Well. It’s happening. IT’S HAPPENING. cue happy tears and awkward dancing while wrapped in a heating pad
The Invisible Illness Club Podcast is officially LIVE! 🎉 This little dream has been living in my heart for a long time, and today it finally gets to live in the real world (or at least on Apple Podcasts and Spotify).
This podcast is for every woman who’s ever felt unseen in the doctor’s office, misunderstood by her friends, or just completely worn out from pretending to be “fine.” It’s honest. It’s unfiltered. And it’s ours.
👉 You can listen to the first episode right here: Click to Listen 🎧
Here’s what you can do to help a girl out:
- Listen to the first episode (or binge ‘em all if you’re feeling spicy).
- Leave a rating and review – seriously, it helps SO much.
- Reply to this email with your thoughts or share a topic you’d love me to cover.
Your support makes this real. You’re not just listening—you’re building something with me. You’re making sure no woman with a chronic illness has to feel invisible again.
Oh! And because I like to keep things interesting… 👀
Coming soon: An episode all about what to do when you’re sick on top of your chronic illness (because yeah, that’s a special kind of misery, right?). It’s one of the most requested topics, and I can’t wait to dig into it.
With so much gratitude and probably too much caffeine,
You can listen to the Podcast on:
LATEST BLOG POST
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ENERGY SAVING TOOL OF THE WEEK:
Earrings by Emma
How it helps:
If you have allergies to earrings like I do, check out Earrings by Emma. They are awesome and now I can wear different styles of earrings that I couldn't wear before.
They are:
✨Hypoallergenic plastic posts for sensitive ears👂🏻
✨Thousands of trendy styles🔥
✨Family owned business🏠
SOMTIMES YOU JUST NEED A LAUGH:
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COMMUNITY SPOTLIGHT
A fellow Spoonie worth following
Meet Evelyn.
Evelyn lives with Multiple Sclerosis (MS). She said "it's honestly hard to sum up my journey because it’s been anything but simple. It took 8 years of symptoms, confusion, and feeling dismissed before I was diagnosed with secondary progressive MS. That diagnosis brought answers, but also grief." Her advice to us is: "You don’t owe anyone proof of how hard it is. It’s easy to feel like you have to justify your symptoms because they’re not visible—but you don’t. Invisible illnesses are real. You are not lazy, dramatic, or making things up. And your experience is valid, even if others don’t understand it.
Evelyn has so many good things to say that I will likely create a post on my blog to showcase all of it.
FOLLOW EVELYN
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"Come to me, all you who are weary and burdened, and I will give you rest."
— Matthew 11:28
