Asking for my adult granddaughter: Is there an Ehlers Danlos Syndrome (EDS) specialist clinic at Mayo? Where? Would they be able to help develop a treatment plan that her local medical providers can follow, since few doctors or therapists know anything about EDS. In fact, most of the doctors during her discovery/diagnosis have been dismissive of the many “mysterious” symptoms. She has had genetic testing done to confirm the diagnosis now. Problems have involved of course joint dislocation and constant pain, gastrointestinal and gynecological challenges. All these frustration are affecting her mental health. Thank you.