APSFA in the Media
Since 2005, the APS Foundation of America has been growing by leaps and bounds, and we’ve been spotted or heard in the media!
If you see us in your local newspaper, in a magazine, or newsletter, please clip the article and send it to us. If you come across an article about us on the web, please also contact us so that we can link to it here. Thank you for your support!
IMD Health Canada
APS Foundation of America and IMD Health Announce Partnership to Improve Quality of Patient Education
August 30, 2022
The Mighty
5 Things You Should Know About Antiphospholipid Syndrome or Hughes Syndrome
September 10, 2020
The World's Video Wiki
6 Organizations Joining The Fight Against Devastating Diseases
July 12, 2020
Patient Worthy
Antiphospholipid Syndrome (APS): Young Women are Five Times More Likely Than Men to Have This Rare Disease
March 9, 2020
Insurance News Net
Hours After Wisconsin Democrats Blast Trump for Social Security, Medicare, Medicaid Cuts, He Doubles Down
March 8, 2020
WISDEMS
Hours After Wisconsin Democrats Blast Trump for Social Security, Medicare, Medicaid Cuts, He Doubles Down
March 6, 2020
Urban Milwaukee
Wisconsinites Blast Trump for Broken Promises to WomenÂ
March 5, 2020
WISDEMS
Wisconsinites Blast Trump for Broken Promises to Women (video)
March 5, 2020
WISDEMS
Wisconsinites Blast Trump for Broken Promises to Women
March 5, 2020
News8000
County Board Chair Johnson Laments Trump’s ‘Broken Promises’
March 5, 2020
Healio
Helio Rheumatology
February 28, 2020
Medical News Today
Antiphospholipid syndrome: What’s to know
January 22, 2018
Wiscasset Newspaper
Wiscasset’s Sharon Jacques joins pageant, spreads awareness on APS
August 2, 2016
Huffington Post
Readers Offer Advice In Blood Clot Prevention
January 3, 2013
Wisconsin State Journal
State health officials hear from both sides of Medicaid debate at public meetings
April 5, 2011
The Rheumatologist
A Catalyst for Antiphospholipid Syndrome Research
March 18, 2011
Townhall
`Wipeout’ TV show player with rare condition dies
November 12, 2009
Cision PRWeb
Antiphospholipid Syndrome (APS) Sufferers Start Non-profit Health Agency
October 27, 2007
Herald-Standard
Sister’s ailment identified
July 23, 2007
The Tribune-Review
Rare condition often overlooked
June 30, 2007
Lupus Foundation of America: Pacific Northwest Chapter
People with Antiphospholipid Syndrome Can Now Seek Support Through New American Foundation
December 2006
American Stroke Association
StrokeConnection Magazine
November/December 2006
Eau Claire Leader-Telegram
New Foundation: APSFA
November 29, 2006
Lupus Foundation of Ontario
Lupus Talk
October-December 2006
Globe Gazette
Rare disorder’s diagnosis draws media attention
November 20, 2005
Our Mission
Founded in 2005, the APS Foundation of America, Inc. is dedicated to fostering and facilitating joint efforts in the areas of education, public awareness, research, and patient services for Antiphospholipid Syndrome (APS) in an effective and ethical manner.
Information Sheets
DISCLAIMER: The 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 doctor. Always seek a trained physician's advice before seeking any new treatment regarding your medical diagnosis or condition. Any information received from the 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 list all donors' or purchasers' names on the donor page of our foundation site. If you do not want your name listed, please get in touch with us to opt-out. If you think you may have a medical emergency, call your doctor or 911 immediately.