Josie and Esten
Our journey began a little over four years ago when, just before my 25th birthday, I had emergency open heart surgery to repair an aortic aneurysm and dissection. I was so young, and what happened was so severe that my cardiothoracic surgeon suspected a connective tissue disorder. After consultations with geneticists and cardiologists, what my surgeon suspected was confirmed. I was officially diagnosed with Marfan syndrome, and I was told that pregnancy would be too stressful for my aorta—the main artery that carries blood from your heart to your body—and there was also a 50-50 chance our children could inherit the disorder. If we wanted children, doctors recommended we create embryos through IVF and have them tested using PGD/PGS before transferring to a gestational carrier.
After completing three rounds of IVF in 2018, we were happy to find out that five of our embryos are chromosomally normal and Marfan-unaffected. We matched with an amazing gestational carrier and completed an embryo transfer in 2020. To our great joy, a son joined our family in the summer of 2021!
Esten and I are so touched and grateful to be the recipients of the Sophie St. Aubin PGD for Life Grant as we have seen firsthand how devastating a genetic disorder can be.