Tuesday, November 17, 2009

we're down to 8 ...

As we headed to Portland today and I looked out the window I couldn't help but smile. Although Connor still has a long journey ahead of him, we are looking forward to celebrating our last day of radiation treatment. When Connor completes his 30th day we will fill up 30 balloons and let him pop them (so if you hear loud popping it's just us in the backyard !!)

My heart aches when I see new children in the radiation office. It's not a place you want to see new faces.

I wanted to thank everyone for purchasing Connor's cards. Everyone has been so kind. One of Connor's nurses has offered to include a basket of his cards on her craft table at the hospitals upcoming bazaar.

His goal is to sell at least 40 cards and Donate a DVD player before Christmas.

Connor was pretty sleepy after treatment today. He took a long nap on the couch after we got home. We spent the rest of the day doing some art, playing UNO, taking a short walk and relaxing.

His appetite is improving, and he was real fond of "breakfast" for dinner tonight. He ate extra maple sausages.

The best part of our day
Sitting and watching our sweet sweet boy sleep, and get some much needed rest.

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