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NEITHER SWIFT NOR EASY

Progress is rarely swift or easy. Especially for the women carrying so much - work, life, motherhood, and beyond

Most of what matters is learned slowly, through lived experiences and the keen desire to learn more about ourselves and keep doing better.

This site began as 'What the CF' - a blog that I started during my child’s diagnosis with cystic fibrosis.

It was a way to learn, cope, and survive a moment that changed everything.
 

Since then, life has expanded.
 

Neither Swift Nor Easy is where this writing now lives.

Essays on motherhood, work, anxiety, identity, and the long work of becoming.

Home: Welcome

How it started

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Cystic fibrosis was the beginning.

My eldest son was born in 2020, during the Covid pandemic - and at just 4 weeks old he was diagnosed with cystic fibrosis.

The early years of motherhood were shaped by newborn magic, lockdown, hospitals, research, fear, growth, gratitude, and learning how to become everything at once: parent, advocate, carer, and still myself.

Those experiences matter. They always will - as they shaped me in ways that have made me better and stronger.


They are part of the foundation of this work.

But motherhood doesn’t stay in one chapter.

What this site is now

Neither Swift Nor Easy is a space for honest writing about life lived under pressure.

Medical 

motherhood

Working

motherhood

Anxiety and mental health

Learning and not always getting it right!

This is not advice. It’s experience, reflected upon.

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"So we found out yesterday that Arlo has tested positive for cystic fibrosis and life has felt pretty surreal since.”

Wednesday 26th August 2020

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Arlo’s Army: We Won’t Stop Until CF Does

There’s no cure for CF yet. Even with groundbreaking new treatments, daily life for people with CF remains a heavy burden and many aren't eligible for these new drugs. That's why we're raising money. To fund cutting-edge research. To support families like ours. To keep pushing until CF stands for Cured Forever.

CF affects over 11,000 people in the UK — and more than 100,000 globally. It impacts the lungs, pancreas, and other organs, turning mucus thick and sticky, and making everyday life a battle for breath.

 

The Cystic Fibrosis Trust is leading the charge to change this. They fund game-changing science, support families, and fight for better treatments, care, and — one day — a cure.


Join Arlo’s Army today.

 

Stand with us. Donate. Share. Fight for a future where no child has to grow up fighting CF.

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