Most Recent Testimonials

The following testimonial is excerpted from pages 429-431 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.

Hi Kerri,

First of all a HUGE big thank you for what you are doing with our children! My daughter has been on MMS two weeks now and she is like a different child!!!!!!!! Every day she gets better…By leaps and bounds. She WILL be one of your recovered ones 😉

UPDATE:

My daughter has now been on MMS for three weeks. ATEC down from 78 to 44. This IS a miracle. We have been in absolute desperation for almost three years trying to figure out what in the world is going on with our child. After hundreds of thousands of dollars, experts all over the world, LA, New York, San Fransisco… and nothing would work. Minor improvements but nothing that I could say really worked. Everyone always agreed that she probably does not have “autism” but what is making her behave that way?!?!?! So a long story short… If I could I would wrap my arms around all of you helping my daughter and so many others through MMS until I was sure you truly understand what your dedication means and that you are saving lives…literally <3 This is by far the biggest thing that has ever happened to my family. We are forever thankful.

UPDATE #2

I sent you my daughter’s ATEC a week ago but redid it today. We started MMS in December and I decided I will do the test every month. Here are the results, 4 more points gone!!!! In 1 month from 78 to 40… Almost half off!!!!!! Her team is blown away 😉 all we need now is that language score to come down… Kerri my goal is to have her recovered by A1!!!

Update #3

We are seeing such amazing improvements every single day. I think the true testament is the daily feedback from people working with her who do not know we are doing MMS. Here is part of a note from her SLP “ her communication on the whole is truly remarkable- words, iPad, eye contact…everything is improving!!!!!!! So exciting. Has anyone told you lately that your daughter is a superstar? You should be so proud. :)” And I am…

Our main challenge has always been anxiety and today we had a breakthrough on that front. Instead of clinging to me for her dear life when I separate from her at school she took her friends hand, waived AND said goodbye and walked away… Here is the best part, she then turned her head, waived and gave me the biggest smile . Her face at that moment is forever engraved to my heart.

Also for the first time EVER my son was able to have a friend come over from school in our car without her having a major meltdown. Instead she shared her iPad with the friend to show him her program and use it TOGETHER!

Honestly I think our major challenge at the moment is for the rest of the family to heal with her… We had lost all hope and settled for life with Autism. We can now look at the future very differently and actually look forward to it! Love our new life

UPDATE #4

I have never really posted gains but this is too huge not to share. We started MMS 3,5 months ago and at that point I could hardly take my daughter to

the grocery store. And even if I did it was a guaranteed meltdown. Well we

just got home from a two week long vacation that included travel by air, time difference, different language, going from hot weather to freezing temps and piles of snow, totally different foods, nothing but strangers to her, visit after visit to new places… The list goes on and on. The BEST part – the vacation was full of excitement, fun, laughter and happiness every single day I have to pinch myself to believe this is my life after such a short time on MMS. Thank you all for your support and guidance I have my life back and can’t wait for the future now! We still have a looooong way to go but we’ll get there.

Today is a wonderful day already.

The following testimonial is excerpted from pages 428-429 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.

Drum roll please…….my son is 17 years old. He’s been on mms for 5 months now, I’m so excited I don’t even know, could it be 6? I think we started late July.

He started with a 63…….he is now a 7. He went from 63 to 25 in just a few weeks, then a 13 a couple months later, now a 7. I feel like I’m cheating every time. I go back and look, argue with myself, nitpick….but whether he’s a 5, 7 or 9, it’s nothing short of a miracle because just one year ago, he was WAY over 100. The ATEC is not perfect, not even close. There are things that the ATEC does not show. All that is true, but this is incredible improvement that no doctor I know would have ever been able to accomplish. Been there, did that, spent the 425K+.

And no, it’s not just MMS, but that has been the main treatment and everything else we do supports MMS and general health because I believe that in the end, it’s a battle between your immune system…and all that’s attacking it. We are winning and I sure do wish they would STOP CALLING IT AUTISM. That alone hurts so many.

Here’s a little background on my son: Matthew was very high functioning from age 6-12. That was after diet since 3, floortime play therapy, some aba, AIT, IVIG, chelation for a year, OIG, years of infusions of glutathione, vitamin C, B-com, etc…immune stuff. Then he did very well GFCF ages 6-12, ran track (very well), 2nd degree black belt, boxing lessons, etc….Then puberty hit, and what I did not know about, Lyme and co-infections RAGED, and for around 3 years, I lost him cognitively, worse, worse, worse. At 15, he was like an advanced Alzheimer’s patient, ADVANCED, he had lost ALL short-term memory, it was horrible, he struggled to think and could not.

He became more and more violent; choking me, kicking me, did I say he was a blackbelt? Even though he lost everything cognitively, like the ability to answer a question, those karate skills popped back into his head and he nearly killed me…. really close a couple times.

That was a year ago when his ATEC was over 100. So, here’s what worked: 1. Low amylose diet helped with the constant urinating. (he acted like a diabetic and had 14 of 16 PANDAS symptoms so auto-immune) 2. Biofeedback helped calm him some. 3. Cholestyramine helped him psychologically – I could see him clear up mentally in minutes. (chemical/mold/dust sensitivities big time) By this time, his doc had him on Ketamine for pain. 4. PEMF (pulsed electromagnetic field device) stopped the pain in 6 weeks, got him off of Vicodin, which was not working anyway at double doses, and all the Ketamine. I hated drugging him. Got him off the psych drugs over 6 months time. Then he got a lot better but communication did not really come around until 5. MMS. BAM. Big improvements in communication and PERSONALITY. With MMS, even his laugh changed to a typical sounding teenager’s laugh, and for the first time in years, he can sit still and stop pacing, pacing pacing….the parasites were eating him alive….and now more recently, I know 6. Hydro-colonics is taking us to another level of clear communication. Now there’s lots of spontaneous language.

I write things on Facebook so that I can remember and maybe write a book one day. I don’t care how bad things get, believe me, your kids can get better and it’s amazing, they really do store up all this info that you didn’t think was there. It is there, and they will share it with you one day.

I hope one day Matthew can share his perspective with others. It’s just that it has taken a very long time for us to help him understand that the things he did back then were not in his control so I’m careful not to talk about it. For months he would out of the blue apologize and feel terrible, over and over. Then there’s memories of his dad losing it also….protecting me.

Thankfully, Matthew has blacked out or forgotten a lot of it. He did say he remembers being locked in his room. We had to turn the lock around and sometimes lock him in there. Bad memories. We were all traumatized. But not anymore. He is a different person today but he’s always been the sweetest boy I know. I knew that, even back then. One day, he’ll probably talk more about it.

7yo with baby teeth had an abscess on both sides of his gums underneath the same symmetrical teeth on both sides of the lower jaw.

In 2 weeks with high concentration CDS gargling (never swallowing high concentration) both abscesses have completely flattened out from their original protruding state. High concentration was 6–10 ml CDS in 150 ml filtered water, 3 times a day.

CDS was also consumed orally but only 2 ml in 150 ml filtered water.

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).

The following testimonial is excerpted from page 428 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.

I found Jim on the Internet 2 years ago, and I immediately started Jim’s protocol for MMS. Unfortunately we were so loaded with mercury, so when I reached 8 drops of MMS, and my son 2 drops (after more than 2 months on slow upgrading) we were really sick again. All the heavy metals that were released with MMS could not get out of us. That´s when I found zeolites, and that was our way back.

Now, two years later, my arthritis is gone, and now I know it was MMS that killed the clostridium bacteria that I had been carrying since I was 13 (I am 52 now).

6 months ago my son fell off his bike and got an open wound. It was infected and some hours later the blood was black in his hand. Now I had a choice, to go to the doctor and give him antibiotics, which I knew would kill the bacteria but make him worse, or do it my own way. I gave him 2 x 3 drops of MMS, and the blood was ok in some hours, I thought.

Some days later he started to wave his hand. I thought he had eaten something else that he could not digest, but it got worse. After 4 weeks he was not only waving/flapping both his hands, but also his head. Then I started get suspicious. I tested him for bacteria (I use a Rayonex PS 10 for testing, bioresonance) and I found Clostridium botulism.

Now I had a choice again. I had a fully booked week, but his father came and took him home to his island, where they could use MMS every day and be in a calm environment. He got 2 x 3 drops of MMS, for 6 days. After 3 days his father called and said “Eva this is scary, the flapping is getting worse”. And I smiled and calmed him down, the bacteria are dying and the toxins are being released, I said. The zeolites took care of the toxins, and after 4 week he was ok again.

My lesson in this was, apart from the clostridium toxins, that I also found an imbalance in my son on Condrogenesis with the Rayonex. When I was 13

I stepped on a rusty nail. The blood was poisoned in the foot, but I did not dare tell my parents. After 3 days the whole leg up to my knee was black. I got antibiotics, of course. At 18 I was diagnosed arthritis in my knee. I think I had small amounts of bacteria left, as my son had, and the toxins from clostridium bacteria degenerates the cartilage near the infection. After some years one develop arthritis. I did, but it’s gone now!

Eva, Sweden