I was diagnosed with Myelofibrosis in 2002 and was told that I had 5>8 years to live and that there was no cure. I stuck my middle finger up at the doctor. I accepted a job overseas and ended up being there for about 13 years and about 3 years ago my spleen had grown to a size where it took about 60% of my stomach cavity and I became quite ill and was suffering all of the side effect that are related with Mf such as excessive sweating, itching, bone aches, headaches, weight loss, anaemia, depression and confusion and others . I heard about the new wonder drug Ruxolutinib so went to Singapore where it was available and started treatment.

The initial results were quite good but about 15 months later, blood transfusions almost every month and close to USD300,000 I gave the treatment away as it was no longer working and had become just too damned expensive as I could not get medical insurance as this was a pre-existing condition. I was then prescribed Hydroxyurea as an alternative but the side effects were worse than the problem so I gave that away as well. I went to China for 1 year and took traditional medicine and that increased my haemoglobin levels but was still costing me about USD2,500 per month.

While there I was still very prone to other infections such as stomach infections, flu, diarreha and I developed serious gout, all the while still with severe headaches 24/7 which had not decreased in intensity over the past 3 years or so, and I was still sweating badly. I came back to NZ in September 2015 and continued to suffer from all of the above afflictions and as I had while in China and was in and out of hospital A&E on a weekly basis. The doctors finally said that they could do nothing for me except control the pain and consequently I was given morphine elixir and slow release tablets.

About 2 months ago I was sent the link to watch the video about MMS and decided to try this stuff, after all, I had nothing to lose. For the first 10 or so days I have never sweated so much in my entire life and I believe that this was my body detoxifying. Since then the headaches that I had suffered 24/7 for the last 3 years plus have GONE. I am not suffering from stomach infections, flu, diarreha or any of the other side effects of myelofibrosis. My spleen, which had grown to such an extent that it was now hard down on my pelvis and extremely uncomfortable, has reduced in size by about 20% and is continuing to shrink in size so if you add all of these benefits together it has given me a new lease on life. Literally.

I am currently still having blood transfusions every month or so but my hg levels are slowly increasing and holding higher levels between transfusions. There is no cure for myelofibrosis but if MMS can relieve or eliminate the symptoms as it has done for me then I am forever grateful. I tell as many people as I can about MMS as I do not believe that anyone yet truly knows the extent of the healing that it can give or promote.