Living with Fibromyalgia

01/02/2026

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28/01/2026

Life doesn’t always give you back the pieces you lost especially when chronic illness rewrites everything. But that doesn’t mean your story is over. It just means you get to create a new one, softer, slower, and still deeply meaningful.

If you feel stuck, scared to start, or convinced your illness disqualifies you from having a life or becoming a creator… you’re not alone.

I’ve built a guided community and a step‑by‑step roadmap to help you move forward gently, sustainably, and in a way that honours your body.

DM me “READY” for more info — I’m only a message away.

Chronic illness has a way of shattering the version of you that used to move freely, dream loudly, and live without calculating every ounce of energy.

And when the pieces fall, it’s easy to believe you’ll never build anything again.

But maybe it’s not about forcing yourself back into who you were.

Maybe it’s about honouring who you are now and writing a completely different story with the chapters you still have left.

A slower story.
A softer story.
A story where creativity doesn’t require perfect health, perfect energy, or perfect timing.

Just honesty.
Just presence.
Just you, as you are.

If you’ve been feeling stuck…

If you’ve been telling yourself you’ll start creating “when you feel better”…

If you’ve convinced yourself that illness means you don’t get to have a life…

This is your reminder:
You don’t need to be fully healed to build something meaningful.
You don’t need to be pain‑free to show up.
You don’t need your old life to create a new one.

Life is short.
Chronic illness taught me that.

But it also taught me that even broken pieces can make something beautiful.

And if you’re ready to start gently, slowly, imperfectly.

I’m just a message away. There’s support waiting for you in the link in my bio.

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28/01/2026

When you’re stuck in bed, watching your life shrink into routines of pain, pacing, and survival… it’s easy to believe the world has moved on without you.

It’s easy to convince yourself that joy, creativity, purpose, all of that is for people with more energy, more health, more freedom.

I used to think that too.
I went from bedbound to slowly, awkwardly, imperfectly choosing life again.

Not because I suddenly felt better.
But because I realised something:

-Life is painfully short.
And waiting for the “perfect moment” is how entire years disappear.

Chronic illness doesn’t mean you don’t get to live.

It means you have to live differently; softer, slower, more intentionally, but you still get to live.

And if you feel stuck…
If you feel like you’re meant to create but you keep talking yourself out of it…

If you feel like your illness has stolen your identity…

Read this carefully:
- You don’t need to be pain‑free to be purposeful.

- You don’t need full energy to start.

- You don’t need confidence to begin; confidence comes from beginning.

You are not alone and feel free to DM Me “ROADMAP,” if you would like to discover how to start Living Well with Fibromylgia & ME/CFS.

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28/01/2026

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Discover even more ideas for you

27/01/2026

If you’ve ever felt like you don’t deserve to enjoy yourself… I get it.

When you’re stuck at home in pain, when your body feels heavy and unpredictable, it’s easy to believe joy isn’t meant for you anymore.

Chronic pain can make the world feel small.

It can convince you that going out, laughing, or doing something for you isn’t worth the energy.

I used to feel that way too, truly.

I went from bedbound to slowly finding pieces of life again.

Not all at once. Not perfectly. Just one tiny moment at a time.

And here’s what I learned:

- You still deserve moments that remind you you’re alive.

- You still deserve softness, connection, and things that make you feel like you.

Even if it’s once a month.
Even if it’s five minutes.
Even if you have to rest for days after.

You don’t have to do this alone.

I’m just a message away and I’ve put helpful resources in my bio for anyone who needs support, guidance, or a gentle nudge back toward themselves.

If you would like to be part of upcoming new new course + community, DM “Roadmap.” - this is where we explore how to live well with Fibro & ME/CFS.

If you are new here welcome fiend, good to connect with you🫶💜

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