← Return to Eagle Syndrome

Discussion

Eagle Syndrome

Ear, Nose & Throat (ENT) | Last Active: Mar 11 6:49pm | Replies (293)

Comment receiving replies
@timber128

I had Eagle Syndrome diagnosed in 2017 and it has become chronic now.
My Family Dr sent a referral to Mayo & after being sent to ENT, then Gastro then Neurology & back to ENT they finally after a month declared they don’t have anyone to help & can’t give me an appt!!! I am frustrated, furious & in pain with NO-ONE to help me!
I have jaw/ear pain, tinnitus, headaches, feeling of something stuck in throat. Gag if I suck through a straw or use a q-tip in my ear. My hearing is bad due to tinnitus.
Tried steroids & shots, Botox, lidocaine, pain meds, but it’s getting worse.
I am at my wits end as I thought Mayo Rochester would at least be able to help or point me in the right direction. But they have failed on both counts.

Jump to this post


Replies to "I had Eagle Syndrome diagnosed in 2017 and it has become chronic now. My Family Dr..."

The University of MN has options for you. I was referred to Dr. Hamar. I have an appt with him next month for the same symptoms. I was diagnosed with ES a few weeks ago.