The Parker Lee Project is named for Parker Lee Reynolds and the idea to create an organization in her honor to help families in need of assistance started shortly before she gained her wings on October 20, 2012. Parker was born June 30, 2010 with Lissencephaly and Microcephaly. Over her short life she acquired many more diagnosis, requiring more and more equipment and supplies. When she passed, she was tube-fed dependent, had a tracheotomy, had countless seizures and was on full time oxygen. Her bedroom looked like a hospital room. During her time as an angel on earth, her parents struggled, argued and pleaded with doctor's offices, insurance companies and DME (Durable Medical Equipment) companies more times than anyone could count.
When Parker was born, an angel graced our earthly planet. She changed the lives of most she met and through us and The Parker Lee Project, she is still able to do so.
Founded in January 2013, The Parker Lee Project has been working tirelessly to help children in need for over 12 years. We have helped thousands of children and their families so far, saving them $6.1MIL in out-of-pocket costs and hope to continue making a positive impact in their lives for years to come.
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