Day 3: Another relatively long day on the transplant floor. Camden and I were shooting hoops this morning after our new child life friend brought us a basketball net for his bathroom door! Today Camden, Ron, and I made the decision to proceed with the NG tube in his nose. This will allow us to give him his oral medications through the tube instead of him worrying and getting upset about taking so many medications by mouth. In time, when he is not eating as much, it can also be used for nutrition supplementation. Praying those little stem cells are working diligently towards engraftment! Lets GO stem cells, LETS GO! Praying, believing, trusting, and praying some more.....
Aunt Donna
9/27/2013 10:35:47 am
I know you made the right decision for him. After your message this morning, I know it wasn't easy to do. Thanking GOD that his count is going down and continues to do so. Also happy he felt well enough to shoot hoops with you. Who won? My love thoughts and prayers are with you always. Wishing you a peaceful, restful night. LOL
Gramma Nanc
9/27/2013 11:49:12 pm
thank you God !! Great to hear he is doing well, Lets Go Stem Cells work hard !!sending Love Hugs & Prayers as always to all of you .:) Comments are closed.
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MommyShe's going to keep everyone up to date about my progress. Isn't she the best mommy ever? Archives
September 2021
Diagnosis: May 9, 2013
Surgery: September 2013 Transplant: September 2013 STRICT ISOLATION UNTIL January 2014 Radiation: November 2013 Antibody: January 2014 END OF TREATMENT June 9, 2014 DFMO Trial: June 2014 (27 months of DFMO) **FINISHED ALL TREATMENT JULY 25, 2016 5 years from diagnosis!! May 9, 2018 5 years from frontline!! June 9, 2019 IN REMISSION: pending (waiting for 5 year mark from maintenance). Benign Tumor: June 2019 |