Solving the challenges of living with complex diseases involves assembling the right pieces of a complex puzzle, bringing patients, advocates, researchers, and industry partners together, and empowering them with advanced tools to conduct clinical research studies.
Count Me In has developed the resources to advance scientific collaboration through partnerships. Through these partnerships and carefully conducted studies, we have generated data that has led to numerous scientific publications and data releases that are improving the complex diseases patients journey.
Partnerships that drive results
>8500
Patients across the United States and Canada have registered to participate in Count Me In research projects.
10
Releases of data into scientific repositories across existing Count Me In projects.
60+
Scientists working in academic and industry settings around the world who are using Count Me In data to catalyze their research.
20
Studies in collaboration with researchers across academia, industry, and patient advocacy groups, resulting in significant translational impacts.
50
Citations of Count Me In datasets to date.
>8500
Patients across the United States and Canada have registered to participate in Count Me In research projects.
10
Releases of data into scientific repositories across existing Count Me In projects.
60+
Scientists working in academic and industry settings around the world who are using Count Me In data to catalyze their research.
20
Studies in collaboration with researchers across academia, industry, and patient advocacy groups, resulting in significant translational impacts.
Count Me In would like to thank each patient and patient advocacy group that has engaged or is participating in our studies. Without your invaluable contributions, achieving our vision of building a platform for the global community of patients and scientific partners that accelerates biomedical research would not be possible.
Patients hold the keys to unlocking insights and advancing research. By collaborating with Count Me In, advocacy organizations can play a vital role in advancing research. Our partnership creates pathways for patients and the scientific community. It empowers patients and their caregivers by providing an easy way to contribute to research that can accelerate discovery and fuel research."
Christina Ip-Toma, Director of Scientific Programs, MIB Agents
