This feature with Round & About Magazine shares my journey of rebuilding life after chronic illness changed everything. We spoke about identity, grief, resilience, disability advocacy, and how community and connection helped me rediscover purpose after losing the career and life I once knew.
You can read the original feature on the Round & About Magazine website here.
I’ve also shared the full feature below for anyone who would prefer to read it here.
The Full Article
Six years ago I was living my dream, training as a professional dancer in London; then, my health changed and took everything.
I was later diagnosed with Ehlers-Danlos syndrome, PoTS, gastroparesis, intestinal dysfunction and many more complex conditions that have brought more than 15 surgeries, two battles with sepsis, and many long hospital stays — including seven Christmases and New Years spent in hospital.
I live with multiple feeding tubes and am connected to a medical pump for 22 hours a day. A quiet reminder of how fragile and precious life can be.
Rather than giving up, I decided to use what I’d been through to help others. I founded milliebridger.com which began as a small personal blog and has grown into a space where people living with chronic illness or disability can feel less alone, understood, and supported.
Through help guides, support groups, advocacy work and an online support community called ‘Finding Happiness, Together’, my goal is to help others rediscover confidence and purpose and to remind them that life can still hold meaning and connection, even when it looks completely different to what they imagined.
I’ve learned that when your world stops, the world around you keeps turning. You don’t get a choice but to keep going. When I lost my health and the identity I’d built as a dancer, I had to rebuild myself from the ground up.
Somewhere along the way, I stopped fighting to be the person I was and started embracing the person I’ve become. I’m still Millie, but now I live slower, smile wider, and find beauty in places I never used to look.
Illness gave me a perspective I never would have found otherwise. I’ve learned that joy can exist alongside pain, that meaning can survive loss, and that strength is often quiet. I’ve found light in hospital rooms, hope through community, and purpose in helping others find a way through their own darkness.
I also volunteer with Ehlers-Danlos Support UK, collaborate with charities and brands on accessibility and inclusion projects, and visit local schools and hospices with my therapy dog, Ralph.
Earlier this year, I joined Champions Speakers Agency to continue raising awareness through public speaking, sharing messages of hope and resilience.
If this guide helped you feel understood or a little less alone, that means everything to me. You’re always welcome to share it with someone who might need it, or continue the conversation over on my socials. If you’d like to support my ongoing medical care, you can visit my JustGiving Page. Your support helps sustain both my health and the work I’m able to do.
If you’d like to stay connected, you can subscribe to my Monthly Newsletter, join our Support Group Finding Happiness, Together, or explore more resources on my website. However you choose to be part of this space, I’m grateful you’re here.
A personal reflection on rebuilding identity and finding purpose after rare and complex illness. Exploring chronic illness, advocacy, community, and the power of turning pain into connection and hope.
