<strong> IF YOUR QUESTIONS ARE NOT GETTING ANSWERED HERE, PLEASE JOIN US AT <a href="
http://www.msplinks.com/MDFodHRwOi8vV1dXLkFQU0ZPUlVNLkNPTQ==">WWW.APSFORUM.COM</a>. THEY WILL DEFINITELY GET ANSWERED THERE. JUST SAY YOU'RE FROM THE MYSPACE GROUP WHEN YOU POST YOUR INTRO. </STRONG> <P>This group is for people who have Antiphospholipid Antibody Syndrome, their friends, family, caretakers...etc. <br>
<br>
Join to meet other people who share your symptoms, and know that you are NOT alone!<br>
<br>
This is a worldwide group.<br>
<br>
<strong>What is Antiphospholipid Antibody Syndrome?</strong><br>
<br>
Antiphospholipid Antibody Syndrome or APS is an autoimmune disorder in which the body recognizes certain normal components of blood and/or cell membranes as foreign substances and produces antibodies against them. Patients with these antibodies may experience blood clots, including heart attacks and strokes, and miscarriages. APS may occur in people with systemic lupus erythematosus, other autoimmune diseases, or in otherwise healthy individuals. <br>
<br>
APS is also known as APLS, APLA, Hughes Syndrome or "Sticky Blood."<br>
<br>
<a href="<a href="
http://www.msplinks.com/MDFodHRwOi8vd3d3LmNhZmVwcmVzcy5jb20vYXBzZm91bmRhdGlvbiZxdW90OyZndDsmbHQ7YnI=">http://www.cafepress.com/apsfoundation"><br</a>>
<img border="1" src="<a href="
http://www.msplinks.com/MDFodHRwOi8vd3d3LmFwc2ZhLm9yZy9zaG9wL2Fwc2NhZmUuZ2lmJnF1b3Q=">http://www.apsfa.org/shop/apscafe.gif"</a>; width="468" height="60"></a><p><a href="<a href="
http://www.msplinks.com/MDFodHRwOi8vd3d3LmNhZmVwcmVzcy5jb20vYXBzZm91bmRhdGlvbiZxdW90OyZndDsmbHQ7aW1n">http://www.cafepress.com/apsfoundation"><img</a> src="<a href="
http://www.msplinks.com/MDFodHRwOi8vaTEwNi5waG90b2J1Y2tldC5jb20vYWxidW1zL20yNDMvaGVpZGlhbm5wL2NhZmVwcmVzc2FuaW1hdGVkLmdpZiZxdW90OyZndDsmbHQ7L2EmZ3Q7Jmx0O3AmZ3Q7Jmx0O3A=">http://i106.photobucket.com/albums/m243/heidiannp/cafepressanimated.gif"></a><p><p</a> align="center"><br>
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.<br>
<br>
<font color="#800000"><b>If you think you may have a medical emergency, call your doctor or 911 immediately.<br>
</b></font>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.<br>
<br>
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.</font></p>