I have struggled with candida (then thrush in mouth) since I was a newborn! My mother told me she could not get rid of it with anything. Finally, the doctor gave me Gentian Rose. I don’t think that is even available anymore. It went away, but I’ve struggled with candida most of my adult life. Last week I had such severe feminine itching that I couldn’t even sleep. That’s when I remembered MMS! We used it initially 6 months ago to fight lyme which my husband contracted from a tick and gave to me. So a few days ago when I couldn’t sleep due to horrible itching to the point of pain, I made up a glass of MMS with 4-5 drops, drank it, and ONE HOUR later there was no itching. THANK YOU, Jim Humble! You also saved my husband from being eaten by lyme and bartonella! THANK YOU, THANK YOU, THANK YOU! I am praying for your protection and for the release of the innocent Daniel from the stasifda.

Four years ago I was bitten by a horsefly. I got a red circle round the bite. My doctor told me it was inpossible I had gone Lyme disease because I wasn’t bitten by a tick. He gave me something for eczema. The circle became bigger every day. After two weeks I went to the doctor again. I insisted on a test for Lyme’s disease. A week later the doctor confirmed I had Lyme. He said I would have to use antibiotics for a long time. I don’t like antibiotics, so I took mms 30 drops a day, for five weeks, then for five weeks 5 drops a day. The circle was completely disappeared two weeks after I started with mms. I am still healty.

I was daignosised with Lyme and Cat scratch/Bartonella Henslae Feb 2016. I was in so much pain I could barely walk, I no longer could think without having difficulty coming up with the correct words, ice pick headaches from the bartonella, joint pain & foot pain. I was given Bactrim DS for 14 days, Azithromycin for another 6 days still no improvement. My doctors said I should be fine but they were wrong. I did not get better so I found and old bottle of Doxycycline and this reduced my symptoms but I still was having trouble with pain, headches, sleeping 16 hrs a day.

I took disability for 2 weeks and only could work part time. Just recently found a pharmacy overseas that I ordered Rifampin from and this was the medication that was suppose to cure me. Took it 10 days and yes it did help some but I still had pain, fatigue & headaches. Ordered every herb I could find for Lyme took them twice a day on an empty stomach, took enzymes, probiotics, antifungals since the fungas started building up from all the antibiotics. 2 months of over 5 antibiotics, antifungals, herbs, apple cider vinegar all helped about 30% but I was still suffering.

On March 23rd 2016 someone posted on facebook that Lyme is found in MS patients so I clicked the link and it said that MMS can cure Lyme disease. I already had it in the refrigerator because I’ve used it for everything else but didn’t want to mix it with all the other stuff I was trying and had planned on using it after I finished the antibiotics. I decided to stop taking everything else because I really needed to try MMS since nothing else was really working.

Today is day 4 March 27th Easter day and I feel like I have Risen from the dead..Literally. 4 days and I feel 90% better. My headaches are gone, my pain is gone, I have not needed anything for pain in over 48 hours. I can feel the bacteria deep in my muscles dying off, it’s a strange sensation. I am using the every 8 hours protocol for LYME. I have histoplasmosis in my lungs also and have been nebulizing it also every hour and I’m coughing up mucous.

I rescue kittens and the kitten was covered in fleas and ended up scratching me while playing and this is how I got cat scratch fever. Well my cats also got infected so I’ve added 1 drop to their water now for the past 2 days and they’re acting better also. It’s like they feel better and more awake. I have suffered from Lyme for I’m not sure how long but have been diagnosised with fibromyalgia but I knew it was not that. I would sleep hours and hours, so much that people thought I was on drugs. This is the first time in literally 40 years that I feel alive.

I have never really known what it is like to be normal. I was bit by a tick when I was around 6 years old then diagnosised with Juvenile arthritis that I would grow out of but never did. I felt like I saved that kittens life and he saved mine. If it weren’t for him making me so sick with Bartonella Henslae I would have never searched out an answer for my Lyme that I really didn’t know I had.

I know it’s earyl yet but I feel I’m cured for sure with no doubts in my mind. I feel like a new person that I’ve never known. I plan to continue with the regimen for the next month because I want to make sure there’s no bacteria hiding out in the biofilms of my joints.

Thank you so much Jim Humble you’re truly an amazing person..Thank you for helping so many people around the world…I will tell as many people as I can.

Gina Barker

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.

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 – JimHumble.org
(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.

Kathleen

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.

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 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.)