Please note that someone may not be here to take you call as we are all volunteers. Please leave a message and someone will get back to you as soon as possible.
Please note that someone may not be here to take you call as we are all volunteers. Please leave a message and someone will get back to you as soon as possible.
Please note that someone may not be here to take you call as we are all volunteers. Please leave a message and someone will get back to you as soon as possible.
Please note that someone may not be here to take you call as we are all volunteers. Please leave a message and someone will get back to you as soon as possible.
Are you looking for Support for Antiphospholipid Antibody Syndrome, APS, APLS, APLA, Hughes Syndrome, or Sticky Blood?
Well you've come to the right place! This is an private forum for people who have Antiphospholipid Antibody Syndrome, friends, family, and caregivers.
If you register and join us you'll find a wealth of information and support on the inside as well as the latest APS and related news articles that you may not be able to find elsewhere. You'll also find friendship.
We strive to ensure that our participants have a safe place that is friendly and supportive because we know how horrible this disease can be.
Come to a place where people understand what you're going through because they've been there themselves. If you join our free private forum, you will finally be "home" where people can relate.
We hope that you'll join us on the inside and we cannot wait to get to know you better!
APS Foundation of America is not intended to replace
standard doctor-patient visits, physical examination, and medical testing.
Information given to members are 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
is not intended to diagnose, treat, or cure. This site is for informational
purposes only. Additionally, while APS Foundation of America, Inc. frequently
updates its content, medical information changes rapidly, therefore some
information may be out of date.
If you think you may have a medical emergency, call
your doctor or 911 immediately.
APS Foundation of America will be building a database with this information for
future mailings. 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. Your information will be kept confidential
and not sold to or shared with any third parties.
If you use the forum or chat room, you are solely responsible for your own
communications, the consequences of posting those communications, and your
reliance on any communications found in those areas. APS Friends & Support and
its licensors are not responsible for the consequences of any communications in
the forum or chat room. If you give your personal information to a host or other
member and later threaten to hurt yourself or others we reserve the right to
contact appropriate authorities, however, no guarantee is made that someone will
contact emergency personnel for you. We are not equipped to handle these types
of crisis situations. You should contact your local law enforcement agency
immediately. If you think you may have a medical emergency, call your doctor or
911 immediately.
This site complies with the HONcode standard for trustworthy health information: 
