Most Recent Testimonials

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.)

I was bitten by a Horse fly age 9 years old. Noone knew anything about Lyme back then. I was left un tested for any spirochete infection. But the infection slowly began to affect my body and my brain from then on, still noone put two and two together. When i was 22 I was diagnosed with Multiple Scelerosis. I have subsequently discovered that M.S is connected to Lyme disease in fact M.S is a spirochete infection not just an autoimmune disease.
 As Dr Lyda Mattman says ‘Multiple scelerosis should be renamed Multiple Spirochetes’.  That is enough for me to know I was infected by the Horse fly.

M.S is chronic untreated  Lyme according to many Doctors out there.

I have been taking MMS for 15 months and wow! I am almost rid of the Lyme disease and co-infections. I say almost because these infections can go dormant for 10,20,50 years if you do not kill it all in the body system.

I am physically stronger, no need for walking aids anymore, my cognetive thinking is now second to none, i have no brain fog, my eyesight is above 20/20 vision, my corodination is brilliant, I can now hold a coversation, I do not have splayed feet anymore (something I have had since the bite age 9) My I.Q has improved by 60% (Lyme and co-infections affect the I.Q.

I am basically a normal healthy human all thanks to MMS and you Jim.

I have been spared a life of ever increasing disability and pain.

My children have congenital Lyme and co-infections and they too have been taking MMS for 15 months (their own choice as they are Gilleck competent)

They are fabulously well and also have cleared their bodies of Lyme and co-infections again they will carry on taking MMS for a while longer as i said because these infections can Lie dormant for a long time and we all want to be sure it is gone for good!

Both have been eyetested and their vision is above 20/20 their eyesight has improved greatly.

My eldest who was a snuffly baby (connected to a spirochete infection) no longer has sinus problems, the eyes are no longer affected (used to have constant eye irratation also connected to a Lyme, co-infection)

Our hair, nails, teeth are brilliant and fabulous with an infection all of these are affected.

We were on a limited time with my children it would only of been a couple of more years (by the time they reached age 18)  that they too would of been diagnosed with an autoimmune disease or become disabled, MMS has saved their lives too!

All of this because of a bite from a horse fly which are carriers of Lyme and other co-infections.

MMS is the saviour as well as Jim of course I am eternally grateful.

I will keep everyone updated about our further progress.

If anyone is concerned about long term use of MMS well if I had of taken antibiotics i would have to take those for up to 10 years causing damage and costing £800 per person per month, as far as i am concerened MMS causes no damage long term, no side affects and is better for the body and costs pence per dose it really is the better option to heal from chronic Lyme.

I can vouch for MMS itself first-hand. It cured my chronic Lyme disease. I have meticulously documented my usage on YouTube and have over 44,000 channel views: www.youtube.com/not2bforgot10.

I took MMS for 3 months, 8 hours per day, every single day and was tested before and after. My actual test results can be viewed on my WordPress blog: not2bforgot10.wordpress.com under 6/17/12: “MMS – Magical Mineral Solution LYME DISEASE test results from IGENIX.”

I have been on Awakenings radio and am a writer, aspiring author, speaker, and wellness coach. I am an avid Facebook blogger: www.facebook.com/emilyannecox and would love for you to subscribe to my channel and blogs.

This product will cure Lyme disease, HIV, herpes, malaria, the flu, etc. It really works!

Emily A. Cox
Author, Speaker, Coach
www.emilyacox.com

Summary:

Emily states that she personally had Lyme disease and believes she fully cured it using MMS, emphasizing that consistent dosing—specifically taking it for about 8 hours a day with strict adherence to timing—was key to their results. They stress avoiding vitamin C and certain foods during dosing, claim MMS only remains active in the body for a short time requiring frequent intake, and strongly endorse it as the primary factor in their recovery based on their own experience. She does give general health advice that might be valuable. She also mentions her schooling.

Transcript:

Hey guys, it’s me. It’s Tuesday, September 10th at 4:40 p.m. I’m currently on Pacific Time on the West Coast and living in Idaho, about a half hour from Spokane.

I just wanted to update you guys. I completed my last semester in my master’s degree and am taking the semester off before starting again in the spring. I’m studying nutrition, alternative medicine, holistic foods, and psychology, including Jungian and transpersonal psychology.

I also want to share that I had Lyme disease and I cured it with MMS (Miracle Mineral Solution). I stand behind that 100%.

I’ve been getting calls from people and even doctors from all over asking about my process. Because of that, I’m planning to write a book about my Lyme journey and would love your questions and feedback.

Lyme disease is systemic. It affects your mind, body, and spirit, so it’s important to take care of all three.

Exercise is important, even if it’s just 20 minutes a day. Nutrition is also critical. You should aim for a diet high in fruits and vegetables, as much raw and organic food as possible.

I recommend researching superfoods such as chia seeds, cacao, goji berries, kale, and spirulina. I also suggest avoiding meat and gluten, as they can stress the body and interfere with healing.

Mindset is also important. The law of attraction and maintaining a positive mental state can help support recovery.

As for MMS, I took it consistently for 8 hours a day, setting an alarm to stay on schedule. I believe consistency is key. I also avoided vitamin C and certain foods during that time because they can interfere with MMS.

MMS stays in your system for a short time, so regular dosing is important. I recommend making it portable so you can stay consistent throughout the day.

I’m not a doctor, just sharing what worked for me. I fully stand behind it based on my personal experience.

I’m currently looking for clients and offering consulting services, and I would love to connect with anyone who has questions or wants help.

Thank you for your support, and don’t hesitate to reach out if you need help.

Hi there,

I’ve been a long time tick host, lived in Germany and last Switzerland, travelled a lot through some european countries and caught most of the local ticks, as I had been straying around in the forests a lot. So no doubt that I must have been pretty loaded with all kinds of parasites. It took many years though to get a diagnosis, so starting from the first erythema migrans, I never have gotten any treatment whatsoever. Somehow I was able to ignore the symptoms by keeping myself active and by a few attempts to shape my immune system (for example with the famous kombucha tea).

However, I got caught in a series of heavy symptoms in the past few years that not only kept me from doing my job, finally I got the worst brain fog that I could every imagine (and I never have been of the depressed, pessimistic type). I was functioning no more, collapsed a few times and scared my dearest human beings around me. They all said my personality was flaky. Hospitals didn’t find anything in my blood, except for a slight hint (when I begged them for a Lyme check), but not enough to get a proper treatment. Generally over all these years, I kept hearing: Well, you’re ok, you’re fit, what do you want from us? Maybe consider seeing a shrink…

So, before terminating myself because I couldn’t take it any longer, I tried various forms of Sodium Chlorite solutions. I had read about MMS, but finally, I was advised by a special therapist, before I took the stuff.

So I began with the advised minimum dose of five drops…and BANG…I was heavily sick for one day. By now, after a 30 day test phase, I could say that the reaction was a heavy Herxheimer reaction to the toxine load and my wrecked constitution. So I could literally keep no food in myself, it splashed out regularely through all possible paths (pardon my descriptive language, my excuse is to not be a native speaker 🙂 )

While being seriously ill, I got aware of another reaction that I had noted earlier: It’s a stinging, short pain that can occur anywhere in the body, and which goes away within a few seconds, then comes back for a few times. The Chlorine Dioxide obviously had triggered something in my head, and since then, it has done it a few times again, but with decreasing intensity.

After the last few times calling ralph by the white phone on that day, I slept a lot. Next day, the brain fog was gone, but my stomach and intestines felt wrecked. So I drank a lot of tea (which I kept inside, this time) and tried to detox myself with a few nutrition additives.

The day after, the brain fog was still gone. How could that be? I was even fit enough to make a walk. Before that, my knees didn’t have any power whatsoever. Somehow, that bit of toxic gas inside my veins must have destroyed a lot of unhealthy stuff that made me sick.

So, since then I am on my little MMS protocol, tried it in various ways (activated, non activated) while monitoring my pH urine level, to see how I was doing with the acids. I have done a lot of research about the pros and cons, honestly I must say it appears to me as one of the least intrusive (let aside the heavy Herxheimer reactions) and best controlleable antibiotics so far.

However, I would not advise anyone to use MMS with a very wrecked immune system and without a therapist-advised strategy on how to get rid of all the toxic waste after the MMS reaction.

After all, I now have my lab diagnosis after more than 10 years of uncertainty, and the funny thing is: I don’t care anymore. Needless to say that the doctors didn’t know what MMS was. Their decision is still not made yet, but the chance is little, that I’ll take their antibiotics advice, once they finally found their conclusion. My hope currently is, that MMS can get rid of the remaining garbage as well. Even if it doesn’t, it got me out of the worst.

Thanks, Jim.