Support

We have many plans for offering support through APSSA. Much needs to be done to achieve OUR AIMS ; we are just starting. Your support, thoughts, ideas and stories are important to us. Please contact us via our Contact Us page.

Please also keep visiting our site where will keep you up to date with how we are progressing and how you can help. We need as much attention and support as possible. If you have any ideas or can help us in any way, again, please let us know. We will be able to offer membership to APSSA shortly.

The following web addresses are of APS foundations and related organisations set up in the UK, the USA and all around the world. These foundations/organisations have been of great help to us and we would like to thank them all for their support.

The Hughes Syndrome Foundation in the UK is an excellent site that has a great deal of information and means of support.

The APS Foundation of America is another excellent site that has a great deal of information and patient support. They would like to welcome you to join their Support Forum, which you can access from their home page.

Please remember we would like to get stories from you for our Personal Stories page. Please write to us at info@apssafoundation.co.za or contact us via our "Contact Us" page. We look forward to hearing from you!