Rodney F. Witcher, II

The BAG Collective is a collective of angel investors from top tech companies and startups that invests intellectual, social and financial capital in seed to Series A startups around the world. Our collective believes in and support founders who build ethical, high-growth technology companies.

About LBDA The Lewy Body Dementia Association (LBDA) is a 501(c)(3) nonprofit organization dedicated to raising awareness of the Lewy body dementias (LBD), supporting people with LBD, their families and caregivers and promoting scientific advances. The Association's purposes are charitable, educational, and scientific. Our Vision A cure for Lewy body dementias and quality support for those still living with the disease. Our Mission Through outreach, education and research, we support those affected by Lewy body dementias. History LBDA was formed by a group of caregivers who met in an online LBD caregiver support group. Discussions about the need of support for LBD caregivers and the lack of public awareness about LBD led to the organization's incorporation. The directors of the LBDA Board are located throughout the United States, and LBDA volunteers are from the United States, Canada, and the United Kingdom. The association consists of a dedicated group of people from all walks of life who understand the struggles of other caregivers due to their personal LBD experiences.

The BAG Collective is a collective of angel investors from top tech companies and startups that invests intellectual, social and financial capital in seed to Series A startups around the world. Our collective believes in and support founders who build ethical, high-growth technology companies.

About LBDA The Lewy Body Dementia Association (LBDA) is a 501(c)(3) nonprofit organization dedicated to raising awareness of the Lewy body dementias (LBD), supporting people with LBD, their families and caregivers and promoting scientific advances. The Association's purposes are charitable, educational, and scientific. Our Vision A cure for Lewy body dementias and quality support for those still living with the disease. Our Mission Through outreach, education and research, we support those affected by Lewy body dementias. History LBDA was formed by a group of caregivers who met in an online LBD caregiver support group. Discussions about the need of support for LBD caregivers and the lack of public awareness about LBD led to the organization's incorporation. The directors of the LBDA Board are located throughout the United States, and LBDA volunteers are from the United States, Canada, and the United Kingdom. The association consists of a dedicated group of people from all walks of life who understand the struggles of other caregivers due to their personal LBD experiences.