The lives of millions of South Africans with a litany of rare diseases can be vastly improved and even saved by addressing challenges in identifying, studying and treating their conditions.
With Rare Disease Day today (February 28), the Rare Diseases Access Initiative (RDAI) is driving an evolution of the country’s healthcare, through innovative strategies to better care for over 4.2 million people living with an estimated 7 000 rare diseases.
“As our healthcare system faces significant changes in the years ahead, it is vital that we also advocate for people living with rare diseases in South Africa, especially those with limited healthcare access,” said Kelly du Plessis, CEO of Rare Diseases South Africa (RDSA), a member of RDAI.
“As part of our ongoing research and awareness efforts, RDAI has conducted an initial analysis of the incidence and prevalence of rare diseases within the country.”
This research will assist in improving access to healthcare, policy development, and patient advocacy while giving critical insight into the challenges faced by patients.
