
Family finds answers to rare, genetic glaucoma
When a father and his two kids developed an array of peculiar symptoms, doctors, Brazilian researchers and the NIH partner
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Imhoff, the team's Diabetes/Endocrinology, Kellogg Eye Center, Nephrology and Rheumatology communicator, joined Michigan Medicine in 2019. She's passionate about storytelling and brand activism. Twitter: @JordynImhoff
When a father and his two kids developed an array of peculiar symptoms, doctors, Brazilian researchers and the NIH partner
Paul DeWyse reflects on being the hospital’s first patient, feeling like a social pariah and how precious life is.
After Shavonn Burgess got her daughter’s diagnosis, she had no idea how her family would cope.
A patient’s genetic makeup and journey with leukemia highlights the need for more gene sequencing in minority children.
A registered dietitian explains how less sugar is key, offering a recipe to try at home.
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