Sarah had her labs drawn again this morning and her important numbers all dropped. Yay, God! So, we will not be enjoying the luxurious accommodations of Seattle Children's Hospital this go-around. Dr. Horslen says we will need to keep her on the regimen of prednisone and have her labs checked out again next week.
Good news - now we can enjoy a three-day weekend together, in our home!
Thanks for the prayers.
Kirk. I happened upon your blog via a link in Google Groups. I want to encourage you in this journey with your Sarah. WOW. I never knew you were going through this with your daughter. I will keep praying for you and Sarah and your wife and family. I'm asking that by HIS stripes your Sarah be completely healed and this liver never be rejected. God Bless you for your honest writing about it. As a mother of a child with a disability it warms my heart. I know I'll never relate on the same level, but there is always a common bond between parents of kids with special needs. There just is. God Bless you!
ReplyDeleteYour Sarah is precious! I would love to add her to our prayers~ what an amazing little girl. God bless you.
ReplyDeleteGigi - that means a lot to me. I don't pretend to relate to what your own experiences have been, but it's true that we share a common bond. Thanks so much for sharing and for your prayers.
ReplyDeleteBrenna - thanks for your kind words and prayers. They are greatly appreciated.