mammananny and CCSVI

This is one of the videos I did pre- procedure for . This is for my friends on Patients Like Me who have been one of my greatest supports for several years. After 17 years with , I am ready to chuck the good life for an ordinary everyday existance without a Power Wheelchair, transfer table, scooter, cooling vest, enough medications to be the envy of my community and handicap parking sticker and plates.I will also learn to live without my rollator and my husband’s cooking. (Great…but not mine!)

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25 pensieri su “mammananny and CCSVI

  1. We all love you Linda. I’m so looking forward to my own treatment. Can’t wait to see you playing with the kids.

  2. @karenems Thanks, I hope so. I hate to think I fell on my butt for nothing!

  3. I am very happy for you! You will be liberated soon! Good luck with everything and thank you for sharing your story with us!
    Take good care,
    hugs
    Angela

  4. Thank you Linda for posting a before video, these videos are doing so much for to help spread the word of CCSVI.
    With prayers and wishes for freedom,
    Susan
    PS Maybe some cart wheels on the grass next update :) just kidding.
    Be safe and well.

  5. You are so Brave Linda to show yourself in such and honest and inspiring way. There is nothing to be embarassed about although I’m sure you’ll have a chuckle and a tear once you are Liberated that you were ever like this at all. Can’t wait to see your update. Good luck and all the best.

  6. You are so Brave Linda to show yourself in such and honest and inspiring way. There is nothing to be embarassed about although I’m sure you’ll have a chuckle and a tear once you are Liberated that you were ever like this at all. Can’t wait to see your update. Good luck and all the best.

  7. i can see the spasms and drop foot *which caused you to hitch at the hip and then fall. being in the grass doesnt help – the path would have been better but at least the grass cushions your fall lol – i saw your after procedure walking and its INCREDIBLE – you are heaps better. Keep posting, please

  8. Thank you for posting. That I know, I only have spinal lesions. So, I have been wondering what CCSVI could do for me…

  9. WOW…….. we aren’t alone anymore! Your fall was NOT embossing but reality. GREAT LUCK on your journey. XOXO

  10. @fridayfc
    Drop foot is such a n annoying and embarassing symptom. Nobody should have to deal with this. Thank you for your post.

  11. @ThePennygirl
    Maybe a cartwhell is a little out of my reach, but I’ll keep trying.

  12. @bazwar6
    Thank you for your best wishes. Things are a bit crazy now, but in a happy way.

  13. Hi!!, Did you have the operation already? How was it? Where? best of luck,
    let us know. I have MS as well, and look forward to your answer! Thanks!!!

  14. oh sweet darling, please dont be embarrassed about your fall! you’re video post is highlighting what millions of MS sufferers experience. i was crying during this video, and your post liberation videos. You are brilliant! never stop educating the MS world!

  15. @MsMezzaa
    Thank you. i am over the embarrassment. I think my last video with me jumping was even more so.I’ll be hanging around until we all see the world embrace the facts about MS and CCSVI.

  16. Yves Savoie’s (president of MS Society Canada) anual salary is $450 thousand as reported by ccsvi Foundation – HOW ON EARTH WOULD SHE WANT A SOLUTION TO THIS DISEASE. HOW DARE SHE EXPLOIT OUR ILLNESS. YOUR LIES AND DECEPTION ARE BLATANT. THE MSS NEEDS TO GO TO HE.!!!!!!

  17. @MrLeooreo
    I sincerely hope that your anger is toward Yves Savoie and not me. I wish I HAD an annual salary.

  18. mammy – OH DEAR NOT YOU – I AM TRYING TO EXPOSE THE DECEPTION OF MSS. I AM SO HAPPY FOR YOU.

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