was diagnosed in 2015 with primary APS ... Because of the stroke paired with APS ... hematologist shared the standard of care for APS ... studies for this topic and people with APS ... complicated by the fact that I have primary APS

He has had APS since 2007.

to check out these 2 discussions on APS ... /connect.mayoclinic.org/discussion/aps

I have small fiber neuropathy plus APS ... knew if my mom was diagnosed with APS

I was diagnosed with APS and was told

Expect with Antiphospholipid Syndrome (APS ... read others' experiences with APS

Eloquis ad advised against anyone with APS

My son has APS too. ... I believe that the APS is a significant ... can’t get his doctors to agree that APS ... I believe the APS (thick blood or like

though your rheumatologist took your APS ... (My doctor deduced APS from a test of ... of autoimmune diseases as well as APS

seems to be my doctors solution to my APS

Curious, do you have APS as a primary ... point they are focused on just the APS

Hello it’s sad when I read about APS ... but I too have APS and so far I’m doing

WAS in 2007 when we learned he had APS ... Since his APS diagnosis 2007, he has ... Just wanted to let all you APS patients ... APS is a horrible autoimmune disease ... He has had APS for 17 yrs.

patients with antiphospholipid syndrome (APS ... I believe fellow APS member @elizabeth513

was on methotrexate 10 years ago for APS

blood work done, but I will see if APS

hearing in both ears supposedly from APS

I have APS and I’m on medication and

If you have tested positive for APS,

I was diagnosed a year ago with APS.