Growing in Empathy: Learning to Take My Own Advice and Seeing the Person Before the Patient

Genetic Counselor Christina Kresge talks about her most memorable cases from providing pediatric and adult genetic counseling services to an underserved population in and around Newark, NJ over the past eight years. She also shares her own recent experience as a patient going through her first pregnancy, grappling with the implications of a positive carrier testing result. Story Reference Points: Patient story #1: Myotonic Dystrophy @ 4:34 Patient story #2: Sialidosis @ 9:15 Patient story #3: A rare recessive condition and an unexpected finding on microarray @ 14:49 Patient story #4: Newborn Screening and Homocystinuria @ 22:49 Patient story #5: Christina’s own story with prenatal carrier testing @ 25:41 Links and Resources Information on Myotonic Dystrophy from the Muscular Dystrophy Association Facebook group for Sialidosis Information and Resources related to High ROH (Regions of Homozygosity) Newborn Screening Resource National Organization for Rare Diseases (NORD) Rare Advocacy Movement (RAM) Check out other Patient Stories podcast episodes. Read other Patient Stories on the Grey Genetics Patient Stories Page Do you want to support Patient Stories? You can now make a donation online! Want to support Patient Stories in a non-monetary way? Leave us a review on iTunes, or share your favorite episodes on Social Media. Patient Stories on Twitter: @GreyGeneticsPod Patient Stories on Instagram: @patientstoriespodcast Are you looking for genetic counseling? Patient Stories is sponsored by Grey Genetics, an independent telehealth genetic counseling and consulting company. Book an appointment with a genetic counselor specialized in your area of concern. Choose from our growing Network of Genetic Counselors. All genetic counseling appointments take place over secure, HIPAA-compliant video-conferencing or by phone.