Moebius Syndrome was something I knew very little about until the age of the Internet. Being able to connect with people from all over the U.S. and throughout the world has been tremendously enlightening. There was a time, however, that I felt alone… I was about seven, after coming home particularly upset because of some bullying at school, my mother explained what little she knew about Moebius. I remember sitting on the stairs with her and listening to her explanation. It wasn’t too detailed, she just said that half of my face was paralyzed. I was certainly different, but I didn’t have much to connect with. Click here to read the rest of her story.