Update on Norah 2
The journey on Norah continues, read the whole story here if you haven’t yet.
So today was another appointment for Norah at the cardiologist. She got weighed again, got another ultrasound/ECHO to checkout how her heart is doing. Not much has changed with her heart. In fact, they believe she has another very small heart issue, however, this other problem is actually benefiting her by lessening the issues caused by the hole in her heart. This other small problem isn’t something they are concerned about and aren’t even treating it. So it’s kind of a blessing in surprise.
So with no change they are once again going to up her medication as well as we are increasing supplemental feeds to help her continue to gain weight. From her previous checkup she had gained weight, just not as much as previous. We got alittle bit more of an answer about possibility of surgery, but the answer was “we’ll wait till January to decide”, so it was really just prolonging this, but it does give more chance to allow her body to “fix” itself so she still has a chance of not needing surgery. So right now we will continue to give medications, extra feedings, extra doctors appointments, extra everything it seems. We are really getting exhausted and could use a night of really good sleep. Please continue to pray for our energy and stress levels as it is all still overwhelming even as it has set in.
The last “fun” thing is that we found out this week about RSV. Before this week I had never even heard of this. Anyways, RSV is basically a type of cold virus. In fact, many adults, and children have had RSV or have at least been a carrier of it without knowing it. They probably just treated it like any other cold. However, to an infant with a Congenital Heart Defect catching RSV could be rather life-threatening. So if you are around us and have a cold we won’t let you hold her. Sorry, it’s not your fault, but Norah could get really sick from you. Don’t take it personally, but our kid is MUCH more important than your feelings. I’m sure you’ll all understand. The good news is that she can be immunized against it. Thankfully Sask Health covers this immunization if your child is “at-risk” like Norah, otherwise it costs $1000 per shot and she will need it every month, especially during cold/flu season. Thanks Universal Health Care!
Thank you to everyone for your prayers and support. As this journey continues we know that we will need more of your prayers and support and know that our wonderful friends will be there for us when we need it.

Just wanted to let all my readers aware of something significant in our lives. Something that is impacting our family right now and something that needs your prayers. On Monday we had a appointment with a pediatric cardiologist. We had been referred to meet with the specialist because our family doctor had noticed what they call, a “noisy heart.” Our doctor was unsure if it was just a loud murmur or what, so off we went. So on Monday the cardiologist did an ultrasound of Norah’s heart and a few other tests. (Thankfully Norah was a pro star during all the tests) They have determined that Norah has a hole in her heart. For those medically in the know, its a VSD. Needless to say this came at abit of a surprise to us, however, we are told it isn’t uncommon. Right now she is on some medication which hopefully will help. But if these drugs don’t work, then she will have to goto Edmonton for open heart surgery. (Which again we are told isn’t uncommon) We are told the surgery is done quite abit and is very low risk. But if you have kids, then you know that open heart surgery on one of your kids is the furthest thing from what you want for your kids. We have another appointment next Monday to see how the medication is working. Please pray with us that the hole in her heart would close and that God would protect her through this. Pray as well for our family during this stressful time.