April Smith | The Thriving Spoonie
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thethrivingspoonie.com
April Smith | The Thriving Spoonie
@thethrivingspoonie.com
84 followers 29 following 130 posts
Helping spoonies adapt and thrive with practical tools, real talk, and community. 👉 Learn more at www.thethrivingspoonie.com
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Such helpful tips for dealing with brain fog! I never considered how morning brain dumps could be helpful - might have to give it a try soon (on days when grogginess isn't winning the game).
Great post with tons of info on how to advocate for #disabilityrights
How to be a disability rights advocate

buff.ly/tE8Yjlx
ID: How to be a disability rights advocate, www. kate the almost great .com
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

bit.ly/46Gbm4R
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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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
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.
100% agree, and that's what inspired the post. 😁
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
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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Completely agree! It took me a while to get the hang of this, but it got easier the more I did it.
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.
bit.ly
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:
ift.tt/lMZeRH1
TW: Suicide

This heartfelt post for World Suicide Prevention Day speaks to the quiet battles so many of us face—and reminds us that reaching out matters. You are not alone.

Read it here:
www.bloomingmindfulness.co.uk/world-suicid...
World Suicide Prevention Day -
It is Suicide Prevention Day today so it's time to change the narrative on suicide and start talking to one another
www.bloomingmindfulness.co.uk