Hi, I am taking mms for 14 days. I started with 4 drops in 1 liter of water 8 times a day and every day I put one more drop. Today I thought 20 drops. In the first week I was weak and tired, couldn’t do anything at the gym, but now I am feeling good. I have acne, candida on my tongue, fungus on my toenails. I’m 50 % cured. Thank you.

Greetings all, I am pleased to say that my bloodwork and medical info have come back all clear, 2015 I was an insulin dependant type 2, Diabetic 4 times a day, metformin etc, suffered from PTSD, restless leg, chronic fatigue, high blood pressure, fatty liver, Global pain syndrome, and Cancer, etc….MMS, DMSO, MMS2 AND THE OTHER Sacraments of the Church have been responsible for a complete recovery and continue to protect me from pathogens, bacteria and viruses. I was so amazed at this I took the course and have helped many others learn to help themselves, If applied to any illness or injury our Sacraments will reverse or assist in the healing of most on the planet.. Everything begins with a thought, So change the way u think, and check out the Genesis2church.is website and help yourself and others. AT this point in my 60 yrs I feel better than I ever have and u will also by following our PROTOCOLS AND TAKING Control of what goes in and out of Your SYSTEM. Regards Wulfric HG Kilburn Health Minister Chapter 313

First I want to dedicate this testimonial to John Darnbourgh who has introduced me to this. When John first met me I was suffering from gastritis and chronic fatigu, constipation and had dark circles under my eyes. Started on the capsules and quite quickly after this noted that I was taking less naps durning the day. Instead of going to the toilet once a week, if that was going every other day. My nails also seemed to start growing and the darkness under my eyes is 90% better. Without the MMS and the advice and dedication of John I would not be where I am lost weight, healthier , happier and can hold down a job so thank you

My 38-yar-old daughter had Epstein-Barr virus with the accompanying fatigue and inability to come alive in the morning. I recommended MMS to her so she agreed try it when she came to visit on her way from collage to her first teaching job. Before she tried it she would sleep till 10 or 11 a.m. and then drag around for another couple hours before she could get woke up enough to function normally. An ordinary cold would drag out for two weeks or more.

The first night she had time for only one dose of one drop each of MMS, citric acid and DMSO properly mixed, with fruit juice (no added vitamin C). The next morning she came cheerily out of her room at 7 a.m. declaring, “Something happened! I NEVER wake up this early.” She continued taking the recommended escalating dosage through three weeks and then decided to really slay the dragon by going another three weeks, ending at six drops for the final week.

Shortly after ending the regimen she began her first year of university teaching, with its guaranteed rotating supply of germs and viruses. She gleefully reported that when some bug was going around, if she got it at all she would have it for only one to three days, like the other staff. “It’s so nice to just be normally sick,” she declared.

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%.

 -= 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 youtube.com/user/Not2bforgot10/videos?query=lyme

Her latest video in two parts on MMS vs Lyme (June 2012):
• MMS UPDATE (1 OF 2) CURES LYME, HIV, HEPATITIS, HPV, ETC
• MMS UPDATE (2 OF 2) CURES LYME, HIV, HEPATITIS, HPV, ETC

Hello,

My name is Teresa, I have 53 years and living in Cadiz (Spain).

In my testimony I want to contribute my little bit to your wonderful work with the MMS.

I had been watching and reading about this, and was able to arouse enough interest in me to decide to try it. Years ago he had suffered from inflammatory rheumatism and several episodes of uveitis that is supposed were related, one day I was desperate enough to move from conventional medicine and explore other possible “therapies” to help me overcome all the pain and suffering. Not to do so long, just say that, going that route, I realized that only I could heal myself and really all we can do when we are able to feel that certainty, and there came a time when I felt healed. I thank with all my heart the experiences, lessons, people …., which made it possible, though I must say that I do not think have gotten anywhere, just try to learn everything with that tune and I think it aportarme something.

In November last year decided to try the MMS, with the aim to clear my body of toxins, metals and other undesirable thing that I assumed would walk swarming my body after years of unconsciousness. And “accidentally” while waiting to receive the order uveitis developed in one of my eyes. I felt that this was a “test” and decided to wait and treat only with the MMS. By the time I started taking my eye was in a sorry state, and even had blurred vision, but I really felt that beyond madness that had a purpose. I took the MMS protocol by 1000 for 14 days, with the first dose and felt relief in inflammation and pain and end of those 14 days my eye was normal and asymptomatic, still looked a little blurry and I decided to just wait until I could rebalance itself, and it did. I’m fine and I share this to give hope to those who may need it. I must say it cost me to take it … I felt horrible taste and suffered diarrhea more or less, half the time, but I saw that really works and I feel wonderful.

Andreas, thank you for what you do, for being brave and for illuminating the Earth.

A hug,

Teresa

I lost my mother to cancer – didn’t know enough about MMS at the time to use it.

Am now trying to help my father overcome cancer of the esophagus. He was diagnosed 18 months ago; he is 82 and the docs were pretty grim faced about it all. But 18 months on here we are. I think the reason he is doing so well is because 2 years before he was diagnosed he was taking MMS off his own back, on the old regime of a 15 drop dose in the morning and one in the evening. I believe that has stood him in good stead. His tumour has not grown or spread since diagnosis. Doctors are a bit confused. BUT the tumour is still there and still dangerous. I have only recently got him back on to MMS – protocol 2000 without the MMS2 as he can’t swallow the capsules. Am persevering but it is hard sometimes and easy to give up when the MMS is making him feel bad. Sometimes the amount of things one could try with MMS is overwhelming too for the carer – should i do this or that etc. MMS1/MMS2/CDS/DMSO…swallowed, bathing, enemas etc. Great to have such choice but overwhelming sometimes too.

my MMS experience

For some reason it popped into my head that I hadn’t gotten around to telling this story yet.

I love curezone, and if people here are getting good results from something, I try it. I do a lot of research before I try anything, and really try to get a solid overview of the patterns and pitfalls with any protocol.

When I was researching MMS, the nearly even balance of positive and negative testimonials was really confusing. I finally decided to at least give MMS a try, because I can’t say something doesn’t work, at least for me, until I’ve given it a fair trial.

Every time I worked up to more than 4 drops of MMS per day, I would feel ill and instinctively back off. “Die off” is one possible explanation. But with many protocols, if I take a day off and start again slower, progress is made and die-off type symptoms are reduced. This didn’t happen with MMS. I would feel sick every time I tried it, maybe 5 times over a 1 year period, and the longer I persisted, the worse I would feel.

So, I finally decided I would just push through the “die off phase” and get to the other side. After about 2 weeks I got up to 5 drops twice per day, and my upper back started to hurt when I would breathe deeply. I stopped the MMS, but the pain under my shoulder blade only got worse over the next couple of days. I started to become disoriented, and out of curiosity, took my temperature. Uh-oh, 104F. A friend took me to the emergency room.

After an MRI and a bunch of blood tests I was diagnosed with pneumonia, possibly mycoplasma. A heavy blast of IV antibiotics got me to where I could be released from the hospital the next day, but I felt like death for about 2 weeks afterwards. A Z-pack finished killing the pneumonia, but turned me into an aggressive know-it-all for about a week, which pissed off a couple of my friends.

While I was in the hospital, I was told that my sodium level was so low that I was in danger of having a seizure. I’d never heard of low sodium before. At that time I was in the habit of taking at least 1/8 tsp of Sea Salt every morning, so something must have really been sucking the sodium out of my system.

So, to sum up, I was taking MMS every day for about 2 weeks and wound up in the hospital with pneumonia and dangerously low sodium. I can conclude that MMS doesn’t work well for me. I’m someone who does anything he can to stay the hell away from hospitals and doctors, and am a little pissed off that MMS landed me right in their clutches.

Anyway, that’s just one story, but I’m sure it’s not the only one. Be careful, everyone!

{followup comment by the same person about the above story…}

…Another acute symptom I forgot to mention from my hospital visit was premature ventricular contractions, happening on average about every other heartbeat. A heart monitor was detecting them, and I could feel them. Disruption of electrolytes by MMS could have contributed to that. In the period prior to the hospital visit, I might miss a couple of dozen beats scattered through the day, but not every other one. That symptom has pretty much gone by now.

I started taking MMS because I’ve got some kind of fibro/chronic fatigue/candida complex of shifting symptoms after being floxed by fluoroquinolones, and am always looking for a way to make it stop. I feel like I’ve tried everything, but there’s always one more thing to try. I gave MMS every possible chance, but it just doesn’t suit my individual chemistry, I guess.