Look at
http://www.marshallprotocol.com
Its based partial on genomics work and molecular receptors.
It a forum and difficult to navigate and find info quickly.
I've got about 20 windows open right now.
Have to go to work, will try to post more specifics later.
Use the search feature.
Look at the required reading section.
http://www.marshallprotocol.com/forum2/
I think one video I watched says it stops fibrotic tissue from being
laid down and maybe reverses it.
It might solve the adhesions problem for you. The Benicar may do that.
Documents
http://www.marshallprotocol.com/forum2/6606.html
Here's one video,
http://www.marshallprotocol.com/forum11/7628.html
but I don't think this is the one that explains reversal of the fibrosis.
I can look later for more info.
Some highlights -
These infections and the "autoimmune" diseases are caused by CWD -
cell wall deficient bacteria.
They are intracellular in macrophages and white blood cells,
They hide from the immune system by producing a metabolite of vitamin D
1 25 hydroxy-<something>
You can do a diagnostic test for the metabolite.
http://www.marshallprotocol.com/forum2/366.html
Or you can just do the protocol and see if you get a herx reaction.
Its complicated. Exclude all sources of vit D, cover skin, wear
special sunglasses indoors and out.
Then take a blood pressure medication, Benicar, which causes the
bacteria to reveal themselves.
This is also the piece of the puzzle about the fibrotic, inflammatory
reactions.
This medication stops that.
Then you take small pulsed doses of minocycline, every 48 hours.
Then over time add two more antibiotics that all work synergistically.
Typical timeline for the very ill. People feel better in 6 months. 2
years symptom free.
3-5 years to a cure.
Looks like it will cure all immune disorders in more than 50 percent of cases.
So I'm checking around about colloidal silver, wild oregano oil, etc.
to see if they might whack these teeny, tiny, intracellular CWD
bacteria without all the hassles of this protocol.
http://www.marshallprotocol.com/forum32/1584.html
Karen
At 12:18 PM 2/25/2007, you wrote:
You might try the deodorized DMSO from
https://jacoblab.com/OrderDMSODusa60.html
It is pricey, but I've been using it and it doesn't produce the BO
in me that regular DMSO does.
And don't forget you can also take/chew chlorophyll tablets when
using regular DMSO. I've done that also. It does help, but
apparently doesn't work for everyone.
sol
[email protected] wrote:
Any suggestions for riding burning scalp muscle adhesions with
trapped edema from a chronic lyme infection? I have tried many
things but nothing penetrates the muscle tissue that has become
fibrosed entrapping fluid. My head is alaways stiff and
crunchy,contracted and burning from head to heels. I have tried
many dressings on my head and done many therapies. DMSO and silver
stinks so bad no one comes near me. All the oils are impossible to
get out of my hair and nothing's changed. I have done many systemic
therapies too but to no avail. The connective tissue in the scalp
muscle has walled off the spirochetes and surrounded my skull with
adhesions. I'm told not to use electrical devices on the head. Any ideas?
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