Most Recent Testimonials

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.

I’ve been using MMS for 7 weeks now. Started with one drop daily, currently at 20 drops. I ran into a little nausea at 8 and 11 drops, dropped down a drop for 3 days, then ramped back up.

These are the benefits I recognize so far from MMS.

I had 3 tiny painful sores on my tongue for about two years now. Nothing I nor my doctor did helped. Trust me, these were very painful. Eating spaghetti sauce became a thing of the past. This past summer, the pain was at its worst. I was sure this was some kind of pathogen, but just couldn’t get rid of it. The pain continued to worsen.

When I started MMS, I decided I would take a sip and hold it in my mouth for a minute or so before swallowing. I no longer have any sores on my tongue. The pain is completely gone. The only change in my treatment protocol was the addition of MMS.

Next and more important, I was dealing with the worst fatigue and brain fog for the past 6 months. Seven weeks of MMS and now my fatigue and brain fog are much better. I can actually do some things again. Walking to the mailbox is now something I can do anytime I wish. Before, most days I couldn’t make that short walk. I’ve been spending some time working out in my yard, something I haven’t done in the past 6 months.

I definitely feel there is a benefit for anyone with Lyme disease using MMS. I am under the care of a few doctors at the Mayo Clinic and just yesterday I had a physical exam of my thyroid. All was normal. I will test for TSH, T4 and T3 at the end of the month. But for what this doctor can tell from all the past TSH tests done there, this too should be considered normal.

This was a Mexican lady about 60 years old. One evening about 6 PM we got a call from a Mexican gentleman who said that he would like to bring his wife over right away. We always try to accommodate anyone that we can and so he was invited over. When he arrived he helped his wife through our door. She could not hold onto the walker that she was using, so her husband was holding her to it from behind. It was a chore to see them squeeze through the door together.
They inched over to a living room couch and sat down. She explained that her right hand was totally paralyzed and numb from the wrist down for over two years, her foot was paralyzed in the same way. The paralyzed hand kept her from holding onto the walker, and the paralyzed foot made it extremely hard to walk even with the walker. In addition she had terrible back pains and leg pains that also limited her walking. She could barely get around the house.
Well, Clara always trains anyone who comes here by first giving them a six drop dose of MMS explaining exactly what she is doing, and then has them wait for an hour. The second dose she has them mix, wait the three-minute wait, and pour their own drink. That is, of course, so they will be able to make their own doses at home. In this case the lady said, about 1/2 hour after taking the first dose, “I think some feeling is coming back to my hand.” She also mentioned that the back pain seems to be less. Clara had the lady mix and take the second dose after an hour.
In just about another hour (it was two hours total) Clara called me. She said, “Jim, come here. You will want to see this. I quickly walked into the room. The lady was exercising her paralyzed hand. All of the muscles were moving correctly, and she had her shoe and sock off and was also exercising all of the muscles in her food. In fact the muscles in my foot don’t move that well. When this lady left our house she was still using the walker, but her husband was not holding her onto it, and one could see that she would not be using that walker for more than a day to two.
Let me say here that so far as I have been able to determine once these things go away, they seldom return. I believe that it is important to continue taking the MMS until one is sure the microorganisms are dead. Then maintenance doses are important to keep the immune system tuned up.