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

Transcript:

My name is Maggie.

My son Gunnar was diagnosed with autism last January. He was four years old. He was born in 2008. Normal pregnancy.

He was born when he had the shakes. And his eyes were darting everywhere. And they were a little bit concerned by the medical staff. They did some testing. And of course they gave him the Hep B vaccine without my consent. Or my husband’s consent, without even telling us.

We brought him home when he was three days old. We got a phone call from the hospital saying he had hypothyroidism. Congenital hypothyroidism. And we needed to start him immediately on Synthroid, on synthetic thyroid medication.

So he was breastfed. But we did have to crush a pill into some formula to give him once a day.

So he was developing normally. We were happy. We wanted him. We willed him to be a boy. He was our beautiful boy.

He was… I’m going to cry… three years old. And I noticed that he wasn’t asking a lot of questions. He wasn’t asking why. He didn’t seem very interested in the world around him. He started to stare off out the window. Hard to get his attention.

I went to his endocrinologist. My husband and I voiced our concerns. And they blew us off. They said, oh, the medication fluctuation, dosage fluctuations cause side effects of fatigue.

Time went on and other caregivers, in-laws, parents, noticed that he was looking out of the corner of his eye a lot. Very picky about foods. Started having some sensory issues.

I took him to the endocrinologist again. And I said, I want an evaluation. And she said, oh, he’s fine. You know, boys are hard to potty train. I said, but he was potty training. And now he’s wetting himself and doesn’t even notice that he soiled himself. This something is not right.

And she had got a page and left the room. And there was a resident in there. And I said, I want an evaluation. So she pulled up a milestones chart and said, is he doing this? I said, he was. He’s not anymore. Is he doing this? No, he never did that. Is he doing this? No, he never did that.

And she went down the list and then she said, Gunnar, can you stand on one foot? And he didn’t even turn. She said, Gunnar, Gunnar, Gunnar. And he didn’t even notice. And she said, I agree with you. He needs an evaluation.

So, it took six months to get the evaluation. They’re so, so very far backed up. It was, and that apparently after talking to other parents, that was pretty quick in comparison. But I kept calling and pushing and pushing to get the evaluation.

So, finally had it in January. He was four years old. And then they didn’t give us a diagnosis that day. They said that they would send it to us in the mail when they concurred with each other.

So, they told us he had autism. So, they wanted us to come back in February for some more in-depth testing.

So, that testing, we had changed diet. We had switched to gluten, dairy, soy-free diet almost immediately after his diagnosis. And we almost immediately saw good things. And his digestive issues were getting better.

And he was waking up in the middle of the night screaming in the fetal position and couldn’t tell us what was wrong. If I touched him, he’d scream, ow! Music was on quietly and he’d cover his ears and turn it down. And he just was uncomfortable in his own skin. He didn’t want to be held. He didn’t want to be rocked. He didn’t want to be sang to. He wasn’t interested in books.

His speech was, want juice, want juice. He wasn’t speaking in sentences.

So, we had him tested and his speech and language was at a 23-month-old level. He was four years old. His gross and fine motor skills are around 26-27 months.

And so, I just went into hyper-research mode. I read everything I could get my hands on. I was up all night, all my free time. I was consumed with, I’m bound to determine to heal my child.

You know, I went into the whole acceptance thing at first because I felt like I was maybe doing a disservice to him. I wanted to change anything about him. I just wanted to get him healthy.

So, I stumbled upon the CD (MMS) protocol and I started watching and started taking notes. And this makes sense to me.

Had some food allergy panels ran, did a comprehensive stool analysis. Actually, both my kids, my neurotypical daughter and my son, and they both tested highly intolerant to gluten, dairy, and soy, among some other things. They both have leaky gut. My son has bacterial dysbiosis, which is leaky gut caused by bacterial overgrowth. And my daughter’s was yeast. She had overgrowth of Candida.

So, the whole family went on the diet. I have hypothyroidism. I had a giant goiter. Within ten days, my goiter was gone.

I decided that this was going to work for us. I just knew it. I just knew in my gut that this was right. I ordered the book. The book came in. And my son was obsessed with the book. My son, who never was interested in books. And our living room is full of books. And his bedroom is full of books. And sister’s bedroom is full of books. And he never wanted to sit down and read a book.

And this came in the mail. And he was obsessed. This book is it. This book is it. Which was the longest sentence he had really said at that point. And my husband and I looked at each other and our eyes filled with tears. And we were like, yeah buddy, this is it. And we just knew.

We just knew in our gut that this was the answer for us. And so, I started with my son.

I did the protocol complete for four months for myself. I saw a lot of improvements in my own health concerns. I had adrenal fatigue and all sorts of things going on. I feel great now.

My son had immediate improvements. He started sleeping through the night. Seven weeks in, he no longer needed his thyroid medication he had been on since he was three days old. Still doesn’t need it to this day.

Started sleeping through the night. Digesting food normally. Eating normally. The sensory issues disappeared. You know, he is affectionate. He is happy. He is healthy.

Sorry. It is just incredible. It is incredible.

Everybody notices how great he is doing. He is just reading books. He is going to mainstream preschool. He is getting ready to go to kindergarten next year.

His ATEC when we started June 23rd last year was an 80 and it is currently at a 5. And there are things that I believe the ATEC doesn’t show. Improvements such as he is asking why questions. He wants an explanation. He wants to play games. He initiates conversation. He jokes.

He is sneaky like a five-year-old should be when he wants something and he bargains. And if I ask him a question, if he doesn’t know it, he says, I don’t know. And then he gives his best explanation. He is healthy. I mean, he is doing incredibly, incredibly well.

I have talked to so many parents that have tried every intervention under the sun and spent beaucoup dollars. And they are not seeing a tenth of the improvement that we have seen in our son. And he is just a little walking miracle and nobody can limit his potential.

He has got a full childhood now. He has got a full life ahead of him. And I am really excited to see what he does with his life. He is really intelligent. He has got a photographic memory. He can memorize things very quickly.

The scripting has slowed. A lot of his speech for a while seemed a little robotic. And now we are getting more and more natural speech. And it is just incredible.

I love helping other parents. This community of parents is just amazing. They are a family. Everybody cheers each other on. Everybody wants each other’s child to improve. Nobody is selling anything. Nobody is trying to make money. Everybody is just trying to heal their children. And we are doing it. And we are all doing it.

It is just absolutely incredible. It is incredible to be a part of. And I am just honored. Very honored to be a part of it.

The following testimonial is excerpted from page 436 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.

My son Nick started MMS just after his 7th birthday. Within 6 months he had cut his ATEC score in half from 66 to 37. Nick showed speech gains from the very first drop of MMS after having made no changes in speech for two years. Really, Nick hadn’t made any improvements at all for two years. He was in a total stall until we began MMS.

We raised Nick’s oral dose of MMS very slowly taking two months to get to his target dose and never experienced die off that was unreasonable.

Three significant changes are obvious in Nick’s health at this point; he has been off of his Mitochondrial cocktail (for several years he has had blood labs pointing towards Mito dysfunction) for over 8 months and we haven’t seen any of the lethargy that used to concern us so much, he was able to wean off of his seizure medication for his absence seizures and we haven’t seen any return of seizure activity, and his thyroid appears to be beginning to shift from his long standing diagnosis of hypothyroid.

The nicest changes we see are in the vibrancy of his health and how happy he is! His eyes sparkle and he has lots of energy for the day. He is no longer sitting on the couch staring out the window waiting for someone to figure out how to help him feel better.

Since beginning MMS, every day Nick shows us just a little bit more of the boy that he is underneath the veil of autism and sickness. He tells us what his favorite things are, what he wants to do, and his sense of humor is coming shining through. MMS has given me a ton of hope that we just might get our boy back!

60 year old female with Long Covid for 2 years. Symptoms – fatigue, brain fog, insomnia, weight loss, neuropathy, autoimmune disorders, hypothyroidism, hormonal imbalance, loss of sex drive. Mast Cell Activation Disorder, chronic Lyme disease, mold issues (CIRS). Unable to tolerate dairy and gluten and many other foods.

I was not helped by 2 years of functional medicine physician including ivermectin and low dose naltrexone.

I started CDS, protocol C and rectal CDS. Within a week I noticed I wasn’t so sensitive to environment exposures such as odors and mold which used to give me a headache and dizziness, no longer bothered me. I tried eating dairy and gluten, no problem! I was amazed!

I am gaining weight and sleeping well again. I am now following Dr. Kalacher’s parasite protocol and am passing small worms in the toilet. I will continue CDS and am trying to get my family members to try and heal their chronic diseases. A Miracle!

Hello,

I am writing to share a testimony from a dear friend of mine, which I believe is quite significant. Along with this message, I am enclosing the relevant blood test results for your review.

My friend has successfully managed to lower her glucose levels, which relate to sugar-diabetes, from an initial value of 124 down to a much healthier 94.

Additionally, her TSH levels, which pertain to thyroid function, have decreased from 7.141 to 2.626. To provide some context, the reference values for glucose range from 60 to 100, while the acceptable range for TSH is between 0.50 and 4.

The initial blood tests were conducted on January 2, 2020, and after following the CDS Protocol C this summer, the follow-up tests were carried out on August 10, 2020.

This improvement in her health markers is attributed to the protocol she undertook.

Warm regards,
Oscar Sanchez

Good Afternoon,

My name is Verónica, and I would like to share my experience with thyroid health that may resonate with you.

Twelve years ago, I was diagnosed with hypothyroidism at the age of 23. For many years, I relied on Levothyroxine to manage my condition, taking a dosage of 125 mcg daily. However, in July 2013, I made a significant decision to stop this medication and explore alternative methods for improving my health.

In November of that year, I underwent a TSH analysis, which revealed a level of 10.79 uU/ml—indicative of my hypothyroid state. Determined to regain control over my health, I began a new protocol, consuming MMS (Protocol 1000).

I was amazed by the results. Just one month later, I had another TSH analysis, and my levels had decreased significantly to 6.15 uU/ml. This marked a turning point in my journey towards better health.

I have attached my studies for your reference. If you have any questions or would like more details about my experience, feel free to reach out.

Thank you for taking the time to read my story.

Warm regards,

Verónica

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I have been taking it for a month after almost two months of flu here in Mexico.

I am immune compromised with neutropenia, Lyme disease and hypothyroidism.

Now the corona virus is coming. So far I am doing well, starting to feel more energy. Would love to know more since I am high risk and lucky to be here. Thank you