We will all learn to live with this illness, Chronic Myelogenous Leukemia, that is in one of us.
I hope to share the journey with others and to make a difference along the way.
Sunday, February 12, 2012
Sometimes my gut still clenches up like this dried up leaf when we are in the waiting phase. Sometimes my heart squeezes tight when I think of others waiting for these results knowing that it probably wont be good, and then I break into a fine sweat, a lady-like one!, just thinking that I don't ever want to be in that position!
Steven looks great and seems great - not too long now, just a week or two, and we will once again know that he is doing great. Please.
This blog is from my point of
view as a mom with an adult
child who has cancer.
In no way do I mean to take away
from what he, or anyone else is
going through. These are purely
my thoughts and feelings at the
time of writing and in no way
suggest treatment options nor do
they offer advice in any way.
This is my way of strengthening
myself, which in turn will
strengthen Steven too.