Date:   7/19/2009 9:01:57 PM ( 15 y ago)
Hits:   20,693
URL:   https://www.curezone.org/forums/fm.asp?i=1459095

Diagnosed with estrogen receptive breast cancer, right breast, 3 yrs ago. Tumour 4X5 in upper half, with 'satellite' in lower right quadrant. I got fired after diagnosis, spent a month watching movies, drinking (rum if you're buying), and smoking weed a lot. Not particularily bothered, 'just another thing'.

This 'dying thing' seemed to be taking a bit long so I thought I should do something before I decided what to do. I started Tamoxifen, and some monthly injection to put me into menopause. I had an appointment with a plastic surgeon who was going to mastectomize me and give me a fake breast at the same time. A date was set for surgery, skipped. Another was set, skipped as well.

Rewind: when diagnosed, I knew there would be no chemo for me. It took them 6 months from pillar to post to kill my father with it, but 10 years later it only took them 6 weeks to get my Uncle. Radiation was mulled about, but I was only willing to evn try it if they would do a 'bracchi-something' which involves inserting a radioactive 'rice kernal' into the tumour to target the radiation. No-go there.

Surgery was never a popular thought as I could not reconcile losing my lymph glands - too stupid for words. I also do not necessarily agree with the removal of tumours in the way it is presently practiced: 'out of sight, out of mind' is the weakest point. Whatever caused the tumour will continue to work unless changes are made. It is rather like having an emergency light in your car going off and when the cause cannot be found, the LIGHTBULB is removed. Also, they say that a much larger area of the tumour must be removed because'cancer cells are so small that if only one escapes, it will possibly mestastise. Funny, they don't seem as concerned about the biopsy needle, spend a lot of time telling you how small the needle is - but neglect to mention any correlation between biopsy's and mestastis.

So, I start on Iscador - European remedy (blah blah blah, look it up).

After 8 months on Tamoxifen and menopause stuff, I quit. A month after I quit, began urine therapy. I had a plan for when I was going to begin: after the drugs had cleared my system to a degree (not worried about the Iscador which I still do), and when I was mentally prepared. I ended up starting earlier than planned when I noticed (or imaged) that my armpits were getting lumps, and were hot to touch.

Now I have been doing urine therapy for over 2 years. I drink it, and lie in the bath with old-urine compresses for 10 minutes every day. I also breath in the steam of old urine occasionally.

Besides the Iscador and the urine Therapy, I changed my diet. Everything I do has to resonate with me, so I thought about why I had this disease. My diet had been VERY low in fat, even as a child. That changed to a lot of good fats, raw if possible, no vegetable oil except olive. My diet had also swayed between vegetarian and vegan for 25 years, so I began to eat meat again. I have since returned to vegetarian because I like it best, but I do eat good animal fats on occasion. (sorry, so much to write, diet is getting a short shrift)

As I have very fair (although olive) skin, I have avoided the sun my whole life. No more. I get sun now for the vitamin D. I also have a Vitamin D skin cream I massage on my breasts. I make my own skin creams, and always remember that the skin eats what it touches - no parabens, other awful things.

Okay, so back to the UT, Amaroli etc...

I decide that I want to inject urine having read up etc. I eventually settle on a method (via advice, research etc) that I do evry couple of weeks or so. It's not intramuscular, but subcutaneous like my Iscador injections. I can't be bothered to try to get the painkiller to go into the muscular injections, and in any event Iwould not be able to do it by myself. So, subcutaneous it is.

The infrequent injections went on for about a year or so. For the last six months I have been injecting 2 or 3 times a week. The breast has 'consolidated', it is half the size of the other breast - very difficult to find bras that wotk, and sometimes to look even. The tumour is obvious (without clothes) and sits high and proud, young looking (making the 'healthy' breast look pathetic and saggy)
There are stretch marks appearing on the top of the breast. It has had periods of itchiness, as one getts before a pimple appears, or a new mole or a boil. Lately, it has been itchy and has a 'burning' in it. I am not worried, it feels as though it is making its way to the surface.

My acupuncturist said he he had never seen anything like it. I stopped seeing my other DRs (GP, Oncologist)as I was no interest to them if I wasn't doing their thing (are they on commission?) I am Canadian, so treatment cost is not an issue.

I am curious what is going to happen. I feel I should also mention that I am not bothered whichever way it goes - but it is interesting.





 

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