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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

From my experience it seems you can take really high oral doses of CDS without problems. I am super sensitive and MMS1 & 2 will give me gut problems. I took 1 tsp (5ml) of 3000 ppm CDS every hr for 8-10 hrs/day for about 10 days and had no nausea or diarrhea. It helped greatly with my symptom which was lung congestion…

To make a long story short. I already did a MMS-DMSO protocol for brain tumor (GBS) cancer which was for my Mom. Everything was going fine until …

Her pain was controlled with xylocaine for another problem she had. When she moved floors at the hospital, they stopped relieving her pain with the xylocaine cream. So, instead, they started giving her morphine and other sedatives until she was no more of this world. The week-end before she was doing so good that we were arranging to take her out for supper. I got the NAVARO test results showing only traces of cancer.

Just started taking the MMS solution a week ago. My parent with Alzheimer’s and I were infested with bird mites since July, and managed to get rid of them through vinegar/soda/borax and zapper. Noticed through the bird mite group that many were using MMS. My blood sugar was sometimes elevated, but my parent had been on insulin for 25 years. I managed to drop her insulin needs by 75%, but never could get her off it. Since taking MMS, her blood sugar 1 hour after meals has been 105-128 at the high end without any insulin. This is almost normal. My parent is speaking to me without stopping to think of the word she wants to say. Her toilet training has improved, and her vasculitis on her legs has improved, and it has only been one week. She is the perfect control case because of her Alzheimer’s. All I can say is that her life has improved, therefore mine has improved – Happy Thanksgiving!

We are taking the 6 drops 3 to 4 times a day. My blood sugar is in the 70’s, making me hungry, but not gaining weight. I don’t think I have ever tested that low. Along with Alzheimer’s, she has Parkinson’s. Her knees are becoming straighter and her heels are flatter making it easier for her to walk. I don’t know how this is all connected, but her skin, and mine have improved too. Her mobility is more work for me, but it is a welcome change. I do worry about her falling.

She is due for an A1C test, so I can get the formal approval of ‘no more insulin’. Her doctor and I understand each other. My mother has always preferred supplements to drugs, so I have continued her wishes. Not only is she talking and making some sense, but she is reading again.

Looking forward to a wonderful Christmas!

Now, this is weird, because I always heard that a ganglion cyst is a mechanical problem, not a bacterial one. Nevertheless, whenever I take a course of MMS, the ganglion that I’ve had for years on the back of my wrist disappears!

The first time this happened, I didn’t even notice it was gone until I was done with the three-week course. Nevertheless, I knew it wasn’t just a coincidence. A couple of months later it slowly started growing back. It’s not a big cyst but it does hurt a bit. The next time I started an MMS course (I do the one that’s two or three drops every hour for eight hours a day) I watched it and saw that in three or four days it flattened out.

Unfortunately, I irritated my throat by drinking my MMS doses one day in a water bottle, which is a new method I’m not sure about. Somehow, the gas built up in the bottle. Maybe I let it wait too long before adding water, or maybe it got too warm in the car. In any case, I decided to cut the course short and try again later. This time, the cyst came back in a couple of weeks.

I have the feeling that if I took MMS every day as Jim recommends for a maintenance dose for older people, that my ganglion cyst would never reappear. But I’d have to have a better reason than that to take MMS orally every day!

I wonder if the cyst isn’t some opportunistic bacteria that colonizes a weakened area, and the MMS attacks it. Now that I’ve heard Bruce’s lecture on using DMSO to carry it in through the skin, I’m going to try that more direct route. (I use medical-grade DMSO).

Since the medical procedure to get rid of a ganglion cyst involves needle aspiration and drugs, and STILL doesn’t get rid of the cyst permanently, oral MMS works at least as well as that! And we can do it ourselves!