Added: 1 year ago
From: mackierojo
Views: 671
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  • Thanks for the update, Jamie....and keeping the neuros on their toes. Keep the updates coming.

  • That is all really great news Jamie. How funny is it that we go back to our neuros with the improvements, they are surprised but not willing to consider why? It has certainly been a ride. Here's to a fantastic 2011. Kerri

  • so happy for you. hope all continues to impove

  • I'm so happy for you Jamie :)

    "There is no reason why it can't be done" -- greed for money... unfortunately.

    I wish for the best and free ccsvi treatment for all of us!

    Love ♥

  • Great results. Great attitude. Couldn't happen to a more deserving person. Keep up the good work.

  • So glad to hear of your wonderful progress, Jamie. Kepp 'em comin' even though you'll be busy enjoying it all!

  • Good to see you enjoying life Jamie :) About SK... I know from friend at the front of the fight... it's still going to take years, even to get to the point of trails for them, and for us in AB, so, it's not really moving forward as they would like us to believe. The powers that be are a sneaky bunch, throwing us a bone here and there when the press gets to them. Keep posting improvements and speaking out when you can

  • Merry Christmas and happy new year to you too, Jamie! I am so thrilled for you on your improvements and new lease on life! 2011 will be a great year! I'm on my way to the US for testing and treatment in January. Wish me luck! all the best (stor klem), Ann

  • Merry Christmas Jamie!

    Thanks for sharing, It's great to hear you're doing so well

    G

  • Merry Christmas Jamie

  • hi jamie, nice to see you again , so happy for you ! you 've done it !

    merry christmas and happy new year

  • All the best to you in the new year too! May 2011 be "the year" Canadian's with MS. I hope we meet again my friend, what would I have done in 2010 without CCSVI in MS in Toronto? Oh yeah, I be in a chair... thank you, God bless you... Dawn

  • Oh Jamie, I just had the most horrific experience at the neurologist today. I cannot believe what I went through today. We have to pay for our own healthcare, as many of us don't have it down here. So we paid for me to be on the defensive for 4/5ths of my appointment. Not once did he speak of medical reasons why ccsvi isn't a possibility but regurgitated all the talking points and wanted to know how I intended to pay for the procedure. Not one comment about physical reasons for MS or me. :/

  • @donotconcede I am VERY glad to know how you are doing and feeling! I'm so glad you did a video. My head is reeling from today. I should have said that first. Everything today was just so surreal compared to the truth in your video. I'm glad to see you and I am so happy for you. I hope you have a very Merry Christmas. :) love you!

    Judy

  • Great to hear how well you are doing.

    Merry Christmas!

    Mark

  • Hi Jamie,

    I am so very happy for you and just a wee bit jealous :-) I wish I had the great improvements you and so many others have had.  You are doing such great work and I hope that maybe in the future I can have the procedure again.

    Go and enjoy your life! Have a Very Merry Christmas and a Wonderful New Year!

    Love,

    Andrea

  • it geat to hear all the good news.. thank you for sharing

    meery xmas and a happy new year

    omario

  • That's awesome news, Jamie. Congratulations! Happy Holidays! Happy Holidays, all the best now and all ways :)

  • Congratulations Jamie! I'm happy that your life is back. Please let us know how you are doing and if there is a restenosis in the future. We are all watching to see how CCSVI can help people. Have a Merry Christmas!

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