It's been 3 years since my AN surgery at Stanford. I had a 1.4 cm AN removed on November 10, 2005, and have resumed life at full steam. The first month post-op was very scary with the balance issues and temporary paralysis on the left side of my face. Most of that is gone now and I am sooooo very thankful to my Drs. and my family for getting me through such a delicate and frightening procedure.
I was back at work by Christmas that year and I got pregnant with my second child just 6 months after surgery. If my daughter had been born a boy, she would have been named after my surgeon Nikolas Blevins (I love him!! - I want to nominate him for sainthood). Instead, her name is Victoria Grace!
I have been very fortunate, and have nothing but nuisance effects to remind me of my AN. They are quite funny actually... (does anyone else have this? ) When I eat, especially spicy food, the left AN side of my face waters/leaks. My eye tears up and my nose runs. But when I cry, the other side of my face responds. It's very odd only tearing up in one eye during a sad movie. Also, the left side of my tongue is kind of numb and doesn't taste anything anymore. So if I accidentally get a green bean in there... I just push it to the left.
problem solved. I haven't tried roller coasters yet to see if they are still exhilarating and fun, or if they'll just make we want to barf. I have noticed that if I challenge my son to a "who can swing the highest" contest, I do get a little whoozy. Otherwise, I have recovered quite completely. I still have hearing in my AN ear (middle fossa approach), a little ringing, some oscillopsia, and a leaky face! What more could a woman want!?
I just found out my high school friend's husband has just been diagnosed with AN. I told her to come to this site and use it. It helped me feel like I wasn't alone when I needed some support. Bless all of you for being a part of this. I just thought I would share my happy ending to the AN and happy beginning to my renewed self with all of you.
Thanks for being here!