I've got an appt with a new doctor that I know will be pro-CCSVI.
Other than "when can I get scanned?", what should I ask?
I'm aware that it may be a while until the facility is available in my area for scanning. Luckily, I guess I can wait a little. But since my annual annual MRI should be done in July, I guess that would be a good time to aim for.
For all you "liberated" folls, what do you wish you had known before you got treated?
Thanks in advance!