# Anyone helped by mayo clinic in mn

**URL:** <https://forum.livingwitherythromelalgia.org/t/anyone-helped-by-mayo-clinic-in-mn/2823>\
**Category:** General\
**Created:** [December 5, 2017, 6:22pm UTC](https://forum.livingwitherythromelalgia.org/t/anyone-helped-by-mayo-clinic-in-mn/2823 "2017-12-05T18:22:06Z")\
**Posts on this page:** 1\
**Page:** 2

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**Author:** ![gwadley](https://avatars.discourse-cdn.com/v4/letter/g/bb73d2/32.png) [@gwadley](https://forum.livingwitherythromelalgia.org/u/gwadley)\
**Post date:** [February 23, 2018, 7:17am UTC](https://forum.livingwitherythromelalgia.org/t/anyone-helped-by-mayo-clinic-in-mn/2823/21 "2018-02-23T07:17:17Z")

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I’ve tried all 3 of the compounding scripts I’ve heard of. Amitrapyline/Ketamine, Voltran, and Midodrine. Thinking if you’ve tried those already and know you have EM (diagnosed at Yale) there isn’t a lot of benefit in goin to Mayo. Any more thoughts as you’ve been there.

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