February 13, 2019
When Stephanie Van Doren came to Mayo Clinic, she never expected to learn she had a genetic defect that raised her risk for a potentially fatal heart condition. But thanks to her physician’s all-inclusive approach, Stephanie and her family now have information they need to live life to the fullest.
February 13, 2018
When Karter Malcomson was born, his care team knew it was likely he had a genetic disorder. But a clear diagnosis was elusive. That’s when the functional genomics team at Mayo Clinic’s Center for Individualized Medicine went to work. And they didn’t give up until they had an answer.
October 5, 2017
After years of dealing with mysterious symptoms, Nicole Rickert was diagnosed with Ehlers-Danlos syndrome. Now she’s working with her team at Mayo Clinic to get the care she needs to move forward into a healthy future.
March 1, 2017
Written by Sanan Malkadjian I was only 14 at the time. I would be ashamed of myself because of how often my stomach hurt. It came to a point where no one would believe the excruciating pain I was facing. This was pain unlike no other. My doctors here in Michigan would blame one another. […]