# UK post…

**URL:** <https://forum.livingwitheagle.org/t/uk-post/16816>\
**Category:** New User Help\
**Tags:** stories, treatment, symptoms\
**Created:** [August 13, 2024, 7:33am UTC](https://forum.livingwitheagle.org/t/uk-post/16816 "2024-08-13T07:33:47Z")\
**Posts on this page:** 1\
**Showing post:** 4

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**Author:** ![Jules](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwitheagle.org/jules/32/404_2.png) [@Jules](https://forum.livingwitheagle.org/u/Jules)\
**Post date:** [August 14, 2024, 6:33pm UTC](https://forum.livingwitheagle.org/t/uk-post/16816/4 "2024-08-14T18:33:03Z")

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Yes, there are definitely long waits for surgery with Mr Axon! Unfortunately we have had a few members who have been refused surgery on the NHS with Mr Axon; it seems he has to get surgery approved by a committee now & there are strict criteria for who he can help.  
@Warrick saw him & did post about which symptoms you need to have before he can do surgery in this discussion:  
[Can anybody help me to confirm if my CT shows elongated styloids? - Welcome / New User Help - Living with Eagle](https://forum.livingwitheagle.org/t/can-anybody-help-me-to-confirm-if-my-ct-shows-elongated-styloids/14963/74)  
So hopefully you would fit into that category!

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