In the summer 2012, I visited my family in Germany. My mom had a caretaker from Poland (61-old woman) who had arthritis in her hands; the index and middle finger on her right hand were stiff. I offered her my traveling pack of MMS and she took 4 drops of 28% sodium chlorite solution mixed with only one (!) drop of 50% citric acid – this is the proper stoichiometric ratio, which I calculated. After only 5 days, the swelling in her finger joints was gone, pain was gone and she could move the two fingers that were previously stiff! I was really surprised. Another lady (72-old, German), a friend of my mom, had rheumatoid arthritis and she also took 4 drops of the sodium chlorite solution, activated with one drop of the 50% citric acid, and after only 2 days, she was pain free – unbelievable! And they are still fine. Once in a while, I have some pain in my hands and I take the same amount as above and the pain quickly disappears. I use MMS to keep my gum healthy and informed my dentist about it. He found the CLOO-SYS toothpaste and oral rinse and uses these in his practice. I wonder if bacteria in the mouth are the cause of arthritis? When I use more than 5 drops I get diarrhea, so I stay with a maximum of 4 drops. Look also into boron – there seems to be a connection between boron deficiency and arthritis.

 15 drops 5 times a day is too much for anybody to handle most cases .

I recomend working up to the 15 drops and then try 15 drops, once a night for two
weeks to two months…..go slow but keep at it in a healthy way that you can
still function. you will eventually clean out your system.
I used to take 10
drops at night, then in an hour from that dose , i would take ten more, then in
and hour again i would take ten more .
Si got to the point I could take 30 drops a nite but sperating it into smaller doses 1 hour apart.

 When i got up to 30 drops like that a nite for one week i began to feel way better.
And my herpes/ skin fungus or whatever the hell I had , dissapeared.Some of the disease I had
came out through my skin around shins and calves. It hardened and i peeled it
away like scabs?.

New skin grew back. I dont know what I had but what ever it was
I believe it was in my intestines and it over spilled into my blood stream.

Maybe it
was candidia over growth.
I think in all it took me about 8 months to
heal.
I took MMS at night and during the day i would take my vitamins and
good bacterias.

Pray and monitor yourself wisely. stay calm. God bless and
God speed to anyone trying to take their health into their own
hands…Triumph…

For years I have had a problem with feeling sick after vigorous exercise. It has gotten progressively worse over time.  I suspected systemic candida, but was never diagnosed. I tried Protocol 1000 and added DMSO.  Three weeks later I was ready to test the effectiveness of this treatment.  I have exercised extremely hard for the past two weeks, with appropriate breaks, and I feel terrific! I have had no indication of my former problems. 

By the way I am 72 years old, but now feel like I’m in my 20’s.  MMS really worked for me.  I have already influenced four others to do the protocol since.

I’ve changed my activator to lime juice and it’s much easier to drink for some reason. The smell is the same but getting it down is really not hard at all – and no real aftertaste. I don’t have the time to mess with adding juice, I just chug it. Also the nausea is not nearly as bad (considering I’m still upping the dose).

The citric acid, though I’m aware is the preferred method, was really not agreeing with me! I’m not sure why, and wonder if others who stopped taking MMS because of the taste have tried different activators?

Anyway, my body continues to “clean out,” showing tons of little strings, along with the yeasty smell, I can only assume is candida hyphae (am trying MMS for deep-rooted candida in fungal form), though who knows for sure. It’s not worms, since I’ve already sliced Tapeworms to death with diatomaceous earth. This is something new, and anything that looks like tons of strings is welcomed out of my intestinal tract! 🙂

Anyway, just thought I’d mention the activator. Oh also eating food any less than 3 hours before or after makes me nauseated, so I can’t do the frequent dose protocol like I originally intended. I’m doing first thing in the morning and when I get home from work, when my stomach is totally empty, so I eat and supplement during the day and before bed.

I’m taking ionic sea minerals, D3, iodine, and cal/mag/zinc pill. Any suggestions are welcome.

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.

I just switched to the 1000+ protocol [every hour with equal amounts of MMS and DMSO] (I have candida/fungal issues, heavy metals, FMS/CFS, GI issues, adrenal/thyroid/hormonals…the list goes on). However, it doesn’t seem to be very effective. I’m up to 6 drops per hour (when you are supposed to do only 3) b/c I’m noticing no difference.

However when I was working my way up to 15 drops twice a day (the old protocol), I seemed to start to get the die-off reactions (it started in my throat: major congestion, phlegm, mucus, raspy voice, tiredness…no diarrhea/vomiting/nausea though, but my stomach felt “odd”). I always took it on an empty stomach (upon awakening and before bed, and i waited at least 2 hours to eat after taking it or 4 hours after eating. I didn’t have to worry about what to eat or what supplements to take b/c I knew I could plan it out so that they wouldn’t interact. (Plus, it is extremely inconvenient to mix a dose every hour…I tried the “pre-mix” idea to carry around all day, but it seemed to lose it’s effectiveness).

I don’t know if this 1000+ protocol works. Like some people have surmised, it seems like a lot of the doses would be useless due to the neutralization effects of food, supplements, etc. This link shows all the foods and substances that can make MMS ineffective: (scroll down to Incompatibilities):

http://bioredox.mysite.com/CLOXhtml/CLOXprot.htm

Should I go back to the 15 drops BID and maybe work up to three or four times a day (take a dose every 3-5 hours)?

Have most people benefited from the old or new protocol?

I appreciate anyone’s advice, for there is not a lot of info about MMS out there.

Thanks!

Hello, I have used MMS orally 1 to 8 drops every hour for 9 hours and I have used MMS in a bag injected with saline water. When I drop off an infection in the face right by where my eye and made ​​me a huge swelling, so I inject the MMS, to my surprise, a look was enough and I was completely cured the infection.

When I felt that MMS inject my face without hurting the liquid passing or hurt me like a spider web. Then I had a little reaction as fatigue or diarrhea, nor I, nor vómitos.Yo MMS1 use for a yeast infection in the lung called aspergillius sp .. We all have this fungus in the intestines, or as not moved to my lungs. Spend 5 times by the hospital and nobody had told me. Thank God I take the MMS every hour in the old protocol. And no need to ask anyone or pay anyone for instructions on the site http://www.jimhumble.com intruccines you can read perfectly and I started with a 1 drop a day, was after he reaches 5 drops I continued to take up to 63 drops per day, taking 7 per hour, I get to the desired reaction was like throwing up (thank God no vomiting) and fatigue that I bounced on the bed. After that I had a kind of detoxification with the same symptoms of an asthma episode but very mild.

Here in Guatemala do not know if there is anyone who sells it, so here I leave my e-mail for which you need to buy, I sell : mariglobal80@gmail.com in Guatemala City.

Greetings MARIA DE GUATEMALA

Autism update

We have some more wonderful news about MMS & Autism!

Here is a letter I received from Kerri working with children with autism – I thought you’d like to read it:

“Well, the past 3 months I have been a busy girl. We visited my good friend Jim Humble the middle of February which was a dream come true. At that time I had about 130+ kids on MMS. Afterwards, we had a conference in Puerto Rico on the biomedical approaches used in recovering children from autism. Directly from Puerto Rico I went to Venezuela where everybody was very excited about MMS and the possibilities of recovering from autism with only pennies a day. While in Venezuela I was able to teach 4 doctors the protocols that I use in my clinic, and share my presentation on the use of MMS for Autism Spectrum Disorders at a conference which 750 people attended. It was a very exciting time to say the least! In the days after the conference I was able to consult 176 families on individual biomedical protocols for their children, including MMS.

Since the conference, there has been much more interest in MMS in Latin America. In particular, I have many families who I help in Spain. I guess word got out, and one of the 2 doctors treating autism in Spain contacted me and asked me to share my protocol with her. The good news is that she is going to use it. Her idea is to apply it as an antifungal for Candida. However, MMS knows no boundaries and will kill all other pathogens at the same time. So, quite frankly, it is of little consequence what she believes she is doing with it, she will be doing far more than she even knows. Combining MMS with diet and hopefully only a few supplements, this doctor should be able to recover some of her kids. Financially speaking, when doctors like her start seeing results they will in turn get more patients and more patients mean more money. So, results coupled with money are a win win situation, and in turn humanity wins as we all grow healthier.

I hope to do a free conference in Spain before year’s end about the biomedical approach to recovering children with autism and autism spectrum disorders. I know that another doctor is using MMS in Italy. Maybe Europe will lead the way to getting MMS into the mainstream biomedical treatments and then the USA will follow. The doctors treating children in the USA with autism are under close watch by the FDA. Anything too “alternative” could cost someone their license. And these people have their own families to feed. So, they have to walk a very fine line. It is sad to see. Because what these special doctors want for their patients with autism whom they are trying to heal is the fastest recovery possible. And if it could be fast and inexpensive these doctors would be happy as well. Unfortunately they have such strict guidelines that it makes doing what they do difficult. Hopefully we could do a double blind study using MMS and autism. I think it would be easy to measure the difference.

On a practical note, many of the parents who have their children on MMS take MMS themselves, frequently out of a necessity to heal some immune issues. They will ask me “Can I take MMS too? I have X”. I always refer to a protocol from Jim’s course, and without fail within the first week I receive an email with some kind of miraculous story as to how “my fibromyalgia went away” “my husband’s sense of smell came back” “my shingles went away” “my Mother’s diabetes is under control”. These and more stories have come from the families of a child with autism. It goes without saying that the affected child is doing much better and having all sorts of firsts of his/her own.

At minimum there are 400+ children on the Autism Spectrum improving steadily, thanks to the help of MMS. These are in addition to all of the other children that these doctors are seeing and treating with MMS. The total including family members could be easily above 1000. The future is bright now that many more healers/doctors have the information on MMS and the knowledge of how to use it. I believe that people like these who see many, many children are an important link that will bridge the gap between “alternative” medicine and “allopathic” medicine, finally bringing MMS to the mainstream. I hope that we have in our hands the missing piece of the autism puzzle, because it sure seems to look that way. Two more children in March lost their diagnosis from autism, which makes a total of 5 children to lose their diagnosis since I began recommending MMS in August of 2010. Not all have recovered. But all are better than they were, and that is a great place to start.

As for now, I receive over 100 emails a day from people using my protocol for MMS. Sometimes we increase the dose, decrease or stay the same. We do protocols that other families and I have developed that add enemas and other elements of timing for the oral administration. The newest protocol that is getting lots of attention is the 72/2. It is a dose of MMS every 2 hours for 72 hours without resting in the night time. So, one parent wakes up every two hours and administers a dose of MMS. We have seen remarkable improvements with the 72/2. Another new protocol is the 12/2. It is taking MMS for 12 days straight then resting 2 days. This way the pathogens living in the gut will expose themselves during the two day rest, and then we hit them with another 12 days of MMS. Using this method we gradually extinguish all pathogens until none remain. When we heal the gut we cure the autism. The MMS enemas have also led to marked improvements for children on the spectrum. The families doing enemas are seeing more language and in general having less conduct issues and a lessening of stereotypical behaviors. When trying these new protocols or any MMS protocols it is a good thing to work in a team situation. Someone like myself, for example or another person who has used MMS knows when and how to avoid Herxheimer’s (die-off) reactions and what they look like. Many times the road to recovery is paved with discomfort, but in the end, it will have all been worth it. Autism means that your child has virus, bacteria, Candida, inflammation, heavy metals and food allergies. Allopathically speaking, you would have to take a drug store to kill all these pathogens, but will MMS, all you need is a little drop of what my husband calls “holy water” and recovery is on its way.

I think to myself that MMS and autism recovery are in their infancy together and wonder where we will be in 25 years. Will we finally, openly acknowledge what is causing the autism epidemic and stop it? Will we all use MMS to cure it? Will we all be hiding our rations of MMS from the authorities who say that we cannot use MMS? The last thought gives me the chills, a harmless oxidizer, yet at the same time potent enough to cure autism? It’s possible to think that it might be held out of a mother’s reach when she needs to heal her child from this devastation. Let’s try not to let this happen, and get everyone we know on MMS. Healing humanity begins with me and begins with you. We can do it. But we need to do it together”.

Best wishes,

Kerri Rivera