Patient advocate shares about her two rare brain tumors and hereditary cancer syndrome.
Daniel speaks about the films to be screened at the festival and the film he produced about his son's rare disease, Menkes Disease.
Her personal journey to become a genetic counselor and advice for students.
Co-Founder/CEO of Kolgene explains the platform connecting clinicians with genetic labs around the world. His company streamlines the process of looking for labs, communicating with them and ordering the tests.
NORD's event in Hartford is recapped including interviews with a patient advocate, Michelle Cotton, and a Connecticut representative, Dave W. Yaccarino.
A Clinical Cytogeneticist talks about the field of cytogenetics which studies chromosomes.
Discussion on the epigenetics of tumor progression in pediatric cancer, how it differs between types of cancer, and using it to diagnosis and alter treatments.
Co-Founder/CEO of Onevoice shares how his new community building software solution supports the rare disease community.
Discuss the subfields of genetic counseling cardiogenetics, hereditary cancer genetics, direct-to-consumer tests and carrier screening.