Treating Autism with MMS - Testimonial (10 of 10)

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.