Now that you have studied the previous Scientific Test of effect of tar and nicotine on mice; make note that mice exposed to radiation had more lung tumors than mice exposed to tar and nicotine.

The following experiment was conducted during a two stage commercial flight from Northwest, AR (XNA) to San Diego, CA. The aircraft were a twin jet engine Embraer to Dallas-Fort Worth and a Lockheed DC-8 to California.

The procedure followed was identical for both stages, with one exception during the stage to CA. Upon boarding each aircraft I stopped and explained to the Captain I was conducting an experiment and asked if he would assist me by checking the flight compartment for presence of electromagnetic fields. Upon agreement I provided the Gauss Meter, explained its operation and proceeded to my seat.

Approximately 20 min after a normal takeoff and climb to assigned altitude, the Captain came back from the flight compartment sat next to me and described how he had operated the meter and that it showed a yellow light in all areas of the compartment except when he placed it below his knees toward his feet, the meter showed red and he was curious as to why. I asked if the weather radar was in the nose section and he replied

that it was. We then talked a few minutes about my research and he returned to the pilot's compartment. After a short explanation to the stewardess I measured the galley area and the only area that measured a emf was near the coffee warmer.

DC-8. The Captain however showed more interest in reason for the experiment and did go back to the galley to advise the flight attendants about my testing. The results of my readings were far more than expected. The Gauss meter showed red when along side seats just forward of the galley and stayed red in every area of the galley. To be sure of the findings, after all trays were returned and the galley was stowed, I returned and checked the galley again and no readings were elevated except directly opposite the coffee warmers. Mission accomplished.

It is safe to say; "there has been no reduction of cancer victims since elimination of smoking on the aircraft". Facts are; there may be an increase as power is added in the passenger area for convenient items.

In considering scientific data presented, pilots and stewards, in my opinion, are in a death trap every flight they make. Crew members and passengers get no benefit from foods served that might have contained oxalic acid since it's been decomposed.

Tobacco like marijuana is a weed and to some degree can relieve pain and discomfort since all weeds contains oxalic acid which does relieve pain. For those who doubt the writings of my findings, for relief of pain buy some bulk green tea and put that in your pipe and smoke it; you will no longer have to smoke the "weed"; oxalic acid in tea is the same as oxalic acid in marijuana. How does it work? When burning, oxalic acid is converted into an ester form ( a very fine powder) carried to the lungs, is picked up by blood and carried to the pain site. Those who doubt it try it. The best is cigar smoke.

All information on this site and coljoe.com as well as the US Patent no. 6133317 was provided years ago to the Arkansas Department of Health under then Governor

MIKE HUCKABEE and absolutely nothing was done and many victims died or suffered indescribable pain and lost every possession they worked a lifetime for.

You need to know the extent politicians (gov),scientists and doctors (pharmaceutical co's) will go to, to prevent any cures for any disceases, major or minor. It is why I refer to them as "stupid politicians" & "brilliant dummies". Most doctors do not know a mean value of "oxalic acid" in the blood of humans. Figure that statistic out. Now go read the letters . Col Joe

I am writing about 3 items I think you will find very interesting. One is a follow-up to my e-mail Thank you; with comments. Second is an item, which may have serious consequences, which I cannot determine; perhaps your spouse Dr. Lincoln would consider evaluating the item. Third is an item I believe could be monumental.

As to the first item, I again express my sincere "thank you" for your action on behalf of the millions of people who will benefit from recognition of my discovery. If it is appropriate I would like to have the opportunity to evaluate Dr. Koplan's response to your request before you reach a position on my research. My reason: previously through Rep. Hutchinson I suggested that the CDC look into the possibility that since oxalic acid kills the rhino (common cold) and flu virus it might be as effective against the virus that causes (BSE) or mad cow disease and Creutzfeldt-Jacob disease (CJD). Dr. Koplan in his answer to Rep Hutchinson said;

"The agent that causes BSE/nvCJD is neither a virus nor bacterium, but an infectious agent called a prion. Prions are infectious proteins that have the ability to alter other proteins in the infectious process"

I do not mean this sarcastically but, Dr. Koplan gave me through Rep Hutchinson the "idiot treatment". What Dr. Koplan did not say was that the agent that infected the protein is a slow virus. My simple logic says if you kill the slow virus there are no infected proteins, and if there are no infected proteins there are no prions, and if there are no prions there is no BSE/nvCJD. Study of the structural proteins of the virus may have been as early as 1954 and in keeping with the new finding the term "virion" was proposed for the complete infective virus particle. But apparently to identify the structure more as a protein then a virus the term "prion" was accepted. I hope Dr. Koplan's knowledge of what causes BSE/nvCJD has greater depth then the :"prion".

The second item which I cannot currently evaluate without extensive research might have very serious side effects in patients receiving treatment for vascular conditions that involve the insertion of metal or plastic devices in the arteries. Oxalic acid as an industrial chemical is used in various solutions as an etchant for stainless steel and there is data that talks of the dissolution of tantalum in oxalic acid solutions. Since oxalic acid is normal in the blood in the anhydrous form (without water), will it etch any of the various materials used in the vascular treatment? If a device is etched, could there be materials released that could be harmful in the blood stream? I have attached copies of 3 reference sheets that describe oxalic acid used in different processes.

The third item is about the very real possibility that clinical studies could be done here in Arkansas, which would place Arkansas in the center of medical science research worldwide. An initial contact with an associate of Mr. James T. Stephens the CEO of Exoemis Inc. and I believe a member of the Arkansas BioVentures Advisory Board, was made.

Given the opportunity in future contacts I will propose Clinical Studies to verify the efficacy of oxalic acid in treating the diseases of Cancer and Arthritis, using the methods described in my Patents, be planned and conducted as quickly as possible.

Use of the Dietary Procedure Plan with carrot juice, recently used successfully, (copy of Laurel J. Lingle and Cindy Monroe e-mail testimony attached) and use of the Dietary Procedure Plan with new therapeutic compositions of oxalic acid providing the increased oxalic acid necessary instead of the concentrated carrot juice will demonstrate that "Integrated Medicine" is not only feasible but very necessary. Integrated Medicine needs an integrator and oxalic acid is that integrator. It is described as such in the Patent claims.

Of equal importaqnce is the part oxalic acid plays in the entire human cycle. Is not the blood of a mother in the blood of a newborn baby? Could a deficiency of oxalic acid in the blood be the reason for cancer in new born babies being treated at St. Jude's? I tried to get my information to those in Administration at St. Jude's without success.

I believe clinical studies of Cancer and Arthritis victims could be conducted simultaneously. And I would disgree with use of placebos. I think it ridiculous in an advanced society to have to accept the deaths of humans, as one does with mice, to know of success with any experiment.

Today when people with a disease go on the Diet and follow it 100%, that is avoiding the blockers, and their bodies have not been destroyed by conventional treatment, there is a 100% cure rate. One of the most devastating conventional treatment is the continuation of radiation treatments after the decision that there is no more hope, it completely destroys the immune system. My opinion is that it is doctor assisted suicide. Isn't that what the latest nuclear weapons are designed to do? Kill people without destroying the infrastructure?

Senator Blanche would you support, perhaps expedite a federal grant, if I am successful in convincing the Arkansas BioVenture Advisory Board,. the CEO of EXOEMIS and the Director of Special Projects, University of Arkansas Medical Sciences in Little Rock to conduct the trials to confirm my findings. Last September an announcement was made, (see attached article) of a $2.4 million grant for several institutions to do research that I have already accomplished. It is estimated to take 3 years to complete. What the research will accomplish is nothing more then confirm my discovery already patented. I have provided Chancellor John White information of the circumstance. Chancellor White did not acknowledge my communication.

Senator Blanche, a conserative estimate is that in 3 years more then a million victims in the US will die from cancer. Many will be Veterans, members of the Greatest Generation just like me, and it tears at my guts that I have been unsuccessful in getting help to prevent it.

After extensive research and testing my findings on individuals knowledgeable and experienced in the appropriate field, I can tell say there is a flaw in the FDA test management program relative to environmental stress on human performance.

The critical item involved in this finding is oxalic acid, a blood borne chemical in the blood of all mammals including humans. A estimated mean value of 288mcg of anhydrous oxalic acid/100ml has been reported for normal human blood.

The decomposition of solutions of oxalic acid has been made a basis of a method for measuring radiation dosage, in the sterilization of food and medical products. The absorbed dose is determined from the decrease in oxalic acid concentration which occurs during irradiation.

If the FDA authorizes a new drug for use on humans or other mammals, where the approved test procedure was directed toward identification of potential failure of the drug and irradiation was used partially or continuously on a mammalian test specimen, the test is flawed. It is possible very serious consequences could develop if a human with a normal or elevated oxalic acid blood level was provided the drug. If oxalic acid and the new drug created a toxic chemical it would not be known. The results could have lethal consequences.

Immediate action should be taken to confirm or deny my findings. Approval of any product where radiation was used during testing should be immediately suspended until the action is completed.