Hello!

Hi! I’m Graham. I’m a dad, a husband and a photographer who was diagnosed with motor neurone disease (MND / ALS) in 2023.

After the initial shock, I threw myself into research to find out what MND is, how it works and what I can do about it. It’s a really difficult diagnosis but I quickly found a few glimmers of hope and I wanted to break away from the established narratives and write a different story for myself.

After 10 months of research, I poured what I’d learned into my book, The 1% Chance: Hope, Wellness and Discovery in the Face of MND. I wanted to pass on hope to the next person who finds themselves where I was 18 months ago.

Now that the book is out, what next? Another book? A podcast? A Youtube channel? How about something simpler? A good, old-fashioned blog where I can share the new things I’m learning on this journey? Posts will be fairly short and I’ll try to add an audio clip to go with each article.

So far, I’ve had really good feedback from the book, which came out a month ago, and I feel like there are more people out there who are looking for ways to support their physical, mental and spiritual health through their diagnosis. This blog is for you.

Check back every week for the latest post, and welcome to the tribe!

The author is not a healthcare professional; this article is for informational purposes only and does not construe medical advice. Please consult a healthcare professional about your own healthcare needs.

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Why The 1% Chance?