New Real-life Stories on OdySMA!
While stabilising treatment for SMA is available, European-wide access is not.
Meet Jana, Julia and Nataliia to understand how access to treatment and care, can impact the lives of people living with SMA!
While stabilising treatment for SMA is available, European-wide access is not.
Meet Jana, Julia and Nataliia to understand how access to treatment and care, can impact the lives of people living with SMA!
We are delighted to invite you to read the latest Digital Spotlight on Spinal Muscular Atrophy by Rare Revolution Magazine.
Today, on Rare Disease Day 2024, we are very excited to launch: "Care for adults living with SMA in Europe: a benchmarking report."
We are delighted to share with all of you the latest article about our 2023 Awareness Campaign: "I am Unique".