United MSD Foundation
United MSD Foundation | Multiple Sulfatase Deficiency | Cure MSD
813669443
2016
Biloxi, MS 39533 USA
curemsd.org
CUREMSD
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News
Are you signed up for our monthly e-newsletter? May's newsletter is out and it's filled with information on our AAV9 gene therapy trials, MSD World Day, and more! Sign up here: (fb)
UMSDF Executive Director Sarah Cortell Vandersypen is at the #ASGCT Annual meeting this week in New Orleans, and is pictured here with Dean Suhr from MLD Foundation and Scott Loiler from National MPS Society. Look for her presentation later this week! #MSD #RareDisease (fb)
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About the organization
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United MSD Foundation Finding a Cure Join the team committed to finding a cure for MSD Zebra Run March 29 2025 Bespoke Award A PublicPrivate Partnership 2024 Conference Recap of the biennial conference Together We Can Cure MSD Founded in 2016 United MSD Foundation is a registered 501c3 nonprofit organization serving an international community of Multiple Sulfatase Deficiency families researchers and care providers. We exist to bring awareness to MSD fund research toward treatment and support families through education resources and community. What is MSD. Multiple Sulfatase Deficiency MSD is a rare genetic progressive neurodegenerative disease caused by the build up of cellular waste throughout the body leading to neurologic regression and multisystemic symptoms.
