I had a dr. appt today and once again, realized that in the past 10 years of all sorts of interventions for FMS, I am the one who proposes the meds or treatments that I get. I saw that ya'll had a discussion about this in August. I have changed drs. often because we were military; either we moved or the dr. moved. I am thankful that the drs. I've had were open to my suggestions, but it confounds me that they rarely have a suggestion. I've always had to carry in an article or a book. Yep! Proactive is the only way to be with this illness. Still, it doesn't seem fair to people who don't speak medical or have computers or just simple folk who trust their physician.