Christmas Light Show
Last night we went for my first adventure post-transplant. We have been seeing ads for a Christmas Light Show and since last night was the final evening, we decided to check it out.
Though I fought to stay awake and did fall asleep on the way home, it was so worth it!
I wish Hannah could have been with us, she would have loved it!
The Home Health nurse will be here at 8:30 to take my blood, so I need to go for now. I know many of you are back at school and work today. I hope you can start this new year with a fresh start and a new found sense of energy!
My love to you all! Nancy
Comments
Your schedule is definately full and I can see how someone could get easily overwhelmed. Is this your permanent schedule or will some of the IVs be phased out as time goes on? You amaze me with your strength, it truley takes great will and an strong spirit to stay on such a strict schedule. If anyone can do it, you can. We will pray that this gets easier for you. Have a super day!!
Lots of love and hugs,
Amy
I cannot tell you how happy I am to see you smile, it brightens up my whole day.
Well, back to work I go--it was so hard to get to school today--I truly miss the kids (even though they drove me NUTS). Love you Nancy!!!!
God Bless,
Bridgette
So glad you were able to get out and see the show. It looks like it was amazing.
Burger King food is consistent in it's taste and sure it was a treat to get out. Thinking of a junior whopper as I write!
Your schedule is a full days' work. Sure among the many other requirements you had to meet to be a transplant candidate they determined that you could and would be able to follow the regime. You and your support folks are amazing. Each day is one step closer to your recovery.
The last four weeks have started you on a new journey. Keep up the great work.
Judy Mark