I was diagnosed with multiple sclerosis at age 40. I’ve been taking monoclonal antibody treatments for the past 12 years to prevent relapse. This causes immunomodulation and makes me more susceptible to infections. Over time my health was steadily declining. Walking and other movements were getting more difficult. I had pathologic fatigue that made it difficult to sit in front of a computer for more than an hour or even get out of bed some days. My lower back would fail if I stood too long, causing my body to bend forward. I could only walk around my apartment by holding onto walls and doors. I could no longer walk to the mailbox, drive a car, or handwrite anything.

Last year I caught something due to my compromised immune system. I spent almost a month in bed. I could not get to the bathroom at all and ended up pissing myself more than once. After the illness passed I could hardly function because my muscles were so deconditioned.

My boyfriend bought a product he hoped would help to protect me from getting sick in the future. I didn’t know what it was but took 8 drops daily. A week later I was just standing in the kitchen without dizziness, without swaying – and then I walked around the apartment without touching anything. I was completely blown away. What were those drops? Chlorine dioxide solution.

I saw my neurologist last month. When performing the walk exam (walking up the hallway and back) the doctor noted I was 8 seconds faster this time. Many of my symptoms were improved. Doctor wanted to know what I was taking….if I told him he would fire me as a patient because the FDA says CDS is poison. He will have to remain baffled.

My current protocol is 11 drops a day split into three doses. I intend to modify this over time and try other established protocols for MS. My brain fog and fatigue is almost completely gone now and I can get around with just one cane instead of two. I am still improving with chlorine dioxide.

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.

I started taking MMS drops in 2020 to prevent getting covid or whatever it is. Anyway, at that time I had gout, sciatic nerve pain to the point I couldn’t even cook a meal with that holding on to the drain board to get through the process. I was actually using a walker in the house I live in I almost didn’t buy 4 years earlier because it had a sunken living room and I knew I was going to end up in a wheelchair. Thank goodness a friend was with me that is a construction contractor he told me that I would be able to put a false floor in if I need to use a wheelchair.

I had an MRI done on one of my knees and it came back saying that there was arthritis, a torn and ripped meniscus, a bone spur and I thought that was my good knee. Both of my knees were so swollen that they were square and my feet were swollen as well. When you can’t move because of the pain then you gain weight and I was very overweight.

I took the MMS drops for 3 years straight I did not use any protocol. I just started with like 3 drops and went up to 12 in time and then I went back down to 8. I would activate it put it in a large glass of water and I would just drink it probably within 15 minutes every day. Jim Humble’s book was sold out when I started this. After getting the book, I changed the way I drank it and I would drink it in a 4-Hour period.

Everything I mentioned above has gone away the only exception is if I get up on a ladder I will have sciatic nerve pain. I believe this has cleaned out my body of all kinds of heavy metals, toxins and parasites. I have also lost 74 lb with no dieting. I had a knot from a car wreck on the back of my neck that is almost gone away. I have seen warts and moles disappear I had a knot in my inner thigh from an ingrown hair when I was real young that’s almost completely gone and it was the size of a golf ball. I also think that this dissolved scar tissue if there is such a thing.

One time I got a illness that had my sinuses and lungs all congested. I did one drop of each and put it in a little water and used a nebulizer several times a day for about 5 days and since then my sinuses and lungs have been really clear and it got rid of cough that I had all of the time.

I believe that the heavy metals, toxins and parasites are the main cause of muscle pain and fatigue. Let me tell you why. I bought a 10 speed bike and I rode it 2 1/2 miles a couple of years ago. My legs were shaking so bad by the time I got back that I had to walk the bike 1/10 of a mile to get back home. I didn’t even know if I would be able to walk the next day since I had not rode a bike in over 40 years. The next day not only could I walk but I was not sore at all.

I am 64 years old now and I feel better than I did when I was 35! I have a little 3 acre farm that I take care of honey bees, goats, chickens, sheep and pigs. I have three different garden areas and I manage all of it by myself. I know I’m missing some of the repair that has happened to my body but all I can say is if you have anything wrong with you give this a try because it really is a miracle mineral. Thank you to all that have done the research and put the information out help save people from an agonizing life.

I’ve been working with MMS since 1995 when I had a bad root canal, and I really hadn’t done a proper protocol.

So in 2011 and 2012, I felt I was dying all the time. I couldn’t get out of bed, I couldn’t sit up, and at that time I was driving a taxi cab.

So there was a point where I just decided, well, why don’t I try and do a bath? So I did a 30-drop bath, and I could not get out of the bathtub after the bath because there was so much activation going on.

And after I did a 30-drop bath and then did another two 15-drop applications orally, the whole thing completely resolved in my body.

Yeah, and I’ve had a bad habit of not doing the proper protocols. But now that I’ve finally gotten to a seminar and I finally got taught something about this, I’m going to actually do the protocol.

I have one other situation with one of my roommates, and she’s a double PhD in pharmacology. She has a bad habit of wanting to try and kill herself all the time, even though she’s all about health. She studies everything that’s about healing, but she is a wreck.

So her foot was swelled up, I would say at least this big. She was crying. She was septic.

She had gone to the doctor, and the doctor had given her antibiotics and sent her home. She said, the pain is terrible, I can’t sleep.

So I said, okay Lisa, let’s treat this with MMS. So I did a 30-drop, two gallon hot water foot [bath], actually put it in a five gallon bucket.

We did two of those treatments. After two treatments, her foot was down to swollen a little tiny bit. On the third treatment, it virtually was gone. Then we did one more treatment and she was completely cured.

She had stepped on something and she walks around barefoot outside. She had [red streaks] going up the leg.

Lisa had one other situation. Her head was swelled up this big. She had four impacted teeth. She was lying on the couch crying, red as a beet.

I said, okay, let’s do MMS together. So I said, let’s do 10 drops together. I sat there and did it with her.

Interestingly, her girlfriend came over with a foot bath, and all the pus that was in here came out into the foot bath.

Then she went down to Mexico, had the teeth out, did some more MMS, and she is completely different now. A new woman.

Summary

A retired teacher from Thailand gives an update after a previous 2013 video about using MMS. He says he stopped taking MMS for about two years after feeling better, but later discovered that his melanoma had returned with serious tumors, severe anemia, weight loss, abdominal swelling, and extreme fatigue.

He describes undergoing hernia surgery, later getting a CT scan, discovering a large tumor in his lower intestine plus additional tumors, and then having major surgery to remove the large tumor and part of his intestine. After recovering, he says he resumed MMS and MMS2, later feeling stronger, exercising again, and seeing tumor shrinkage on a follow-up CT scan.

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Transcript

Hello, everybody.

This is another update on my last one. I did another video in, I think it was March of 2013. I’m that teacher from Thailand. I’m no longer a teacher. I’m retired.

But in the interim, I got another… I had another problem with cancer.

I did… last time that you heard from me, I was steadily doing MMS. And because my health got better, and because I had no known symptoms from my tumors, I stopped doing it for about… I did it until about 2014 and I stopped. And I didn’t do it for about two years.

So we’re looking now at the beginning, middle of January… beginning of the year in 2000, middle of the… towards the middle of the year of 2016. Right now it’s 2018. So we’re talking about a year ago, basically. A little more than a year ago.

Anyway, I’m just going to give you a quick update what happened. Because it came back. It came back.

And as I said, I wasn’t doing MMS maintenance dose, and I should have been. I realize that now. And I wasn’t looking after my body and listening to the signs of my body and what was going on. So those are my bads. And so I advise anybody to not make that same mistake.

So here’s what happened. About the middle of 2016, I started getting bad heartburns. Heartburn at night. And I tried different things like peppermint leaves. And, you know, a doctor would give me some antacid stuff. And nothing really worked. I was just still getting them at night.

So I didn’t know what to do. And it wasn’t severe enough where I really wanted to delve in it deeper. I was just looking for like little band-aids. So that went on for about two months.

And in that two months time, so we’re talking maybe around August of 2016, I coughed one time when I had this kind of gas in my stomach from this, you know, heartburn. And I had a severe pain around my groin area. And it turns out that I had a hernia. That cough, which was very painful, caused a hernia.

I didn’t know about any of this at the time. So I went to see a doctor. He looked at me. Boom, he knew right away what it was. So he rushed me in. And they did a blood test. And they said, Oh, well, you’re pretty anemic as well. You’re very low anemia. I said, Well, I don’t know why that is.

So anyway, so he did the operation and successfully they got that hernia taken care of. Now I don’t know if you know this, but hernia is a kind of a painful operation. It takes a while to recover. And consequently, it took me a while to recover.

Now, during this time, I was having it was getting was causing me more tiredness. I was sleeping more during the day. And I thought that was a consequence of the hernia operation.

And I went back to the doctor and he said, Well, you should be getting feeling better by now. So anyway, this is about October now. And I wasn’t feeling any better. And I was still getting gas in my stomach, which was unrelated to the hernia, obviously.

So I went to the anemia lady. She did another anemia test and I had about one third a normal reading I should have for a normal anemia, right? So I was very deficient in red blood cells.

So she suggested that I go and I get I think it’s called colonoscopy, where they stick the tube down there and they take a look at your intestine. I’m not sure what it’s called, but it’s that it’s where they stick the little video camera down in your intestine and make sure there’s nothing wrong with you.

Because a lot of people that have anemia, very high anemia like I had, it turns out it’s a ulcer or something like that in their intestine. And that’s what they’re checking for. They didn’t find anything clean as a whistle.

So back to stage one. So I go and I just for the next month, I keep doing what I’m doing and it keeps getting worse. And then what happens is I start to get this big swelling in my stomach, like a like a beer gut. I’m not a big beer drinker.

And I went to the doctor again, the anemia lady, same lady. And she said, Oh, well, right away, she says, Have you ever had cancer before? I say, Yeah, I had I had cancer. She goes, I think you might have your cancer. I go, Well, I don’t have any other symptoms.

She goes, Well, let’s just check it out. Because, you know, now that I know you have cancer, I think the two are related. Sure enough, she goes in there and has me do a CT scan.

And I do the CT scan. And it’s bad. It turns out that I had a grapefruit size tumor in my lower intestine, which you can see very easily in the CT. And I had a bunch of look like the hanging gardens of Babylon. You know, all the little trees and stuff.

They were like grape size. They were probably about eight or nine, maybe 10 grape size tumors. And they were still kind of small. But there were a lot of them. And I had another tumor.

So once inside my intestine, and I had another one on a vein that was probably about this big.

Now that when I found out about this, I knew that the really big tumor, which is about six, six centimeters at the time, I knew that needed to come out. Okay, I knew it needed to come out.

Now, you’d ask, why not just take MMS and try and get that tumor down? Well, as this tumor was growing, it was starting to grow at a very rapid rate. I was losing at the time that I had this CT scan done. I was losing about a pound a day.

So I went from virtually maybe 180 pounds down to 130 pounds in about a month, maybe, maybe a little longer, right? But I was losing weight at a rapid rate.

And I was also getting all that fluid, like I said, where they pumped out three liters of fluid from my chest, which is giving me the beer gut, three liters of fluid with that lady. So I knew I had some serious problems.

Now apparently that was, she suggested that was a complication from the big tumor. I don’t know. That’s what she said. And I believe it. So anyway, I was in pretty bad shape.

Another side effect, and everybody should be aware of their body, is that I was really tired. Now I was also tired from the anemia, because that’s what anemia is basically, but I was really tired all the time. And that was from the tumor. So really the anemia was caused from the tumor. That’s what I think.

So anyway, so then I thought, well, talk to my wife, and we had to go see a doctor about a surgeon. It turns out that this lady’s husband was an oncologist, and she wanted to have him look at me. But I said, not not having any of that.

Because as I’ve said on my last video, I don’t believe in doing the whole chemo nor radiation. I think they’re a waste of time. But everyone’s got their own opinion, but I wasn’t gonna do it.

So anyway, so I went to see some doctors, and I was blown away because they wouldn’t respond well. They said, oh, no, your anemia level is way too low. We don’t want to do this.

So I got knocked back about two or three times from people just saying, no, your tumor is too big. Your anemia is too bad. We’re not going to operate because we think you’re going to die on the table.

At the meantime, this this oncologist is trying to contact me and say, well, come see me and I will I will help out with the pain. So they’d written me off, basically.

So I couldn’t find a doctor to operate on me. Finally, we went to a local hospital here, and we had some good hospitals, and it was a good local hospital. I found a guy really good doctor who said, yeah, I’ll operate on you.

OK, that’s great. So he saw my CT scans. He knew what he was getting into. And he was OK. He was game.

So OK, let’s go. So this is about November, I guess, maybe early December. And we’re getting all set. And it turns out that he’s got a week conference. So that pushed everything back a week. And this tumor is getting bigger.

I can feel it because my stomach’s getting more extended. And I know it’s getting bigger. And it was big to start with. Like I said, it was the size of a grapefruit to start with.

So my energy level was nil. I was on the ground. I couldn’t because I lost so much weight. I couldn’t really sit in a chair because my my backbone would would hurt so much because I was sitting on my ass bone. Right.

And when you lose all this weight, it you’re right on your spine and you can’t really sit for long. So I had to lie down. So consequently, I was lying down every every 20 minutes, every half hour, basically falling asleep because my energy level was flat.

So I knew at the time I had maybe two or three weeks to live. I’m positive. That’s my gut level. I’m really sure that that’s what would happen. Now, this was confirmed after the operation, but that I’ll get to that.

So anyway, we get we’re at the hospital. We’re getting everything set up. I’m going to be going into the operating room in 20 minutes. And, you know, when you’re getting ready to go on operation and it’s a life threatening operation, you kind of get psyched out.

And I didn’t know whether that’s going to die on the table or not. You know, I was really kind of upset about it. But what can you do?

And then so I psyched myself up. I’m getting ready for this operation. The doctor comes in and he says, we can’t do the operation.

I said, what do you mean you can’t do the operation? He says, well, the anesthesia, anesthesia, whatever the person does, the noxia out anesthesia, I think it’s called.

She has decided that you’re too. It’s too risky. She’s the only one. She’s not going to do it. Not until we can bring up my iron levels.

So anyway, then I had to go and get some pints of blood. So she stuck three pints of blood in me and it brought the levels up a little bit. But anyway, I guess not enough for the anesthesiologist.

So anyway, I said, listen, I’m either going to die on the table or I’m going to die from this tumor because I just knew in my gut. Literally in my gut.

So anyway, so like I said, it was in the lower part of my abdomen and in the intestine. So anyway, finally had to sign a lot of papers and and they said, OK, you’re cleared.

So they rushed me up to the operating room and they did a really long operation and they pulled what looks like just a massive blood and fat out of my intestine and they cut out a foot.

So I lost if I I’m operating on a foot less intestine than most of you, which doesn’t really have an effect. I guess maybe I got to eat more, a little more food to get the nutrients. I don’t know. But it’s to me, I don’t really notice any effect.

So I have a little bit less intestine. So it was a major operation.

I went through eight pints of blood during the operation and I woke up in ICU with a bunch of tubes down my throat breathing for me. You know, the ventilators, which was the worst experience I’ve ever had in my life, actually.

But after about two hours in ICU, I could breathe. They let me breathe again on my own. I got a big scar from where they pulled the tumor out.

And then after six days, I came home from the hospital. OK, after I could prove to them that I could walk for, you know, 20 feet or whatever.

So anyway, I came home and that was a huge bonus. And I went straight into the MMS, straight into it because I knew that’s what allowed the tumor to build over those two years. Maybe I have a bad DNA. I’m not sure what it is, but I got it again.

OK, and I knew I put all my faith in MMS because I didn’t know anything else. I knew chemo wasn’t going to work. I knew radiation wasn’t going to work. I knew I wouldn’t be here now. And I said it’s just all or nothing.

So I’ve been just in this past week was the year anniversary of basically doing MMS that whole time. And I do my protocol right now is probably I do eight drops at a time, maybe six, seven times a day.

So I’m getting in maybe eight sixes or what? 48. Yeah, maybe 50 drops per day of MMS. I’m doing MMS2 as well. OK, the calcium hypochlorite, I think that’s called. I’m doing that as well.

So that’s my protocol. And I’m doing great. I’m doing great now. OK, like I said, I was very close, but I’m doing fine now. I don’t know. I guess I look healthy. I don’t know my colors back.

I’m riding a stationary bike. I’m doing today. I did 10K. So I do that three times a week. And I’m just eating normal. I haven’t changed my diet at all. I eat pretty well.

I don’t eat a lot of junk food. We eat a lot of rice. That’s probably the worst thing we eat. But I’m feeling good.

I got a little bit of a cold now, which I’m surprised because usually when you do MMS, you don’t get a cold. But I got a little bit of a head cold, but nothing major. A little phlegm, which I’m probably going to do the gas method to get rid of.

But other than that, I feel good. Real good.

So that’s kind of my message. My message to you is don’t let something carry on long enough before you get a CT. Because CT scan, or maybe even a PET scan, pretty much tells it all. They’re pretty good tests.

And I kind of got fooled, like I said early on, because of the hernia operation. And that threw me back. And I thought that’s why I had the anemia, blah, blah, blah.

So that was my screw up. Hopefully you won’t screw up. Just follow your body. If you start to get really tired and things like that, go see somebody that’s going to give a CT exam. Or I don’t know if an MRI would work. I know a PET scan would tell you as well.

I’ve had blood tests at hospitals and I’ve had where it showed negative, no cancer. But it turned out I ended up having a tumor in my lung. That’s from the last story. So I don’t really rely on a blood test.

I think CT scan, they can see it. Now, you probably ask, well, don’t you have those tumors still inside you?

Well, I did a CT exam about four months after my operation. And the doctor looked at it and said, yeah, you’ve maybe lost about 30 percent of your old tumors.

Now, you still have the one on the vein, which was one of the tumors. It was pretty big. That shrunk, once again, about 30 percent.

So they’re not all gone. But they’re definitely a lot better than before.

So do I still have some tumors in my body? Yeah, I probably do. But I don’t think they’re very big. And I might not even have some tumors. I don’t know. I haven’t had a test for a while because I don’t have insurance right now. So it can be expensive due to CT tests.

But I’m judging by my health. Can I pedal a bike at double my heart rate for 30 minutes without any issue? Yeah.

Am I feeling good? Am I eating good? Am I sleeping well? All these positive health effects I’m finding are what I’m experiencing now. So I think I’m pretty good.

I’ll get a test in a while. I was going to do it for a year, you know, after a year of being on MMS. But I just haven’t gotten around to it because honestly, even if I don’t have any tumors in there, I’m going to keep doing MMS because I’m scared.

I’m scared that the cancer is going to come back. This was the third time I had this cancer. Melanoma. And I’m scared it’s going to come back.

So I don’t really care. I’m just going to keep doing MMS no matter what. So it really doesn’t matter if I do another test and I have little tumors in there. I’m not going to change what I’m doing. I’m going to keep doing MMS.

Now, the only other thing I would suggest that I would do, at least from my research, is if I could ever get a hold of it, I’d probably do some cannabis oil too. But that’s another subject.

If you’re going to do MMS, don’t make the mistake of stopping completely. That’s what I did. I thought I was over it. Obviously, I wasn’t.

And I think once a day, three drops or something like that, or maybe it’s three times a week. I’m not sure what exactly the protocol is.

You know, I wish I had did that because I think probably it wouldn’t have gotten a handle on me again, this cancer. But it did. I had those experiences. They’re not good experiences. But I survived it. And here I am.

So, just as an aside, what I do is I do the eight drops. I hold my nose. I drink it. And then I still am holding my nose. I drink just a little bit of chocolate milk.

And I find that if I swirl that chocolate milk in my mouth, it completely gets rid of the taste.

Now, you might ask, well, what are you using? Are you using citric acid? Are you using hydrochloric acid? I’m using the 4% hydrochloric acid.

So, yeah, there is still some taste when you do that protocol. But I find that the chocolate milk is just amazing the way it gets rid of the taste. And I haven’t had any real issues on that front. Not at all.

The general feeling I wanted them to get out of that is that, check your body. I didn’t do that. I mistakenly thought it was from my anemia and my tiredness. It was from my operation. That’s where I screwed up, from my hernia operation.

I wasn’t listening to my body. I didn’t get a checkup. I just assumed. And you know what happens when you assume stuff, okay?

Am I still sold on MMS? Absolutely. Am I going to keep doing it probably until the rest of my life? I’m 59 years old now.

When I have good experiences through doing MMS, which I’ve had lots of, I want to share these with other people. And what I find is that they’re very optimistic when they talk to you.

And they say, oh, well, you know, you cured cancer with it. And I say, yeah. And they say, yeah. You know, how did you do that? Blah, blah, blah. I tell them the whole story. And they’re very psyched.

Now then they go home and they get on the Internet. And then they come across these articles that say, MMS is bleach or MMS is going to kill you and blah, blah, blah. And they end up not taking it for whatever reason.

And that’s fine. That’s their choice. It’s always their choice. But I’ve found if they’re pretty religious about how they take it and they take it in the proper dosage, in the proper timing, we’ve had people from having, you know, stage two diabetes to people that have had all kinds of stuff wrong with them.

And it, you know, headaches. My wife was getting headaches regularly. She did the MMS protocol. Boom, headaches gone.

And there’s been lots of other experiences like this. Someone had really bad… Lady in Perth, Australia had really bad liver failure. And she started doing MMS and her liver test just went through the roof as far as being positive.

So if you do it correctly and if you, you know, you don’t have to be exact, exact. But if you do it close, you know, like every hour to every hour and a half, something like that, you should find good results.

But when they start getting on the Internet and believing everything they read, well, that’s another story because then they just don’t want to know about it.

So ask people to be informed. Don’t believe the first thing they read when they get on the Internet. Have them look at some of the videos and there have been some good ones.

There’s a lot of people. This is a big grassroots project. And there’s a lot of people being helped by this stuff. And, you know, you can’t… there’s just so many ways it’s helping people. I can’t even name a fraction of them.

But try it. Try it.

Because when I… Well, my experience with allopathic medicine is that they want to get you under the knife, radiated and chemoed as quick as possible when they find cancer in you.

And as I said in the last video thing we did, if you do that, that quick, without doing any research, I don’t think you got a lot of chance. I don’t think the odds are good doing the chemo and the radiation.

Just check it out. Other things. Try other things. You usually have a lot more time than you think. They’re going to tell you, the doctors are going to tell you, you got to do this yesterday.

That’s what they’re going to tell you. You got to go upstairs right now and get some chemo in you or radiation or whatever. I mean, it’s like leading cattle to a slaughter. It really is.

And part of my advice is, you usually got a little more time than you think. Research it. Check it out. Try different things. There’s lots of alternatives. MMS is one that I think works well. But you might want to try something else.

I have a friend, now in her 40’s, who in highschool always had bad bronchitis. She and I went separate ways for many years and in the last 3 years we began talking again.  Turned out she had been suffering from asthma (puffer 8 times an hour), chronic back pain, extreme fatigue, and sinusitis.

I explained MMS to her and left it in her hands to take action. 3 months passed. In speaking with her again, her asthma had progressed to the strongest medication and medical dr’s said the next step was an oxygen tank. I asked what was holding her back from trying MMS. A chemist ‘friend’ told her it was a form of bleach and to stay away from it. I almost fell off my chair!  Staying calm I re-explained MMS and once again left it to her and prayed for her life.

Two weeks later she called and said she had received an order of MMS and could I help her.  On the phone with her I walked her through taking 1 drop of activated MMS in a glass of water.  She felt slightly nauseated but ok. I encouraged her to take 1 drop every hour and I would check with her later. Three hours later I talked with her again.  She was very excited to report she hadn’t used her puffer more than once an hour and her ability to taste was returning. The next day I called again to find out she had been raking leaves for 2 hours, cleaned the main floor of her house, and could jog the stairs without being out of breath!

She continued the 1 drop an hour for a few days and increased to 2 and 3 drops gradually. She is now on maintenance and tells everyone I saved her life. She no longer uses a puffer, can smell and taste everything, and can participate in her 3 sons life once again.  Thank you, Jim for sharing the information about MMS and saving my friends’ life.

Dear Jim,

I just had to tell the World… I was suffering from coronary artery disease since 1996 after having 2 heart attacks – 6 months apart. Doctors were offering a partial bypass surgery but I wasn’t satisfied with opening my chest just to partially and temporary fix my heart so I was looking into all sorts of unconventional procedures and treatments.

I had Chelation Therapy; Chelation Therapy with Plaquex (that actually made things allot better); Oral Chelation from several places; ongoing vitamins and minerals, CQ10, lots of garlic, Straus Drops etc. Nothing actually did more then make me feel a touch better and I still had to take my medication and my Nitro Patch daily.

Just recently I came across your MMS solution. I was fixing a computer for some old guy and he mentioned MMS. We got talking and he gave me a bottle of MMS and a bottle of Citrus and I promised I would give it a try. And I am so happy that I did.

I have to say, I may be a little premature in saying certain things but the way I feel I just couldn’t keep it locked inside any more. I was scared, to be honest, so I started very carefully with just a drop every hour but not more then 8 times a day. Then I started to take 2 drops every 2 hours again up to 8 drops. I was about to start taking more (after 2 weeks) when a started to feel exceptionally better.

You have to understand, I was living with a daily dose of Angina Pains for years. I would go to bed at night and first had to wait for my heart to calm down enough not to echo inside my ears and to slow down so that I can fall a sleep. I could not walk more then a block and a half without having to stop and wait for pain to go away…

But now, after just 2 weeks, I started to feel totally different. I was not having any pain. At first I couldn’t believe it but then I started to test myself. I would walk faster and further – nothing. I would walk up stairs – nothing. I would then run upstairs and NOTHING! No pain.

I knew I needed to get into shape because I was loosing my breath but there was no pain. There was only a great feeling of happiness for feeling like I use to when I was younger…

I know that MMS did this. There is nothing else that could have been making this turnaround in my health. I want to tell everyone. I want to tell people and I wish someone could show me the best way to do that in a way that people would believe me and not think that I am just trying to sell them something.

In any way, I thank the person whom computer I fixed and who gave me the Miracle Solution and I thank you Jim for coming up with this brilliant solution and for giving it to the World unselfishly.

Neb Radojkovic

I have over the last 8 months removed Aluminium 97.739 mcg/l., Barium 205 mcg/l., Beryllium 0.225 mcg/l., Cadmium 0.225 mcg/l., Lead 37.21 mcg/l., Mercury 35.237 mcg/l., Nickel 11.112 mcg/l., Palladium 6.002 mcg/l., Platinum 4.157 mcg/l., Silver 60.227 mcg/l., Tantalum 0.54 mcg/l., Thallium 0.104 mcg/l., and Tin 10.737 mcg/l.

It was a saliva test. Aluminium and barium don’t belong in the make up of what was in my mouth, 6 gold plates of which no gold is present, 4 amalgam fillings, Tantalum also doesn’t belong there, it’s only found in mobile phones, computers, and flat screen TVs.

I can take you through every aspect of what it does to your body, in conjunction with what you put in your mouth will determine the effects and how long it takes to turn you into a candidate for the asylum.

10 yrs in the hands of the experts and told I was unstable (and I was, I was a danger to myself and everyone around me), given the tag of PTSD/combat stress, diagnosed with a multitude of illnesses. So where have all the nightmares and the rest gone? MMS has blown them away.

It hasn’t just been MMS. I have got a procedure that will clean out the body, then it has to be built up from cell and mineral level. I now have 10 previous sufferers at different stages of recovery. They cannot change what’s already on our medical records. I want them to explain what magic wand has started to reverse the lot.

Learn what MMS is, how it works, but most importantly make decisions for yourself. This can only be done by having the information required.

My eyes have kept me alive throughout many different crazy situations. One look into Jim Humble’s eyes gave me all the answers I needed. You have got no problems with MMS harming you. Take it for a few weeks. Life will change. All it is doing is removing the combinations that are destroying the human body, the mind and memory problems which are a symptom of a body that is slowly disintegrating from the inside out.

22 yrs of military, lead from weapons, mercury from amalgam fillings and as a leaving present, 6 gold plates put in 10 months before leaving but there is no gold. They consist of 7 different metals.

I became a plumber, heating engineer and gas fitter. That knowledge has saved my life, also nearly cost me it. The system ensures tests are inadequate. I had to play them at their own game to get answers. Combat stress, doctors and dentists all denied this was happening but they could diagnose PTSD.

Even now the metals are visible throughout my whole body. The difference is they are out of my main organs and I am in control. NO HELP FOR HEROES should be the slogan.

It cost a few thousand pounds to get tests done (Germany). I had to sell what I had to get answers. Even now when I put the results down in front of the doctor he never gave them a second glance, but hey they said I was mentally ill.

I will go into roleplay to trigger actions. When a doctor wants to take blood to test for lead after giving him the results, when I pointed out that it will not be found in my blood and his answer was “well where is it?”, he had to be told that he was a threat to my life.

After surviving 22 yrs infantry I find that the most dangerous people I have ever met are the ones who are supposed to help.

PTSD = HEAVY METAL and CHEMICAL POISONING.

People are looking for what is there, the most important factor is what and how your internal workings are slowly destroyed. As time goes on what you put in your mouth completes the combinations required.

No problems (for permission to use this testimonial), my experiences and knowledge gained are all personal. MMS is just part of what has had to be done to get me to this stage. MMS 2 has been used also, the results phenomenal.

Only after or during me carrying out medical experiments on myself and monitoring every reaction, observing carefully what is departing my body and by which method I was then able to work out the causes, and the process of all illness.

There has been no help from anyone. In fact, doctors, veterans agencies etc. all closed the doors when I mentioned mercury.

My body is now 9 stone soaking wet, 2 stone muscle tissue eaten away.

What I really need is someone to take the words from my mouth and put them in an order people can understand. There is so much more that happens inside.

The key things that happen are that metals keep you acidic. This feeds Candida. Candida eats cells destroyed by acid. The immune system uses calcium from bones to balance pH, this is deposited internally in most organs and pipes, causing blood to thicken and a lack of oxygen.

Calcium in this state is as toxic as lead. Once in this condition, anything that goes in with a pH of less than 7.365 requires to be alkalised and the immune system uses anything at hand. Behaviour etc. is a manifestation of this process.

June 6 … an update

The confirmation of the ability of MMS1 came when after getting a 2nd test done after a chelation drip and the strongest chelation method available, on receiving my results my doctor called to enquire the name of the substance I had been using other than what he had prescribed.

What he did not know was that I only used MMS for 3 wks and none of the chelation prescription.

Mercury was down from 37 mcg/l to 1.75 mcg/l and the rest were gone or way down.

Thanks to MMS 2, lead buried deep in my hips, knees and big toe was removed and injuries that have been there for years have gone, bent knuckles are now straight, joints are pain free.

I went at it with the view that I have nothing to lose. The medical system wasn’t helping and it can do no harm. My body knows exactly what it is doing.

MMS is the cleaner.