What is the Cytoluminator Cancer Treatment 

The Cytoluminator Cancer Treatment is not static, they continually add, improve, and meet challenges faced by those they treat. Some of the challenges are of those with prior chemo damage or radiation damage; other challenges are understanding how to overcome the release of toxins held inside the tumor tissue.

Once you arrive, we will do extensive testing using unconventional methods as well as conventional methods when needed; blood tests are a common occurrence.  When your baseline is done we will monitor your progress.  Select supplementation is used based on the administrating doctor's assessment of what the body needs.

You will begin your three weeks stay, undergoing extensive Rife work.  The first portion of the Rife work will be done exploring and scanning the patient for all viruses, fungi, bacteria, and parasites; these are often a catalyst to your cancer; the cause of cancer is an accumulation of many such factors creating the 'perfect storm' for cancer.  After such a scan, the Rife machine will then be used to eliminate them, this can take several hours.  This scanning and treating will be repeated throughout your stay to determine what is released from the tumors as they are exposed, and the cancer killed. Many bacteria, viruses, fungi, and parasites live inside tumors and are not detected until they are exposed or released; if not killed off they will go on to make the patient sick.

4th Generation PDT will be used alongside your Rife work specially formulated sensitizer is administrated. This formula is stronger than any other known to be used across the globe. The sensitizer is teamed synergistically to special laser lights designed by the researcher to operate at a hundred times stronger than any other PDT light known, the reason other PDT's do not work below the skin layers and why the researcher calls it 4th Generation PDT.  When the lights meet the sensitizer cancer cells begin to die.  The most significant occurrence is an immune response, making the patient immune to their cancer.  This means the body will build immune data against the cancer, every cell that it encounters containing the DNA markers of your cancer will be automatically killed off. No recurrence.

In the first days a nano formulation is given, this formulation is designed to go directly into cancer cells only and prevent them from gaining energy for life and reproduction.  The cancer cells cannot live through administering of this solution. Without being able to 'feed' they die quickly. No healthy cells are harmed. We will determine how long to administer this serum.

At the end of your treatment, a second serum, x-gly, may be given. The team here will determine if you need this based on how you are doing. This serum is able to stop all blood flow to tumors and kill off more cancer cells. A very advanced cancer may need this to help the body further.

During treatment, many pains, and discomforts from the cancer are alleviated. As the body begins to recognize stray cancer cells, the body will send out a response in the form of inflammation this usually occurs after leaving because it takes a few days or weeks for the immune system to find such cells. We note - do not be surprised to find soreness or pain from inflammation in areas that you did not know you had cancer, this is NOT cancer spreading, on the contrary it is the body finding cancer where conventional medicine did not; the body is far superior. 

While we kill off most all cancer while you are with us, the possibility of stray cancer cells are real; the body will be set to a mode of curing itself.  Most see tumors shrink within a short time, some lesions may disappear while there; large amounts of cancer and large tumors take time for the body to eliminate from the body. The body works systematically and can only eliminate a certain number of cells at a time; it took a long time to make the cancer, it will take a long time to remove it. .  If you have blood work done upon returning know that cancer as it is killed releases certain elements into the blood, dead cancer releases antigens. Numbers can significantly rise; it is NOT a sign of cancer going wild, this is a sign of the body finally beating the disease. As the dead cells are cleaned up the numbers will drop.  Detoxing is an essential part of your healing process. Supplements will be suggested and changed as you go through your healing process. You will be referred to After Care monitored by Jesicha's Hope, their expertise we support.

We here at Cytoluminator want you to understand this is a unique treatment and it not found or known elsewhere because it is completely created and researched by our Scientist and founder. We are not a 'clinic' in the sense most think; you are seen in a private setting, the mini-clinic is private; your stay is in ’Patient' houses that are nearby within the private gated community located outside the city. If you are looking for out of the ordinary, complete scientific but non-invasive approach to curing yourself of cancer, or autoimmune disease, we believe this is the place.

You leave after three weeks of treatment, your after care or beyond cancer journey is just beginning.  Some that are advanced or have many metastases are encouraged to stay for three weeks. Many children are there for four weeks to be sure they are doing well.

We will NOT recommend any PET, CT or MRI scans after leaving as these scans cannot tell the difference between, dead or living cancer, inflammation or infection.  It is understandable people are in fear still and they are taught these types of scans are reliable, but they are not. Resist for your own good. These scans also promote cancer growth and clumping of stray cancer cells making them harder to remove by the body. Ultrasounds, naturopathic testing, including Kinesiology are safe and reliable, the body knows.

And what if for some out of the ordinary reason there is a slight recurrence or that not all cancer is dealt with from the immune response. If this rare occurrence happens you can go back at no charge and we will repeat the protocol. This is so rare never yet has anyone returned for recurrence of cancer. If you have had extensive chemotherapy or radiation within a few months prior to going for Cytoluminator  treatment a secondary cancer can occur, the is due to the secondary cancer has not yet begun yet from the chemo or radiation damage therefore the 4th Gen PDT did not create an immunity against it. In these cases we will treat you at a significant courtesy discount. Some become so reliant on our services and protocol that they want to return for checkups.  We arrange check ups at a very small cost.

Questions and answers below are directly related to explaining the Cytoluminator Cancer Treatment  for other questions and answers go to our Q and A page.

The answers below may be quite scientific they are answered by Scientist Wright of Cytoluminator

What type of cancers does this protocol cure?

The treatment is non-type specific; because of how it scientifically works this protocol works with any type of cancer, any stage that your doctor claims you are. We want you to note, that stage four is considered when the cancer has spread beyond the originating area. When you are diagnosed - everyone is stage four - once one cell has entered your blood stream, wherever the blood travels so does the cancer - everywhere in your body the cancer travels and cells are deposited.

Explain what the x-gly is-

Oncologists cannot afford to have their patients cured, it is a danger to their income. Studies have discovered something called bromopyruvate. This chemical stops the cancer food manufacture. You've probably heard of glycolysis, the conversion of sugar to energy through fermentation. That is how cancer produces adenosine triphosphate (ATP), the basic food for all cells. The molecule interferes with that only in the cancer, so it stops the cancer's energy production and replication stops so eventually the cells just die of starvation. This has a stunning effect on cancer, but as used before [see below chart] it is unstable and not as powerful as it could be. To make it really useful they had to go beyond the current design and create a new molecule. According to basal metabolism tests, their version of this molecule is over 2000 times more powerful than the material discussed below. They have been using a highly modified version of this for over a year and see incredible results on all cancers, including brain cancer. The small green curve on the chart below is the result of the first modification of 3BP and it is about 50 times more powerful than the original molecule discussed below. Their latest version is over 400 times more powerful, so it is about 2000 times stronger than the molecule of the bromopyruvate.

gly chart

Tell me about PDT? And what makes this PDT different than other PDT's offered in other clinics around the world?

The principle is simple.  A sensitizer is put into the body and, if it is designed properly, it goes to bad organisms like cancer bacteria and viruses.  When a light of the right wavelength activates it, it converts the oxygen near it to a very toxic form of oxygen which kills the bad organisms.

Like any technology, PDT has been improving with time as new advancements are made in the sensitizers and lasers.  The first-generation sensitizers, photofrin and ALA, had big problems which they could never overcome.  They accumulate in the skin heavily, are activated by UV, and their activating wavelength is absorbed heavily by blood.  Consequently, patients had to have ZERO sunlight for a full month, they could not be treated through the skin so surgery was necessary to get the light in, and most importantly they could not kill more than 3mm of tumor at a time.  In short, they were pretty worthless but even, so they got the ball rolling to stimulate further advancements. Second generation sensitizers, notably the chlorin and chlorin derivative molecules solved some of the problems, but they had poor selectivity and a number of other limitations, including an improved but still unacceptable penetration depth. There are in the my opinion as the scientist and developer of the 4th Generation PDT we use, only two, third generation sensitizers, their molecules and a similar molecules which has low selectivity issues.  It also is not convenient to "functionalize" so it does not lend itself to targeting specific tissues, so it cannot be used for most of their applications. There is only one fourth generation sensitizer in existence because no other provider has created a perfect nanomolecule shell for their sensitizer.  The nanomolecule is critical for targeting cancer well enough to treat deep into the body. I did it ! And this is what will KILL your cancer!


So what makes this different than other PDT?

The light source is critical. It needs to be concentrated and exactly the right wavelength (color) and of high intensity to work. A bed similar to the one shown below is being used by Noel Campbell and other SonoPhotoDynamicTherapy providers. Noel is under investigation by the Australian TGA and other agencies and accused of fraud. The second is the light source used by another SPDT user in Mexico. This light is about 30% as powerful as the one used in Australia and the researcher's investigation proved the Australian SPDT light was totally worthless. He estimates about 2000 hours for 1 cm penetration.

noels bed


At the Cytoluminator Cancer Treatment center, we use 3 different light sources, all custom made to be an exact match to our sensitizer. Instead of a $100 array of fluorescent bulbs we use high power lasers and even higher power arrays which cost between $10,000 and $35,000 each. These allow us to get all the way into the center of the body. This is where most cancer is found.


The graph above is the amount of light hemoglobin your blood absorbs at various wavelengths. You can see minimum absorption is at 685 (our wavelength) so that color penetrates best. This is a logarithm scale so at 600 nm 40 times as much light is absorbed. Ten centimeters into the body only 0.1% as much light reaches the cancer.


The above chart shows the sensitizer actually used by SPDT done in Mexico, even though they think it is Chlorin E6 [shown in chart below]. As you can see it absorbs at 632 nm, which makes it the worst sensitizer in the world, it can only penetrate 5 mm even with good lights, which they don't have. As the Scientist at Cytoluminator  I  have taken spectral absorption readings from many of their samples and they are wrong about what they are using. Of course, the doctor has no idea of this, they are not scientists. What SPDT uses is a cheap drug for hemochromatosis.


The above chart is Chlorin E6, what SPDT in Mexico thinks they have but they are wrong, but it is what NextGen [in UK]uses with a small addition that helps it get into cancer better. Biggest problems with these are no penetration, because wrong wavelength, it leaves the body very fast and it is only 5 times as much in cancer as in normal cells, which is why some patients have to have surgery to remove the healthy cells they kill.


The above chart is Cytoluminator's sensitizer. It has many advantages, 2 times higher quantum yield, exactly the right wavelength and does not leave the body until the cancer is dead, so you don't need recurring dosage at a high cost. Most importantly, it is a nano particle which results in 85 times more in the cancer than in normal cells

What is even more important than all of the above is the fact that nobody else uses nano particles and if they do not use nano particles there is no way they can treat metastatic cancer.

And what are nano particles?

There is currently a lot of effort put into nanotechnology, the study and development of nanoparticles and most of this centers around cancer research. Nanotechnology at present focuses a lot on gold nanoparticles, because they are easy to make, and carbon nanotubes. Unfortunately, there is building evidence that carbon nanotubes have major drawbacks when put into the body. 

We succeeded at this about 8 years ago and have been using it regularly and expanding on it to make new alternative medicines. Our nanotechnology has developed into an array of nanoparticle based medications that are incredibly effective against cancer. Several researchers around the world are trying to develop nanoparticle encased sensitizers, because they target cancer far more specifically. We have already achieved that goal with our present sensitizer. While it is not difficult to create nanoparticles, it is quite difficult to control their size and how they aggregate and assemble. It is also important to control how well the nanoparticles penetrate cancer cells. We use a nanoparticle that enhances the sensitizer uptake. Other researchers are working with gold nanoparticles, because it is the easiest nanoparticle to make, but ask yourself this, does cancer have a desire for gold bling? Probably not, your girlfriend may like gold, but cancer prefers sugar. Our nanoparticles look like sugar to the cancer.

The Cytoluminator  nano particles are about 25 nanometers. Cancer cells can take this size nano particles in, and they are less likely to cross into normal tissue. This is because of what is referred to as the leaky vasculature limited lymphatic perfusion trap. (patent pending).

"Our Nanoparticles Kill Cancer Even Without PDT to our surprise it turns out that the nanoparticles alone, without sensitizer or laser, kill cancer cells to about the same degree as chemotherapy, but the nanoparticles cause NO damage to healthy tissue. We make the oral nanoparticle solution available to cancer patients for follow up after PDT. The nanoparticle solution has no taste and is made from things you eat all the time, a meat preservative and a filler compound use in ice cream and yogurt."


Normal liver cancer cells before treatment    Same liver cancer cells after Nanoparticles

We have known since the early 70's nanoparticles were vital for cancer management, in those days they called nanoparticles the magic bullet because they can target all cancer specifically and they promised they would be in use in ten years, the same old thing they always say. Now, 43 years later, who is using nanoparticles for cancer treatment? I don't mean researching them, I mean using them. The reason nanoparticles are SO important for cancer is simple. you put the medication in the nanoparticles and inject them into the blood. You know food and nutrients penetrate the blood vessels, right? That is how all food and oxygen get to the cells. But nanoparticles are TOO BIG to get out of normal vessels. So, what happens is normal tissue never sees the nanoparticles or the medication inside them. When the nanoparticles find cancer, it is a different story. Cancer, like all scar tissue, builds leaky vasculature the space between the arteries and veins cells is greater and larger things can get out, so the nanoparticles flood into the cancer eagerly. When the nanoparticles are perfectly designed, they have a positive charge which causes cancer to pull them in like a star trek tractor beam and when the cancer tastes them, OUR nanoparticles taste like sugar. Cancer does not build lymph vessels, which are what removes things from the body, hence the term leaky vasculature limited lymphatic perfusion trap the term used to describe the method by which nanoparticles target cancer. Most photosensitizers are only 3 to 6.8 X selective, they only go into cancer 6.8 times more than normal tissue. Therefore, nobody else can treat deep metastatic cancer, because the normal tissue would be damaged. Our sensitizer is 85 X selective, which is a massive improvement that nobody else can come close to. As you can see in several places on this site, thanks to our nanoparticle technology we can treat down to the center of the brain, treating kidneys and colons is not a problem. When you are looking for alternative cancer treatment, always put a high importance on nanoparticles designed to treat cancer.

This treats all types of cancer, but what about terminal cancer like brain cancer, or osteosarcoma, angiosarcoma, ovarian cancer, skin cancers, etc - this will treat all those?

YES - if you understand the above information you should realize no cancer can hide from this protocol - NONE.