Re: I have a theory....are there any Dr.s that would entertain it?

[Guest guest]

I think the enzymes that you are talking about are serrapeptase and nattokinase.

I've taken serrapeptase for a long time off and on, lately on. I haven't had an

exacerbation since the one that took my mobility away years ago. If not for

that I would consider myself to be doing well.

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[Guest guest]

Thank you !!!

I've heard about another taking the Serrapeptase, with good results That is one

leg of it that I've not started. Yesterday I aslo found this enzyme that may

help Plasmin. I found yesterday that

" Strickland and colleagues studied nerve regeneration in mice lacking fibrin.

Strikingly, the mice lacking fibrin regenerated crushed nerves significantly

faster than mice with fibrin.

After further investigation, the researchers discovered that this is possible

because fibrin normally plays a role in keeping sheath cells in an immature

state in which they are not capable of regenerating the intact myelin sheath. In

the absence of fibrin, sheath cells are able to mature more quickly and can more

efficiently remyelinate damaged nerves. " website:

http://www.mult-sclerosis.org/news/Mar2002/FibrinMyelinRegeneration.html

and so this other " plasmin " may be a bit better. I'll be trying to find out

more today.

The final part of it is to get the proper protien going so that the Myelin can

regenerate. Yesterday I put a call into the Lab where they did the animal

studies to approve the Epicore. I pray they call. I don't have a way to access

the entire articles of the medical journals, nor the knowledge. Someone will

help!!!

Have you got a Physcian that is open to the enzymes?

Again, thanks for responding I'm so glad someone else is looking at things and

being proactive!!!

ette

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doing.

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[Guest guest]

I have only seen a doctor a few times since I was diagnosed with MS and I only

had blood tests taken. One time I went for a broken leg but I waited for three

weeks to go (I thought it was a sprained ankle)and it was already healing in the

correct position. I have been self treating for 7 years. I have made mistakes

along the way. I have also had success.

I had a hair mineral analysis done and I learned my metabolic type. A Dr.

who treats cancer and MS uses enzyme therapy for people with my m.

type. I follow his enzyme protocol to some degree. I started taking serapeptase

long before I knew the information about fibrin or Dr. . I thought it

would digest scar tissue, lesions.

I used to be a raw food vegan, big mistake for me. I thought the food would

provide the enzymes. It doesn't. The enzymes in the food were good for the

plant but not for a human.

I take lots of enzymes now, proteolytic, probiotic and digestive, several kinds

of each.

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being proactive!!!

> ette

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[Guest guest]

I haven't repeated the MRI to know what the lesions are doing but my arms and

hands move normally and they used to be shaky, unstable. I still don't always

get a signal from my brain to my legs. I do sometimes. Serrapeptase helps the

swelling in my feet to ease up. I take it all the time now because of the CCSVI

video that was posted here. I want to keep fibrin under control. I had sticky

blood when I was tested a few years ago.

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[Guest guest]

How encouraging!!!

I really feel that there are 3 approaches, the enzymes to disolve the scar

tissue, the imuno modulators to stop the t1 cells from damaging the mylean in

the first place, then finding the right stuff to ingest to rebuild the myelin.

I've not heard from anyone doing all three...have you? I am so glad things are

working for you.

I began taking colostrum before my first MRI but 7 months after my " big MS "

symptom appeared. It was an impulse going from my neck down my leg. the MRI

showed a lesion on my spine, however they said that it did not " light up " as an

active MS plaque.

I did the evoked response vision test, and what they said about it confused me.

they said it showed my optic nerve was stable. I need more information, however

I wonder if the 2 immuno modulators stablized my nerve responses.

Continuing on my quest, we really need someone who can look at this and see if

the imuno modulators are deactivating the MS lesions and plaques, and if the

enzymes (which should arrive this week) will begin to disolve and begin to

reverse the scarring.

I have called the lab that did the testing for Epicor to see if they'd be

willing to look at this further, but no reply. I will not give up...

ette

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[Guest guest]

I drink raw goat's milk, eat free-range eggs, grass-fed meat, organic produce,

EVCO. Some of those things I eat fermented. This is a natural probiotic but I

take others as well. Immuno modulators didn't seem to make a difference for me.

They help other people but I think that eliminating free radicals by taking

digestive enzymes and not eating fake food takes care of an immune response.

Immuno-modulators would be good before the other things take hold. I don't take

LDN but other people take it and love it. I've tried all of the things that

you've mentioned. I have improved a lot but not as much as I want to. There is

more than one way to skin a cat! I want to win a lottery and have CCSVI!

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