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Jun 1, 2016 Latest post:
Mar 14, 2018
David was born 6 May 2016 with a rare form of Hirschsprung Disease; he was born with only 15cm of intestine with the nerve cells that allow food to move through his bowels.
Right now, David is home after living his first 9 months in the hospital! He still faces an uncertain road ahead as we try to preserve as much remaining bowel as possible for food absorption, other bodily organ sustainability, and immune health. Infections, organ failures, and intestinal blockages are common for children with this degree of severity. David's entire large intestine, half of his small intestine, his gallbladder, and appendix have been removed. He is fed with IV nutrition and tolerates some milk through his g-tube.
Some ask, why not get a transplant? Well...small bowel and liver transplants are never desired, because success rates are iffy, about 50/50 long-term survival rates with small children, but sometimes it becomes necessary. David is doing very well with what he has right now! We hope to have David's intestines work for him for a great many years and for a miraculous healing/regeneration!
We are so grateful for the outpouring of support and prayers for David and our entire family this past year. Thank you friends, family, coworkers, doctors, and nurses! Without a doubt, God has a plan for David and us. It's been a wild ride, and hopefully, this is just the beginning of our wonderful life with this adorable child.
We are praying for David's miraculous healing through the intercession of Michelle Duppong, a former FOCUS missionary who bravely and faithfully battled colon cancer and passed on Christmas of 2015. (We have some prayer request cards made and she had a caringbridge site.)
We also request our friends and family pray the Divine Mercy Chaplet for David's strength and for the conversion of souls.