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it. This protein 'web'—actually, a fungus—shot up and encapsu- and then went all over the place and grew again—just this one lated the tumour. Within a few days, there was a little bit of the cell, the spilt cell." One cell or a few cells get loose and the dis- cancer left. A couple of weeks later, no cancer—just the fungus! ease comes back. This may account for some of the cancer recur- So what this does is it gives us this new therapeutic modality. rences, but to try to explain all cancer recurrences that way, the This nemesis organism can now give us highly specific chemicals medical term for that is "crap"! that it used to kill the cancer, but which can be made so they do What we know from those leukaemia trials is that they wiped not attack any other sort of tissue. Two, it can give us tagging out the patient's bone marrow. There was nothing left! They complexes which stick to the outside of the cancer and make the — gave him someone else's bone marrow. Six months later, the cancer highly visible to the immune system. And three, it can leukaemia came back. Now, if it was a leftover cell, then when give us a complete range of digestive enzymes which are specific you check that leukaemia cell you should find that it's the same as for digesting the cancer and the cancer alone. So this little baby the leukaemia you treated before the patient went into remission, not just kills the disease, it also cleans up after itself! true? It should be the same cell come back. However, when they With use of the tagging system, if the immune system looks at ran DNA checks, they found that not only wasn't it the same cell, this fibrillary network of protein stuck onto but it belonged to the donor. It was the the outside of the cancer, it doesn't see can- donor's bone marrow that had turned into cer; it sees a bug and it wants to go after the leukaemia cells! bug. Now, you don't inject the bug; you purify the protein extract that sticks to the This finding has been published in the conventional medical literature, and it You and I have no cancer and you re a ee sucks trouble getting rid of trans thay cancer the cisease 6 not cancer to the cancer in the body. The body can then . the cell. There is something in the body of a see it and recognise it because it's tagged a cough ora cold In patient which regenerates and augments with bacterial, fungal or viral protein. a a week or two. cancer, the cancer cell. And if you don't You and I have no trouble getting rid of a address that, then you won't get rid of the cough or a cold in a week or two. We can disease. get rid of cancer: make the cancer look likea | Vf n ri f ncer: cough or a cold by sticking cough or cold e ca get d SU Clie o there I was, with all these little make the cancer look bottles, cooking up these nemesis particles on it, and the body will attack it, destroy it and remove it. like a cough ora cold organisms and tagging them, but However, there were instances where aoe something kept showing up over and patients had a regression several by sticking cough or over and over again which was driving months or years after treatment of their cold particles on it me nuts. I would incubate the cancer tumours with a tagging complex. This ie with another organism—say, an E. and the body will coli—and I'd find other organisms attack it, destroy it and remove it. suggested that tagging the cancer was not the be-all and end-all, that tagging growing when the cancer cells died, that I hadn't put in there. They would the cancer cell still didn't cure cancer the disease. There was another factor at usually be staphylococcal or strepto- coccal in appearance. Acid-fast bacilli work. An interesting observation was made sometimes would show up, depending on what culture medium was used and about 20 years ago when leukaemia patients were treated by wiping out for how long I cultured them. their bone marrow and then giving Now this is really interesting. What them somebody else's bone marrow. It was found that the you notice is what some people would call "pleomorphism" in leukaemia would invariably recur. And you know how they say progress. A couple of elements would develop these elongated how cancer comes back? Well, the doctor says: "Sorry, Mr rodlike structures, and you could actually see a coccal form Jones; it seems that when I was operating on you and I was giving changing into a rodlike form. Pleomorphism in action. you the chemo and the radio, one cell spilt, and this one cell hid I went to my colleagues and said: "Look, why do I keep getting these bugs? It's a sterile cancer I'm putting into the bottle, for goodness TABLE 1: CASE STUDIES OF AIDS PATIENTS TREATED WITH sake. I'm incubating with some- INDUCED REMISSION THERAPY thing completely different, and these bugs keep showing up." And CASE #1 (32-YEAR-OLD MALE) they said: "Well, Sam, you know what you're like. You probably Before entering into therapy: After one week: sneezed and contaminated the Viral count 312,000 Viral count 10,000 | whole lot!" Then I said: "It's hap- T-helper count 150 T-helper count 650 pened over and over and over again. So it's contamination?" CASE #2 (49-YEAR-OLD MALE) "Yes, yes, absolutely." Before entering into therapy: After one week: A hundred years ago, everybody Viral count 78,000 Viral count 7,000 | Dlamed this contamination as the T-helper count 89 T-helper count 438 ture. There were thousands of arti- cles written on bacteria—bacterial trouble getting rid of a cough or a cold in like a cough or a cold by sticking cough or cold particles on it, and the body will attack it, destroy it and remove it. TABLE 1: CASE STUDIES OF AIDS PATIENTS TREATED WITH INDUCED REMISSION THERAPY After one week: Viral count T-helper count After one week: Viral count T-helper count 7,000 438 38 = NEXUS JUNE - JULY 1998 You and I have no a week or two.