Hi & welcome to the site!
I’ve not seen this mentioned much at all; I found one discussion where a couple of members were talking about their experience, so here’s a link:
Undiagnosed, New to ES - General - Living with Eagle
There’s certainly not any documented link between palate expenders & ES that I can recall, although it seems logical; many members have had jaw issues so there seems to be a link there…
Have you explored treatment for your ES? Dr Hepworth is very experienced with vascular ES, so would be good to see if you haven’t already? As your jugular compression is from the skull base down they would need to be removed right to the skull base to help resolve symptoms.
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