Dylansmom
02-28-2007, 10:02 PM
Hello ~
I am Brittany, mom to Dylan. We live in Kendallville, Indiana. Dylan is a 5 year old who is currently still trached. He has lots of energy, and keeps me very busy.
He was born at 37 weeks with mid-line anomalies. Dylan was born with 2 ASD??s, PDA, pulmonary stenosis, cleft lip and palate, small right kidney, subglottic stenosis, bronchial & tracheomalacia, TEF, & bilaterally deaf. He was just currently diagnosed with CHARGE & immunodeficiency.
Dylan was in NICU for 27 days came home for 23 hours, and then went back to PICU for 5 months. He originally was only on o2 via a nasal cannula, then had his trach placed at 1 ?? months old due to his malacia. He became vent dependent around 3 months old, and was taken off to just CPAP at night around 2 ?? years old. He gets all of his nutrition through his G-tube.
Dylan just had his 5th birthday, attends a regular preschool, wears hearing aids bilaterally, just starting wearing his PMV, loves basketball, tee-ball, running around outside, and going to the park. ??--- This sounds like a personal ad?? Any one looking for a stud? ?? http://www.tracheostomy.com/iB_html/non-cgi/emoticons/upsidedown.gif
I am a RN but only work PRN at night-around 6 days a month. I have found this board to be very helpful and comforting to grow friendships with members on this board.
Brittany ??http://www.tracheostomy.com/iB_html/non-cgi/emoticons/hug.gif
http://i78.photobucket.com/albums/j85/dawn_250/Pro%20pictures%20of%20Dylan/Mail0145.jpg
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I am Brittany, mom to Dylan. We live in Kendallville, Indiana. Dylan is a 5 year old who is currently still trached. He has lots of energy, and keeps me very busy.
He was born at 37 weeks with mid-line anomalies. Dylan was born with 2 ASD??s, PDA, pulmonary stenosis, cleft lip and palate, small right kidney, subglottic stenosis, bronchial & tracheomalacia, TEF, & bilaterally deaf. He was just currently diagnosed with CHARGE & immunodeficiency.
Dylan was in NICU for 27 days came home for 23 hours, and then went back to PICU for 5 months. He originally was only on o2 via a nasal cannula, then had his trach placed at 1 ?? months old due to his malacia. He became vent dependent around 3 months old, and was taken off to just CPAP at night around 2 ?? years old. He gets all of his nutrition through his G-tube.
Dylan just had his 5th birthday, attends a regular preschool, wears hearing aids bilaterally, just starting wearing his PMV, loves basketball, tee-ball, running around outside, and going to the park. ??--- This sounds like a personal ad?? Any one looking for a stud? ?? http://www.tracheostomy.com/iB_html/non-cgi/emoticons/upsidedown.gif
I am a RN but only work PRN at night-around 6 days a month. I have found this board to be very helpful and comforting to grow friendships with members on this board.
Brittany ??http://www.tracheostomy.com/iB_html/non-cgi/emoticons/hug.gif
http://i78.photobucket.com/albums/j85/dawn_250/Pro%20pictures%20of%20Dylan/Mail0145.jpg
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