I’m a senior network quality assurance engineer from Scandinavia. In February 2014 I desperately needed to find solutions for a series of symptoms. At the time I felt the life was running out of me despite dozens of alternative treatments for many years.

In my search I accidently stumbled over MMS. That probably saved my life. Today I have been on MMS since mid March 2014, thus in treatment with Protocol 1000 for 4 months. I’d like to express my gratitude for letting me learn about this divine treatment and to let you know what it did for me.

After a short time everything inside you feels natural, like something you have been waiting for for a long time. All human needs change. Sleep gets better. The need for eating and drinking changes to natural. You might even change personality. I did. I don’t know if it was for the better, but I certainly changed beliefs about many things.

The healing process is like a movie playing backwards, for good and bad. That means you will feel the pain and discomfort of diseases experienced earlier in life but fortunately it won’t last that long.

The process of taking MMS is, sad to say, dreadful when having a job and social life to attend to. I wish an easier but still as cheap method could be found. But I held my spirits up high when I by accident misinterpreted Clara’s Protocol (6×2) and took 6×6 (6 drops per hour in 6 hours). When taking that lot in the early stage it later turned out that this can be used as indication for what the solution can do for you.

In this case some very annoying conditions would disappear: pain in feet, neck, back and shoulders, the fog in my brain. And it did. While it did I was so relieved and so happy one might think I was on drugs. What a feeling. Though returning to normal after a couple of days, I had a taste for more after that experience as I knew everything was going to be better.

The easiest way to describe the healing powers of MMS is to show my own list of symptoms with comments.

Small Fiber Neuropathy – Unnatural pain in hands, arms, legs and feet. Trouble walking. Restless legs and feet make it almost impossible to fall asleep at times. Dozens of doctors were involved in the diagnosis. It turned out to be inflammation in the nerve fibers that transmit thermal information to the brain. It is connected to diabetes, which I didn’t have. Not cured but relieved to be endured. MMS was able to remove the pain and most of the restlessness in less than a month. Currently the condition is like when it started years ago with only disturbance in the feet.

Hypothyroidism – Low energy, bad digestion, ennui. Treated with T4 medicine which turned out to be insufficient but not recognized by endocrinologists. Only with T3 supplement the jar over my head went away, but life was still a struggle. Last check and bloodwork showed no change in readings. MMS cleans up a lot and life is easier already.

Paradentosis – Sore and bleeding gums. Loose teeth for years. Brushing, flossing, rinsing with chlorine, strong antibiotics, vitamins and minerals, even ultrasound treatments at dentist didn’t help. I would inevitably lose my teeth. Almost cured after less than a month without mouth rinses with MMS. The dentist had never seen anything like it.

Hypertension – No symptoms. Blood pressure is lowered around 15% which makes me believe that I can start removing some of the medicine.

Deafness in left ear – Due to inflammation of the eustachian tube connecting the inner ear with sinuses. Had it for years. Sometimes tinnitus with both high and low sounds. Cleared up the day after first dose of MMS.

Nasal congestion – In the left nostril only. Cleared up the day after first dose of MMS, though it returned occasionally during treatment.

Swollen eyelids after Graves Disease – Before hypothyroidism I had Graves Disease for a couple of years. The disease made my eyes almost pop out of the skull and left damage in the eye sockets. MMS removed the inflammation in about 5 weeks.

Strange pressure under left ribs – A disturbing condition examined earlier by my doctor without findings. No improvement the first month. The second month I coughed a lot and tightness in the diaphragm ceased. The third month it got worse with more diarrhea and coughing. By the fourth month it was better than ever.

Muscle and joint pain – Aching muscles and joints for years, probably related to hypothyroidism and calcium metabolism problems. Reduced about 80% in three months.

Confusion and lack of concentration – Episodes of mental numbness and difficulty concentrating on complex tasks. Disappeared in about two weeks.

Exhaustion – Only willpower allowed me to do daily activities. Energy returned partially after one month and continues improving.

Trouble falling asleep – Sleep sometimes took several hours to arrive. This is now much better.

Nightmares – Vivid dangerous dreams occurred twice a month. Experienced only once at the beginning of treatment.

No libido – The desire was gone. After about three months a small sign of recovery appeared.

Depressive state – Felt hollow, like a zombie living in a filthy and creepy world. After four months this feeling is almost gone.

Fungal attack – Frequent fungal attack on the left side of palate starting with sore scalp. Appeared only once during treatment and much milder.

Abscesses – Boils in different places. None experienced during treatment.

Bonking – Need for sugar after several hours without food, sometimes leading to near fainting. Has not happened for months even though my need for food has reduced.

EM

Summary:

Sue describes her daughter Natalie’s lifelong health struggles, including mitochondrial disease, repeated infections, hospitalizations, cognitive regression, autism diagnosis, aggressive behavior, immune problems, and seizures.

After years of medical treatments, DAN doctors, special diets, immune globulin therapy, and rotating medications, Sue says she discovered antiparasitic treatment and later the MMS protocol connected with Kerri Rivera. She reports rapid signs of calmness and awareness after the first very small dose, followed by gradual improvements, reduced medications, lower ATEC score, and longer seizure-free periods.

Transcript:

My name is Sue and my daughter has been very ill all her life, from birth actually.

She started, gosh, she started getting really ill at about two weeks of age. Pneumonia, different things happening to her, many hospitalizations, ear infections, many hospitalizations.

At any rate, we were told to get a muscle biopsy and we learned through that muscle biopsy that she has mitochondrial disease.

So we of course sought out the best doctors that we could seek at that time, that we could find at that time, excuse me. And we employed many, many different medical treatments on my daughter to try to help her feel better.

And part of those treatments were a lot of antibiotics, a lot of antibiotics over the years. And also the mitochondrial specialists at the time were telling us that you really should make sure that every single year you give that girl a flu vaccine and your entire family. Because, you know, she has mitochondrial disease and so she’s going to be more susceptible. She’s, you know, going to want to protect her.

So we did this. And every single flu vaccine that she was given, she ended up in the pediatrician’s office the day two later. And she somehow bounced back, you know, a little bit. But she was always weak, always fragile, always sick.

Ear tubes, always occupational therapy, speech therapy, you know, everything. She started to kind of get a little bit better with a lot of in-home nursing care and my quitting my job and a lot of care.

Somewhere around 2003, and we were getting more help for her. We were really excited. 2003, 2004, like, hey, she’s getting prepared to go into kindergarten, a special needs type of kindergarten, one for mildly cognitively impaired children, but nonetheless, a kindergarten in a general ed setting. And she was happy.

And we gave her another flu shot in 2005.

[Crying]

She regressed so rapidly. She went from being, you know, mildly cognitively impaired, I’m sorry, to severely, multiply impaired classification in the school.

Sorry, I wasn’t prepared for this. Severely multiply impaired. She could no longer be in that mild kindergarten anymore. Mildly impaired kindergarten anymore. She could no longer be integrated with normal children. Not even the least bit.

She had to be moved to an autism classroom. And it was, you know, a classroom of five children and three adults. And she was the worst one in that group of five children. She could not function at all. Barely at all.

So everything fell apart. And this happened, it was September of 2005, she got that flu shot. And she was rapidly degressed. By October, November, December, she had fallen apart within a couple months.

And the school systems take a while to make the adjustments. But by that April of 06, they did make the adjustments to that very heavy, intense need for her supports. And in 06 of April, we got an autism diagnosis.

So we had the medical side and we had the school side of her deterioration.

So of course I sought out the DAN doctors and we went that route for years, very diligently for years. And actually I started the gluten-free diet in 05 because I was already sensing and researching, you know.

And so gluten-free, casein-free diet in late 05 and then 06 became all the DAN supplements folded in and all that, you know. And, you know, there was some improvement initially, but then it just seemed like over the years things weren’t improving. They were getting worse and worse and worse.

07, 08, more aggression, more irritability, not only towards the caregiver myself, attacking kids at school, attacking them, attacking para-educators. My little, at that time, probably roughly 45-pound little infant girl, excuse me, infant girl, was attacking like an animal and could barely stay in school.

We had to switch school systems to try to find even more support for her. So I was really frustrated.

Things degraded even more to the point where she needed immune globulin therapy every four weeks. She’d get an injection of immune globulin into her vein to try to give her some immune support to try to combat these illnesses that kept on reoccurring in her.

And then the DAN doctor at the time, very generous and kind man, he was trying so hard for her, he said, well, let’s try every three weeks now. That still didn’t do it.

So we made another change. We said goodbye to that doctor, thank you for all your efforts. We made another change to the local hospital because we felt that we needed the local hospital support in case things continue to get worse for her.

[Crying] Excuse me.

We got her with an immune specialist and he put her on weekly immune globulin, which is subcutaneous. It’s less invasive. You don’t have to find a vein. You just go under the skin. So then weekly therapies.

Still didn’t do it. She was still attacking. She was still uncomfortable, still not sleeping well. She was not having a quality of life at all that she deserved.

And I was on Facebook, not on Facebook, on email, a Yahoo group, a support group of moms that I try to research like all autism moms do. And this one gal was talking about the moon.

She seems like she’s lost it. I mean, I thought I had already lost it. And she’s talking about the moon. Okay, whatever. And I’d see her emails periodically.

And one time, there was this one evening that Natalie had such a bad evening of weird crying, weird crying in a way that we had never heard before. Almost like a possessed kind of cry before bed.

And I looked at her dad, my husband, I said, this is weird. Something’s weird. And that email I had just read, again, the earlier in the day, I ran down to my computer at that very moment. And I went to Farmer’s Almanac.

And it’s full moon. It’s full moon. And that’s that crazy, crazy laughter. And it’s full moon. I knew that that crazy lady, that crazy mom wasn’t so crazy.

So then I knew what I was dealing with, at least to some degree. And I contacted her doctor. And I was emphatic.

Her pediatrician, I said, we need to, we need to give her an antiparasitic. This is what I think is going on based on all the research I had done. Give her an antiparasitic medication.

Things started to improve. Reports home from school. Natalie did this or Natalie did that where she hadn’t been doing things before. She hadn’t had behavior of hitting or pulling someone’s hair or biting or pinching or kicking. Oh, I could name the behaviors.

So we were onto something. I was really pleased. And we kept on with these antiparasitic meds. We’d rotate very various ones.

I was lucky enough to have found a doctor who was willing to see my passion and trust me. And I told that doctor, I will bring her in for as much blood work as you want me to bring her in. You have to do this for me.

And so there was a relationship where he allowed me to rotate various antiparasitic and sure enough, she improved.

But there was still some strain there. And I couldn’t figure it out what it was. Why? Why it was still going on?

Well, of course, she was still on antifungals daily, antibiotics daily, antivirals daily, and now an antiparasitic daily, rotating whatnot. So she had very complicated medical life.

And I ran into a friend of mine at Costco, an acquaintance who also had a special needs child with autism. And we were just chit-chatting back and forth over the Costco shelves.

And I told her, I said, no, we’ve been doing some antiparasitic on Natalie and they seem like they’re helping. I said, but I was expressing to her, you know, that some kind of strain is still there. I can’t.

And this friend of mine explained, she said, you know, maybe they’re having a hard time coming out. I didn’t really know what that meant. Because I hadn’t had that much time to research coming out.

She goes, you know, coming out, coming out of, you know, in the poop.

So I said, well, she goes, you know, there’s this, this, this woman who I’ve connected with Sue on the computer and she’s from Mexico.

I’m like, I said, I think, I think I know who you’re talking about. I said that to my friend, because I had just again been on Google and I was looking for mineral water, because I felt like, well, maybe this missing piece is maybe Nellie’s not getting enough minerals supplementation.

You know, you’re on the gluten-free diet. You don’t know. You want to make sure that she’s safe.

And I had Google mineral water and up pop Andreas Kalcker video. And I watched these videos. One, this was, this would have been November of 2011.

And I watched these videos around Thanksgiving and I saw this Andreas Kalcker talking and talking. And everything he was saying was making sense to me somehow, even though I didn’t understand the science. It was making logical sense to me, but I didn’t know, can I put, employ that, that technique, that product on someone so sick as this little girl, so sick? I didn’t know.

And I had actually again Googled again on a different evening, sometime around November or early December timeframe of 2011. Mineral water, because I thought, I want to look into that a little bit And Kerri Rivera popped up.

And she was, she had a tropical background. It was a nice, she was pouring and mixing and showing, displaying how to mix this product that Andreas was talking about. I didn’t know that they knew each other necessarily at this point, because I was still learning.

But when my friend at Costco said to me, hey, I know this woman. I said, is she, she has this beautiful face and she’s smiling like this in her video. She goes, yeah.

I said, and she said, Kerri Rivera. I said, yes, that’s who I was talking to, or who I saw in the video.

Anyways, within a week, that friend at Costco got me connected with another friend who had some spare MMS. And I went over to her house and she showed me how to mix the first drops.

And it was July 9th of 2012. And I’ll never forget it, because I’m sorry.

One eighth of a drop. One eighth. She took that afternoon at my friend’s house and we came home.

And I was in the kitchen getting ready to prepare dinner. And Nellie was watching me. She was watching me. Sitting there calmly, calmly sitting and observing me.

And I had never, never witnessed that ever in my life from her. And I knew, I knew from that moment, that moment I saw her, I said this, there’s something to this.

And we found a way to help my daughter finally feel better. I knew.

Anyways, the shock of it all, but delight too at the same time. She went and I had her go jump on the neighbor’s trampoline like she always liked to do. And she jumped.

But it was different. I was watching her from the kitchen, you know, and make sure she was safe and netted trampoline, of course. She stopped jumping.

She was looking around and she looked in the neighbor’s house. She looked up at the birds. She looked down at the grass. And it was different. It was different. Ken, this is just one-eighth of a drop.

Normally, on the trampoline, she would just be constantly bouncing, constantly flapping, looking, you know, never ever ability to focus, not one iota. You know, she could never attend to occupational speech therapy very well, hardly at all, because of that too, you know, in her past.

But yeah, so she came in from the trampoline. I said, Natalie, what are you doing out there?

Because I did see her doing a little bit of what is referred to as tick spitting. She has a little, you know, so I did see that she would kind of spit towards the sunlight, but it wasn’t consuming her, which was amazing.

She came, I said, I said, what are you doing out there? She goes, it’s sensory. She said to me about the spitting. It’s sensory.

Sensory. So what this tells me is she, all those years, and I’m talking with occupational therapists or teachers and trying to explain to people that all that spitting thing is a sensory input thing. She needs that, you know, visual stimming and oral stimming. And it’s a sensory thing.

She’s, you know, she was hearing me all those years. And she told me, it’s sensory, mom. Never had she ever said before. Anyways, more confirmation.

So from there, the story continues, of course, that I employed the MMS protocol of Kerri Rivera’s. I took out all the antioxidants from the DAN protocol. It was basically you’re doing a 180 away from DAN to the Kerri protocol and took some time.

This takes time, especially with a fragile one, as fragile as my Natalie. And we started seeing more, more good reports coming from home.

It’s a little rocky because with someone so sick, you have to move very, very slowly up on the drops. I could only go up, you know, I couldn’t go up as fast as some children could go up.

But I was able to go up and, you know, pretty fast and correlate it with the parasitic protocol and adding those also in slowly.

She started July 9th was the first drop and her ATEC was a 79, I believe it was. And she’s still a work in progress. And it is currently, what is it, May 25th of 2013.

But she hasn’t had a full year because it was such a slow ramping up. She has not had that many parasite full protocol rounds yet. But she’s already at about a 40, I think the last measurement was a 46, I believe, ATEC, somewhere around there.

She is off of antifungal med. Again, she used to take it daily. She is off of antibiotics. Again, she used to take them daily and rotate them because they weren’t working.

She is off of antiviral. She is off of low-dose naltrexin, which is an immune modulator type technique …that is employed by the DAN [protocol]. She’s off of that.

She is… her seizures used to happen grand mal tonic-clonic, which is a very dangerous kind of seizure. They used to happen every two and a half to three weeks. Terribly dangerous.

She has had seizure-free days now. Her largest streak of seizure-free days was 105 days. Then she had a seizure, but we know what it was related to. It was related to a stop in an antiparasitic med that was too fast.

But now she is, again, ramping back up. She’s at seizure-free day 69 right now. And she’s going to continue to go. I feel pretty good about that.

We are lowering her seizure med. We have to go very slow. But the dream is that she will be off that seizure med next too. And then the dream after that is that someday maybe she will be off that immunoglobulin therapy, which would be awesome for her.

So she’s a very complicated case. And being 14 years old and highly compromised in many ways, highly infested. Well, whatever.

She takes a lot of time, but she’s getting there. And so we’re really excited and really hopeful now. We’ve never had this before in our life. Never thought we would ever see her feeling better and coming off of all these medications like this.

So that’s my story, and I’m sorry for crying so much.

The following testimonial is excerpted from pages 425-426 of Healing the Symptoms Known as Autism, 2nd Edition by Kerri Rivera, published in 2014.

The book outlines a protocol in which chlorine dioxide is a key component. More recent editions have since been released with updated information.

A link to the full book in PDF format is provided at the bottom of this page.

Drum roll….

I have been dying to share…

Been off MMS for a few weeks…AND HOLY SMOKES we are ALLLLL GOOD!!!!!!!!!!!!!!!!!

Summary…

My daughter—PANDAS—MAJOR sleep issues—fluctuate between diarrhea and constipation

Me—Acne—horrible—and nail fungus

ALL GONE. ALL.

NOBODY could EVER, ever, ever tell me why I broke out so much esp. with our squeaky clean diet.

First PP, OMG it was REALLY bad—worst ever—and became cystic—painful— so for SURE worse before better in my case BUT believed in protocol and KEPT GOING.

By month 4, GONE and yet to return

Fungus—gone in month 1, never to return

My daughter:

Well, you know, AMAZING!!!!!

YOU, Kerri, YOU helped me figure out FINALLLLLY after a zillion docs, WHY MY KID could NOT SLEEP! EVER! 7 LONG years… long long—exhausting years—and it was PARASITES NO DOUBT in my mind! Month 1 of PP, literally like a light switch, SLEEPING —falling asleep ON HER OWN—(not with a circus routine to “get her to sleep”) AND staying asleep ALL NIGHT LONG! UNREAL! This is HUGE!

AND bye bye PANDAS (Silver/Aloe nipped it, MMS maintained her gains, BEAUTIFULLY!) SO I do believe in our Silver Aloe protocol for PANDAS, 100% worked for us! AND MMS. Both.

AND since OFF MMS, my daughter is 100% pooping NORMAL—OMG first time in her WHOLE LIFE!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! (on MMS it was still fluctuating…) AND she is eating things she would have NEVER ever touched! EVER! Raw veggies, nuts, trying EVERYTHING I make… unreal… this is HUGE too… the “healthier” you get, your tastes DO change… and one becomes less “picky”

I have learned that SOME probiotics can literally throw a child into a PANDAS rage—and also brought back MY symptoms—literally within 12 hours of consuming. (Like “Regarding Caroline” posted) This clearly happened to us. Mental note: NOT all prob’s are appropriate for everyone. We react to fermented food—so I am going to experiment with no prob’s and with THeralac __ONLY THeralac BTW

Now,

We are back to silver/aloe, daily, as prevention

We will still take DE (prevention)

Vit D3

Trace Mineral Drops

Enemas as needed

AND I am going to go BACK to the herbs for 3 months around full moon “just in case”—

I CANNOT WAIT to meet you in person, THANK YOU, and share our story with EVERYONE that will “hear me”.

Again, my daughter did not have ‘autism’ per se, but autoimmune issues, meaning that, perhaps, her treatment protocol is ‘shorter’ then someone who is “more sick’ etc. if that makes sense.

We also did a boat load of work prior to this. Meaning diet in place, for instance, for 4 years already—so healing began. This was the final layer for us. The frosting on the cake!!!!!

I have 2 brand new bottles of MMS in my cabinet 🙂 AND will ALWAYS have it on stock!

With MUCH LOVE and respect to you Kerri. -Jeni, IL, USA

I am a man in my 50’s and a few months ago I thought I had an ingrown hair on my scrotum. Before long I had a grossly swollen, painful, inflamed scrotum. Within a couple of days my chest erupted into a rash.

Within two days this rash reddened into what looked like a large burn and rapidly moved from my sternum all the way to my elbow, including my armpit. The rash produced a scalded appearance and then erupted into sores. The pain and exhaustion were unrelenting and I could not rest. I was racked with pain and malaise.

Soon an itch started on my calf and there began the third location. I tried every topical essential oil that could be beneficial and was losing ground, so I went to my physician. He started me on antibiotics and ordered lab tests.

I went to the lab, they took scrapings and blood samples, and almost three weeks later the state lab reported that I had MRSA staph and an unidentifiable gram-positive bacterial infection that turned out to be strep.

As a side note, I had also been unable to breathe through my nose for many months. It was so occluded that I had to breathe through my mouth, which created shortness of breath when I ate and caused severe sleep apnea. I was already in a state of exhaustion before the infections set in.

I had been fighting a long-term battle with mycoplasmas and would take doxycycline for that, which is the only drug that would keep it in check. I was also plagued with prostate problems and had the resulting urination difficulties.

My doctor prescribed sulfa, cyclines and cillins to be staggered to hit the staph and the strep. Topically I used colloidal silver, essential oils including oregano, tea tree, lavender and chaparral, fresh aloe vera, hydrogen peroxide, goldenseal, slippery elm and lidocaine for the surface pain. Internally I used probiotics, olive leaf, goldenseal, aloe vera juice, digestive enzymes, amino acids, vitamin B’s and other supplements, along with pain medication.

Although I was holding my own, I was not returning to good health. I was becoming depleted, sleepless and fatigued, had chills and what felt like fever. I had to continue to work. The infection seemed to go away, although now I know it was only in remission.

During this remission time I had a muscle spasm in my other leg that caused me to fall, injuring my muscles, ligaments and tendons. The infection invaded the damaged tissue and became another site of infection and I had another 8-9 weeks of severe illness.

Later the outbreak returned on my face, primarily my nose. The second site was chest and armpit and the injured leg became painfully swollen again.

I enlisted the assistance of the QX system of bio-radionics. There was an identification of mycoplasma pneumoniae, MRSA staph and Group A strep erysipelas.

At this time two friends brought MMS to my attention. A friend brought me a bottle and the book. Thoroughly understanding the chemistry, I started taking it immediately. Since I was so seriously ill I did not start gently.

I started with 12-15 drops three times a day.

Results:

Reduction of swelling of the prostate and increased urine flow without pain. Sludge-like material passed in urine.

Complete clearing of nasal and sinus congestion that had plagued me for months. Puffiness in my face around my eyes went away.

Sharp stomach pains and nausea occurred. Despite warnings in the book I did not reduce the drops. I began vomiting on day three. On the third day of vomiting I passed what I believed to be a parasitic infection which took three more days to pass entirely.

The treatment stabilized the sores and swelling and prevented the advancement of the infection.

Edema and inflammation in extremities cleared, including severe leg and back spasms.

I was able to reduce pain medication due to the reduction in inflammation.

The whites of my eyes became extremely white and my vision somewhat improved.

My skin healed and re-formed. The new skin on my nose and face was smooth and healthy.

Inflammation throughout my body reduced significantly and my swollen calf returned to normal by day three.

I stopped taking MMS after two weeks as I was feeling so well. The following week after a minor injury to my thigh the infection appeared again, this time localized to my thigh.

I resumed MMS at 6-10 drops once every 24 hours and gradually increased the frequency to twice per day.

I believe MMS has been helping my immune system tremendously. Although another outbreak occurred, it remained localized instead of spreading as before.

I am recovering and very grateful to Jim Humble and the work he has done.

Rick

The following testimonial is excerpted from page 419 of Healing the Symptoms Known as Autism, 2nd Edition by Kerri Rivera, published in 2014.

The book outlines a protocol in which chlorine dioxide is a key component. More recent editions have since been released with updated information.

A link to the full book in PDF format is provided at the bottom of this page.

So I just redid my daughter’s ATEC. She was a 71 a month and a half ago and is now a 60!!! I thought she was making nice improvements but it really set in when I saw her score.

Some things that have changed for her are now she is pooping on the toilet every day and telling me. She used to just go every few nights in her diaper. There’s no more diarrhea, she’s not constipated, she’s sleeping great.

She is just starting to show signs of imaginative play and a big one for us is that she just learned to blow. She couldn’t blow no matter what we did to try to teach her. Now she’s got it.

Hopefully more good things to come

I have taken MMS for 18 months at 6 drops twice per day. I do not have any mouth ulcers or herpes outbreaks anymore!

I also noticed I sleep much better and breathe much better. Though it has not cured me of my fibromyalgia, it has helped.

I will try the DMSO with MMS1 very soon for several months.

My brother had a bad case of intestinal flu for a week and popped over one day. I said, “Give this MMS a try!”

He took 2 drops and went straight home. He phoned me back 20 minutes later saying all his discomfort had gone somehow.

So he came over for some more just in case, but he never needed any more.

Brian Adams
(UK Bournemouth)

Took MMS for 2 months which got rid of an impossible sinusitis condition that made me feel like I had allergies yet I didn’t test allergic to anything. I had incredible congestion, sinus inflammation causing breathing problems and sleep disturbances FOR 50 YEARS!!. Once or twice I took a bit too much which caused a bit of nausea and diarrhea but I just backed down a bit and no other issues. I’ve had more reactions from eating too many fruit than taking too much MMS. My husband reduced his back pain (he’s had spinal fusion surgery almost 2 decades ago) by about 90% ..he always complained about the pain and never does now.

I have been taking all kinds of medication for schizophrenia, but did not lose my cognitive abilities. After 5 years on such meds all other small issues become life threatening, and tons of complications with my health made search and try anything and it was very hard to do physically. I found MMS and Jim’s videos and site, read his book while waiting for the MMS to arrive. I needed one certain medication to fall asleep and still do need it if I want to sleep for a long time and completely relax and rest, but I hope to find a solution to such insomnia soon. So, I started taking MMS, I knew it would flush out medication that is stuck anywhere in the body along with other pathogens, but I would take MMS during the day and medication late at night before bed. I had plenty of detox reactions, and they were not pleasant but some can be scary, but when you are facing early death like me, MMS cleanses very fast and the amazing relief is experienced shortly after. I took MMS protocols for about 4 month almost no stops and I became alive again, and started to search for more healing methods. I found information that one old doctor left after his death, his name is Dr. Abram Hoffer. I found interviews and webpages, and decided to follow the vitamin regimen he used and developed since like the 70s to treat early cases of schizophrenia with success. Mainly it was a certain type of vitamin Niacin in larger doses along with other vitamins and better diet. By that time I only took MMS as necessary because I figured that taking vitamins has to be first after enough MMS, and I was worried that MMS may destroy some artificial vitamins. I took about 2 weeks on Dr. Hoffer’s vitamin regimen and I started to feel much much better in my mind. So, I continued vitamins in moderate doses and sometimes took a day or two and would take MMS as much as I thought I needed. I continued my search. I knew about Rife Machines, but did not have my own, but I did find a clinic that had professional BICOM Rife Machine. I was treated with that machine before with success about other issues, but they had some frequency programs for schizophrenia and I tried that, but in my case it would work but the mind / brain would rearrange itself back like it was, but bipolar issues were fixed. However, later I got my own Rife Machine, it is called Spooky2. I am not affiliated with Spooky2 rife machine retailers and I am not recommending them, but I believe they offer the best equipment for a relatively low price. I tried many healing programs on that machine and some did have good results, however, rife machines are considered “experimental equipment” and using one is one’s personal responsibility. Eventually I connected an attachment to the Spooky2 machine and did so called BioFeedback Scan and software found the issues in the body, but looks like software does not name what they are, but did let me save the list of frequencies that suppose to heal the found issues, so I ran them on the machine and in few days I noticed some improvement with schizophrenia along with other found issues. BioFeedback I did repeat every 4th day and in a couple weeks things would get even better. And I would have one day of vitamins, one day of MMS, and a third day with Spooky2 treatments because few hours of frequencies may cause discomfort. I would also do bentonite clay detox for intestines due to the fact that plenty of debris gets dumped there during the cleanse. And vitamin Niacin is great for the skin so I noticed that my skin became shedding old layers faster, so I had to get that female skin scrub to cleanse my skin. It has been a year and a half with all these alternative treatments and the only issues I am still trying to resolve is my insomnia. I tried CBD and a few other things like Melatonin, and it did help a little but not a lot and I find CBD to be a very costly solution because I can take a lot without predictable effect, so I still take this one psych pill at bedtime so I could get enough rest at night.