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I woke up on a Sunday morning not being able to feel the left side of my body from my lower back to my feet. I shrugged it off at first, but on a Monday - the next day - I decided to check myself into the emergency room. I’m so glad I did. Every doctor told me most people would have just dealt with the numbness and wouldn’t have bothered checking to see what’s happening. Probably because our healthcare in the United States is robbery - but that’s another topic for another day. This is my new diagnosis and it’s flipped my world upside down. But the only way forward is to accept it, learn all I can and to try to thrive with my disease the best I am able! I truly appreciate you sharing your experiences, and I never want to discredit your stories. However, I kindly ask that you refrain from sharing worst-case scenarios or horror stories about this disease. I’ve already read many difficult accounts, and right now, I’m choosing to focus on hope. I fully understand the potential complications, but for the sake of my mental health and my struggles with anxiety and depression, I need to stay as optimistic as possible. Hope is the one thing I can control, and I appreciate you respecting this boundary. Thank you for your understanding and support! ❤️ When I come back from my social media break, my name is @shayleejustshaylee on Instagram and TikTok.