MSD World Day
July 30th is MSD World Day, and as a genetic counselor and board member of the United MSD Foundation, I'm reaching out to my colleagues in the field. Multiple Sulfatase Deficiency (MSD) is incredibly rare – so rare that many of us may never encounter a case in our practice.
Despite its rarity, the impact on affected families is profound. With long diagnostic journeys and no treatments available, there's an incredible opportunity for us, as a community, to drive awareness and support the vital work of organizations like the United MSD Foundation to find solutions.
Here’s how you can make an impact right now:
Donate to accelerate research and help families access life-changing clinical trials: https://secure.qgiv.com/for/2025msdworldday/
Wear BLUE or grab MSD World Day gear to show your support: https://curemsd.org/msd-world-day/
Follow @CureMSD on all social media platforms and share their content to raise awareness
Thank you, Michelle Fox