Not much news to share today. Teags was started on a heart medicine to try and reduce her runs of 'SVT' she's been having. (super ventricular tachacardia) Basically she's been having small runs of super fast heart rythms over the past few days that they're trying to control. Other than that we're still watching her wrist for signs of improvment and we started training her for some oral feeds this afternoon! Sorry no pics today!
We started this blog to share the latest happenings at the Maxwell house and our daughter Teagan's 'heart journey'. Teagan was born March 21st 2008 with a congenital heart defect called Critical Aortic Stenosis which led to Hypoplastic Left Heart Syndrome. (HLHS)