Today is National Lewy Body Dementia Day—and unlike many "National Days," this is not one anyone wants to celebrate. Lewy Body Dementia is a little-understood yet common form of dementia. It often affects younger people but can strike at any age. Tragically, its symptoms progress more rapidly than other forms of dementia, making it a particularly devastating diagnosis for those affected and their families. If you’ve encountered Lewy Body Dementia, you’ll know just how life-changing it can be. My father-in-law Jon, is currently suffering from LBD. It's been a difficult time for everyone. No more so than for Jon. Currently, there is no cure. However, there is hope. There is a community offering vital support, and at the forefront is @lbsorg. Last week, the Society delivered a petition to Parliament urging the government to provide greater support for families navigating this incredibly challenging journey. Based on my own experience, I can’t stress enough the importance of early diagnosis and equipping yourself with as much information as possible. A book that particularly helped me understand the illness better was 'Living With Lewy Body Dementia' (linked below), and I highly recommend it for anyone seeking understanding and practical advice. Supporting the charity was one of three reasons behind my December 2025 ocean rowing challenge: 3,000 miles across the Atlantic in an attempt raise £100,000 for The Lewy Body Society. It’s a tough journey, but one that pales in comparison to the daily battles faced by those living with this condition and their loved ones. We’ve made a start, but there’s still a way to go. If you’d like to support this cause, you can find my GiveStar link in the comments. Finally, if you or someone you know is struggling, please know that help is available. Reach out to The Lewy Body Society—they’re there to guide you and offer the support you need. Together, let’s raise awareness, offer hope, and make a difference.