I am newly diagnosed MGUS, though I wonder if I'm smoldering. But, for purposes of my question, that part isn't important. And I will apologize now if this isn't the right forum for this question!
My question is: Does anyone have any personal experience with, or heard anything about, the Cleveland Clinic and where it ranks as far as multiple myeloma?
So many trials and specialists seem to be out of MD Anderson, Sloan, NIH, Dana Farber, Mayo, etc. Just not sure if I will be in good hands or if I should be looking elsewhere.
Thanks in advance!
