It is the end of a long week, but not quite. Sarah still has an appointment tomorrow. It is a short one (90min) but still requires us to go to the clinic. Lilly wants to come along. She got a pez dispenser while we were in UT and she was told that the clinic has a wall of pez dispensers. She wants to go see them. Since most of Sarah's appointments are during school time, this might be one of the few times she is able to go.
Gus is trying to walk everywhere. He loves to stand in front of the toy kitchen and pull things out of the sink. He pulls himself up on his stroller because he wants to always go. He is an active kid.
We are so grateful for all the support that we have been given. It is so nice to have a meal brought or have Jess just be able to take one out of the freezer. We have gotten a number of cards and people telling us that they are thinking of us. It helps our spirits and helps us to stay positive. Thank you so much.
I had a friend in Highschool whose little brother was diagnosed with Luekemia. It was crazy, he was just under 5 years old. I remember his treatments lasting for a couple of years and us always thinking and worrying about little Dougie. He is Cami's age (22) and we haven't hardly thought of his cancer at all for all these years. For him it was the initial fight...and that was kind of it. Lets hope for the same thing with little Sarah!
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