Ardent Cerebrations: Musings of Lupus Survivors!

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APSFA

13th International Congress on Antiphospholipid Antibodies

13th International Congress on Antiphospholipid Antibodies
"Antiphospholipid by the Beach"


When: April 13-16, 2010

Four days of the most up-to-date evidence-based medicine and state-of-the-art scientific sessions on Antiphospholipid Antibodies and the Antiphospholipid syndrome.

Participants included: rheumatologists, hematologists, OB-Gyn specialists, neurologists, dermatologists, cardiologists, pathologists, researchers, laboratory scientists and clinicians dealing with Antiphospholipid Syndrome, SLE and other related autoimmune diseases.

There will be a patient session on Wednesday April 14, 2010 from 5:00-6:30PM CT

URL for more information on costs, hotels & location here: http://www.utmb.edu/apla2010


Keywords: APSFA, APS Foundation, antiphospholipid antibody syndrome, lupus, stroke, dvt, pe, thrombosis, clot, migraine, hughes syndrome, miscarriage, america, usa, anticoagulant, heart attack, APS, APLA, conference, CME, international

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Angie Comment by Angie on October 26, 2009 at 12:50pm
This is encouraging. Maybe it will be sooner that that doctors, nurses and healthcare know what APS IS when I tell them I have it. I just made appointment with rheumy thats listed on APSFA list. He was recommended by facebook friend, Debbie from Kingsport. I am so blessed...his office is in my zip code!

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