What should I ask my new neurologist?

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.

What should I ask my new neurologist?

Postby Rosegirl » Sat Mar 13, 2010 3:39 pm

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!
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