The regional structures came into existence before the national body was formed, and therefore most activities are driven by the regional bodies, with the national body (SACFA) being more of an umbrella body, which monitors regional developments and handles issues which need to be addressed at national level. The Medical & Scientific Advisory Committee for cystic fibrosis (MSAC) was formed under the auspices of SACFA. MSAC is an active and representative panel of experts in the various aspects of cystic fibrosis management.
The national body (SACFA) is made up of a President and 2 representatives from each of the 3 regions.
The SACFA national executive is made up of:
President : Alan Dunn – 083 285 5853
The regional associations have been in existence for over 30 years, and are:
- Cystic Fibrosis Association Central Region (based in Gauteng)
- KZN Cystic Fibrosis Association
- Cape Cystic Fibrosis Association
They are all registered NPO’s and have 3 main objectives:
- To provide emotional support to families when their child has been diagnosed with cystic fibrosis.
- To promote early diagnosis and so have a positive impact on the progression of the disorder.
- To ensure that all those with cystic fibrosis receive proper treatment.
Summary of funding requirements
The regional associations raised funds for their own regions, and these are the main areas where the funds are applied.
- Funds are required to support the cystic fibrosis clinics around the country which are open to anyone with cystic fibrosis.
- Funds are needed to sponsor essential equipment for daily use by patients with financial constraints.
- Funds are required to promote public awareness, thus facilitating early diagnosis.
- SACFA Association supports the work done by the Medical & Scientific Advisory Committee (MSAC).