We are home....again! Teag was discharged from Children's Tues. afternoon and we made it home around 6. She is already acting like she feels better and is slowly getting back to her normal self. She's still in some pain from the surgery,cath and chest wound but hopefully she won't need her pain meds for much longer. We had our first cardio appt. today already with Dr. Sesslar. Everything looked good (sats,hr, etc...) so we don't go back for a month! Now we're just focusing on getting rid of the NG tube again and letting her enjoy life outside the hospital! Thank you all for checking in on us and for all of your continued prayers!
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)