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National MPS Society

The National MPS Society is a US-based charitable organization dedicated to curing, supporting and advocating for people with mucopolysaccharidoses (MPS) and mucolipidosis (ML). MPS and ML are rare genetic lysosomal storage diseases (LSD) caused by the body’s inability to produce specific enzymes. The Society funds researchers worldwide working on MPS and ML at all career stages.

Challenge: Rare Diseases

Recipient Citizenship: Global

Host Location: Global

Grant Opportunities:

Research Grants (rare diseases: MPS)

Final closing date: September 15, 2022

Research Grants (rare diseases: MPS research fellows)

The opportunity is currently closed. Sign-up for grant alerts to be informed when the grant re-opens.

Final closing date: May 15, 2022