My pain doctor referred me to a doctor today who is doing oral ketamine for crps/rsd patients that are not having a lot of success in other areas. Y'all have seen my struggles of late in finding relief. Has anyone tried this? Please give me good and bad experiences. I've been reading research that make it seem like giving it a try is worthwhile, but I am not sure as it doesn't seem like they have been using it long.

Also, it seems like insurance doesn't pay as it is "off label" use for crps.

Any help would be appreciated!
Thanks. I hope everyone is having low pain days!!

TK