AW: Re: Help with CCSVI questions please

[Guest guest]

Thank you all for the answers.  I agree that we each have different problems

with different causes and I'm sure there is an answer somewhere.  Diet(s) did

not work for me, so I'll keep looking.  If only to feel better, not necessarily

cure.  And I'll continue to worry over this CCSVI and see where my thoughts

lead me.  I still feel it could help and will keep you posted if I actually

give it a go. 

 

Sheila

--- eapsystems schrieb am Mo, 14.3.2011:

Von: eapsystems

Betreff: Re: Help with CCSVI questions please

An: mscured

Datum: Montag, 14. März, 2011 12:38 Uhr

 

My take on this is that those who have reversed their ms with diet obviously do

not have physical deformities like webs, nonfunctioning valves or crimps due to

external pressure because no diet or blood thinning supplement can fix those

problems although they may improve flow a bit and for PWMS, even a small

improvement is a big thing. But if there is a physical problem adversely

affecting bloodflow, getting it fixed would offer far greater benefit and then

supporting it with the diet/supplements.

Also, for what it is worth, one of the most common improvements at this point in

time is cogfog and fatigue, followed by bladder, mobility is more difficult,

although it can happen.

> >

> > Hi Sheila

> > I think it's best to move further forward with your CCSVI investigations as

when one has stenosis/narrowing/blockages nothing will really help while those

vascular issues are still there.

> >

> >

>

> Response to above: Sometimes people are tested and found to have blockages but

get treated with CCSVI and have no improvement. There are people such as

Kopera, Yvette our moderator, Terry Wahls, Sue Ellen Dickinson, Grace,

Ken Presner, Dudley Delaney, Ann Boroch, Professor Jelinek, others I know

only by first name,such as (stem cells), (raw foods), and Cara

(chelation and candida cleansing), Ann Sawyer and Crystal (BBD), Kathy (cal EAP

injections 3x per week for 7 years) and others who are in remission (or very

near full remission) without having ever been tested and treated for CCSVI....

>

> What I am saying is CCVI may help some but there are other ways that people

have recovered from MS. CCSVI is not the only way. But it is an option for those

who have tried so many things that haven't worked.

>

> I am still very much on the fence about CCSVI. I can still walk and drive and

do all my basic daily activities of living independently, although I cannot work

due to fatigue, cog fog, vision, and pain. So I am really on the fence.

>