Just a quick note to say that if any friends or family feel like you would like to share something, a story, a memory, a perspective, or a challenge after learning about my diagnosis – you’re more than welcome to contribute to the site.
I would like this to be a place for connection around MND. If there’s something on your mind that you’d like to put into words, I’d be honoured to include it here.
No pressure, of course but if you’re interested, Matthew will help get it posted. He plans to add his own posts over time too.
Thanks for reading and being part of this.
