# Official diagnosis!

**URL:** <https://forum.livingwitherythromelalgia.org/t/official-diagnosis/1357>\
**Category:** Blog\
**Created:** [June 2, 2012, 4:19am UTC](https://forum.livingwitherythromelalgia.org/t/official-diagnosis/1357 "2012-06-02T04:19:29Z")\
**Posts on this page:** 2\
**Page:** 1

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**Author:** ![Rachee\_Rache](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwitherythromelalgia.org/rachee_rache/32/132_2.png) [@Rachee\_Rache](https://forum.livingwitherythromelalgia.org/u/Rachee_Rache)\
**Post date:** [June 2, 2012, 4:19am UTC](https://forum.livingwitherythromelalgia.org/t/official-diagnosis/1357/1 "2012-06-02T04:19:29Z")

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Well, after over a year of dealing with this I FINALLY have an official diagnosis to what is causing my EM and Sjogren's Syndrome (SHOW-grins)...LUPUS!

Not "excited" that I have Lupus, but I'm very relieved to finally know the primary auto-immune disease causing these secondary issues.

I have even more blood drawn today for her to review and discuss at my treatment options appointment on Tuesday morning.

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**Author:** ![lauraflora1](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwitherythromelalgia.org/lauraflora1/32/38_2.png) [@lauraflora1](https://forum.livingwitherythromelalgia.org/u/lauraflora1)\
**Post date:** [June 25, 2012, 8:27pm UTC](https://forum.livingwitherythromelalgia.org/t/official-diagnosis/1357/2 "2012-06-25T20:27:27Z")

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Glad you finally found out the primary cause, I've been waiting for over 4 years and still nothing. Good luck in finding best treatment options.
