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APS can be a confusing, frustrating disease and it helps to talk and share experiences with people who have gone through what you're going through and understands.

We've collected some links and information on different ways to meet other people who have APS.

The APSFA has an online support forum with the latest news articles on APS and related diseases as well as APS chat, general chit chat, & Foundation information. We currently have over 1500 members and we are HON Code Certified. We'd love to get to know you better on our forum as well as offer the support and information you're seeking. Click the graphic below to join our forum.

Some of these groups are very active and some are not active. APSFA does not endorse nor is affiliated with any of these groups, they were recommended to us by others. The only support group that APSFA is affiliated with is APS Friends & Support Forum.

Page updated on: 05/04/08

The APS Foundation of America, Inc. website and forums are independently funded and maintained by Heidi and Tina. We do not receive any funding from advertising. 

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Website created and maintained by Heidi P.

DISCLAIMER: APS Foundation of America, Inc. website is not intended to replace standard doctor-patient visits, physical examination, and medical testing. Information given to members is only an opinion. All information should be confirmed with your personal doctor. Always seek the advice of a trained physician in person before seeking any new treatment regarding your medical diagnosis or condition. Any information received from APS Foundation of America, Inc. website is not intended to diagnose, treat, or cure. This site is for informational purposes only.   If you think you may have a medical emergency, call your doctor or 911 immediately.