You can contact the APSFA through our contact form or through written correspondence to the address below. The APSFA is a volunteer run organization. Please keep in mind that many of our volunteers are living with APS and other autoimmune disorders themselves, work full time jobs, attend college classes, and have families.
Please allow 5 business days for online replies. We ask you to make sure that you have read the website before asking questions as many of your questions can be answered on the website.
Frequently Asked Questions:
I need a Antiphospholipid Syndrome (APS) doctor. Where can I find a list. Click Here
What is Antiphospholipid Syndrome (APS), exactly? Click Here
Where can I find support for Antiphospholipid Syndrome (APS)? Click Here
How do I donate to this cause? Click Here
Contacting the APSFA Online
Please use the form above to ask general questions about the foundation, to add/remove doctors to our doctors list, request information packets, or for comments/concerns. Questions or discussions about your specific APS symptoms would be better asked and answered on our support forum and you will be directed there in our reply. Please direct website questions and/or broken links to the webmaster.
Please note that we cannot answer specific medical questions.
Please also note that the APSFA does not provide financial assistance or scholarships at this time.
The phone field is optional. The reason we are asking for home addresses is to build a database with names and addresses of people to send out APS related information to. Your personal information is kept confidential and will never be sold to a third party. You may opt out at any time by filling out the form above and letting us know you would like to be removed.
Requirements to Add a Doctor
Please try to provide as complete information as possible as it is hard for us to verify doctor’s names when we do not get a full name, correct address and phone number. Please DO NOT use ALL CAPS when filling the form out. All incomplete forms will be deleted. Thank you.
**Please be sure that your email address is correct and that you add @apsfa.org to your safe list so our reply doesn’t end up flagged as spam. Thanks!**
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.