DADA2 Foundation

The DADA2 Foundation aims to find innovative ways for patients & families, physicians, researchers, non-profits, government, academia, biotech and pharma, to work together to accelerate research into the rare disease Deficiency of Adenosine Deaminase 2, to raise awareness about the condition, and to improve the lives of DADA2 patients around the world. 

We feel that establishing our large network of patients and families, physicians and researchers is the secret sauce to moving fast as possible toward a cure for DADA2 and improving the lives of DADA2 patients around the world.
Key tenets to our strategy today include:
Convening
Curiosity
Collaboration
Consensus
Communication

Please go to our website www.dada2.org for more in-depth information about DADA2 as well as resources for patients, families, physicians and researchers.