About Us
Building Partnerships for Better Health
Who is Disease Management Network?
At DMN, our approach involves an integrated system of education, interventions, measurements, and refinements of healthcare delivery designed to optimize clinical and economic outcomes for individuals within specific rare or chronic disease communities. With over 20 years of experience with a peer-to-peer disease management model, we are uniquely equipped to share our successful approach with disease communities, their patients, advocates, and medical partners.
The DMN Team
Get to know the dedicated individuals behind Disease Management Network, working tirelessly to provide expert care, support, and innovative solutions for better health outcomes.
Mark Delvaux
Robert Sandhaus, MD, PhD, FCCP
DMN Board of Directors
Discover the accomplished leaders who guide and shape the vision of Disease Management Network, driving strategic decisions and fostering excellence in healthcare and disease management.
Robert Greene, Jr.
Miekeleen Hart
Grant Wood
Dell Witcher
Marcia Ritchie
Charles “Tim” Frost
AlphaNet Case Study
AlphaNet, a non-for-profit organization, works to serve individuals with Alpha-1 Antitrypsin Deficiency. In partnering their Alpha-1 community leaders with leaders in the pharmaceutical industry, they were able to provide disease management services for increased compliance, better Alpha-1 patient outcomes, lower health costs, and improved future support to the Alpha-1 Foundation.
How DMN Supports Rare and Chronic Disease Communities
Every solution we provide at DMN is supported by medically reviewed information through our Medical Team. Using customized data gathering, monitoring, and reporting, our team helps to improve the quality of life for patients, develops comprehensive educational reference guides, and generates donations that go directly to your community from our foundation.
Reach out to learn more about partnering with Disease Management Network.
We are a not-for-profit organization that builds partnerships with patient communities and health care entities to provide peer-coordinated, data-driven disease management services for patients with rare or chronic conditions.