Donate to the APS Foundation of America, Inc
Founded in 2005, the APS Foundation of America, Inc. (APSFA) is a volunteer run, 501(c)3 public charity. Without your generous donations, the APSFA could not continue to provide APS patients and their families with the information on our foundation page and social media pages, support Antiphospholipid Syndrome (APS) research – both adult and pediatric, obtain education on APS and related disease through various mediums and share that with the APS community and the general community as a whole.
In addition, we are developing a strategic plan for the future course of the APSFA and plan to raise money towards our long term goals.
Make a Donation to APS ACTION Core Laboratories
International Congress of Antiphospholipid Antibodies (ICAPA)
In 2022, we were able to provide six scholarships to the Silvia Pierangeli Young Scholar Award at the 17th International Congress on Antiphospholipid Antibodies. We were thrilled to have representation there and have been invited to attend the next congress which in 2022 located in Cordobo, Argentina.
We have estimated that the APSFA will need to raise $10,000 over the next three years to meet our obligations for the 18th International Congress in Kyoto, Japan. We will also be providing several Silvia Pierangeli Young Scholar Awards. We will be attending virtually to defray our costs and spend the donated dollar wisely.
Attending these congresses and other events of this type allows the APSFA to build a positive relationship with physicians and APS patients from all over the world and keeps us abreast of what is happening with APS research and allows our clients voices to be heard.
APS Research (Adult and Pediatric)
We would also like to raise monies to assist in funding research. In the past, we have given money to research groups such as APS ACTION, CARRA, APSCORE, The Rare Thrombotic Disease Consortium, Genetic Alliance, EURORDIS, and AARDA Autoimmune Summit. We have also sponsored medical students to attend specialized training dealing with APS. However, we have never raised money specifically for research in the form of a grant.
Over the course of the next 5 years, we will be setting aside 10% of our donations for Antiphospholipid Syndrome (APS) research. This money will go to a researcher, group of researchers or facility that is doing APS research. There will be an application process for those who are interested in our funding. We will review it as a board of directors, with 2 medical advisors that do not have a conflict of interest in the funding and 2 outside APSFA volunteers.
In 2022, the APSFA plans to award a college aged student a $1,000 scholarship. Pending funding for this scholarship, there may be more than one awarded per year. This is something we would like to do yearly. This will be a one time, non-renewing scholarship that will be granted to someone who is going to Medical or Nursing School. There will be an application process for those who are interested in this scholarship. More information will be available soon where we will explain the qualifications, application process and how the recipient will be chosen.
How Else Are Donations Spent?
Your donations also fund our yearly foundation expenses. These include: annual registration fees, legal fees, accountant fees, bank fees, insurance, postage and printing fees, rent share and cellphone. Services such as internet connections, electric, sewer, water, lawn & snow removal and heat are donated by our volunteers. Since, we are completely volunteer run we don’t have any payroll costs. We also do not use professional fundraisers to raise funds for us. We have also saved hundreds of dollars by creating our own brochures and newsletters.
We research ways (and use coupons where we can) to save money on administrative office supplies & printing expenses so we can apply as much of our donations towards our misson and goals. We have already done so by selling awareness items through our CafePress store and our Zazzle store which totally eliminates overhead costs.
If you have more ideas on how to save, feel free to contact us. We always welcome more ideas on how to save money.
If you’d like to make a donation by check* or money order, please click here to download our donation form. Once completed, please send to:
APS Foundation of America, Inc.
Post Office Box 801
LaCrosse, WI 54602-0801
We are also able to take donations directly over the phone, just give us a call at 608-782-2626 (voice/text) and we will be happy to assist you.
Thank you very much for your kind donation!
*There will be a $25.00 returned check fee plus bank fees.
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.
APS Foundation of America, Inc.
P. O. Box 801
LaCrosse, WI 54602-0801
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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.