
In early February she got to remove her own mic-key button from her tummy since she didn't need tube feeds anymore.
Then before we knew it we were off to the Child Cancer Foundation's sunshine lodge for a week.

This was amazing, because after 9 months of Zoe not being able to really go anywhere or even having the energy to, we did something new every day for the week, just me and Zo. It was amazingly restorative.
We had and end of treatment party and then Zoe got to celebrate her 4th birthday. On her third birthday, 3 days after she was diagnosed, we didn't know if that would happen.

April brought a second clear MRI. Zoe returned to daycare and it was like she had never been away. She loves it and is looking forward to school. She's also back to swimming lessons which she adores.
Zoe's most recent clear MRI was followed 2 days later by an operation to remove her portacath (the device they deliver chemo through). That was a big milestone too and that's it she's holding in her hand in this photo.
Her hair is coming through wavy, which she wasn't too happy about, but is getting used to.
We enjoy the small pleasures. We dance. We ditch the housework in favour of going to the zoo and visiting friends and family a little more often. We drink lots of fluffies - don't hold the chocolate fish thanks.
And it looks like the Make A Wish Foundation is about to give Zoe a very special experience. She doesn't know about it yet, but it looks like she is going to get to meet her hero Dr Harry Cooper, the TV vet, in October.
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