....mommy's tired and is going to just post a picture. This is from tonight :)
Thank you Lord for this sweet little miracle....
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About Me
- DevonLeah
- Camden James joined our family on January 22, 2009, weighing approx 8-9 pounds and measuring around 22 inches with an UNKNOWN congenital diaphragmatic hernia. He joins his father, Marcus and I and three brothers and a sister.He has a trach and has been off ventilator since winter of 09. He gets all nutrition from a gtube.Life is not what it was, but we are adjusting to our new normal and trusting God as He continues to guide.... *Camden had his first "reherniation" diaphragm repair on Oct 30 2009, patched with gortex.* Some colon had made its way in chest cavity, behind his heart.*He was hospitalized due to his first sickness resulting from a cold(we think) for the first time on Jan 6 2010, at almost one year old.*REASONS FOR BLOGGING? Obviously to keep close friends and family updated but more importantly to help others with special needs children. Other blogs encourage me, give tips, and help me realize that I am not alone on this journey.I hope to do the same for them.*Camden was decannulated on June 2, 2010!!!*UPDATE for 2011 He finally took interest in eating, but it isnt possible due to his nissen surgery being too tight. New hurdle to overcome..
Awww, Mr Camden is getting cuter and cuter.. what a sweetie..
ReplyDeletehey cutie pie you gotta a girlfriend??? ya want one ;-)
ReplyDelete12lbs!!!! all that pumping is paying off:) He is going to end up being a chunky little thing after all! So good to see some chub after all those skinny days! To see the progress Camden has made in 3 months has been like witnessing an incredible miracle for sure! His eyes talk to you!!! Nana misses you buddy every day I am not there:(~
ReplyDelete...never ceasing to pray for lung power that shocks all the doctors!!!!love & blessings xxxooo