This Is MS Multiple Sclerosis Knowledge & Support Community

Hi all,
Down the road to me is a hospital that provides chelation therapy using EDTA.
It is administered intravenously.
I have read some positive reviews about it but also some very worrying things.

Has anyone personally had this treatment?

I think once I have had the CCSVI treatment, that perhaps chelation is the way forward.

Any thoughts?

.

You are probably right Bob. I have a tendancy to do too much. If the CCSVI thing works that should be enough. If I still feel like I am progressing 2/3 months after the procedure then maybe I will look into it again.
Its just so hard to know what to do! Wierdly enough the only things I know I am staying away from are the proven treatments for MS. I think they are all poisons (accept for copaxone but I still don't fancy injecting everyday)

LR1234
you might want to check out this tread on chelation, it's in the CCSVI topic

http://www.thisisms.com/ftopict-9034.html