A lot has happened since my last post. I talked to my oncologist at UofM and they were “pushing” me into a particular clinical trial. They told me that after analyzing my old biopsy sample, they found the cancer cells expressed an HER2 Low, androgen negative oncogene. Armed with this information, they sought to put me on a breast cancer chemo drug; trastuzumab deruxtecan. Even though it’s described as a “smart bomb and not a carpet bomb, there’s still quite a few side effects. Additionally, while participating in the clinical trial, I could not do any of the “alternative or functional” treatments I’m doing now, or have planned.
They said it “could” extend my live up to 36 months or so – and reiterated that it “was not a cure”. I can only imagine the treatment being worse than the disease. It didn’t sound like anything I wanted to try.
I went to Sloan Kettering in NY for a second opinion. The oncologist there was straightforward and up front. They have a clinical trial there as well, a new drug called AVA6000, a tumor targeted form of doxorubicin that has been chemically modified to reduce side effects by targeting the release of the active chemotherapy to tumour tissue.
The oncologist at MSK also said I could continue with Active Surveillance. So I’m pursuing alternative treatments while actively surveilling my status.
I’ve been taking all the metabolic “enhancers” that are familiar to the Peat world… 4g Aspirin, Biotin, Niacinamide, Thiamine, QOQ10 (similar to the Georgi study, as well as Vitamin K, Curcumin, Meldonium, VitD, and Doxycycline.
I’m juicing every day with Tumeric, Garlic, Onion, Kale, green apple, lemon, oranges, carrots and broccoli sprouts.
I’m also looking at a clinic in Mexico called Sanoviv. It’s a three week treatment with several interesting therapies like Hyperthermia, Vitamin B17, Vitamin C, Mistletoe, hydrotherapy/colonics, massage/meditation, and hyperbaric O2 and others.
Now I like some of those treatment ideas at Sanoviv, but it has some glaring issues – 1. Expensive, 2. In Baja Mexico, 3. Low Dose Cisplatin during Hyperthermia, 4. Chelation with EDTA
As an option, I may recreate this at home, some where I can control more of the treatment. I found a clinic here in Michigan that does a test called RGCC+, that tests for:
-Circulating tumor cell (CTC) count
-Genetic and physiological expressions of your cancer cells
-Effectiveness of 90+ chemotherapeutic agents and targeted therapies on your cancer cells
-Effectiveness of 50+ natural substances on your cancer cells
This will let know which natural food substances are effective against my cancer (Allicins, Sulpurophane, etc). They also do blood tests at the beginning for a baseline, mistletoe/Iscador, Hyperbaric, HOCATT , Ozone treatment, Chelation, and more.
If I go this route, I may purchase a sauna with red light, altitude tent, grounding pads, linen sheets etc.
I do have one question… I started taking some Methylene Blue, but I stopped until I could find out more about the dosage.
I found this 2024 trial for Ovarian Cancer, done In Vitro on Mice
2024 Ovarian Cancer Metabolic Therapy
Study: da Veiga Moreira et al. – Carboplatin-Resistant Model
🔸 In Vivo Dosage:
50 mg/kg/day continuously via drinking water
🔸 In Vitro Dosage:
50 μM in cell culture (selected for 50% viability response)
🔸 Delivery Methods:
In Vivo: Oral administration through drinking water
In Vitro: Direct addition to culture medium
🔸 Timing Protocol:
Treatment initiation: When tumors reached 200 mm³
Duration: 22 days continuous treatment
In vitro assessment: 4 hours (mitochondrial assays) or 24 hours (proliferation assays)
🔸 Key Result:
Significant tumor growth inhibition vs. carboplatin chemotherapy
THAT’S A LOT OF METHYLENE BLUE!
Human dose would be:
For an 88 kg Human
4.07 mg/kg × 88 kg = 358 mg/day
Can anyone help confirm this, or supply an alternate dosing strategy?
Author
