Rare Diseases South Africa NPC

Best Patient-Led Health Advocacy - South Africa
<p>Founded in 2013 by Kelly du Plessis, Rare Diseases South Africa is a non-profit organisation that has been successfully working to ensure that people living with a rare diseases and congenital disorders experience better recognition and support, improved health service and a better life overall. Today, as a voice for the vulnerable communities, RDSA advocates the right to medical advice and assistance &#8211; playing a fundamental role in bridging the gap between vulnerable communities and innovation.</p>