We need innovative solutions when it comes to the rare (disease) community

February 28th is Rare Disease Day. Twenty-five to 30 million Americans live with a rare disease. For more facts and figures related to rare diseases, check the NORD website. This podcast episode catches up with Aditi Kantipuly, a physician and advocate, immersed in the rare disease community. As a young girl Aditi learned about a child born with osteogenesis imperfecta – a rare bone condition – and has been captivated ever since. Her journey includes a masters program in public health, a Fulbright scholarship to small villages throughout India, and medical school. Currently she's exploring the roles of health equity and social immunity. For earlier podcast episodes related to rare disease, It's not that easy being rare, Rare disease and the need for research, and Rare and invisible disability + spoon theory. Check this webpage for a list of other podcast programs related to rare disease.