MMS users

[Guest guest]

anyone doin MMS can you share what company you bought it from?

i have used MMS in the past but am thinking about trying a new bottle as i saw

some negatives with the one I have... i have heard the MMS can difer depending

on who made it. so im hopin to find a better experience with new company.

thank you guys.

channa

[Guest guest]

I wonder if I could get that info please too .we have used .MMS in the past and I think will revisit it even if its just for oral hygieneThanksLet your email find you with BlackBerry® from VodafoneSender: mb12valtrex Date: Tue, 13 Mar 2012 11:58:57 -0000To: <mb12valtrex >ReplyTo: mb12valtrex Subject: Re: MMS users Hi Channa, I can email you a link to the 2 US sources recommended by the MMS expert. If you are on FB, friend me I go by Madre Orion. I will add you to the secret MMS group. She now has 28 recovered.>> anyone doin MMS can you share what company you bought it from?> i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.> thank you guys.> channa>

[Guest guest]

thank you so much Caryn!!!

i cant go on facebook for safety reasons....which really stinks as i feel like i miss out on a lot of support that way..

yes if you could send me the 2 links I would be so grateful.......i am just barely keeping my sons PANDA like symptoms under control with the strongest natural bacteria fighters and the strongest natural antinflammatorys....

I am really desperate at this point as I dont do RX and I need something strong enuff that could tackle this bacteria issue he has...he is becoming violent and aggressive and i am beyond desperate to help him at this point..

channa

To: mb12valtrex Sent: Tuesday, March 13, 2012 7:58 AMSubject: Re: MMS users

Hi Channa, I can email you a link to the 2 US sources recommended by the MMS expert. If you are on FB, friend me I go by Madre Orion. I will add you to the secret MMS group. She now has 28 recovered.>> anyone doin MMS can you share what company you bought it from?> i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.> thank you guys.> channa>

[Guest guest]

Hi,I got it from: http://www.mineral-solutions.net/mms-1No problems whatsoever, it even passed customs(its banned in canada for oral consumption) with no extra charge (canada).Remember to use the protocol: http://autismo2.com/protocolos.htmlThere are reported around 20 recoveries with this, along with taking minerals, probiotics, clay baths, GFCFSF diet, therapy and whatever your child lacks, like carnitine or food sensitivities and things like that, but, the less supplements the better.If you get too dizzy, just back up or have some vitamin c to cut

the effect, I got dizzy just one time and just ate something and I felt super fine afterwards. I've seen many improvements with this in my son, but my husband didn't like the idea of giving it for too long(5 months) and he also believes that mms could oxidize our son's body more, so now we are taking a break. You have to take a lot of time to give this thing so many times per day, but it is worth it.When giving MMS remember to give probiotics, theralac and custom probiotics d-lactate are the ones I give.Just my situation here.Sasha To: "mb12valtrex " <mb12valtrex > Sent: Tuesday, March 13, 2012 8:59:25 AM Subject: Re: Re: MMS users

thank you so much Caryn!!!

i cant go on facebook for safety reasons....which really stinks as i feel like i miss out on a lot of support that way..

yes if you could send me the 2 links I would be so grateful.......i am just barely keeping my sons PANDA like symptoms under control with the strongest natural bacteria fighters and the strongest natural antinflammatorys....

I am really desperate at this point as I dont do RX and I need something strong enuff that could tackle this bacteria issue he has...he is becoming violent and aggressive and i am beyond desperate to help him at this point..

channa

To: mb12valtrex Sent: Tuesday, March 13, 2012 7:58 AMSubject: Re: MMS users

Hi Channa, I can email you a link to the 2 US sources recommended by the MMS expert. If you are on FB, friend me I go by Madre Orion. I will add you to the secret MMS group. She now has 28 recovered.>> anyone doin MMS can you share what company you bought it from?> i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.> thank you guys.> channa>

[Guest guest]

thank you sasha!

[Guest guest]

Hi sashaWhen you say recoveries do you mean from autismLet your email find you with BlackBerry® from VodafoneSender: mb12valtrex Date: Tue, 13 Mar 2012 08:51:07 -0700 (PDT)To: mb12valtrex <mb12valtrex >ReplyTo: mb12valtrex Subject: Re: Re: MMS users Hi,I got it from: http://www.mineral-solutions.net/mms-1No problems whatsoever, it even passed customs(its banned in canada for oral consumption) with no extra charge (canada).Remember to use the protocol: http://autismo2.com/protocolos.htmlThere are reported around 20 recoveries with this, along with taking minerals, probiotics, clay baths, GFCFSF diet, therapy and whatever your child lacks, like carnitine or food sensitivities and things like that, but, the less supplements the better.If you get too dizzy, just back up or have some vitamin c to cutthe effect, I got dizzy just one time and just ate something and I felt super fine afterwards. I've seen many improvements with this in my son, but my husband didn't like the idea of giving it for too long(5 months) and he also believes that mms could oxidize our son's body more, so now we are taking a break. You have to take a lot of time to give this thing so many times per day, but it is worth it.When giving MMS remember to give probiotics, theralac and custom probiotics d-lactate are the ones I give.Just my situation here.Sasha To: "mb12valtrex " <mb12valtrex > Sent: Tuesday, March 13, 2012 8:59:25 AM Subject: Re: Re: MMS users thank you so much Caryn!!!i cant go on facebook for safety reasons....which really stinks as i feel like i miss out on a lot of support that way..yes if you could send me the 2 links I would be so grateful.......i am just barely keeping my sons PANDA like symptoms under control with the strongest natural bacteria fighters and the strongest natural antinflammatorys....I am really desperate at this point as I dont do RX and I need something strong enuff that could tackle this bacteria issue he has...he is becoming violent and aggressive and i am beyond desperate to help him at this point..channaTo: mb12valtrex Sent: Tuesday, March 13, 2012 7:58 AMSubject: Re: MMS users Hi Channa, I can email you a link to the 2 US sources recommended by the MMS expert. If you are on FB, friend me I go by Madre Orion. I will add you to the secret MMS group. She now has 28 recovered.>> anyone doin MMS can you share what company you bought it from?> i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.> thank you guys.> channa>

[Guest guest]

Hi sasha,I just read about MMS and my mind is exploding with all the stuff that is out there, I'm chelating my son with AC protocol can I use MMS?and when do you use MMS2?I was about to buy Immusist and now this MMS makes me think which one I should do first.Thanks Lili From: S M

To: "mb12valtrex " <mb12valtrex > Sent: Tuesday, March 13, 2012 11:51 AM Subject: Re: Re: MMS users

Hi,I got it from: http://www.mineral-solutions.net/mms-1No problems whatsoever, it even passed customs(its banned in canada for oral consumption) with no extra charge (canada).Remember to use the protocol: http://autismo2.com/protocolos.htmlThere are reported around 20 recoveries with this, along with taking minerals, probiotics, clay baths, GFCFSF diet, therapy and whatever your child lacks, like carnitine or food sensitivities and things like that, but, the less supplements the better.If you get too dizzy, just

back up or have some vitamin c to cut

the effect, I got dizzy just one time and just ate something and I felt super fine afterwards. I've seen many improvements with this in my son, but my husband didn't like the idea of giving it for too long(5 months) and he also believes that mms could oxidize our son's body more, so now we are taking a break. You have to take a lot of time to give this thing so many times per day, but it is worth it.When giving MMS remember to give probiotics, theralac and custom probiotics d-lactate are the ones I give.Just my situation here.Sasha To: "mb12valtrex " <mb12valtrex > Sent: Tuesday, March 13, 2012 8:59:25 AM Subject: Re: Re: MMS users

thank you so much Caryn!!!

i cant go on facebook for safety reasons....which really stinks as i feel like i miss out on a lot of support that way..

yes if you could send me the 2 links I would be so grateful.......i am just barely keeping my sons PANDA like symptoms under control with the strongest natural bacteria fighters and the strongest natural antinflammatorys....

I am really desperate at this point as I dont do RX and I need something strong enuff that could tackle this bacteria issue he has...he is becoming violent and aggressive and i am beyond desperate to help him at this point..

channa

To: mb12valtrex Sent: Tuesday, March 13, 2012 7:58 AMSubject: Re: MMS users

Hi Channa, I can email you a link to the 2 US sources recommended by the MMS expert. If you are on FB, friend me I go by Madre Orion. I will add you to the secret MMS group. She now has 28 recovered.>> anyone doin MMS can you share what company you bought it from?> i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.> thank you guys.> channa>

[Guest guest]

Hi sasha,What improvements did you see with it,we gave it for a few months but did not notice anything much having said that it does deal with yeast well, I think our sons problem is that where a lot of things help him detox it just becomes overload and he can't get it out of his system despite all the liver kidney lymph adrenal support. Our son is 8 next week still non verbal,just love to hear what good things you seenLet your email find you with BlackBerry® from VodafoneSender: mb12valtrex Date: Tue, 13 Mar 2012 09:29:42 -0700 (PDT)To: mb12valtrex <mb12valtrex >ReplyTo: mb12valtrex Subject: Re: Re: MMS users Hi sasha,I just read about MMS and my mind is exploding with all the stuff that is out there, I'm chelating my son with AC protocol can I use MMS?and when do you use MMS2?I was about to buy Immusist and now this MMS makes me think which one I should do first.Thanks Lili To: "mb12valtrex " <mb12valtrex > Sent: Tuesday, March 13, 2012 11:51 AM Subject: Re: Re: MMS users Hi,I got it from: http://www.mineral-solutions.net/mms-1No problems whatsoever, it even passed customs(its banned in canada for oral consumption) with no extra charge (canada).Remember to use the protocol: http://autismo2.com/protocolos.htmlThere are reported around 20 recoveries with this, along with taking minerals, probiotics, clay baths, GFCFSF diet, therapy and whatever your child lacks, like carnitine or food sensitivities and things like that, but, the less supplements the better.If you get too dizzy, justback up or have some vitamin c to cutthe effect, I got dizzy just one time and just ate something and I felt super fine afterwards. I've seen many improvements with this in my son, but my husband didn't like the idea of giving it for too long(5 months) and he also believes that mms could oxidize our son's body more, so now we are taking a break. You have to take a lot of time to give this thing so many times per day, but it is worth it.When giving MMS remember to give probiotics, theralac and custom probiotics d-lactate are the ones I give.Just my situation here.Sasha To: "mb12valtrex " <mb12valtrex > Sent: Tuesday, March 13, 2012 8:59:25 AM Subject: Re: Re: MMS users thank you so much Caryn!!!i cant go on facebook for safety reasons....which really stinks as i feel like i miss out on a lot of support that way..yes if you could send me the 2 links I would be so grateful.......i am just barely keeping my sons PANDA like symptoms under control with the strongest natural bacteria fighters and the strongest natural antinflammatorys....I am really desperate at this point as I dont do RX and I need something strong enuff that could tackle this bacteria issue he has...he is becoming violent and aggressive and i am beyond desperate to help him at this point..channaTo: mb12valtrex Sent: Tuesday, March 13, 2012 7:58 AMSubject: Re: MMS users Hi Channa, I can email you a link to the 2 US sources recommended by the MMS expert. If you are on FB, friend me I go by Madre Orion. I will add you to the secret MMS group. She now has 28 recovered.>> anyone doin MMS can you share what company you bought it from?> i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.> thank you guys.> channa>

[Guest guest]

Please email me, too. Unfortunately, I just purchased some over the web last night so I hope I got the right stuff.sally To: mb12valtrex Sent: Tuesday, March 13, 2012 6:58 AM Subject: Re: MMS users

Hi Channa, I can email you a link to the 2 US sources recommended by the MMS expert. If you are on FB, friend me I go by Madre Orion. I will add you to the secret MMS group. She now has 28 recovered.

>

> anyone doin MMS can you share what company you bought it from?

> i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.

> thank you guys.

> channa

>

[Guest guest]

Wow that's exciting our sons 8. Non verbal will look into getting approved stuff Thanks jLet your email find you with BlackBerry® from VodafoneSender: mb12valtrex Date: Wed, 14 Mar 2012 11:26:43 -0000To: <mb12valtrex >ReplyTo: mb12valtrex Subject: Re: MMS users The reports from the MMS group is that if nothing is happening you might have ineffective MMS or you might be coadministering with something that makes it ineffective, like vitamins or citrus fruit/juice. There are test strips you can buy to make sure your mixture is effective.BTW, on Kerri 's group there are now 18 recovered kids. The kids recovering have been as old as 8 and mostly severe/nonverbal.There is a link to youtube videos with an interview with Kerri . She has pictures of massive biofilm and worms that passed from the bowels of a child after a MMS enema. Fascinating.Caryn> >> > anyone doin MMS can you share what company you bought it from?> > i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.> > thank you guys.> > channa> >>

[Guest guest]

What exactly does this mms do & how do you dose it?Sent from my iPhone

There are moms chelating on the MMS group and they do not coadminister MMS and ALA. I am not sure if they just use on seperate days or just keep doses away by an hour or so. I have heard that DMPS and DMSA are OK with MMS.

> >

> > anyone doin MMS can you share what company you bought it from?

> > i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.

> > thank you guys.

> > channa

> >

>

[Guest guest]

Since MMS is so effect at killing off the bad stuff, I have to wonder if it kills off the good stuff as well.....if that makes sense. Do any doctors recommend MMS? How do you monitor your child on it? Any type of tests/testing used in conjunction with MMS? Is it safe for liver & kidney function? Does it kill off good bacteria along with the bad? I am glad people are having success with it, but I'd need to research it more before giving it to my child. The negative things I have read about it so far through googling are sort of scary. However, there are many positives as well, but the positives seem to be mostly from parents & the guy who discovered it. Any other sources out there??? To: "mb12valtrex " <mb12valtrex > Sent: Wednesday, March 14, 2012 8:03 AM Subject: Re: Re: MMS users

What exactly does this mms do & how do you dose it?Sent from my iPhone

There are moms chelating on the MMS group and they do not coadminister MMS and ALA. I am not sure if they just use on seperate days or just keep doses away by an hour or so. I have heard that DMPS and DMSA are OK with MMS.

> >

> > anyone doin MMS can you share what company you bought it from?

> > i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.

> > thank you guys.

> > channa

> >

>

[Guest guest]

That and the Camel Milk will be big presentations for sure. I hope they stream them live. Thanks for the info! To: mb12valtrex Sent: Wednesday, March 14, 2012 8:52 AM Subject: Re: MMS users

Here is the link to th youtube video with one of the few english speaking interviews with Kerri . This is almost a year old. She discusses 4 recovered kids. The number today is 18.

There is a dosing schedule that I have heard is to start with 1 drop once daily. Then on day 2 give 1 drop twice daily. Then on day 3 give 1 drop three times daily. Keep increasing by 1 drop a day until you get to 8 doses a day. If your child has symptoms of die off, go back to the previous days dose and stay there for several days before trying again. I think for kids over 25 pounds, start increasing to 2 drops, one dose/day for 8 days until you are on 2 drops 8 times daily. For kids over 50 pounds can do the same practice to get to 3 drops per doase. I am not sure if 4 drops is for kids over 75 or 100 pounds. There is also instructions on giving MMS enemas.

Like you, I am researching this protocol and am very interested. However, I have not started my son on this and therefore am not recommending this to others. Just sharing the excitement. I know that many parents feel her presentation is the highlight of the Autism One conference. I am sure the room will be packed.

I think that another mom on this group, , used this and recovered her son. She no longer posts much.

Caryn

> > > >

> > > > anyone doin MMS can you share what company you bought it from?

> > > > i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.

> > > > thank you guys.

> > > > channa

> > > >

> > >

> >

> >

>

[Guest guest]

Thanks caryn,do you mind asking those mom for me why , or maybe I can join the group?ThanksLili To: mb12valtrex Sent: Wednesday, March 14, 2012 7:43 AM Subject:

Re: MMS users

There are moms chelating on the MMS group and they do not coadminister MMS and ALA. I am not sure if they just use on seperate days or just keep doses away by an hour or so. I have heard that DMPS and DMSA are OK with MMS.

> >

> > anyone doin MMS can you share what company you bought it from?

> > i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.

> > thank you guys.

> > channa

> >

>

[Guest guest]

Hi everyone,Like I said I used it for several months with great results, the oral and the enemas, unfortunately there is some people in Spain that started to discredit the MMS, because lets be frank it is said that because it works thru oxidation, many are afraid it can be dangerous for the body(too much oxidative stress, which our kids already have too much), so my husband saw this comments and he asked me to give my son a break, in my family this is how we work things out, we are in this together and we do things that we both agree to. I'm planning to reintroduce it again soon as I think it really fit my son, I never saw any kind of negative side effect.You do have to follow the protocol for MMS, IT DOES NOT INCLUDE MMS2,

DON'T USE IT, JUST MMS1, the liquid that needs to be activated with citric acid right before you drink it.Kerry is a mom of a child in the spectrum that met Dr. Rimland on 2006 and he ask her to translated the DAN protocol to spanish and help the people in latin america. She've tried all kind of things trying to recover her son, and this is far the most successful, according to her comments. She's been attacked by many people for "treating" with MMS (with the guidance of Jim Humble), anyway, she is a great person and has helped my paisanos in Mexico and latin america, she owns a clinic for kids in the spectrum and she doesn't charge a dime,I call her on her phone and she is the nicest person always willing to help, she provides all kinds of therapies when she can and HBOT, and many times she even provides the supplements for poor children, like I said she is no doctor but I guess

that for most parents on this list it is not big deal, we know that a lot of doctors don't have a clue about autism, and many parents have way more knowledge about recovering or at least help with healing. this is her website http://autismo2.com/english.htmlI stopped all supplements before started it, when I did start my son had severe eye stimming and almost no comprehension of language, even when he had a few words. His eye contact came back, his eye stimming went away, his tantrums went away, his stools are not stinky foul like they used to be, he lost almost every food sensitivity(this along with probiotics), it is like a chain, he gets better in something and then something else follows in getting better, He reads now, he is 5 years old. I only gave him MMS, minerals (drops), probiotics(theralac and/or custom probiotics), clay baths and of course a GFCFSF

diet.Again this does not "cure" by itself but it is a big, big help in the road to recovery. Nothing else I tried before worked like this for us, talking about antifungals and antivirals.There are many things out there that help recover our children, I love this list because we are not "canned" in just one option, I understand that our kids are all different, but I do know first hand of children that are recover mainly thanks to MMS.The protocol can be found at Kerri's website, email her, english is her first language.http://autismo2.com/protocolos.htmlSashaPS What MMS does is it kills pathogens, kills virus, parasites, fungus and it crosses the BBB (blood brain barrier) that is why the kids start to lose their "fog" very quickly. The effect it has goes beyond of just killing bad stuff I

wish I could explain it better, but killing bad pathogens is its main thing and from there like I said is like a chain effect, killing fungus helps get rid of metal, etc. It only kills bad stuff, my son never felt better nor look better, like I said I'll start it again, as soon as I convince my husband to do it. To: mb12valtrex Sent: Wednesday, March 14, 2012 8:52:52 AM Subject: Re: MMS users

Here is the link to th youtube video with one of the few english speaking interviews with Kerri . This is almost a year old. She discusses 4 recovered kids. The number today is 18.

There is a dosing schedule that I have heard is to start with 1 drop once daily. Then on day 2 give 1 drop twice daily. Then on day 3 give 1 drop three times daily. Keep increasing by 1 drop a day until you get to 8 doses a day. If your child has symptoms of die off, go back to the previous days dose and stay there for several days before trying again. I think for kids over 25 pounds, start increasing to 2 drops, one dose/day for 8 days until you are on 2 drops 8 times daily. For kids over 50 pounds can do the same practice to get to 3 drops per doase. I am not sure if 4 drops is for kids over 75 or 100 pounds. There is also instructions on giving MMS enemas.

Like you, I am researching this protocol and am very interested. However, I have not started my son on this and therefore am not recommending this to others. Just sharing the excitement. I know that many parents feel her presentation is the highlight of the Autism One conference. I am sure the room will be packed.

I think that another mom on this group, , used this and recovered her son. She no longer posts much.

Caryn

> > > >

> > > > anyone doin MMS can you share what company you bought it from?

> > > > i have used MMS in the past but am thinking about trying a new bottle as i saw some negatives with the one I have... i have heard the MMS can difer depending on who made it. so im hopin to find a better experience with new company.

> > > > thank you guys.

> > > > channa

> > > >

> > >

> >

> >

>

[Guest guest]

I just want to clarify that my son is not recovered yet. we still deal with many social issues, sometimes when he gets sick he turns totally into "autism mode". When I stop something I move to another thing, like right now, when my husband said lets have a break of MMS, now I'm going to try the SCIA protocol, as soon as I get a doctor willing to help.At home I keep on teaching him things. It is like it never ends, we accomplish something and then there is something else I want him to achieve.So the bottom line is that you have to keep doing things, if you tried something and it didn't worked, maybe it was bad timing, some things are worth to try again. And keep up the good work!!

:)Sasha

[Guest guest]

Yes, I agree, you should always research something before you give it to your child.Apparently that is the beauty of this, it won't kill your good probiotics from your gut, it only kills bad stuff, like I said I wish I could explain it better, it has something to do with its strength and the ph and the electricity, that is why you give minerals to help with conduction. It is recommended the quinton isotonic and hypertonic water, is like clean ocean water.There is a scientific the explains this call s Kalcker.Many people also treats cancer with this as it is suppose to work at cellular level and kill the cancer cells with no damage to the normal cells.Sasha To: "mb12valtrex " <mb12valtrex > Sent: Wednesday, March 14, 2012 8:41:55 AM Subject: Re: Re: MMS users

Since MMS is so effect at killing off the bad stuff, I have to wonder if it kills off the good stuff as well.....if that makes sense. Do any doctors recommend MMS? How do you monitor your child on it? Any type of tests/testing used in conjunction with MMS? Is it safe for liver & kidney function? Does it kill off good bacteria along with the bad? I am glad people are having success with it, but I'd need to research it more before giving it to my child. The negative things I have read about it so far through googling are sort of scary. However, there are many positives as well, but the positives seem to be mostly from parents & the guy who discovered it. Any other sources out

there???

[Guest guest]

this is the most amazing group ever and it is because there is so many diffrent ideas, viewpoints from people ..and people are accepting of others beliefs.......

channa

To: "mb12valtrex " <mb12valtrex > Sent: Wednesday, March 14, 2012 10:15 AMSubject: Re: Re: MMS users

[Guest guest]

Thank you for all of the info you provided. I will definitely keep an eye on this and research it more. Do you know if the lectures at Autism One will be streamed? I definitely would like to see the one on MMS.

Yes, I agree, you should always research something before you give it to your child.Apparently that is the beauty of this, it won't kill your good probiotics from your gut, it only kills bad stuff, like I said I wish I could explain it better, it has something to do with its strength and the ph and the electricity, that is why you give minerals to help with conduction. It is recommended the quinton isotonic and hypertonic water, is like clean ocean water.There is a scientific the explains this call s Kalcker.Many people also treats cancer with this as it is suppose to work at cellular level and kill the cancer cells with no damage to the normal cells.Sasha To: "mb12valtrex " <mb12valtrex > Sent: Wednesday, March 14, 2012 8:41:55 AM Subject: Re: Re: MMS users

Since MMS is so effect at killing off the bad stuff, I have to wonder if it kills off the good stuff as well.....if that makes sense. Do any doctors recommend MMS? How do you monitor your child on it? Any type of tests/testing used in conjunction with MMS? Is it safe for liver & kidney function? Does it kill off good bacteria along with the bad? I am glad people are having success with it, but I'd need to research it more before giving it to my child. The negative things I have read about it so far through googling are sort of scary. However, there are many positives as well, but the positives seem to be mostly from parents & the guy who discovered it. Any other sources out

there???

=

[Guest guest]

SCIA? Do share!

I just want to clarify that my son is not recovered yet. we still deal with many social issues, sometimes when he gets sick he turns totally into "autism mode". When I stop something I move to another thing, like right now, when my husband said lets have a break of MMS, now I'm going to try the SCIA protocol, as soon as I get a doctor willing to help.At home I keep on teaching him things. It is like it never ends, we accomplish something and then there is something else I want him to achieve.So the bottom line is that you have to keep doing things, if you tried something and it didn't worked, maybe it was bad timing, some things are worth to try again. And keep up the good work!!

:)Sasha

=

[Guest guest]

I am on many groups and this and the TACA groups are my favorites.

this is the most amazing group ever and it is because there is so many diffrent ideas, viewpoints from people ..and people are accepting of others beliefs.......

channa

To: "mb12valtrex " <mb12valtrex > Sent: Wednesday, March 14, 2012 10:15 AMSubject: Re: Re: MMS users

=

[Guest guest]

Hi all,

We have been " pulsing " MMS, taking breaks to do chelation. My son really has

done well on it. Improvements in eye contact, language. We have only done 2

" rounds " of MMS, one that lasted for 10 days and one for 5 days.

So far I have only gotten him up to 1/2 drop 4x/day. He weighs 32 lbs.

I am taking it with him, as is my NT 7 year old girl. She has made some

improvements on it as well, like better eye contact and interaction.

My brain feels much " younger " since I started the MMS.

Bethany

>

> > this is the most amazing group ever and it is because there is so many

diffrent ideas, viewpoints from people ..and people are accepting of others

beliefs.......

> >

> > channa

> >

> >

> > To: " mb12valtrex " <mb12valtrex >

> > Sent: Wednesday, March 14, 2012 10:15 AM

> > Subject: Re: Re: MMS users

> >

> >

> >

> >

> >

> >

> >

> > TODAY(Beta) • Powered by Yahoo!

> > Youngest Natl. Spelling Bee contestant

> > A 6-year-old spells " vaquero " to snag a spot at the Scripps National

Spelling Bee.

> > Privacy Policy

>

[Guest guest]

bethany, do you do the mms thru the night too? or just day?

To: mb12valtrex Sent: Wednesday, March 14, 2012 7:46 PMSubject: Re: MMS users

Hi all,We have been "pulsing" MMS, taking breaks to do chelation. My son really has done well on it. Improvements in eye contact, language. We have only done 2 "rounds" of MMS, one that lasted for 10 days and one for 5 days.So far I have only gotten him up to 1/2 drop 4x/day. He weighs 32 lbs. I am taking it with him, as is my NT 7 year old girl. She has made some improvements on it as well, like better eye contact and interaction. My brain feels much "younger" since I started the MMS. Bethany>

> > this is the most amazing group ever and it is because there is so many diffrent ideas, viewpoints from people ..and people are accepting of others beliefs.......> > > > channa> > > > > > To: "mb12valtrex " <mb12valtrex > > > Sent: Wednesday, March 14, 2012 10:15 AM> > Subject: Re: Re: MMS users> > > > > > > > > > > > > > > > TODAY(Beta) • Powered by Yahoo!> > Youngest Natl. Spelling Bee contestant> > A 6-year-old spells "vaquero" to snag a spot

at the Scripps National Spelling Bee.> > Privacy Policy>

[Guest guest]

Channa,

Can I just say I love reading all your posts? You are awesome, and I've learned

so much from you.

We dose upon awakening, then 10 am, 1pm, and 4pm. Then I give any supplements

like vitamin c 4 hours later. Here is a really good website that tells you what

foods and supplements interact:

http://bioredox.mysite.com/CLOXhtml/CLOXprot.htm

I'll be really interested to learn more reports from the upcoming events.

I do want to keep adding doses until we get to 8 a day, we're just taking our

sweet time.

Bethany

> >

> > > this is the most amazing group ever and it is because there is so many

diffrent ideas, viewpoints from people ..and people are accepting of others

beliefs.......

> > >

> > > channa

> > >

> > > From: S M <s.ash_a@>

> > > To: " mb12valtrex " <mb12valtrex >

> > > Sent: Wednesday, March 14, 2012 10:15 AM

> > > Subject: Re: Re: MMS users

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > > TODAY(Beta) • Powered by Yahoo!

> > > Youngest Natl. Spelling Bee contestant

> > > A 6-year-old spells " vaquero " to snag a spot at the Scripps National

Spelling Bee.

> > > Privacy Policy

> >

>

[Guest guest]

oh Bethany, you have no idea how good that makes me feel.....i am tryin to get a blog set up where i will have everything i have learned on one site......I want to also do phone consults for the newbies just getting into biomed...I want this to be my lifes work spreading the news and healing other peoples kids as well as my own.

I have a lot of doubts but your words ...really meant a lot right now:)

thank you

channa

To: mb12valtrex Sent: Thursday, March 15, 2012 10:56 AMSubject: Re: MMS users

Channa,Can I just say I love reading all your posts? You are awesome, and I've learned so much from you.We dose upon awakening, then 10 am, 1pm, and 4pm. Then I give any supplements like vitamin c 4 hours later. Here is a really good website that tells you what foods and supplements interact: http://bioredox.mysite.com/CLOXhtml/CLOXprot.htmI'll be really interested to learn more reports from the upcoming events.I do want to keep adding doses until we get to 8 a day, we're just taking our sweet time.Bethany> > > > > this is the most amazing group ever and it is because there is so many diffrent ideas, viewpoints from people ..and people are accepting of others beliefs.......> > > > > > channa> > > > > > From: S M <s.ash_a@>> > > To: "mb12valtrex " <mb12valtrex > > > > Sent: Wednesday, March 14, 2012 10:15 AM> > > Subject: Re: Re: MMS users> > > > > > > > > > > > > > > > > > > > > > > > TODAY(Beta) • Powered by Yahoo!> > > Youngest Natl. Spelling Bee contestant> > > A 6-year-old spells "vaquero" to snag a spot at the Scripps National Spelling Bee.> > > Privacy Policy> >>