My doctor mentioned on my last visit that he thought the president of our National Fibromyalgia Association was not helping our cause. I didn't realize there was an association nor a president. Her name is Lynne Matallana . My doctor said she flys from one conference to another, all nicely scheduled and looking good and talks to medical people about our disease. My doctor said he doesn't have a single fms patient that could handle that kind of travel schedule, stress and acitivity. I put in google the National Fibro Association and found this woman says we are celebrating our tenth anniversary!