Talk Lupus to Meg

Because you deserve more than just survival mode.

Six women standing outdoors at sunset, with their arms around each other's waists and holding hands behind their backs, viewed from behind.
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Practical tools, comforting hacks, and a little humor to help you live (and laugh) through chronic illness.

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Hey, I’m Megan.

Talk Lupus to Meg is your space to feel seen, supported, and less alone in your chronic illness journey.

After living with lupus and overlapping autoimmune conditions for over two decades, I’ve learned that healing isn’t linear and survival mode can take over fast. TLTM exists to make chronic illness life easier, softer, and funnier. Here, you’ll find digital guides, comfort hacks, and honest conversations that help you rebuild trust with your body and your voice, one small step (or nap) at a time.

Why trust me?

Because I’ve lived it, studied it, and survived it (more times than I can count). Everything here comes from real trial and error, not recycled wellness advice.

I built Talk Lupus to Meg to make the hard days softer and to prove that rest is productive.

Take a look around and see what speaks to you.

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Interested in working together? Fill out some info and I’ll be in touch shortly. I can’t wait to hear from you!