What I Wish More People Knew About Lupus (Bonus Episode – Lupus Awareness Month)

Whew… this one’s close to my heart. In today’s bonus episode, I’m
sharing the raw, behind-the-scenes truth of what it really looks
like to live with lupus — especially the things most people don’t
see.


This isn’t about complaining… it’s about naming the
invisible.
The fatigue. The body changes. The mental load. The quiet moments
when you feel like you're just trying to hold it together.


I opened up about what I personally wish more people understood —
not just about the illness itself, but about the constant
adjusting, the mental toll, and the strength it takes just to
show up. If you’ve ever felt unseen in your journey, this episode
is for you.


Real-Life Reminders:




Fatigue from lupus isn’t regular tired — it’s
body-shutting-down tired.




Just because someone looks okay, doesn’t mean they’re not
battling silently.




Life with lupus means constantly adjusting — physically,
emotionally, spiritually.




We need support that honors our full selves, not just our
symptoms.




Lupus doesn’t define us — we’re still worthy, valuable, and
called to live fully.



Sound Bites:


“Fatigue is not just about being tired.”
“Don’t give up. Keep the faith.”
“Life with lupus can still be beautiful.” Let’s Keep This
Conversation Going:


If this episode spoke to you, I want to invite you into the
Chronically Planned Inner Circle — a 6-week
space for women who are ready to plan their life around what
really matters, not just their diagnosis. We meet weekly, share
tools, and support each other in real time.
Click here to join or learn more


Need a little more personal support? You can also book a
1:1 Planning Power Hour with me. We'll map out routines,
content, or just make sense of the chaos — together.
Book a session with me here Be sure to subscribe so you don’t
miss the next drop — new episodes are coming every
Friday during Lupus Awareness
Month.