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» LymeNet Flash » Questions and Discussion » Medical Questions » MMS test by a natpath via live blood

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Author Topic: MMS test by a natpath via live blood
jamescase20
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Ok, I have been on mms for about 7 days. Def felt like massive herxing the time.

Anyway, this is what we did to "attempt to test" mms.

First, I am on abx too.

My 1st smear showed a few lyme babies, thats about it.

2nd smear, we touched a needle that had a small drop, actually not even a drop. of diluted mms to the blood smear (this is about 1 drop of blood) We guessitmate that it would be about 20x stonger then the bodys level of mms taken as directed.

What we saw was a reaction, and its not scientific and its also not conclusive. And it may be invalid since its not taken via the stomach.

We witnessed tons of bugs come crawling out of the red blood cells, tons.

The smear went from 1-4 lyme babies, to 100s after the mms was applied.

Jim humble the author of the book on mms, said that the MMS is absorbed into the red cells and "taz" comes out to kill them, inside the pathogens feeding grounds, the red cells.

Jim humble also said that MMS stays out of plama unless you use it in IV format.

This test seems to help confirm his claims.

My nathpaths take is similar to mine, she feels that the bugs leaving the cells at such an instantanious rate indicates if not outright killer, certainly a deserving more study, or even perhaps an adjucnt to tx.

Ok, well, my bodys response to MMS so far?

Feels like a massive herx, and I feel like things are turning around faster. I feel I leap frogged into further recovery. I am also using paxil, ceftin, doxy, MMS, and um. prilosec

BTW, the bugs leaving my cells, we tested this on this first smear, waited 24 hours for the blood cells to die, and no come crawled out, so the claims appear true...mms turns your red cells into killer cells. naturally.

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lymie_in_md
Frequent Contributor (1K+ posts)
Member # 14197

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James -- another great post, it is the best research on a supplement many are interested in. I suppose the only way to get some kind of research on it, is to fund it by those with chronic diseases. This includes lyme, morgellons, CFS, MS, parkinsons, ALS, to name some of them. Unless we unite our causes and resources we'll never get the type of information we need to clearly understand how best to utilize this tool and others like it.

--------------------
Bob

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troutscout
Frequent Contributor (5K+ posts)
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So....I forget exactly what this MMS is...some form of chlorine....but what is the name?


Trout [Wink]

--------------------
Now is the time in your life to find the "tiger" within.
Let the claws be bared,
and Lyme BEWARE!!!
www.iowalymedisease.com
[/URL]  -

Posts: 5262 | From North East Iowa | Registered: Sep 2002  |  IP: Logged | Report this post to a Moderator
troutscout
Frequent Contributor (5K+ posts)
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How do you take it, etc?


PM Me please


Trout [Wink]

Major fungal issues....need to get at it.

--------------------
Now is the time in your life to find the "tiger" within.
Let the claws be bared,
and Lyme BEWARE!!!
www.iowalymedisease.com
[/URL]  -

Posts: 5262 | From North East Iowa | Registered: Sep 2002  |  IP: Logged | Report this post to a Moderator
   

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