Most Recent Testimonials

I have taken MMS and I have seen my doctor for numerous blood tests and I am negative; IE cured !

My wife and children are using the CDS and I am using the MMS. We are all feeling a lot better, it is a miracle.

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.

Hello everyone. I just wanted to share my latest experience. I live in Jakarta Indonesia and it’s very hot and humid here. I have been using a fragranced alcohol based under arm deodorant spray that has worked fine for me here for almost 2 years. The other day however, I started to get a rash in my left arm pit and it seemed to be getting worse day by day as I used my normal deodorant. So one morning last week I decided to try using my mms skin spray which is a 10 drops per once solution. I sprayed each arm pit as I normally do at about 5am. I then went to work – I’m a school teacher here, teaching English. It happened to be my big day of the week which is I leave at 6am and get back home at 9:30pm – so that’s 15.5 hours. During the day the AC was off at times in my classrooms or weren’t sufficient to properly cool the rooms I teach in because it’s been rather hot lately. During my evening classes at one time the power went off for about 45 minutes and it really got hot and I sweated quite a bit.

So how did the mms work you ask? Absolutely NO smell. I couldn’t believe it and thought there must be something wrong with my nose so I asked my wife to please smell my arm pits for the sake of humanity and experimentation – but she declined 🙁 . Later she did kind of smell from a distance and said she couldn’t smell anything.

I told my dad about it and he suggested that I see how long it would last on just the one morning spray. I told him that, for the sake of humanity and experimentation I would do just that (to the dismay of my wife 🙂 ) Guess what, after 2 full days (and no shower during that time either :ohmy: ) there was still NO smell at all. I’m amazed.

So, it’s not a medical breakthrough – but I think it’s pretty cool. By the way, the rash is going away too and I have not experienced any irritation at all using mms under my arms 😛 .

That’s all for now. Keep mmsn!

Oh, one last thought. And this may become a common proverb in the future so I’d like to claim credit for it right now 😛 :

You can lead someone to MMS, but you can’t make him drink it.

Hi there, My partner has a Kidney transplant of twenty years now and she regularly takes CDS for various things like urinary tract infections and to nip colds and flues in the bud. She has numerous blood tests and they can detect antibiotic like activity. Her transplant was under stress five years ago and deteriorating, but since CDS/MMS she has become very stable and the doctors are very happy with her progress. At twenty years she is now one of the longest in New Zealand. Before CDS/MMS, the use of antibiotics always had a bad effect on her health. She would have to rest for two days after one good day out. Now she never needs rest days at all. I make the CDS as she prefers it to MMS, as we both did the old high dose protocols and she got heartily sick of the MMS -citric acid taste. She now is up early, rides her horse, walks the dogs an average of 6 kms a day and cooks the evening meal. Every day!!! So from five years and first hand experience with MMS/CDS, we know that it is very beneficial and does not interfere with transplant drugs. Hope this helps.