People always ask what they can do for us. We do appreciate your prayers and service in our behalf. We'd also like to ask you to leave comments on the blog or directly in our email sometimes. Just a little note so that we know that you've been here and know what's going on. For Jon & I it is these little reassurances that we are not in this alone that mean the world.
Wednesday, February 11, 2009
It's Back
Here's a phrase that had gotten phased out, but it's back:
"Jacob, go brush your hair." I posted this picture because it gives a side view. He had the top combed with gel. The sides reveal his waves. It was like that when he was a baby.
Jaylynn pasted the computer and said, Hey he looks like Jacob again. I have to agree. Not only is his hair back, but the light in his eyes are back too.
Jacob was diagnosed with Embryonal Rhabdomyosarcoma (ERMS) Stage 1 in July 2008. His tumor was completely removed with clear margins. He had a port surgically placed in his left chest where he receives received all of his medicines and where blood is drawn. He has been following finished a 24 week treatment protocol of chemotherapy in January. He returned to 3rd Grade at his Elementary School in March 2009. He will see his oncologist monthly until his surgery is scheduled to remove his port-a-cath. We want him to swim all summer (needs to take a two week break for surgery site to heal), so we will wait until school starts again. He has follow up scans (ie. CT & chest x-rays) every 3 months.
Jacob's port was removed October 2009. This eliminated the need for a monthly flush of his port at the oncology clinic. He now goes in every year for a check up and blood work.
1 comment:
Jaylynn pasted the computer and said, Hey he looks like Jacob again. I have to agree. Not only is his hair back, but the light in his eyes are back too.
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