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*In the News & Community - APSFA
Michigan Proclamation for 2007
Written by: Charles Strickler. What is APS? How do we increase awareness of APS? What research needs to be done to improve treatment options? These were some of the many questions discussed at the awareness and fundraising dinner that was hosted by me, my wife, Mary Strickler and our co-hosts, David and Kim Penberthy. We held the dinner May 17th, and it seemed more than appropriate to have such an event just prior to APS Awareness Month in June!
APSFA Press Release - January 2008
On April 22nd the APSFA made an appearance at the annual March of Dimes WalkAmerica event in Springfield, Virginia.
APSFA Press Release - Week 4 - 2007
APSFA Press Release - Week 2 - 2007
Written by: Seren Estrada Thanks to the support of the APSFA, I expect to continue my education with the help of the DSSO. It also goes to show that the APS Foundation of America, Inc is truly dedicated to advocating for people with APS
written by Tina Pohlman
Written by: Tina Pohlman
The APS Foundation of America, Inc. (APSFA) has declared June as National Antiphospholipid Antibody (APS) Awareness Month. We are educating the public and medical community about this disorder, urging people to Get in the Flow!
APSFA Press Release - Week 1 - 2007
The APS Foundation of America, Inc. (APSFA) has declared June as National Antiphospholipid Antibody (APS) Awareness Month. We are educating the public and medical community about this disorder, urging people to Get in the Flow! 2009
Written by Dana Stuart. "Mo-Kan" is a phrase commonly used in the Missouri-Kansas region to describe various missions or goals that Missouri and Kansas businesses and residents CAN accomplish together. Frequently used for public service announcements, advertisements, and other miscellaneous uses, "Mo-Kan" has become the unofficial slogan for several alliances, which have formed for some very worthy causes. Now "Mo-Kan" spreads APS Awareness!
Written by: Dana Stuart
written by Michelle LaRue
written by the APS Foundation of America, Inc. Full archive of all of our newsletters available for download for free, no membership necessary.
07/23/2007 - By Christy Murdoch, For the Herald-Standard
APSFA Press Release - Week 3 - 2007
written by Heidi Ponagai. The National Alliance of Thrombosis and Thrombophilia (NATT) and the MSU Center for Bleeding and Clotting Disorders held an education day on March 24th in Lansing, Michigan for people who have had blood clots, who have clotting disorders, and their families and friends. We were fortunate enough to get a booth at the seminar to display and distribute APSFA brochures and booklets to people.

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The APS Foundation of America, Inc. website and forums are both volunteer run and funded by donations to the APSFA.
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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.
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