01/27/2026
Bringing this post from last year back, because I think it's a valuable topic more people need to understand.
"Informed consent" is a term we hear often in healthcare, but do we really understand what it means, or how often it’s done poorly?
Informed consent is a process to ensure you fully understand what’s happening and why, not just a checkbox. It comes down to five key components: the explanation, risks, benefits, alternatives, and consequences of not proceeding. If any of these are missing, you don’t truly have informed consent.
Risks are what could go wrong–short- and long-term– to help you make an informed decision (not to scare you)).
Benefits need to go BEYOND “this might help.” What are the goals? Are the outcomes likely or just possible?
And understanding alternatives matter too. Is this the only option? Are there other treatments, even if less common?
Finally, what happens if you do nothing? Understanding the consequences of not proceeding is just as important.
This is top of mind because, even as a healthcare professional, I didn’t receive proper informed consent for this procedure I received last year. I got a basic overview but not enough to fully understand what I was agreeing to. I had to Google it to fill in the gaps and to know what questions to ask my doctor. That’s not okay. And if it’s happening to me, I know it’s happening to others.
And I don't blame providers for this either! Most aren’t dismissive on purpose, but in a system stretched thin, with routines and time constraints, it’s easy to overlook how significant a “routine” procedure is for the person experiencing it.
So, if you’re facing a medical decision–surgery, an injection, a manual therapy technique, even a skin treatment–ask the questions.
What are the risks?
What are the benefits?
Are there alternatives?
What happens if I don’t do this?
If the answers aren’t clear, keep asking. Your health isn’t routine. You deserve to feel informed, heard, and respected.