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Antiphospholipid Syndrome awareness, education, research, and support

Who Is AAPSA Print E-mail

Mission Statement

The American APS Association is a not-for-profit organization with a mission focused on awareness, research, and education of Antiphospholipid Syndrome. AAPSA provides support for those affected by APS, including but not limited to the diagnosed, their family and friends; such support is given in cooperation with other organizations that have a positive effect on the lives of APS patients in the USA.

Volunteer Staff

The volunteer staff manage the American APS Association in all aspects of business including the editing of this website, printing educational materials, promoting awareness campaigns, representing the AAPSA at medical conferences and much more. Some of the volunteer staff are as follows:

Seresa Crowson, President and Founder This e-mail address is being protected from spambots. You need JavaScript enabled to view it

Barbara Novy, Vice-President This e-mail address is being protected from spambots. You need JavaScript enabled to view it

Ali Smith, Treasurer This e-mail address is being protected from spambots. You need JavaScript enabled to view it

Kibby Smith, Secretary This e-mail address is being protected from spambots. You need JavaScript enabled to view it

 

Last Updated on Monday, 17 May 2010 00:44
 

Disclaimer

The American APS Association is volunteer run by APS patients and their supporters. Although we have a Medical Advisory Board to make sure the information is correct, the information provided by the American APS Association is meant for educational purposes only. It is not intended as medical advice. If you need specific advice about your medical condition or symptoms, please seek the assistance of your care provider.