Most Recent Testimonials

Although I remain a big supporter/believer in MMS and what it can accomplish in the body,

I am going to go off it for a while (at least.) At only 6 drops once a day, it seems the MMS is

neutralizing blood sugar and blood pressure medication because both are going up.

I have been feeling more pain and other all-over crappy feelings, easily stressed out, with

palpetations at times.

My bp has been inching up steadily with no change in medicine. I have had my blood sugar medicine

changed because the one I was on was causing pitting edema. It seems that the new medicines have

had no effect since I was on the MMS at the time of changing.

Since I feel so bad, I am dropping the MMS and continuing with other good supplements.

Hopefully, this will help.

Just a “heads up” to those on medication.

I have reported before that MMS made my breathing easier. Here’s what happened last night.

I was born with asthma. Had it all through my childhood and though I outgrew it as a young adult it left my lungs compromised–meaning that if I exerted myself I wouldn’t be able to breath deep. There were many times that I’d still have asthmatic spells of short duration. If I was in a damp environment it would be hard for me to breath.

I started taking MMS, only 6 drops a day. I noticed better breathing in just 2 days, but in only less than 3 weeks I am now able to breath all the way to lung capacity. I can fill my lungs completely with air and not cough or have that catch that happens. And last night I went to a concert held in an underground cave. It was quite a ways down–and going down is always easy. 😉 But coming up, I pushed myself to keep up with the group as we were leaving so as not to block anyone behind me.

When I got to the surface I had to sit down and catch my breath for 3 to 4 minutes before breathing slowed down to normal. BUT–the whole time I was puffing and panting was just from being physically out of shape and had nothing to do with my lungs, because I miraculously was breathing deeply, filling my lungs, no catching, no heat/pain in the lungs from exertion, no coughing. I was pretty darn impressed!! That has never happened to me before in my life.

I also experienced that same thing using MMS for lyme. I worked to 15 drops twice a day and was fine for a while and started to notice fatigue and nausea building and stopped the mms after about a month. It became tough to tollerate the mms. 5 days later I started it up again because the fatigue worsened. 4 days after that i started feeling ok again. At 10 drops a day I leveled off as it was to much to go to 15 drops again. I finished half the bottle and have stopped for now. Most of the infections I have had are gone. After dermal testing the lyme was gone also but may be dormant. I had a lyme test three weeks ago to verify that I have beaten the bug.

If MMS can beat lyme this would be god sent.

I’m using MMS for Lyme. I started it on 10/4/07, worked up to 15 drops 2x a day, am & pm. When I experienced no nausea or diarrhea, I began to wonder if it was doing anything. Well, 15 drops 2x day didn’t last long. Walking got more difficult, started taking 2 hr naps, lots of pain in jaw/teeth/neck area and down spine, swelling in cheek, nerves in limbs screaming. Agony everywhere! Well, maybe not everywhere. It just felt like everywhere. But at least it became obvious it wasn’t doing nothing. Dropped back drastically on # of drops and some days went off entirely. Dropped salt/vit c protocol and supplements. I couldn’t think what to take or not to take or when to take it and couldn’t keep track even when I tried.

What I think is happening is that the MMS got to the spine where the dastardly little beasties had been successfully hiding out escaping the salt/vit c. I also consider this experience further confirmation that it was dental work that provided the major opportunity for this invasion. (If it hadn’t been for our ‘state of the art’ American medical profession I’m sure I could have negotiated this life much more successfully. Grrr!!) Anyway, I’m still miserable. but plodding on. Presently doing 15 drops once a day. Would like to try fewer drops at a time and more often during the day, but the taste/smell grosses me out so that I prefer to do it once and get it over with. I also added to my misery by using the Indian Herb, (otherwise known as black salve) recommended by Jim Humble on a couple of little crusty spots on my skin which, judging from how angrily they are reacting, I’m now convinced they are skin cancers. I also got the life-line water from the Indian Herb lady in hopes it will help hydrate as she says it will. So the experiment goes on.

Thanks to all of you for being here.

I have used MMS for symptoms of Multiple Sclerosis for almost 2 months. I am getting symptom relief. Has anyone else with Multiple Sclerosis been using MMS protocol? Have you experience any symptom relief?

I can see natural signs that I attribute to less Mercury, pathogens, yeast and mold (old hard sore’s are healing and soft) No longer have digestive problems and breathing is much better. Lymph glands are getting softer and I am losing weight.