The Month of February is Congenital Heart Disease Awareness Month. Today had me thinking about the last 3 years and everything we have been thru. Honestly, I don’t know how I got thru it. From getting the devastating diagnosis that kept getting worse every single time we saw a new doctor, to having to rock him in […]
Read moreBaby Pierce Update
Just got off the phone with Jessamyn and Pierce is doing astoundingly well. For a family that was told surgery would most likely be a death sentence things have really turned around since Pierce was in Boston. Pierce had surgery on Monday afternoon, went in around 1pm and came out around 8pm and has since, […]
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Meet Baby Pierce
Meet Baby Pierce. He has a very similar type of Heterotaxy that Logan has. Jessamyn (Pierce’s Mother), myself, and many others fought like mad to get him transferred to a heart center that has more experience with these types of children. That was going to be his only shot at living. Pierce is so sick […]
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Open Heart Surgery…again
Well this has been one hell of a week. Logan did great on the plane, slept the entire time. We arrived in Boston at 7pm and took Logan to the ER just like we were told to do. We were under the impression that it was going to be just checking his pulse ox and […]
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February 2, 2013 





