In our culture, there is a pervasive fear of fever.

Many people see fever as the cause of illness, rather than the body’s natural attempt at healing. While fever racks the patient, the mother, father, lover, friend, or caretaker stands by, feeling powerless. It is no wonder that at the first sign of a fever, we quickly reach for medications such as aspirin or Tylenol
(NSAIDS—non-steroidal, anti-inflammatory drugs).

The medicine represents hope and recovery. Giving medication implies a cure. (And so does the advertising.) The message is:
If you can just reduce the fever, the disease will go away. So the caretaker feels empowered by giving fever-suppressing medication. There is the belief that reducing the fever is a way of fighting the illness.

Ironically, the fear of fever is misplaced. Unless the fever is too high (104 °F (40.0 °C) or above over weeks at a time, no harm occurs. Fever signals the immune system to mount an increased defense and sets the process of healing in motion. In fact, fever is the natural response of all mammals to infection or illness.

This is true for cats and dogs, elephants and tigers, horses and humans. Research has made it clear that fever is not the enemy; it is the friend of healing. This scientific rationale, supported by thousands of research studies, provides the basis for hyperthermia treatment at the Medical Center Cologne and other medical centers in Europe, Japan, and world-wide.

A number of researchers have tracked this issue in large clinical trials over the past 100 years, starting with published reports in 1854 that many cancer patients have a “remarkable disease-free history.”

Several later studies confirmed this, reporting that people who developed cancer were rarely ill before their disease. If it seems surprising that this premise would have gone unrecognized for 150 years, consider the fact that scurvy among seaman caused by lack of vitamin C was not acknowledged for more than 100 after it was first confirmed by a ship’s physician.

The doctor’s recommendations were adopted 105 years later when another naval physician reported a similar finding. In a similar pattern, studies on the importance of fever in a strong immune defense against cancer were published in the medical literature in 1854, 1910, 1934, and 1936, each study involved hundreds of patients. Researchers consistently found increased cancer risk for patients who had no history of infectious illness or fever. The majority of more recent studies have corroborated these findings:

• German research published in 1983 found that cancer risk more than doubled in patients who had not experienced major infectious diseases (2.6 times greater risk). Cancer risk was more than five times higher in patients who had never experience the common cold (5.7 odds ratio), and there was a 15-fold increase for those who had never experienced fever (15.1 odds ratio).
• A study of skin cancer patients, published in Melanoma Research in 1992 reviewed the medical histories of 500 comparable patients, with and without cancer. Researchers found that the patients who had experienced infections accompanied by fever had a much lower incidence of malignant melanoma.
• Research published in the journal Cancer in 1992 evaluated the medical histories of more than 200 patients with brain tumors, who were compared with over 400 similar but non-cancerous patients. Those who had experienced infections and colds had a 70% lower risk of cancer.

NIH Report on Fever

One of the most insightful looks at the role of fever has come from a research team from the National Institutes of Health.
The researchers performed an in-depth review of the medical literature on cancer risk. They reported that risk appears to be increased in individuals who have experienced fewer infections. They noted “an inverse correlation between the incidence of infectious diseases and cancer risk.

” In other words, people who have not experience common childhood illness and fever seem to have a greater risk of cancer. Averting fever by the frequent use of aspirin or antibiotics may actually impair immune function.

The NIH team concluded that, “the occurrence of fever in childhood or adulthood may protect against the later onset of malignant disease.”

They also pointed out that “spontaneous remissions are often preceded by feverish infections.”[vi,vii] Their final report includes hundreds of references from the medical and research literature.[vi]

In a newborn the immune system is immature and underdeveloped. For example, protective antibodies are not made by the infant’s body, and the baby relies on those transmitted before birth by the mother to her infant through the placenta. These maternal antibodies become depleted by the time the baby is about 6 months old. At this point, the immune system of the child must learn how to respond to invasive infections such as bacteria, viruses, and parasites and to threats from within the body such as abnormal and cancerous cells. Like any other organ system, the immune system must develop and mature if the child is to remain healthy.
On average, each newborn develops about seven viral infections in its first year of life. Researchers now view fever as a “necessary attempt by nature” to support immune system development and have confirmed that it is the process that activates the immune response.ii,iii,iv Cohort studies have also shown that a child needs at least 4 to 5 episodes of high fever before age 6 to develop an adept immune system.
The development of immunity can be compared with the maturation of the muscles and skeleton, which only develop correctly if they are used all the time, and experience periodic exertion from activity and play. That is why we encourage children to participate in sports. A child who is bed-bound or wheel-chair bound does not have the opportunity to develop a proper skeleton and musculature as a result of disuse.
The immune system can only develop fully if it is put under “stress” by defending the child against invading microbes such as viruses and bacteria. When a child experiences any type of infection, the immune system must augment its defense mechanisms and step up its activities and metabolism. In childhood, fever is important because it plays a role in immune development and maturation so the system can function properly life-long.
A number of researchers have suggested that averting childhood infections and fever through inoculations for benign illnesses such as chicken pox and rubella may be a factor in increased vulnerability to cancer in adulthood.

• A British study published in 1977 of 300 women with ovarian cancer found lower incidence of measles, mumps and rubella compared to non-cancerous patients.
• Another study published in The Lancet in 1985 of 500 patients reported that approximately 6% of cancer patients had not develop measles in childhood compared with less than 1% of noncancerous participants in the study.
• A third study in the American Journal of Epidemiology (1986) reported that children with leukemia had experienced fewer infections in their first year of infancy, suggesting the importance of stimulating the immune system early in life.

When fever is blocked with medication such as aspirin, Tylenol, or antibiotics, that appears to compromise long term health by impairing immune development.

Absence of fever in cancer patients —In clinical cases evaluated at the Medical Center Cologne, the vast majority of cancer patients report that they are never sick and they never missed a day at work. Typically, they may have had a few days when they experienced a sore throat, a cold, or a cough, but it was never accompanied by fever. When fever did develop, it was suppressed with aspirin, Tylenol, or antibiotics.

Most cancer patients also have a reduced core body temperature and lack of circadian temperature rhythm.[xxi ] These are indications of the inability to raise temperature to a level necessary to activate the immune system.[xxi]
It is possible that we have unknowingly conditioned the immune system not to respond, through our use of fever suppressants with our children.

Interrupting the fever mechanism —Surprisingly, the immune system can be trained to turn on or off in response to repeated cues, for example in response to certain medications. This trained or “conditioned” response was demonstrated in the work of Dr. Robert Ader and colleagues, published over a period of 25 years. Researchers found that the immune system could actually be deactivated through “classical conditioning.”

Applying this finding to the use of fever suppressing medications with children, the implication is that over time the fever response can be permanently inactivated by the frequent use of medication. Childhood fevers are also prevented when vaccines are used to avoid common childhood infections. From that point on, whenever the child develops a fever, the fever process is aborted.

Suppressing the immune response —In time, the body becomes conditioned to suppress fever at the slightest hint of a fever. Since fever is the cue that activates many of the key defenses of the immune system, this also means that immune response is cut short and never activated.

Loss of defenses against cancer —We now know that our bodies develop cancer cells every day of our lives. When we have periodic bouts of cold or flu, if we allow our bodies to experience a fever, that provides an additional opportunity for clearing malignancies and l ingering infections. If the immune system is never activated, we have lost these opportunities to destroy cancer cells while their number is still small.

Increased risk of chronic infection —Suppressing fever may also enable bacterial and viral infections to become chronic. Without fever, some of the infectious cells escape destruction, linger, and start increasing in number. Note that although we think of antibiotics as our primary protection, it is actually the immune system which protects us. The antibiotics simply lower the infectious load so the immune system can handle it more easily.

Infections linked to cancer —Specific types of chronic infection have been linked to the localized development of cancer, including human papilloma virus, viral hepatitis, and H. pylori bacteria. In the peer-reviewed literature, more than 20,000 articles address the link between cancer and these three infectious agents.

• Chronic human papilloma virus infection is implicated in about 40% to 80% of
  all cervical cancers.
• Various forms of hepatitis viral infections are associated with the development of liver cancer.
• H. pylori bacterial infections have been identified as a causal factor in an estimated 40% to 80% of gastric cancers.

Allergies, asthma, and cancer —Among children who never developed a high fever, about 30% develop food allergies, hay fever, and contact dermatitis (atopic dermatitis). In children who experienced episodes of childhood fever, only 5% develop these allergic reactions. Overuse of fever-suppressing medications has been found to increase the risk of allergies and autoimmune conditions.[xx]

Increased incidence of asthma —A recent study on the effects of Tylenol exposure in childhood published in the British journal Lancet in 2008 reported on the health of 205,487 children ages 6 to 7 years old, from 31 countries.
The study found that exposure to Tylenol (acetaminophen) during intrauterine fetal development or during the first year of infancy was associated with an increased risk of asthma symptoms. The risk was “dose-dependant”—the more frequent the Tylenol use, the greater the likelihood of asthma. Tylenol use, both in the first year of life and in children aged 6 to 7 years is also associated with an increased risk of symptoms of rhinoconjunctivitis and eczema. This data suggests that by suppressing fever, the immune system becomes compromised and less functional.

Nothing led me to suspect that I had breast cancer. I’m a strong woman. I’ve always been strong and active… I’ve always done my work with energy and commitment. (I’ve always been very health—one of those people who never misses a day of work.)

I was initially diagnosed with breast cancer in the summer of 2005 and had breast surgery, 8 sessions of chemo, 25 sessions of radiation, and medication. Although I went into remission and felt better, in 2007 I learned that the cancer had metastasized to my bones and my oncologist told me that it was incurable.

I see cancer as a disease I have to deal with. But I want to live. If other people can survive cancer, so can I. My attitude is that I will do whatever it takes.

In August 2008 I began treatment at MCC, despite severe bone pain. At that point I had nothing to lose and everything to gain, so I decided to do the hyperthermia and dendritic cell treatments. The treatments at MCC had no significant side effects, although the two hours of hyperthermia were tough for me. The localized was no problem at all. I experienced the dendritic cell vaccinations as a severe flu with headaches and nausea that lasted for about 6 hours. It was unpleasant but I knew it will be over after just a few hours

After three treatments the pain went away. It was totally gone and I stopped taking pain killers. I have felt good ever since.

Four months after my first treatment at MCC, I went for a checkup with my original oncologist and they did a PET scan. The bone cancer was gone. There was no trace of the cancer visible on the scans—they had disappeared and in September 2010 another PET-CT Scan still showed no recurrences and I am still in complete remission. Now I am hopeful about the future. God will decide when my time has come. But I know that I will live for many years to come.

Fatima Galamba, a patient with metastatic breast
cancer and now in complete remission for more than
two years and who was treated with the Gorter Model.

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When I arrived at the clinic for my hyperthermia treatment, the nurse checked me in and then helped me settle into the hyperthermia chamber, which is essentially a light box heated by infra-red lighting as shown in Fig. 6.2a and 6.2b.




My head was outside the box, comfortably supported by a pillow, which avoids any sense of claustrophobia. The doctor then began an IV infusion of electrolyte minerals to assure that I would not get dehydrated. The infusion included antioxidants, particularly vitamin C and selenium. An electronic thermometer was provided rectally so that my core temperature could be monitored continuously. To monitor my heart rate during the treatment, the nurse also placed a few electrodes on my skin, attached with gel. (This is another step provided to assure the safety of all patients.)

The lights inside the light chamber gradually increased my temperature. However, because the container is relatively air-tight, perspiration did not cool my body, which was also covered with heavy towels to retain the heat. My temperature gradually increased. After about three hours, the lights were turned off, but my temperature continued to increase for a while because the blood just under the surface of my skin was still warmer than the rest of my body. Once my skin began to cool, the returning blood began to cool and my core temperature very slowly began dropping naturally.

For me, the worst side effect of hyperthermia treatment was boredom and the inability to turn over while lying on my back for four and a half hours. My major concern occurred about 2 hours into the treatment, I had to urinate. This was solved by urinating into a special container. When the treatment session was finished, I took a shower, shampooed my hair, and felt comfortably warm, very relaxed, and ready for a meal. I went downstairs to the hospital cafeteria and ate a large salad and a delicious dessert. This is a very different experience than I imagine I would have had with chemotherapy or radiation.

Erik Peper, PhD

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I was diagnosed with colon cancer and that spread to my liver. Although I did well on the chemotherapy, the oncologist made it clear that treatment was palliative and not a cure. So we made an appointment for a consultation in Cologne. When we learned that Dr. Gorter’s treatment could be used together with chemotherapy, we decided to do that as well.

I began the total body hyperthermia and dendritic cell therapy in Cologne. Once you’ve received the treatment, you know what to expect. It’s not painful and I was hardly sick at all. I usually feel worse after the dendritic cell vaccination, but only for one day. Every nine weeks a scan is made and they show that there are no new tumors and the liver tumors are getting smaller. The fact that my cancer has stabilized is remarkable.

Truus Kleij-Swan, more than five year long-term survivor of
intestinal cancer, metastasized to the liver, lymph nodes
and peritoneum.

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Twenty years ago, Teun van Vliet was twice an indoor world champion cyclist and in 1988 wore the yellow jersey in the Tour de France. In 2001 he was diagnosed with a brain tumor and in 2006 an inoperable recurrence of the tumor was detected. Teun had another round of brain surgery (“debulking”) and also received radiation treatment.

This caused him to lose his power of speech, and to some degree he also lost memory and coordination. Within conventional oncology, nothing could be done for him. He was told that he had a year left to live at the most. Teun and his girlfriend decided to seek a second opinion and they went to Cologne to consult with Dr. Gorter, who advised him to do localized hyperthermia in combination with immune therapy. Teun’s partner soon noticed beneficial changes in his health:

“The first thing we noticed about these treatments was that they really improved his speech. He is much more lively; more active. I have my old buddy back, really. When he comes home from Cologne, his speech has improved, his motor skills have improved, he feels more energetic. Nothing but improvements. The quality of his life is definitely better. In April 2010, a new MRI scan confirmed that there is still no recurrence of the cancer and Teun has been clinically cancer-free for more than four-and-a-half years.”

Partner of Teun van Vliet, Tour de France
Champion Cyclist, survivor of brain cancer.

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