Our oldest son has a condition known as pectus excavatum. This blog is to record our journey through diagnosis, treatment/surgery, and recovery. It is our hope that our experiences will help educate and encourage others dealing with this condition. This is not a substitute for medical treatment or advice; it's just our experience.
Thursday, August 14, 2014
A Quick Update
Just a quick update to say that CJ is continuing to do well! He's still on the oral antibiotic 3 times a day, and the healing at the incision sites is progressing. His last lab work showed everything staying in normal ranges. We go back to the Infectious Diseases doctor next week. I'll post again after that.
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