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.

I’m a 25 year-old woman who is on the spectrum with many autoimmune symptoms, chelating to remove mercury using Andy Cutler’s protocol. That protocol helped reduce my symptoms immensely, but I felt I was at a plateau so I used MMS2 for about two weeks and it helped substantially in lowering the pressure and anxiety in my brain. I’m going to try MMS enemas very soon and will give updates.

From Jim Humble’s MMS Newsletter:

You may recall that our Minister of Health in Mexico, Kerri Rivera, has been ministering to over 400 autistic children by working with their mothers using the Church’s cleansing water (MMS) and the Church’s Sacraments. Kerri has developed a number of her own improvements to the sacraments which have made them more effective, one of which is that:

Her mothers have been giving the drops for more than the 8 or 10 hours suggested in the sacraments. This seems to have an even better effect. You might be interested to know that Kerri is now working with more than 1000 mothers and all the children are getting good results. The treatment has been extended to ADD, ADHD, and Asperger’s Syndrome. The results throughout the world are fantastic. Kerri said that it would be alright to give you her email address so here it is: kerririvera@yahoo.com

Autism update

We have some more wonderful news about MMS & Autism!

Here is a letter I received from Kerri working with children with autism – I thought you’d like to read it:

“Well, the past 3 months I have been a busy girl. We visited my good friend Jim Humble the middle of February which was a dream come true. At that time I had about 130+ kids on MMS. Afterwards, we had a conference in Puerto Rico on the biomedical approaches used in recovering children from autism. Directly from Puerto Rico I went to Venezuela where everybody was very excited about MMS and the possibilities of recovering from autism with only pennies a day. While in Venezuela I was able to teach 4 doctors the protocols that I use in my clinic, and share my presentation on the use of MMS for Autism Spectrum Disorders at a conference which 750 people attended. It was a very exciting time to say the least! In the days after the conference I was able to consult 176 families on individual biomedical protocols for their children, including MMS.

Since the conference, there has been much more interest in MMS in Latin America. In particular, I have many families who I help in Spain. I guess word got out, and one of the 2 doctors treating autism in Spain contacted me and asked me to share my protocol with her. The good news is that she is going to use it. Her idea is to apply it as an antifungal for Candida. However, MMS knows no boundaries and will kill all other pathogens at the same time. So, quite frankly, it is of little consequence what she believes she is doing with it, she will be doing far more than she even knows. Combining MMS with diet and hopefully only a few supplements, this doctor should be able to recover some of her kids. Financially speaking, when doctors like her start seeing results they will in turn get more patients and more patients mean more money. So, results coupled with money are a win win situation, and in turn humanity wins as we all grow healthier.

I hope to do a free conference in Spain before year’s end about the biomedical approach to recovering children with autism and autism spectrum disorders. I know that another doctor is using MMS in Italy. Maybe Europe will lead the way to getting MMS into the mainstream biomedical treatments and then the USA will follow. The doctors treating children in the USA with autism are under close watch by the FDA. Anything too “alternative” could cost someone their license. And these people have their own families to feed. So, they have to walk a very fine line. It is sad to see. Because what these special doctors want for their patients with autism whom they are trying to heal is the fastest recovery possible. And if it could be fast and inexpensive these doctors would be happy as well. Unfortunately they have such strict guidelines that it makes doing what they do difficult. Hopefully we could do a double blind study using MMS and autism. I think it would be easy to measure the difference.

On a practical note, many of the parents who have their children on MMS take MMS themselves, frequently out of a necessity to heal some immune issues. They will ask me “Can I take MMS too? I have X”. I always refer to a protocol from Jim’s course, and without fail within the first week I receive an email with some kind of miraculous story as to how “my fibromyalgia went away” “my husband’s sense of smell came back” “my shingles went away” “my Mother’s diabetes is under control”. These and more stories have come from the families of a child with autism. It goes without saying that the affected child is doing much better and having all sorts of firsts of his/her own.

At minimum there are 400+ children on the Autism Spectrum improving steadily, thanks to the help of MMS. These are in addition to all of the other children that these doctors are seeing and treating with MMS. The total including family members could be easily above 1000. The future is bright now that many more healers/doctors have the information on MMS and the knowledge of how to use it. I believe that people like these who see many, many children are an important link that will bridge the gap between “alternative” medicine and “allopathic” medicine, finally bringing MMS to the mainstream. I hope that we have in our hands the missing piece of the autism puzzle, because it sure seems to look that way. Two more children in March lost their diagnosis from autism, which makes a total of 5 children to lose their diagnosis since I began recommending MMS in August of 2010. Not all have recovered. But all are better than they were, and that is a great place to start.

As for now, I receive over 100 emails a day from people using my protocol for MMS. Sometimes we increase the dose, decrease or stay the same. We do protocols that other families and I have developed that add enemas and other elements of timing for the oral administration. The newest protocol that is getting lots of attention is the 72/2. It is a dose of MMS every 2 hours for 72 hours without resting in the night time. So, one parent wakes up every two hours and administers a dose of MMS. We have seen remarkable improvements with the 72/2. Another new protocol is the 12/2. It is taking MMS for 12 days straight then resting 2 days. This way the pathogens living in the gut will expose themselves during the two day rest, and then we hit them with another 12 days of MMS. Using this method we gradually extinguish all pathogens until none remain. When we heal the gut we cure the autism. The MMS enemas have also led to marked improvements for children on the spectrum. The families doing enemas are seeing more language and in general having less conduct issues and a lessening of stereotypical behaviors. When trying these new protocols or any MMS protocols it is a good thing to work in a team situation. Someone like myself, for example or another person who has used MMS knows when and how to avoid Herxheimer’s (die-off) reactions and what they look like. Many times the road to recovery is paved with discomfort, but in the end, it will have all been worth it. Autism means that your child has virus, bacteria, Candida, inflammation, heavy metals and food allergies. Allopathically speaking, you would have to take a drug store to kill all these pathogens, but will MMS, all you need is a little drop of what my husband calls “holy water” and recovery is on its way.

I think to myself that MMS and autism recovery are in their infancy together and wonder where we will be in 25 years. Will we finally, openly acknowledge what is causing the autism epidemic and stop it? Will we all use MMS to cure it? Will we all be hiding our rations of MMS from the authorities who say that we cannot use MMS? The last thought gives me the chills, a harmless oxidizer, yet at the same time potent enough to cure autism? It’s possible to think that it might be held out of a mother’s reach when she needs to heal her child from this devastation. Let’s try not to let this happen, and get everyone we know on MMS. Healing humanity begins with me and begins with you. We can do it. But we need to do it together”.

Best wishes,

Kerri Rivera