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I love it! I was going to have a heart ablation done STV and was 18.000 pvsc a day and now I am healed. No medicine and my blood pressure is awesome. THANK YOU!

BP 206/180 (12/11/22)… 110/71 (12/28/22) in 18 days on MMS starting protocol.  Amazing !!!

WHAT HE IS VERY FAST TAKEN TWICE A DROP FIRST AND THEN TWO. On day 3 I felt much better, no fatigue, improved pressure, and I have an incredible feeling.

Only energy.

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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.

I am so glad that I got to know MMS. This miracle remedy not only cured so many diseases for my own, but it also helped a lot with my dog. I have a 6-year-old pug. I treated her several times with the MMS 6+6 protocol.

I remember one time she was coughing and gagging all day. Then I gave her 1 drop activated MMS with 1tbsp water and added it to her food. She had no problem taking it. It seemed she was not bothered by the strong smell. Just after 2 doses 1 hour apart, her discomfort disappeared completely. She was healed.

This time, a couple of days ago, I noticed she may have some blood in her urine. Yesterday, she started to pee much more often, and it took her a long time to finish, plus she had to go 2 to 3 times for one potty trip. I knew she had some urine tract infection going on, even though she didn’t show too much discomfort or had to pee at night. Just peed frequently, had long urination time, and had pink urine.

So last night, I gave her one 6+6. I followed the directions in Jim Humble’s MMS Health Recovery Guide Book, There is a special section for animals (trust me, this book is well worth the money to buy, having a physical book like this is always handy). I also gave her 500mg D Mannose in case. My dog likes milk. So mixing the MMS1 (activated MMS) with a little bit of milk made it so easy to feed her.

Last night she didn’t need to wake up to pee, so she slept all through the night. I took her to pee outside. She has shown significant improvement already. Her urination time was back to normal length, and she didn’t go pee again after that. Her urine was dark yellow instead of pink.

So I gave her another 6+6 this morning, and another 500mg D Mannose (I don’t think this is necessary but I just had some on hand.) Then she peed after 4 hours since the morning one, this time it was even better, and her urine was back to normal light yellow color. About 4 hours later, I gave her another 6+6 (no D mannose) to make sure everything was cleared up.

She peed again after almost 4 hours and a half (a lot less frequent than yesterday, yesterday she could go every 1 hour or 2). It seems she is healed. But I will keep giving her the maintenance doses for the next 5 days.

I noticed that when I treat my dog with MMS or homeopathic remedies, she recovers way faster than human beings. I think that’s because the animals don’t have the mindset to question or doubt if they will be healed or not.

Btw, if the dog’s UTI is more severe, adding DMSO to MMS works even better and faster. (DMSO itself works for UTI too).

Note:  This is a combination of 3 testimonials by the same person as they produced updates.

March 31, 2015

Hi,

My name is Gerald McClellan and I am 72 years old of Monroe, NC. I was diagnosed with prostate cancer in Nov 2011 and my doctor said that my prostate had a PSA reading of 5.89 and was over 80% infected with cancer and he suggested that I have it removed or I would not live more than 5 years.

Well believing in my doctor I agreed to have it removed and they did remove it in Jan of 2012. I had been scheduled to have a PSA reading done every 3 months to see if my cancer was gone and it wasn’t so they scheduled me for 37 treatments of radiation, which was completed in July of 2012.

From that point on my PSA readings, which were low but not gone, were doubling every 3 months until I learned about MMS in Jan. 2014. My son ordered it and I started on Jim Humble’s protocol 1000+ and when I had my April PSA reading my cancer had reversed for the first time in two years and now is gone.

My readings had always been pretty low but not the 0.00 reading I should have had being I don’t have a prostate. Well I have documented readings which prove that the MMS did in fact reverse my cancer and got rid of it.

I also was using Vitamin B17 between my April reading and June reading to find out if it also worked and it did and my cancer kept going down.

So between my June reading and Oct reading I was just taking the MMS2, pill form, and found out that the hydrochloric acid thickened my blood, even though I was on Coumadin because of having AFib. And I suffered with a mini-stroke that affected my right eye making me cross eyed to over 18 degrees off center.

I could see out of the eye OK but not both at the same time. I went to an eye doctor and had some medical tests done. My eye doctor said that I might possibly have to have an operation on the eye but wanted me to wait and see if it got better on its own. If no changes were seen by 6 months then the operation would have to be scheduled.

Well I knew that my MMS worked for my cancer so I thought that it might work as well for my stroke also. I made up an activated 10 drop solution and put it with distilled water in a spray bottle and made up a 70/30% solution of DMSO and sprayed it on my whole right side of my head and around my eyes two to three times a day.

I told my eye doctor what I did and I noticed improvement after 3 days and my eyesight returned to normal within 10 days. My eye doctor couldn’t believe my rapid recovery and wanted to know what it was that I did so I told her about MMS and how I used it to recover.

I had her make notes of my use of MMS and had her put them in my medical record and gave her a CD with all of the information about MMS. I also had my urologist put my taking MMS in my medical records he has.

Neither doctor would admit that this use of MMS would really work. But the records of recovery speak for themselves.

Signed Gerald D. McClellan

Hi this is Gerald McClellan of Monroe, NC and this is a followup of my posting to Jim Humble’s site in March 2015. I am now 79 yrs old and will be 80 in June.

It was Jan. 2014 that I received Jim Humble’s book Master Mineral of the 21 Century and when I first learned and started using the drop per drop method of CD but being that I have A-Fib and am on a blood thinner, I couldn’t do the recommended protocols when I tried like I mentioned in my previous posting.

So I tried other natural remedies to fight my cancer. I was skeptical at first with CD until I started using Kerri Rivera’s method of drinking it from a baby bottle and did until I learned the VA Oncology’s protocol.

And then on the newest method that is Chlorine Dioxide Solution (CDS) with no side effects and neutral PH of 6.7 to 7.4, a alkaline base that made it very easy to consume. I learned of this when accessing Andreas Kalcker’s web site and used it to control and rid my body of a very aggressive Gleason 8 prostate cancer that metastasized first to my lymph nodes then to my bones creating me to stage 4 prostate cancer and creating a very high PSA reading of 38.

On Webster Kehr’s web site I found out all about what cancer really was.

Being I have A-Fib which earlier forced me off of the old drop per drop method CD protocol in 2015 to 2016 and I was not taking much CD and my cancer metastasized from my lymph nodes to my bones and then in 2017-2018 and I recovered down to a 0.45 PSA reading from just being on the Bitter Apricot Seed vitamin B17 protocol for 6 weeks.

Then after several months of not taking anything and as I mentioned earlier I found my cancer was getting really aggressively bad again from the Sept bone and body scans done by the VA hospital my PSA reading grew back up to 38.

Then in late 2018, by the advice of my VA oncologist, I went on a protocol of Abiraterone Acetate, 5mg of Prednisone and a hormone injection (that caused me to gain 20lbs).

The Abiraterone Acetate is a low dose chemo pill that at first caused me to suffer of liver damage putting me in the ER at the Presbyterian Hospital of liver damage. My dosage was then lowered from 1,000 mg a day to 500 mg while being closely monitored by the VA then to 250 mg which I was on from early 2019 to April 2020.

Now is the PSA a true marker for cancer? This is a question I am not truly believing in and having several different thoughts with my oncologist and him explaining to me that testosterone is what really feeds cancer cells.

But after reading the findings on the referenced web site of what caused me to question my oncologist’s explanation and description of cancer, I had body imaging and bone scans done in Sept., 2018, 2019, the cancer kept growing to almost all of my bones even though the hormone injections did lower my testosterone and PSA readings.

Then in April of 2020 I stopped the VA protocol and on May 17 of 2020 I started on the newly form of taking CD which was CDS and by Sept of 2020 and of only being on CDS for 4 ½ months my cancer showed from the Sept scans that it has regressed to almost half.

And now in the most recent scan of Sept 2021 it showed my cancer being undetectable.

Oct 28, 2024 Update

Written by Gerald McClellan a 82 year old USMC Veteran of the Viet Nam Era from 1961 to 1966. I was a Helicopter Mechanic and stationed at New River Air Station, New River, NC from April 1962 to my discharge from active duty on April 28, 1966. My email: gdmcc8008@twc.com

I was diagnosed with Prostate Cancer in Nov of 2011. I learned about CD from a book given to me in Dec of 2013 called ‘Cancer Step-Outside the Box’ written by Ty Bollinger and bought my products from https://discovermms.com and started using it in Jan of 2014, which was difficult to take because of the chlorine smell and side effects from the drop per drop method and took awhile to get used to. The term CDS didn’t get its name until 2012 and 2013 by Charlotte Lackney of https://mmsinfo.org and Andreas Kalcker of https://andreaskalcker.com. At that time it was called CD and named MMS (Master Mineral Solution) by it’s rediscover Jim Humble in 1996. In 1984 NASA named it The Universal Antidote. You can learn all about it at https://theuniversalantidote.com or on Rumble.com

CDS (Chlorine Dioxide Solution), which is a gas put into distilled water is an Oxygen Alternate Carrier in the blood, that I call The Fountain of Youth Water it improves the health and life extension of humans and animals. In 2014 when I first started using Chlorine Dioxide (CD) with the acidic drop per drop methods of PH 5 mentioned in Jim Humbles book “Master Mineral Solution of the 21st Century” and could only use it from time to time because of the chlorine smell and the acidic side effects. So I tried other natural remedies to fight my cancer.

I was skeptical at first and until I learned of the newest method which is Chlorine Dioxide Solution (CDS) by Andreas Kalcker with no side effects I started using it on 17 May of 2020 which has a neutral PH of (6.7 to 7.4) and used it to control and rid my body of a very aggressive Gleason 8 Prostate Cancer that metastasized first to my Lymph Nodes then to my bones and created a very high PSA reading.

On Webster Kehr’s web site https://www.cancertutor.com I read all about what Cancer really was and learned about the Intracellular Micro-Parasites called Microbes being the root cause of Cancer and several other diseases and was mentioned as a Theory but I never learned on how to rid the body of these parasites not realizing that CDS was the best way to do that and forgot all about it for a few years.

Being I have A-Fib which forced me off of the old drop per drop CD protocol from 2015 to 2016 and in which I was not taking CD and my cancer metastasized from my Lymph Nodes to my bones and then in 2017-2018 and I then recovered down to a 0.45 PSA reading from just being on a Bitter Apricot Seed Protocol (Vitamin B17) for 6 weeks eating 45 seeds per day and then wasn’t taking anything because I thought I was OK but after several months not realizing that the micro-parasites eggs hatched I found out that my cancer was getting really aggressively bad again from the yearly VA Sept bone and body scans done by the VA hospital.

Then in Dec of 2018 all of 2019 until April of 2020, by the advice of my VA oncologist, that believe Testosterone feeds cancer but the microbes that invade the cells of your body in fact eat Glucose Not Testosterone that is what feeds these Intercellular Micro-Parasites. By per-pressure of threatening me of not doing any more scans from the VA Oncologist I went on a protocol of Abiraterone Acetate, which is a low dose chemo pill that at first caused me to suffer of liver damage with a bilirubin reading of 3 times what it should be and putting me in the ER with a 103 degree temp.

My dosage was then lowered from 1,000 mg a day to 500 mg then to 250 mg which I was on from the end of 2018 to April of 2020 plus 5mg Prednisone and a Hormone Injection every 3 months, from the VA Hospital. Now is the PSA a truly a marker for cancer? This is a question I do not truly believing in. I had body Imaging and bone scans done in Sept., 2018, 2019, the cancer kept growing to almost all of my bones.

Then in April of 2020 I stopped the VA protocol and on May 17 of 2020 I started the newly form of taking CD which was CDS (Chlorine Dioxide Solution a CD gas infused in water) and by Sept of 2020 and of only being on CDS for 4 ½ months my cancer was half gone taking CDS into 2021 (My VA PSA reading of 0.01 or below the hormone and predisone lowered my PSA but did nothing for my cancer) But after being on CDS my cancer regressed to almost half in 2020 then gone in 2021, which I stated earlier in this writing showed that my cancer has regressed so low that it is unrecognized.

Then in Sept of 2023 my scan showed that I was Stage 4 again with a PSA reading of 200 and the cancer this time was in my Lymph Nodes, T10, T11 and T12 plus in my right Femor. My VA oncologist wanted to put me on a cancer protocol but I refused and only accepted the hormone pill called Relugolix 120mg, and wasn’t told of the side effects which did have some major side effects of bone and muscle pain and loss, in order to reduce my PSA reading.

It did drop my PSA to about 70 at our next appointment then down to 13 and back up to 16 and I stopped taking this drug on May 16 of 2024 because of these side effects that cause me to suffer from a muscle tear (twice) in my lower back and bone deterioration and pain. After watching Dr. Lee Merritt and Dr. Jane Ruby on Rumble.com I learned that having a steady intake of a parasitic drug will not kill all of the parasites and now am on 32oz of CDS for 7 days then off for 4 then on a anti-parasitic drug called Artemesinin for three days then off again for 5 days.

Because when you kill the mother micro-parasite you lose the hormone that keeps the eggs (20,000 to 200,000 per day) from hatching that she excretes while she is alive. This protocol is what I am on right now and I can say that my muscle strength is returning and my cancer is almost gone again per my most recent VA Scan on Aug 12, 2024.

Please share all this with other family members and friends. Go to Amizon.com and search for a book called ‘The Cancer Microbe’ written by Dr. Alan Cantwell, Jr. M.D. The first discovery of the Intracellure Micro-Parasites was in 1890 by Dr. Russell William, M.D.

Check out all the testimonials on Jim Humbles site: https://mmstestimonials.co/ Do not try to access this site with Google, or Chrome, Internet Explorer, Plus or other Microsoft browsers because it is being censored and blocked or will cause either a 404 code or misreading the site. You must download the latest Brave or Tor Browsers and DuckDuckGo for the search engine.

I get my products at https://discoverwps.com. You will have to buy a $10.00 life time membership to access the site but the prices are cheaper than on Amazon. On Amazon it is sold as a water purifier and not as CD. It is set up this way to keep the FDA / Gov. from shutting it down to protect Big Pharma and Major Medical.

Watch the video called ‘Video Proof that Intracellular Parasites Cause Cancer’ or go to Rumble.com and search for micro-parasites or true pathfinder the people who released the video in Feb of 2018 and has been updated for over 20 years.

My VA Oncologist won’t write me Nexus Letter so as to increase my VA Disability because of the Contaminated Water at Camp LeJeune. From the first time we met in 2017 and he became my VA Oncologist he tried to make me believe that Testosterone was what feed cancer cells but in fact via the German Doctors of the video say it is Glucose that feeds them. Well I didn’t believe him about the Testosterone and made vocal my disbelief.

At that time in 2018-2019 they were wanting to schedule me for a bone hardening injection that would permanently calcify my bones causing me to have teeth pulled with minor decaying in preparation because my bones would be too brittle.

I after talking with a Veteran Dentist decide to not go through with the injection and refused it. Then as the years went by and the continued pressure by my Oncologist who threatened me to not be able to have any more scans if I did not accepted another Experimental Testosterone reducing pill called ORGOVYX (relugolix). I was told that if I didn’t accept something from them then they wouldn’t give me any more scans so I accepted it.

The side effects of this pill from only being on it for 2 1/2 months had caused me to tear my back muscle twice and lose strength causing me to walk with a cane and cause me to have even more cancer which was killing me and in the (August 2024 scan) which now was in my back and several new tumors in my pelvic and lymph nodes in my chest until I stopped taking it completely with the objection from VA Oncologist Doctor.

Well long story short my VA Oncologist won’t make me a Nexus Letter because I am recovering from my cancer by getting rid of these Intracellular Microparasites. [When a Proctologist would examine the tumors of the dead they would see these microbes and called them Extracellular Vesicles (their medical term)]. Since I stopped taking their Testosterone reducing Relugolix medicine my strength has restored with only a minor pain in my lower back muscle. It takes a long time for muscles to heal.

I am almost back to full health because after stopping their med’s I started on a parasite protocol as mentioned above of CDS for one week then nothing for 3 or 4 days to allow the eggs from these parasites to hatch then hit them again with the consumption of Artemisinin 1800mg (Anti-Parasitic medicine) for only 5 days then nothing again for 3 to 4 days and then back on CDS for another week. This is my protocol now and I feel great.

Anyway I just wanted you to know about this and think that this information should be given to all.

Sincerely Gerald McClellan

The following testimonial is excerpted from pages 419-422 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 now 8-year-old daughter was dx with autism at 18 months old. Started GF/ CF diet and started with a DAN! She slowly made progress with speech, had a few words, a few 2 and 3 word sentences, and despite having autism, she was always a happy, calm, sweet little girl. Shortly after her 3rd birthday, she “changed.’ She became more of a Jekyll / Hyde personality, and all progress in speech and improvements in eye contact and sociability started to fade. Seemed like everything we did was just like yo-yoing back and forth between improving, and then crashing yet once again.

Last year at this time, we had just left the doctor we had been taking her to. For years she was on antivirals, antifungals, antibiotics on and off, SSRI’s, Tenex, and when her violent SIB had become so bad the second year into treatment with him, he put her on Abilify. SSRI’s and the Abilify did nothing for her except make her behave worse. Neither did any of the other things he had her on. The first year she was doing pretty good, but possibly because the antivirals were acting as an anti-inflammatory. She always had chronic constipation with loose stools/ diarrhea. Nothing helped that either. We finally left that doctor who yelled at us in his office for 20 min straight, in front of my daughter, because he did not like that I had been challenging him on all of this for the past 6 months. I was no longer going to let him put the blame on us and everyone else… that her ABA and speech therapists didn’t know what they were doing, and telling us she acted out this way because we didn’t know how to give proper time outs or how to correctly give “pep talks” at bedtime. I was convinced that she had PANDAS/PANS and/or parasites that were causing her ever increasing SIB, loss of all progress she had made in speech over the past 4 years, and the fact that she had not grown in 4 years…did not gain 1 pound, feet did not grow at all, and she only grew 1/2 inch in height in that 4 year span. We had taken her to a very well respected endocrinologist the previous summer who ran all the tests. Could find nothing wrong as to why she wasn’t growing. But he decided to put her on HGH anyway. Thankfully, we left and decided not to give her the HGH. We also took her to one of the best Ped Psychiatric doctors at UCLA who specialized in autism that summer. He observed her, her SIB happened right there in his office for him to see. He said her SIB is coming from pain, discomfort, something medical going on inside, most likely stemming from her gut. He suggested we get her scoped upper and lower. So we did. The only thing that came up was on the upper endoscopy, and that was that she had esophageal gastritis. So the GI dr gave her Nexium.

All the parasite stool tests we had done over the years had always come back neg except for one at age 3 came back with Giardia. But that was it. So last January, when we had finally left that her doctor of 3 years, her liver AST and ALT were at 130 and 135, her Creatinine (kidneys) were severely elevated at a dangerous level, she now had hypothyroidism, and after testing her cortisol thru blood and saliva we discovered she was barely making any at all. She had dark circles under her eyes, grinding her teeth for 3 years now, and agitated beyond belief ALL the time. Mind you when we started with him 3 years prior, her thyroid, liver, and kidneys were all in normal range. She did have dark circles, many many food allergies, some SIB, but nothing compared what we were dealing with now, or what was to come.

So now, what to do. We took her to a very highly recommended Pediatric GI in Los Angeles who was very nice. Listened to what we had to say. Ran the most sensitive and comprehensive stool analysis. Came back with nothing at all. Then took her to the head of pediatric Infectious Disease at Cedars Sinai. She obviously had her mind made up before she even walked in the door. She saw the word AUTISM on my daughter’s chart, and that was it. I showed her every blood and stool test, explained the not growing at all for 4 years despite all the endocrinology labs said everything related to growth was in normal range, her severe SIB. She said to us…”I know you want to help your child. You want to find something “medical” that has caused her autism so you can fix it. But the truth is, your daughter has autism. You need to accept that, and take her to a pediatric psych dr who can help her with these SIB’s. There are lots of meds that can help her be calmer.” Had she not listened to one damn word I told her!!! All the meds we had tried in the past did nothing, already took her to a psych dr who specialized in autism telling us something internal was wrong. She would not run any blood tests, or any other kind of Infec Disease tests. So with that, my husband, my sister, and I completely dumbfounded started to walk out. The dr then had the nerve to say…”She hasn’t been vaccinated since 18 months (she was 7 here) Let’s get her caught up right now before you go. I can give her 6 vaccines today.” I looked at her and said you have got to be crazy! I am not giving my very sick child vaccines full of the poisons that did this to her.”

So a month later we started with doctor who “gets it.” Who listens, and treats parents with respect. Values their opinions. And the networking I had been doing for the past 6 months on a few different bio-med autism groups with other moms was paying off. The moms are the ones who KNOW!!! That’s how I found my daughter’s current doctor and how I found Dr Maile Pouls last June to help her with nutritional and metabolic healing. Dr Pouls ran a $100, 24 hour collection urine analysis, and we found out she had severe malabsorption, Ph was too Alkaline, she was catabolic, extremely electrolyte and mineral deficient, severely Vit C and D deficient, and had severe bowel toxicity. Working with Dr Pouls and her new doctor lead them to suspect parasites/worms. I was encouraged to look into mms, but of course I had heard nothing but bad things like it’s bleach. I was very hesitant to try it, but I researched it, and sought out other moms on Facebook who were doing it. The toxins from the parasites had completely taken over her body and brain. She was SIB almost all day, every day by now. It was pure hell. We thought we were going to lose our minds it was so bad. We had stopped taking her anywhere but school and dr’s appointments for the past 2 years because she would just suddenly out of nowhere, for no reason, violently freak out and there was no way to help her calm down. Her doctor said she’s so toxic, and her body is so sick that she can’t detox. That the mms will not only help kill, but will neutralize the toxins and help her calm down. So we started mms, and I could not believe how much calmer, happier, and more present she was in just a week. MMS is literally saving her life, and bringing her back to us. Before starting mms, we did just parasite meds like Alinia and Mebendazole. The parasite meds alone did not help her, even though she was dumping worms, but she was still completely psychotic, and getting more crazy and manic every day. Since starting mms she has dumped hundreds of worms, some 10-12” long, ascaris eggs, TONS and TONS of the shedded skins of the worms, tons of liver flukes, and hundreds of tapeworm segments. We had not done any PP yet. This had all been with MMS only! We actually started Albendazole for treating tapeworm about a month ago and saw immediate improvements with it. It really seems like this is her biggest beast right now to deal with.

These are her labs from before MMS, and after starting MMS:

2/7/2012 – one month after leaving scumbag dr of 3 years

AST = 79 ALT = 108 Creatinine = 1.24 EOS = 11.2 Sed Rate = 9 ~ Started MMS 11/23/2012 ~

12/4/2012

AST = 73 ALT = 64 Creatinine = 1.32

1/15/2013

AST = 61 ALT = 60 Creatinine = 1.30

2/27/2012

AST = 51 ALT = 42 Creatinine = 0.92 EOS = 5.1 Sed rate = 12 Ref Range for AST is [15 – 46] ALT is [3 – 35]

Ref Range for Creatinine (kidney) is [0.60 – 1.20] Shows how well kidneys are working. Anything close to or over the 1.20 is considered to be of serious concern

Ref Range for EOS (eosinophils) is [0.00 – 3.0] * High EOS are always seen with parasites

Ref Range for Sed Rate (marker for inflammation) is [0 – 10]

Her doctor said her Sed Rate is likely high because when killing off pathogens and detoxing, inflammation will go up temporarily.

So I say never give up. Don’t listen to doctors who don’t listen to you. Kerri, thank God you saw those bottles of MMS at the clinic that day and asked what they were. And that you bought some out of curiosity and tried it. And that you selflessly have taken what you’ve learned and experienced, and shared it. Given so much of your time to help others, to help heal and recover their kids. You are truly an amazing person. We finally have the answers to our daughters autism after almost 7 years of numerous doctors and specialists, so many tests, so much money and valuable time wasted… and now we finally have real hope…real results. We know without a doubt she is going to get healthy, which will in turn

give her the happy joyful life back that she once had before she got “autism.” ~

xoxo

On Saturday last weekend, I began to have sudden, strong pain in my right side.

I also had trouble breathing, as it hurt more if I took normal breaths.

I was at a basketball game for my grandson, along with my wife. I didn’t want to alarm her, so I didn’t tell her.

I made it through the night with little sleep, and Sunday morning I thought I needed to go to the ER, the pain was so bad.

I also ran a fever.

However, I remembered I had bought MMS several years ago, and it had sat on a shelf in our basement since then.

I took 2 Ibuprofen to deaden the pain and began looking at what my problem might be.

I narrowed it down to appendicitis or a kidney stone.

But there was no blood in the urine, and I had passed a kidney stone some years ago, and it didn’t feel the same.

I then went to look again at MMS on the computer.

I found a testimonial for a young girl who was relieved of her appendicitis, so I decided to use Protocol 1000.

I took 3 Ibuprofen before bed Sunday night, and that helped, but the pain soon returned Monday morning.

So I took 2 more Ibuprofen and began the protocol Monday morning, my first ever experience with MMS.

I took two more Ibuprofen before bed Monday night and was prepared to take two more when the pain returned Tuesday morning.

The pain did not return.

In one day on the protocol, I felt normal again.

However, I am going to finish the 7-day protocol (3 drops every hour for 8 hours a day, for 7 days), just to be sure.

I did not want surgery, as we are scheduled to have two of our grandchildren over for the weekend, and I did not want to cancel that, so I turned to MMS.

Glad I did.

Translated Transcript from Spanish:

Hello. Today we are speaking with Dr. Icce Hernández Galán, a licensed homeopath with 22 years of experience in private practice using homeopathic metals, Bach flower therapy, emotional and mental therapy, and homeopathy for physical illnesses.

Today she brings a testimony about her own mother.

My name is Icce Hernández and I am speaking from León, Guanajuato, Mexico.

A few weeks ago my mother experienced an ischemic event, a cerebral infarction (stroke). She is 79 years old and had no illnesses and was not taking any medications.

On Thursday, August 13, she suddenly developed symptoms of a stroke. She lost her speech and had difficulty performing normal functions such as eating, writing, walking, and reading. She also had confusion and did not know what date it was.

She had difficulty coordinating movements and experienced memory loss, which made it difficult for her to take the CDS that we began trying to give her on Friday, August 14.

On Saturday, August 15, I attempted an enema with 10 milliliters of CDS but she could not tolerate it.

On Sunday, August 16, I asked my mother to try writing. The results showed she could barely write. She could not write her name or correctly trace numbers. I gave her exercises like those given to small children in kindergarten.

On Monday, August 17, laboratory tests were done including blood tests, urine analysis, and an electrocardiogram because I suspected cholesterol or triglycerides might have caused a blockage. However, all the tests were normal and the electrocardiogram was perfect.

On Tuesday, August 18, I decided to administer CDS intravenously. I prepared 400 milliliters of saline solution with 48 milliliters of CDS at 3000 ppm and administered it slowly.

Within about thirty minutes my mother began speaking again. She even began telling me about a movie she had found and was watching.

After that infusion I gave her another saline solution to hydrate her and allowed her to rest.

On Wednesday, August 19, we had our first appointment with the neurologist. The diagnosis was a cerebral ischemic event, but the neurologist did not find neurological damage.

After the first treatment my mother’s writing improved significantly. Her letters became clearer and more recognizable.

On Thursday, August 20, I administered a second intravenous infusion using 500 milliliters of saline with 60 milliliters of CDS.

Her speech improved further and we continued working on memory exercises.

After that I began giving it orally. I placed 15 milliliters of CDS into one liter of water. She drinks this mixture slowly every five to ten minutes during the morning and again in the afternoon.

Since that time my mother has improved every day. Her cognitive abilities have increased. She now speaks fluently, goes up and down stairs, and performs activities around the house that she had not done before. She no longer uses a cane.

Fifteen days after the event she was able to read and write normally again.

Here is her writing today. It says:

“Good morning. My name is María del Refugio Galán Gómez. I was cured with chlorine dioxide. Thanks to my daughter.”

This is what happened with my mother. It is emotional for me to share this because I was very worried about her.

In my practice as a homeopath I treat patients based on their symptoms rather than simply treating diseases. I applied this same philosophy in deciding how to use CDS with my mother.

I have also used similar treatments with patients who had COVID and low oxygen levels. They recovered quickly when taking it orally.

One of the principles of homeopathy is that the first duty is to preserve the life of the patient. We can use whatever therapeutic methods are necessary to save the patient’s life.

Thanks to this treatment my mother is now alive, coherent, mobile, and able to climb stairs in our four-story home.

Health Issues Mentioned:

Primary testimonial:

• Stroke / cerebral infarction (ischemic stroke)
• Loss of speech (aphasia)
• Memory loss
• Loss of coordination
• Cognitive impairment
• Difficulty walking
• Difficulty writing and reading

Associated symptoms:

• Confusion about time/date
• Reduced motor coordination
• Need for a cane

Other conditions referenced in discussion:

• COVID with low oxygen saturation
• Dementia prevention (mentioned)
• General neurological impairment after stroke