After many years of feeling lethargic, addicted to snuff tobacco for pick me ups after meals, blurred vision, terrible night vision, joint pain from football injuries and just a general feeling of total crap, I knew I needed to try this.

Whatever my problem was it has virtually been eliminated in 2 weeks with only 3-4 drops twice a day, sometimes less.

God only knows what the longterm effects of this is, I swear on a stack of bibles this concoction has changed my life in 2 weeks.

I don’t have cancer that I know of.But I have been devastated by something that is killing me. Extreme fatigue, Brain fog, Locked up lower back, Recently thinning hair and blurry vision, and many more
symptoms.I have been told I have mercury poisoning from the pretty silver fillings in my teeth which I intend to remove when I can afford it. I have been taking MMS for about 6 or 7 weeks, And it is lowly cleaning this junk out of me.

It has not been overnight, And There has been a few times I had to slow down a little, Because of high pressure bathroom visits. There is definitely something in my body MMS doe’s not seem to care for. It is ‘unlocking’ my lower back, And I am sleeping great compared to the virtual insomnia I used to have. I have a better sense of well being. I am sure it is just a matter of time that it will get me where I want to be, As well as using other things that are specific to my needs. I also gave some MMS to my cousin who was recently told that she has fibromyalgia. She was almost to the point I was, She even needed help bathing and getting undressed, She had what you could say was an overnight sucess with MMs. A few days,She’s back to work. I was amazed to see it work that fast on a person. She is still having smaller problems, Such as her bowels are still cleansing. (She has an extended tummy), Causing me to suspect a plugged bowel. This seems to work well on plugged bowels.

I just sent $10 [to the US~Observer MMS Defense Fund] and I’m not a rich person, but an organic farmer in Kansas. We are a small oasis surrounded by ‘Round-up’ and have natural crops where thousands of birds and bees hang-out regularly on our one acre farm. I can also assure you I write about one letter like this every ten years. I’ve worked for a federal agency (and I’m proud of the work done there) and I’m the son of a private land owner (also proud of that work). IN BOTH cases though, we working citizens with educations and aspirations are always getting screwed over by someone ‘in Washington or on Wall Street’ (a.k.a. big business).

In Feb 2011, I contracted what is likely to be Lyme Disease and after having correlated symptoms (and wasting a few thousand dollars on THREE doctors in two states), I found myself in a ‘haze’ where my vision was suddenly going fast AND Tinnitus occurred in my left ear OVERNIGHT. The left side of my head then had (and to this day still has) ‘something’ attacking it as I also had blurred vision, a pain deep in the center of the left eye, and daily discharges of heavy amounts of thick, disgusting phlegm. Even after biking 100 miles a week (rock steady for two months) the phlegm (to this day) occurs first thing EVERY morning when I awake and sometimes throughout the day.

‘Neural Lyme’ is the best guess but my Blue Cross insurance can’t help me due to the ancient test they go by AND they won’t allow NEW tests that are 98% (Vs. 40%) accurate to be run– why? Nobody knows how to fix healthcare, but we do know WHY it’s broken: ‘big oligopolies working for an oligarchy of the few,’ and this is even mentioned by a former WTO economist (among others one might hear speaking at TED). A good friend (and MD) I hunt with says, ‘we really are great at ‘preventative’ and ’emergency’ medicine in the USA- BUT we suck in the middle.’ I also should add than he is a surgeon who doesn’t HAVE to work ‘in the middle’ (and he is glad for that fact). He is scared for his children and being a kid off the ranch, like me, he himself doesn’t have a plan for his children WHEN they get bitten by that tick.

After all else was tried, money and jet fuel were wasted, and frustrations were hitting peak levels in my life– a friend of my mother’s mandated I try MMS as she had used it for HER Lyme for years and controlled it ever since while hoping one day for a cure she still can not find after many years of (like all of us) waiting. But she was happy and said that when using the MMS correctly, she was very little effected by her Lyme. So I did order and try it– that was 19 months ago and I CAN say it works pretty good. I still have the phlegm hack (no matter how hard I work out) and the tinnitus is often still there but slight WHEN I use MMS regularly. This last Spring I ran out of the MMS product I purchased (from one of the ‘approved’ sellers) and had to go three weeks without it. I thought that maybe whatever I had been ‘killing off’ might be finally gone– but it was not and it returned with a vengeance. I found myself back to that starting point where my head rang like a jet was right outside my back door; my eye was full of puss in the mornings, the shooting pains came back; and I generally felt as I had over a year prior before I started using this stuff.

Read full article.

(Taken from ‘MMS and doctors who can’t evenpractice what they learned in school…‘,
A Letter to the Editor, By Russ Davenport, posted on USobserver.com.)

Hello,

My name is Teresa, I have 53 years and living in Cadiz (Spain).

In my testimony I want to contribute my little bit to your wonderful work with the MMS.

I had been watching and reading about this, and was able to arouse enough interest in me to decide to try it. Years ago he had suffered from inflammatory rheumatism and several episodes of uveitis that is supposed were related, one day I was desperate enough to move from conventional medicine and explore other possible “therapies” to help me overcome all the pain and suffering. Not to do so long, just say that, going that route, I realized that only I could heal myself and really all we can do when we are able to feel that certainty, and there came a time when I felt healed. I thank with all my heart the experiences, lessons, people …., which made it possible, though I must say that I do not think have gotten anywhere, just try to learn everything with that tune and I think it aportarme something.

In November last year decided to try the MMS, with the aim to clear my body of toxins, metals and other undesirable thing that I assumed would walk swarming my body after years of unconsciousness. And “accidentally” while waiting to receive the order uveitis developed in one of my eyes. I felt that this was a “test” and decided to wait and treat only with the MMS. By the time I started taking my eye was in a sorry state, and even had blurred vision, but I really felt that beyond madness that had a purpose. I took the MMS protocol by 1000 for 14 days, with the first dose and felt relief in inflammation and pain and end of those 14 days my eye was normal and asymptomatic, still looked a little blurry and I decided to just wait until I could rebalance itself, and it did. I’m fine and I share this to give hope to those who may need it. I must say it cost me to take it … I felt horrible taste and suffered diarrhea more or less, half the time, but I saw that really works and I feel wonderful.

Andreas, thank you for what you do, for being brave and for illuminating the Earth.

A hug,

Teresa

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 ?

{Part of original post}

I am a seriously ill person who has been diagnosed with both ALS and Lyme Disease…

I thought I had better qualify my previous statement. I now realize it sounds like I have both diseases whereas it is actually more of an either/or situation:

I am not sure if I have ALS or Lyme disease. I was diagnosed with ALS by a neurologist last May but 2 months later, I took antibiotics for an unrelated ailment (swollen glands) and I had a “Herxheimer reaction” (which should not happen to an ALS patient). Since August, I have been also given a working diagnosis of Lyme by an infectious diseases doctor (it can sometimes imitate ALS) and have recently had a weak/borderline positive Lyme test result from IgeneX labs in CA. So, my feeling is that I do have Lyme (with severe neurological manifestation of symptoms) and not ALS, even though I have been diagnosed with both.

{2/8/08}

I have been taking MMS for 1 month now. Currently, I am at 10 drops twice a day. I have had to stop and re-start twice due to extreme “herx” reactions. My goal is to get up to 15 drops 2x a day WITHOUT nausea. I got up to 15 drops before and had a violent reaction (the usual- vomiting and diarrhea) BUT I felt great for several days after the reaction subsided. I DO feel like it is getting to something toxic in my system and killing it.

I am still weak, have trouble walking and my hands are crippled from nerve damage. I do notice that some of my other symptoms are better or gone.

Better: fasciculations (twitching muscles), fatigue

Gone: tingling, facial numbness, blurred vision

I don’t have cancer that I know of.But I have been devastated by something that is killing me. Extreme fatigue, Brain fog, Locked up lower back,Recently thinning hair and blurry vision,and many more symptoms.I have been told I have mercury poisoning from the pretty silver fillings in my teeth which I intend to remove when I can afford it. I have been taking MMS for about 6 or 7 weeks, And it is slowly cleaning this junk out of me. It has not been over night, And there has been a few times I had to slow down a little, Because of high pressure bathroom visits. There is definitely something in my body MMS doe’s not seem to care for. It is “unlocking” my lower back, And I am sleeping great compared to the virtual insomnia I used to have. I have a better sense of well being. I am sure it is just a matter of time that it will get me where I want to be, As well as using other things that are specific to my needs.

I also gave some MMS to my cousin who was recently told that she has fibromyalgia. She was almost to the point I was, She even needed help bathing and getting undressed, She had what you could say was an overnight sucess with MMs. A few days,She’s back to work. I was amazed to see it work that fast on a person.

She is still having smaller problems, Such as her bowels are still cleansing. (She has an extended tummy), Causing me to suspect a plugged bowel. This seems to work well on plugged bowels. I am sure every ones needs are different,

But here is a list of my suggestions to you.I have had swollen lymph glands for years. Sota’s magnetic pulser worked great for this condition, As well as MMS. My next step is Enzymes, There is a great post here in this forum about them.Also I intend to get a stirwand to oxygenate water. These are available from http://www.globallight.net/ . Please make sure you have no metals in your mouth. Do a heavy metal detox. Globallight has free cd’s and dvd’s explaining many of these. You might want to look at ENGERG-IODINE™,

http://www.angelfire.com/mb2/montereybayholistic/EnerG-Iodine.html.

Hope this helps. You can beat this, Yes you can, Hang in there!! I’ll say a prayer for you.

Bob.

I am getting dry eyes after using MMS for several weeks. I also get blurry vision, just like when I swim in a pool that has too much chlorine.

Is it possible to get too much chlorine dioxide? I don’t have any diseases.