Alan's Reflections

First of all, I would like to thank you for your prayers and concern for us - Judy and me. Your prayers are especially appreciated because through prayer and God's help anything is possible. Faith, determination, family, and friends are going to be the anchors that pull me through this difficult time. (I am a Navy guy, you know.)

Some of you like to give me a hard time, that is appreciated too! I know you are just doing so because you care. I look forward to many more fun times with each of you. May God bless and keep you.

Signing off with the name my grandchildren call me,
Dude

Showing posts with label SECOND CHANCE...We Want to Make the Most of It. Show all posts
Showing posts with label SECOND CHANCE...We Want to Make the Most of It. Show all posts

Wednesday, October 22, 2008

We are HOME!!!!! (Apartment in Durham)

I am so happy to say we are out of the hospital and back at the apartment. We thought we would get to come home on Tuesday, but the infectious disease folks wanted to keep us an extra day because of the ecoli. They needed time to study the cultures of the ecoli and determine what type of ecoli it was and which antibiotic would be the best to treat it. Yesterday he got his first IV of the antibiotic, Ertapenem. The transplant coordinator had to come before we could be discharged and go home, she was there from 4:30p - 5:30p, and we left the hospital around 6:45pm. We had to drop prescriptions off at the drugstore. I hadn't eaten since breakfast, because I was afraid I would miss the coordinator, so I grabbed a sandwich at Wendy's. Alan had all 3 meals at the hospital. We went by the apartment to unload and for me to eat. Alan went back to the drugstore with me and went in. When we got back to the apartment, he walked across to the mailboxes to check the mail for the first time since we have been here. Before transplant he did not have the energy to walk over to the office and check our mailbox. I am going to like having my husband back. Since we have been here I have pretty much done everything by myself, now I have my best friend back. JOY! JOY! JOY! JOY! Down in my heart, down in my heart to stay.

His insulin is up since surgery as are all (most?) transplant patients. So he came home on insulin. Very small doses. Last night we were too tired to even try to figure out the machine to check blood sugar levels. So this morning we hit the floor running, he had to have meds at 8a, we worked on the machine and figured out how to do the test, only to realize we had no syringes to administer the insulin. Meanwhile the home health care nurse showed up to train me on giving the IV of anitbiotic for the ecoli and how to flush his picc line. She left at 12p and we ate breakfast, and then I went back to the pharmacy to get the syringes to give the insulin. Got home and we tested his glucose levels and he gave himself the shot.

Now he is napping, and I am blogging. But I have to get busy on organizing everything. This is very much like bringing a newborn baby home from the hospital. Everything is new. I am grateful he did not have to go back to the Center for Living (fitness center) today, that will happen tomorrow, and we can have today to get a handle on everything.

WE APPRECIATE EACH AND EVERONE OF YOU WHO ARE TRAVELING WITH US ON THIS AMAZING JOURNEY. OUR SECOND CHANCE IS BECOMING REALITY.