I've had RSDS for about 12 years. I live in Colorado but grew up in southern New Jersey. I've had ketamine and lidocaine infusions....they sort of helped. However nothing in neurology is ever cured so RSDS is what it is. Medical cannabis took me from being bedridden to having a somewhat normal life. I'm still on SSD but at least I can do the basics now and I continue to improve. Stay strong.