First, I want to apologize for not updating sooner. Every March since Caleb died has been rough for me, and I tend to avoid the internet as much as possible. With that said, March is over and it's time to fill everyone in on the latest.
From Oct 2010 - Mar 2011, this blog chronicled my son Caleb's journey with DIPG. Afterwards, it became an outlet for me to share how I was doing. Now, the blog takes a new direction. A new beginning. A new journey. The URL will remain the same, but the story is new.
Showing posts with label congestive heart failure. Show all posts
Showing posts with label congestive heart failure. Show all posts
Saturday, April 13, 2019
Update Time
Thursday, February 21, 2019
Heart Cath Results
Dad was feeling a bit weak yesterday morning and actually requested a wheelchair when they first arrived at the Cath Lab for his heart catheterization.
Sunday, February 17, 2019
Update as of 2/17/2019
After Dad was released from the hospital for the double pneumonia, he developed an issue with severe edema in both of his legs to the point that you couldn't tell where his calf ended and the ankle began. Then he had a rash form along his calves and ankles right where his socks normally sit. We called the cardiologist and Dad was advised to wear compression socks to help with the edema and increase the fluid pill they put him on while he was in the hospital.
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