BEST WISHES, DR. SCLAFANI
BEST WISHES, DR. SCLAFANI
.
Your symposium will be wonderful, Superstar.
Best wishes,
~Pamela
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Your symposium will be wonderful, Superstar.
Best wishes,
~Pamela
.
It's tomorrow, isn't it?
You have my best wishes as well. Thank you for bringing your knowledge and experience and open-mindedness and ability to work with other doctors.
You have my best wishes as well. Thank you for bringing your knowledge and experience and open-mindedness and ability to work with other doctors.
"However, the truth in science ultimately emerges, although sometimes it takes a very long time," Arthur Silverstein, Autoimmunity: A History of the Early Struggle for Recognition
A million thanks Dr. Sclafani to you and all the others who take the time to attend, to work on our behalf and to OPEN their minds to new ideas. Wish I could be there, hope there will be a press conference and a video perhaps posted..if possible. We are all behind you. Best of luck.
Onthelake
I am a great believer in luck, and I find the harder I work, the more I have of it. Stephen L.
I am a great believer in luck, and I find the harder I work, the more I have of it. Stephen L.
- blossom
- Family Elder
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ccsvi
dr. sclafani, thank you so much for everything you have done for us in the past the present and the future. the best of everything to you not only with the meeting but the best to you in life. you are one of those people that defines what it means to be a true and dedicated individual and doctor. thank you from my veins that feed my heart. blossom
- ozarkcanoer
- Family Elder
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Dr Sclafani, I wish we could all be at your symposium. It would be so wonderful to hear all the IRs and other experts share their experiences with CCSVI treatment. You and all the other doctors will be in our thoughts tomorrow as you talk about this procedure that has the potential of changing so many of our lives from hopeless to hopeful again. I hope we get to see and/or hear and/or read some of the highlights of the meeting. On this board you have learned how much it means to us when we can be involved in our own treatment. It gives us a sense of power over a disease that can be very cruel.
ozarkcanoer
ozarkcanoer
Re: Best wishes, Dr. Sclafani
...and if that doesn't work, "make them an offer they can't refuse."Onthelake wrote:A million thanks Dr. Sclafani to you and all the others who take the time to attend, to work on our behalf and to OPEN their minds to new ideas.

NHE
Here is a link to some live updates on how the symposium is going:
http://www.facebook.com/pages/CCSVI-MS- ... all&ref=mf
http://www.facebook.com/pages/CCSVI-MS- ... all&ref=mf
"However, the truth in science ultimately emerges, although sometimes it takes a very long time," Arthur Silverstein, Autoimmunity: A History of the Early Struggle for Recognition
A report by Wheelchair Kamikaze covering the symposium can be found here:
http://www.wheelchairkamikaze.com/2010/ ... osium.html
--Frank
http://www.wheelchairkamikaze.com/2010/ ... osium.html
--Frank
Treatment: Gilenya since 01/2011, CCSVI both IJV ballooned 09/2010, Tysabri stopped after 24 Infusions and positive JCV antibody test, after LDN, ABX Wheldon Regime for 1 year.
Re: Best wishes Dr. Sclafani
Girlgeek's videos of the conference can be found at the following link. 
http://s112.photobucket.com/albums/n167 ... Symposium/
NHE

http://s112.photobucket.com/albums/n167 ... Symposium/
NHE