Note: Difficult to understand video. Source unknown.

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

English Translated Transcript:

My name is Paola Cruzco.

About four years ago, I became pregnant, but unfortunately I lost my baby.

After undergoing medical tests, I was diagnosed with polycystic ovaries. I later learned that this condition was the cause of my miscarriage.

I began researching the reasons behind my loss and discovered that polycystic ovaries can prevent pregnancy or increase the likelihood of miscarriage.

I then started taking MMS.

After some time, I became pregnant again, thank God.

Today, my baby has been born and is now six days old.

Original Spanish:

Hola, mi nombre es Paola Cruzco.

Hace algunos años, hace más o menos 4 años, salí embarazada, pero lamentablemente perdí a mi bebé.

Luego de hacerme el rétrovíx, me detectaron que tenía ovaris poliquísticos y a raíz de eso se presentó el aborto.

Yo estuve investigando las causas de mi aborto y me di cuenta que fueron por los ovarios poliquísticos y que estos mismos no permitían que quedara embarazada o que, si quedaba embarazada, tenía la posibilidad de perder a mi bebé.

Empecé a tomar MVMAs y salí embarazada, gracias a Dios.

Y hoy en día, mi bebé nació, tiene 6 días de haber nacido.

Okay, we’re in Freeport, Texas, the seminar here, and Bobby wants to tell everybody in the world about what’s happened with him in MMS, his experiences.

Go ahead.

I found out about MMS about three and a half years ago from a friend of mine. He had cancer. At the same time, my mother-in-law had a pink yard of cancer. His daughter was in Germany. I heard about MMS from a friend, sent us the link to Genesis 2, started studying it, got the MMS, and took it for about six months and was having some results but not doing too well until we figured out we were taking bottom and C with it and doing some things wrong.

But finally figured it out and man, he had six months, the doctors gave him six months to live and he didn’t take the chemo, he didn’t want to do that, and it was pretty amazing. He kept her off. I’ve got a CT scans in his blood work and…

Good.

Acreotic cancer.

No, that was my mother-in-law who had pancreatic cancer, but I didn’t get it in time and she passed away.

But I’ve had seven members of my family that have died of cancer since I was a young kid. I was very interested in figuring out why I might have a family that has died.

Now your buddy, what kind of cancer did he have?

He had throat cancer and it took, after the six months of doing things wrong, and we were taking the 15 drops twice a day, it was doing pretty well. He did real good. Then we started the MMS too, and we’re doing real well.

I had read Jim’s book and after about two weeks of doing the MMS too, he had the Hirxheimer reaction, which scared me to death because I’m telling him what to do and what to take, but it cured his cancer.

As time went on, he was having trouble breathing. The doctors, he would go to MD Anderson to get his blood work and we saw that his blood count came down and all back to normal levels and it was great to see all that. So I knew that it was working and that it cured his cancer, but he had it in his lungs, his breast, his lymph nodes, and we had biopsies done again, and all of a sudden there was none in his lymph nodes anymore.

But the one in his throat, finally he couldn’t breathe anymore, and he went back to MD Anderson and the doctors was going to cut it out, and the sad part is they took his voice box out with it, and they tested it and it had no cancer on it, but they took it out anyway.

I’ve had people tell me that they took out all the lymph nodes out of a woman, and they said, good news, there wasn’t any cancer in the lymph nodes.

Yes, but you know what, he’s three and a half years, he’s healthy as a horse, he’s 76 years old now, and he comes by about two or three times a week.

How about you had other things you were talking about?

Oh gosh, I’ve used it on kids from sunburns to wasp stings to, we’ve taken off stuff, you know, different gross on the head and the face of my brother and just different family members, we’ve used it for a lot of different things now.

And I had people come by with cancer, it seemed like once a week.

Come by your work now?

Yes, they come by more talking about cancer. I just refer them to Yosemite.

That’s great, that’s great.

So you had the seminar, you learned more?

Oh yes.

Kind of fine-tuning some things?

Yes, that was the thing, learning, you know, not to take things right way and doing things the wrong way, and I’m lucky I figured out that if they’re not getting better, there’s something they’re doing wrong, and you’ll find out it’s either they’re taking vitamins, vitamins seem like…

Anti-oxidants?

Any of those, yeah, it definitely will stop and you’ll be like, man, it’s not getting better, it’s not working, why?

Yeah, because you put two people together and you go, why is this guy’s leukemia gone? This one’s not.

Obviously you deal with two different types of people, two different people, but if you hit it hard enough, long enough, it’s going to kill it all. And usually they’re neutralizing it somehow.

Right, but both my parents, my dad’s 80 and my mom’s 78, you know, they take MMS every day and they’re doing great. They’re healthy as can be.

Yeah, no one’s died from MMS. They only get better.

Great, man, I appreciate it. Thank you.

Translated Transcript:

Hello, my name is Gino Greco Todorovich Lavalovic. I am a television producer and scriptwriter. I have written scripts for almost all the comedians in Chile. I spent 27 years in Chilean television with Rupert Rupertina, El Japonín con J, and now I work with Dinamita Show, Los Locos del Humor, and the young clowns of Viña.

Countless comedians have worked with me, and of course I have worked with them as well.

One day while watching a television program on La Red with Salfate, they were talking about pharmaceutical companies and how they prevent new medicines from entering the market, logically because of business reasons, because it could also take away their customers.

Suddenly Pato Sotomayor said, “Yes, MMS has helped me a lot and now I almost have no pain.” They stopped him at that moment and said they would talk about it later, but the comment stayed in my mind and I kept thinking about it.

So I went onto the internet and saw testimonials from many people. I also saw how this created controversy, because many people did not believe it. I was one of those people too. I kept thinking, how could someone accept something like that?

I kept researching until I came across Ms. Angélica Costa Correa here at Colón Altura 7000.

I had a problem that I had carried for many years, which was my teeth. I spent a lot of money on dentists. When I was a child I had surgery for a tracheoesophageal fistula in Argentina, and they gave me many medications orally, which severely damaged my teeth. I had many cavities and had lost my dental enamel. My teeth were dark almost all the way down.

On the internet I also saw that this treatment could help teeth, because Jim Humble, while helping many indigenous people in jungle areas, discovered something interesting. Many of them came back and told him that besides helping them with things like cancer or AIDS that they had, it also whitened their teeth. They said their teeth had become white and no longer had cavities.

Through the experiences of his patients, he realized it was also effective for treating many dental problems. He began to investigate and came to the conclusion that a certain amount of MMS with pure lemon juice, with a slight effervescence and then a rinse, could improve dental health.

I tried it myself. I’m going to show something that might make some people uncomfortable, but I want to show my teeth. Down here in the middle I had a hole. It was not just a cavity, it was a hole where you could easily insert a needle, and not a small needle but a large one. It could pass through that cavity. It was tremendous.

I followed the treatment for about two months and began to notice that from here upward my tooth started to whiten. For 10 or 15 years I had tried to get dentists to fix this problem, and in two months it was already improving.

The cavity hole began to disappear and the dental enamel started to regenerate, which dentists say is impossible. However, what prevents enamel from regenerating is the cavity bacteria themselves. Those microbes prevent enamel from reproducing and regenerating. But without cavities and without those microbes, the enamel can regenerate again.

In my case it not only regenerated, but it also eliminated the cavity. The large hole I had here disappeared.

I had to stop the treatment for a while because of an illness my son had, and I had to focus on him. But the dark areas that I had on my teeth had already moved upward. I don’t know if you can see it.

Now I can continue the treatment and I know that in two or three more months my teeth will be white and free of cavities.

The breath also improves greatly. It’s incredible how much better your breath becomes.

Medical Categories Discussed

• Dental cavities (caries)
• Tooth enamel damage
• Dental enamel regeneration
• Dental discoloration / tooth whitening
• Tracheoesophageal fistula (childhood surgery)
• Oral medication damage to teeth
• Halitosis (bad breath)
• Bacterial infection of teeth
• Cancer (mentioned in testimonials)
• AIDS (mentioned in testimonials)

Transcript:
So, about a year ago, I was so upset that I didn’t get to come to Autism One. And I was spending an awful lot of time online reading everybody’s story. And there was huge, huge grinding and gnashing of teeth and drama about this woman who was telling people to bleach their children. Horrible, horrible fights in the autism community. And you would think of all communities that we would be more open-minded to things like that. But something I have learned is that when there is so much anger about something and so much passion, there’s probably something there. There’s probably something going on. And so I watched the presentation that Kerri had put out last year at Autism One. I went, hmm, that kind of makes sense. And I got online and I looked at a bunch of forums and I went, we’re going to try MMS, chlorine dioxide. And I spent a little bit of time getting my son off all of the supplements that he was on because that step one is to get off the supplements. So I spent a couple weeks tapering him off because you don’t ever want to cold Turkey anything. And then we started. It was a rough couple of weeks when we ramped up from one drop to his full dose, which is 18 drops. Very rough couple of weeks. We saw so many improvements. But at the same time, we saw a lot of die off. We saw a lot of herxing. We saw, I mean, he, I left a soda can. He was so aware. I left a soda can out in the backyard. He stuck his finger in it and cut it and ended up with three stitches. And it took three adults to hold him down to get the stitches. But he was aware. He’d never been aware before. I could leave something around. He would never notice it. He stuck his finger in once this and then he got it stuck. It was awful. But anyway, so we saw instantly, we saw awareness. We saw more focus. We saw a little bit more, more verbal. In January of 2012, he was speaking. The Therapy Center had him at about eight or nine three-word utterances per three-hour window. That was in January of 2012. We started the chlorine dioxide in June. In January of 2013, in a three-hour window, he was averaging two hundred three-word sentences. That’s the difference in speech we got. Now, he’s kind of stuck on three-word sentences. We’re having a hard time getting to four. But that’s the difference from a couple to two hundred in the same amount of time. That’s the data we kept. Right, so the enemas are magic. It’s just a couple of, couple tiny little bit of MMS in a liter of water. And it’s an enema and stops behavior, stops some cold. He has gone, his ATAC, which is the Autism Treatment Evaluation Checklist score, which is kind of how we keep track of how they’re doing, was a 25 when we started last summer. It bounced down in the fall to around a 15. It bounced back up to a 23 around Christmas because, well, they bounce. That’s what they do. We’re a 10. We’ve got him down to a 10. I have no doubt that it’s going to bounce back up, but it’s coming down. We’re going to get him there. All that’s left, really, is speech. The behavioral stuff for the most part is gone. He’s focusing better. He’s listening. The goo that has come out of him is astonishing. It’s just awful. I’ve never seen anything like this stuff. It’s so cheap. It is so easy. It’s so accessible. It works. I’ve taken it myself for colds. It will stop them just like that. We have been doing CDS as well as just straight MMS. I like CDS better myself. That’s not something that’s broad on the forums yet. We haven’t, you know, kind of broadcast it from the mountaintops because it’s a little complicated to make. But the CDS has been really good for Dominic because we’ve been able to get his dulcet higher. We haven’t had to worry so much about the actual physical pieces because with the CDS you just take the gas and it’s in water and it’s very pure. It’s great stuff. I don’t see us. I don’t see us needing to change anything. I like it and it’s going to get my kid back. It is so rare in this day and age to find someone who is as dedicated and selfless as Kerri has been and sharing this protocol with all of us to give so much of her time and her energy to individually work with families and kids to get these children back. I will be forever grateful to her for having the… for being so brave, for having the balls to do this because it takes so much to to put this out there. She’s so brave and she’s so selfless and I will be forever grateful for that. So thank you, Kerri.

Transcript:

Hello, I’m Dan Bender.

Every day, a countless number of individuals receive a diagnosis that includes a word such as incurable, terminal, or perhaps inoperable. Most of us reluctantly accept such a diagnosis, while a minority has the tenacity and strength to seek out a solution.

I’m here in beautiful Puerto Vallarta, Mexico, to report on the heartbreaking challenge of a local family, how they dealt with it, and how their experience is now having a positive impact on thousands of other families around the world. Join me.

On August 12, 2000, Patrick Rivera was born. He started life as a healthy, eight-pound, one-ounce baby boy, always ready to give anyone who held him a big, bright smile.

But something changed suddenly on August 13, 2002, that would forever change the course of the Rivera family. The thing that was most noticeable was his lack of eye contact. He had almost no eye contact whatsoever. He almost looked through people, and he stared at the TV until he pretty much fell asleep.

At the time, Patrick’s aunt Kim was living in the same house and also worked at Patrick’s preschool as a teacher. In some ways, it seemed that he had reverted back to behaviors he had when he was a baby. He was not responding to his name. He was running around in ways that were not appropriate for children of his age, not to mention flapping, squealing, the ambulance sound we called it, excessive drooling.

All the while, his pediatricians were saying to my sister, don’t worry, this is just a phase, he’ll eventually outgrow it. Patrick didn’t outgrow this strange behavior and was eventually diagnosed with autism, a neural development disorder now afflicting about one in 88 children in the U.S.

Patrick’s family was devastated. Emotionally, it’s very difficult to have a sick child, especially when you had a neurotypical child and then something happens to your child and you don’t really know what it is that happened to your child. But somehow, your life as you knew it changes drastically overnight. And then, of course, when the child stops being loving and the child stops looking for you, all those kind of things also are very distracting for the bond between a mother and her child.

Autism put a tremendous amount of stress on our entire family. I remember waking up pretty much every night to either Patrick crying or him running around. Then I would hear my sister come down the stairs, have to prepare him a bottle, try to sit with him, soothe him, get him to go back to sleep, which was nearly impossible.

Patrick’s brother Alex experienced life with autism firsthand and has had to learn to live with the limitations of his sibling. Like, if I ask him, hey, why don’t I go and play a video game with me? He just won’t do it, so that’s a bit frustrating.

According to experts, autism is incurable. But Kerri wasn’t ready to accept that as the final word.

So what made you believe you could cure Patrick when the accepted medical belief was, and I suppose still is, that this can’t be done?

Within a week of having had the diagnosis, I ran into a lady that I knew from tennis, and I told her exactly what happened. And she says, I have a friend who started the early autism center in Toronto, Canada, and I’m going to have her email you. Well, within 24 hours, I had a very long email from this wonderful angel, and she told me all about what happened, and she told me where to go to get help, and that autism is curable, that they’re curing kids all the time, and this fabulous guy is here, and you’ve got to go see him.

This started a six-year odyssey of treatment protocols and therapies that were administered by numerous doctors and therapists. We went to the recommended doctor, the Defeat Autism Now doctor, and we did everything from diet, supplements, chelation, hyperbaric, and other things with him, and we did notice an improvement with the diet. We were able to recover three words that he’d had prior to getting sick, and so we had recovered some speech, so we knew that the diet did work. And then we did the hyperbaric oxygen treatment, we also noticed that we had improved language as well.

The financial cost of autism is staggering. According to the CDC, the cost of care generally ranges from 40 to $60,000 per child per year. It’s ironic that we’ve spent about a million dollars trying to recover a child in the past eight years, and the ironic thing is that the majority of the things that were inexpensive like diet and supplements, and we were able to do them at home were the things that gave us the most bang for the buck.

Kerri and her husband, Guillermo, were fortunate in that they could afford to spend that kind of money to try and help their son. The family operates a successful advertising business, which of course had to keep operating during all the turmoil. Yeah, we definitely spend a lot of money, and I wish we knew then what we know now.

Autism also impacts the relationship between parents. We almost became a statistic. Basically when you have a child with autism, the first five years you have about an 80% chance of getting a divorce, and when the first 10 years of diagnosis you have about a 90% chance of getting a divorce.

Fortunately, hope was not lost. So in late 2005 I was told by the doctor that we were seeing at the time that the new fashion in autism recovery was going to be hyperbaric.

Kerri was put in contact with Bob Sands, a world-renowned expert in hyperbaric engineering. He advised Patrick receive 40 treatment sessions. Kerri followed his advice and the results were impressive. Within about two or three weeks after finishing our first set of 40 sessions, my son started to get more speech. So we knew that the hyperbaric chamber was a really good thing.

A hyperbaric chamber is commonly used aboard diving ships to help divers who come up too fast from developing the bends, which are bubbles of nitrogen in the blood. In recent years, it is also being used in medicine as a way to increase oxygen levels in the body to help alleviate various conditions.

Patrick’s positive results led the family to set up an autism clinic and install a hyperbaric chamber of their own. Not only would it help our son get well, but it would help other people heal themselves from whatever disorders that they had. And then, of course, other children without the ability to use a hyperbaric chamber financially would be able to have access to that for free.

Patrick now receives a cluster of 10 treatments over a period of 10 days every three months.

Patrick’s aunt Kim, once again, appears in his life, this time as his certified hyperbaric technician. Patrick’s in the hyperbaric chamber right now. He’s doing one session that’ll take 90 minutes, give or take about 15-20 minutes for the pressurization and depressurization. The environment inside is 100% oxygen, and he’s just hanging out in there watching his favorite Muppets movie.

We did notice over the first three years that we had the clinic that pretty much diet supplements and maybe some hyperbarics or a little chelation really didn’t recover the majority of the children. So what happened next?

In 2009, I went to visit a doctor in Guadalajara, and he at the time was doing IV chelation on children that we were treating. And in walked his nurse with all these little cute bottles. There were a bunch of green bottles and blue bottles, and I asked him what that was. And he told me that it was detoxification drops, and so I told him I wanted 10 of each. So I took 10 of each home with me, and I tried them out, and I broke out in a rash, so I figured that was probably a bad thing. And so I shelfed them.

The cute bottles turned out to be MMS, the street name for sodium chloride, which when mixed with citric acid turns into chlorine dioxide. So I started using MMS, these detoxification drops that I had found a year prior in about 20 months ago that was in the summer of 2010 that I started to use them. And I started to use them on my son after my husband had tried a few days of them, and he was fine. And so when we started them on my son about seven days later, my son turned to me and asked me things that he had never said before. Like, I want to take a bath, I want to brush my teeth, things like that that he just didn’t say before. And he was doing it all while he was looking me in the eye, and he just was so alive and so in his body. It was sort of like his soul had returned to his body for the first time in eight years, and it was really exciting to see.

And of course, over the next 20 months, and not only did we use it with him, but sharing that same information with other mothers and them doing the exact same things in their homes, 38 children, 20 months of using MMS have recovered and lost their diagnosis and are now neurotypical children in regular schools having friends and having full lives because of having used MMS.

And in a nutshell, how are you using MMS with these kids?

In autism, anything in autism, whether it’s a supplement or whatever it is, we go low and we go slow. It’s always low and slow because then you get less aggravations and you can actually sort out what you’re seeing because if you go too fast with anything, whether it’s a good thing like zinc or vitamin C or whatever the supplement might be, the best thing you can do is go very low and very slow.

And so I started to take that same approach with MMS because with my son I’d gone too fast and so I got a lot of detoxification, I got a lot of herksheimers, so there was nausea involved and which is not something we’re looking for. So if we start, if we go very slow and we raise it as the body’s able to tolerate it, then we get only positive changes, which is nice because we’re killing off the pathogens, iterate the body’s able to keep up with it.

And what about your success rate? Are you seeing results with every child?

I don’t think that anything will give you the desired results in every case because everybody’s different. I mean anybody can take it for any reason and still have different results. But what I have noticed is that you can say that everybody that I’ve ever seen take it that does it correctly has improvements. And then of course there are certain people that are going to have recoveries in shorter periods of time, then there are certain people that are going to get desperate and they’re not going to see recovery in the first two or three months and they’re going to run and try the next amazing cure-all that’s out there.

So if in fact we really focus on what autism is and why the chlorine dioxide molecule helps to cure it, it has to do with the fact that everything is based in pathogens and MMS is directly a killer of pathogens and nothing else. So that’s how we’re able to have and repeat the good results in many of the children.

Do you have any idea why it works better for some than others?

With everything, the application is the most important thing. Not any two parents are exactly the same, not any two children are exactly the same. So there’s some people that are giving it with juice and the juice doesn’t work or some people giving it with anti-oxidant supplements like Vitamin C, Meringa, CoQ, Diet 10. There’s a lot of different supplements that will kill off the MMS because MMS is a low potency oxidizer whereas pretty much anything that’s anti-oxidant will kill it. So there’s a lot of reasons why it doesn’t work and then of course there’s a lot of people that just don’t even follow the diet on a seven-day basis. So there’s some basic things to recovering autism that have to be in place for everything else to work.

What impact does the age when you start the protocol have on the success rate? Does it help to start earlier or later?

A young child can recover faster in many cases than an older child. We’ve seen this a lot in autism recovery. We’ll see two or three-year-olds start diet, a few supplements, maybe some methyl B12 shots and just pop right out. They’re talking, they’re playing with their parents, they’ve pretty much returned to what would be normal. Neurotypical as we like to call it.

But then there’s children also that they don’t seem to make that exact same type of recovery. So I think it goes back to the individual child because I’ve also had some children that were older, some nine-year-old children and 12-year-old children that have improvement very quickly because of course the child is ready for it, the body is ready for it, it is applied correctly. Every situation is a little bit different but we will typically see some of the younger children that are recovering faster because they’ve been sicker at less time is kind of the basic idea as well.

So are you still seeing improvements with Patrick now that he’s 11 years old?

Absolutely, I would say probably every week we’re seeing something that’s just a little bit different than the week before and it’s very encouraging to see that there’s still improvement and of course Patrick’s been sick for a long time. So Patrick is going to be the slow road back as he’s turning out to be. I would like one day just to find a magic bullet, give it to him until his recovery and everything will just be behind us. But until that day I know that every time I give him more MMS we’re killing down more pathogens and Patrick returns to us drop by drop every day.

For assistance, Kerri turned to Jim Humble, the man who discovered MMS in 1997 and has been researching and promoting its many uses ever since. I’m really quite impressed with what Kerri is doing with autism and how she’s using MMS and the results that she’s getting has been quite phenomenal.

Jim Humble has certainly stirred up a substantial amount of controversy over his MMS discovery. Some call it snake oil while others say it is no different than household bleach and will cause the very ailments Mr. Humble claims it will cure.

It’s crazy to say that MMS is the same as a laundry bleach. It isn’t even the same chemical. Even table salt has chlorine in it. Just because something has chlorine in it does not make it a bleach.

Although Humble’s critics are outspoken, countless individuals around the world consider him a godsend and he is frequently invited to speak at well-attended conferences the world over.

Kerri Rivera is also no stranger to conferences. Good morning. Today we’re going to talk about autism recovery.

On May 27th, 2012, she spoke at Autism One, the most recognized conference in the autism field. Although extremely well received by the MMS at the event, once word got out that she was given such a legitimizing platform, the blogosphere and media went into a tailspin attacking her use of MMS on children while completely ignoring the ever-growing number of recoveries as a result of Kerri’s protocol, including these children that appeared in a South American autism organization’s commercials.

So what do you tell those people who are critical of you using MMS on children?

I think it’s totally ridiculous. We have 38 children recovered in less than 20 months of using MMS to heal, cure and recover children from autism. And these children, when they recover from autism, are healthier than the general population. So I ask those people, why wouldn’t you use MMS to cure autism?

The cause of autism is heavily debated among the experts. But if you ask the moms, a particular observation is heard quite often.

Those people who say that autism is caused by vaccinations, so what’s your feeling about that?

I can’t speak for everybody. But in the case of our son, it was very noticeable that after a vaccine that he changed dramatically. But we have two choices. We can either focus on where autism came from or focus on the future and the healing from autism. And so I choose to work towards autism recovery.

Whatever the actual cause, whatever the ultimate perfect cure, there is no question that Kerri Rivera and her efforts have made an ever-growing positive dent in the autism community.

Transcript:

Hi I’m Michelle and I have been taking the product MMS Miracle Mineral Solution and actually I think the name has changed to Master Mineral Solution.

For seven days I’ve been taking it. I’ve been taking three drops an hour and that’s the one-to-one ratio.

What else? Let’s see. I’ve had a little diarrhea, a little nausea, but mostly I haven’t had any issues.

I do feel like I have a little bit of energy compared to normal, but at the same time I, especially at night and in the morning, I feel sick, like kind of like a cold, respiratory type cold. I don’t know if that’s to do with the MMS, but I do feel a little more energy and I have noticed that my skin is clearer.

So that’s nice. I’ve actually been making a small solution and wiping it on my face, you know, a couple times a day and if my skin gets too dry then I’ll skip a day.

So as of now things have been going great.

I’m going, actually today I’m trying a new way. I’m going to do, raise the amount of drops every hour. So the first hour today I took three drops and I just took my second hour of drops and that’s four drops. So I’ll just increase it hourly for eight hours or ten hours, somewhere around there.

The only issue that I am having is the eating thing. You’re not supposed to eat with it. It’s supposed to be like an hour or two hour window when you’re eating and so it’s really hard when you’re on the protocol of taking it all day to be able to eat.

Because I think that some of the food kind of deactivates, or not necessarily deactivates, but the MMS attacks the food instead of the pathogens in your body.

So anyways, like I said, that’s about my only issue right now.

I will check back in with you as soon as I get a chance and I will keep you updated.

Thanks. Bye.