Medical Stories - CDKL5 Deficiency Disorder (CDD): Judith's Story скачать в хорошем качестве

Medical Stories - CDKL5 Deficiency Disorder (CDD): Judith's Story

According to the Epilepsy Foundation, CDKL5 deficiency disorder (or CDD) is a genetic condition that manifests in several ways, including triggering seizures in infants just weeks, days, or even hours after they’re born.  Kaitlyn, 33, learned that her daughter, Judith, had CDD when she had convulsions shortly after her birth. Along with her epilepsy, Judith, now 11, also has trouble focusing on faces, moving on her own, and speaking with others. Although Kaitlyn initially felt overwhelmed as a new mother, she shares with Medical Stories how her family's support gave her the strength she needed to care for her daughter. Featuring renowned experts: Elia M. Pestana Knight, Pediatric Epilepsy, Cleveland Clinic Epilepsy Center; and Orrin Devinsky, director of the NYU Langone Comprehensive Epilepsy Center. Please subscribe to our YouTube channel and look for Medical Stories on your Public Television station. Check your local PBS listings today! Or visit https://medicalstories.tv/ to learn more about this very popular documentary series. Follow us on Facebook:   / medicalstories.pubtv.pbs   Check us out on Instagram:   / medicalstories_pubtv_pbs   Subscribe to our YouTube Channel:    / @medicalstories   #MedicalStories #MedStoriesTV #rarediseases #cdd Chapters: 0:00 Judith’s Story 3:04 What Is CDKL5 Deficiency Disorder (CDD)? 3:55 Early Seizures and Developmental Delays 4:37 Becoming a Single Special Needs Mom 5:42 Living With Uncontrolled Seizures 6:13 The Honeymoon Phase and Setbacks 6:56 Managing Seizures With the Ketogenic Diet 7:39 Communication, Personality, and Daily Life 9:50 Hope for Research, Gene Therapy, and the Future