Cure MSD
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Multiple Sulfatase Deficiency (MSD) is a rare, genetic condition that affects children. It is a monstrous disease that is extremely progressive, similar in effect to Alzheimer's or Parkinson's. Children born with MSD suffer from loss of motor skills, speech and cognitive abilities, inability to swallow, blindness and ultimately death. While this disease is rare, with only approximately 100 known c
14/05/2026
More inspiring voices joining our 2026 MSD Virtual Summit speaker lineup 👇
We’re honored to welcome leading researchers advancing the future of MSD treatment and understanding through innovative pharmacological chaperone research:
🧬 Dr. Matt Baud & Dr. Hugh Britton from the University of Southampton
🧬 Dr. Hartmut Niemann from Universität Bielefeld
During our Scientific Day, these experts will share the latest developments in pharmacological chaperones and their potential role in treating MSD, including efforts focused on stabilizing the FGE protein as a therapeutic strategy.
We’re also grateful to recognize the important support of the MSD Action Foundation and the Health Research Board (HRB) Ireland, whose funding has helped advance this promising area of research.
Together, these collaborations reflect the power of global partnership, innovation, and relentless hope for the MSD community. More speakers and details coming soon!
🗓 September 18–19
💻 ZOOM | FREE to attend
Learn more here 👉 https://curemsd.org/2026-virtual-summit/
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Opening Hours
| Monday | 08:00 - 17:00 |
| Tuesday | 08:00 - 17:00 |
| Wednesday | 08:00 - 17:00 |
| Thursday | 08:00 - 17:00 |
| Friday | 08:00 - 17:00 |
