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*In the News & Community - APSFA


Antiphospholipid Antibody Syndrome Awareness Month

Michigan Proclamation for 2007

APS Awareness Starts Here

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!

APS FOUNDATION OF AMERICA, INC. JOINS WITH NORD TO CELEBRATE THE 25th ANNIVERSARY OF THE ORPHAN DRUG ACT

APSFA Press Release - January 2008

APS in the Community

On April 22nd the APSFA made an appearance at the annual March of Dimes WalkAmerica event in Springfield, Virginia.

APS is a snake in the grass and can bite or kill without warning

APSFA Press Release - Week 4 - 2007

APS Linked to Birth Difficulties

APSFA Press Release - Week 2 - 2007

APSFA To the Rescue

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

Eau Claire, Leader-Telegram, November 29, 2006, Page 1C


Grand Rounds at Marshfield Clinic

written by Tina Pohlman

June is APS Awareness Month ~ Get In the Flow!

Written by: Tina Pohlman

June is APS Awareness Month: Get in the Flow!

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!

JUNE IS APS AWARENESS MONTH: GET IN THE FLOW!

APSFA Press Release - Week 1 - 2007

JUNE IS APS AWARENESS MONTH: GET IN THE FLOW!

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

Lupus Foundation of America: Pacific Northwest Chapter: In the Lupe! December 2006, Page 5


Lupus Foundation of Ontario: Lupus Talk, October 2006 to December 2006, page 5


MO-KAN Spreads APS Awareness

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!

One Fine Day

Written by: Dana Stuart

Our Journey with Mystery Diagnosis

written by Michelle LaRue

Quarterly Newsletters "Antiphospho....What?"

written by the APS Foundation of America, Inc. Full archive of all of our newsletters available for download for free, no membership necessary.

Sisters' ailment identified

07/23/2007 - By Christy Murdoch, For the Herald-Standard

Social Networking for APSFA


Strokes and heart attacks could be caused by APS

APSFA Press Release - Week 3 - 2007

Thrombosis Education Days ~ MI & Chicago

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.

State health officials hear from both sides of Medicaid debate at public meetings - 4/2011


Orangeville woman's misdiagnosis leads to debilitating effects - 3/2011



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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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