Most Recent Testimonials

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.

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

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!