💖 Our Legend, Our Maya 💟
- dellanienash9
- Nov 2
- 2 min read
Three weeks to be confined in hospital — and still, this little warrior keeps shining through it all.
🩺 Friday 31st October: IV fluids all day. Cyclophosphamide (1 hour) + Fludarabine (30 mins).
She missed celebrating her sister Lola’s Halloweeny birthday again, just like last year — but still found a way to smile.
🩺 Saturday 1st November: IV fluids all day. Cyclophosphamide (1 hour) + Fludarabine (30 mins).
🩺 Sunday 2nd November: Bloods, fluids finishing after 24 hours, and possibly de-accessing her port around 1pm.
She’s not allowed to go out yet, only short walks within the hospital — but she still makes the best of every step.
🩺 Monday 3rd November: Rest Day (and maybe re-access her port in the evening).
🩺 Tuesday 4th November: CAR-T Cell Day — the big day! Photos will show you how Car T Cell are meant to help Maya fight neuroblastoma cells.
Through it all, Maya never loses her smile, her spirit, or her spark.
She plays, she laughs, she finds joy even in the smallest things.
“How can you fall apart when your child keeps smiling, keeps fighting, keeps living her life however she can?”
Please, if you’re reading this — click the heart and please share Maya’s story.
Every share helps her voice reach a little further.
Every donation helps keep her treatment and travel possible.
Every act of kindness gives us hope on days when it’s hard to find any.
Please help
us keep Maya’s fight going — one share, one prayer, one act of love at a time.
Our girl is pure courage. A true legend. 💜























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