Episode 127 – Finding body confidence when living with chronic illness

In my latest podcast episode, I’m talking about something that’s been on my mind a lot lately—body confidence when you’re chronically ill.

When your body feels unpredictable and limits what you can do, how are you supposed to feel confident in it?

I talk about how:

 To stop comparing yourself to others or who you used to be.

 To change your self-talk. 

 To listen to your body as a partner, not an enemy.

 You don’t need validation from others.

 To let go of who you were. 

Real confidence doesn’t come from your body working perfectly. It comes from recognising your strength, honouring your journey, and treating yourself with the compassion you deserve.

Body confidence with chronic illness is a daily practice. Some days will be easier than others—and that’s okay. 🤍

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Transcript of episode

Hello loves, how are you today?

Today I want to talk about something that’s been on my mind a lot lately – again…. body confidence when you’re living with chronic illness.

I know this might feel like an impossible topic. When your body feels like it’s working against you, when it’s unpredictable, when it limits what you can do – how on earth are you supposed to feel confident in it?

But here’s what I’ve learnt through my own journey: real confidence doesn’t come from how we look or even how well our bodies perform. It comes from changing our relationship with ourselves, and letting go of certain behaviours that chip away at our self-worth.

The Comparison Trap

Let me start with something I struggled with for years: comparing myself to others.

Social media wasn’t really a thing when I was diagnosed in 2009. However, I have still been susceptible to the “I used to be able to do that.”

Here’s what I’ve realised: comparison when you’re chronically ill isn’t just unhelpful – it’s particularly cruel to yourself. No two bodies are the same, and no two chronic illness experiences are identical. Your body is fighting battles that others can’t see. 

The only person you should compare yourself to is who you were yesterday, and even then, be gentle with yourself about it.

The Voice in Your Head

Then there’s the internal dialogue. For the longest time, my inner voice was absolutely vicious. “You’re broken.” “You’re a hindrance.” “Your body has let you down.”

Would I ever speak to a friend with chronic illness that way? Never. So why was it acceptable to speak to myself like that?

I had to consciously change the narrative. When negative thoughts crept in – and they still do – I’ve learnt to counteract them. Instead of “my body is failing me,” I try “my body is doing its best under difficult circumstances.” Instead of “I’m useless because I can’t do what I used to,” I remind myself “I’m adapting and finding new ways to live my life.”

The way we talk to ourselves matters enormously, especially when living with chronic illness. You need to be your own cheerleader, because some days, you’re all you’ve got.

Learning to Listen

Perhaps the biggest shift in my journey has been learning to actually listen to my body rather than seeing it as an adversary.

For so long, I pushed through pain. I ignored warning signs. I’d compare myself to healthy people and try to keep up, only to pay for it later with flare-ups and crashes.

Living with chronic illness forced me to completely reframe my relationship with my body. I had to start treating it as a partner, not an enemy. If it needs rest, I rest – without guilt. If it’s having a good day, I celebrate that rather than trying to cram in everything I’ve been unable to do.

This isn’t giving up or giving in. It’s actually the opposite. It’s respecting what your body needs so you can have more good days overall.

The Validation We Seek

Here’s something I didn’t expect to struggle with: how much we seek validation from others about our illness.

I’d find myself either downplaying my symptoms to seem more “normal,” or over-explaining them to justify why I couldn’t do something. I was constantly feeling like I had to explain that my illness was “real enough” or that I was “sick enough”.

Mine then became more complicated when I wasn’t able to have children, and being put into medical menopause. The changes in how my body looks is still something I am getting used to. It took a long time to be able to look at my scar. There are times in the month when the scar itself feels uncomfy, and if something brushes over it, even slightly, it feels like it’s burning or being pricked with needles.

The truth is, you don’t need anyone else to validate your experience. You know what you’re going through. You know what your body feels like. That’s enough.

Your worth isn’t determined by how sick you appear to others, or by how well you’re coping. You don’t have to perform your illness to prove it’s real.

Letting Go of Who You Were

One of the hardest things about chronic illness is grieving the body you used to have. I used to hold onto these insecurities about what I could no longer do, comparing my current self to my past self constantly. When I started running again it was far too easy for me to beat myself up and think how slow I am now. I got to a space where I was able to separate my running personal bests into pre-diagnosis and post-diagnosis PBs.

But holding onto that grief was exhausting. It kept me stuck.

I’ve had to accept that I’m not the same person I was before my diagnosis. My body has changed. My capabilities have changed. And that’s not a failure – it’s just reality. Now, over 15 years later, my menopausal body is after smashing those post-diagnosis PBs. I would love to smash them before I turn 50. I have two years, I figure it must be doable… We are aging, which is a blessing as it means we are still here, and there’ll always be something to come along in life to change it. It’s what should happen.

You are not your past self. You’ve adapted, you’ve survived, you’ve learnt so much about resilience and strength that you never knew you had. It’s time to let go of who you were and embrace who you are now.

Practising Self-Love (Even When It’s Hard)

Finally, and I won’t lie – this is the hardest one – self-love.

Self-love when you’re chronically ill doesn’t mean pretending everything is fine. It doesn’t mean toxic positivity or forcing gratitude for lessons you never asked to learn.

It means treating yourself with kindness on the difficult days. It means recognising that your body is doing its absolute best, even when it doesn’t feel like enough. It means understanding that you are worthy of love and respect, regardless of what your body can or cannot do.

Moving Forward

Building body confidence with chronic illness isn’t about achieving some perfect state of acceptance. It’s a daily practice. Some days will be easier than others.

But by letting go of comparison, changing your self-talk, listening to your body, seeking validation from within, releasing past insecurities, and practising self-love – you’re not just changing how you see yourself. You’re transforming your entire relationship with your body.

Your confidence doesn’t need to come from your body working perfectly. It comes from recognising your strength, honouring your journey, and treating yourself with the compassion you deserve.

This is one of the pillars in my SHIFT to Alignment coaching programme, empowering you to live life on your own terms. Not mine. Not someone else’s. Yours.
To take back the life a chronic illness stole from you.
Every step of the way is about finding clarity, allowing and creating intention, and taking action as we work through your mindset blocks into the most aligned, powerful and magical version of yourself. And now you can have a taster of that in a free mini SHIFT that I’m creating. Five bite-sized units that you complete at your own pace. You can get on the waitlist at lifeinalign.com/minishift.

Thanks for listening to this episode of the Life in Align podcast. I’d love to hear your experiences with this – feel free to reach out and share your story.

And remember, you are worth it, and you get to choose.

Have a lovely day.