I have, thank you so much for your time and help. I am just really frustrated, and was hoping to find more specific answers about the CFS specialist/treatment at the Rochester clinic, but have had no luck. I was diagnosed with CFS at the Jacksonville clinic, and went through what I think is similar (or exact) to the Rochester clinic's "self management sessions." My husband contacted the Rochester clinic because they have a CFS specialist (Jacksonville doesn’t), and we both feel I may benefit from seeing one. The Rochester clinic did accept me as a patient. My husband expressed to the Rochester scheduler that we did not want to incur all of the expenses that traveling to their location would require (including medical) if it would be no different than what we learned at the Jacksonville clinic. I feel that is a valid concern. The scheduler in Rochester said I would not have been accepted for an appointment if they didn’t feel they had something beneficial to offer me, but that is all they will tell us. When we were at the Jacksonville location, I asked them about seeing a CFS specialist (not necessarily at Mayo), and I was told that I might get more information, but the treatment would be the same. So here we are wondering if we should spend more money (which is already tight since have not been able to work) based on conflicting information/basically a gamble. My husband pleaded for just one tele-medicine appointment with the CFS specialist in Rochester to find out more information; just enough information to see if we should make the trip. Jacksonville clinic did this for us, the Rochester location will not. We aren’t asking for a comprehensive visit, just enough to help us determine what we should do. When you are a person struggling to feel well again, this doesn’t feel just, and is frankly heartbreaking. If you know anyone else I can contact that would be a blessing. Thank you.