2021 was another challenging year for many, but once again, MDA’s grassroots advocates were relentless in ensuring lawmakers heard their voices. Throughout the year, our volunteers emailed, called, and met with important decision-makers urging them to act on vital public policy that will improve the lives of people living with neuromuscular disease and their families. . . .
Researchers at the Icahn School of Medicine at Mount Sinai are seeking disability advocates to participate in a survey about the current state of genetic counseling for the disability community. The goal of this survey is to help understand gaps in knowledge among genetic counselors regarding life with disability and to evaluate educational opportunities, such as . . .