Partial Anomalous Pulmonary Venous Return
In my mailbox this morning: “My daughter Madison has just been diagnosed with Partial Anomalous Pulmonary Venous Return. I’m so glad I found your story. Please keep Madison and our family in your prayers!” I will. Nathan had cardiac catheterization at two, and it was determined that his PAPVR needed to be addressed surgically. A [...]
In my mailbox this week: “I’m just 30 weeks pregnant and my baby has been diagnosed with TAPVD/R. Please pray that the next scan shows that there is nothing abnormal and that it was a misdiagnosis. We have waited so long for her and can’t even start to believe it.” I pray that this is [...]
I have been contacted by a loving, concerned parent whose son will have heart surgery to correct PAPVR (Partial Anomalous Pulmonary Venous Return). She has three requests: Pray that Joshua will make it through. Pray that he will come out healthy and strong. Ask for others to pray, too. Sending love and prayers your way!
I received this prayer request last night: My daughter Rosabela just turned 4 years old a few days ago. She went to have a procedure to fix the SVT (Supraventricular tachycardia), and that became unsuccessful. It was discovered that she has PAPVR (Partial Anomalous Pulmonary Venous Return). We are awaiting final diagnosis. Please pray for [...]
Broady Doland will have surgery to correct his congenital heart defect, Partial Anomalous Pulmonary Venous Return (PAPVR), on May 5, at Children’s Hospital in Pittsburgh. Like my son, Nathan, Broady has Scimitar Syndrome. A nice article, “Benefit Aids Vandergrift Boy’s Family,” appeared today in the Valley News Dispatch. Family and friends have rallied to support [...]
