NEW ORLEANS – A Rochester, New York, researcher will receive a $263,622 grant to continue his study of injury to brain cell connections (synapses) in multiple sclerosis (MS) through the American Brain Foundation (formerly the American Academy of Neurology Foundation) and the National Multiple Sclerosis Society Clinician-Scientist Development Award.
Matthew Bellizzi, MD, a Fellow in experimental therapeutics and neuroimmunology at the University of Rochester, was awarded the fellowship for his work investigating progressive degeneration of the brain in MS patients and in MS models.
The three-year award is designed to encourage MS clinical research with the goal of providing better treatment, prevention or cure of the disease. Clinical research is the fundamental transition stage between discovery and treatment. Clinical research provides the scientific basis for all forms of care, addresses patient and caregiver needs and is the backbone for drug development and cost-effectiveness studies needed to improve lives. Fellowships provide recipients with up to three years of “protected time,” with salary that allows them to continue important research projects in their chosen interests.
Multiple sclerosis is an unpredictable disease of the central nervous system that disrupts communication between the brain and other parts of the body. MS patients experience muscle weakness in their extremities and difficulty with coordination and balance, among other symptoms. The progress, severity, and specific symptoms of MS vary from one person to another. There is no known cure for multiple sclerosis at this time, but there are therapies available that may slow the disease and improve quality of life.The American Brain Foundation, the foundation of the American Academy of Neurology, supports vital research and education to discover causes, improved treatments, and cures for brain and other nervous system diseases. Learn more at http://www.CureBrainDisease.org or find us on Facebook. The National MS Society addresses the challenges of each person affected by MS by funding cutting-edge research, driving change through advocacy, facilitating professional education, collaborating with MS organizations around the world, and providing programs and services designed to help people with MS and their families move their lives forward. The Society is dedicated to achieving a world free of MS. For more information about the National MS Society, visit www.nationalMSsociety.org.