RE: Re: help starting Wahl's (Russ)

March 3, 2012

Has your wife tried CCSVI treatment? That is the one thing that has helped me

more than anything else. It could be that in my case, CCSVI was high on my list

of " MS " symptoms (along with mercury poisoning, candida, food allergies, stress,

....) CCSVI is real, not just someone trying to sell you something, it is a

clinical condition. If one has a compromised jugular (/azygous) no amount of

specific diets can 100% " cure " you.It works for some and not others depending on

the severity of their CCSVI, how and where the malformation is and the skill of

the interventional radiologist. Some veinous problems are in awkward places

near the bone where ballooning is difficult or not possible. " MS " could well

have wreaked havoc on the body prior to CCSVI treatment and what has been zapped

is probably gone. I got so much out of the treatment and am still experiencing

changes for the better 16 months later. ALL my senses are back 100% but my

mobility is still compromised. I am happy with what I got out of it and am

continually working to keep my veins open and healthy. I may not be walking but

so what! I presume your wife has had an ELISA food intolerance test and any

amalgams removed? Another two that helped me a little.I am still BBD and will

be for life. (No point in changing direction when something is working.) It is

so sad to hear of someone in her condition, especially as you have done so much.

If people can afford it, and I think you lucky people in the States can get

often get it covered on your insurance, I sincerely think CCSVI treatment is

well worth a try.Janet.

Recommended Posts