Sunday, July 11, 2010
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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..
Holy cow he walked a long way! I love how cautious and slow he went, looked like he's been walking forever!
ReplyDeleteAmazing! He looks like an old pro already!
ReplyDeleteThat's my boy!!! Camden you defy words just like our God! Awesome doesn't nearly describe what He has done through YOU!!! I only wish I was there to see you in person but YEA for video~ Keep on strutting for Jesus! XXXOOONana
ReplyDeleteThank you for this post. It was so awesome to see Camden walk. I knew he would do it. It was just a matter of time. Stephen says - ooh how exciting to see you walk (lol). Once again God is soooooooooo good.
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