Hi there, My name is Angie. I've recently been diagnosed with Eagle Syndrome, & would love o meet others who also have it, or have had surgery to correct it. Looking forward to chatting. Cheers

Hi Angie. I just found this site and have just been diagnosed. I'm in the southern US. Can't find a surgeon to speak with about helping relieve this pain. What about you?

I live in North Alabama. I was diagnosed with Eagles about 4 years ago. Mine had calcified and was sharp as a needle. It was causing neck and jaw pain and eventually it started poking me. I was referred to an ENT at UAB in the Kirkland Clinic. He removed my right styloid and tonsil. I have had no more pain once I healed.