This past week, I had an appointment with my GI doctor to go over my ongoing symptoms and feeding tube situation. Right now, I still can’t eat or drink, and that hasn’t changed in quite a while. It’s honestly exhausting—not just physically, but emotionally too. After discussing everything with my doctor, we’re planning to change my current PEG tube to a GJ tube. This should hopefully help with some of the issues I’ve been having, especially around tolerance and gastric motility. But like most things in the medical world, it’s a waiting game. We’re also waiting to hear back from a multi-disciplinary clinic in Toronto. It’s supposed to be a more comprehensive setup, where multiple specialists can weigh in, which gives me a bit of hope. I’m really hoping this will bring some answers—or at the very least, a more holistic plan moving forward. I’ll be honest, it’s been hard. Living without the ability to eat or drink feels incredibly isolating at times. I miss the simple things—grabbing a coffee with friends, sharing a meal with family, even just sipping water without worry. But I’m trying to stay grounded and hopeful while we wait on the next steps. Thanks to everyone who’s checked in or sent kind words lately. Your support means the world. I’ll keep you all updated as things unfold. 💛