Dynamo

My little dynamo!

I had the intention of updating the blog throughout Bridger's recovery, but obviously life at home with 3 little boys is busy. Baby Bridger is doing fantastically. He seemed uncomfortable the first few weeks at home and wasn't his typical, active self. That changed about 6 weeks post-op and he began sleeping better, rolling over again, and was much happier. Now he is sitting up and even scooting around on his belly- backwards- but scooting nonetheless. He is very motivated to crawl after those brothers. His weight gain has been slow but steady and he's done pretty well with starting solids. The interval between cardiology appointments has increased from 3 weeks to 6 weeks. We have never had that much of a break between appointments! His right branch pulmonary artery is still very narrow, but the docs tell us that pulmonary artery stenosis often improves on its own, over time. Blood pressure is still on the high side but not too much of a concern. Med wise, he is only on aspirin.

I decided at the very last minute that Bridger and I will head down to Littleton tomorrow for the Williams Syndrome walk. It is Williams Syndrome Awareness week and the walk will help to raise money for the WS Association- and amazing organization that provides support to WS individuals and their families. The WSA has provided us with a great deal of information and has connected us with many other families. If anyone feels compelled to donate to the WSA, check out www.walk4williams.org.

One of the other mothers that I've found through the WSA is named Ruth. Her baby, Corbin, was born in February and has spent most of his life in the hospital. Yesterday, he had his second open heart surgery. He is in critical condition and needs prayers. This little baby is a fighter, and his mom is incredible. Check out www.caringbridge.org/thecorbinstory.