AdvocacyJun 21, 2024
New publication at Rarity Life magazine!

We are delighted to share with you the latest article published by Rarity Life magazine.
We are delighted to share with you the latest article published by Rarity Life magazine.
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."