# Rough road...not sure where to go now - are these styloids 'normal'?

**URL:** <https://forum.livingwitheagle.org/t/rough-road-not-sure-where-to-go-now-are-these-styloids-normal/9486>\
**Category:** General\
**Tags:** stories, symptoms\
**Created:** [June 21, 2021, 9:58pm UTC](https://forum.livingwitheagle.org/t/rough-road-not-sure-where-to-go-now-are-these-styloids-normal/9486 "2021-06-21T21:58:32Z")\
**Posts on this page:** 1\
**Showing post:** 20

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**Author:** ![alawton3214](https://avatars.discourse-cdn.com/v4/letter/a/dbc845/32.png) [@alawton3214](https://forum.livingwitheagle.org/u/alawton3214)\
**Post date:** [July 28, 2021, 8:17pm UTC](https://forum.livingwitheagle.org/t/rough-road-not-sure-where-to-go-now-are-these-styloids-normal/9486/20 "2021-07-28T20:17:47Z")

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Hi kforssen & Snapple2020,  
I am new to ES and also from the Seattle area. I am having similar issues with doctors/specialists in the area who have even heard of ES. I had an appointment yesterday with a pain management doc (probably the same one you saw for PRP/prolotherapy) who I have been seeing for a while. I brought up ES with him because he has it listed as a condition that he treats on his website. He completely disregarded it as a possibility and wants to look at other issues. Finding someone who can even refer me for a CT has proven difficult. Any recommendations you have for docs in the area that might refer for a CT would be greatly appreciated. I have only been following this community for a couple of days, but it is amazing how many people are following similar paths because of this crazy condition. Hang in there!

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