
Has anyone ever actually been cured of or into remission cancer using Gerson Therapy?
All the research I can find says that the Gerson Institute never follows up any cases, yet claims lots of successes, and when clients were followed up, over 5 years, 20 of the 21 cases followed up were dead, and the remaining survivor still had cancer.
A friend of mine has embarked on using Gerson Therapy to treat her breast cancer (stage 1) and is not having any conventional treatment for it and I am terrified for her.
You are right to be frightened for her; with conventional medical treatment Stage 1 Breast Cancer has a near 100% 5 year survival rate. Your friend’s cancer will, if she pursues Gerson, be untreated and may spread and progress.
No, there is no evidence at all of Gerson treatment having effectively treated a single case of cancer.
It sounds as if you have read good information about this quack treatment; if you haven’t seen these, they may be useful. the first is about Gerson’s famous 50 ‘best cases’, only four of which appear anything like credible
http://www.users.on.net/~pmoran/cancer/Gerson.htm
http://www.quackwatch.org/01QuackeryRelatedTopics/OTA/ota03.html
I have actually tried this regime, briefly.
I was diagnosed with stage 3 grade 3 breast cancer almost 7 years ago. At the time I had been a vegan for 6 years (and a vegetarian for most of my life) and was a juicing enthusiast; I started most days with green juice. I mention this because an almost entirely vegan diet and frequent consumption of fresh juice is the basis of the diet Gerson followers claim will cure cancer.
I was also something of an alternative medicine enthusiast at the time, and frantic to avoid harsh treatments. I visited (among other alternative practitioners) a nutritionist, who guided me in starting a diet almost identical to to Gerson’s, recommended by a British nutrition organisation whose name I’ve forgotten .
I wasn’t willing to pay the few thousand pounds the organisation wanted for providing the information, visiting me and providing the food, vitamins etc I would need for two years, but the nutritionist agreed to give me the basic diet and guide me through it. I intended to follow it as a substitute for chemotherapy, and spent a couple of hundred pounds on vitamin pills and supplements. I passed on the enemas; the nutritionist was concerned thought this might be ok as I was taking milk thistle.
A couple of days into the regime, drinking juice every hour and consuming enormous amounts of vitamin pills caused me to vomit regularly, and in the end my stomach turned even as I contemplated the dreary routine of making and drinking the juices (it put me off juice for years). . There were nights when I went to bed weeping with hunger because I couldn’t face the bland and repetitive food I was ‘allowed’ on this restrictive (even for a vegan) diet. My weight plummeted and I felt very ill. I lasted two weeks and felt so much better when I started eating what the hell I wanted.
I’ve only known one person who followed the Gerson diet to the letter; she was a contributor to a breast cancer forums whose prognosis was almost as poor as mine. She was a fine, strong woman who had surgery but refused further conventional treatment.
She had a recurrence after a year or so; she continued with the Gerson diet and seemed to be doing well. A year or so later she stopped posting; I have no idea why, and it’s always a worry on a cancer forum when you stop hearing from someone suddenly. I emailed her and, very uncharacteristically, she didn’t email back. A website she ran on alternative Cancer Treatments came to a full stop too. I hope she’s still fit and well, but I fear the worst.
Yes, anecdote; but it’s impossible to provide anything else, either way, in the absence of proof.
I went on to have conventional treatment, and am fit and well and have been in remission for over 6 years.
I hope you may find some of this helpful to pass on to your friend
Interview w/ Dr. Contreras – Breast Cancer – Part 1
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Angiotensin-(1-7): A novel small molecule for the targeted treatment of triple negative breast cancer. $49.99 Triple negative breast cancer (TNBC), an aggressive breast tumor that disproportionately affects young and minority women, is associated with a poor survival rate regardless of stage at diagnosis due to development of distant metastases. Tumors from women with TNBC lack estrogen receptors and progesterone receptors and have basal expression of the human epidermal growth factor receptor 2 (HER2), severely limiting therapeutic strategies. The purpose of this study was to determine whether angiotensin-(1-7) [Ang-(1-7)], an endogenous peptide hormone that activates the AT(1-7) receptor mas , inhibits the growth of triple negative breast cancer cells and tumors and identify the molecular mechanisms for the inhibition of cancer cell growth. Injection of MDA-MB-231 cells into the mammary fat pad of athymic mice resulted in triple negative breast tumors that were treated for 28 days with either saline or Ang-(1-7). The average tumor volume from mice treated with the heptapeptide was approximately 3-fold less than the size of tumors from control animals (170.8 +/- 21.4 mm3 vs. 546.7 +/- 87.9 mm3; n = 5, p < 0.05) and tumor weight was reduced from 1.0 +/- 0.2 g in the saline-treated mice to 0.5 +/- 0.1 g in Ang-(1-7)-treated mice (n = 5, p < 0.05). The reduced size of Ang-(1-7)-treated tumors was associated with low immunoreactivity to Ki67, a proliferation marker (84.2 +/- 8.2 compared to 41 +/- 7.6), suggesting that Ang-(1-7) attenuates cell growth. Activity of the MAP kinases ERK1 and ERK2 was reduced in tumors of Ang-(1-7)-treated mice which was associated with a receptor-mediated increase in the MAP kinase phosphatase DUSP1 (1.01 +/- 0.1 relative gene expression in tumors from saline-treated mice compared to 1.78 +/- 0.13 in tumors from Ang-(1-7)-treated mice). The decrease in tumor growth of Ang-(1-7)-treated mice was also associated with a reduction in the endothelial cell marker CD34 (a decrease in vessel density from 87.8 +/- 6.4 in tumors from saline-treated |
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