Re: Re: Testing: TNF, MSH, MMP9...? (CSM)

[Guest guest]

THANKS, SHAKER!

VICTORIA

[] Re: Testing: TNF, MSH, MMP9...? (CSM)

I've only taken it a few times. However, I can report that I think

it reduces some of my pain symptoms significantly. For example, I

try to take walks for exercise, and I am able to walk longer and

faster with much less pain in my lower legs after the CSM. I should

try increasing to the four daily doses that I believe Dr. S

recommends, but I don't know how I'm going to manage that.

I've looked through the old posts on CSM, and there doesn't seem to

be many experiences shared. I will try to start a survey-type

thread, where maybe we can hear more about people's experiences with

this stuff. If it's the only answer out there for reducing

mycotoxins, I would think some of the 1471 people on this forum would

be trying it. And if there are other answers, I would love to hear

about them.

> > > In Desperation Medicine, Dr. Shoemaker says:

> > > " Measuring TNF in serum can give us an idea about how many

toxin

> > > molecules are activating DNA transcription, but the

corrrelation

> isn't

> > > 100 percent. Research shows clearly that the rise in TNF-

mRNA in

> the

> > > bloodstream following CSM dosing is a better measure of toxin

> activity

> > > on nuclear receptors. " (p. 265)

> > >

> > > Has anyone had TNF-mRNA testing done to show toxin activity?

Or

> MSH or

> > > MMP9, which I've read are more recent tests used by him?

I've

> read

> > > sick people generally have a low MSH (bad sleep and chronic

> pain), and

> > > high MMP9 (inflammation).

> > >

> > > I'm wondering if there is any test he uses now (other than

the

> visual

> > > contrast sensitivity test, or symptom changes) to measure

toxin

> load

> > > and patient progress.

> > > Thanks!

>

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