-The Alliance incorporates and becomes a 501(c)3 nonprofit

-The Alliance creates a website, www.ccsvi.org, featuring clear and objective discussions of CCSVI research, diagnosis, and treatment.    All medical content is reviewed by a world-class team of medical professionals.  The website also offers resources to assist patients in discussing CCSVI with their medical team, as well as patient perspectives.  It provides a database of research abstracts, links to all IRB and N.I.H. approved CCSVI clinical trials and a growing catalogue of exclusive video interviews with some of the world’s leading CCSVI scientists and treating physicians.

- CCSVI Alliance becomes a member of the Endovascular Forum, www.endovascular.org, where it hosts a CCSVI group for the professional and medical community.

-The Alliance makes connections across disciplines to advance research in CCSVI on behalf of Hubbard Foundation, International Society of Neurovascular Disease (ISNVD), and Society of Interventional Radiologists (SIR)

-The Alliance is recognized by the National Multiple Sclerosis Society (NMSS) as a valuable, balanced, and accurate resource for people affected by MS who are seeking information on CCSVI and related treatment.  As a result, ccsvi.org is the first CCSVI organization linked to by the NMSS. 

-The Alliance is represented at CCSVI medical conferences in Brooklyn, and Albany, NY,  and at the annual MS Consortium meeting

-CCSVI Alliance is hard at work preparing for upcoming events, including the educational seminar at Brandeis University with Dr. Michael Dake, The Walk 'n Roll fundraiser in Florida, the 23rd Annual International Symposium of Endovascular Therapy and more.

Thank you for supporting us, helping us grow, and entrusting us to work for you.

Here's to 2011!