Support Our Team, Team Lexie

2019 Eversource Walk for Boston Children's Hospital

Sunday, June 9, 2019 | -188 Days to Go!

Team Captain:

Raised So Far: $7,358.69

Fundraising Goal: $5,000.00

Why We Walk

Team Roster Amount Raised

2019 Walk


Team Lexie

Thank you for visiting our page in support of Team Lexie!

THANK YOU to our family and friends for their donations and support these past 2 years. Our walks have been such a success - we’ve raised over $10,000 for BCH! We are teaming up again this year to support the Boston Children's Hospital Eversource Walk for Kids in honor of our daughter, Lexie (age 3.5).

Lexie was born with a congenital heart defect. Her pediatrician detected a suspicious heart murmur at 3 weeks old and we were referred to a local Cardiologist a few weeks later. Lexie was completely thriving and otherwise "healthy" so we were sent home without much concern, except to follow-up in 4 months when Lexie was 6 months old.

That started our journey to cardiologists and tests such as EKGs, ECHOs, Chest CTs and Lung Scans. She eventually had a Diagnostic Cardiac Cath performed on July 13, 2016, when she was almost 10 months old, to determine her diagnosis: PAPVR (Partial Anomolous Pulmonary Venous Return) which explained the defect and she also had PAS (Pulmonary Artery Stenosis).

A multidisciplinary team met afterwards to review Lexie's case and discuss her path of care. It was decided that she should first undergo open heart surgery to fix the PAPVR, a structural issue where 2 of her pulmonary veins were misplaced. In her case, all 4 pulmonary veins were dumping into the right side of the heart creating extra blood flow requiring that side of the heart to work harder. It was also insufficient in supporting the oxygenation to the lungs. While it's an important diagnosis, it's not usually an issue that requires urgent fixing and she was also asymptomatic. However, she also had extensive PAS where her pulmonary arteries, including many distally located, were stenosed (narrowed) and insufficiently allowing blood to flow through to the lungs. The medical team decided to fix the PAPVR first to normalize the blood flow to see if that may better improve the PAS.

Lexie underwent open heart surgery on October 14, 2016. Dr. Chris Baird at BCH was her surgeon and an expert on congenital heart valve issues. Those were the longest few hours of our lives, including the 45 minutes where they had to stop her heart and put her on the heart-lung machine. The surgery was a success (!) and we were sent off to the BCH ICU. Lexie was only 14 months old and had just started walking and learning words. She got "mommy" and "ow" down during her stay and even began singing "Twinkle Twinkle Little Star" with me. She recovered really well and after a few days we were able to take walks around the ICU floor and then eventually moved to the inpatient floors where she could walk her way down to the Cardiac 8East activity room (while still hooked up to the drip lines) and play with all the toys other people had donated to the hospital. We were discharged a week later, on October 19th and sent home without many restrictions, except for having to scoop when picking her up, to limit any tear on her sternum. We were given time to recover and had check-ins with her local cardiologist. Just a few months later she was scheduled for another Cardiac Cath to check the status of her PAS and likely do an intervention.

Fast forward 2 years, since her open heart surgery, Lexie has had 5 interventional cardiac catheterizations where they had to balloon dilate her pulmonary arteries, including the placement of 2 stents into one of her main arteries where the balloon dilations just weren't enough. Each time involved 3 days in the hospital, including the pre-op rodeo, the day of the procedure where we'd stay one night and then discharge the following day. All along, through the needle-poking, boo-boos, and sleepless nights, Lexie has been an inspiration to us and anyone who knows Lexie. She truly is our hero.

Today, Lexie's pulmonary pressures are considered to be at a "safe" number so that we don’t need procedures every few months, rather, we can wait a year in between. The Cardiac team has been telling us at the last couple visits that ultimately the goal is to wait years between procedures, but we're not quite there yet. Her PAS is still quite extensive and they want to continue monitoring it each year until it’s more stable.

Lexie's next procedure will come up this fall. We've been very fortunate these last 3 years to have the best medical teams at BCH care for Lexie to get her to this point.

Thank you for reading Lexie's story and considering to support us as we walk to support Boston Children's Hospital and the exceptional care they provide to kids like Lexie and families like ours across the world.

If you're interested in joining our team, just register within this page.

Thank you,
Jay & Lauren Leavitt (daddy & mommy)

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