5 comments
I really am getting fed up with raising untold amounts of money for the ms society and not getting the help when I need it, which is now the scan on my veins and the CCSVI locally.
They did buy a scooter for me 8 years ago but I did take part with Dr. Paty to develop the MRI as THE Dx for ms. Before that it was a hit and miss afair for dx.
I am very frustrated and disapointed with the ms society and the ms clinic at UBC, they have done very little for ms'ers to help them deal with this disease.
