I kept a journal but got discouraged when I could not break through the barrier of 12 drops twice a day. When the Navarro test came back unchanged, I knew I had to try something else before the cancer cells get time to multiply and spread more.
It was a sad day for me because I believed so firmly in what the MMS was capable of doing for me.
The aversion to the drops was another problem, I could not eat because of the nausea and did not feel like anything, and I mean literally nothing, not even fruit or yogurt.
It was the worst 2 months since I got diagnosed because I believed so much in it that I bought a lot of product, and could not even use up one bottle.
