suggestions for American journalists?
- cheerleader
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I know Johnson and Johnson (Cordis stents) has given $ to Dr. Zamboni to help fund his research..peekaboo wrote:Ditto Sharon's post
What about getting stent mfgr's a heads up? They could be the industry back up and $$$
Hey! I made a Facebook page Jimmy suggested it, and I thought that was a terrific idea.
It's fun and easy....and I just started, so don't be too critical
It's called "CCSVI in Multiple Sclerosis" (to make it easy for folks searching to find it.) It'll get better, but I only had a half hour today.
link
Jamie...you ol' softy. We gotta put pressure on the docs to get moving on this. Everyday that passes, more people are diagnosed, more families are affected, people are progressing. There's no time to waste.
Thanks, Sharon. It'll be a quick trip to Bologna (never been before-done Milan/Venice/Firenze) for some good food and interesting conversation. Two of my favorites!
busy fingers... (idle fingers are the devil's workshop )
cheer
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
- cheerleader
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Nice to hear from you, javaneen...javaneen wrote:Any luck finding any US reporters to go to the Conference in Sept?
Haven't found anyone to specifically come to the conference, but I do have confirmation for a feature this fall from a national journalist. Will update once more is known. I'm hoping some of the news wires will have their Italian desk medical writers in attendance. Lots of folks will be in Germany for ECTRIMS the following days. There is an official press conference with patients and doctors speaking as part of the Bologna event.
cheer
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
- javaneen
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just a though incase you haven't already found someone...what about Dr. Marie Savard. She is ABC's Good Morning America Medical Contributor. She is a big advocate for taking charge of our own health. She would love you Cheer and everyone on TIMS and all that they have done for themselves and loved one. You can reach her through eileen@drsavard.com
http://www.drsavard.com/index.php
Let me know if you need me to write any letters. You guys may already have someone lined up.
http://www.drsavard.com/index.php
Let me know if you need me to write any letters. You guys may already have someone lined up.
javaneen
The Hilarscere Foundation has spent millions of dollars on the CCSVI research. They no doubt have a detailed plan on how this is going to be released to the international press. It is going to be interesting to see how the medical community reacts. This research is not going to be an easy "sell"......I plan on doing my part in spreading the word.There is an official press conference with patients and doctors speaking as part of the Bologna event
Sharon
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I hope so Jamie! I just checked out the ECTRIMS conference schedule and the only mention I see at all of CCSVI for the entire 4 day conference all about MS is in two poster sessions. I am suprised that there is not even a lecture or class about this. Maybe perhaps because there are a lot of neurologists there?
Here's the link...tell me if I am looking at it wrong.
http://www.congrex.ch/ectrims2009/
click on Scientific programmee to see all the topics for everyday.[/url]
Here's the link...tell me if I am looking at it wrong.
http://www.congrex.ch/ectrims2009/
click on Scientific programmee to see all the topics for everyday.[/url]
javaneen
This is exactly what our neurologist asked me "why isn't it (CCSVI) being presented at the ECTRIMS conference in Germany." Big conference, so on, and so on.
He didn't say this because he thinks the procedure should be on the schedule, but because he feels that if it is so promising, it would be.
Maybe next year it will be.
He didn't say this because he thinks the procedure should be on the schedule, but because he feels that if it is so promising, it would be.
Maybe next year it will be.
- CureOrBust
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