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| Pediatric Tracheostomies For parents and caregivers of children with tracheostomies. Please limit discussion to seeking and sharing of information pertaining to tracheostomy care, medical issues, special needs, disabilities, networking and moral support. |

08-27-2009, 10:01 PM
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Senior Member
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Join Date: Oct 2006
Location: Ontario Canada
Posts: 1,921
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Good News
Hurrah, Jacob can now safely swallow thin purees/thickened formula!  He is still aspirating thin liquids, but they feel confident this will come with time, as he adjusts to feeding orally again. So, no G-tube.  The plan is to keep him on the N-G tube for now, as he transitions back to oral feeds and can take all his calories by mouth. It was so great to feed him some mashed potatoes with gravy tonight!!
Now, we wait for his ENT to book his bronch and see if he's ready for the big "D".
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Mom to Jacob, 26 Weeker - Our miracle boy, hero  and the light of our lives  Born 06/25/06; trached 10/17/06 for bilateral vocal cord paralysis, laryngomalasia, tracheamalasia, acquired subglottic stenosis, Failed Double Stage LTP 2009, Failed Single Stage LTP 09/16/10, Retrached 10/03/10;CP.
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08-27-2009, 10:12 PM
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Senior Member
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Join Date: Jan 2007
Location: Colorado
Posts: 3,979
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Kim... I am so glad you posted!!! I am even more happy to hear that you got the OK for Mr. Jacob to eat!!! Congrats!!
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Dawn

former 26 weeker -- 4/2006 -- trach, g-tube, nissen; came home 1/07 vented 24/7; Successfully decanned 8/8/2008 - 
Follow decan at: http://sleepy-dogs.blogspot.com/
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08-27-2009, 10:26 PM
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Member
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Join Date: Jan 2009
Location: Portland Oregon
Posts: 662
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This is GREAT news!!!!!
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08-27-2009, 10:29 PM
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Administrator
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Join Date: May 2002
Location: Phoenix, Arizona
Posts: 7,320
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Yeah!  I hope the big "D" happens soon.
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08-27-2009, 10:44 PM
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Senior Member
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Join Date: Feb 2009
Location: Carnegie, PA
Posts: 2,041
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Wow! that is great news! (and great that he wanted to eat after not doing it for so long!) I'll be keeping my fingers crossed that the bronch goes well !
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 Lynn, mother of Brooke(19), Haely(17), Sydney(12)Dominic(1) and Joseph(DOB 11/03/06)DX:Jeune's Syndrome:trach 12/12/06:vent depend: Sprinting 12 Hrs a day!!!!EE:GERD:Hydronephrosis:Situs Inversus:Aortic Stenosis:Myocardial Hypertrophy:Kidney Transplant 08/18/10 http://www.caringbridge.org/visit/josephmollica
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08-28-2009, 06:34 AM
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Senior Member
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Join Date: Jun 2005
Location: Minnesota
Posts: 4,726
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Katie-mom to Mitchell, DOB 12/16/04 trisomy 13 mosaic, severe laryngotracheobronchomalacia trached 5/04, cleft lip and palate DECANNULATED 12/16/10 A GREAT BIRTHDAY GIFT!
www.caringbridge.org/mn/mitchelljohncragg
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08-28-2009, 07:31 AM
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Senior Member
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Join Date: Apr 2008
Location: Virginia
Posts: 2,664
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Yay! 
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Karin
Alex's Mom
Alex born 6/19/2007, PRS, Trached and GTube at 3 weeks, palate repaired 12/20/2007, failed decannulation 5/7/08 due to undiagnosed suprastomal collapse, jaw distraction 9/9/08 (insertion) to 10/30/08 (removal). Single Stage LTP 2/17/09 and now member of the Naked Neck Club. Need a laugh? Check out http://itsallgoodtoday.blogspot.com/
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08-28-2009, 07:36 AM
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Senior Member
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Join Date: Jul 2007
Location: Vienna, VA
Posts: 2,227
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I am so happy for you that is truly great news!!!
Michelle
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Grand Ma (or Nanou French version of Nana) to Cedric born on August 5, 2006, Trached on October 16, 2007 because of subglottic stenosis due to 27 intubations for debridment of polyps
https://www.babiesonline.com/babies/c/cedric1/
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08-28-2009, 07:41 AM
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Senior Member
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Join Date: Apr 2007
Location: NJ
Posts: 2,549
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Wahoooooooo!!!!
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Angela - mom to Zach 14, Jake 12, Nick 9, & Kate 9/28/06 Pierre Robin Sequence, Stickler Syndrome, decannulated July 4, 2008 -- Kate's blog http://pieceofkateb.blogspot.com/
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08-28-2009, 08:28 AM
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Senior Member
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Join Date: Nov 2006
Posts: 1,391
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Yay!!
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Has a daughter who is vent dependent.
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