As I’ve mentioned a few times on this blog I’ve been working in healthcare information is some form or another for over a decade now.
In my days as a opinion researcher with people in pain a theme regularly came up in interviews of how many people felt – both powerless and overwhelmed by chronic pain.
So I was very interested when one of my readers sent me this infographic which offers some ideas for “A Chronic Pain Personal Bill of Rights”.
I must admit that while I agree with the sentiments of the infographic I have to say I don’t really see how it could be described as a Bill of Rights. No mention of access to decent pain management for instance.
But really that is just me.
What do you think of it? And what would you add to a “Chronic Pain Personal Bill of Rights”? Please do share you thoughts in the comments section below.
Many thanks in advance.
Click on the image for the full version!
From Visually.