I was very lucky in my diagnosis journey, my GP suspected MG from my very first visit back in Jan 2012. The hardest part of this disease is the limitations it puts on your day to day life, and learning to accept them has been my biggest challenge. I have found great joy in celebrating the new and creative things I can do rather than focusing on what I have had to give away. My message for the world is that MG is a crazy condition that effects each person so differently.