Great that you are looking for support on the Internet.

Could I suggest you also try some other bulletin boards:

The DMRF one, which is for dystonia generally:

http://www.dystonia-bb.org/forums/asd/

then specific ones for cervical dystonia (aka ST = spasmodic torticollis) and blepharospasm:

http://www.blepharospasm.org/forums/beb/

http://www.a-zdoctor.com/cgi-bin/dcforum/dcboard.cgi

and

http://www.torticollis.org/ - click on message forum. The user name is NSTA and the password is "torticollis"

Each of these have distinctive styles - you should find at least one of them a useful forum for discussing common problems, symptoms, treatments and coping.

This bulletin board here is for spasmodic dysphonia (SD) which is a form of focal dystonia that affects the vocal cords - making the voice effortful and broken. You're welcome to read posts and post here of course, but you'll find that most of our readers are SD patients rather than cervical dystonia, Meige syndrome or blepharospasm.

Good luck in your search for answers