Avery Alexandra was born on October 14, 2009. She has had many health issues to battle in her short life and this blog is for our family and friends to stay updated on her progress. We also want to document this process for other families to view who may be going through the same experience. We thank you all for your continued love & support..♥♥

Tuesday, March 2, 2010


We met with the Cardiologist today and he said we only have to give her the heart medication 3 times a day. No more waking her in the middle of the night (she slept 11-12 hrs before I had to start waking her to take her meds). He also said that around 8 months of age, she will go off her medicine, get an EKG and see if the SVT is recurrent. 1 out of 3 times, it does recur (and she may have a higher likely hood of it recurring since it did already from when she was in-utero). Otherwise, it may occur around 7-8 years of age. At that time, she can handle the episodes herself with various techniques.

The picture above is of my son, Kyler checking Avery's heart ;-) He said "Don't worry mama, she's all better"!!! He is such a great big brother.


  1. Oh my gosh... Kyler is such a cutie! Making sure that his little sister is all better! Sending our love and prayers. Love, Josh, Leandra & Caleb

  2. This is the sweetest picture. Avery looks like such a happy baby despite everything that is going on. My thoughts are with your family :).