United States

California

Ultraviolet Blood Irradiation

Supportive Oligonucleotide Technique (SOT)

Pulsed Electromagnetic Field Therapy is a painless, non-invasive way to address abnormal resonance in cancer cells. In addition, PEMF has been shown to assist in making cell membranes more permeable. PEMF also is non-toxic to healthy cells. By inducing a mild electrical magnetic current into damaged cells, PEMF therapy slows or stops the release of pain and inflammatory mediators, increases blood flow of the cells, and re-establishes normal cell interaction. PEMF is not intended to treat a specific condition, however, it is more as an optimizer for the body’s natural functions of self-healing and self-regulation.

**Additional Resources:**
- <https://pubmed.ncbi.nlm.nih.gov/33675261>
- <https://pubmed.ncbi.nlm.nih.gov/34311647>
- <https://pubmed.ncbi.nlm.nih.gov/34368353>
- <https://pubmed.ncbi.nlm.nih.gov/26143265>
- <https://pubmed.ncbi.nlm.nih.gov/26762464>
- <https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119968>



Pulsed Electromagnetic Field Therapy (PEMF)

Prolozone is a treatment that injects ozone and nutrients into your joints to speed healing. This connective tissue injection therapy of collagen-producing substances and ozone gas can reconstruct damaged connective tissue in and around joints. These substances are injected into the connective tissue to rebuild the damaged areas.


Prolozone

Prolotherapy, which has been used since the 1950s, is based on the theory that chronic pain is often caused by the laxness of the ligaments responsible for keeping a joint stable. When these ligaments and associated tendons become loose, the body is believed to compensate by using muscles to stabilize the joint. The net result, according to prolotherapy theory, is muscle spasms and pain. Prolotherapy involves injections of chemical irritant solutions into the areas around the ligaments. These solutions are believed to cause tissue to grow quickly, which would increase the strength and thickness of the ligaments. This presumably tightens the joint and relieves the burden on associated muscles, stopping muscle spasms. Prolotherapy is used to treat many conditions, including back pain, osteoarthritis, fibromyalgia, plantar fasciitis, sciatica, sports injuries, temporomandibular joint disorder (TMD), tendinitis, and tension headaches.


Prolotherapy

Poly-MVA

Ozone (O3) is a close cousin to Oxygen (O2). The extra molecule makes O3 highly reactive and a powerful healing substance. Ozone is able to oxidize plaque and break down matter such as blockages inside blood vessels. It also can destroy cancer cells. O3 acts to strengthen healthy cells and destroy pathogens, including cancer cells, through several means, including activating the enzymes involved in “free radical destruction,” enhancing metabolic detoxification, increasing red blood cell pliability and blood fluidity, increasing the production of white blood cells and strengthens their effectiveness in detecting and destroying foreign matter, disrupting the cell wall of pathogenic cells. Ozone also is a strong anti-bacterial and germicide, both externally and within the body, and stimulates the immune system in general.

**Additional Resources:**
- <https://pubmed.ncbi.nlm.nih.gov/33850923>
- <https://pubmed.ncbi.nlm.nih.gov/33802143>
- <https://pubmed.ncbi.nlm.nih.gov/33932964>
- <https://pubmed.ncbi.nlm.nih.gov/33176412>


Ozone Therapy

Low Dose Chemotherapy

Laser therapies are medical treatments that use focused light. Unlike most light sources, light from a laser is tuned to specific wavelengths. This allows it to be focused on powerful beams. Laser light is so intense that it can be used to shape diamonds or cut steel. In medicine, lasers allow surgeons to work at high levels of precision by focusing on a small area, damaging less of the surrounding tissue. If you have laser therapy, you may experience less pain, swelling, and scarring than with traditional surgery. However, laser therapy can be expensive and require repeated treatments.


Laser Therapy

When you look at the evidence with IV Vitamin C, the volume dwarfs much of the research that pushes many prescriptions drugs today. The published evidence for the benefit of IV Vitamin C in cancer includes a reduction in pain, decreased cancer-associated inflammation, prevents cancer-associated sepsis, reduces side effects and toxicity of chemotherapy and radiation, augments the cancer kill rate of chemotherapy and radiation, and kills cancer stem cells (CSC). However, IV Vitamin C is not created equally for all cancers and is not a one-size-fits-all approach. The patient size, tumor burden (amount of cancer present), metastasis or spread of cancer, the type of cancer, the aggressiveness of cancer, and whether the cancer is the primary presenting tumor or is recurrent all play a role in determining the dose and the frequency of the Vitamin C.

IV Vitamin C

NAD regenerative therapy boasts a wide range of benefits by delivering the oxidized form of a coenzyme called nicotinamide adenine dinucleotide (NAD+) directly into the bloodstream. While research is still ongoing and more studies are needed to fully understand the impact of the NAD+ coenzyme on various conditions, scientists have found a connection between this enzyme and cardiovascular and metabolic diseases. Lowered levels of NAD+ have been linked to diabetes and fatty liver disease, among other conditions.


IV NAD Therapy

Hydrogen peroxide is widely found in nature and is a cheap and readily available chemical compound with many applications. At low concentrations in cells, it is important to maintain a range of normal cellular functions. At higher concentrations in the body, hydrogen peroxide can trigger apoptosis, a type of programmed cell death, which could be used to treat cancer, as well as acting as a source of oxygen and free radicals that can enhance the effect of radiotherapy. A small clinical trial showed that injecting a solution of hydrogen peroxide into tumors could kill cancer cells and also make them more sensitive to radiotherapy. Twelve patients with inoperable breast cancer who were treated at The Royal Marsden were given injections of the hydrogen peroxide mixture directly into their tumors, before receiving standard radiotherapy. The study showed that the injections were safe to be given to patients, and blood samples showed markers linked to cancer control and cell death. Hydrogen peroxide makes cancer cells more sensitive to radiotherapy thereby killing more cancer cells.

**Additional Resources:**
- <https://www.ncbi.nlm.nih.gov/pubmed/30779017>
- <https://www.ncbi.nlm.nih.gov/pubmed/30034255>
- <https://www.ncbi.nlm.nih.gov/pubmed/31083324>
- <https://www.ncbi.nlm.nih.gov/pubmed/26823956>
- <https://www.ncbi.nlm.nih.gov/pubmed/30378035>
- <https://www.ncbi.nlm.nih.gov/pubmed/26343967>
- <https://www.ncbi.nlm.nih.gov/pubmed/27633575>
- <https://www.ncbi.nlm.nih.gov/pubmed/32290499>
- <https://www.ncbi.nlm.nih.gov/pubmed/28049396>
- <https://www.ncbi.nlm.nih.gov/pubmed/29433327>
- <https://www.ncbi.nlm.nih.gov/pubmed/25830649>
- <https://www.ncbi.nlm.nih.gov/pubmed/28088622>
- <https://www.ncbi.nlm.nih.gov/pubmed/29161882>
- <https://www.ncbi.nlm.nih.gov/pubmed/27130805>
- <https://www.ncbi.nlm.nih.gov/pubmed/27375834>
- <https://www.ncbi.nlm.nih.gov/pubmed/26117330>
- <https://www.ncbi.nlm.nih.gov/pubmed/28744456>
- <https://www.ncbi.nlm.nih.gov/pubmed/26927177>
- <https://www.ncbi.nlm.nih.gov/pubmed/30018566>
- <https://www.ncbi.nlm.nih.gov/pubmed/27842920>
- <https://www.ncbi.nlm.nih.gov/pubmed/31415727>
- <https://www.ncbi.nlm.nih.gov/pubmed/29325444>
- <https://www.ncbi.nlm.nih.gov/pubmed/32231263>
- <https://www.ncbi.nlm.nih.gov/pubmed/27461591>
- <https://www.ncbi.nlm.nih.gov/pubmed/27338365>
- <https://www.ncbi.nlm.nih.gov/pubmed/25950600>
- <https://www.ncbi.nlm.nih.gov/pubmed/27353526>
- <https://www.ncbi.nlm.nih.gov/pubmed/26369938>
- <https://www.ncbi.nlm.nih.gov/pubmed/31103570>
- <https://www.ncbi.nlm.nih.gov/pubmed/28587525>
- <https://www.ncbi.nlm.nih.gov/pubmed/28936716>
- <https://www.ncbi.nlm.nih.gov/pubmed/28062361>
- <https://www.ncbi.nlm.nih.gov/pubmed/25942353>
- <https://www.ncbi.nlm.nih.gov/pubmed/31678843>
- <https://www.ncbi.nlm.nih.gov/pubmed/25827425>
- <https://www.ncbi.nlm.nih.gov/pubmed/31453999>
- <https://www.ncbi.nlm.nih.gov/pubmed/28382202>
- <https://www.ncbi.nlm.nih.gov/pubmed/29145191>
- <https://www.ncbi.nlm.nih.gov/pubmed/27293512>
- <https://www.ncbi.nlm.nih.gov/pubmed/26881027>
- <https://www.ncbi.nlm.nih.gov/pubmed/31440046>
- <https://www.ncbi.nlm.nih.gov/pubmed/30728893>
- <https://pubmed.ncbi.nlm.nih.gov/33200159>
- <https://pubmed.ncbi.nlm.nih.gov/33334271>
- <https://pubmed.ncbi.nlm.nih.gov/33665502>



IV Hydrogen Peroxide

Glutathione is a powerful antioxidant made up of three amino acids – cysteine, glutamic acid, and glycine. Antioxidants connect themselves to damage-causing free radicals and escort them from the body, reducing their ability to cause disease and discomfort.  A glutathione IV is good for administering this tripeptide directly to your bloodstream. The body does not absorb glutathione well, so using an IV drip helps spread the antioxidant more effectively, allowing it to provide immune and anti-aging support. Many people believe glutathione is the best way to remove toxins from their bodies and bring balance to the immune system.


IV Glutathione

Curcumin, a polyphenol first extracted from Curcuma longa in 1815, has gained attention from scientists worldwide for its biological activities –antioxidant, anti-inflammatory, antimicrobial, antiviral –among which its anticancer potential has been the most described and still remains under investigation. The present review focuses on the cell signaling pathways involved in cancer development and proliferation, and which are targeted by curcumin. Curcumin has been reported to modulate growth factors, enzymes, transcription factors, kinase, inflammatory cytokines, and proapoptotic (by upregulation) and antiapoptotic (by downregulation) proteins. This polyphenol compound, alone or combined with other agents, could represent an effective drug for cancer therapy.

**Additional Resources:**
- <https://pubmed.ncbi.nlm.nih.gov/33631231>
- <https://pubmed.ncbi.nlm.nih.gov/33684680>
- <https://pubmed.ncbi.nlm.nih.gov/34627097>
- <https://pubmed.ncbi.nlm.nih.gov/34621313>
- <https://pubmed.ncbi.nlm.nih.gov/34704580>
- <https://pubmed.ncbi.nlm.nih.gov/34697839>
- <https://www.ncbi.nlm.nih.gov/pubmed/18588355>
- <https://www.ncbi.nlm.nih.gov/pubmed/29802852>
- <https://pubmed.ncbi.nlm.nih.gov/30466988>
- <https://pubmed.ncbi.nlm.nih.gov/28872903>
- <https://pubmed.ncbi.nlm.nih.gov/33095554>
- <https://pubmed.ncbi.nlm.nih.gov/31988047>
- <https://pubmed.ncbi.nlm.nih.gov/33099272>
- <https://pubmed.ncbi.nlm.nih.gov/33130987>
- <https://pubmed.ncbi.nlm.nih.gov/32961574>
- <https://pubmed.ncbi.nlm.nih.gov/32942023>
- <https://pubmed.ncbi.nlm.nih.gov/33039729>
- <https://pubmed.ncbi.nlm.nih.gov/32934709>
- <https://pubmed.ncbi.nlm.nih.gov/33179087>
- <https://pubmed.ncbi.nlm.nih.gov/33125518>
- <https://pubmed.ncbi.nlm.nih.gov/33280258>
- <https://pubmed.ncbi.nlm.nih.gov/33275041>
- <https://pubmed.ncbi.nlm.nih.gov/33105719>
- <https://pubmed.ncbi.nlm.nih.gov/33270200>
- <https://pubmed.ncbi.nlm.nih.gov/33118292>
- <https://pubmed.ncbi.nlm.nih.gov/33207594>
- <https://pubmed.ncbi.nlm.nih.gov/32945513>
- <https://pubmed.ncbi.nlm.nih.gov/33316116>
- <https://pubmed.ncbi.nlm.nih.gov/33152486>
- <https://pubmed.ncbi.nlm.nih.gov/33142257>
- <https://pubmed.ncbi.nlm.nih.gov/33124505>
- <https://pubmed.ncbi.nlm.nih.gov/33283585>
- <https://pubmed.ncbi.nlm.nih.gov/32919003>
- <https://pubmed.ncbi.nlm.nih.gov/33108717>
- <https://pubmed.ncbi.nlm.nih.gov/33113417>
- <https://pubmed.ncbi.nlm.nih.gov/33595796>
- <https://pubmed.ncbi.nlm.nih.gov/33602218>
- <https://pubmed.ncbi.nlm.nih.gov/32466578>
- <https://pubmed.ncbi.nlm.nih.gov/32721631>
- <https://pubmed.ncbi.nlm.nih.gov/33530098>
- <https://pubmed.ncbi.nlm.nih.gov/33217990>
- <https://pubmed.ncbi.nlm.nih.gov/33092261>
- <https://pubmed.ncbi.nlm.nih.gov/33781887>
- <https://pubmed.ncbi.nlm.nih.gov/33507691>
- <https://pubmed.ncbi.nlm.nih.gov/33513394>
- <https://pubmed.ncbi.nlm.nih.gov/33767985>
- <https://pubmed.ncbi.nlm.nih.gov/33511113>
- <https://pubmed.ncbi.nlm.nih.gov/33667554>
- <https://pubmed.ncbi.nlm.nih.gov/33721752>
- <https://pubmed.ncbi.nlm.nih.gov/33457406>
- <https://pubmed.ncbi.nlm.nih.gov/33466849>
- <https://pubmed.ncbi.nlm.nih.gov/33450110>
- <https://pubmed.ncbi.nlm.nih.gov/33433509>
- <https://pubmed.ncbi.nlm.nih.gov/33387125>
- <https://pubmed.ncbi.nlm.nih.gov/33310285>
- <https://pubmed.ncbi.nlm.nih.gov/33894206>
- <https://pubmed.ncbi.nlm.nih.gov/32723255>
- <https://pubmed.ncbi.nlm.nih.gov/33912467>
- <https://pubmed.ncbi.nlm.nih.gov/33917379>
- <https://pubmed.ncbi.nlm.nih.gov/34000462>
- <https://pubmed.ncbi.nlm.nih.gov/34015183>
- <https://pubmed.ncbi.nlm.nih.gov/34028111>
- <https://pubmed.ncbi.nlm.nih.gov/34082400>
- <https://pubmed.ncbi.nlm.nih.gov/34098006>
- <https://pubmed.ncbi.nlm.nih.gov/34131980>
- <https://pubmed.ncbi.nlm.nih.gov/34181321>
- <https://pubmed.ncbi.nlm.nih.gov/34299604>
- <https://pubmed.ncbi.nlm.nih.gov/34209461>
- <https://pubmed.ncbi.nlm.nih.gov/34471000>
- <https://pubmed.ncbi.nlm.nih.gov/34347326>
- <https://pubmed.ncbi.nlm.nih.gov/34188448>
- <https://pubmed.ncbi.nlm.nih.gov/33182828>
- <https://pubmed.ncbi.nlm.nih.gov/33095554>
- <https://pubmed.ncbi.nlm.nih.gov/34485117>
- <https://pubmed.ncbi.nlm.nih.gov/34473898>
- <https://pubmed.ncbi.nlm.nih.gov/34498308>
- <https://pubmed.ncbi.nlm.nih.gov/32814463>
- <https://pubmed.ncbi.nlm.nih.gov/34456716>
- <https://pubmed.ncbi.nlm.nih.gov/34361819>
- <https://pubmed.ncbi.nlm.nih.gov/34375483>
- <https://pubmed.ncbi.nlm.nih.gov/34146588>
- <https://pubmed.ncbi.nlm.nih.gov/34522447>
- <https://pubmed.ncbi.nlm.nih.gov/34539398>
- <https://pubmed.ncbi.nlm.nih.gov/34559416>
- <https://pubmed.ncbi.nlm.nih.gov/34637800>
- <https://pubmed.ncbi.nlm.nih.gov/32951583>
- <https://pubmed.ncbi.nlm.nih.gov/34671398>



IV Curcumin

There are two basic approaches to immunotherapy for cancer. One is the isolation of some proteins of the patient’s cancer, which are then used to stimulate the immune system and attack it. These forms of immunotherapy are highly effective on cancers such as prostate, colon, kidney, breast, skin, and others. A second approach is to build a viral “smart bomb,” by engineering certain viruses to selectively invade and kill cancerous cells. When lysis (or cell breakdown) occurs, antigens then release express GM-CST, which further improves the immune response against that cancer.


Immunotherapy

Hormone Therapy

Electromedicine is a general term for any form of “energy medicine” that uses electromagnetic fields, which is based on the belief that all living organisms are controlled by electrodynamic fields. Electromedicine includes the use of stronger, to extremely small, electric direct current (DC), alternating current (AC) and electromagnetic fields, applied to the human body in a variety of ways, for a wide range of therapeutic effects. Among the uses of electrotherapy are the relaxation of muscle spasms, increase of local blood circulation, muscle stimulation and rehabilitation, increasing range of motion, the management of chronic pain, and stimulation of muscles to prevent venous thrombosis.


Electromedicine (RIFE)

An extensive body of literature describes anticancer properties of dichloroacetate (DCA), but its effective clinical administration in cancer therapy is still limited to clinical trials. The occurrence of side effects such as neurotoxicity as well as the suspicion of DCA carcinogenicity still restricts the clinical use of DCA. However, in the last several years, the number of reports supporting DCA employment against cancer increased also because of the great interest in targeting the metabolism of tumor cells. Dissecting the DCA mechanism of action helped to understand the basis of its selective efficacy against cancer cells. Successful coadministration of DCA with conventional chemotherapy, radiotherapy, other drugs, or natural compounds has been tested in several cancer models. New drug delivery systems and multi-action compounds containing DCA and other drugs seem to ameliorate bioavailability and appear more efficient thanks to a synergistic action of multiple agents. The spread of reports supporting the efficiency of DCA in cancer therapy has prompted additional studies to find other potential molecular targets of DCA. Interestingly, DCA could significantly affect cancer stem cell fraction and contribute to cancer eradication.

**Additional Resources:**
- <https://pubmed.ncbi.nlm.nih.gov/27437085>



Dichloroacetate (DCA)

Iron chelators for human disease has focused primarily on their use in the treatment of secondary iron overload, chelators also may be useful anti-tumor agents. They can deplete iron or cause oxidative stress in the tumor due to redox perturbations in its environment. Iron chelators have been tested for their anti-tumor activity in cell culture experiments, animal models, and human clinical trials. Largely for pragmatic reasons, clinical studies of the anti-tumor activity of iron chelators have generally focused on desferrioxamine (DFO), a drug approved for the treatment of iron overload. These studies have shown that DFO can retard tumor growth in many different experimental contexts. However, the activity of DFO is modest, and advances in the use of chelators as anti-cancer agents will require the development of new chelators based on new paradigms. Examples of iron chelators that have shown promising anti-tumor activity (in various stages of development) include heterocyclic carboxaldehyde thiosemicarbazones, analogs of pyridoxal isonicotinoyl hydrazone, tachpyridine, O-trensox, desferrithiocin, and other natural and synthetic chelators. Apart from their use as single agents, chelators may also synergize with other anti-cancer therapies. The development of chelators as anticancer agents is largely an unexplored field but has extraordinary potential to impact human cancer.

**Additional Resources:**
- <https://pubmed.ncbi.nlm.nih.gov/34071479>
- <https://pubmed.ncbi.nlm.nih.gov/34536548>



Chelation Therapy

BioMats are used for pain and stress management. Combining far-infrared rays, negative ion therapy, and the superconductive healing properties of pure amethyst, the mats are used to treat a range of health issues. The most common treatments focus on stress, insomnia, sprains and strains, post-surgical healing and scar reduction, joint and muscle soreness, chronic neck and back pain, heavy metal toxicity, inflammation, arthritis, Lyme disease, and circulatory issues. Far infrared rays also have been found to prevent metastatic cancer and target cancer cells, providing patients with an alternative to radiation or chemotherapy treatments.


BioMat

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