I too believe we are a wealth of information. The members here are from every demographic type, women of all ages, men of all ages, types of treatments, different geographic areas, and the list goes on.

To correlate this wealth of information could help shed light on directions to take research, or turn the lightbulb on for doctors. Maybe we can determine common threads of meds that work nearly the same on everyone.

We need to have compassion for all of our RSD family. We are unique in that we all have been labeled with this monsterous disease, disorder, dystrophy or what ever they finally decide to call it.

It is written things dont change if you always do the same thing you always do. It changes when you decide to do something different from what you always did before. We can make a difference.