Welcome to The Notebook, a blog about Hannah Rose her journey and the awareness we’ve gained along the way. We never intended to create a website; we simply wanted answers. When we discovered Arthrogryposis, we had to figure everything out on our own. Now, everything we’ve learned is here for you, for us, and for anyone who needs it.

The Notebook

It’s honest, sometimes messy, and filled with love and hope. If our story can help even one family, it will be worth it. You’re welcome to walk this path with us you’re not alone, and every step matters. xx

The things we carry
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The things we carry

There’s the obvious stuff we carry the kind of things every parent knows by heart. The baby bag that somehow weighs more than the baby, packed for every possible situation. Paracetamol and Brufen for before casting appointments. Teething gel Jack and Jill’s, the one that actually helps. Extra nappies and bottles.

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What we gained when plans changed.

What we gained when plans changed.

Somewhere between those endless Tuesdays and the smell of fibreglass, a quiet doubt started creeping in. We’d sit there watching her tiny legs wrapped again and again, and sometimes we’d look at each other and think, this isn’t what it’s supposed to look like. It wasn’t ungratefulness it was instinct. Something in us knew there had to be more.

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When the world started listening.
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When the world started listening.

A few days after the Givealittle page quietly went live, something unexpected happened. We weren’t prepared for it, not mentally, not emotionally, not in any way. Dan’s phone buzzed with a message from a reporter at the Otago Daily Times. He explained that he’d come across Hannah-Rose’s page, read her story, and felt moved enough to reach out. He wanted to help us share her journey with people who weren’t on social media, people who lived offline, the ones who could easily miss stories like ours unless someone physically put it in front of them.

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The Casts, the Hospitals, and the Little Wins

The Casts, the Hospitals, and the Little Wins

After the birth, everything blurred. One minute we were still taking in the tiny perfection of her toes, the next we were being handed a schedule that felt like it belonged to someone else’s life. Hospitals became our second home before we’d even settled into our first.

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The Question that collapsed America.
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The Question that collapsed America.

After our meetings, calls, and new connections, the plan to get to America felt like it was finally becoming something real. We had support. We had advice. We had direction. And slowly, piece by piece, we started lining up what we needed to make it happen.

We contacted our GP to request a letter supporting travel for medical reasons.

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Supports, Advocacy & Grace

Supports, Advocacy & Grace

It took me a good two weeks to even say the word arthrogryposis. After hearing the devastating news to abort, it felt like I didn’t sleep for weeks. Everything felt heavy. The air, the noise, even time. I remember sitting there wondering how something I’d never heard of could suddenly become my whole world.

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THEY SAID SHE WOULD NEVER MOVE HER LEGS..she missed the memo

THEY SAID SHE WOULD NEVER MOVE HER LEGS..she missed the memo

It was one of those dark days that feels like it will never end. I thought I understood what the doctor was saying at first arthritis and I pictured my nana sitting in her chair, her bones sore, and I thought maybe my baby would feel the same. That was all. I didn’t understand the weight of the words coming next. Then the doctor came back in, papers in hand, calm as if she was asking about lunch, and said, “We can arrange a room now for an abortion and sterilization.” I froze. Pardon me?

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UNDERSTANDING ARTHROGYPOSIS

UNDERSTANDING ARTHROGYPOSIS

The name Arthrogryposis comes from Greek arthro meaning joints, and gryposis meaning curved. It’s a word that sounds complicated, almost scary, but at its core, it simply describes stiff or curved joints. For us, it’s the word that first knocked the wind out of me, the word that entered our lives and changed everything.

When Hannah-Rose was diagnosed, it wasn’t just a medical term. It was a label that came with fear, confusion, and a thousand unknowns. What I learned quickly is that understanding it doesn’t make it any less overwhelming, but it does give you something solid to hold onto something to guide you through the uncertainty.

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