Lyme Disease

My Lime Disease Story

First let me say that I am not a doctor, nor do I play one TV. But the Doctors have sure seen a lot of me!!

Like most people with Lyme disease I went years without being diagnosed. Over my first 20 some years of life my parents or I had removed about half a dozen or so ticks. Most had no rash or noticible effects on me.

The first unusual tick bite was while hiking in the mountains of Northern California or Nevada way back in 1975. The tick was black with a white star on it, and was very difficult to remove. Back in those days I burned them off, that is the wrong way to remove them. We tried burning, cutting all sorts of things to get the critter off of me. The correct method is to use tweezers as close to the head as possible and gently rock it side to side. After removing it I developed a rash that some jokingly called "Rocky Mountain Spotted Fever". Now I know that it could not have been RMSF, RMSF is found on the East Coast. Recently they have discovered that ticks in the Northwest do carry a form of Babesia called "WA-1"

The next tick problem was when I went to a wedding in the spring of 1978 in Massachusetts. On the way back from the wedding the car broke down on I-95 in eastern Connecticut. I will give you three guesses as to where that put me. Somehow in the process of fixing the car or just goofing off I scratched my left arm. The scratch healed except one end of the scab did not come off. Someone at work convinced me to see a doctor about it. The doctor examined it then he removed it with tweezers. He told me it was a very tiny tick and asked if I could see its legs. I could not see the legs, the tick was way too small!

I returned to the doctor a couple of weeks later with a circular rash. He called it "Ringworm" and gave me something for it. I asked why it had formed right around where he had removed the tick. He said the tick could not have caused the rash. The Ringworm treatment did not work and it grew and spread.

The following spring I was almost kicked out of the Navy when the doctors found a giant bulls eye rash about 1 foot by 8 inches in size on my back. They had me look in a mirror to see it, at first I thought it was some sort of a trick, but it was really there. They asked me what countries I had been to and what girls I had been with. I told them I had never been out of the US and I did not even have a girlfriend. They put me on benadryl for a possible allergy. I returned for another physical a few weeks later and the rash was gone, so they let me stay in the Navy.

At that time the doctors diagnosed first a bladder infection, next tennis elbow and then "likely polyalthralgia" because I ached all over. Over the next 20 some years I saw dozens of doctors and was diagnosed with Severe allergies, Mitral Valve Prolapse, Acid reflux disease, Constipation, Irritable Bowel Syndrome, Migraines, Depression, Eye problems, etc. Eventually it reached the place where walking was very painful, there was blood in my BM and urine, and I felt like I was going to die. The docs all assured me there was nothing seriously wrong with me.

Finally A Diagnosis

One day while working with a friend I had to sit down, I could not take another step. He suggested I look into Lyme disease. I told him it could not be that, because those people are all in wheelchairs. A few days later I came across a Lyme disease Brochure and opened it up because of what he had said to me. I saw pictures of the rash and started reading. I still had the rash several times a month after all of those years. The brochure said the rash was "Pathogenic" for Lyme disease. I looked it up and found out that the CDC says if you have the rash you have Lyme disease. With this new understanding of my illnesses I went to see the doctor but received a very cold reception. Blood tests quickly proved that it was not Lyme disease. But how do you explain the rash? So I continued to researched Lyme disease and found a web site where you can ask questions of others with Lyme disease. It is at http://www.lymenet.org

Eventually I changed doctors and got on Doxycycline. At first I was much worse, but after 3 weeks my health started improving. I am still doing lots of research on Lyme disease. My hope is that the PCR DNA test will eventually be accepted as a better test for Lyme disease. In my opinion the current tests are almost worthless.

My Research

My research into Lyme disease is out of my desire to do two things.

First is to try to find a cure for this disease.

Second is to make that cure available to everyone free of charge.

Here are two important links. The first shows that blood parasites like Malaria and Babesia are susceptible to magnetic fields. The Iron in the red blood cells builds up in the blood parasite. Iron is highly magnetic. Cancer is also very high in Iron. If this is the case, then magnetic mattress pads and other magnetic devices may play an important role in the treatment of diseases.

http://www.washington.edu/newsroom/news/2000archive/03-00archive/k033000.html

The second link is to show that treating blood parasites may be important in chronic diseases. They put a big strain on the spleen and may even lead to it failing. H-pylori is a spirochete bacteria similar to the one that causes Lyme disease. This study shows that healthy spleen cells help in fighting disease. So then blood parasites must be treated first, before the Lyme disease can be effectively treated.

http://unisci.com/stories/20012/0426014.htm

I have what is jokingly called "Not Lyme" disease. "Not Lyme" disease is when all the symptoms are the same but every doctor says it is "Not Lyme". That is even though a doctor removed the tick and called the rash "ringworm". The first thing I had do was to prove to myself was that I actually have Lyme disease. To do this I used a microscope with 600 X magnification to look for the spirochetes. Then a Sony Camcorder with 15 X zoom is focused into the microscope. The video output is then run to a "Snappy" video capture device plugged into the parallel port of a computer.

During this research I take several pictures and find out what ones look best later. I tried to find them in my blood, tears, urine, and saliva. At first the possible spirochetes were only visible in my urine. Even there they are hard to find, as they are almost transparent. Later I caught one amoung my Red Blood Cells while looking for parasites. I did see blood parasites, they appeared as three or four black dots in about 1 out of 10 red blood cells but I did not get any pictures of them. Now I know that what I am seeing in the picture is too large to be spirochetes, but what are they?

My research has continued to discover that ticks also cary small worms. Some worms are known to attack the eyes and may be responsible for some of the things in the eyes appearing just like what is seen in the picture. I have read where they discovered that American visitors to India already had small worms when they arrived. That comes from a study of people before and after they visited India. The study was supposed to see how many people picked up worms while visiting India.

My treatment protocol once used ALL of the following medications, but I am NOT a doctor, see your doctor first! I was taking Doxycycline, Flagyl (Tinzandole), Garlic, Quinine, Silver water (Called "Ionic Silver"), and Bismuth (Pepto Bismol). Now I am just using an electromagnetic Coil device, my high voltage zapper, drinking tonic water, taking wormwood, and taking some supplements! I take benadryl to fight the allergies and to help to get to sleep at night. A good supplement is called "Ambrotose" it has glucosomine for your joints, Aloe Vera for your stomach, and Arabinogalactin to boost your immune system. I also drink lots of Green Tea.

In My Opinion.......

Over 90% of illnesses are caused by viruses, bacteria, and parasites.

Technology WILL someday make "Star Treck" like treatments of diseases a possibility.

"Autoimmune" diseases are really caused by allergic reactions to infections.

Natural antibiotics will always outperform synthetic ones (Contrary to "Evolution").

Some examples of natural antibiotics are Aspirin (White Willow bark), Quinine (Chincona bark), Penicillin (Mold), Wormwood (Artemesia), Garlic and Green tea (Plants). "The leaves of the tree were for the healing of the nations" -Revelation 22:2

Lastly I do not believe there is any such thing as "autoimmune" diseases! The PCR DNA tests have shown that arthritis is an allergic reaction to an infection. Previously attempts to culture bacteria from arthritic joints proved negative and so the idea of "autoimmune" diseases arose. Now we know better, yet some doctors still claim that "autoimmune" diseases are the plague that is sweeping across this country, with more than 100 of them "discovered" since we cut back on using antibiotics. In my opinion you can control the allergic reaction by destroying the immune system and killing the patient, or you can fight the infection!

If you watch TV any you will know that they are even pushing treatments for arthritis and other so called "autoimmune" diseases that do nothing but supress the immune system. If you do a search of medicines approved in the early 1900's they included medicines made from arsenic and mercury. In the short term they likely worked, but in the long term they killed the patient. Are the perscription medicines they are pushing today any better? Listen to the side effects during the commercials, how many include the side effect of death? How many of these drugs require regular testing to try to prevent liver or kidney failure?

Finally it has been said, and I will repeat it, that if illegal drug users knew what legal drug makers make they would stop selling their illegal drugs and start working at a phermacy.