Through an Intimacy with All of Life

My MMS Protocol for Curing Lyme Disease

Overview

I cured my Lyme disease primarily through using MMS or Master Mineral Solution or Miracle Mineral Supplement. This anti-microbial compound was discovered as a health agent by Jim Humble who was using it to sanitize drinking water and found that it cured malaria. MMS works as an oxidant, much like ozone, and has the ability to target pathogens. You can read all about it in the resources I’ve listed below.

This product is controversial and you’ll have to listen to your own intuition and take your own chances. Most Lyme sufferers are so desperate that they are willing to try anything. This was the case for me. And I’m so grateful that I did try it. I only wish I had done so sooner. And skipped the antibiotics.

Decision

After a year of being on antibiotics, my health was the same or worse, and the side effects from the drugs were getting to be too much for me. The year of treatment was brutal and wrecked havoc on my digestive system, which was already struggling from years of Lyme. I was so reactive to the drugs that I started breaking out in mouth ulcers and had to discontinue their use.

I had read about the MMS years before but it was at this juncture that I had nothing else to loose. I was completely done with the antibiotics and I knew the Lyme wasn’t gone. So I figured it couldn’t be worse than what I just went through.

Treatment

I really hate the taste of the MMS and I was working full time so taking something every hour, as advised in the Protocol 1000 through 4000, was unrealistic. I had also read the enemas can be as powerful as intravenous without having to go to a health care practitioner. I’m all about DIY and wanted to try something strong at home.

I resolved to do enemas every 36 hours for as long as it took to get rid of the Lyme. It ended up being three months. Every 36 hours gave my body a chance to heal from the last treatment and but it was soon enough that the infection couldn’t take over again.

To Purchase

  • MMS. I buy here but there are lots of options. Look around online.
  • Enema Bucket. Example here. Buy plastic, not metal. They say not to use metal of any kind but I’ve was using a stainless steel enema bucket and it seemed fine. To be sure, use glass or plastic.

Protocol

  • Warm up a pint of water to slightly above body temperature and put it in a quart jar. It will be half warm water and half empty. Because a pint is half of a quart.
  • In a separate glass container (with a little nipple at the bottom so the solutions can mix) put in one drop of sodium chlorite and one drop of activator (HCL in my case). Let it sit for 30 seconds. This makes the chlorine dioxide solution.
    • See resource section below for videos about mixing and other protocol suggestions.
    • I started with one drop and worked my way up to 15 drops over three months.
  • Add a pint of room temperature water to that now combined (and amber color) chlorine dioxide solution in the glass container. Add this mixture to the warm water in the quart container. Now you have a quart of water (a pint from the warm water and a pint from the MMS solution).
  • Make sure the temperature is warm enough to feel soothing in your body but not too warm to burn you. Adjust the temperature as needed. You will get the hang of this after a couple of tries.
  • Add this quart of water with the MMS (should look yellowish) to the enema bucket.
  • Give yourself an enema.
    • Use some kind of lube on the insert end. Coconut oil is fine. I use Emu oil.
    • I would often do the quart in two sessions – one that would come out fairly soon and the second one which I could hold in for longer.
    • Hold as long as comfortable. You can work your way up to holding longer over time.
    • Do something enjoyable as you are holding the enema water. You want to make this a pleasurable experience.
    • If the body needs to evacuate, let it. That’s why it’s great to do a 2nd round because it’s easier to hold that round for 10-20 minutes or even longer.
  • Let yourself rest during and after the enema.
  • Do enemas as often as you feel you can tolerate.

Other Thoughts

  • MMS is not bleach. Many people have cured many illnesses using this treatment and no one has been harmed or died from MMS. That’s not something the medical community can claim for its treatments. Do your research. There’s much controversy out there but the effectiveness of this treatment for others convinced me.
  • I did enema‘s every 36 hours because when I tried every day it was too much (drained and wrung out feeling).
  • Try not to eat a big meal before doing the enemas although I feel fine eating afterwards.
  • My body would sometimes go into a series of big spasms after an enema. I sense it was reacting to the MMS. The MMS is harsh. For sure. And so is Lyme disease. I believe it took that level of harsh treatment to expel it.
  • It’s good to really look at your poo because I (https://skepticink.com/health/2014/08/14/rope-worms-cest-la-merde/and others on MMS) have had long stringy mucous things come out that some people call “rope worms.” Rope worm information here, and here, and here, and here. I don’t have an opinion on this and I can believe that it’s mucus and I can also believe that it’s something more. Find out for yourself.
  • I got nearly immediate relief of symptoms (within a week).

Resources

Overview Video(I recommend starting here).

Equally inspiring is Kerri Rivera who has been curing kids of autism with MMS and completely banned from youtube: https://cdautism.org/videos.

Banned Video about MMS curing Malaria

Facebook support group

Jim Humble’s Book can be found here and here. Jim Humble’s Website: http://jimhumble.co/

How it works, some scientific articles here and here

Protocols:

Other Lyme Related Articles

enema, Lyme, mms, protocol, treatment


Lee Warren

Lee Warren is reclaiming wisdom through conscious relating with self, land, and others. She has 25 years of experience envisioning, designing, and living innovative solutions to mutually empowered relationships, land-based food systems, residential community, non-violent communication, and sustainability education. She is the principle and founder of Reclaiming Wisdom, a co-founder of SOIL, School of Integrated Living, and a proponent of regenerative systems, consent culture, and authentic living. Lee is a writer, teacher, and activist, with an passion for embodiment practices, rural wisdom, sustainable economics, conscious dying, and community of all kinds.

Comments (27)

  • Thanks for sharing your journey!

    Did you feel any different regarding your symptoms when doing mms-enemas compared to drinking it?

    I am both drinking and experimenting with enemas to help me with my remaining symptoms from covid(strange throat sensations + occasional fatigue triggered by exerceise and stress), but I’m thinking I might also have lyme at the same time(I have a strange mark on my skin looking lymish), confusing my recovery journey.
    But, I’ts more of a project doing the enemas and sometimes leaves me drained. I would rather avoid it, but if it is worth the effort I might continue experimenting with it. I am using cds, but I’m not sure which form of mms is more effective for enemas.

    Did you ingest any mms between your enemas?

    Also, you are still well?

    Thanks. =)

    • I had a hard time taking it orally because I really HATE the taste of it. So it wasn’t sustainable for me. I read somewhere that Jim Humble suggested that enemas are as close to intravenous as you can get in an at home DIY situation, meaning most effective.

      I am now doing MMS orally but I put it in capsules and swallow them. I’m doing this for health maintenance and to continue to eliminate candida or Lyme or whatever is still happening for me in my upper gut area.

      Yes, enemas are a project but I had IBS as part of my symptom picture so I was really motivated to get my bowels functioning properly again.

      I’d say go with what’s easiest and most desirous for you. That will be the most sustainable. Ongoing consistency is key so making sure you are on board with your own treatment protocol will create long term “compliance.”

      I am using MMS – combined drops of sodium chlorite and hydrochloric acid. I get my sacraments from my MMS church. You can find on my resources page.

      I am better than ever and I never thought I would get here. So many things are better and I can do most everything in life that I want to. Still on a long road of recovery of my most robust self but that’s to be expected.

  • Hi! Thank so much for sharing this resource.

    Has your lyme been permanently cured since doing this? Have you had any relapses? Did you completely stop MMS after 3 months?

    • A few caveats:

      1. Chronic Lyme Disease has not been researched or funded thoroughly so much of the time all we can do is guess.
      2. The tests are inaccurate and unreliable.
      3. The solutions are as varied as there are people.
      4. The human body is still a mystery to us – what we know can be represented by a pinprick on a sheet of paper.

      Further, I don’t use the word cure, ever, to indicate my situation because it’s a paradigm I don’t subscribe to. I believe we evolved with pathogens including bacteria, viruses, and fungi. They are a part of the biome inside and outside of us.

      All that being said, I no longer experience the most extreme symptoms of infectious Lyme that I used to. The tingling nerve ending sense that something is active in me that is not to my wellbeing, the lying in bed due to exhaustion and pain, and the coinfections that seemed always be present. I have recovered from lifelong irritable bowel syndrome and the chronic pain is no longer an issue.

      I still have a long slow road of rebuilding and recovery and I still have to rest often. I still have food sensitivies and I still have candida or other complications along those lines. But that all makes sense since I was struggling with Lyme for 30+ years.

      I do six week rounds of enema’s every six months or even just one here and there when I feel that I need them. I am doing MMS orally for what seems like candida and it’s helpful.

      I’m still on a long slow road of recovery but gratefully so much better than when I had a more active infection.

      Hope that’s helpful.

  • Hi Lee, thank you for this site it is wonderful!

    A few MMS enema questions:

    Once you get the MMS solution in the bag how long is the solution potent for? It seems that it starts losing
    power the moment it is in the enema bag, so I am wondering if it makes most sense to have the first enema
    be the longest? How long did your enemas last once you got used to them? Do you have a recommendation
    for how long to hold it? Thank you so much!

    • Mixing the solution and using it right away when it is fresh is really best. If I remember correctly I believe Jim Humble says that after an hour it’s no longer good/viable. If I have content in my colon I sometimes can’t hold it very long so I’ve sometimes done a smaller amount of liquid (either with the MMS or even without) to clean out the colon and then once it’s empty I can hold it longer. Sometimes I just don’t worry about it and do what I can trusting that the MMS is getting into my system. I have found that my body wants to expel the MMS especially (because it’s harsh) as I increase the number of drops. The harshness of the treatment is what has contributing to eradicating Lyme so it’s part of the effectiveness in my opinion. Overall go easy on yourself. Do what you can and experiment and work up slowly. You want it to be sustainable for the long haul. If you can only hold a couple of minutes, that’s fine. Try again and again over time and you’ll get the hang of it for your body. For me the shortest hold was probably two minutes and the longest hold probably 30 minutes.

      • I was a hard-core and very strict carnivore from Fall of 2016 to Spring of 2022. I’m now mostly carnivore but have added more range into my diet. I can tolerate more and I’m healthier.

  • Hi Lee. Thanks for the MMS info. Fellow Chronic Lyme and co-infection human. I will follow your protocol and let you know how I do. I wanted to share something with you too since we are all just trying to help one another along. I have been researching molecular hydrogen “Brown’s Gas ” (George Wiseman). I ordered my machine and It seems to be a real game changer. Check it/him out. https://youtu.be/olFIXa2Lr2Q. Also check out Vitality detox drops https://youtu.be/mJ7JQO0_pck. Natural Zeolite that helps detox lyme bi-product from the body along with heavy metals and toxins. just wanted to share. Blessings – Kerri

    • Hydrogen gas is making a HUGE difference for me too! Mood, appetite, bowels. I would not have had a chance to really try it had I not gone to a clinic in Europe and had a few hours a day there for an affordable price with everything else I was doing. I recently used my tax return to buy my own machine for at home use for my family and it is making a big difference for me.

  • Have you read Andreas Moritz book “Timeless Secrects of Health and Rejuvenation”? And do several liver flushes…
    Highly recommended! Best Luck!

  • Hey Lee!

    Im so happy i found you!

    ive been struggeling with lyme since i was around 8 years old.. im 30 now.

    Could you tell me what kind of water you use for the enemas?

    Should i boil it first?

    Thank you so much for sharing! I feel so alone sometimes and this gives me energy and hope to keep going and heal myself 😀

    Much love,

    Luka Pollmann

  • Hi thanks for sharing! If you hate the taste of MMS make it into CDS which is Andreas Kalckers new way of making it.CDS is much better absorbed by the body and lasts longer in the water unlike MMS which needs to be taken witthin a few minutes. I did a 2 month 1000 protocol and knocked out Lyme and EBV its a miracle… also i followed a cancer diet while doing it, no sugar, wheat dairy etc now i am rebuliding my minerals and strentgh working with Morley Robbins the root cause protocol 🙂 check these guys out on youtume, bitchut, rumble….

    • Can you tell me the difference between mms and cds. I thought they were the same thing. And where do I get cds? Also a Lyme sufferer. Thx

      • It’s the same. Chlorine Dioxide is made by combining sodium chlorite and an activator. MMS is the same thing as Chlorine Dioxide. You can look at my links for where to buy.

  • Mel, so glad for your success! I’ve suffered with lyme for 28 years. I ordered and received the cds plus 250 mls. I don’t know what the 2 month 1000 protocol is. I’ve searched for a dosage but this site is the closest I’ve found. Would sure appreciate any help. Thanks in advance.

  • Hi Lee, in this protocol you say use one drop of each ingredient. If you worked your way up to 15 drops, dos that mean 15 drops each of each ingredient? Thanks!

    • To make one drop of chlorine dioxide solution / CDS, start with 1 drop of sodium chlorite solution and 1 drop of an activator.

  • Did you ever post your original symptoms? Has this protocol kept them away to date? Did you experience any side effects? I tried orally and haven’t had much success. Mainly loose stool for awhile after I do the regular daily dosing schedule.

    • My original symptoms were intense digestive issues, fatigue, full and new moon suffering of staggering proportions, extreme food allergies and got down to eating one food only, headaches, and more.

      The protocol has been life changing. I treat regularly to keep things in check. As needed.

      Side effects of using MMS, for me, were much less than antibiotics but it’s an intense process and sometimes painful and draining.

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