RE: CCSVI & MS: FIbrin, Sleep apnea, systemic proteolytic enzymes, venous stenosis

October 11, 2010

Thanks

As I believe I've always said, people MUST do their research!! The procedure is

not a 'cure' and will involve their effort and commitment for it to be

successful.

This is not something which is a quick-fix! It will take committing to a

healthier way of living and doesn't have the same outcoms for ALL! Once people

have done their research, and know the ins-and-outs of the causitive reasons

behind CCSVI, they'll start to realise what they can expect from it and what

THEY (individually) will need to do for themselves for best reults.

It will be best for those who are not a long way down the track and for those

who follow a truly 'healthy' lifestyle and dietary road....remembering that it

cannot 'fix' what is irreversible damage.

Also, the body needs time to heal. Remember that CCSVI is a congenital condition

and so for example, I have been living with it ALL my life and that therefore, I

have 36 years of 'damage' to reverse - THAT'S not going to fix itself and it

won't be quick!

I'm committed to doing as much as I need to in order to give my body the helping

hand it will need to get me back to functioning well.

Take from that the recommendation of RESEARCH, RESEARCH, RESEARCH if nothing

else.

'What we do in life, echoes through eternity.'

MARCUS AURELIUS (121 - 180 A.D.)

From: moochbay@...

Date: Sun, 10 Oct 2010 12:26:39 +0100

Subject: RE: CCSVI & MS: FIbrin, Sleep apnea, systemic proteolytic

enzymes, venous stenosis

Thank you for your reply and good wishes.

I must however emphasise that my post was not in anyway intended to be negative.

The simple answer was asked. Is it likely that the procedure will have to be

redone or possibly be of no tangible benefit? The answer is simply yes.

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