Hi all, want to provide an update in the hope of giving someone some encouragement around this issue. In July 2013 I was diagnosed with APS and Lupus following the loss of our son at 24 weeks. Symptoms began at 17 weeks when I developed this bizarre joint pain in my toes. I was eventually referred to a rhematologist who discovered the telltale indicators for the disease in my blood. I was put on clexane 40mg and aspirin 100mg but unfortunately the intervention came too late. Progressed to severe pre eclampsia and the baby's growth had been restricted. We were devastated at the loss of our son and unsure if we would ever be able to have a child. (Previous miscarriage at 15 weeks)
Earlier this year I fell pregnant again and this time I was monitored from day 1 by the high risk OB and the immunologist. I was put on aspirin and clexane again and doses were increased over the duration of pregnancy. We expected that I would develop preeclampsia at some point and the goal was to get to at least 30 weeks. Miraculously the meds kept everything in check and neither disease caused any issues. I was induced at 37 weeks and delivered a healthy baby girl (2.3kg). We are besotted with her!
Hopefully my story will bring some encouragement that having a baby is possible with this illness under the right care and management.