Hi,
My sister was born with a ventricular septal defect in the early 1960s in the Twin Cities (Minneapolis/St. Paul). I am trying to learn what type of options she would have had at the time, and as a child. She never had heart surgery, and died at the age of 40. I am trying to learn if she could have gotten help at some point, and what that would have been. She mentioned she might have been a candidate for a heart & lung transplant as an adult, but never had serious enough symptoms (so she said) to warrant getting a transplant. I do not have her medical records; I'm just starti
