Hi.
I thought I couldn't access my blog anymore for some reason,
but it seems that I can!
All is well 2.5 years after completing treatment.
Dr. Ewa told me on Tuesday that it's probably time for me to stop keeping track of Jaxon's bloodwork results. They've been normal and "in the black" with no caution flags for ... a long time.
We'll see. I do like to track his height and weight. He's perfectly within the 50th percentile for his age group and thriving at school and his new passion - hockey!
I'm hoping to finish up a few posts that have been sitting in my "drafts" folder for a long time, especially as there is some exciting news to share as a result of the study Jaxon was on for his treatment ... and some other progressive steps in the treatment of his diagnosis - Standard Risk Pre-B Cell Acute Lymphoblastic Leukemia.
Next quarterly appointments are March and June 2020.
Then he'll move to biannual visits in December 2020, June 2021, December 2021, June 2022.
Then annual from June 2023 until he's old enough to make his own medical decisions.
More to come.
While you wait, I encourage you to find somewhere to donate blood!
www.blood.ca
Please leave a comment so I know you're reading. :)
