Has anyone seen Dr, Davis at Mayo?

Did he help at all or mostly diagnose the EM?

I am so scared to make that long trip just to have a diagnosis. I already have that.

So confused.

I just ran a site search on Dr Davis Mayo Clinic and here is the link to the results where members have previously posted http://www.livingwitherythromelalgia.org/main/search/search?q=dr+davis+mayo+clinic

Hope this helps Twinkle Toes.

Thanks very much Jules,