Thanks very much for the kind words. They mean a lot to me.
I just posted this at another thread, but it seems pertinent here: My daughter has CH (I don't). Six years ago, people here helped us learn how she could manage it, after she had been misdiagnosed and mistreated for years by some "highly trained" neurologists. That's why I'm here -- out of gratitude; to keep learning as much as I can; and to try to help keep anyone I can from going through what she went through.
The heroes of this board and the CH community are too numerous to mention. In my view, everyone who fights CH is