Ethan, the eldest son of the family, was born on May 15, 2000. He was compassionate, loving, and genuine, and dreamed of becoming a rap artist. At age six, he started a long journey with a low-grade brain stem glioma.
Ethan’s tumor was discovered after he started having blurry vision, a hard time hearing, and would wake up in the middle of the night vomiting. After he was diagnosed at six years old, he had his first surgery to relieve a buildup of fluid in his brain called hydrocephalus. This surgery left Ethan visually impaired. He later had his first craniotomy and was set up with a treatment plan. He endured 18 months of chemo, ending when he was eight years old.
This process was difficult for his family who had to navigate learning about brain tumors and visual impairment in tandem. They did a lot of research on their own for services to help with modifications at home and school. Ethan didn’t like using a cane, so his family stuck with sighted guides.
Once he was done with treatment, Ethan was able to attend school more often since he no longer had side effects from chemotherapy. He used modifications like enlarged printing for his schoolwork and was able to play with modified card and board games at home.
When he was in fourth grade, Ethan’s school taught him braille, which was much easier as the large print was becoming too difficult for him, and many of his friends at school sight-guided him. He started showing interest in rap music, writing lyrics from age 12 to 17.
“He was very resilient, relentless, determined, and motivated to not let the disease or his blindness stop him from doing as much as he possibly could with his life and enjoying as much as he possibly could with his life. He never gave up. The disease just basically became more than he could fight,” says his mother, Vicki.
The smart, social, and determined Ethan was excited to start high school when a routine MRI showed his tumor was growing again. When he ended up with hydrocephalus, doctors did another craniotomy, which left him completely blind.
Children with brain cancer can’t wait another week, another day, another minute for your support. When you donate to the Pediatric Brain Tumor Foundation, you help fund life-changing research and provide families with the resources and support they need. Don’t let pediatric brain cancer steal another future.
Ethan spent his freshman year in and out of the hospital after the shunt doctors put in became infected. His sophomore and junior years were better – he was able to go to school more regularly and had a social life with his friends.
A few months into his senior year of high school, a second tumor was discovered. At first, doctors were not worried about it, but Ethan started fainting and having seizures. In March 2017 at seventeen years old he ended up in the hospital from a seizure. After he returned home from the hospital, he had to learn how to do some tasks like how to walk with a cane. However, he was also partaking in new eighteen-year-old activities like opening his own checking account.
In September, the day after Labor Day, Ethan was non-responsive after a hemorrhage. Doctors didn’t think he would make it through the night, but he did. After additional procedures and monitoring, his doctors suggested that he enter a nursing home so he could have skilled care and build enough strength to come home.
Months later in May doctors discovered the tumors had spread through his brain and there were no more treatment options available. He entered hospice and one month later passed away at age 18. Vicki shares that Ethan was never expected to pass away. His prognosis was that his tumor would dissolve or stabilize by the time he was 23.
Ethan left a huge impact on the world, and any recognition and remembrance of him is very comforting for his mother and family. Through her grief journey, Vicki found the most support from other parents in the Pediatric Brain Tumor Foundation’s peer-to-peer mentoring program, her online Cancer and Afterlife groups, and grief therapy.
“Everyone grieves very differently and everyone’s experience after they lose their child is very different. Some parents have found that they pretty much would lose everybody from their families and friends, and that’s been the case for me mostly. For those types of families, I would say to really reach out to providers who specialize in grief and get involved in support groups for grieving parents. Sometimes you make new friends in those groups too.”
No parent is prepared to hear their child has a brain tumor, and the journey can be overwhelming and lonely. Through resources like our peer-to-peer mentoring program and virtual support groups, the Pediatric Brain Tumor Foundation is there for families every step of the way.
You can bring hope and healing to more families by donating toward our year-end campaign at www.curethekids.org/holiday2022. If you or a family you know need support this holiday season, contact us at 800-253-6530 ext. 3 or [email protected] to speak with a member of our Family Support team.
My brain tumor experience is something I think about every day of my life, but the outside world likes to erase that and pretend it didn’t happen. It’s too “taboo” or “uncomfortable.” So, this year, on the 7th anniversary of my surgery, I want to talk about it.
In June 2018, Valentina was diagnosed with a pediatric low-grade glioma with a BRAF mutation. At the time, she was only one year old. Surgery was not an option, so her family had two choices for treatment—traditional chemotherapy or an experimental treatment suitable for her type of mutation.
Combining her love for reading and desire to give back to help kids with brain tumors like her, Zoe created Books 4 Brains to raise money for pediatric brain cancer research. Join her upcoming Books 4 Brains read-a-thon and support the Pediatric Brain Tumor Foundation's research funding efforts.
The Pediatric Brain Tumor Foundation (PBTF) proudly announces an infusion of $1 million to help researchers, led by Dana-Farber Cancer Institute’s Drs. Pratiti (Mimi) Bandopadhayay and Rameen Beroukhim, launch a study into a novel therapeutic target and expand their research into overcoming treatment resistance and rebound growth.
Recently, the Accelerating Kids' Access to Care Act gained significant momentum in Congress when Charlie, a 12-year-old brain tumor survivor and advocate with the Pediatric Brain Tumor Foundation, testified to the U.S. Senate Finance Committee about the hurdles families face when seeking treatment for their child. Now, to see it become law requires your immediate action.
