Re: anyone taking MMS

[Guest guest]

I am taking the MMS myself for a month now to test it for effectiveness against lyme before giving to my son with autism.The first week on MMS was filled with nausea and fatigue.  The second week no nausea but more fatigue plus diarrhea.  The third week less fatigue and less diarrhea.  Now I'm in my fourth week and my bowels are almost normal, the fatigue is gone, and the terrifying and debilitating lyme symptoms are so much better.  I could barely move my head and neck and spine from inflammation and this was building up over the course of a year and reached a crisis point when I started the MMS.It tastes like poison but I am extremely happy with the results so far.   I feel that it works better and faster than salt/c and rife, although I still do both because after what happened to me recently, I want to make sure I'm always a step ahead of the Bb bugs and their friends.I think it's a must to buy the book and educate yourself first (I didn't do this because I was in crisis and couldn't read much), but now that I'm feeling better I've ordered the book.   I think it's a must to start with only 1 drop and then still only drink half of the final solution so that you are only getting half a drop effectively.   I was incapacitated for a day on just one drop.   I'm up to 15 drops now and this is over the course of 4 weeks but I've heard that many cannot tolerate the higher doses so be sure to individualize the protocol. Hope this helps.LydiaMMS stands for Miracle Mineral Supplement.   I was at an autism summit (think tank of sorts) with some absolutely fabulous and famous doctors.  One doctor pulled me aside and said that this product- he's seen incredible results with kids on the spectrum.  I'm not recommending it because I don't know any more than this...but he was adamant.   So I'm wondering if anyone on this board is using it and if you can share? Also...it made the short list of things to consider because it's dirt cheap....he said like $20 per year! Tami DuncanPresident and Co-Founderwww.liafoundation.orgPlease help our mission of research, awareness and education by participating in our "Holiday Giving Program" Click here for details: http://www.firstgiving.com/liafoundation For online shopping at your favorite stores, join iGive and a donation will go to LIAF just by shopping for the Holiday's. http://www.iGive.com/LIAFoundationDelicious ideas to please the pickiest eaters. Watch the video on AOL Living.

[Guest guest]

May I ask what book you are referring to? Thanks, Lydia Flynn wrote: I am taking the MMS myself for a month now to test it for effectiveness against lyme before giving to my son with autism. The first week on MMS was filled with nausea and fatigue. The second week no nausea but more fatigue plus diarrhea. The third week less fatigue and less diarrhea. Now I'm in my fourth week and my bowels are almost normal, the

fatigue is gone, and the terrifying and debilitating lyme symptoms are so much better. I could barely move my head and neck and spine from inflammation and this was building up over the course of a year and reached a crisis point when I started the MMS. It tastes like poison but I am extremely happy with the results so far. I feel that it works better and faster than salt/c and rife, although I still do both because after what happened to me recently, I want to make sure I'm always a step ahead of the Bb bugs and their friends. I think it's a must to buy the book and educate yourself first (I didn't do this because I was in crisis and couldn't read much), but now that I'm feeling better I've ordered the book. I think it's a must to start with only 1 drop and then still only drink half of the final solution so that you are only getting

half a drop effectively. I was incapacitated for a day on just one drop. I'm up to 15 drops now and this is over the course of 4 weeks but I've heard that many cannot tolerate the higher doses so be sure to individualize the protocol. Hope this helps. Lydia Delicious ideas to please the pickiest eaters. Watch the video on AOL Living.

Never miss a thing. Make Yahoo your homepage.

[Guest guest]

It's the inventor of MMS , Jim Humble's  book.   It's called "Breakthrough".   The website is www.miraclemineral.org.  I ordered my MMS from www.globallight.net  and I ordered the citric acid powder from bulkfoods.com My son is doing the Cowden herbal protocol right now (into the 5th month) so I'm going to finish the protocol through the sixth month and then start him on the MMS provided I continue to do well with it.    LydiaMay I ask what book you are referring to?Thanks, Lydia Flynn <bflynn2optonline (DOT) net> wrote:I am taking the MMS myself for a month now to test it for effectiveness against lyme before giving to my son with autism.The first week on MMS was filled with nausea and fatigue.  The second week no nausea but more fatigue plus diarrhea.  The third week less fatigue and less diarrhea.  Now I'm in my fourth week and my bowels are almost normal, the fatigue is gone, and the terrifying and debilitating lyme symptoms are so much better.  I could barely move my head and neck and spine from inflammation and this was building up over the course of a year and reached a crisis point when I started the MMS.It tastes like poison but I am extremely happy with the results so far.   I feel that it works better and faster than salt/c and rife, although I still do both because after what happened to me recently, I want to make sure I'm always a step ahead of the Bb bugs and their friends.I think it's a must to buy the book and educate yourself first (I didn't do this because I was in crisis and couldn't read much), but now that I'm feeling better I've ordered the book.   I think it's a must to start with only 1 drop and then still only drink half of the final solution so that you are only getting half a drop effectively.   I was incapacitated for a day on just one drop.   I'm up to 15 drops now and this is over the course of 4 weeks but I've heard that many cannot tolerate the higher doses so be sure to individualize the protocol. Hope this helps.LydiaDelicious ideas to please the pickiest eaters. Watch the video on AOL Living.Never miss a thing. Make Yahoo your homepage.

[Guest guest]

Interesting...well maybe it's something to keep on our radar and see how people are doing on it. Thanks everyone for sharing.

Tami DuncanPresident and Co-Founderwww.liafoundation.orgPlease help our mission of research, awareness and education by participating in our "Holiday Giving Program" Click here for details: http://www.firstgiving.com/liafoundation For online shopping at your favorite stores, join iGive and a donation will go to LIAF just by shopping for the Holiday's. http://www.iGive.com/LIAFoundation

I ordered it for my daughter who has lyme and autism. I took it myself first to judge the side effects. I started with the 2 drop level and worked up to 6 drops a day before I had a 24 hour herx reaction that felt flu like. What it did was clear up a herpes infection that would come and go under stress. It caused the herpes spot to flare up, then bleed briefly, then go into remission which seems to be lasting, about 6 weeks now. I haven't started my daughter yet but I intend to do so.Kay-- In BorreliaMultipleInfectionsAndAutism , Lydia Flynn wrote:>> It's the inventor of MMS , Jim Humble's book. It's called > "Breakthrough". The website is www.miraclemineral.org. I ordered > my MMS from www.globallight.net and I ordered the citric acid powder > from bulkfoods.com> > My son is doing the Cowden herbal protocol right now (into the 5th > month) so I'm going to finish the protocol through the sixth month > and then start him on the MMS provided I continue to do well with it.> > Lydia> > > > > >> > May I ask what book you are referring to?> > Thanks,> > > >> > Lydia Flynn wrote:> > I am taking the MMS myself for a month now to test it for > > effectiveness against lyme before giving to my son with autism.> >> > The first week on MMS was filled with nausea and fatigue. The > > second week no nausea but more fatigue plus diarrhea. The third > > week less fatigue and less diarrhea. Now I'm in my fourth week and > > my bowels are almost normal, the fatigue is gone, and the > > terrifying and debilitating lyme symptoms are so much better. I > > could barely move my head and neck and spine from inflammation and > > this was building up over the course of a year and reached a crisis > > point when I started the MMS.> >> > It tastes like poison but I am extremely happy with the results so > > far. I feel that it works better and faster than salt/c and rife, > > although I still do both because after what happened to me > > recently, I want to make sure I'm always a step ahead of the Bb > > bugs and their friends.> >> > I think it's a must to buy the book and educate yourself first (I > > didn't do this because I was in crisis and couldn't read much), but > > now that I'm feeling better I've ordered the book. I think it's a > > must to start with only 1 drop and then still only drink half of > > the final solution so that you are only getting half a drop > > effectively. I was incapacitated for a day on just one drop. > > I'm up to 15 drops now and this is over the course of 4 weeks but > > I've heard that many cannot tolerate the higher doses so be sure to > > individualize the protocol.> >> > Hope this helps.> >> > Lydia> >> >> >> >> >> Delicious ideas to please the pickiest eaters. Watch the video on > >> AOL Living.> >>> >> >> >> > Never miss a thing. Make Yahoo your homepage.> >> >> Delicious ideas to please the pickiest eaters. Watch the video on AOL Living.

[Guest guest]

I ordered it for my daughter who has lyme and autism. I took it

myself first to judge the side effects. I started with the 2 drop

level and worked up to 6 drops a day before I had a 24 hour herx

reaction that felt flu like. What it did was clear up a herpes

infection that would come and go under stress. It caused the herpes

spot to flare up, then bleed briefly, then go into remission which

seems to be lasting, about 6 weeks now. I haven't started my daughter

yet but I intend to do so.

Kay

-- In BorreliaMultipleInfectionsAndAutism , Lydia

Flynn wrote:

>

> It's the inventor of MMS , Jim Humble's book. It's called

> " Breakthrough " . The website is www.miraclemineral.org. I

ordered

> my MMS from www.globallight.net and I ordered the citric acid

powder

> from bulkfoods.com

>

> My son is doing the Cowden herbal protocol right now (into the 5th

> month) so I'm going to finish the protocol through the sixth month

> and then start him on the MMS provided I continue to do well with

it.

>

> Lydia

>

>

>

>

> >

> > May I ask what book you are referring to?

> > Thanks,

> >

> >

> > Lydia Flynn wrote:

> > I am taking the MMS myself for a month now to test it for

> > effectiveness against lyme before giving to my son with autism.

> >

> > The first week on MMS was filled with nausea and fatigue. The

> > second week no nausea but more fatigue plus diarrhea. The third

> > week less fatigue and less diarrhea. Now I'm in my fourth week

and

> > my bowels are almost normal, the fatigue is gone, and the

> > terrifying and debilitating lyme symptoms are so much better. I

> > could barely move my head and neck and spine from inflammation

and

> > this was building up over the course of a year and reached a

crisis

> > point when I started the MMS.

> >

> > It tastes like poison but I am extremely happy with the results

so

> > far. I feel that it works better and faster than salt/c and

rife,

> > although I still do both because after what happened to me

> > recently, I want to make sure I'm always a step ahead of the Bb

> > bugs and their friends.

> >

> > I think it's a must to buy the book and educate yourself first

(I

> > didn't do this because I was in crisis and couldn't read much),

but

> > now that I'm feeling better I've ordered the book. I think it's

a

> > must to start with only 1 drop and then still only drink half of

> > the final solution so that you are only getting half a drop

> > effectively. I was incapacitated for a day on just one drop.

> > I'm up to 15 drops now and this is over the course of 4 weeks

but

> > I've heard that many cannot tolerate the higher doses so be sure

to

> > individualize the protocol.

> >

> > Hope this helps.

> >

> > Lydia

> >

> >

> >

> >

> >> Delicious ideas to please the pickiest eaters. Watch the video

on

> >> AOL Living.

> >>

> >

> >

> >

> > Never miss a thing. Make Yahoo your homepage.

> >

> >

>

[Guest guest]

Hi, my son is 32, with downs syndrome and autism and was diagnosed with

early onset dementia.

I am trying the drops myself. Am up to 13 drops once a day. When you

get into the book, it says you actually need to be building up to 15

drops finally three times a day, for a week, before dropping back to a

maintenance dose of 6 drops a couple times a week. Its tricky for me to

get in multiple dosings, since

you can't take vitamin c with the drops. Ascorbic acid deactivates the

drops. I use mega doses of ascorbic acid at this point, so take the

vitamin c in an eight hour window, from 12 hours after the drops, till 4

hours prior to the next dose of drops. Jim Humble suggests 3-4 hours

after last ascorbic acid (powder/supplement, or even orange juice or any

juice with added vitamin c). Once you take the drops they are active

for about 12 hours, most intensely so for first 2 hours, but then

continues for another 10 hours, and the continued work will be stopped

by vitamin c. The good news is that the ascorbic acid will counteract

the drops, if you accidentally get too much for some reason, or simply

get too sick from them. Some people don't get nauseus or diarhea at

all, others get quite sick. When you do, he suggests backing off a few

drops, staying on lower dose a little longer, gradually building up to

the higher dose. One other thing is that the dose is for an average

adult. For a child or for a heavy adult, the dose that you are building

up to should be 3 drops for each 25 pounds. You need to get the book -

first part, with directions for use, is free, available from

http://www.miraclemineral.com Second part, with more in depth

instructions costs 10 bucks. But you really need to read the book, get

the thorough instructions.

I'll be slowly starting my son after I get up to one dose of 15 drops.

I'll let folks know what I see.

Sara

[Guest guest]

I believe in the product and took it for two months. I believe it

works for a lot of pathogens and it works for awhile on fungi. The

only thing I would add is that I heard from another MD that fungi can

build a resistance to it and I ran it by my MD and she said that it

made sense. I told her how I sincerely felt that it lowered my

pathogen burden and helped my immune system in the process.

I will not take antibiotics again as I have the MMS and will try that

first before anything else. I am also taking Oil of Oregano for

awhile in case I still have colonization of mold in my body. I will

then go back to MMS again for another round. Although I am not

totally healed because I have Secondary Adrenal Insufficiency from

mold exposure I believe this product is something everyone should

look into as something they have in their medicine cabinet (my

opinion). I have a life time supply and I have not been sick since I

started taking it.

Also mold releases mycotoxins and mycotoxins = antibiotics (some).

For me antibiotics are not an option as I have an inability to filter

these toxins.

It is good that this product is getting out there from doctors. I'm

happy about that.

>

> MMS stands for Miracle Mineral Supplement. I was at an autism

summit

> (think tank of sorts) with some absolutely fabulous and famous

doctors. One

> doctor pulled me aside and said that this product- he's seen

incredible results

> with kids on the spectrum.

>

> I'm not recommending it because I don't know any more than

this...but he was

> adamant. So I'm wondering if anyone on this board is using it

and if you

> can share?

>

> Also...it made the short list of things to consider because it's

dirt

> cheap....he said like $20 per year!

>

> Tami Duncan

>

> President and Co-Founder

> _www.liafoundation.org_ (http://www.liafoundation.org/)

>

> Please help our mission of research, awareness and education by

> participating in our " Holiday Giving Program " Click here for

details:

> _http://www.firstgiving.com/liafoundation_

(http://www.firstgiving.com/liafoundation)

>

> For online shopping at your favorite stores, join iGive and a

donation will

> go to LIAF just by shopping for the Holiday's.

> _http://www.iGive.com/LIAFoundation_

(http://www.iGive.com/LIAFoundation)

>

>

>

> **************Ideas to please picky eaters. Watch video on AOL

Living.

> (http://living.aol.com/video/how-to-please-your-picky-eater/rachel-

campos-duffy/

> 2050827?NCID=aolcmp00300000002598)

>

[Guest guest]

Could you expand on the absorbic acid vs citric acid? I thought all

citrus fruit contained Vit. C But the following quote is from the

directions on the MMS web site and why would Vit. C deactivate the

drops if it needs citric acid to activate it?

" Always activate the MMS drops with one of the food acids, either lemon

juice drops, or lime juice drops, or citric acid solution drops (to

make citric acid solution add 1 level tablespoon of citric acid and 9

tablespoons of water. "

If it gets results I have no problem giving this a try and not giving

vitamin C, I am just confused about why orange juice is bad but lemon

or lime juice would be okay.

Thanks,

Sue

>

Its tricky for me to get in multiple dosings, since you can't take

vitamin c with the drops. Ascorbic acid deactivates the drops. I use

mega doses of ascorbic acid at this point, so take the vitamin c in an

eight hour window, from 12 hours after the drops, till 4 hours prior to

the next dose of drops. Jim Humble suggests 3-4 hours after last

ascorbic acid (powder/supplement, or even orange juice or any juice

with added vitamin c).

> Sara

>

[Guest guest]

>Could you expand on the absorbic acid vs citric acid? I thought all

citrus fruit contained Vit. C But the following quote is from the

directions on the MMS web site and why would Vit. C deactivate the

drops if it needs citric acid to activate it?>

I wondered, too. Citric acid is not the same thing as ascorbic acid,

though all citrus fruits

contain some of both. Orange juice has higher level of vitamin c than

do lemon and lime

apparently, or perhaps he is talking about frozen or reconstituted

orange juice, which always

has additional ascorbic acid added. Orange juice, even fresh, does also

not have the

needed citric acid to activate the MMS. Apparently in lemon and lime it

is at a much higher

level and works more effectively in the activation. In part 2 of the

book, the part you have

to pay for, he goes on to say that further studies have shown that the

pure citric acid

solution is far more effective in activating the MMS than the lemon,

lime, or vinegar. It is

the preferred activator. The citric acid in some form is necessary for

the activation. Any ascorbic

acid present limits the effectiveness of the drops, and at high enough

levels will deactivate them

completely. I don't pretend to understand the chemistry. It is easy to

demonstrate though.

I use 10 % citric acid solution (one tablespoon of citric acid - you can

buy at a health food store - to

nine tablespoons of distilled water). You can see and smell when the

drops become activated.

Add a few drops of a similar ascorbic acid solution and the solution is

deactivated. Jim Humble,

the fellow who discovered these drops, says that leaving three to four

hours after the last

ascorbic acid supplement or any juice or food with added ascorbic acid,

is sufficient to cause no

interference with taking the drops. Hope that helps. Sara