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9:00 a.m. Drag out of bed to do IV therapy, my breathing treatments, and my VEST.
9:45 a.m. Breakfast downstairs in the Dining Room.
10:30 a.m. Another IV treatment.
11:15 a.m. Bath and an attempt at washing my hair by kneeling in the tub and running my head under the sink. (While on IVs I can't shower.)
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12:00 p.m. Lunch.
12:30 p.m. More respiratory treatments.
1:00 to 3:00 p.m. Rest Time.
3:00 p.m. Another IV treatment.
4:00 p.m. If the weather is nice, we try to sit out on the front porch and read until dinner.
6:00 p.m. Dinner.
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7:15 p.m. Breathing treatments and VEST again.
9:00 p.m. IV therapy.
10:00 p.m. Bedtime!!!! Start my feeding tube treatment (that runs through the night).
2:30 a.m. IV therapy.
3:15 a.m. IV therapy.
9:00 a.m. It starts all over again! See, nothing boring about my day! : - )
Thursday, May 15
I had an appointment with Dr. Pilewski this afternoon. It went well. We decided to continue IV therapy for at least another week. He is such a wonderful man and started the appointment by apologizing that I didn't have lungs yet. Can you imagine? That is just the kind of caring person he is, I am very lucky!
Hannah and Scott come tomorrow, hooray!!!
Love to you all! Nancy
3 comments:
Just another example how you truly AMAZE me! Enjoy your time with your hubby and beautiful daughter. I love you!
Love,
Debbie
Wow Nancy,
It takes a special kind of person to have such stregth and the ability to smile through it all. Have a wonderful weekend. Tomorrow is almost here!!! It must feel like Christmas eve!
Lots of love and hugs,
Amy
Hey, Nancy,
Well, by now you're enjoying the company of your family. I'm sure it's a wonderful feeling. I'm so glad they're there with you this weekend. (Have you stopped hugging Hannah?) I can't help but think you're surmising the idea of camping. After reading what your day entails, please don't camp. Instead, have Scott and Hannah set up camp in your apartment. (Good thing I'm not there to direct things.)
Thinking of you and praying ever so strong...
Love you, my friend!
Deb
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