Dealing with Joint Pain
The worst thing about Lyme disease for me is the joint pain. I don’t like taking medication, so I asked for something much weaker than the Percocet that was initially recommended. I’m taking what amounts to an extra strength Aleve and it pretty much does the job. However, I’ve had tears in my eyes after it wore off more than once during “strenuous” activities like sitting at a table for four hours. I’m thinking about investing in one of those massage chairs you see at the mall or moving into a family member’s hot tub as additional pain management techniques.
Anyone have some good tips for dealing with joint pain?