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Hello - Hope everyone is doing well!!I have a question - is anyone here using MMS? Where can I get more info? We are considering it for my 7 year old son.Thank you!in MISent from my Verizon Wireless BlackBerrySender: BorreliaMultipleInfectionsAndAutism Date: Thu, 7 Jun 2012 10:07:29 -0400 (EDT)To: <BorreliaMultipleInfectionsAndAutism >ReplyTo: BorreliaMultipleInfectionsAndAutism Subject: Re: Re: Interesting call from the FDA thank heidi, i declined. i never answer phone surveys and this was no exception.you're right, remembering those studies from my psych 101 days.Roseann Re: Interesting call from the FDABy law, people have a right to know about the study they are in, so ask lots of questions. The only things that can be kept from them is stuff that has to be kept from them in order to not influence the results. For example, if you are doing on study on smiling when asked a question, the person can't say, "I'm doing a study on smiling upon asked a question" because that would influence whether or not the person smiles. But. . . .a person can say that it's a study on people's reactions to questions. Anyhow, I say all this to say that you do have the right to decline being in research, and you do have a right to know general information about the study.Love and prayers,Heidi NI just received a call from someone taking a research study on vaccination rates for the FDA. Wanting to talk to the person responsible for any child in the homes vaccination.anyone else receive a call like this?Roseann------------------------------------

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I know there is a secret Facebook page that you need to be invited to. If you

go to the mb12 valtrex Yahoo group, there are a bunch of people there who can

invite you. I bought the MMS, but haven't used it. My husband isn't on board

with the MMS. We're giving our LLMD's protocol a chance to work first. Kerry

seems to have recovered many kids using MMS, so it sounds very tempting.

http://www.genesis2forum.org/media/kunena/attachments/284/MMS_English%20kerri%20\

rivera%20powerpoint.pdf

http://keavyscorner.com/

http://www.health-recovery-info.com/2012/05/mms-curing-autism/

>

> Hello -

>

> Hope everyone is doing well!!

>

> I have a question - is anyone here using MMS? Where can I get more info? We

are considering it for my 7 year old son.

>

> Thank you!

>

> in MI

> Sent from my Verizon Wireless BlackBerry

>

> Re: Interesting call from the

FDA

>

>

> By law, people have a right to know about the study they are in, so ask

> lots of questions. The only things that can be kept from them is stuff

> that has to be kept from them in order to not influence the results.

> For example, if you are doing on study on smiling when asked a question,

> the person can't say, " I'm doing a study on smiling upon asked a

> question " because that would influence whether or not the person

> smiles. But. . . .a person can say that it's a study on people's

> reactions to questions. Anyhow, I say all this to say that you do have

> the right to decline being in research, and you do have a right to know

> general information about the study.

>

> Love and prayers,

>

> Heidi N

>

>

>

> I just received a call from someone taking a research study on

> vaccination rates for the FDA. Wanting to talk to the person responsible

> for any child in the homes vaccination.

>

> anyone else receive a call like this?

>

> Roseann

>

>

> ------------------------------------

>

>

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Guest guest

Hi Everyone..

I actually attended the conference in person.

I have talked Kerri as well email her on and off

Here's the information for the person who want to see on the videos

for th MMS I hope you all watch it and lt me what you guys think

part 1: http://livestre.am/3VW8E

part 2: http://livestre.am/3VWaQ

part 3: http://livestre.am/3VWhx

part 4: http://livestre.am/3VWn5

here the MMS protocol

http://www.autismo2.com/PDF/MMS_English.pdf

and the keycorner to get the MMS is right. I just got my today.

The protcol does say to use Ocean Water abou 20 ML a day forever. Can any one

give me feedback if they are using it

>

> Hello -

>

> Hope everyone is doing well!!

>

> I have a question - is anyone here using MMS? Where can I get more info? We

are considering it for my 7 year old son.

>

> Thank you!

>

> in MI

> Sent from my Verizon Wireless BlackBerry

>

> Re: Interesting call from the

FDA

>

>

> By law, people have a right to know about the study they are in, so ask

> lots of questions. The only things that can be kept from them is stuff

> that has to be kept from them in order to not influence the results.

> For example, if you are doing on study on smiling when asked a question,

> the person can't say, " I'm doing a study on smiling upon asked a

> question " because that would influence whether or not the person

> smiles. But. . . .a person can say that it's a study on people's

> reactions to questions. Anyhow, I say all this to say that you do have

> the right to decline being in research, and you do have a right to know

> general information about the study.

>

> Love and prayers,

>

> Heidi N

>

>

>

> I just received a call from someone taking a research study on

> vaccination rates for the FDA. Wanting to talk to the person responsible

> for any child in the homes vaccination.

>

> anyone else receive a call like this?

>

> Roseann

>

>

> ------------------------------------

>

>

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  • 1 month later...
Guest guest

5-27-12 rm e 918 ‎5-27-12 rm e 918on autism one on Livestream - Watch live streaming Internet TV. Broadcast your own live streaming videos, like autism one in Widescreen HD. Livestream, Be There. http://www.autismo2.com/PDF/MMS_English.pdf To: BorreliaMultipleInfectionsAndAutism Sent: Thursday, August 2, 2012 10:37 AM Subject: Re: Nicotine Patchs

So as per experience, nicotine didn't do much for concentration or hyper...

What is MMS ?

>

> oh no I don't know when we will stop the mms..it's has been nothing but good results. I was answering the e mail regarding the use of the nicotine patches for hyperactivity, concentration, etc....basically used as an ADD drug. We have only been using mms for a month and like I said, nothing but good results. We are not even up to full dosage yet. is on 16/16 drops and he needs to get to 24/24 at least to be on full dosage. There is also a "parasite protocol" with the mms that I have not read yet but I know we are killing parasites. Deb

> Nicotine Patchs

>

>

>

> Hello all,

>

> My son is 6.5 yrs old and autistic.. Last time when we met Dr.klinghardt, I was asking him about his lack of concentration and hyper.. He asked to try Nicotiin patch and also said it will facilitate growth of brain...

>

> Any one using this, then please share your experiences(positive or negative)...I want to try it , but side effect of addiction worries me.

>

> Thanks for help...

>

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The PDF link is already dated. Kerri does not use DMSO anymore. For up to date

information www.MMSAutism.com.

I use MMS so feel free to ask me.

> >

> > oh no I don't know when we will stop the mms..it's has been nothing but good

results. I was answering the e mail regarding the use of the nicotine patches

for hyperactivity, concentration, etc....basically used as an ADD drug. We have

only been using mms for a month and like I said, nothing but good results. We

are not even up to full dosage yet. is on 16/16 drops and he needs to

get to 24/24 at least to be on full dosage. There is also a " parasite protocol "

with the mms that I have not read yet but I know we are killing parasites. Deb

> > Nicotine Patchs

> >

> >

> >

> > Hello all,

> >

> > My son is 6.5 yrs old and autistic.. Last time when we met

Dr.klinghardt, I was asking him about his lack of concentration and hyper.. He

asked to try Nicotiin patch and also said it will facilitate growth of brain...

> >

> > Any one using this, then please share your experiences(positive or

negative)...I want to try it , but side effect of addiction worries me.

> >

> > Thanks for help...

> >

>

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