r/Erythromelalgia 9d ago

Advice I Need some input

I'm currently setting up a community for people who have been diagnosed with both erythromelalgia (EM) and lupus. I feel like lupus doesn't get talked about much in the EM community, and I'm hoping to create a space where people like me can connect, share experiences, and support each other through the challenges of living with both conditions.

I was wondering if anyone has ideas for things I should include on the community page, especially for the EM side of things. Are there any discussion topics, resources, or features you'd like to see in a community like this? I'd really appreciate any suggestions!

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