Support Owen Brenna and his family

Please help Graham and Allyson as they temporarily relocate their family to Boston, giving their son, Owen, the best chance at a healthy future. Your contribution will help cover crucial medical expenses, travel, extended stay, and any unforeseen needs during this challenging time.

My nephew, Owen, at just two and a half years old, has courageously battled health challenges from the start. Born with tracheoesophageal fistula (TEF), tethered cord syndrome, and intestinal malrotation; his journey has been a series of surgeries, procedures, and complications.

Now, we turn to Boston Children’s Hospital for a comprehensive solution to address his recurring fistula and tracheomalacia. My brother's family is already in Boston meeting with the doctors to determine the next steps before surgery. The road ahead is not without financial strain.

Please share Owen's story with your network, and let's unite to give him the care he needs. Your contribution, no matter the size, will make a significant difference, providing Owen and his family with the means for what we hope will be a permanent resolution.

Your support and prayers mean everything. Thank you for being a part of Owen's journey to a healthy future.

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Here is a post from my brother from November, 24:

Owen Matthew Brenna. What a strong and courageous young boy. I’m so thankful for you, your sister Hailey, and your wonderful mother who has taken on the enormous challenge of being your medical care quarterback. At just two and a half years old, Owen has faced challenges beyond what any child should endure.

On May 7, 2021, at 5:21 PM, Owen entered the world. Shortly after, we discovered a rare condition called tracheoesophageal fistula (TEF) type C. His esophagus wasn't directly connecting his mouth to his stomach. At 3 days old, Owen underwent successful corrective surgery. However, we later discovered he also had tethered cord syndrome, leading to another surgery at 7 months old.

Complications persisted. In the summer of 2022, pneumonia, ER visits, and recurring fistulas challenged Owen and our family. In the summer of 2023, Owen underwent surgery to correct intestinal malrotation, discovered through an accidental x-ray wide-shot a few weeks prior. His resilience and the bond with his sister, Hailey, are our sources of strength.

After unsuccessful procedures to close his TEF, we contacted Boston Children’s Hospital after learning it’s a top hospital for TEF kids. Their experienced surgical team offered a comprehensive plan addressing the recurring fistula and tracheomalacia. We knew we had to get him to Boston after hearing the hundreds of surgeries they’ve completed had no recurrence (something we’re all too familiar with).

We are anxious but hopeful.

Our family will need to be in Boston for 2 to 4 weeks, with return follow-up visits.

For those who've followed Owen's journey throughout the years, or if you’re just hearing it now, we'll keep you updated. Details are pending and your prayers mean the world to us. We appreciate you.