Seeking Participants: Pregnancy and Antiphospholipid Syndrome (APS) Study

WHO: We are looking for people who have primary APS, are 18-45 years old, and have been or are considering becoming pregnant. You are eligible if you have ever been pregnant, regardless of how the pregnancy ended (such as miscarriage/stillbirth, live birth, abortion).

WHY: To help us understand the experiences, priorities, and concerns surrounding pregnancy for individuals with APS

WHAT: Online survey and potentially a Zoom interview

HOW: Fill out your contact information using this link or the QR code below so we can follow up with you


Alexandra Harper, PhD, OTR/L, CPHQ
Jason Knight, MD, PhD
Susan Murphy, ScD, OTR
Justine Wu, MD, MPH


Our Mission

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.


APS Foundation of America, Inc.
P. O. Box 801
LaCrosse, WI 54602-0801

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.