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*In the News & Community - APSFA
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These are air checks that are currently hitting the DC Metro Area. About 1 million listeners at any given time.
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(c) APS Foundation of America, Inc. Special thanks to Jeff Cecil of JMC Creative for producing the audio.
Bill Sparks said in a statement that doctors have determined that Tom's stroke was probably caused by a condition called antiphospholipid antibody syndrome (APS), a disease that causes unnatural clotting of the blood. In lieu of flowers, the family has asked that donations in Tom's memory be sent to the APS Foundation of America, the only nonprofit organization in the country dedicated to bringing awareness to APS.
By Shannon Farr, Saturday, June 30, 2007
These are air checks that are currently hitting the DC Metro Area. About 1 million listeners at any given time.
(c) APS Foundation of America, Inc. Special thanks to Jeff Cecil of JMC Creative for producing the audio.
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PSA airing on 93.3 WFLS- Real Country Variety, Fredericksburg, VA
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(c) APS Foundation of America, Inc. Special thanks to Jeff Cecil of JMC Creative for producing the audio.
Michigan Proclamation for 2007
(c) APS Foundation of America, Inc. Special thanks to Jeff Cecil of JMC Creative for producing the audio.
These are air checks that are currently hitting the DC Metro Area. About 1 million listeners at any given time.
June is Antiphospholipid Antibody Syndrome (APS) Awareness month.
Published: Sunday, November 20, 2005 12:03 AM CST. A Ventura teen's struggle to obtain a diagnosis for a relatively rare auto-immune disorder will be featured on the Discovery Health Channel. Angie Abbas, 18, who has Antiphospholipid Antibody Syndrome (APS), will be featured in a segment of "Mystery Diagnosis" in early 2006. The date has not been determined. Angie's diagnosis was difficult because APS mimics other disorders, LaRue said. In addition, Angie's primary symptom, a severe twitching of the head and neck, is not typical. In the meantime, producers of "Mystery Diagnosis" had learned about Angie through the APS Foundation of America, a relatively new organization in which Angie and her mother had become active.
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VENTURA — A program featuring a Ventura teen's struggle to obtain a diagnosis for a relatively rare auto-immune disorder will be aired March 6 on the Discovery Health Channel, the show's producers have announced. Angie Abbas, 18, who has Antiphospholipid Antibody Syndrome (APS), will be featured at 9 p.m. Central Standard Time on March 6. "Mystery Diagnosis" is a series that tells the stories of how real people have obtained difficult diagnoses. It is produced through True Entertainment LLC of New York City. The program was filmed in October at a Minneapolis production studio, Mercy Medical Center-North Iowa in Mason City and Angie's home in rural Ventura. The Discovery Health Channel is Channel 203 on Mediacom's digital-plus package or Channel 93 through CL Tel.
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Surgeon General Announces Call to Action at VDC Meeting Members of the Venous Disease Coalition (VDC) and the Office of the Surgeon General came together at the VDC Annual Meeting in Washington D.C. on Monday, September 15th. Acting Surgeon General Rear Admiral Steven K. Galson issued "The Surgeon General's Call to Action for the Preventionof Deep Vein Thrombosis and Pulmonary Embolism," which combined affect hundreds of thousands of Americans each year. Dr. Gale McCarty & Dr. Tom Ortel represented the APSFA at this annual meeting.
The APS Foundation of America, Inc. is the only United States nonprofit health agency dedicated to bringing national awareness to Antiphospholipid Antibody 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.
Press Release - October 27, 2007 on PRWEB

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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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