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Pathways to Cures Research RoadmapInvesting in the next generation of MS researchers and clinicians: Advanced training fellowships and early-career awards are now accepting applications from MS researchers and physicians. The opportunities differ in duration (ranging from one to five years) and scope (covering both basic science and clinical research). All awards are designed to invest in emerging talent to build the skills needed to drive future breakthroughs in MS. We also are accepting applications for awards to train board eligible/certified neurologists or physiatrists in specialized MS clinical care . Advancing women’s health in MS: When Society staff identify gaps in the Pathways to Cures Research Roadmap, targeted funding opportunities are created to increase awareness and research in those specific areas. The Society recently highlighted priority research areas related to women’s health in MS that remain largely unexplored. In response, the Society is requesting grant applications for proposed research that addresses the knowledge gaps in women’s health issues for people with MS. Deadlines for these funding opportunities are in August 2025. Details about each of the awards are available on our website: Training fellowships and early-career awards Specialized MS clinical care opportunities Targeted funding opportunity: advancing women’s health in MS Pathways to Cures Research RoadmapInvesting in the next generation of MS researchers and clinicians: Advanced training fellowships and early-career awards are now accepting applications from MS researchers and physicians. The opportunities differ in duration (ranging from one to five years) and scope (covering both basic science and clinical research). All awards are designed to invest in emerging talent to build the skills needed to drive future breakthroughs in MS. We also are accepting applications for awards to train board eligible/certified neurologists or physiatrists in specialized MS clinical care . Advancing women’s health in MS: When Society staff identify gaps in the Pathways to Cures Research Roadmap, targeted funding opportunities are created to increase awareness and research in those specific areas. The Society recently highlighted priority research areas related to women’s health in MS that remain largely unexplored. In response, the Society is requesting grant applications for proposed research that addresses the knowledge gaps in women’s health issues for people with MS. Deadlines for these funding opportunities are in August 2025. Details about each of the awards are available on our website: Training fellowships and early-career awards Specialized MS clinical care opportunities Targeted funding opportunity: advancing women’s health in MS nationalmssociety.org, Facebook , X (formerly known as Twitter), Instagram , YouTube or 1-800-344-4867 . " c-nmssatomrichtext_nmssatomrichtext-host="">About Multiple Sclerosis Multiple sclerosis is an unpredictable disease of the central nervous system. Currently there is no cure. Symptoms vary from person to person and may include disabling fatigue, mobility challenges, cognitive changes, and vision issues. An estimated 1 million people live with MS in the United States. Early diagnosis and treatment are critical to minimize disability. Significant progress is being made to achieve a world free of MS. About the National Multiple Sclerosis Society The National MS Society, founded in 1946, is the global leader of a growing movement dedicated to creating a world free of MS. The Society funds cutting-edge research for a cure, drives change through advocacy and provides programs and services to help people affected by MS live their best lives. Connect to learn more and get involved: nationalmssociety.org , Facebook , X (formerly known as Twitter), Instagram , YouTube or 1-800-344-4867 . nationalmssociety.org, Facebook , X (formerly known as Twitter), Instagram , YouTube or 1-800-344-4867 . " c-nmssatomrichtext_nmssatomrichtext-host="">About Multiple Sclerosis Multiple sclerosis is an unpredictable disease of the central nervous system. Currently there is no cure. Symptoms vary from person to person and may include disabling fatigue, mobility challenges, cognitive changes, and vision issues. An estimated 1 million people live with MS in the United States. Early diagnosis and treatment are critical to minimize disability. Significant progress is being made to achieve a world free of MS. About the National Multiple Sclerosis Society The National MS Society, founded in 1946, is the global leader of a growing movement dedicated to creating a world free of MS. The Society funds cutting-edge research for a cure, drives change through advocacy and provides programs and services to help people affected by MS live their best lives. Connect to learn more and get involved: nationalmssociety.org , Facebook , X (formerly known as Twitter), Instagram , YouTube or 1-800-344-4867 .
Spring 2025 Funding Opportunities