Neutropenic basically means your white blood cells are zero and you are unable to fight infection. Dave has reach netropenia today from the high dose chemo that he has been recieving. He was sick this morning but seems to be feeling a little better now and has been able to keep his meds and some food down. We did get special permission to go home and watch the BYU game Saturday night since our hotel doesn't have versus:) We want to let our neighbors know how much we appreciate the meals and acitivities for the kids. They are enjoying them so much. We also want to let friends, co-workers and family know how much we appreciate thier thoughtful gifts, packages, phone calls, posts, and emails. We feel so blessed to have such a supportive and loving fan club for Dave. We have felt your prayers for us. We have truly felt comforted day and night. Even when things feel overwhelming or unsure around us I love the peace that comes through the Spirit and the Savior carrying us through.
Thursday, February 3, 2011
Tuesday, February 1, 2011
Stem Cells Back Today
Dave has been tolerating the chemo pretty well. The nurses says that he will probably be the most sick over the weekend and the early part of next week. Even though Dave has not been sick he somehow has lost another 10 pounds=( Poor guy is doing his best to eat. Since Dave's white blood cell count isn't too low yet the doctor has given us permission to go home and visit the kids. We have gone home Sat, Sun, and Mon and spent the afternoon, eaten dinner, and i got to put the kids into bed. It's amazing how meaningful that becomes to you. A once mundane task that I often couldn't wait to get over with and relax has become the highlight of my day. To be able to scratch my kids backs, sing to them, and assure them that I love them even when apart has been priceless. Each hug and kiss feels so good. My sister Kimberly is there with them this week. My mom and Rod are at home recovering from a long weekend that is more than they are used to. My mom said they took over a 4 hour nap the minute they got home. She says she has a renewed appreciation for the work that young mothers do. Today is our longest day ahead of us. Dave will be getting his stem cells back. They will be given them through his port in his chest. He then will recieve platlet and red blood cell transfusions from donors as needed throughtout the week. We have loved reading the comments on the blog posts. Thanks again everyone for your thoughts and prayers we can feel the support.
Friday, January 28, 2011
Chemo and Cafe Rio
Dave got his first experience with chemo today. He recieved it through the port in his chest. We were at the hospital for about 5 hours. Afterward we picked up our load of medications and I have been trying to sort them out using a pill box that a friend sent me:) Dave isn't feeling the effects of chemo yet and we moved in to our hotel room downtown. We are required to be close to Huntsman in the event that anything goes wrong. My mom and Rod brought Cafe Rio and the kids to come visit us tonight. It was so good to hug and kiss them. It is crazy how time warps. I felt like I hadn't seen them for days. They had a great time playing on the bellhop cart. Well now we sit and wait and watch for Dave to get sick and then we endure it and then we watch him get better. Sounds simple right? I love how trials can make you remember what is most important and how to cherish the simple yet meaningful things in our lives. Life is precious and beautiful. Thank you again to everyone walking with us every footstep we take. We love you.
We had some additional supporters join in on the head shaving fun. I will post the pics as I receive them. Thanks to everyone for your support. Matt from Portland....
Saturday, January 22, 2011
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