My grandfather passed away today from stomach cancer.
He was 84 years old, and was diagnosed with stage 4 stomach cancer with liver metastases. He had no symptoms besides general fatigue, it was found after a blood test showed a low iron level and they eventually figured out he was bleeding from the stomach cancer. Insidious fucking thing.
He had six cycles of chemotherapy (oxaliplatin), but we decided to make him fast for 48 hours before each infusion. There's some recent studies showing it reduces the side effects significantly and actually increases the effectiveness of the treatment. Typically you're told to eat as much as you can because you're probably not gonna feel like eating for the next couple of weeks.
He actually had very few side effects from the chemo, probably due to fasting. He didn't lose his hair, he didn't vomit, he didn't get nausea or mouth ulcers or anything like that. He did develop some nerve damage in his extremities that gave him pins and needles all the time. The sixth cycle really knocked him down though after his electrolytes severely went out of balance. After he recovered from all the chemo, we were told the cancer was about 90% gone which was an amazing result considering how advanced it was.
Unfortunately it only took about a year and a half for it to come back with a vengeance, and he finally passed away last night. He lasted about 2 years which is pretty darn good, with no actual problems with his stomach until the very last few days. He could still eat and be normal for the most part.
You're all talking about special diets, fasting is a contender.
Dr. Valter Longo - Fasting Cycles Retard Growth of Tumors - YouTube
In a nutshell, low carb ketogenic diet gets the same benefits as fasting. While you can only fast for a short period of time, a low carb ketogenic diet can be used indefinately.“CHO restriction mimics the metabolic state of calorie restriction or – in the case of KDs (ketogenic diets) – fasting. The beneficial effects of calorie restriction and fasting on cancer risk and progression are well established. CHO restriction thus opens the possibility to target the same underlying mechanisms without the side-effects of hunger and weight loss.”
your daddy goes to a clinic and they blast him with a ct. because they dont have an mri. or a pet. or because hes not important enough for them to waste 10k on. how about you visit a real fuckin doctor before you go on "alternative"..
Are you dense?
An MRI scan costs something like $200-400 everywhere but in the extremely corrupt US health care system.
its not corrupt. hospitals bill what they can bill. free market dream.
Are you dense?
An MRI scan costs something like $200-400 everywhere but in the extremely corrupt US health care system.
Here is the protocol my Dad is on:
1. Low carb high fat diet
2. Vitamin D
3. Ubiquinol
4. IP6 + inositol
5. Vitamin C
6. Chlorella vulgaris
7. Zinc
8. Beta Glucan
9. Serrapeptase
10. B17
11. B15 + mixture of minerals (magnesium, potassium etc)
Already started 1-9. 1-8 started one and half weeks ago. 10 started on Friday. 11 will come in next week.
just like that. you dont understand metabolism. quit trying to help people youre making it worse.
your daddy goes to a clinic and they blast him with a ct. because they dont have an mri.
How are your dad's liver enzymes? Ubiquinol is excellent due to dad's age, but I would also take the redox (ubiquinone) in coconut oil. Melt 14 oz of coconut oil on the stove under low-heat and put it back in the bottle. Add 56oz of CoQ10 powder. 500mg/tsp, twice daily. It's freely converted (cell), even if he has liver-involvement.
IP6 is phenomenal.
While coenzyme Q10 may show indirect anticancer activity through its effect(s) on the immune system, there is evidence to suggest that analogs of this compound can suppress cancer growth directly. Analogs of coenzyme Q10 have been shown to inhibit the proliferation of cancer cells in vitro and the growth of cancer cells transplanted into rats and mice.
In patients with cancer, coenzyme Q10 has been shown to protect the heart from anthracycline -induced cardiotoxicity (anthracyclines are a family of chemotherapy drugs, including doxorubicin, that have the potential to damage the heart)[3,16-18] and to stimulate the immune system.[19,20]
Ubiquinol Cancer Related StudiesIn view of these findings, it has been proposed that analogs of coenzyme Q10 may function as antimetabolites to disrupt normal biochemical reactions that are required for cell growth and/or survival and, thus, that they may be useful as chemotherapeutic agents.
Over 35 years, data and knowledge have internationally evolved from biochemical, biomedical and clinical research on vitamin Q10 (coenzyme Q10; CoQ10) and cancer, which led in 1993 to overt complete regression of the tumors in two cases of breast cancer. Continuing this research, three additional breast cancer patients also underwent a conventional protocol of therapy which included a daily oral dosage of 390 mg of vitamin Q10 (Bio-Quinone of Pharma Nord) during the complete trials over 3-5 years. The numerous metastases in the liver of a 44-year-old patient "disappeared," and no signs of metastases were found elsewhere. A 49-year-old patient, on a dosage of 390 mg of vitamin Q10, revealed no signs of tumor in the pleural cavity after six months, and her condition was excellent. A 75-year-old patient with carcinoma in one breast, after lumpectomy and 390 mg of CoQ10, showed no cancer in the tumor bed or metastases. Control blood levels of CoQ10 of 0.83-0.97 and of 0.62 micrograms/ml increased to 3.34-3.64 and to 3.77 micrograms/ml, respectively, on therapy with CoQ10 for patients A-MRH and EEL.
In a clinical protocol, 32 patients having "high-risk" breast cancer were treated with antioxidants, fatty acids, and 90 mg. of CoQ10. Six of the 32 patients showed partial tumor regression. In one of these 6 cases, the dosage of CoQ10 was increased to 390 mg. In one month, the tumor was no longer palpable and in another month, mammography confirmed the absence of tumor. Encouraged, another case having a verified breast tumor, after non-radical surgery and with verified residual tumor in the tumor bed was then treated with 300 mg. CoQ10. After 3 months, the patient was in excellent clinical condition and there was no residual tumor tissue. The bioenergetic activity of CoQ10, expressed as hematological or immunological activity, may be the dominant but not the sole molecular mechanism causing the regression of breast cancer.
Tumour angiogenesis is a complex mechanism consisting of multi step events including secretion or activation of angiogenic factors by tumour cells, activation of proteolytic enzymes, proliferation, migration and differentiation of endothelial cells. Both primary and metastatic tumours in the breast are dependent on angiogenesis. In the present study, 84 breast cancer patients were randomized to receive a daily supplement of CoQ(10) 100 mg, riboflavin 10 mg and niacin 50 mg (CoRN), one dosage per day along with tamoxifen (TAM) 10 mg twice a day. Serum pro-angiogenic levels were elevated in untreated breast cancer patients (Group II) and their levels were found to be reduced in breast cancer patients undergoing TAM therapy for more than 1 year (Group III). When these group III breast cancer patients were supplemented with CoRN for 45 days (Group IV) and 90 days (Group V) along with TAM, a further significant reduction in proangiogenic marker levels were observed. Supplementing CoRN to breast cancer patients has found to decrease the levels of proangiogenic factors and increase the levels of antiangiogenic factors. A reduction in proangiogenic marker levels attributes to reduction in tumour burden and may suggest good prognosis and efficacy of the treatment, and might even offer protection from cancer metastases and recurrence.
CoQ10 levels were significantly lower in patients than in control subjects (t test: P < .0001) and in patients who developed metastases than in the metastasis-free subgroup (t test: P < .0001). Logistic regression analysis indicated that plasma CoQ10 levels were a significant predictor of metastasis (P = .0013). The odds ratio for metastatic disease in patients with CoQ10 levels that were less than 0.6 mg / L (the low-end value of the range measured in a normal population) was 7.9, and the metastasis-free interval was almost double in patients with CoQ10 levels 0.6 mg/L or higher (Kaplan-Meier analysis: P < .001).
Over ca. 25 years, assays in animal models established the hematopoietic activities of coenzyme Q's in rhesus monkeys, rabbits, poultry, and children having kwashiorkor. Surprisingly, a virus was found to cause a deficiency of CoQ9. Patients with AIDS showed a-"striking"-clinical response to therapy with CoQ10. The macrophage potentiating activity of CoQ10 was recorded by the carbon clearance method. CoQ10 significantly increased the levels of IgG in patients. Eight new case histories of cancer patients plus two reported cases support the statement that therapy of cancer patients with CoQ10, which has no significant side effect, has allowed survival on an exploratory basis for periods of 5-15 years. These results now justify systematic protocols.
IP6 is phenomenal.
It is. Did you do research into it during your doctorate? I'm in contact with the lead IP6 cancer researcher Dr Shamsuddin.
ubiquinol is great stuff, no doubt. Now, The studies are contrasting the plasma conc. of a ubiquinol suspension (gel cap containing soy oil) vs. ubiquinone capsules containing powder (no carrier). 'ol is more quickly absorbed during the passive transport phase (diffusion) due to it's being more hydrophilic. It will achieve a significant plasma conc. faster, for sure.
'ol is the reduced form. Many supps are converted through first-pass in the liver. Ubiquinone is freely converted in the cell to a eq. state in complex three of ETC/mitochondrial redox. Kaneka is largely responsible for funding research into 'ol use as a retail supplement. A conflict of interest, but I don't doubt the results.
'ol is very unstable and it degrades rapidly. Yes, it's more bioavailable, but IMO the cost benefit isn't there.
I owned a board in which we had another doc who was involved in the debate. He did 1g/day of ubiquinol daily for a week and then drew blood for analysis six hours after the last dose. He waited a month-off and then took 1g of the ubiquinone bound to coconut oil. Samples taken six hours after the last oral dose of ubiquinone. An HPLC test was performed on both samples.
The plasma concentration was virtually identical. They ran each test twice. Understand that ubiquinone bound to coconut oil is ideal. I wouldn't cook it, but no damage will be done. Melt the oil slowly on low heat -> back in jar -> add powder. Now Foods sells a 28g bottle of pure powder.