Has anyone gotten surgery for Eagle Syndrome?
I just got diagnosed today. My PCP is worried the bones are touching arteries and nerves causing a laundry list of symptoms that mimic heart failure even though I’ve been completely cleared by a cardiologist. I’m kind of relived that this isn’t “just anxiety”. But I’m also scared because I have PTSD from 2 failed spine fusions.
I live near Philadelphia and it looks like there are some doctors who are familiar with Eagle Syndrome.
Does anyone else have this? Did you get the surgery for it? If so, how was it? Is it a huge scary ordeal or is it like getting your tonsils out?