📣 Learn more about what disruptions in federal funding can mean for #myotonicDystrophy research. 🔬🧬 MDF surveyed experts in DM research to understand how funding uncertainty may delay the timeline for treatments & a cure. 🔗 Learn more: https://t.co/jevEyYyiMt
Honored to present my research findings at the @MDAorg Conference on their 75th anniversary! Grateful to contribute to the fight against neuromuscular diseases. Huge thanks to Professor Berglund for all your support! #MDAConference#75YearsOfMDA#BerglundLab
Excited to kick off the Muscular Dystrophy Association’s 75th Anniversary Conference with an engaging Trainee Networking Session! Honored to share insights on my MDA Development Grant project and connect with brilliant minds dedicated to neuromuscular research.
Today is International myotonic dystrophy awareness day! Happy to be contributing to myotonic dystrophy research and spreading awareness online and in my local community.
Today is #InternationalMyotonicDystrophyAwarenessDay. Watch Sarah’s story to learn about her diagnosis, the impact #DM1 has on her and her family, and why a transformative therapy is urgently needed for this progressive disease: https://t.co/UpApkeDpnj #myotonicdystrophy
#myotonicDystrophy symptoms usually become more severe with each generation, yet there is currently no cure and there are no approved treatments. Help us get closer to better care and a cure by spreading #myotonicDystrophyAwareness on September 15! https://t.co/NQ5hsCpjJO
Dear Air India, your passenger deserves better service. Look at the seat condition that I forced to use for my journey to India from JFK airport, New York(flight number AI102).
Dear Air India, your passenger deserves better service. Look at the seat condition that I forced to use for my journey to India from JFK airport, New York(flight number AI102).