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Close your eyes. Imagine you could live anywhere in the world. Money isn’t a consideration, logistics? No problem. Whatever you fancy is available… Got it? Let me guess what you got… a golden sandy beach? Sun rays warming your face? A sangria in one hand with a cabana boy fanning you from the side? Bingo. This is what I envisioned when I decided to move to the South of France with my, at the time, 9-month-old bundle of joy (baby, not a puppy, just to clarify).

My name is Liam Virgo, and I am an advocate for functional neurological disorder (FND), pushing to raise awareness for this life-changing condition. For the past ten years, I have been fighting a quiet, gruelling war to reclaim my body and my identity after a sudden illness turned my teenage world upside down. While the physical realities of severe FND are devastating, the profound mental health struggles, emotional scars.

Overnight, at the age of nine, I went from an energetic, sociable child to housebound and isolated as Myalgic Encephalomyelitis (ME/CFS) and other comorbidities shrunk my world to my bedroom. ME is a chronic, fluctuating disease that causes symptoms such as severe fatigue, post-exertional malaise, pain, sleep problems, and brain fog. It can leave people bed or housebound, and there is currently no cure. As the years passed, I tried every form of low‐energy activity that I cou