Bri’Ellas Fight Against Aplastic Anemia

04/24/2026

HELLO EVERYONE
It’s been a while! Bri’Ella has been doing good, we were able to go Home HOME. She still has some bumps on the road. But is doing well. She’s rocking it!

02/19/2026

One year ago, our world changed forever.
The day Bri’Ella was diagnosed with Severe Aplastic anemia felt like the ground disappeared beneath our feet. We went from ordinary routines and future plans to hospital rooms, lab results, and words we had never imagined would become part of our daily vocabulary. Fear settled in quietly at first and then all at once. The uncertainty was overwhelming. The waiting was unbearable. And the helplessness as a parent… that is something you can never truly prepare for.
This past year has been the hardest of our lives.
There were days filled with tears, exhaustion, and questions without answers. There were long nights listening to the sounds of monitors, holding her hand, trying to be strong for her even when we felt like we were falling apart inside. There were moments when hope felt fragile. Moments when courage felt borrowed. Moments when we had to take it one breath at a time.
But in the middle of all of it, there she was.
My baby is brave in ways most adults will never have to be. She faced needles, treatments, and endless appointments with a strength that humbled us. She learned medical words no child should have to know. She endured more in one year than many do in a lifetime and yet she still found ways to smile. To laugh. To be light in the darkest rooms.
This year has tested our family in every possible way, but it has also revealed a strength we didn’t know we had. It has taught us gratitude for small victories stable numbers, good days, quiet nights. It has taught us to celebrate progress in inches instead of miles. It has shown us the depth of love that carries you when you cannot stand on your own.
One year later, we are not the same people we were before. We are softer in some ways, stronger in others. We understand fragility. We understand courage. And most of all, we understand that our daughter is one of the strongest people we know.
Aplastic anemia tried to take so much from her.
But it did not take her spirit.
It did not take her light.
And it did not take her fight.
One year down.
And she continues to show us every single day what true strength looks like. 💛
Here’s a video with pictures throughout the year.
I’m glad I was finally able to do something and be her donor after a long 9 months of waiting.

01/29/2026

Bri’Ella was admitted to the hospital a few days ago. I’m asking to please keep my baby in your prayers. It breaks me to hear her plea with me that she don’t want to be sick anymore or she wants to be the old Bri’Ella. Please , Please keep praying.
Thank you.

01/13/2026

Hi Everyone. Bri’Ella wanted to share this video with you all. She is now comfortable sharing her hair loss. She’s got to meet lots of beautiful kids who also have lost their hair so she now understands that it’s okay and she don’t have to be embarrassed or insecure. Please share and help Bri’Ella spread awareness. Especially now when kids are so vulnerable to all the illnesses going around.
Thank you ❤️🤍

01/01/2026

2025 was one of the hardest years my family has ever faced. It tested our strength, our patience, and our hearts in ways we never imagined. Everything shifted when my daughter was diagnosed with aplastic anemia. From that moment on, our lives became filled with hospital rooms, difficult conversations, and a kind of fear you can’t fully prepare for as a parent.
The journey led us to a bone marrow transplant—a road filled with hope, uncertainty, and courage. Being her donor was one of the most emotional experiences of my life. It was overwhelming, humbling, and powerful all at once. As a parent, you’d do anything to protect your child, and this was my way of fighting for her, of giving her a chance at healing.
Through the hardest days of 2025, our family learned what resilience truly means. We leaned on love when we were exhausted, on faith when answers were unclear, and on each other when the weight felt too heavy to carry alone. It was a year marked by pain and fear, but also by bravery, sacrifice, and an unbreakable bond that carried us through. Goodbye 2025 you are one to remember . Hello 2026

12/28/2025

Bri’Ella’s counts have been up and down. Her blood counts are still very low. Her doctor says it’s normal for it to be this way. But knowing that she will have this the rest of her life, everything worries me! She has good days and bad days. But one thing is for sure… She is a Fighter.
Parents, when you feel something is wrong with your child dont walk away! Push those Doctors to test everything!!! Please, continue sharing Bri’Ella’s story it may be helpful to someone else who is going through something similar.

12/24/2025

12/20/2025

Bri’Ella’s Christmas wish is to be home for Christmas with her family. Will Santa grant this for her?

We wish you all a Merry Christmas. May God bless you in the New Year. Please hug your loved ones and let them know how much they mean to you.

12/18/2025

Please do not bring gifts to Bri’Ella without letting me know first. When my mom is not with me I cannot leave the room. There are gifts being left and by the time I get told about it someone has taken them. If you’d like to gift Bri’Ella anything please reach out to me, my mom or sisters to meet up with you. We appreciate all that you guys have done for us. More than I can ever explain. We Thank you so much for all the love and prayers 🥹 We love you all 🙏🏼

12/14/2025

Bri’Ella’s reaction to the Christmas Tree Lighting last night at Phoenix Children's 🥹❤️🤍

12/11/2025

Good Morning ❤️🤍
has really changed our lives and robbed my baby of her life. Lately Bri’Ella has not been happy. She starts crying out of nowhere, her eyes are very sensitive and she’s been super itchy. Last night I laid her back in the shower and let the warm water run on her head to relax her. Being in the hospital has taken its toll on us. There’s times when my mom and I cannot even leave the room. I won’t ever take being home and having home cooked food for granted again 😩 Thank you to everyone who is sending Christmas Cards and gifts to Bri’Ella and my family. We really appreciate it.
We love you all. ❤️🤍

12/04/2025

I know a lot of you have been messaging us about Bri’Ella’s condition.

It’s been a very emotional time for us. Bri’Ella had been very tired and in a depression over losing her hair. So we have just been trying to keep her spirits up. She thinks she looks ugly and like a boy. We let her know how beautiful she is and how much we love her. We read to her all your messages. (Which she loves)
Please continue the prayers for Bri’Ella. Also for those that have asked yes we do have the gofundme and Bri’Ella has her cashapp. We really appreciate all the support you all have given us. It helps so much. I can’t Thank you all enough!!!! 🥹❤️🤍