I live with Ehlers-Danlos Syndrome and polymyalgia rheumatica: chronic pain and fatigue that nobody can see while everyone expects me to just "power through." I know what it's like to look fine but feel terrible, and how exhausting it gets explaining why some days I can function and others I can't. And the constant unsolicited advice? Exhausting. I'm here for the real conversations about living with invisible illness. The guilt from canceling plans again, the frustration of medical gaslighting, the isolation when people don't understand that "getting better" isn't always the goal. No forced positivity, no pressure to be grateful for "lessons." Just honest talk about navigating life when your body doesn't cooperate and the world isn't built for people like us. I know how lonely chronic and invisible illness can be. You're not alone.