The description fits. I wish there was a way to escape this story. Can't I write my own ending?
(Photos on this post are from my walk "around the block." Watching spring emerge these last weeks has been restorative.)
Ed's MRI this week showed significant growth in the new tumor in the center of his brain. Because of the physical and cognitive decline we've watched this last month, I wasn't surprised. Still, it is hard to see confirmation of our fears.
Old barn covered in wisteria
Ed's seizure on Monday left him even weaker on his left side. At first he could not move his fingers or lift his arm. He has regained a little movement, but still can't use his left side much.
My brothers and Ed's brothers take turns coming every morning and evening to help Ed dress and shower. With the children's help, I can move him from his wheelchair to the recliner, but it isn't easy. I'm so glad to have the help of family.
Road-side poppies
In the past two years we've thrown a lot at Ed's cancer including multiple surgeries, chemo, radiation, diet, and experimental treatments. We knew Ed had the most aggressive form of glioblastoma multiforme, which has dismal statistics. But Ed had nearly two years of good quality life after his diagnosis, for which we are thankful.
But now we feel it is time to change tactics. We've stopped all treatment and are focusing on caring for Ed. Brain cancer patients rarely experience pain, and Ed appears comfortable and worry free. Our palliative doctor and home-care nurse have been helpful in giving us the needed equipment and information.
I don't know what the coming weeks hold, but I know that we'll need to hold onto God.






