Erythromelalgia treatment and autoimmune
Hi all,
I (31, F) have been experiencing Erythromelalgia for about 1.5 years. I was diagnosed officially about 6 months ago.
-Asprin didn’t help
-Magnesium does seem to help.
-I have symptoms the worst in my hands, then feet, and also at times get redness on my face and ears as well.
I’ve had various other random symptoms over the last 10 years which lean towards being possibly autoimmune related. Because of this, I recently was referred to a rheumatologist who flat out denied that Erythromelalgia is related to or coincides with autoimmune conditions. I was flabbergasted by this.
So now I’m at square one, and am receiving no treatment for my EM. Any insights or suggestions? I feel stuck and frustrated.
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
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We talk a lot about different drugs for EM in our TEA Zoom monthly meetup. One things I have learned is that there is no one size fits all. For non-inherited EM everyone has a different recipe that works. Come join the group and you’ll learn a lot.
Thank you. I will join the group.
Can you send the link??
@clint81 thank you so much. Do you live in the vicinity of John’s Hopkins? It would mean a plane trip for me. That doesn’t really matter. I just need help.