Wait and See
We’re sliding into fall, and I’m racing to squeeze in the last joys of summer—one more pool day, one more pontoon ride, one more adventure on the calendar. Everything feels rushed, as though there’s so much I want to do and see before the season slips away.
And yet, my doctors’ message is the opposite: “wait and see.”
Wait? Me—wait? That’s never been my strength. But this cancer journey is on a timeline of its own, and I’m learning to surrender to it. For those curious, here are a few updates.
In August, I quietly celebrated a milestone: three years since my diagnosis. That’s nearly two years longer than the doctors expected – and I count that as a gift. My mobility has shifted, and I now use both a walker and a wheelchair. But the important thing is: I’m still moving. These changes could be lingering effects of radiation, or the brain tumor itself, or most likely a bit of both. For now, it’s another season of “wait and see.”
Another change is with my career. After ten incredible years at Milliken—years full of teamwork, growth, and accomplishments—it’s time for me to step away. I recently transitioned to disability status.
But enough about the challenges—here’s the good news!
I’m still deeply engaged with The Cure Starts Now, an organization that funds vital brain tumor research. Through my personal fundraising page, I have contributed nearly $150,000, much of it through the sale of my paintings. To everyone who has donated or purchased art: thank you. I hope your homes are brighter with my work on your walls.
This year also brought an exciting partnership with Love From Companies, a Minnesota-based retail store. Their “Art For Good” campaign pairs artists with nonprofits, and I was honored to be chosen as their first featured artist. My designs have already raised more than $1,500 for The Cure Starts Now.
In July, Calvin, Dave and I traveled to Banff, Canada, for a brain cancer symposium sponsored by The Cure Starts Now. We met doctors, researchers, and families—all united by the mission to advance pediatric brain cancer research. Again and again, I saw proof of the extraordinary impact this organization is having and the urgent need to continue funding.


On September 6, another wonderful organization, Humor to Fight the Tumor hosted their annual gala. With more than 800 in attendance, the organization raised a record-breaking amount of money – more than $1 million! I’m so grateful for the love of family and friends who bought tickets, filled tables, and donated auction items. Your support makes such a difference.



In mid-September this year I attended the annual American Brain Tumor Association conference in Chicago. The event featured a gathering of patients, caregivers, researchers and advocations dedicated to advancing brain tumor research and treatment.
So while I’m often told to “wait and see,” I choose instead to feel lucky—for each day, each experience, and for each of you who continue to walk this journey with me.
With gratitude and joy,
Lisa