Hi! I am new to this site and web forums all together. I am a 34 yr old disabled RN and mom of 2 great kids. MS has robbed me of my ability to work outside my home for the past 3 years. I recently had a baclofen pump placed, then removed 18 months later. I am so curious about CCSVI and if it really works. I am scared to get my hopes up, I did for the pump and was disappointed. Anyone that has had the procedure please share info, I'm just at a standstill on what to try next. I am on betaseron and a ton of oral meds, and am sick and tired of being sick and tired. Any advice/insight on CCSVI would be helpful. Thanks!