On November 21, 2025, a local news station spotlighted Jax’s life-changing journey: the brave 4-year-old who was diagnosed with Severe Aplastic Anemia is now preparing to embark on his Make‑A‑Wish Foundation adventure.
A Diagnosis That Changed Everything
It’s been a tough path: what started as a routine check-up led to the life-altering diagnosis of severe aplastic anemia — a condition where Jax’s bone marrow stopped producing enough blood cells. His family, his younger brother (who became his donor), and the community rallied behind him.
From Treatment to Trip
Now, thanks to the power of hope and community, Jax and his family are preparing to set out on their Make-A-Wish trip—a moment that marks not just a getaway, but a milestone in recovery, in joy, in simply being a kid again.
Why This Matters
- Healing in action: This trip isn’t just fun — it’s a symbol that treatment is working, that Jax is reclaiming childhood after serious illness.
- Visibility for rare illness support: The story reminds us how important donor registration, research, and community support are for conditions like aplastic anemia.
- Empowering the family’s voice: With each interview, each smile from Jax, the family strengthens their role as advocates — showing other families they are not alone, and there is hope.
What Comes Next
The journey continues with follow-ups, care plans, and of course more “just being a kid” moments for Jax. The family plans to use this trip to recharge, celebrate, and continue sharing their story — so that when others face similar diagnosis, they know: there is light ahead.
How You Can Help
- Share Jax’s story, and link back to his COTA page so more families are reached.
- If you haven’t already, register as a donor (bone marrow/cord blood) to broaden the pool and opportunity for others.
- Reach out and support families navigating rare illness — sometimes a message or a share is the hope they need.