Welcome

Thank you so much for visiting our blog. As you all know, Bill is loved by so many, in so many countries across the world - and we want to make sure you are up to date on his health. The support we have received from our family and friends is truly a blessing and we want to thank you so much. On this blog, I will be giving regular updates on Bill. Please feel free to share comments/ask questions and I will get back to you asap.

Love,
The Deane Family

Wednesday, June 17, 2009

Day + 15

I see Kaitlyn got to the blog before we did tonight. What a doll. Can't wait to see her.

This has been a long day! Bill and I got to the hospital this morning at 11.00a.m. and did not leave until 10.00p.m. Bill needed I.V. fluids and two units of magnesium. Each took four hours to infuse. At the end of this he was exhausted. His white blood count was 3.0 and he did not need blood or platelets.I guess this is one way to learn patience!

Each day we will have to go to the hospital. We are hoping it will not be for this long each day.

It was wonderful to be in our own space last night. Bill slept for 11 hours solid.

Thank you again for your prayers. Please keep them up. Bill has his first bone marrow biopsy on June 29th. Please God it will bring good news.
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