Rare Diseases South Africa turns 11

Introduction to the Rare Disease Partnership Programme

Access Dialogue - Access to Innovation

Patients attending and participating in Scientific Conferences: what is it all about?

Interstitial Lung Disease and Pulmonary Fibrosis: Managing Treatment

Exploring Inherited Metabolic Disorders in South Africa

Interstitial Lung Disease and Pulmonary Fibrosis: My Patient Journey

Rare Disease Day 2023

Letsatsi la Mafu asatlwaelehang la 2023

Usuku lwezifo ezingavamile 2023

Rare Diseases Access Initiative Stakeholder Symposium 2022

#Ride4Rare Ride Joburg 2022

You Think Your Body Hurts?

Meeting the Unmet Needs of IPF Patients

Interstitial Pulmonary Fibrosis: Patient Community Impact

Myelofibrosis Unmasked

ITP: Can You Hear Us?

Harnessing Social Media for Better Advocacy

Importance of Newborn Screening for Inborn Errors of Metabolism

What is Interstitial Pulmonary Fibrosis?

RareActivists Ride4Rare 2022

Rare Diseases South Africa: What We Do

Introducing the Rare Registry

Make your voice heard: Take the global Rare Barometer survey and share your diagnosis experience!

Let's Talk Genetic Counselling

Celebrating Rare Disease Day

#RareAware 2022 Kelly Du Plessis School Video

#RareAware 2022 - Megan Hunter

#RareAware 2022 - Sharon Pruss

#RareAware 2022 - Kelly du Plessis