A rambling collection of thoughts as we’ve hit the one year post-treatment point.
MRI day # 8 is tomorrow. It isn’t really much easier yet.
For this first year after treatment scans are scheduled every 3 months. We just finished the 2nd set of those.
An unfortunate reminder of the lingering effects of cancer popped up on the playground.
A too-long post about how mom is feeling about upcoming scans
A month ago today we celebrated Joanna’s NED status with her bell ringing at the Jimmy Everest Center for Cancer and Blood Diseases in Children. Yay for celebrations! So, I thought I’d take a moment to give a bit of an update about how things are going. This means we’re one month closer to that… Continue reading It’s been a month
Last week was the last scheduled chemo. Just blood work today.
There are just 4 more weeks left in the 24 week plan to treat Joanna’s cancer! Now, 24 weeks isn’t the whole plan, there were lots of appointments and 5 surgeries before that countdown started. And, once it’s done there will scans each three months for awhile, and then more scans, just spread out a… Continue reading Four More Weeks
We’re making progress through the treatment plan!
Week 15 of treatment had a new low.