2012 Angioma Alliance Patient & Family Conference

Yes!!

June 22-23, 2012 in Santa Fe, New Mexico. The conference is being co-hosted by Angioma Alliance and the University of New Mexico, Department of Neurology.

Check it out here.

Is it me, or do those pictures not make Santa Fe look like the quaintest place ever???

New Facebook Group for Parents & Kids

One thing you can never have enough of is support. I don't care who you are, or what you're dealing with. It's invaluable. And the best part of technology is that it opens up the world to you, esp when it comes to others facing the same issues you are dealing with...

Check out the new Facebook page Angioma Alliance for parents and children.

2011 Angioma Alliance Pathobiology of Cerebral Cavernous Malformations Scientific Workshop

I hope you've been following Connie Lee's live blogging from France. (If not, go here.) Make sure you check out her final take away message from the Workshop here as well.

 “Without you, there can be no cure”...

Her words are poignant, and necessary. 

Live Blogging from Scientific Workshop

Join Conne Lee on the Angioma Alliance blog as she live posts from the three day 2011 Angioma Alliance Pathobiology of Cerebral Cavernous Malformations Scientific Workshop in France. 


Her intro is here and Day One is here and here. 


Day Two.


Day Three.


You don't want to miss it!