Our Generous Donors
Without your donations, the APS Foundation of America, Inc would still be just a support forum and informative website. We’ve grown immensely in the past 5 years and we hope, with your support, we will be able to continue to grow as a foundation and bring much needed awareness to APS.
Please note, we generally do our book keeping on a quarterly basis, which may delay the posting of donor names. Tina does our book keeping and she is also an APS & Lupus patient. Your patience and understanding is greatly appreciated!
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
[ Contact Form ]
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.