“An integrated approach to treating Cancer”
My treatment approach to cancer is based on the fact that cancer is a mitochondrial metabolic disease. Cancer cells use fermentation to generate energy, meaning they produce energy without the use of oxygen. This is the result of damage to mitochondrial respiration. Mitochondria are the powerhouse of the cell, responsible for producing ATP, the primary source of cellular energy. When the mitochondria become dysfunctional, they revert to fermentation fuels that don’t require oxygen, such as glucose and glutamine. If you want to kill cancer, you must deprive it of its fermentable fuels, glucose and glutamine. As you degrade the tumor by restricting glucose, your other cells will continue to improve in health as they rely on fatty acids. Normal cells are very flexible in the fuels they can use, while cancer cells are restricted to just two fuels, glucose and glutamine, because their oxidative phosphorylation system is corrupted.
1) Starve the cancer of its two fuels, glucose and glutamine. We deprive the tumor of glucose by following a strict Ketone diet. To get patients into ketosis quickly, we start with a water fast for 3-7 days. Fasting starves cancer of glucose, its primary source of energy. It also triggers autophagy (your body's cleanup system), which helps clear out damaged cells. We simultaneously deprive the cells of glutamine by administering glutamine blockers throughout the day. Once you understand the origin of the disease, you can manage it without toxicity.
2) We then administer Ivermectin alternatively with Fenbendazole throughout the day. These two drugs facilitate apoptosis, or programmed cell death, by inhibiting the microtubules of cancer cells. These drugs inhibit glucose uptake in cancer cells, which are 200 times more dependent on glucose than normal cells. They reactivate the p53 gene, also known as the cancer suppressor gene. These drugs are a form of chemotherapy that targets cancer cells, while sparing normal cells. These have been used effectively in the treatment of various diseases, including the eradication of parasites from the body.
3) We then flood the system with oxidative treatments that create an oxygen-rich environment. This inhibits cancer growth as they thrive in an oxygen-poor environment. These oxidative treatments can boost your energy level and immune function.
4) It is essential to manage cancer and support your immune health, allowing it to effectively engage in destroying cancer cells. We do this by ensuring your vitamin D level is over 100. Vitamin D is not a vitamin but a hormone that regulates 2500-2800 genes that control your immune system. Additionally, I encourage Regular physical activity, which has been shown to improve cancer survival rates and enhance quality of life. Both aerobic exercises and resistance training can help reduce inflammation, boost immune function, and combat fatigue caused by cancer and its treatment. This is particularly beneficial, as it allows the muscles and brain to take priority, depriving the tumor of its fuel when there is extra sugar in the system. Stress management is also essential, as chronic stress elevates cortisol levels, which can weaken the immune system.
Integration with traditional treatment: Some patients may choose to continue pursuing traditional treatments. It should be noted that the above therapies enhance the effect of conventional chemo and radiation.
These treatments degrade the cancer
1) Starve the Cancer of its two fuels, glucose and glutamine
2) Destroy the cancer with Ivermectin, Fenbendazole, or Menbendazole
3) Create a hostile environment for cancer to survive
4) Build up your immune system to better protect healthy cells and degrade cancer cells
When cancer is in a weakened state and is more susceptible to both chemo and radiation, it requires fewer and shorter-duration treatments. I encourage patients undergoing traditional therapy to consider adding these integrative therapies, especially if they are vaccinated for COVID, as the vaccine can potentially activate the P53 cancer suppressor gene. Ivermectin reengages the P53 cancer suppressor gene.
NOW AVAILABLE, Thomas Seyfried’s Press-Pulse Therapy is an innovative metabolic strategy for treating cancer, developed from his research at Boston College on the metabolic theory of cancer. It is rooted in the idea that cancer is primarily a metabolic disease—caused by dysfunctional mitochondria and reliance on fermentation fuels (glucose and glutamine)—rather than a purely genetic disease.
Here’s a clear breakdown:
Core Concept
Cancer cells survive and proliferate by fermenting glucose and glutamine. Healthy cells, however, can adapt and thrive on ketones and fatty acids when glucose is restricted. Seyfried’s therapy uses a “press” and “pulse” approach to weaken and destroy cancer cells while protecting healthy tissue.
The “Press”
The press is the constant, ongoing metabolic pressure that stresses cancer cells:
Ketogenic diet: severely limits carbohydrate intake to reduce glucose availability.
Caloric restriction/fasting further lowers glucose and insulin levels, while increasing ketone levels.
Lifestyle/metabolic strategies: exercise, stress reduction, sleep optimization, and exogenous ketones.
This creates an energetic stress on cancer cells that can’t efficiently use ketones, forcing them into metabolic crisis.
The “Pulse”
The pulse is an intermittent, targeted strike to push weakened cancer cells over the edge:
Drugs or natural compounds that block glutamine metabolism (e.g., DON or other inhibitors).
Oxidative therapies like hyperbaric oxygen, ozone therapy, or high-dose vitamin C — exploiting cancer cells’ inability to handle oxidative stress.
Other repurposed drugs (fenbendazole, ivermectin, metformin, etc.) that add metabolic stress selectively to cancer cells.
The pulses are given intermittently so the body can recover, but the cancer cells—already under constant press—cannot adapt and eventually die.
The Goal
Starve cancer cells of their two key fuels (glucose + glutamine).
Exploit their defective mitochondria and poor antioxidant defenses.
Protect and even strengthen normal cells by keeping them nourished with ketones and amino acids.
Create a reproducible, non-toxic framework that could work across all cancer types, not just one.
Why It Matters
Unlike chemotherapy and radiation, which damage healthy cells, Press-Pulse Therapy selectively targets cancer metabolism. Seyfried believes this approach should form the future foundation of cancer treatment, integrated with other supportive therapies.
Links:
Targeting the Mitochondrial-Stem Cell Connection in Cancer Treatment:
Fasting for 72 hours is the best medicine on Earth
Scientists Announce Major Breakthrough as Ivermectin Nanoparticles Destroy Brain Cancer Cells:
New Study: Ketogenic Diet Without Chemo or Radiation for Control of Mutant Glioblastoma
Avoid Radiation with Glioblastoma patients:
Clinical research framework proposal for ketogenic metabolic therapy in glioblastoma:
Premium FenBendazole no fillers
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