons directed against the tumor and the cancer cells. However, the latent pathological processes preceding and producing the manifestation of the tumor, remain chronically active, even after elimination of the tumor; hence the high rate of recurrence after standard cancer treatment.
Standard cancer treatment is based on the "localistic" concept that views the malignant tumor as the beginning of a disease which progressively spreads throughout the body. This interpretation of cancer makes all measures of treatment concentrated on the tumor, seem causal and exhaustive. They are exhaustive in those cases in which the immune system is capable to recuperate after alleviation from the tumor load (Rubin).
The holistic concept views cancer as a systemic disease from the onset and the tumor as its late stage symptom. This concept, therefore, calls for a holistic strategy in order to achieve optimal treatment results.
Based on the holistic concept, the Issels Treatment has two main lines of approach to cancer which complement each other:
A. Treatment aiming at the removal or reduction of the tumor :
Surgery Radiation Chemotherapy Hormonetherapy Hyperthermia and other non-toxic modalities Specific Immunotherapy. B. Non-specific immunobiological basic treatment aimed at the restoration of the impaired defense, repair and regulatory functions of the tumor host.
The basic treatment is modified to suit each individual patient's needs. It includes:
Elimination of all seizable exogenous and endogenous causal factors that may lead to an impairment of the immune functions and may contribute to a transformation of symbiotic microorganisms into pathogens: a) Malnutrition to be replaced by a diet designed to meet the special needs of the individual cancer patient (Budwig, Gerson, Hildenbrand), with supplementation of vitamins, anti-oxydants, minerals, trace elements, enzymes;
b) Abnormal bacterial intestinal flora to be normalized by diet and long term ad- ministration of coli cultures (Nissle) and probiotic cultures;
c) Head foci of infection such as dental, alveolar and tonsillar foci to be removed by surgical intervention (Issels, Pischinger);
d) Fields of neural disturbance to be neutralized by neural therapy (Huneke). Neural therapy and acupuncture are also administered in conjunction with conventional pain therapy;
e) Hereditary allergoses and toxicoses to be treated by administration of specific colloids (Issels, Spengler);
f) Environmental and occupational factors and addictions to be rectified by change of life style;
g) Psychic stress to be relieved by psychological guidance, in single and group therapy, biofeedback, relaxation techniques, meditation, visualization;
h) Physical therapy, hydrotherapy, breathing techniques, massage, lymph drainage etc.
Treatment of secondary damage and metabolic disturbance to restore normal function of organs by: a) Activation of cellular respiration by oxygen-ozone therapy in various forms, ultraviolet blood irradiaton;
b) Regeneration of organs and compensation of losses by administration of organ extracts or organ hydrolysates, (e.g. liver extract, thymus peptides);
c) Therapy to improve detoxification, i.e. elimination of toxins resulting from oncolysis, and of metabolic residues by activation of liver and kidney function assisted by herbal extracts and high fluid intake, colon hydrotherapy, enemas;
d) Enzyme therapy with lytic enzymes to eliminate immune suppressive factors such as immune complexes;
e) Homeopathy, Isopathy.
Stimulation of immune response by: a) Hyperpyrexia, i.e. the injection of bacterial lypopolysaccharides, e.g. an autolysate of streptococci and bacterium prodigiosum (Coley), to raise body temperature up to 104 F. Hyperpyrexia fights latent infections, loosens regulative blockades, improves detoxification, damages cancer cells, temporarily raises the white blood count up to 30 - 40,000 and increases the release of interferon and interleukin. Over the past 40 years more than 100,000 applications were given in the Issels Hospital and Clinic in Germany without any adverse side effects.
Biological Response Modifiers, Autologous Vaccines. The vaccines were developed in the Microbiological Department of the Issels hospital. From 1958 until 1973 Dr. Franz Gerlach was its director of research. He was a Professor of the University of Vienna, a researcher of the Pasteur Institute in Paris, well published in peer- reviewed medical journals, and internationally renowned for his research on mycoplasma and cancer. In the Issels hospital, thousands of mice served for a variety of studies, all of which confirmed that mycoplasma species can be causative or co- factors in oncogensis.
To quote Gerlach: "Mycoplasmas are, synergistically with other factors, essential and obligatory for oncogensis". For example, after cell free depot inoculation of mycoplasmas under the skin of 209 albino mice, 90.9% developed all types of malignancies, whereas of 600 control animals which were not inoculated, only 0,83% developed cancer.
Over the last hundred years, other scientists have as well associated microorganisms with oncogenesis. Recent research by reputable US scientists confirms the involvement of certain mycoplasma species in cancer (S.C.Lo et al.), the Gulf War Syndrome, Chronic Fatigue, Fibromyalgia and Rheumatoid Arthritis (Nasralla M., Nicolson G.L.et al.)
The mycoplasma vaccines developed in the Issels hospital were administered within the comprehensive treatment program.
Clinical observation showed that even in an advanced stage of malignant disease an immune reaction with complete long term remission can be achieved. The basic therapy seems to improve the immune reactivity of the body and the efficacy of applied tumor antigens. This may explain why tests in some cancer centers where only tumor antigens were given without the basic treatment, did not achieve the same results and led to such statements as " tumors of a certain size cannot be influenced immunologically".
The importance of the basic therapy can be seen in the fact that with its use immune paralysis simulated by intoxication could be eliminated within a few days and a sufficient immune response was achieved. In the Issels Hospital and Clinic it was repeatedly observed that by the elimination of foci, above all infected devitalized teeth and chronically infected tonsils, or with an active fever therapy, a blockade of the neuro-hormonal systems was broken.
Table 3 - Table 4 - Table 5 - Table 6
Especially during the first years of the development of the Issels Treatment, it became evident: Specific immunotherapy was more effective when causal factors could be eliminated systematically and detoxification mechanisms and herewith the endogenous environment, the "milieu", could be normalized.
The normalization of the detoxification processes is an essential part of basic therapy. This is generally ignored in research and practice. Despite all efforts, even to-day many patients are lost who respond well to the tumor antigens, but who are not able to excrete the products of tumor lysis. Without sufficient detoxification neither immunotherapy nor chemotherapy will achieve long term results.
In patients with a rapidly growing tumor who cannot expect immediate help from long term immunotherapy, the latter is combined with chemotherapy according to the morphology of the tumor. Thus the progression of the tumor growth can be stopped and the patient gains time to respond to immunotherapy. In qualified cases, cautious short term administration of chemotherapy avoids the severe immune suppression associated with prolonged use of these drugs (Frei). Experience of 40 years has shown that chemotherapy combined with basic therapy, has less toxic side effects, and in special cases, when given in lower than the standard doses, it has the same cytotoxic effect. Thus many patients can be helped who would die, if only one of these therapies were used.
It has also been observed that through comprehensive immunobiological treatment alone or in combination with chemotherapy, a variety of inoperable tumors can be rendered operable. Blocked ureters or gall bladders can be freed, making it possible to continue treatment of patients who would otherwise be lost.
A decisive improvement of cure rates can be achieved through comprehensive immunotherapy as follow-up treatment shortly after standard treatment, such as surgery, radiation and chemotherapy. The restoration of the immune functions can reduce the incidence of recurrence from about 50% (World Statistics) to 13% by combined conventional treatments and comprehensive immunotherapy.
Josef M. Issels, M.D. reported in "Immunotherapy in Progressive Metastatic Cancer, A Fifteen Year Survival Follow-up" 1970, Clinical Trials Journal , 7(3): 357-366, London, a peer reviewed paper, that of 370 patients with various types of cancer who were given immunological treatment shortly after surgery or radiation therapy, 322 (87%) were alive and well after five years without recurrence or detectable metastases.
An independent statistical study by A.G. Audier, M.D., University of Leiden, Holland, "Immunotherapie Metastasierender Malignome" , 1959, Die Medizinische 40: 1860-64, Stuttgart, a peer reviewed paper, reported a 16.6% cure rate of histologically verified metastatic malignomas by the Issels comprehensive immunotherapy. The study comprised 252 patients with various types of cancer after all conventional methods were exhausted (World wide cure rate is 2%).
John Anderson, M.D., Teaching Professor at King's College Hospital, London, reported 17% cures of histologically verified metastatic malignomas by the Issels comprehensive immunotherapy. The independent randomized study comprised 570 patients with various types of cancer after all conventional methods were exhausted (General Practitioner, 1971 : 15-16, London).
The Issels Treatment opens up the following therapeutic possibilities:
Treatment of cancer of all types and stages offering a considerable chance of recovery even for patients in advanced stages who have exhausted all standard treatments. Follow-up treatment to reduce the risk of recurrence after standard cancer therapies through restoration of the patient's defense and repair functions. Nontoxic preventive treatment for patients at risk (genetic predisposition coupled with environmental challenges), and those with precancerous lesions. Preparatory treatment prior to surgery, radiation, and chemotherapy to reduce complications and in qualified cases, to render inoperable tumors operable. Treatment of chronic degenerative diseases which are untreatable by standard methods. A system of monitoring regulatory functions on a day by day basis is used to evaluate the effectiveness of the treatment.
It is not the purpose of immunotherapy to replace surgery, radiation and chemotherapy. These "localized" treatments have their place within the integrative approach to cancer. On their own, however, they cannot be expected to be the answer to a chronic systemic disorder, although they have given their utmost in removing its symptom, the tumor. Therefore, interdisciplinary collaboration should no longer be subject to the primacy of surgery, radiation and chemotherapy under the exclusion of immunotherapy.
It is the integrative approach to cancer based on the h o l i s t i c concept that will bring physicians and scientists closer to their goal : More Cures of Cancer.
About the author Ilse Marie Issels was the wife and for 40 years the closest collaborator of Josef M. Issels, M.D. (1907 - 1998). His continuous research until his recent death enabled him to integrate advanced state-of-the-art technologies into his comprehensive treatment program. Mrs. Issels follows this strategy. As the president of the Issels Foundation she carries on Dr. Issels legacy. Mrs. Issels is a consultant to hospitals and clinics implementing the Issels Treatment. For more information: Internet: www.issels.com, Email : issels@...
References
Alexander P. In: Prog Emp Tumour Res. 1968; Basel and New York; Karger; 10:22.
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for more information, one should be able to find both radio, and other archives on Dr. Issels at http://www.garynull.com
on garynull's radio show, i heard probably 30 shows on cancer, and other conditions,were dr. issel's approaches to illnesses where discussed in great detail.
GiGi
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Prof. Issels was forced out of Germany many, many years ago because of constant persecution. He continued his work in Mexico. Not much has changed. Thinkers are not wanted in many parts of the world.
Take care.
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I find Issels book very interesting for all chronic diseases. This is long but good! It was written in the 1970's
Sunny thoughts, Wallace Cancer: A Second Opinion, Chapter 8, Focus on Foci Focus on Foci
The "focus" has been described as a chronic, abnormal, local change in the connective tissue, capable of producing the most varied distant effects beyond its immediate surroundings, and therefore in constant conflict with local and general defence (Pischinger and Kellner). By this definition, even a fully-healed scar may sometimes act as a focus, spreading disease to distant parts of the body. But the foci we shall now examine will be confined to those of the teeth and tonsils - in my view, the most lethal of all foci.
The emphasis I place on the removal of devitalised teeth and chronically-diseased tonsils is one of the better-known aspects of my work, but also one of the most criticised and misunderstood. I do not, for instance, recommend that healthy tonsils and teeth be removed from a healthy person. But I believe if they are diseased, they cause the body's natural resistance to be lowered, thus acting as an important contributory factor to tumour development. In these cases, I insist on their removal.
It is sometimes argued that to carry out such operations on seriously ill patients is unnecessarily cruel, even irrelevant. There are some unpleasant side-effects, but in my opinion, the benefits - which I will describe - more than make up for any temporary discomfort. It is further argued that in the cancer patient, as much lymphatic tissue as possible should be preserved, and therefore tonsillectomy should not be carried out because even a diseased tonsil may retain some useful defence potential. I used to believe this was so. I do not any longer for reasons which will be evident.
The beneficial results of tonsillectomy with cancer patients were first brought to my attention in 1953, and by chance. A tonsillectomy was performed on an incurable cancer patient in my clinic who had severe rheumatic pains and a long history of tonsillar disease. The operation was done to relieve the woman's pain, but it was remarkably successful in other ways as well: general toxic symptoms disappeared and, most important of all, her pathologically rapid pulse rate was reduced. Many cancer patients have a high pulse rate, reaching 140 and even 160, and this always leads to a poor prognosis, but in the case of this woman, it was almost normalised. Soon her tumour began to regress, and ultimately she recovered from her cancer.
This unexpected but welcome result encouraged me to arrange for tonsillectomies on two further patients with tonsillar ailments, who also had therapy-resistant cardiovascular disorders and toxic symptoms. In these cases as well, following surgery, cardiovascular and many other symptoms virtually disappeared. A positive "re-tuning" of natural defence and a certain inhibition of tomour growth was also observed. This improved situation naturally allowed more time for active immunotherapy to work.
These early successes encouraged me to persevere with tonsillectomies. Before making them virtually obligatory in my clinic, forty percent of those who died there did so from heart attacks. Afterwards the figure dropped to five percent. This, I contend, is incontrovertible proof that tonsillogenic toxins find their way into the bloodstream and eventually can cause, for instance, a fatal myocardial disease. This is one reason why more people die from heart disease than from any other.
In addition, my experience shows a direct connection between dental and tonsillar foci and many of the illnesses responsible for early debilitation and untimely invalidising.
It has long been generally accepted that head foci may give rise to almost all kinds of chronic, and certain acute diseases, such as-to mention a few-the manifold varieties of rheumatic and cardiovascular conditions. The removal of such foci is today a routine part in the conventional treatment of those diseases. However, the fact that head foci are also a contributory cause in the development of neoplasia, by lowering resistance, has received all too little acknowledgement.
The extent of the disease-provoking activity of a focus in distant parts of the body depends on whether the body is able to oppose the focus with its own defence mechanism. As long as the focal situation is kept under control by the local defence mechanism, no focus-induced remote effects will arise. On the other hand, distant effects will arise when the body's resistance has more or less broken down: control of head foci will then gradually collapse, and there will be consequential gradual increase in generalized focogenic intoxication. This will cause an inevitable deterioration of the body's defence power with a concomitant promotion of malignant growth.
Nearly everybody is confronted with dental problems at some time in their life, and even the most scrupulous dental care cannot guarantee dental health. Endogenous factors, such as prenatal damage to the embryonic dental tissue, as well as exogenous influences, such as malnutrition and toxins, must essentially be held responsible for the great number of dental diseases, be they a weak, susceptible gingival, or gum; or teeth which are malpositioned, barreled or impacted; or, worse of all, a disposition to decay.
Despite its porcelain-like surface, the crown enamel of the tooth is vulnerable to decay. Enamel defects develop especially in the grooves of the crown or on the adjacent surface of neighbouring teeth which are difficult to clean.
Decay is not painful so long as it is confined to this nerveless enamel layer. The onset of a toothache is the first noticeable sign that the decay has invaded the dentine body of the tooth which, unlike the enamel, does have nerves. If this decay is allowed to continue, sooner or later the dentine will be completely penetrated, and the pulp inside the tooth will then become inflamed.
As long as only the outer enamel and dentine are affected, the tooth can be preserved. But a tooth with an inflamed pulp can no longer be saved, and must be extracted without delay.
In an understandable desire to preserve as many teeth as possible, to maintain the masticatory apparatus and its functions, attempts are often made to save teeth which are in fact lost. There is a widespread conviction that this can be done without risk by the sterile evacuation of the pulp, and then refilling the cavity. For decades, the erroneous belief was held that, after such treatment, the tooth is an isolated, lifeless thing, no longer involved in any of the body's processes. This assumption was originally based on the premise that the pulp cavity had only one orifice to the apex of the root below, and by filling, this opening was sealed. However, the dentinal canal does not end in just one opening; instead, it resembles a tree with many branches which penetrate the tooth's body in all directions.
The finer details of the entire dental structure have been exhaustively studied by Austrian researchers. They have established that there is a lively metabolic interchange between the interior and exterior milieu of the tooth, and that this two-way process takes place along many thousands of hyperfine, capillary canals joining the pulp cavity to the exterior surface of the tooth.
Very careful conservation measures may possibly seal off the vertical central-medial-tube of the dentinal canal, but it will never reach the lateral "twigs" branching off from this tube. Nor can it ever close off the innumerable capillary canals. Some protein will always remain in these secondary spaces. If this protein becomes infected, toxic catabolic products will be produced, and conveyed into the organism.
It was established in 1960 by W. Meyer (Goettingen) that within devitalized teeth the dentinal canals and dental capillaries contain large microbial colonies. The toxins produced by these microbes in a tooth with a root filling can no longer be evacuated into the mouth, but must be drained away through the cross-connections and unsealed branches of the dentinal and capillary canals into the marrow of the jawbone. From there, they are conveyed to the tonsils, and thus the flow systems of the body. In fact, the conservation treatment may literally convert a tooth into a toxin producing "factory".
A devitalized tooth is no longer able to perceive and control inflammatory processes even when suppuration has invaded the surrounding bone spaces of the tooth's socket; it rarely gives warning signals, for instance through pain, and therefore there is nothing to induce the patient to have this dangerous toxic foci removed. It then may be left to develop its devastating effect on the organism for decades or even for a lifetime.
When the inflammation spreads to the marrow of the tooth socket, it can cause osteomyelitis. Its further course is determined by whether and for how long the local defence is able to keep the focal disturbance under control.
If the body's local resistance is intact, the inflammation is enclosed by a capsule of connective tissue known as the dental granuloma. This membranous cyst prevents its toxic contents from spreading into the organism. Radiographs of these teeth show granuloma cysts as more or less marked transparencies at the apex of the root. This type of tooth is called X-ray positive.
If the body's local resistance is weakened to such an extent that the inflammatory process cannot be encapsulated by the granuloma cyst, the toxins will be able to advance unhindered into the marrow spaces, the tonsils, and into the body. In this case, it is proof that - as stressed by Pischinger and Kellner - the organism has become largely incapable of reaction. Radiographs of these teeth as a rule show no transparencies, and are therefore called X-ray negative.
In my cancer patients, I have found that such non-encapsulated foci - that is those who show X-ray negative - were particularly common, as one would expect from people whose body resistance has been lowered.
Today there is general agreement that dental foci should be cleared away, and it has become usual to diagnose them by X-ray. Unfortunately, only some of the dental foci can be discovered by this means. Encapsulated foci can be recognized only if large enough, and if not concealed by the tooth's shadow. And definite X-ray signs are much rarer in non-encapsulated osteomyelitic processes. It is therefore the most dangerous of all dental foci which most frequently prove X-ray negative. Even with X-ray positive dental film, only those foci can be recognized which happen to be situated outside shadows. Since X-ray negative foci often escape treatment - and they are the ones the body has failed to resist effectively - they can continue to develop their destructive effects unhindered.
My clinical experience has produced evidence of a causal connection between foci and tumour development, and in this respect, the results obtained with the aid of an infra-red test are especially significant.
Any inflammatory disease focus creates on its corresponding skin surface a pathological increase of infra-red emission; the higher the activity of the focus, the more pronounced it is. Using an infra-red sensitive instrument (Schwamm's infra-red toposcope), the intensity of this emission can be continuously monitored and measured. Observation shows a close interrelation between the infra-red emission of head foci and that of the neoplasial region. That is, after treatment, a decrease in the infra-red activity of dental foci was as a rule accompanied by a decrease in infra-red emission over the tumour areas.
From this it is clear that the advisable treatment for devitalized teeth is extraction.
But even this is not always enough. My experience has further shown that also living teeth may sometimes be so damaged that their pathogenic potential almost equals that of devitalized teeth. For instance, latent chronic pulpitis may arise in a tooth that appears outwardly healthy, thus having a focal effect.
The diagnosis and treatment of dental foci remains generally unsatisfactory. A survey conducted at my clinic found that, on admission, ninety-eight percent of the adult cancer patients had between two and ten dead teeth, each one a dangerous toxin producing "factory". Very often we are confronted with X-ray negative dead teeth, root remnants, and residual ostitis which had not been diagnosed and therefore had not been removed.
Only total, thorough dental treatment will really succeed in giving the body's defence a chance. In addition to X-ray diagnosis, it is therefore necessary to use other diagnostic aids, such as infra-red techniques, tests, to estimate tooth vitality and periosteal resistance, and other electrometric methods.
The diagnosis of foci in teeth had been greatly improved by electro-acupuncture. It is now possible to differentiate foci not only with regard to their type and position, but also to their virulence and pathogenic efficacy. The result of focus treatment can consequently be observed and improved, before, during, and after dentistry, to an extent never known before (Kramer).
If total treatment is to be performed, it is necessary to remove not only any devitalized teeth but also any hidden dental foci remaining in the jaw.
Further, total removal of devitalized teeth and their roots must not be the end of the dentist's activities. Each alveolus - the tooth's socket in the jaw - should be radically cleared down to the healthy bone. In that way the development of the residual ostitis or of a cystoma may be prevented. It is not only the tooth which may be a focus, the but the adjacent tooth-fixing apparatus as well.
There are four different ways by which dental foci - and indeed all foci - can affect the organism and contribute to the development of secondary damages:
1. The "neural" way of affecting the organism.
When a focus develops anywhere in the transit tissues, the mesenchyme, the process is centripetally projected from the terminal neural organs around the irritated area, along the neural ducts, up to the corresponding control cells within the central nervous system. The irritation originating from a focus can, under certain conditions, trigger off the mechanism of a neural dystrophy - a slow degeneration - which may show itself in localized effects in other areas, but also in a generalized dystrophic disturbance.
In the 1950s it was shown that these manifestations are based on depolarizing processes in the affected neural cells, and in the corresponding tissues of the body's periphery (Fleckenstein and Ernsthausen). By elimination of the focus, the affected tissues may be repolarised. The most striking example of this repolarisation is called "second-phenomenon".
Ferdinand Huneke, the founder of neural therapy whose remarkable contribution in this regard we shall look at in detail later, discovered over forty years ago that injection of a local anaesthetic near a primary focus may immediately remove any symptoms of distant disease induced by the focus. This effect - the second-phenomenon - usually takes place only a few seconds after the anaesthetic injection, and lasts for hours, days, or even for a lifetime. Naturally the improvement occurs only in those regions influenced by the injected focus. Nevertheless, the measure has therefore a remarkable diagnostic value as well.
Since neural therapy only neutralizes the neural effect of a focus, the focus itself must, of course, be removed after such treatment, in order to eliminate its latent toxic or allergenetic action. Conversely, any focal surgery must be followed by desensitizing and neural-therapeutic measures.
The only exceptions to this rule are, for instance, featureless scars or other spots with no inflammatory change which produce only neural distant effects without at the same time causing any toxic, microbial, or allergic secondary phenomena.
2. The "toxic-way" of affecting the organism.
The toxic activity of odontogenic foci is probably far more perilous for the organism than their neural effects. The mechanism of this distant toxic activity, as well as the characteristics of the toxic compounds involved, have been largely ascertained.
Odontogenci compounds are the gangrenous contents of an inflamed pulp cavity and its adjoining spaces. It consists of detritus and decaying, formerly vital substrates which have been necrobiotically altered - commonly found in tissues destroyed by inflammation, liquefaction and microbial putrefaction. Thus there can be little doubt that they are genuine necrogenous toxins, including for instance autologous proteinic and higher-molecular fission products resulting from enzyme cleavage and other biogenic conversions.
The identity and chemical struction of certain of the biogenic amines were mainly clarified in the 1950s by Schug-Koesters, Hiller, Gaebelein and others of the University of Munich. Following similar findings in America, the metabolic and exchange processes in solid dental structures were further investigated by the German researcher Spreter von Kreudenstein. He showed that drugs injected intravenously were, four to five hours later, discernible within the intradental capillary ducts or even devitalized teeth, and in a concentration only slightly lower than in the blood.
That endodental exchange may also take place in the opposite direction has been reported by Bartelstone (USA) and Djerassi (Bulgaria). If radio-iodine, I-131, is deposited in an evacuated pulp cavity which is then sealed off with a filling, the iodine will appear in the thyroid some twenty hours later, as can be demonstrated by taking a scintograph of the thyroid region. Similarly, dyes can be washed out of a sealed pulp cavity.
All these findings prove conclusively that within solid dental structures, there may proceed an unimpeded substantial interchange in either direction. Consequently, odontogenic toxins, wherever they may have been produced, are able to diffuse and circulate within the organism.
The pathogenic significance of these "endotoxins" has been investigated by the German study group of Eger-Miehlke. They examined the changes in healthy experimental animals after injection of accurately defined, minimal quantities of the endotoxins from an odontogenous granuloma.
A single injection of a minimal dose seemed to develop a defence-activation effect. But after repeated injections, there was severe liver damage, and the animals died within weeks. Apart from the fatal liver damage, inflammatory and degenerative changes were found in all other organs, especially in the joints, muscles, and blood vessels.
These results brought clear experimental proof for the first time that focogenic toxins act as causal agents for severe diseases in animals corresponding to similar chronic conditions in man.
The most dangerous of all odontogenous toxins are undoubtedly the thio-ethers, for instance dimethylsulfide. In a series of tests performed at my clinic, it was observed that patients with odontogenous and tonsillar foci had a heightened level of dimethylsulfide in their blood. After intensive treatment of the foci, this level returned to normal in just a few days.
Thio-ethers are closely related, both in their structure and their effect, to mustard gas and other poison gases used in the First World War. The extreme toxicity of the poison gases and thio-eithers can be attributed to the following properties:
They are weakly basic, therefore "electro-negative", and thus they are deposited particularly in "electro-positive" cells such as those of the transit tissues as well as those of the defensive tissues.
They are soluble in the lipids, and therefore have a pronounced tendency to enrich themselves in the lipoid-containing cellular structures, especially in mitochondria.
These subcellular organelles, attached to their lipoid membranes, contain the enzymatic structures responsible for the maintenance of aerobic metabolism - a precondition for full functioning power in all the body's cells and tissues. If these indispensable units are damaged, the most serious consequences will follow. Because they are the most vulnerable cellular organelles, mitochondria are a favourite and almost exclusive target for thio-ethers. The action of thio-ethers is effected in three main ways:
Since thio-ethers tend to combine with electro-positive metal ions and many bio-elements which act as co-effectors or activators of numerous enzymes of absolutely vital importance, and as our present-day average diet is deficient in essential substrates such as vitamins and bio-metals, this deficiency is enhanced. Much of the daily intake of bio-metals, usually deposited in the fluids of a focally affectd organism, will be made permanently ineffective; the more foci, the greater will become the deficiency.
Thio-ethers are "partial" antigens, haptens, and thus they also tend to combine with the normal proteins in the body, "denaturising" them. Such denatured proteins become "non-self" agents which the body must deal with as such. The production of antibodies adapted to the situation will be provoked, and they will home in on the target antigens wherever they are. The process of "auto-aggression" will be set in motion: self-destruction of agents alien to the organism. Extensive structural cellular damage will result, increasing with age.
The famous biologist, Otto Warburg, twice winner of the Nobel Prize, has shown that aerobically-blocked cells - as caused by thio-ethers - will increase their anaerobic metabolism in an attempt to maintain their vigour. In doing so, they acquire the characteristics of malignant cells. Therefore, chemical agents capable of inactivating the aerobic process while increasing the anaerobic process are usually classed as carcinogenous compounds. Druckrey (Heidelberg) found inter alia that transformation of a normal cell into a malignant cell requires a certain quantity of a carcinogen -the carcinogenic minimum dose. It does not matter whether this quantity is supplied in a single dose or in a number of smaller doses, because the toxic effects of each dose are stored, and accumulate without loss. The carcinogens held primarily responsible for the development of spontaneous cancer in man are those:
Which inhibit the aerobiosis even in minimal quantities without at the same time immediately destroying the cell, and, which are constantly present in the organism in this minimal concentration of either endogenous or exogenous origin; they can therefore accumulate during the normal life expectancy gradually and unnoticeably until the total quantity necessary for malignisation is reached.
There is hardly a carcinogen which so completely fulfils these conditions as do thio-ethers. Incessantly, from the moment the pulp is removed, hour by hour, year by year, minimal amounts of these most virulent of all the odontogenous toxins will be released into the circulation - minimal doses, but nevertheless sufficient to more or less totally paralyse the aerobic action of the cell.
The nervous system is thus doubly affected by focal intoxication. Firstly, by the increasing destruction of the neural ducts which mediate between the control centers and the peripheral areas, thus sometimes initiating neurogenic dystrophy. And secondly, by the immediate intoxication of neural cells caused by the toxins spreading through the liquid vehicles of the flow systems, such as the blood and lymph.
The more mitochondria a cell contains, the more it will be damaged by the enzyme-inhibiting effect of thio-ether compounds. Therefore it is the vital organs - the liver, nervous system, endocrine glands, heart, and reticuloendothelial system - whose cells may consist of up to one-fifth of mitochondria, that are primarily affected. Apart from disturbing regulatory control, odontogenous toxins will also cause additional damage almost throughout the body. Naturally, the higher the book-level of focogenous toxins, the more severe will be their effect.
The close interlacing of the lymphatic and endocrine systems in the head, make it unavoidable that brain cells are more intensively toxified by the circulating focogenous agents and may suffer particularly heavy damage. The lymph ducts of the head region join Waldeyer's tonsillar ring, and if there is such congestion, waste fluids will be pressed through the porous base of the skull into the lymphatic spaces of the brain. Toxogenous changes, especially within autonomic nuclei, are regularly found in cancer patients, as verified in the 1930s by Muehlmann (USSR), and they may be a consequence of a life-long inhibition of cerebral aerobiosis due to focogenous intoxication.
The cerebral damage (diencephalosis) and the subsequent loss of vitality in cancer patients is accompanied by the number of other symptoms. The emission of hypothalamic energy impulses, recordable by a Voll's electro-acupuncture device, are reduced in patients with focal disease. The autonomic vigour is relaxed, creating "regulation rigidity": carcinomas tend to parasympathicotonic derailment; in sarcomas and systemic diseases, as a rule the opposite is found - sympathicotonic derailment (Regelsberger, Gratzl-Martin, Rilling et al). the diurnal, circadian regulation of the acid-base balance is lost (Sander). At the same time, there will exist a distinct inhibition of other diurnal control functions, for instance of blood sugar, cholesterol, and mineral metabolism, and many other metabolic parameters are greatly restricted (Hinsberg).
The lack of vigour and control efficiency is not, of course, without effect on the patient's psychic condition. Vegetative disorder is therefore generally accompanied by neurasthenic dystonia - characterized by the diminishing vitality and autonomic instability.
3. The "allergic" way of affecting the organism. The toxic effects of thio-ethers overlap those caused by higher-molecular odontogenous toxins as already described.
Antibodies are formed to fight these substances, eventually leading to the destructive processes in toxified cells. Since the organ-destroying antibodies or defence enzymes are excreted by the kidneys, they can be diagnosed in the urine by the abderhalden test. In this way we can precisely deduce, in most cases, which organs have suffered secondary damage (Abderhalden, Dyckerhoff et all).
The extent of secondary lesions can also be demonstrated indirectly by vaccine treatment. Using desensitizing vaccines made from focogenous agents, reactions are caused in regions affected by distant focal effects which may become evident in regional as well as general symptoms.
It is thus clear that the development of cancer disease is, in more ways that one, closely linked with focal events.
4. The "bacterial" way of affecting the organism.
Bacterial dissemination from primary dental foci as a rule takes place with barely perceptible symptoms, and may be followed by the formation of "secondary foci" in other regions. These include, inter alia, foci in the paranasal sinuses, gall-bladder, appendix, prostate, and renal pelvis.
Above all, bacterial dissemination tends to produce microfoci or microthrombi in veins, and they in turn have a tendency to thrombosis or thrombophlebitis, possibly with concomitant embolism.
Thrombophlebitis and thrombosis, so common in cancer patients, and generally regarded as resulting from disordered metabolism, are due not only to the dyscrasia of those patients, but also to the manifold effects of dental foci.
Shakow (Moscow), in collaboration with several clinics, has carried out an interesting investigation involving more the 1200 young pupils at a boarding school. Over a period of six years, it was seen that students with devitalized teeth had three times as many illnesses as those with healthy dentition. By removing devitalized teeth in these young patients, up to eighty percent of their illnesses were cured.
We have now seen how decisively the entire organism is affected by dental foci not properly treated, and what catastrophic results destruction of the pulp may entail. Dentists must, therefore, bear in mind that there is no root treatment which does not inevitably produce foci.
The dentists' task is only secondarily cosmetic; primarily it must be preventive and curative. The over-riding consideration must not be conservation of the tooth but preservation of its vitality. If this is impossible, even the most beautiful crown must not delude us that the lifeless tooth beneath is anything other than a "corpse in a golden coffin", whose decomposition toxins slowly but surely are destroying the organism (Bircher-Benner).
Other foci in the jaw, for instance ostitis, cysts, foreign bodies, gingivitis, and malposition of teeth may also develop focal effects. It goes without saying that these foci and centers of irritation must be removed.
The dentist should always remember that he has a vital role to prevent the development of chronic illness and, most important of all, to decisively reduce the hazard of cancer.
Now let us turn to tonsillar foci.
Chronically inflamed tonsils are primary head foci which sometimes have an even more damaging effect on the organism as a whole than dental foci. They can participate in the development of chronic illness, including cancer, by the four ways already described for dental foci: by neural, toxic, allergic, and bacterial means. There are also similar connections between the development of cancer and tonsillar foci as there are between cancer and dental foci. For instance, after removing the tonsils, there is a decrease of infra-red radiation over the tumour, and sometimes even a shrinking of the tumour.
The three tonsils in man, that is, the naso-pharyngeal tonsil, or adenoid, and the two tonsils proper, the palatine tonsils in the pockets between the anterior and posterior palatine arches in the back region of the mouth, together with other seemingly insignificant lymphoepithelial organs, form Waldeyer's tonsillar ring.
The tonsils are excretion organs by which the lymphocytes, microbes, toxin-laden lymph, and other matter, are discharged (Roeder). Even in healthy people, the tonsils may contain plugs - sometimes wrongly described as pus - which consist mainly of fatty acids, cholesterol, and other slag substances clearly characterizing them as excretion. The pale-coloured plugs form in the shallow depressions on the tonsils' surface - the tonsillar crypts - and are expelled into the oral cavity and swallowed. The excretions of the tonsils may also contain dental toxins.
The tonsillar crypts have been described as the places where the physiologically obligatory bacterial flora are hatched. This flora colonises the mucous membranes of the nose and throat and the other air passages. The tonsils also produce antibodies, and undesirable microbes and their toxins are rendered harmless. Thus they have an immunizing or detoxicating purpose and must be regarded as a functional analogue of the lymph organs of the intestinal mucous membrane, and, like the latter, as an important part of the body's defence system.
Healthy tonsils have a pale, pink, surface, and are normally almond or bean-sized. Their size and reaction capacity are determined not only by functional demands and loads, but also to some extent by each individual's inherited constitution. With an inherited disposition to lymphatic diathesis, due mainly to heavy hereditary infection, there is regularly found a congenital enlargement or hyperplasia of the tonsils. This is always accompanied by an increased disposition to inflammatory reactions. Inflammatory reactions are also caused by their physiological function. A normally subliminal, and therefore symptomless tonsillitis, thus belongs to the "normal bodily state of man" (Leuscher).
Whenever large quantities of toxic and waste substances have to be excreted, the blood perfusion and inflammatory activity of the tonsils will increase. This state is often accompanied by painful swelling and reddening of the tonsils, and is described, depending on its subsequent course, as acute, sub-acute, or if occurring repeatedly, chronic tonsillitis.
I shall now concentrate on chronic, and especially on degenerative tonsillitis, because, under certain conditions, dangerous focal processes develop from it which are of causal importance for the origin of all chronic illnesses, including cancer.
Although each case of chronic tonsillitis is due to the same mechanism, it is possible to distinguish between three different groups. The first group includes those chronic tonsillitis cases which arise in healthy tonsillar tissues capable of response, following frequent attacks of acute tonsillitis, or angina; they have been called upon to repeatedly react to infective irritation, and to excrete toxins. Each new attack leads to an increase in volume, perfusion, and activity. They are then in a high state of readiness for defence. But if such inflammations occur with increasing frequency, the tonsils gradually lose their reaction capacity and defensive power, and atrophy. Too much has been asked of them.
The second group includes those tonsillar foci which develop under certain conditions from congenitally enlarged or hyperplastic tonsils. This kind of hyperplasia can be so extensive that the fauces are completely obstructed. Unfortunately it is still common practice to reduce their size by partially lopping off these hyperplastic tonsils. The tonsils are thereby deprived of the shallow depressions - the crypts - so indispensable to their purpose; the excretory function cannot take place without an intact surface with open crypts. After a tonsillotomy lopping-off operation, the remaining crypts are always narrowed or closed by scar tissue, the substances to be excreted are cut off from their air supply (Voss), and are therefore un-aerobically decomposed with the formation of toxic decomposition products. It follows that lopping-off should not be performed. These tonsils should be totally removed, even if they are not yet causing any recognizable distant effects.
The third group of tonsillar foci, in cancer patients the most common, comprises the seemingly healthy, but small, congenitally underdeveloped and functionally deficient tonsils. A history of tonsillar symptoms is usually absent in these patients. Their tonsils are "unremarkable" , but firmly fused with their base, and cannot easily be dislodged.
What these three main groups of chronic tonsillitis have in common is a focal-toxigenic effect progressively increasing with age, and a tendency sooner or later to atrophy. This process will be accelerated if there is an additional and continuous passive exposure to odontogenous toxins.
The close connection between teeth and tonsils was proven when it was observed that Indian ink injected into a sealed dental cavity appeared as spots on the tonsillar surface in about twenty to thirty minutes. These experiments showed that pathogenic substances from the jaw region, including toxins from devitalized teeth, are conducted to the lymphatic tonsillar ring, there to be detoxicated and excreted. Besides their "natural" physiological load, the tonsils are thus additionally exposed to continuous attack by odontogenous toxins provoked by the devitalisation of teeth.
We have already seen how dangerous these dental toxins are. It is inevitable that they eventually have a severe effect on the active lymphoepithelial tonsillar tissue. So long as the cells destroyed by dental toxins can be regeneratively replaced, the functional capacity of the tonsils will not be seriously impaired. But if the destroyed lymphoepithelial tissue is increasingly replaced by inactive scar tissue - by tissue unable to execute its defence function - the excretion, detoxication, and defence capacity of the tonsils will progressively diminish and eventually be extinguished.
With the loss of reactive lymphatic tissue, the tonsils lose their ability to give warning signs by inflammation; they not longer offer this usual signal for trouble. According to Kellner, this lack of symptoms signifies a definite inability to continue to further reaction. In such tonsils, the attacking toxins are no longer excreted; on the contrary, they are channeled into the organism via the vascular system.
It goes without saying that this development will take place far more quickly when less lymphoepithelial tissue is still present. In congenital tonsillar deficiency, there is, a priori, so little active tissue that its complete destruction can in certain cases be accomplished in a relatively short time. Normally developed, or hyperplastic tonsils if not lopped off, will withstand the dental infection considerably longer. But they too will sooner or later succumb.
The final stage of all three forms of chronic tonsillitis is therefore "atrophically degenerating tonsillitis". On medical examination, the findings here are small, atrophic tonsils which show no sign of inflammation but, unlike healthy tonsils, they cannot be dislodged by the surgeon's spatula. When removing them, they have to be dissected from their bed, so firmly fused are they to the surrounding tissue. Whereas with healthy tonsils the colour of the anterior palatine arch does not differ from that of the oral mucous membrane, in atrophically degenerating tonsillitis there is a bluish discoloration of the palatine arch. The uvula is mostly gelatinously thickened. The tonsils themselves, however, may still appear externally healthy.
Even normal-sized or enlarged tonsils may already have extensive degenerative changes and consist mainly of hardened scar tissue which of course is unable to neutralize toxins. There then follows the formation of usually quite latent and painless chronic tonsillar and retrotonsillar abscesses. Here we find the highly pathogenic beta-haemolytic streptococci of Group A - responsible for many chronic illnesses, and whose toxins spread through the organism and contribute to the development of secondary lesions, of resistance deficiency, and of the tumour milieu.
Apart from the directly allergenic and toxinic activity of these products, continuous toxic attack always leads to an alteration of the tonsillar (lymphoid) cells. Their proteinic structure is so altered that the organism is induced to form antibodies against these, its own, cells which have become foreign to it, antibodies which finally turn against healthy lumphocytes as well, and thus considerably weaken the lymphatic defence system of the whole organism.
With the decline of the active tonsillar tissue, its biological power is also exhausted. Active detoxication, toxicopexis, and excretion of toxic substances and wastes through the tonsils is no longer possible. In the tonsillar crypts, the physiologically essential symbionts are no longer hatched. Instead, dangerous pathogenic organisms are able to spread through the body because the immuno-activity of the tonsillar barrier is lost with the destruction of the lymphoepithelial tissue.
When the dental toxins are no longer neutralized and excreted, they will infiltrate even the last remnants of functioning tonsillar tissue and cause them to die. This creates high- and low-molecular necrotoxins which, as we have already seen, are similar or identical to odontogenous toxins. Toxin formation is inevitably increased.
All these toxins, no longer inactivated in the tonsillar ring or excreted, have to be conducted to other "vents" by way of the blood circulation. Toxinaemia and secondary lesions are increased, and the humoral milieu and the body's resistance deteriorates further. The process has become a deadly vicious circle.
Since degenerated and chronically inflamed tonsils are such dangerous toxogenic foci, like dead teeth and other dental foci, they must be removed. With previously lopped tonsils, there is also a clear case for tonsillectomy.
The focogenous toxicopathy caused by necrotic-atrophic tonsillitis is of course far more dangerous than the toxi-infectious effect of a hyper-reactive tonsillitis in childhood. And if the need for tonsillectomy is accepted in children, in cases of rheumatism and other comparatively harmless diseases, should it not be obeyed all the most urgently in tumour disease, especially as a causal connection between focal and tumour events can no longer be denied?
During more than twenty-five years of clinical experience, I have found that painful, enlarged tonsils and other symptoms of chronic tonsillitis were evident in less than one-third of my cancer patients. This suggested to me early on that the others might have silent tonsillar foci in the form of atrophically-degenerating tonsils. In these patients with subjectively quite unremarkable, small, featureless tonsils, I examined their case histories, and searched for silent tonsillar foci with the aid of the infra-red toposcope, the electrodermatometer, and other methods. These observations showed that, although most of them had never suffered from tonsillitis, there were clear findings of a tonsillogenic focal toxicosis. Whenever this was compatible with the condition of the patient tonsillectomy was performed.
The findings in these healthy-looking tonsils were incomparably more serious than even those in the obviously diseased tonsils removed in usual ear-nose-and-throat practice. The tonsillar capsule always proved to show callous thickening, and was so firmly adherent that the tonsils could only be dissected out. In about five percent of the patients there were fairly large peritonsillary or retrotonsillary abscesses which had caused no symptoms. Far more frequently there were several abscesses as well as cysts often the size of cherries, full of liquid or condensed pus. The tonsillar tissue was spongy, slushy, and had a putrid smell. Histological examination of these tonsils always showed severe degenerative changes, and in the majority of cases, a complete atrophy of lymphoepithelial tissue.
All these "featureless", clinically unremarkable, small tonsils proved without exception to be foci of the most dangerous kind which, like the silent dental foci, had probably been present and unrecognized for years or even decades.
These pronounced positive effects of tonsillectomy make it mandatory to always follow dentistry with treatment of the tonsils. In every tonsillectomy performed in my clinic subsequently, we found through biopsy severe or very severe destructive tonsillar processes with more or less virulent tonsillogenic focal toxicosis.
The flourishing of patients after tonsillectomy is impressive and has been demonstrated to my clinical satisfaction again and again.
Toxins constantly circulating in the blood in degenerative tonsillitis cause a permanent spasm of the blood capillaries, seen outwardly in the poorly perfused, pallid skin of many cancer patients. After tonsillectomy and the consequent elimination of the toxins and their neural effect, there was frequently an immediate improvement of the circulation and a simultaneous improvement in the general condition of the organism.
As already mentioned, before I began paying special attention to the tonsils, I lost many incurable patients, not as a result of cancer, but through acute cardiocirculatory failure. After introducing tonsillectomy, such deaths became much rarer.
Toxic circulatory death, however, is only one of the many dangers constantly threatening the life of the chronically sick. Phlebitis, thrombosis, embolism, pneumonia, pleurisy, and cystitis all too often complicate the course of treatment. In my experience, these, too, became noticeably rarer with the introduction of routine tonsillectomy.
Another observation, one I believe very important for cancer treatment, is that often following tonsillectomy, in a large proportion of patients, I have found that the tongue, not coated before the tonsillectomy, later has a marked yellowish, brownish, or blackish coating. Experience shows that the canalizing activity of the intestinal mucous membranes is indicated by the surface condition or coating of the tongue; a change in this coating suggests that a previously blocked "gut filter" has been opened, leading to the conclusion that tonsillar foci also disturb the detoxicating and excretory activity of the gut. Restitution of this function is of crucial importance in the treatment of cancer because the largest proportion of the necrogenous toxins which develop during tumour solution is excreted by this route.
The widespread opinion that degeneratively destroyed tonsils may still be of importance for cancer patients as detoxicating and excretory organs and must therefore be preserved at all cost has, in my experience, been quite clearly refuted. Anyone, having seen the degenerative destruction in the tonsillar tissue of cancer patients, will be convinced that, on the contrary, these tonsils have contributed in potentiating the virulence of the tumour milieu and the defence deficiency. Tonsillectomy must be followed by desensitization with vaccines obtained from dental and tonsillar foci. Neural treatment of the tonsillar bed concludes this treatment.
The increased tendency towards thrombosis in cancer patients has been reported by many clinicians. It can be assumed there is a causal connection between the two diseases. My experience is that this tendency is reduced by treatment of the head foci. I have treated cancer patients who were being given anticoagulants permanently because of their thrombosis; after treatment of the head foci, as a rule, they were able to discontinue these drugs.
In some cancer patients there is a secondary finding of therapy-resistant hypertension. Here too, following treatment of the head foci, the blood pressure generally returns to normal.
The growth of the tumour itself is very often distinctly slowed down by focus treatment. Now and then tumour development stops altogether, and sometimes even regresses. The head foci therefore seem not only to contribute to the development of secondary lesions, to the origin of cancer disease, but also to exert a direct influence on tumour growth by stimulating it. Many tumours seem to respond to immuno-therapy only when foci have been removed. The subsequent improvement in the body's defences clearly shows itself in the response to immunizing vaccines.
Nevertheless, my own unhappy experience shows that with cancer patients, foci treatment has generally been left to a very late state. In the vast majority of the patients I have treated it is quite clear that foci treatment should have been carried out years before - and certainly long before the manifestation of the tumours.
That this was not done is a sad reminder that far too many doctors and dentists fail to recognize a fundamental truism: untreated foci can be linked to the development of cancer.
There are also other facets of our every day life-style that indirectly play their part in how the disease can progress.
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