You can contact the APSFA through our contact form or by 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, and have families.

Please allow five business days for online replies. We ask you to ensure that you have read the website before asking questions, as many of your questions can be answered on the website

Thank you.

Common Frequently Asked Questions:

Please make sure you look through the frequently asked questions, as many of your questions can be answered there.

I need an Antiphospholipid Syndrome (APS) doctor.  Where can I find a list?

What is Antiphospholipid Syndrome (APS), exactly?

What are the Frequently Asked Questions?  

Where can I find support for Antiphospholipid Syndrome (APS)?  

How do I donate to this cause?  

Requirements to Add a Doctor

Please try to provide as complete information as possible, as it is hard for us to verify doctors’ names without a full name, correct address, and phone number.