Hi. I was wondering how people explain crps to others. I moved to australia 4 years ago and am due to go home to the uk for a wedding next year. My concern is that when i left my crps was very mild and most people didnt know i had anything out of the ordinary wrong with me. After a flare up a few years ago the crps has spread. I walk with a very noticeable limp and sometimes use a cane. I have limited use of the effected arm. But my main concern is the permenant tremours and speech problems. I should be feeling excited about seeing my family and friends but i am dreading it. Does anyone have any advice