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.
Friday, January 28, 2011
Posted by Caroline Welsh at 6:52 PM 0 comments
Saturday, January 22, 2011
Thanks so much for everyone who participated today near and far. It was a lot of fun. Thanks Jeffrey, Jasen, Ryan P., Bishop, Carter, Scott, Dave B., Dan, Steve, Bud, Sam, Zac, Dave M., Austin, Jared, and Higgins.
Posted by Caroline Welsh at 4:53 PM 3 comments
Sunshine and Rain
Posted by Caroline Welsh at 2:37 PM 1 comments
Friday, January 14, 2011
Day One of Many Days to Come
Dave got his central line and his temporary line surgically inserted today. These line are ports that are used for removing stem cells out of his body and to put the chemotherapy in. Dave had a great attitude today and kept joking around. My personal favorite was when he was coming out of recovery he said "I have the power" refering to He-Man and then started singing the Thundercats theme song. He remembers none of this and is unsure that I am telling the truth. I am. He gets a long weeked of R&R to recover and get some shots to increase his white blood cells and then mobilize them into the bloodstream. Tuesday, Wednesday, and maybe Thursday he will be at the Huntsman Cancer Hospital all day to remove the stem cells.
He is resting and still a little out of it. Ally and Grant went to open gym at Ally's gymnastics tonight. We are trying to get the wiggles out before our 2 months home bound starting Jan.31.
Dave and I will be moving downtown in a hotel while the kids stay at home with my mom and my sister Kim. Thank goodness for family and friends.
Posted by Caroline Welsh at 7:10 PM 14 comments





