RE: Myasthenia Gravis with Thymoma

[Guest guest]

Kachina,

Bruce Chesley would be the go-to guy for that, and he is on this list. He is

doing it now . Your first application transdermally is to see if you are

allergic to it. Start at 50% in a very small area and give it 1/2 hr to cause

reaction. Transdermal use is commonly done at 70% strength. I use it full

strength as a pain killer, but not on sensitive skin. It does dry the skin so

use Emu oil in between applications for restoration of skin oils to area

treated. You will smell like you have been eating garlic. That is the sulphur

I think. Small price for relief and tiny price for a cure ?

Kindest regards,

Gerry

Myasthenia Gravis with Thymoma

Thanks for the earlier responses about tumor reduction with DMSO. Have not yet

tried it as I am still looking through old posts to find what would be the best

SB:DMSO ratio to begin with. If anyone would like to throw out some suggestions

that would be great, it will be used on the sternum targeting a thymoma. From

what I gather it would be best to start with a low DMSO/distilled water

solution, like somewhere between 5 & 20%, does this sound correct? And the

amount of SB?

I am only just learning about Myasthenia Gravis and the importance of avoiding

certain drugs/substances has been emphasized so I typed 'DMSO Myasthenia Gravis'

in a google search and much to my surprise there were older articles about the

potential benefit of DMSO for the illness though it looks like the studies never

made it past the rats.

As I am quite overwhelmed at the moment I thought I would check in here to see

if anyone already had information or experience with this. Or, if someone here

more experienced with DMSO might take a look at the information with a

discerning eye and provide some feedback.

Any thoughts are much appreciated!

[Guest guest]

What about hyaluronic acid? Perhaps that could prevent the dryness without

making the oil into a barrier (never tried this, just throwing some ideas

around).

From: DimethylSulfoxide-DMSO

[mailto:DimethylSulfoxide-DMSO ] On Behalf Of G Simpkins

Sent: 06 December 2009 11:30

To: DimethylSulfoxide-DMSO

Subject: Re: Myasthenia Gravis with Thymoma

Kachina,

Bruce Chesley would be the go-to guy for that, and he is on this list. He is

doing it now . Your first application transdermally is to see if you are

allergic to it. Start at 50% in a very small area and give it 1/2 hr to

cause reaction. Transdermal use is commonly done at 70% strength. I use it

full strength as a pain killer, but not on sensitive skin. It does dry the

skin so use Emu oil in between applications for restoration of skin oils to

area treated. You will smell like you have been eating garlic. That is the

sulphur I think. Small price for relief and tiny price for a cure ?

Kindest regards,

Gerry

Myasthenia Gravis with Thymoma

Thanks for the earlier responses about tumor reduction with DMSO. Have not

yet tried it as I am still looking through old posts to find what would be

the best SB:DMSO ratio to begin with. If anyone would like to throw out some

suggestions that would be great, it will be used on the sternum targeting a

thymoma. From what I gather it would be best to start with a low

DMSO/distilled water solution, like somewhere between 5 & 20%, does this

sound correct? And the amount of SB?

I am only just learning about Myasthenia Gravis and the importance of

avoiding certain drugs/substances has been emphasized so I typed 'DMSO

Myasthenia Gravis' in a google search and much to my surprise there were

older articles about the potential benefit of DMSO for the illness though it

looks like the studies never made it past the rats.

As I am quite overwhelmed at the moment I thought I would check in here to

see if anyone already had information or experience with this. Or, if

someone here more experienced with DMSO might take a look at the information

with a discerning eye and provide some feedback.

Any thoughts are much appreciated!