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Re: Question for Tom

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Hello Tammy,

In studies with rats it was found that chlorite does pass the blood brain

barrier. While this has not been studied in humans, I would be surprised if it

didn't.

One of the concerns with oxidation therapy is oxidation damage. When people are

exposed to high concentrations of chlorine dioxide, they suffer brain impairment

for a while and then the brain seems to go back to normal function. Once

chlorine dioxide enters the body it is quickly transformed to chlorite, so it is

reasonable to speculate that it is able to cross the blood brain barrier. It is

also speculated that long term oxidative damage from chlorite may manifest

itself in a loss of cognitive function.

I think that DMSO is an anti oxidant and that would work against the chlorous

acid solution. There were a series of tests done with MMS and DMSO which were

applied transdermally for treating cancer. I don't believe there was much

success using it.

The studies with rats indicated that chlorite was present in all the organs

within a couple of hours, so I am not sure DMSO is needed. From a chlorite

perspective, I don't think there is much difference between rats and humans...

It is all about the details. Too much and you do oxidative damage. Too little

and it is ineffective. If you get it just right you have the best chance of it

working.

Tom

>

> My one daughter has a lot of mental issues from her infection whether it is

> the Bartonella, Lyme, whatever. She has had huge improvement using the MMS

> but if I understand correctly, MMS does NOT cross the blood-brain barrier.

> I have been reading about another product called DMSO which DOES cross the

> barrier and is said to carry the MMS with it. Could you give me your

> opinion on this? Here are a couple links in case you are not familiar with

this:

> _http://www.dmso.org/articles/information/muir.htm_

> (http://www.dmso.org/articles/information/muir.htm)

> _http://www.bevanpotter.com/DMSO.html_

> (http://www.bevanpotter.com/DMSO.html)

>

> Thanks very much for your help!

> Tammy

>

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Oh thank goodness! To tell the truth I was kind of freaking out about this as

all my infection is in my brain....and people improving with neurolyme disease

on MMS, it just has to cross the BBB.

Tom do you have an opinion as to whether the 30 drops a day target dose is too

much or too little? Is that what most on here are doing?

> >

> > My one daughter has a lot of mental issues from her infection whether it is

> > the Bartonella, Lyme, whatever. She has had huge improvement using the MMS

> > but if I understand correctly, MMS does NOT cross the blood-brain barrier.

> > I have been reading about another product called DMSO which DOES cross the

> > barrier and is said to carry the MMS with it. Could you give me your

> > opinion on this? Here are a couple links in case you are not familiar with

this:

> > _http://www.dmso.org/articles/information/muir.htm_

> > (http://www.dmso.org/articles/information/muir.htm)

> > _http://www.bevanpotter.com/DMSO.html_

> > (http://www.bevanpotter.com/DMSO.html)

> >

> > Thanks very much for your help!

> > Tammy

> >

>

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Hello ,

I don't have Lyme disease, and no one in our group has it either. The cases I

have followed have all taken a similar path. At around 4 - 6 drops, there seems

to be an increase in energy and a reduction in symptoms. As the number of drops

is increased, there seems to be little improvement. At 30 drops the person is

suffering from discomfort and does not seem to be getting much better.

I am aware of a couple of people that claim they have been cured. In each case,

MMS was one of several treatments used, so the effectiveness of MMS is

uncertain.

This is not to say that it doesn't work, just that it doesn't work as

advertised.

I think there is a benefit in the 4 - 6 drop range. I also think that there is

a benefit from pulsing. Beyond that, I don't know.

In medicine, one of the big problems in clinical trials is the placebo effect.

Often this accounts for about 30% of the success of a treatment. This does not

mean that the people are not suffering from an illness. It means that some

people can concentrate and overcome their illness when they focus. The placebo

acts as a focus.

With MMS, I have not been able to verify a 30% success rate. I don't know

exactly what that means, but it does cast some doubts with the current protocol.

My suggestion is to contact Jim Humble and see if he will put you into contact

with someone that has been cured of Lyme using MMS. This way you can compare

notes and adjust doses to those that are most effective.

Tom

> > >

> > > My one daughter has a lot of mental issues from her infection whether it

is

> > > the Bartonella, Lyme, whatever. She has had huge improvement using the

MMS

> > > but if I understand correctly, MMS does NOT cross the blood-brain

barrier.

> > > I have been reading about another product called DMSO which DOES cross

the

> > > barrier and is said to carry the MMS with it. Could you give me your

> > > opinion on this? Here are a couple links in case you are not familiar

with this:

> > > _http://www.dmso.org/articles/information/muir.htm_

> > > (http://www.dmso.org/articles/information/muir.htm)

> > > _http://www.bevanpotter.com/DMSO.html_

> > > (http://www.bevanpotter.com/DMSO.html)

> > >

> > > Thanks very much for your help!

> > > Tammy

> > >

> >

>

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