I wanted so badly to improve my life and connect with resources that would support me.
I must have been living in a bubble.
I had no idea the stigma and discrimination against those living with an SMI diagnosis was coming from the very folks contracted to provide necessary services.
The excuses for the clinic's 's lack of quality care are becoming just that, excuses.
If anyone would like I gather and come up with a way to at least start effectively communicating correct, current and accurate information not only regarding process and policy but also ensuring correct, current and accurate documentation I would live to advocate for better care providers with you.
The phrase, "If it's not written down it didn't happen does not equal If you write "whatever down it's true and real.
I'm pissed and for good reason.
Who's listening?