Lesotho Support Groups and Charities

Rare Diseases Lesotho Association

Nthabeleng Ramoeli is Founder and Chairperson of Rare Diseases Lesotho Association (RDLA). Having been misdiagnosed for years and eventually receiving his diagnosis of EDS, he created Rare Diseases Lesotho, an NGO that was formally registered and founded in October 2017, with the core fundamentals of aiding all those afflicted with rare conditions in and around Lesotho, Africa, and the world at large, through awareness campaigns and effective dialogue. www.rdla.africa and mramoeli@gmail.com. Please follow us on Facebook at Rare Diseases Lesotho Association and on Instagram at rare_diseases_lesotho.


 




To add your EDS support group or charity, please complete the Support Group Listing Request form. To become an affiliate of the Society, please visit the Global Affiliation Program page.