She had an EEG to measure seizure activity. Her seizures were confirmed, and she started a new medication to help manage them. The seizures are still present, so the medication will need some tweaking, but none of it is interfering with her days.
|Wired up for EEG. She was sleep-deprived for several hours the night before to help increase the likelihood of catching a seizure during the test - torture for her and us!
|Ice cream parlor for mommy's birthday
|She has a new fascination with purses - carrying her own and emptying mommy's!
|New occupational therapy goal: dressing herself. We have a ways to go...
|Carousel ride at Happy Hollow
We went to Jack's Camp with other brain tumor families. It was a great weekend!
Scarlett did several Easter Egg hunts in the last week. By the time Easter actually arrived, she was starting to get it, and enjoyed opening her eggs (filled with stickers!) She got dressed up and played with her cousin Caleb.
|Helping daddy blend her meals for the week.
The biggest new development is that Scarlett is walking independently!! She has been taking a few steps between people for a while, but last week, she set her mind to it and just started walking around the house.
She started with a few steps (surely in part because of her fancy cape from Cape4Heroes!)
Then, last week, we snuck around the corner of the living room to see this:
Now, she's on the move everywhere she goes! At school, she follows the other kids around and does a good job dodging them as they play around her. She can stand on her own, pick things up and carry them. She tries to sign while she walks, but still needs her arms for balance. I am not sure what finally changed after a year of using the walker, but she decided she was ready. Yesterday at physical therapy, we officially returned the walker, and even got the OK to have her wear regular shoes (without braces or inserts) for a while!
Last week, my article was published in the Narrative Inquiry in Bioethics journal. It's one among a collection of stories from parents who have children with pediatric brain tumors. I am very proud to have contributed to this, and hope that doctors and other professionals will read it and gain some insight into parent experiences that will benefit families who go through the same things in the future. If you are interested in reading the journal, you can access it here or with Project Muse access (with a university or library affiliation). Just for fun, I searched for myself in Google Scholar...
Tomorrow, we visit the neurosurgeon to discuss plans for her next surgery to continue rebuilding her skull. We're hoping that he can continue to wait into the summer, when our schedules all calm down a bit...we'll see how patient he can be. The idea of surgery now - days (weeks?) in the hospital, trying to keep this new walker from escaping her crib...ugh. Procrastinating won't help, but it is the least amount of fun I can imagine for our summer.