Meet Other APS Patients – Online Support Groups
APS can be a confusing, frustrating disease and it helps to talk with people who have shared experiences. We’ve collected some links and information on different ways to meet other people online who have APS.
In 2016, the APSFA has migrated our online support forum to Facebook, since it is an active social networking website. We may return to a separate online forum in the future if there is a need to do so.
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 & Family.
Founded in 2005, the APS Foundation of America, Inc. is dedicated to fostering and facilitating joint efforts in the areas of education, public awareness, research, and patient services for Antiphospholipid Syndrome (APS) in an effective and ethical manner.
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APS Foundation of America, Inc.
P. O. Box 801
LaCrosse, WI 54602-0801
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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. Please note that we will be listing all donor or purchaser's names on the Donor page of our foundation site. If you do not want your name listed, please contact us to opt out. If you think you may have a medical emergency, call your doctor or 911 immediately.