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Moyamoya Related Topics >> Moyamoya Related Information and Support >> International Moyamoya Symposium June 2009 http://www.moyamoya.com/cgi-bin/yabb2/YaBB.pl?num=1246442891 Message started by Little Luca on Jul 1st, 2009 at 6:08am |
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Title: International Moyamoya Symposium June 2009 Post by Little Luca on Jul 1st, 2009 at 6:08am
I'm looking for the link to the video. Kim's posted a link to the website, but I'm not seeing the video link.
Help? Here's the link to the website: http://neurosurgery.stanford.edu/m_program.html Mark (Luca's Dad) |
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Title: Re: International Moyamoya Symposium June 2009 Post by Mar on Jul 1st, 2009 at 7:45am
Michelle posted the Link in the news section
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Title: Re: International Moyamoya Symposium June 2009 Post by Little Luca on Jul 1st, 2009 at 9:37am
The link is here:
http://www.moyamoya.com/cgi-bin/yabb2/YaBB.pl?num=1246058737 |
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Title: Re: International Moyamoya Symposium June 2009 Post by Entesar S. on Jul 3rd, 2009 at 9:51am
Thank you Mark :)
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Title: Re: International Moyamoya Symposium June 2009 Post by LA on Jul 3rd, 2009 at 11:41am
Hello~
The symposium was incredible. Just a note on the Stanford reunion and the Moyamoya symposium. I posted this in another section but feel it pertains here as well. I am filled with appreciation for everyone who's involved with mm. Stanford reunion---Being with people who share life with mm, have experienced the search for answers and help, the knowledge of being in such a small 'club', the notion of helping others now, was such a gift. Dr. Steinberg, Nadia, Teresa, Jill and many of the Stanford folks were there. Was a tremendous feeling of camaraderie for Jack and I. We were able to attend the afternoon sessions of the symposium. Nadia played a large part in making it happen ~ along with Dr. Steinberg. Hearing the world experts discuss the various aspects of this relatively knew and unknown disease from management to research, surgical methods to patient care and awareness was beyond incredible. Having lived with mm for the past ten years, seeing these committed efforts being made was heart (and brain!) warming. Just want to toss in my appreciation, support, and care for people who live with mm, help others with mm with our personal knowledge, and for the world wide efforts being made on our behalf. Linda (LA) |
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Title: Re: International Moyamoya Symposium June 2009 Post by Little Luca on Jul 6th, 2009 at 5:24am LA wrote on Jul 3rd, 2009 at 11:41am:
LA wrote on Jul 3rd, 2009 at 11:41am:
I second that, well said Linda Mark (Luca's Dad) |
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