On Wednesday, June 1, Ayanna Bradford lived a normal life for a 5-year-old girl. She played outside with her friends and rode her bike. She complained of a little tummy ache, but nothing out of the ordinary. That night she went to bed, excited for her pre-kindergarten graduation.
On Thursday, June 2, Ayanna’s world stopped being normal and became a chaotic mess.
Ayanna, or Yaya to her friends and family, woke up at 5:30 a.m. Thursday morning. While getting ready for the day with her mom and sister, the usually cheerful little girl was complaining that her tummy and head hurt. Even a warm bath didn’t make her feel better.
She stayed home with her dad, Brian, while her mom Mandy went to work at a hospital near Cook Children’s. Only an hour after Mandy arrived at work, her husband called to tell her something was definitely wrong with their daughter.
Ayanna woke up screaming, the left side of her face was drooping and her eyes “were going every which way,” and not focusing. Mandy told Brian to meet her at Cook Children’s and he rushed their daughter into the Emergency Department. After a quick look at Ayanna, she was taken in to the Trauma bay.
A battery of tests followed including an X-ray and ultrasound of her abdomen, a chest X-ray and CT and MRI scans of her brain. The news was not good for little Yaya.
She suffered a stroke that attacked the right side of the brain.

While still reeling from the news of the stroke, the family found out Ayanna suffered heart failure as a result of myocarditis, a disease that attacks the heart. They later learned that it was most likely the result of the Parvo B-19 virus, which children commonly get in day care or schools (not the parvo from a dog). Usually, it causes cold like side effects, but nothing serious. Usually. But for Ayanna, it was another blow to her already fragile little body.
Cardiologist Corey Mandel, M.D., gave the family a 40-percent chance that their daughter would need a heart transplant, a 30-percent chance she would need either a pacemaker or defibrillator and another 30-percent chance that she would return to a completely normal state.
“I never would have thought in a million years that a child could have a stroke,” Mandy said. “My husband and I were talking and I said you know everything happens for a reason good or bad and if she didn’t stroke she may have been the child that had the heart attack and died on the playground and you would’ve never known what caused the heart attack. That’s a blessing in disguise. As difficult as this is, she’s still here.”
Donald Murphey, M.D., an Infectious Disease physician at Cook Children’s started Ayanna on an antibody regimen to fight the virus. The antibody regimen worked.
“Her heart today is 100-percent normal,” Mandy said. “Miracles do happen and Ayanna is a walking one.”
Ayanna needed a few miracles while at Cook Children’s. Richard Roberts, M.D., a neurosurgeon at Cook Children’s, told the family that their daughter’s stroke was so severe her brain was swelling at a significant rate. Without something to minimize the pressure on her good side, Ayanna would be brain dead.
That Friday morning, Dr. Roberts performed a decompressive craniectomy where he removed the right portion of Ayanna’s skull to allow her brain to expand. The swelling continued into the next day until a sodium IV regiment flushed the extra fluid out and once again, a crisis was averted.
If the sodium regimen had not worked, Ayanna would have received a right hemispherectomy, which would have required the removal of the right side of her brain. Instead Dr. Roberts removed her skull to allow for the swelling to go down. Ayanna was fitted with a special helmet to protect her head. She will need another surgery in about a month, after the swelling goes down, to reattach her skull.

Ayanna is currently in the Transitional Care Unit at Cook Children’s, which provides rehabilitation services to children recovering from illnesses and injuries. Her face on her left side is still drooping and she can’t move her left arm, but has regained movement in her left leg. Improving her left side is the focal point of her rehabilitation at Cook Children’s.
Now, Yaya faces another challenge. Among her many battles, she acquired gall stones and pancreatitis. She had her gallbladder removed and is working with the gastroenterology physicians at Cook Children’s to get the enzymes her pancreas creates a regular number. The numbers are extremely high right now and if they can’t be brought down to normal, she faces the danger of getting diabetes.
Today, the Bradford’s anything but typical day includes the care of an array of physicians, nurses, rehab therapists and Child Life specialists.
And with everything going on with their youngest child, the Bradfords continue to try to make life as typical as possible for their three other children, as they all deal with what has happened to their Yaya.
“You either go to the negative and fear for the worst or you go for the positive,” Mandy said. “I have my mini breakdowns. Yesterday I had to go for a little walk. I thought nothing’s getting better, but the truth is she’s here and she is getting better. You can’t be sad that she’s here. God gave me my baby and that’s all that I wanted. The day we walked into Cook Children’s was the worst day in my life, knowing how close she was to passing and that she wasn’t breathing on her own. It was more than difficult. It was very hard, knowing that she’s here and that she is just a kid. Like I told my husband I don’t care how she is. She can never walk again, even if she can’t talk again, I’m taking her just the way she is. She’s here and I get to hold her, squeeze her and kiss her until she’s blue in the face. As long as she’s here you can’t be anything, but happy.”



8 comments
Mandy Bradford says:
Aug 11, 2011
Yaya is doing GREAT, thanks to all the wonderful nurses, physicians and therapists here at CookChildrens. We were blessed to be so close to this facility during our time in need. CookChildrens saved my daughters life and we are forever thankful.
Sara Quiroz says:
Aug 11, 2011
What a wonderful story about a beautiful little girl. She makes my heart smile everyday with her continued hard work and updates from her loving family.
Dora Phillips says:
Aug 11, 2011
Jeff -
What a wonderful article, Thanks for bringing Yaya’s trek to the fore front so other can share in this extraordinary, beautiful little girl’s grit and her parent’s fortitude. Fort Worth is fortunate to have this extraordinary children’s hospital and its support group.
Sekeitha Jones says:
Sep 6, 2011
Thanks for sharing.. although this has brought me to tears, i’m scared for one that this could happen to a perfect, beautiful little girl…It hits close to home since I do have a 7 year old beautiful little girl of my own. I’m also crying because i’m so happy for the family of this loved little girl. I can tell in the pictures just how loved she is. A picture says a thousands words… and all of her pictures say LOVE… I met her grandmother at her job and when she ask that I pray for her little grandaughter before she could finish speaking I said done.. Thanks for sharing and I look forward to seeing her continue to get stronger and better each and every day.
Monica Galvan says:
Sep 27, 2011
We are still praying for little YaYa. It was such a blessing to meet her and the family. She is a little angel that God is using to show what a true miracle really is!
Love and Prayers,
Intense Student Ministries
Laurie Dirks says:
Dec 16, 2011
What an amazing family you are! Mandy and Brian are the most patient parents I have ever seen! They always kept a smile on their faces even when they were going through the toughest times imaginable! Yaya has so much fight in her and will to survive and she is truly a courageous little girl! I am so glad she is now at home with her family! They became part of our family at Cooks!
Love,
Nurse Laurie
xitclalli says:
Jan 15, 2012
i like it it made me sad
Regina Smith says:
Jan 15, 2012
Dear Mandy,
The last paragraph says everything that I felt as I sat with Adam in ICU reminding him to breath. He also had the saline solution and Dr. Roberts was also our surgeon. He stayed on call and at the hospital for first 48 hours of Adam’s stay at Cooks. He told us on the morning after Adam’s first night that they had not expected Adam to make it thru the night. It is very difficult to think of my 17 year old son missing almost all of his cerebellum and part of the brainstem is dead. His recovery does not match the images and damage that show up on the scans. Your story is so inspiring and your positive attitude is so contagious. YaYa is so precious, so beautiful. She just radiates joy and love. I am so excited to have found you! Praise God. He knew I needed someone and how lonely I have been since our move and he brought me you! Thank you Jesus!