What We Do
OUR VISION
Every person affected by GBS, CIDP, MMN, or related syndromes will one day have access to early and accurate diagnosis, appropriate treatment, and knowledgeable support services.
OUR MISSION
We seek to improve the quality of life for individuals and families affected by GBS, CIDP, MMN, and related conditions. Our unwavering commitment is built on four pillars:
Support
Nurturing a local network of volunteers, healthcare professionals and industry partners to provide them with critical, timely, and accurate information, with support on each from GBS | CIDP Foundation International.
Awareness & Education
To create awareness of these diseases, get people registered, give them access to information and avenues for treatment and help. To help doctors, clinicians and caregivers increase their awareness and understanding.
Research
Tap into research funded locally through grants in Centres of Excellence, as well as internationally. To continue to seek out other appropriate avenues to identify the causes of and discover treatments.
Advocacy
At the HPCSA, Medical Aids and grassroots levels, to educate policymakers and help them make informed decisions that benefit our patient community.