I was born on May 5th, 2023. The doctors diagnosed me with Hypoplastic Left Heart Syndrome, Shone's Complex, and Noonan Syndrome.
I spent 7 months making friends in the CVICU at Children's Minnesota in Minneapolis with my parents Daniel & Kelsey Collins. I fought hard everyday to get better, but I went to heaven on December 2nd, 2023.
Levi was the most amazing little human. Our story is Levi's story. The impact he had on us will last forever and we want to share his life, his story, however we can.
In May 2024 we're taking a memorial trip over his first birthday. You can follow the journey through our stories.
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