frodo wrote:Very soon everybody in USA will be treated thanks to this.
There are 500,000 people with MS in the US. It will take a while. Plus repeat venoplasties! Thank goodness they are started on it.
CCSVIhusband, that is good news too. Can't wait to see all the dots red. This is different than our regular treating doctors, wtih this registry all the data will be captured and will be used for publications and research. Clinically the docs are ahead of the game, we need that research to support what they're doing.
David, great news!