Alaura’s Light — The Little Girl Who Refuses to Fade.2942
💗 Alaura’s Light — A Little Girl’s Fight to See the World Again 💗
Alaura was the kind of child who filled every room with sunshine.
She was bright, funny, endlessly curious — a seven-year-old who loved stories, silly jokes, and anything that made her mom laugh.
But this September, her world began to dim.
It started with her vision.
First, small things — missing a step, squinting to see her toys, hesitating when walking across the room. Within days, she was bumping into walls. By the time her mom, Ruth, rushed her to the ER, Alaura could barely see at all.
Scans revealed what no parent is ever ready to hear: a tumor, three centimeters wide, pressing against her brain and blocking the flow of spinal fluid.
The pressure had built so high it was damaging her optic nerves — stealing her sight, her balance, her childhood.
Ruth says she felt the world tilt that day.
Of all the fears she carried as a mother, this was one she had never imagined.
💗 The First Surgery
Doctors moved quickly. Within days, Alaura was in the operating room.
The surgeons worked to remove as much of the tumor as they could and relieve the pressure building inside her skull. The goal was to save her vision, but it was already slipping away.
She woke up with a scar curving across her small head and a quiet bravery that stunned everyone around her.
Even through the pain, she was sweet and chatty, asking for her favorite music and reminding nurses, “No pinches, no pokes, no drops!”
Her humor, her spark — still there.
💗 The Second and Third Surgeries
When the swelling didn’t subside, doctors realized she would need another surgery — this time to insert a VP shunt, a tiny tube to drain excess fluid and keep her brain safe.
By the end of September, Alaura had endured three major brain surgeries. She now carries five scars — three on her head, two on her abdomen — each one a symbol of survival.
The pathology report came back: astrocytoma.
Cancerous, but slow growing.
There would be no chemotherapy for now — just time, monitoring, and hope while doctors searched for targeted treatments.
💗
When Alaura’s bandages came off, she smiled. She thought maybe the blur around her would fade.
But the world stayed dim.
Tests confirmed the damage — her optic nerves had been permanently injured. Her eyes themselves were perfect, but they could no longer send messages to her brain.
She can see shapes and shadows, a little color, and some light from her left eye. But beyond ten feet, the world disappears into fog.
Ruth held her hand as the ophthalmologist explained.
She didn’t cry then — not until later, when Alaura reached out, feeling for her mother’s face and whispered,
“It’s okay, Mommy. I can still see you here.”
And she touched her chest.
💗 A Mother’s Love in the Dark
Ruth has not left her daughter’s side since that first ER visit.
She learned how to clean surgical wounds, monitor the shunt, and recognize pain from tiny changes in Alaura’s expression — because Alaura, who is level 2 autistic, struggles to describe what hurts.
Their days are a careful rhythm: medications, therapy, follow-ups, and rest. Their nights are softer — stories whispered in the dark, fingers tracing patterns across blankets, a mother reminding her child that even when sight is lost, light can still be found.
💗 The Road Ahead
Alaura’s recovery will take months — maybe years.
She’s learning to walk again, to balance, to live in a world she can no longer fully see. Adaptive tools, home therapy, and travel to specialists are now part of their new normal.
Ruth has taken unpaid leave to stay home with her, stretching every dollar to cover gas, food, and the endless medical bills that never stop coming.
But this campaign — created by friends, by a community that loves them — is helping keep them afloat.
Every donation, no matter the size, goes directly toward Alaura’s care:
🩷 Travel to appointments and specialists
🩷 Adaptive items for vision loss
🩷 Wound care and recovery supplies
🩷 Daily living expenses as Ruth remains her full-time caregiver
💗 Her Village, Her Hope
Through every update, Ruth’s strength shines:
“My girl is sunshine and silliness,” she wrote. “She’s still laughing. Still singing. She’s my miracle.”
Alaura may have lost much of her sight, but her light hasn’t dimmed.
She still giggles when nurses make funny faces. She still insists her stuffed animals have voices. And she still greets every visitor with a shy smile that feels like sunrise after a storm.
💗 A Promise
When asked what she wants to do when she’s “all better,” Alaura said,
“I want to help people who are scared, so they don’t feel alone.”
That’s who she’s always been — a child who brings comfort even when she’s the one in pain.
And with every act of kindness, every message, every shared story, you’re helping her and her mom keep going.
You’re proving that even when the world goes dark, love finds a way to shine through.
✨ Because this is not just a story about illness — it’s a story about light.
About a mother and daughter fighting side by side.
About the power of community.
Alaura’s world may look different now, but it’s still filled with color —
the color of courage, the color of hope, the color of love that refuses to fade.
Easton’s 200-Day Fight: A Child’s Courage Shines at Cardinal Glennon.738

After more than 200 days within the walls of Cardinal Glennon Children’s Hospital, little Easton has become more than just a patient — he has become a symbol of what true courage looks like. His journey has not been easy, but every day he shows the world that bravery doesn’t always come from soldiers or heroes in capes; sometimes it shines brightest through the smile of a child fighting for his life. 💛
When Easton was admitted, his heart was too weak to carry him through each day on its own. To keep him alive, doctors placed a Berlin Heart — a mechanical device that gives his heart the chance to rest while keeping his body strong enough to grow. For months, Easton has lived with wires and machines by his side, but he has never allowed them to define him. Instead, he greets each new morning with determination, ready to take one more step toward healing.
This week marked a milestone. For the first time in a long while, Easton was able to spend an afternoon outside on the playground, not just as a patient but as a child — laughing, climbing, and playing with his mom and his extended Cardinal Glennon family. His mother, who has been by his side every single day, watched with tears in her eyes as Easton took cautious but joyful steps, balancing his fragile condition with his boundless spirit.
The moment was powerful, not just for Easton’s family, but for the doctors, nurses, and therapists who have walked this road with him. Each member of the healthcare team has poured their skill, patience, and love into helping Easton reach this point. They have cheered at every small victory — from his first strong breath to this day on the playground — and they continue to fight alongside him as his journey unfolds.
For more than 200 days, Easton’s life has been defined by hospital routines, medical equipment, and constant uncertainty. Yet through it all, he has managed to remind everyone around him of the strength that comes from hope. His bravery is not loud or boastful; it is steady, gentle, and inspiring. He fights quietly, with every heartbeat, showing resilience far beyond his years.
Today, his story is not just about survival — it is about thriving, even in the face of hardship. Easton’s fight has become a beacon for other families enduring long hospital stays, proving that joy can still be found even when life seems overwhelming.
To the world, Easton is a patient connected to a Berlin Heart. To his mother and those who love him, he is simply a little boy who wants to play, to laugh, and to live. His courage is matched only by the compassion of those surrounding him at Cardinal Glennon, making every step possible. And as the sun set on his playground adventure, it was clear: Easton is not just surviving — he is showing us all what it means to be brave. 💛