Transcript:

Hello, my name is Kenneth Bingham and this is my mother, Phyllis Bingham. I want to take a few minutes to talk about what MMS has done for her.

I had an upper respiratory infection that was almost like pneumonia or the worst flu that anyone could ever have. I couldn’t breathe. My head was so full of congestion I couldn’t even blow my nose, nothing would come down. I was in bed for two weeks with this same ailment.

So he said, well I’ve got something that will help you if you’ll take it. I told him I’ll take anything because I was feeling at that point that there was no help for me.

So my daughter went over and he made up the solution for me to take the MMS and the carrier. He told me how to take it. I was to take one drop of each in a glass, swirl it around until it began to change colors to like an amber color, about 30 seconds, then add water, about four ounces, and then drink it.

When I first drank it, the smell is one of the things that kind of threw me back a bit, so I just held my breath and drank it straight down. Then I went to bed.

The next day the congestion began to loosen up. I was able to blow my nose. I used about four boxes of tissues. The coughing ceased and I just took the regime like he told me, every hour.

Within one night of taking MMS, after about four hours before going to bed, the next day I felt almost 60% better.

Then I started the daily regime, taking two drops every hour for eight hours. I’m still on the same two drops and will probably increase it next week.

Yes, I’m still taking MMS. It’s right here in my kitchen by the sink where I can grab my glass and water.

It works, and I do not take chemical medicine. It worked for me.

It definitely works for infections, flus, and colds because that’s what I had, an upper respiratory infection. It even helped my post-nasal drip that I used to have every morning. I don’t even have that now.

I’m going to continue taking MMS.

Transcript:

I’m here in Calgary, Alberta, Canada, with Pedro. Pedro Acuna.

So I was 35 years old when I actually got the flu vaccine, and I was also traveling. So I got the required vaccinations when you travel to another country, yellow fever, Chagas, three different vaccinations.

Until then, I would say that I had pretty good health. Sometimes I got a cold, but nothing that really made me feel sick.

Probably between three to six months later, I started developing the first symptom of psoriasis. My arm, my shoulder, my hip, all on the right side.

Every time it started getting worse and worse. I didn’t know what it was, so I went to the doctor. After two or three months, I was diagnosed with psoriasis.

I started getting all kinds of creams. I started cortisone. Nothing helped me, and the psoriasis kept coming back continually. So I was one week fine, another week really bad, but every time it kept getting worse.

Then I started developing a sinus infection. The symptoms were really slow at first, two or three days, then a week. Then there was a moment when I was really sick. I couldn’t work anymore.

I remember being in my house for a week in bed with a lot of pain. Every time I coughed, I felt like my eyes were going to explode.

So the infection was really, really bad. That was the moment I started taking pharmaceutical drugs to deal with it. It helped me for one month, but then it came back, and every time it came back, it came back stronger.

So I needed more and more antibiotics. I was in that situation for two to three years.

My psoriasis was treated with drugs, and the sinusitis as well. Then I moved to Canada because I thought maybe healthcare would be more advanced. But it was the same solution, more drugs, just dealing with the symptoms.

The psoriasis and sinusitis kept getting worse and worse.

Until one day I needed to replace my prescription. I went to the doctor, and that day the doctor treated me really badly. I felt humiliated.

And I said, this is enough. I’ve been in pain all these years, worse and worse, no solution.

That day I left the clinic and said, I will find a solution by myself.

At that moment I was working in a research department in an IT company, so I had time to do research. I started researching many different sources, and one of them was Jim Humble talking about MMS.

For about a year, I read everything on the internet about MMS. I read so much that I knew every article that was available at that time.

Then I decided to contact Jim Humble to verify that it was real. He answered my email, and I arranged to meet him in Mexico, in Puerto Vallarta.

I traveled there, learned about MMS, and started doing my own protocol. At that time, we didn’t have the protocols that exist today.

I did my own protocol. I had a strong Herxheimer reaction, but after each reaction I started feeling stronger and better.

The symptoms started disappearing. At the same time, I was also researching diet, so I completely changed my diet.

In a period of six to eight months, I completely cleaned my body. The sinusitis was gone, psoriasis was gone, and they never came back again.

Today my skin is completely clean. No itch in my sinuses.

I also noticed more energy. I wake up every morning at five a.m. with a lot of energy. I feel like I slept until ten a.m. because of the energy I have.

I believe this is because I continuously use MMS to maintain my health.

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.

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.

Transcript (Edited for clarity):

We are in Vilcabamba, Ecuador, with Gurpal from Canada. He came down for the seminar and wanted to share his testimony.

I had a condition called pinguecula. It is a chronic condition where a small growth forms on the eye, and my eyes were always red. People constantly asked if I was smoking weed.

I wasn’t able to play sports, and I had to quit several jobs because of my eyes. I was told I would have this condition for the rest of my life, so I started looking for answers on my own.

I began reading many books, contacting authors, and trying different therapies until I found something that worked.

I first tried hydrogen peroxide, but it was too oxidizing for my body and was hard on my digestive system. Then I came across MMS. I followed the protocols and began seeing similar benefits without the negative effects on my system.

I also used it on my eyes, which I could not do with hydrogen peroxide. I continued with MMS, and I have not had any symptoms since. It has now been about five years.

People who knew me before, and knew I had to quit jobs because of my eyes, noticed the change and asked what I had done.

I have since shared MMS with others. The key is to stay consistent, use the correct product, and follow the protocol properly.

This experience changed my mindset and gave me a sense of control over my own health.

Transcript:

Hi, I’m Bishop Jan here with the Genesis II Church of Health and Healing. And I’m here in Ecuador with Sabina, and we’re talking about Sabina’s use of MMS.

Sabina, you were using MMS about a year ago, is that true?

I think it was a year ago. I remember we met on the bus. And I had bad weeks, or I think months, with infections on my leg and on my hand, with pus. I didn’t know what it was and how to react.

And then at the end I had diarrhea for a long time, I don’t know, many weeks. And I took antibiotics and it didn’t work.

So I met Jan on the bus and she told me about MMS. And I’ve heard about it, but I never really knew anything about it. And I thought, okay, let’s try it.

We met. I came to her office and we started. And that took three or four weeks. I took… I don’t know how much. How much did I take?

Well, I think we started you out with the starting protocol. So that’s a really nice, gentle way. So anybody that’s taken MMS in the past and remembers, you know, some kind of harsher protocols, it’s very easy to take now and it’s very smooth.

So we started her out on the starting protocol. And I don’t know, we were talking, I don’t know if you remember, but what I remember about your case was that we started you out in the daily bottle. So we started you out at a quarter of a drop dose.

And I remember you saying that you felt your head clearing. You could actually feel that quarter of a drop dose.

So we started with that. And then you moved to the, worked up to the protocol 1000. And that’s three drops every hour for eight hours a day for three weeks. So I think we had you on it for about a month.

Okay, yeah, three, four weeks.

After that, my diarrhea was gone. And since then, I didn’t have anything with infection anymore.

I didn’t have to take it anymore, but I would take it again. Of course, if I have an infection, I take MMS.

Great. Great.

So you feel it made you healthier and you’re not getting sicknesses, colds and flus and stuff as much. Maybe it boosted your immune system.

Could be the case.

Very good. All right. Thanks for watching.

Summary:

A mother shares her journey with her son, who was diagnosed with autism around age two. After the initial diagnosis, the family actively pursued various approaches to help him, including dietary changes (eliminating wheat and dairy), chelation, and the Son-Rise Program, which helped improve connection and interaction over several years.

Later, they discovered a chlorine dioxide (CD/MMS) protocol through a book and online community. After starting the protocol, they noticed gradual improvements, beginning with subtle changes that became more significant over time. The early stages included what they describe as detox reactions, but they continued with the approach.

One of the most meaningful changes for the mother was emotional connection—her son began expressing affection more directly, including spontaneously saying “I love you,” which he had rarely done before. She describes ongoing progress, feeling that her son is “blossoming” and revealing more of his personality.

Overall, the testimonial reflects a long journey through multiple therapies, with the family attributing their son’s continued improvements and increased emotional expression to the later introduction of the CD protocol, along with strong support from a community of other parents.

Transcript:

Okay, so in a nutshell, here is our story. My son is now 12 and a half years old, and we discovered at a pretty early age, around age two, that things were just not adding up. And we got a diagnosis of autism, and we had our short little pity party, and then we decided we were going to dive right in and just figure out what we can do to help this boy.

And we tried, fortunately we got hooked up with a chiropractor from the get-go that helped us with, first thing he said is, this boy needs to stay away from wheat and dairy. So that was one of the first things that we did. And he did improve from that.

We also, somewhere in there, we started doing some chelation. And, I mean, my gosh, we’ve done so many things, it’s hard to keep track of everything. At some point we did, we learned about Son-Rise in 2006, and that has been an amazing and wonderful tool to help us connect with our son. And we ran a Son-Rise program for probably three or four years, pretty full time, and we had some wonderful improvement with that.

And I’m really fast-forwarding here, but then we heard about Kerri’s protocol of the CD, Healing the Symptoms Known as Autism, her book that she wrote. And a great, great friend of ours sent that book to us in the mail because it was so important that she said, she didn’t just say, you’re going to go get this book, she sent us the book and said, you are going to read this book. And so then we got on the CD Autism Facebook page and started perusing that, and we knew immediately that it felt right, and it felt good, and we couldn’t get our stuff fast enough, and we started right away.

And what I can tell you is we started to see improvement right away. It was just little stuff, very subtle stuff, stuff that even an ATEC test would not necessarily pick up on. And then he, you know, actually the first couple of months were, they were kind of rough in their own way because there was a lot of die-off and detoxing. He had the rash that comes and goes with that, but you just kind of power through and you keep going.

And we just kept going and we formed these most amazing relationships and friendships with other moms that are doing the protocol, and it’s just been absolutely an amazing journey. And here we are right now in Chicago. It’s Memorial Day weekend 2014, and we’re at the Autism One conference, and I’m meeting many of my amazing, what I call my warrior moms, superheroes. That’s why I’m wearing this amazing cape, because we’re all superheroes, and it’s just been an amazing journey.

My son is literally blossoming. I am seeing who he really is for the very first time. It’s just so encouraging.

Backing up just a little bit, when we were first doing this, my son never, when I say never, I don’t really mean never never, but hardly ever would say, I love you. Now I know he knows what that means, but he would always say, when I would say, I love you son, he would say, yes you do. So that was his way of telling me the same thing.

And within about three weeks or so of being on the CD, he for the first time, unprompted anything, he just blurted out, I love you mom. And they’ve just been coming in tidal waves ever since. And he has, he’s literally, I’m seeing who my son is for the first time. It’s just been an incredible journey.

And I feel so blessed to have met so many people and for all that Kerri has done to get this information out to people. And it’s just been incredible.

Transcript translated from Spanish:

For the same reason as she did, I want to give my testimony because I am also here now.

I was diagnosed with diabetes about 17 years ago. When they diagnosed me, my blood sugar was 350, which means the diabetes had probably been developing for years already. We started with pills, but after some time my blood sugar reached 500 and they put me on insulin. I have been on insulin for four years, but I could never accept the idea that one day my pancreas simply stopped working. I just could not get it into my head that I had to be diabetic for the rest of my life. No matter how many times they insisted, it never made sense to me.

Two months ago, through the son of a very good friend of mine, I received a video from Andrés. As soon as I heard it, I said to myself, “This is for me.” The next day I ordered the book by Jim Humble without hesitation, and within weeks I was already taking MMS.

Since I’m a bit of a daredevil and I’m tired of so much nonsense, I started quite aggressively. Yes, I had my vomiting and everything that comes with it, but I kept insisting and continuing. About two weeks later I also did a parasite cleanse, and I passed some worms that were really something to see.

After about one month of taking MMS, my blood sugar levels began dropping dramatically. Before that I had to inject 18 or 20 units of insulin in the morning, 18 at midday, and 20 at night. Today I no longer inject insulin at midday. In the mornings I take only 4 units and at night I take 6. I cannot say my illness is completely gone yet, but it has improved tremendously.

Something very important also happened. After about 6 or 7 days of taking MMS, the diabetic gingivitis in my mouth disappeared. After about 8 or 9 days, the numb padded feeling that some diabetics get in their feet also began to change. The first thing that disappeared was the pain, and little by little the numbness faded away. Now I can feel my feet touching the ground again, something I had lost before. Conventional medicine has nothing for that.

So it not only improves diabetes, but it also corrects many of the complications caused by high blood sugar.

I thought it was important to talk about this because if there is a plague in our countries today, it is diabetes. Many people are condemned to live with something that, with proper parasite cleansing and taking a few drops regularly and with discipline, could possibly be solved. We do not necessarily have to be diabetic our entire lives.

There is a huge business built around us — tests, pens, strips, insulin, pills — things meant to keep us dependent for life. And that is all I wanted to say.