It will be 4 years in May (2010) since I was diagnosed with multiple myeloma (bone cancer) and I continue to have no symptoms except for the actual presence of the cancer cells. Every lab test I have taken since I have been diagnosed has shown a decrease in the number of cancer cells!

I have had several bone surveys so far (last one March 2010) and all show no bone damage or "holes," to the amazement of my oncologist. Yes, I am seeing an oncologist and have since I was first diagnosed but I have not accepted any of the "normal" cancer treatment. At first, when I would not accept treatment, the oncologist was angry, in fact very angry! But my point in going to him was for him to continue to monitor my cancer. Was the natural way I was choosing really working or not? The lab tests and the bone surveys were two ways to test this.

On this site I want so share those things I am doing that you might consider for yourself if you also are facing with dealing with multiple myelome. I am not a doctor but I have done a lot of reading and research. I have not gone this direction lightly and I have always been prepared to follow my oncologist advice if my way wasn't working. The last test I had to check on my "M-Spike" showed a drop from 3.4 to 3.2; this happening over a six month period (of heavy stress). My oncologist continues to be amazed at my progress--or maybe better said, at my lack of progress towards the normal progression that comes with bone cancer.

I am "attacking" my cancer from three different directions: diet, juicing and a special drink that I have most days--and, exercise.