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4 Responses to “About”

  • DebJC:

    Hi, I just read your May 29th posting. I am not sure where you live. CCSVI has been around for a couple years now. GOOGLE or use your fave Search Engine and see if there is a clinic near you–it’s worth it! I live in Arizona and I have been treated in Calif. 3 times in the last 9 months. The first time gave best results. I was able to WRITE again-hand tremors gone. My walking time doubled from 5 min. to 10 min. , with a walker. I was able to empty my bladder better, but this Good Stuff only lasted a few weeks. I want THAT Again and more! I insisted all clinics bill Medicare. So far I am only out $3,000. Usual charge in $8,000. I feel sorry for Canadians who have to bring CASH. The docs that do this are Interventional Radiologists. These procedures have been in use for Other Conditions for awhile now. I say to all MSers to GET TESTED-! I went to San Diego and tested with Hubbard Foundation.

  • Wow,
    A muscian friend of mine on Indaba.com just introduced me to this! I was not even aware of it. Now here you are telling me that I can go to San Diego and get tested.

    Now how are we to tell everyone we know who has MS about this? Got any ideas?! Thank you so very much for the information!


  • Wow! This could be one of the most helpful blogs we have ever come across on thesubject. Actually wonderful article! I am also a specialist in this topic therefore I can understand your effort.

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