I’m late to the party on this conversation, but… I just recently completed one. I didn’t have any issues with it for this particular person (I had discharged them a month or more prior) but I’m curious, who would fill it out if not the treating provider? I don’t have the directive on hand but clearly I missed the part where it says treating provider shouldn’t fill it out. Does that mean not to complete it only if you’re actively seeing them *now*?
I get asked about social security disability forms more often and my supervisor’s hard line has been under no circumstances should be complete them, since it’s asking us to make medical determinations outside the confines of our roles as psychotherapy providers. It’s saved me from having to deal with patient reactions to my real answer, which is that except in extreme cases, I don’t think someone is permanently disabled because of (whatever diagnosis) for the rest of their life. I’ve yet to come across someone in my current role I believe was severely disabled such that they couldn’t work at all.
In other news, I was recently smacked upside the head with some fierce burnout that felt like it came out of nowhere. I’ve been extremely happy with my current role and I can’t get articulate where this came from. But I have been on the prowl for and have applied to a few jobs that are mental health related but more in the program development/public health realm. Advocacy has always been my passion and while I love clinical work, I am getting tired of the repetition of addressing the same problems on an individual basis a million times over. A couple of my patients have told me I look tired lol.