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Eagle Syndrome

Ear, Nose & Throat (ENT) | Last Active: 6 days ago | Replies (307)

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@taml

Hi. Just found out I have ES. after 50 yrs of TMJ diagnosis. Just joined Mayo connect and totally confused. Why is there no information about Mayo doctors and ES. Haven't seen any mention of Mayo docs for neck pain, ear pain and vision problems due to ES. or Mayo doctors for anything. Really confusing what Mayo has to do with this site. Sorry. Also most ES info is from 2018..... confused. Thank you.

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Replies to "Hi. Just found out I have ES. after 50 yrs of TMJ diagnosis. Just joined Mayo..."

Hello @taml, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others. @travelgirl shared a post earlier in this discussion to a support website that you may find helpful for resources - https://livingwitheagle.org/t/4-10-15-updated-doctor-lists/774/41/ The support site lists discussions as late as Aug 2021.

I know it's frustrating not being able to find current information. Another source that you might find helpful is Google Scholar (https://scholar.google.com/) as it allows you to filter results by year so that you can find the latest medical research information. Here is a search done using "Eagle Syndrome treatment" sorted for 2021 -- https://scholar.google.com/scholar?as_ylo=2021&q=eagle+syndrome+treatment&hl=en&as_sdt=0,24

May I ask what confuses you the most?