The G Word: Episode 96

Julia Vitarello, Rich Scott and Ana Lisa Tavares: Treating Mila - Lessons for those living with rare conditions

29 February marks Rare Disease Day. This day is an opportunity for the rare community to come together to raise awareness of the common issues affecting those living with rare conditions. A rare condition is a condition that affects less than one in 2,000 in the population, and although rare conditions are individually rare they are collectively common. It is estimated that there are over 7,000 rare conditions. Around 80% of rare conditions have an identified genetic origin.

In this episode of the G Word, our host Julia Vitarello, Founder and CEO of Mila’s Miracle Foundation, is joined by Rich Scott, Interim CEO for Genomics England, and Ana Lisa Tavares, Clinical Lead for Rare Disease Research at Genomics England, as they discuss challenges for those living with a rare condition and the work being carried out across the genomics ecosystem to support them.

Science Straight Up: Episode 23

JUDY MULLER AND GEORGE LEWIS

July 25, 2023

Our experience with mRNA vaccines during the COVID pandemic showed us the possibility of  designing other RNA-based drugs in a flexible and efficient manner. Dr. Athma Pai of the UMass Chan Medical School talks about how her research into RNA therapeutics and the immense promise it holds for conquering a wide range of diseases, from. cancer to sickle cell anemia, and more.  Veteran broadcast journalists George Lewis and Judy Muller moderated the session with Dr. Pai, recorded at the Telluride Conference Center in Mountain Village, Colorado

The G Word: Episode 88

Julia Vitarello and Dr. Tim Yu speak with Richard Scott of Genomics England about Mila’s powerful story - her diagnostic odyssey and bespoke treatment, the importance of newborn screenings for rare disease drug development, and their continued pursuit to pave a path for more n-of-1 treatments like milasen - as they move from Mila to Millions.