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Eagle Syndrome

Ear, Nose & Throat (ENT) | Last Active: Dec 6 8:32am | Replies (308)

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@jenlink

@abby4paige I am also in MN and about to lose my mind trying to find a dr that will help me! I think the problem is that so few dr's have a clue about ES so they tell us all it's in our head and we shld seek counseling or my favorite..... you just need physical therapy and reduce your stress! UGH!!!!! I recently had several medical professionals within the same office tell me that they don't believe in ES causing pain!!! And I needed to look into a more mind and body approach to heal myself!!! Tell that to the bone and calcification in my neck that keeps me up at 3:00 AM and is destroying my life!
Did you make it to your appt at the U of M? Curious to hear about your experience if you did and who you saw!

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Replies to "@abby4paige I am also in MN and about to lose my mind trying to find a..."

I’m also being told that.. it’s been 6 months of Doctors telling me I’m ‘the picture of perfect health’. Finally, last week, a new female ENT told me it MAY be Eagle’s Syndrome and I’m getting a CT scan on Monday.. I’m 99% sure I auto-diagnosed myself months ago but nobody would listen. Wishing you the best on your recovery!