The article points to concrete ways research benefits could be more fairly shared with disabled communities. This includes ensuring that findings are published in accessible formats (plain language, captions, screen-reader compatible documents), reducing financial barriers to treatments by advocating for insurance coverage or sliding-scale pricing, and designing interventions with accessibility built in from the start. Redistribution also means prioritizing disabled communities when research leads to new programs—such as ensuring clinical trials are followed by community rollouts in disability-centered clinics or schools.