Most Recent Testimonials

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.

My experience with MMS has been so pleasant; I am on my second go. The first was about a 10-day trial, and then I got nervous about taking it, so I stopped. However, with this start I am having nothing but great feelings of health. Today I am at 5 drops with lemon and I take it 2 x per day. One of the coolest feelings has been in my brain area. A feeling of tingling, like a clearing sensation.

I have been using MMS for MS symptoms just over 2 months and am seeing things which I love. For now what about the reduction of the skin lymph glands? I think this is a major sign of what may be happening inside all the other organs and glands. I had enlarged lymph below my breasts, under my arms and stomach. My holistic dr said they were swollen lymph glands. The computer allergist specialist said they had strep, mold and other virus and bacterial overloads. These glands are a part of the skin and look like fat deposits. I have had lymph massage drainage and this helped but nothing permanent. They the Lymph deposits on my trunk underarms, and lower stomach look like they are disolving. I also have small tumors around these lymph glands and they are too getting smaller. Does anyone know of anyone else with this experience. I think if it is doing this to my outsides it is also doing this to my pancreas, bowels (are loaded with glands, immune glands,)Brain in MS, and thyroid one side was swollen last week when I saw the dentist. I am also regaining better function with my Lungs. I would appreciate any support on this issue. Links experiences ect. Thank You