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ABOUT US

We have funded over $500,00 in APS Type 1 related research through restricted grants with the National Organization of Rare Disorders (NORD); a $100,000 research RFP is awaiting final selection of a recipient by NORD. We will continue our work with NORD but since the establishment of our own foundation we are now pursuing opportunities to support critical
APS Type 1 projects including this symposium, the study currently being conducted at the NIH by Dr Lionakis and his colleagues and the creation of a natural history on-line registry. 
 
We hope you consider supporting us not only with your time, your prayers for all those challenged with this difficult condition, but financially as well. You can make a contribution by clicking here.

The APS Type 1 Foundation, Inc. is an established 501 (c) 3 not for profit. The goal of the foundation is to support the following areas related to APS Type 1...Education, Awareness, Fundraising.  We strive to:

  • Provide a centralized registry that will unify all those who have the disease so that we can find and communicate with one another.

  • Help educate and support those that have been recently diagnosed, and their families, about this rare disease.

  • To raise money for research that will improve treatment and hopefully, find a cure for those who are living with this disease.

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Click here to view the APS Type 1 Foundation website.

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