Why We Started The Parker Lee Project
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 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.
Provide needed medical equipment and supplies to families of children with special needs and who are medically dependent.
An educational resource for families while they navigate the system for their loved ones.
Advocate and provide emotional support to families struggling to care for their special needs child.