I was diagnosed with CRPS 9 years ago and the pain doesn’t get better. Unfortunately, for me, it has spread to my other leg, and to 1 arm. My doctor believes it’s in my spine also but at this point it’s kinda like whatever. My life forever changed bc of this disease, I am no longer able to work, so on disability. I miss/grieve the person I used to be, my depression has gotten worse, I honestly want to amputate my legs and one arm, doctors don’t take me seriously saying then you will have phantom limb pain. You find out very quickly who truly cares about you and who doesn’t. Best of luck to anyone diagnosed with this disease, you have to be your own advocate bc most doctors don’t know anything about it, heck haven’t even heard about it. Going to the ER, as soon as you tell them you have CRPS, even if that has nothing to do with why you are there, they label you as wanting pain meds. Trust me, you have to advocate for yourself, educate yourself as much as possible. Find support groups. 💕