To support and advocate for equitable diagnosis, access to appropriate quality health care and treatment for Rare Diseases patients.
To offer patients and families affected by rare diseases the necessary support and maintain their dignity and respect.
To work closely with the Ministry of Health in Botswana in policy development and any necessary documents that guide in management of rare diseases in Botswana.
To be the primary source of information on rare diseases in general and in Botswana. In addition the society will develop and disseminate information to patients, parents, carers and the general public about rare diseases.
To facilitate capacity building and networking opportunities for health care professionals to ensure better identification and management of rare diseases in Botswana.