ALso was told that it is unlikely that my facial nerve is still recovering almost 3 years out. (will be 3 years this July) What a bummer!
Angie,
I am carefully documenting my face with photos (and some videos) . Almost at 3 years post op and I'm STILL have
NEW movements come in (albeit some are weird with the synkenisis etc
) You can see more of my upper teeth in my smile than a few months ago
. These are steps slower than a banana slug crossing a tennis court on a rainy day in the Pacific Northwest...
nevertheless these
micro-steps are still happening.
Please also know that by an uh-hum "expert"
I was told I could never ride a bike and sightsee at the same time again. Well I cannot just do that- but with no hands. Truth is the "expert" is just reading some textbook... the same textbook that says if their is no movement at 6 months there probably won't be. (Which many of us have already proven to be
bogus.) I hope that you will be the one to show photos that will update the expert and their outdated information.
One thing I started to do was practice chewing on my AN affected side by sticking a piece a gum in my mouth every time I get into drive the car (that way no one can see my weird chewing action.
) I have to concentrate on chewing without eye involvement as to see out the windscreen ... Low and behold the skill was mastered and now the upper lip is starting to fire up. I cannot make the whistle sound yet but it is almost there when it was not 6 months ago. I am actually making a windy sound when before-
nada nothing.
My 11-year-old has mastered the unicycle. I really want to see if I can do this too. My goal would be to ride right into the experts office, who said I would not be able to ride and sight see at the same time, and blow a big ole bubble in his face- with chewing gum.
Angie are you seeing a neuro muscular facial re-education (re-animation) therapist (NMFRT) at all? They know much more than the neurotologists who study everything from ear wax to CSF leaks to how to tape the eye
incorrectly ... the NMFRT spend years just studying everything related to the facial nerve
specifically. When I was getting frustrated with the DR's I posted here and someone led me to Jackie Diels. I contacted her and she led me to one of her graduates. Have you contacted Jackie at all?
Neuromuscular Retraining Clinic
Dept. of Rehabilitation Medicine
University of Wisconsin Hospital and Clinics, Research Park Clinic
Madison, Wisconsin
H. Jacqueline Diels, OT; Facial Rehabilitation Specialist
608-263-7271
Here is my therapist here in the west- Wanda Crook
Movement Learning Center
San Diego, California
Wanda JK Crook, PT, GCFT
760-315-2599
send an email
California Facial Nerve Center (diagnostics, acute care, NMR, reanimation surgery)
La Jolla, California
Ritvik Mehta, MD
Wanda JK Crook, PT, GCFT
Anshu Gupta, MD, FACS
858-909-0770
http://californiafacialnerve.org/meet-our-team.htmDHM