About PKANDAO
Last updated
Last updated
PKAN(Pantothenate Kinase-Associated Neurodegeneration) DAO provides financial, emotional, and informational support to individuals affected by PKAN and their families. Increasing public awareness about PKAN for early diagnosis, and fostering a supportive community. Creating a strong and connected community of patients, families, researchers, and stakeholders to facilitate collaboration, knowledge sharing, and mutual support.
In essence, the PKAN DAO's mission is to leverage the principles of decentralization and community to combat the challenges posed by this rare disease PKAN. By empowering stakeholders and transparently managing resources, We aim to make a significant impact on the lives of those affected by PKAN
The DAO aims to explore innovative ways to accelerate the development of therapies for PKAN, potentially through funding early-stage research, supporting clinical trials, and incentivizing pharmaceutical Labs.
Increasing public awareness about PKAN is crucial for early diagnosis, attracting awareness, and fostering a supportive community. At PKAN DAO we undertake initiatives to educate the public and healthcare professionals about the disease.