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

[Guest guest]

i've had ms symptoms for 30 years. i was diagnosed 19 years ago and on

8/27/2010 i received ccsvi treatment. it was by far the best thing i've ever

done for the disease. i was lucky to be able to drive to phoenix to the arizona

heart institute, have the procedure, then go home. it was covered by blue cross

and i'm feeling so much better. i'm still using my scooter and my recovery is

somewhat slow but it feels so much better than being ill all of the time. ccsvi

is great!!

Re: CCSVI & MS: FIbrin, Sleep apnea, systemic proteolytic

enzymes, venous stenosis

Great post. There are a few things that I have in common with the guy who made

the video. I take serrapeptase because it digests scar tissue and apparently

fibrin. I take horse chestnut, a vasodilator. I take protealytic (pancreatic)

enzymes. And I smoke medical marijuana, less now because it makes me weak and I

prefer to be strong. I have also seen improvement. I'm not sick but I'm not

walking.

CCSVI is looking better to me after seeing this video.

>

>

> I saw this and thought that it should be brought to peoples attention, it may

ring bells with people or offer up more info that makes sense on a personal

level..

[Guest guest]

>

>

>

> i've had ms symptoms for 30 years. i was diagnosed 19 years ago and on

> 8/27/2010 i received ccsvi treatment. it was by far the best thing i've ever

> done for the disease. i was lucky to be able to drive to phoenix to the

> arizona heart institute, have the procedure, then go home. it was covered by

> blue cross and i'm feeling so much better. i'm still using my scooter and my

> recovery is somewhat slow but it feels so much better than being ill all of

> the time. ccsvi is great!!

>

> Re: CCSVI & MS: FIbrin, Sleep apnea, systemic

> proteolytic enzymes, venous stenosis

>

> Great post. There are a few things that I have in common with the guy who

> made the video. I take serrapeptase because it digests scar tissue and

> apparently fibrin. I take horse chestnut, a vasodilator. I take protealytic

> (pancreatic) enzymes. And I smoke medical marijuana, less now because it

> makes me weak and I prefer to be strong. I have also seen improvement. I'm

> not sick but I'm not walking.

>

> CCSVI is looking better to me after seeing this video.

>

>

>

>

> >

> >

> > I saw this and thought that it should be brought to peoples attention, it

> may ring bells with people or offer up more info that makes sense on a

> personal level..

>

>

[Guest guest]

go for it...you won't regret it.

Re: CCSVI & MS: FIbrin, Sleep apnea, systemic proteolytic

enzymes, venous stenosis

A young woman came into our store walking with a cane, so my mother asked her if

she had MS (after telling her about me). The woman said that she had a shunt

put in her neck and was in a wheelchair before the treatment. Now, of course,

my mom wants me to check into it. I surprised her by telling her all about it.

The woman had CCVSI in Tulsa but they are also doing it in Dallas and probably

all across the country. I lived in the Phoenix area for a long time. I miss

it!

>

>

> i've had ms symptoms for 30 years. i was diagnosed 19 years ago and on

8/27/2010 i received ccsvi treatment. it was by far the best thing i've ever

done for the disease. i was lucky to be able to drive to phoenix to the arizona

heart institute, have the procedure, then go home. it was covered by blue cross

and i'm feeling so much better. i'm still using my scooter and my recovery is

somewhat slow but it feels so much better than being ill all of the time. ccsvi

[Guest guest]

i would think that as the blood enters the brain and refluxes many of the

products in the blood would drop out and with the damage to the blood brain

barrier it would have to cause many of the problems we experience in ms.

Re: CCSVI & MS: FIbrin, Sleep apnea, systemic proteolytic

enzymes, venous stenosis

I got to wondering if stenosis causes mercury and other heavy metals, besides

iron, to pool in the body. I have an abundance of copper and though I haven't

been tested in a long time, I had an overload of mercury at one time. I had

aluminum show up in a hair mineral analysis. And is metal the only toxin that

gets blocked? Can this cause food intolerence and allergies?

>

> go for it...you won't regret it.

>

[Guest guest]

I am a bit confused. I had read on this site a while aback that CCSVI treatment

was only available in the U.S. in two places: one place in CA and one place in

NY,  but then both of those closed down. and that it was not available in the

U.S. at all .... But now people have been writing that they are getting the

treatment (not just the testing) in various places in the U.S. such as NY,

Phoenix, and several other places in the U.S.

So is this treatment available in the U.S. now, and how does one who lives in

the U.S. go about finding the closest center to get not just the testing but

also the treatment?

Thanks.