Hi there,
It has been quite a while since I visited the site, still amazes me how so many are being diagnosed with AN. I am 3 years post-op AN (4 cm), with SSD on the left. To all the newbies, this is great site to get info and people with knowledge that I wished I had before my surgery. I found this site after my surgery, it helped me to learn what I could expect or experience. I didn't post often, more or less just read. I have gone through ALOT since my surgery. I did go through the depression and angry phase, sometimes, still do. Not even a year after my surgery, I lost my mom to breast cancer, then a few months after that my fiance broke off our engagement. Seems like I lost everything all at once, my hearing included. I still pop in a read in the forum, it has been helpful in many many ways. It helps to know that you are not alone. Everyone's words of wisdom and encouragement, has gotten me through some rough days, and even though I am not quite out of the woods yet, I know i can always come here to this forum and find that silver lining. So, thanks to this forum and the caring people that do know what you are going through.
Leah