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MDF Board of Directors Approves Over $1 Million in Myotonic Dystrophy Research Funding

Published on Wed, 01/22/2025

We are thrilled to share that the Myotonic Dystrophy Foundation (MDF) Board of Directors recently approved an additional $805,000 in funding towards 2025 myotonic dystrophy research grants and fellowships, bringing MDF's 2024 total research grant investment to over $1 million! MDF's two groundbreaking initiatives, the Research Fellowship Program and the Early Career Grant Program, are made possible by the generous support of the DM donor community.

Record-Breaking Interest in MDF Funding Opportunities

The global response to these research funding programs was overwhelming, with applications from doctoral students, postdoctoral scholars, and early career researchers from institutions around the world. The proposals were competitive, showcasing innovative studies aimed at unraveling the complexities of DM, including investigations into pathogenesis, disease progression, clinical management practices, and advancements in therapeutic and diagnostic development.

In a rigorous review process held in November 2024, a committee of over 20 members, including MDF's Scientific Advisory Committee (SAC) and other expert reviewers, evaluated the applications. Their recommendations led the MDF Board of Directors in December 2024, to select five exceptional applicants for the two-year MDF Research Fellowship Program and two outstanding individuals for the Early Career Grant Program. Additionally, two early career applicants were recognized with short-term awards for their promising contributions.

Investing in the Future of DM Research

MDF's grant programs would not be possible without the incredible support received from our incredible donor community. Thanks to their generosity, these research initiatives are now poised to make significant strides in the field and support emerging leaders in DM research. The funded studies will encompass a wide range of topics, from testing the feasibility of remote assessments to exploring new models and therapies for myotonic dystrophy.

This investment in cutting-edge research and emerging leaders reflects the collaborative dedication of the entire DM community. We eagerly anticipate the transformative impact these studies and the scholars leading them will have on the lives of those affected by myotonic dystrophy and the broader scientific community.

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