Amy,
I agree it was a tough year. My timeframe for diagnosis to surgery was 34 days.  I think I am finally finally coming to terms with my new face and other physical issues or b.s. ÂÂ
I am in my second year, and at my one year anniversary in May, I found out my facial paralysis was permanent. Talk about having all your hopes dashed in one fell swoop!  Anyway, in August I had the 12/7 nerve switch surgery.  I think I am less droopy, but still have little or no movement.  Dr. says at six months should see movement. So watching and waiting.
I did have coffee with Kathy, (Obita) a couple weeks ago, and she swears she saw my upper lip move a few times, so again I am very hopeful. ÂÂ
I HOPE AND PRAY YOU HAVE A BETTER 2007 AND YOU SEE IMPROVEMENT IN YOUR SITUATION ON A DAILY BASIS. ÂÂ
I have been keeping a journal since my diagnosis and when I read my previous entries, I do see improvement in my symptoms and in my abilities to control my physical issues.  When I found this site after my surgery, everyone was saying patience it is a slow recovery, well, unfortunately, they were RIGHT!!!  Recovery is a long long process, it is easy to be down and loose hope, especially around the holidays.  But, thank goodness this site is here and there are so many others that understand what its like.
Have faith, Amy, we are all here for you!!!!!
Denise