Doing a 14 drop glass right now. This stuff really works! I used to drink quite a bit of colloidal silver and one of the first effects that I noticed was that my pee was silvery-even the bubbles (ok not a lot silvery, but definitely noticable).

Yes, it has a chlorine smell, but I’m not as psychologically sensative as most and I can deal with it.

So the claims about chelation-I suspect they are right. I’m not a chemist, but what made sense to me was the chemical recombination into silver chloride(?). I’m sure that this would help those with argyria.

It would be nice to know if probiotics are needed after mms treatment. On the whole it seems to be good stuff, but what effects if any would come about long term are still to be discovered. It seems every wonder suppliment or medicine has a potential dark side, the light has yet to be shined into the dark corners of this treatment. Sure seems worth a go at this point though, given its potential for removing heavy metals and subsiquent benefical effects upon the cardiovascular system and body as a whole.

I’ll be on mms for one more week before going to a 5 drop once weekly maintenance dose. I do intend to use kefer as a probiotic/prebiotic and see what restorative effects wheatgrass juice has upon a “clean” system. My only problem was a little bit of sinusitis. To be honest, I am breathing better. I’ll check my bp and pulse rate after this mms loading is complete since a few reports indicated significant improvements. I have noticed that my strength is improving (I do three sets of push ups every other day), my sense of smell is better and ease of breathing has greatly improved. I ride a stationary bike apx. six times per week and it seems a little less effortless although my routine is not one where I go for maximum exertion.

I consider this substance to be better than colloidal silver overall, primarily because an electrical source is not required to produce it and quite honestly it seems more effective and beneficial than even nano partical col. silver. Though I never thought of myself as having any degree of brain fog, there does appear to be minor improvements in cognitive functioning as well-we all have residual traces of mercury, aluminum, lead and neurotoxins from microorganisms. Increased systemic oxigen and nutient uptake weigh positively into the balance as well.

I have chronic Neuro Borreliosis, in other words Lyme Disease in third stage.

The symptoms (some but not all) are severe headaches, especially in the back of the head. These headaches are caused by massive amounts of ammonia that is produced by the the Borrelia bacteria.

Furthermore pains in mussles, strong morning chills, low temp feavers, very!! foggy brain, paralizing feeling in palm of hands, changes in perception of length of extremities, stumbling walk, loss of congnitive function.

I am using MMS now for two months. The great thing about this product is that it kills the Borrelia quite fast and sufficient to have much less pain in the brain. I have been on painkillers for 18 months and had to stop, so fortunately MMS came allong.

At this moment I use 7 drops 5 to7 times a day, so that is quite a lot.

The last few days I started to note a difficult feeling in the liver, as if too much chlorine (or some chloor product) was accumulating in the liver.

That is why I have started to research what the long term negative effects might be of taking this amount of MMS.

7 times 7 drops is a little more that Mr. Humble suggests, for strong treatment protocol. So I’m taking this daily to have the pain reduced, it is one of the other at this moment.

I have heard and experienced that Phenylbutyrate (Brands: Buphenyl and Ammonaps) is very good in reducing the ammonia ammount in the brain, it really helps. However Phenylbutyrate is expensive – you need 500 – 1000 mg a day – and can only be supplied through MDsubscription.

But MD’s are not knowledgable in this area and refuse to supply this to me. I live in Amsterdam, The Netherlands

So I’m looking for supplier or MD that is willing to sent it to me without subscription for a reasonable price.

Will continue use of MMS, I use ozone sauna for 2 hours a day to feel better when too much regular MMS is getting me ill.

My experience so far is that MMS does reduce very well the pain in the brain but has very little effect of killing the CWD forms as well as the cysts and spores forms that Borrelia uses to hide itself in the body. So it does kill the spyrocheet forms, but leaves the rest allone. This means that after about 3 hours you have to take it again to reduce the pains

I’ve been using it for 5 days now, and I’m upto 7 drops. After the first set of drops my brain fog, which I didn’t realise I had, completely disappeared. I can now think straight and remember things. My skin has cleared up (small acne patches since I was 14, I’m now 29). And I feel like a different person.

I would rather live my life as I feel now, than how I was.

Maybe MMS is bad for you, maybe it isn’t, I’m not stupid enough to claim either way. All that I know is, it’s helped me. I’m only going to do it for a week anyway and see how long the affects last.

I don’t care what you say/think/speculate MMS works – END OF STORY!!!!!!

I started MMS about a week ago. I am up to 10 drops twice a day and have started to notice nausea and slight diarrhea. (BTW, I just saw the ‘rice’ in the toilet, I wonder what it is?)

So far I have noticed that my breathing is better and my sinuses are clear. I had been diagnosed with sleep apnea. I told several doctors and ENTs that I don’t snore when my nose is clear but they all ignored me. They suggested losing weight and using a CPAP machine. I tried the machine two times, but it couldn’t push the air past my plugged nose.

I also suspect that I have candida. I never even believed in it before, but the more I read about the symptoms the more I believe that I have it. I’ve had athletes foot since junior high school (40+ years). I’ve had jock itch for the past ten years. I had a bad case of ringworm for two years (one doctor told me it was a rash from my pants rubbing, in the meantime it spread from about the size of a quarter to cover most of my thigh). I also got toenail fungus about 10 years ago.

Last year my saliva started to get “weird”. It got thicker and kind of sour tasting. I also had a few sessions of extremely dry mouth to the point where I had to get out of bed to drink water because my mouth was totally dry. I think these might be candida related. I also have the brain fog and feel tired and have low energy all the time. About the time my saliva changed I got really run down. One day I sent out and dug up a lot of dirt and wheelbarrowed it to another location. A week later I could barely lift the shovel.

So far on the MMS I’ve noticed my saliva is becoming more normal. I am sleeping better. My nose is clear at night and I don’t snore. Brain fog was getting better at first, but now I may be herxing so it is back but different.

I have also been applying MMS topically. I soak my feet in it and the athletes foot is clearing up. My toenails are no longer yellow (probably due to the bleaching effect). I forgot to mention that I have several patches of dry skin. They may be eczema or psoriasis. The rub the MMS on these areas and they are clearing up. I had one very dry and itchy spot between my eyebrows that is completely gone. I applied it directly to the jock itch and it is much better. Had a lot of skin slough off from that.

To make the foot soak I mix up a two drop dose and then add it to my soak water. I also mix up a one drop dose and add it to my Water Pik tank.

Also noticed that some joints work better. I probably have the beginning of arthritis in my hands. I can now make a fist much easier than before. There is an intersection nearby where you have to turn almost all the way around to watch for traffic. I went through yesterday and noticed turning my head was much easier.

So far I am pleased with the results.

An holistic healer friend of mine sent me a bottle of MMS and powdered citric acid a year ago when I found out I was HIV+. I shelved the remedy, and elected to go with traditional medication to keep it in check. Now a year has passed, my health is good, but I found out that MMS can be used for general detox purposes, something we can all use. I’ve also had a nasty case of athlete’s foot for probably 8 months that will NOT go away, no matter what I use to treat it — antifungal sprays, tea tree oil, colloidal silver, and hydrogen peroxide have all been useless.

So I’m on day #5 now, rocketing from 2 drops on Wednesday to 13 drops today. Already I’ve noticed BIG changes in regard to the athlete’s foot, but also some distinct improvements in my mood and brain function. I played a small acoustic show yesterday at a coffeehouse (first one in several years), and had practically no stage fright, which is extremely odd for me. I’ve been getting out of bed around 8:00 feeling refreshed and somewhat chatty (also unusual), and getting tired around 11:00 at night. Is the chlorine dioxide possibly regulating my sleep cycles? I’ve had some D, and a bit of nausea, but it feels good knowing that it’s part of the healing process.

Can anyone tell me if they also get blurry vision, blood in stool and a foggy head and extreme fatigue? 7th day, 7 drops. Stumbled upon this a few weeks ago while trying to research parasite cleanses (possible morgellons??)and thought it might help. I’m hoping symptons above will get better as I continue to take , but also wondering if I should stop. no blood, foginess, tiredness or blurred vision prior to mms. I am optomistic about mms . any thoughts ?

Hi. My name is Victor Summers and I am suffering from HIV, Severe COPD, as the doc describes it, with emphysema and other stuff I will share as time goes by. Today I started with my first dose of the mms. I have read about half of the posts made and will finish them.

I wanted to use this thread as a way to keep record of my progress and let others use it as a testimonial.

I have been on HIV meds for two years and my viral load is <50 (under 50) which is considered undetectable. My Tcell count is at 500 and something. I just happen to have noticed I have thrush today so instead of using the thrush meds I will look to see the progress I will make with mms. I will also be looking for my COPD to improve which is the biggest thing to me at this point because the HIV is under control but my COPD is really causing me lifestyle problems like being out of breath all the time, plus my chest is very tight to the point it hurts. I also have an enlarged prostate gland and I feel sharp pains coming from that area often (a few times a day.) So will also be looking for that to improve. I would like for this to be documented in the greatest way possible so I will cooperate with anyone in making that posible so we can have the proper documentation to prove the claims I believe I will be making :) I'm going to stay on my HIV meds for now just to see how this first step goes. I took 1 drop in citric acid with apple juice about three hours ago now and will determine tomorrow if I am going to increase it or not and will keep my progress posted here. There are other things wrong too and will mention them as I discover them improving (like my energy.) After reading so many of the posts already, I feel I know some of you and I am very impressed and am so very happy to make your aquaintance. {5/1/08} Day 2 of my MMS experience. Well, I woke up this morning feeling like crap. I could barely get out of bed. After taking my son to school I came home and slept till 2:45 pm. I havn't slept so soundly in a very long time. It reminded me of how I slept when I was a teenage boy. After being awake for a while I started feeling better and I also noticed my lungs seemed to be working better. I have not taken any of my albuteral today, which is highly unusual. I decided not to take my Spiriva and see what tomorrow is like. While writing just now I realized that the tightness in my chest is also much better. I also coughed up some nasty mucus today. My sinuses are dripping I think. There is a weird feeling in them anyway. My joints are hurting also. I had a white spot on my uvula which I noticed yesterday while checking to see if this weird looking bubble was still on my uvula, which it was, but the white spot is gone. The bubble (which looks like a blister) looks the same. It has been there for many years now. My doctors could not tell me what it is. They didn't have a clue. I had a brainstem stroke in 1999 so am anxious to see if my brain improves as a result of taking MMS. I have also been diagnosed with Peripheral Vascular Disease and my legs hurt most of the time and both of my feet have numbness in them. I will see if I experience any improvement in that area as well. I am sticking to one drop until I start feeling better. I'm still tired and feeling blah, like you do when detoxifying. The most important thing for me is getting relief from the COPD and emphysema. My lungs do feel better and I haven't ran out of breath today. And I walked up a hill at my son's baseball practice too. I wasn't even sure I was going to go because of how badly I felt this morning when I woke up, but by 5 pm I actually wanted to go with him. For any readers who may think it may be in my head, I don't care if it is so long as I get relief. I'm serious! LOL {5/4/08} Well, this is May 4th, and I am up to three drops and am feeling very well. Still sleeping like a log but my energy is back up. My COPD acted up yesterday and I had to use my albuteral, but today my lungs feel better again. I seem to be able to breath better -- like my lungs are bigger, if that makes any sense. Oh, well that may be because the tightness in my chest has subsided. Still coughing up green mucus, which started soon after I started using the mms. I feel my strength returning. Feeling more normal and more alive too. My brain fog, which I wasn't that aware of, is lifting and I am thinking better. Just now I noticed I am typing this note without any difficulty or hesitation on my brains part happening. I decided to stop taking my HIV meds. I hope that was a wise choice. But I can always resume them. I have stopped them before and restarted them. I have had chronic diahrea for several years so, for me, I will be seeing if in the long run that improves as well. I hope to see dead parasites soon :) I am also entering into this with a good mental state of mind so I have that on my side. I have a doctor's appointment coming up in a couple of weeks so it will be interesting to see what happens when they give me the "blow" test. Not sure what that is called, but it measures your lung capacity by blowing into this contraption. I failed it so badly the last time that I was diagnosed with SEVERE copd. You know. I am a happy fella and I don't like talking about myself so this is a labor of love, in a way, in hopes that it may help others if it helps me. I don't want people to look at me and think I am ill when my state of mind is so positive and, the truth is, I am not afraid of death. I do, however, want to see my little boy raised.

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.