April Smith | The Thriving Spoonie
@thethrivingspoonie.com
81 followers 29 following 120 posts
Helping spoonies adapt and thrive with practical tools, real talk, and community. 👉 Learn more at www.thethrivingspoonie.com
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Learning to pace with #chronicillness isn’t about doing less—it’s about doing differently. In this post, I’m sharing the simple weekly check-in that helps me prevent burnout, plan around unpredictable energy, and stay grounded in what my body actually needs.

#lifewithchronicillness

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How to Catch Yourself Before You Burn Out: Pacing With Chronic Illness Made Simple
Learn simple ways to pace with chronic illness using a weekly self-check-in to manage energy, prevent burnout, and plan with awareness.
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What if living authentically with chronic illness isn’t about being bold—but about not abandoning yourself?

New post on the quiet, complicated truth of showing up as you are.

#chronicillness #spoonie #disabledvoices

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What It Really Means to Live Authentically With Chronic Illness—And Why It’s So Hard to Do
Discover what it really means to live authentically with chronic illness—and why it’s so challenging to let go of expectations.
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September is Pain Awareness Month 💜 Living with chronic pain isn’t always visible—and that’s what makes it so often misunderstood. Community, advocacy, and compassion matter more than ever.

#PainAwarenessMonth
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I love that you called attention to the humility it takes to do things this way! I've felt it, but couldn't articulate it. And I agree about courage - doing things this way goes against the grain of society, and any kind of push back on that take courage for sure.
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100% agree, and that's what inspired the post. 😁
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The hardest part of chronic illness fatigue isn’t always the crash itself. It’s the spiral that follows—guilt, shame, feeling like you’ve failed.

Your worth isn’t measured by your energy level. A bad day doesn’t erase your reliability, your care, or your value.

#ChronicIllness #SpoonieLife
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Anaphylaxis is terrifying on its own—add a rare reaction to a chronic illness treatment, and it’s a whole new level.

This powerful story from @achronicvoice sheds light on the risks, the aftermath, and the resilience it takes to keep going.
An Anaphylaxis Reaction from Rituximab in Between Shady Years
The medications we tried were not much use for Lupus and its comorbidities. Here's what an anaphylaxis reaction from Rituximab feels like.
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thethrivingspoonie.com
Completely agree! It took me a while to get the hang of this, but it got easier the more I did it.
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Energy crashes aren’t just physical—they take an emotional toll too. The guilt, shame & self-doubt can feel heavier than the fatigue itself.

I wrote about how I stopped blaming myself for unpredictable energy & started rebuilding self-trust.

Read here 👉 bit.ly/42tPzLp

#ChronicIllness #SpoonieLife
The Emotional Toll of Unpredictable Energy (And How I Stopped Blaming Myself)
Learn how to manage the emotional toll of fatigue and build self-trust with chronic illness energy management.
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Chronic pain isn’t just physical—it’s emotional, mental, and deeply complex.

This post explores the layers of living with pain that others often overlook, and why compassion matters more than ever. Read it here:
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So many #chronicallyill activists helped build the #disabilityrights we rely on today—but most of us were never told their stories.

This post explores their powerful legacy, the quiet ways they made change, and what we can learn from them now.

📖 Read here: bit.ly/3K90GCR
The Powerful Legacy of Chronically Ill Activists—and Why Disability Rights Are Still Under Threat
Discover the powerful legacy of chronically ill activists in U.S. disability rights history—and why their fight still matters today.
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