Route position 48 · Planned public waypoint
Bone Marrow Awareness Day — Quilcene
A day standing still, in Quilcene
Quilcene, Jefferson County, WA
This experience shows the planned public route and reviewed editorial progress. It is not live location tracking and does not show where Jeana Moore is now.
One of the walk's ten Bone Marrow Awareness Days. No miles are walked. Jeana stays in Quilcene and spends the day talking with anyone who stops — about donors, transplants, and how and why to join a registry.
Ten of the walk's forty-five days are Bone Marrow Awareness Days, and this is one of them. In Jeana's own words: "I stay where I am to educate about donors, transplants, how and why they should join." That is the entire plan for the day. No mileage, no schedule to keep, no stage. She stops moving so that people have somewhere to find her.
If you stop, here is what she will actually go through. What a match is: for HLA matching, doctors look at up to twelve markers on your DNA and generally want eight to ten of those twelve to match. Why family is usually not the answer: three quarters of patients have no fully matched donor among their own relatives, which is what makes strangers the whole story. What donating is really like: nine donors in ten give blood stem cells through an IV over a few hours with no surgery, one in ten donates marrow, nearly always under general anaesthesia, and NMDP covers all donation and travel costs either way. And what joining takes, which is a free swab kit, a cheek swab, and a prepaid envelope.
She will also tell you about Jada, who was diagnosed with acute myeloid leukemia at one month old and had her transplant at seven months, and about Torsten Huber, a stranger in Germany enrolled by DKMS — one organisation founded in 1991 that has now facilitated some 135,000 stem cell donations. That is not a story about luck. It is a story about how many people had to have already said yes for one of them to turn out to be the right one.
What this day is not: it is not a registration drive run by the foundation, and nobody registers here. The Jada Bascom Foundation does not run a registry, does not mail swab kits, does not perform HLA typing and does not decide who is eligible. If you decide to join, Jeana will point you to the registry that serves where you live, and that registry does everything that follows. Coming over to talk costs nothing and commits you to nothing. The exact public spot in Quilcene will be posted by JBF once it is confirmed; her lodging and her precise position are never published.
Find the official registry for your country
JBF is a registry referrer. Choose a country to visit the official organization that decides eligibility and handles registration.
United States — NMDP
NMDP currently lists ages 18–35 for joining its U.S. registry.
Optional age guidance
NMDP join the registry guidance · verified Aug 1, 2026
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Eligibility rules can change. Confirm the current requirements with the official registry before joining.
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