I wish I could go. Where is it being held anyway? At Hopkins?
I'd consider aking him how he personally feels about diagnosing MS on clinical grounds with people who have a clean MRI, LP, EPs, etc. It would be interesting to see what a Hopkins guy says thinks about this.
Hope you have a good time and bring back info for us.
Julie
what does he think of the ccsvi treatment? what does he think about people that pay to leave there country and have the ccsvi treatment?
Hi there... are there any new treatments for SPMS and PPMS?
Are there more people getting DX with these?
is it true that many people Dx with MS could have something other then MS but they just can't find the right answers, so they say MS? I've had friends Dx with lets just say "Parkinsons" and 6 months later were told...no it's cancer not parkinsons
I've had a few friends ask me these questions?
looking forward to your update after this session.
thanks alot
wobbly
I can't think of anything specific, but please give us the scoop on what you learn. I need to look into finding some conferences, seminars or something around my area.
Even if I don't get diagnosed, my sister is and it couldn't hurt me to be well educated.
Have fun
Paula