# Implanation case study

**URL:** <https://forum.livingwitherythromelalgia.org/t/implanation-case-study/1775>\
**Category:** General\
**Created:** [July 5, 2016, 6:58pm UTC](https://forum.livingwitherythromelalgia.org/t/implanation-case-study/1775 "2016-07-05T18:58:32Z")\
**Posts on this page:** 3\
**Page:** 1

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**Author:** ![rfordham811](https://avatars.discourse-cdn.com/v4/letter/r/58f4c7/32.png) [@rfordham811](https://forum.livingwitherythromelalgia.org/u/rfordham811)\
**Post date:** [July 5, 2016, 6:58pm UTC](https://forum.livingwitherythromelalgia.org/t/implanation-case-study/1775/1 "2016-07-05T18:58:32Z")

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Just found this yesterday.

[http://www.epostersonline.com/nans2015/node/8](http://www.epostersonline.com/nans2015/node/8)

if you click the pdf button you can read it more clearly

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**Author:** ![Miss\_Patti](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwitherythromelalgia.org/miss_patti/32/734_2.png) [@Miss\_Patti](https://forum.livingwitherythromelalgia.org/u/Miss_Patti)\
**Post date:** [August 12, 2016, 2:08am UTC](https://forum.livingwitherythromelalgia.org/t/implanation-case-study/1775/2 "2016-08-12T02:08:36Z")

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Thank you for posting this! I’m going to try to contact the NANS to find out if this is something that I could try to have performed. If you hear anything more about this I would appreciate you posting it. I’ve had it for 16 yrs & each year it progresses. Now I am in a wheelchair. I really need help if it’s out there. Thanks, again.

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**Author:** ![rayofhope](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwitherythromelalgia.org/rayofhope/32/2077_2.png) [@rayofhope](https://forum.livingwitherythromelalgia.org/u/rayofhope)\
**Post date:** [August 15, 2016, 6:34pm UTC](https://forum.livingwitherythromelalgia.org/t/implanation-case-study/1775/3 "2016-08-15T18:34:11Z")

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I tried lidocaine therapy but the pain clinic did not know I had EM even though I had the pictures and symptoms. But he said you have “crazy” pain. Ok. Now I am diagnosed with EM. But I had the lidocaine therapy one day a month for two months. The relief in my hands was great but short lived. Within a few days full return. We tried again. Same thing. So it did work for the pain in the hands but I cannot say if the redness was gone because at that time I didn’t know I had EM. But it was short lived. This is interesting. Interesting read, thank you for posting. Keeping in my research.