1) To increase widespread awareness of rare diseases and ways for their
early detection & management and ensure education in related issues
such as newborn screening, prenatal diagnostics and genetic
counseling among all relevant stakeholders.
2) To advocate for stronger policy support, funding and interventions
necessary for rare disease management in the country
3) To help improve the standards of care for patients – including improved
diagnostics and treatment in India.
4) To collaborate with important stakeholders that can strengthen the
cause of rare diseases.
