APS Foundation of America, Inc. (APSFA) is the only United States nonprofit health agency dedicated to bringing national awareness to Antiphospholipid Syndrome (APS), the major cause of multiple miscarriages, thrombosis, young strokes and heart attacks. We are a volunteer run, community based 501(c)3 non-profit Public Charity organization and is dedicated to fostering and facilitating joint efforts in the areas of education, support, public awareness, research and patient services. They also offer information and education. Their website contains a glossary, links to videos on YouTube, online support, newsletters and more. You can sign up to receive their newsletter.
P. O. Box 801
LaCrosse, 54602, WI
Accessible Location: No
Type of Organization | Nonprofit (501c3) |
---|---|
Categories | Disability Specific, Emotional Support, Other |
Services offered in Spanish? | No |
Newsletter? | yes |
Child Care Available? | No |
Age Range | All Ages |
Disability Categories | Medical Condition |
Does this organization belong to all disabilities? | No |
This organization belongs to these diagnoses | Antiphospholipid Syndrome (aPL) |
Is this a statewide service? | yes |
Website | https://apsfa.org/ |
Contact Name | Contact form online |
Email Address | |
Phone Number |