I know this is unrelated to the above post, but I'm curious if there has been any news about what will happen to the EDS Clinic at Mayo Jacksonville when/now that Dr. Knight leaves his position, and the patients established with and waiting to be seen? I've been very transparent about not having the most positive experience, mostly because of organizational challenges, but they were always kind to me when we were able to overcome the communication and administrative challenges. And as a patient, we were always told we could contact the clinic to return if and when we experienced a significant life change that affected our condition. I'm disappointed Mayo didn't or couldn't invest more in EDS and POTS care.