I just want to vent a bit and perhaps get your individual feedback, if you share the same 'type' of experience as me.
I switched neurologists from Dr. F* (for very obvious reasons, as I was unable to deal with his 'God Complex').
The neurologist I have now is much more personable and understanding. However, everytime I visit him, I leave his office feeling so sad and down on the future of CCSVI. He always makes me feel as if it is just a random phenomenon and that all the patients he has that have done the procedure, have not really improved that much! Furthermore, that the decrease is vein width is due to age and the progression of the disease...which thus makes us MSers, less reliant on our jugular/other veins.
Then the conversation always switches to new drugs on the market and how CCSVI is so risky. He does not seem like a 'conspirator' against CCSVI, just so skeptical, even though he has had lengthy coversations with Dr. Zamboni and other CCSVI champions.
I just feel totally deflated and that the only real goal of the various IR's is to make $$.
So confusing
