Lately I'm seeing a common issue with regard to CP patients receiving adequate pain control after an acute episode like surgery. Having recently gone thru it myself, I'm curious how many others this has happened to and if there's a solution. Most of us can't really advocate for better pain control when we can barely move after surgery, much less discuss the problem with hospital staff without appearing to be a nuisance. If I or someone I know is in a similar situation again, what is the best way to approach staff and achieve positive results? I'm very interested in this as it has happened several times with my elderly father, myself (2 months ago), and others on this wonderful site.
Any thoughts, suggestions, experiences?
Thank you for taking the time to read this, and my prayers are with those that are just trying to get through each day
PS I'm writing this on a smart phone & tried to edit the subject but it's not working. Sorry if it doesn't make sense...
Post Edited (1 day at a time) : 1/11/2013 3:37:50 PM (GMT-7)