GFM

Lucas Wayne

Lucas made us parents on October 18, 2009.    He had a bit of a rough start with jaundice and trouble latching/sucking, but with time and perseverance we managed to work it out.  After 11 weeks of supplementing with pumped milk, I managed to wean him completely to nursing at the breast.




One Year Old 2010

September 13, 2011 Lucas had a pH probe and endoscopy to rule out GI/Reflux issues causing his "seizure like episodes".  He spent one night in the hospital.


Two Years Old 2011

February 29, 2012-Lucas had his ear tubes put in.

Three Years Old 2012

July 16, 2013 Lucas had his ear tubes removed and replaced with a new set.

July 18, 2013 Lucas broke his foot while playing with his cousin.  He was casted on July 24.

Four Years Old 2013

Five Years Old 2015


In August of 2014 we took Lucas to the Orthopedic Surgeon because he was "toe-ing" in & his running was unbalanced.  Dr. St. Remy suggested that Lucas was "hypermobile" and advised us to look into Ehler's-Danlos Syndrome.  

In November of 2014 (after meeting with a geneticist) we saw a cardiologist to do an echo-cardiogram as part of the diagnostic process for EDS.  The results of the test were that Lucas has a bicuspid aortic valve, or a mild congenital heart defect.  


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